학술논문
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'학술논문'
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1~20
Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Eoli A; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Popp B; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Strehlow V; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Wittekind DA; Department of Psychiatry and Psychotherapy, University of Leipzig Medical Center, Leipzig, Germany.; Institue for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig Medical Center, Leipzig, Germany.; Vuorinen AL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Faculty of Social Sciences, Unit of Health Sciences, Tampere University, Tampere, Finland.; Aldhalaan HM; Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.; Baer S; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; de Saint Martin A; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Herman I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Hornemann F; Department of Pediatrics, Klinikum Chemnitz, Chemnitz, Germany.; Ingebrigtsen T; National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et Génétique (IPG), Charleroi (Gosselies), Belgium.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Marafie D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Mathot M; Neuropediatric Unit, CHU UCL-Namur, Namur, Belgium.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratory, Houston, TX, USA.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Schelhaas HJ; Department of Neurology, Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.; Stillman C; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Orsini A; Section of Pediatric Neurology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.; Patel AD; Division of Pediatric Neurology, Nationwide Children's Hospital, Department of Pediatrics, The Ohio State College of Medicine, Columbus, OH, USA.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Veggiotti P; Neuroscience Research Center, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Pediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Vlaskamp DRM; Department of Genetics and Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands.; Weckhuysen S; VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium.; Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Traynelis SF; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.; Center for the Functional Evaluation of Rare Variants (CFERV), Emory University School of Medicine, Atlanta, GA, USA.; Benke TA; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany. Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.
Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE; In Process
Academic Journal
Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Eoli A; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Popp B; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Strehlow V; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Wittekind DA; Department of Psychiatry and Psychotherapy, University of Leipzig Medical Center, Leipzig, Germany.; Institue for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig Medical Center, Leipzig, Germany.; Vuorinen AL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Faculty of Social Sciences, Unit of Health Sciences, Tampere University, Tampere, Finland.; Aldhalaan HM; Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.; Baer S; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; de Saint Martin A; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Herman I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Hornemann F; Department of Pediatrics, Klinikum Chemnitz, Chemnitz, Germany.; Ingebrigtsen T; National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et Génétique (IPG), Charleroi (Gosselies), Belgium.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Marafie D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Mathot M; Neuropediatric Unit, CHU UCL-Namur, Namur, Belgium.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratory, Houston, TX, USA.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Schelhaas HJ; Department of Neurology, Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.; Stillman C; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Orsini A; Section of Pediatric Neurology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.; Patel AD; Division of Pediatric Neurology, Nationwide Children's Hospital, Department of Pediatrics, The Ohio State College of Medicine, Columbus, OH, USA.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Veggiotti P; Neuroscience Research Center, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Pediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Vlaskamp DRM; Department of Genetics and Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands.; Weckhuysen S; VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium.; Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Traynelis SF; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.; Center for the Functional Evaluation of Rare Variants (CFERV), Emory University School of Medicine, Atlanta, GA, USA.; Benke TA; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany. Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.
Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE
Academic Journal
Wanner JS; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Germany (J.S.W., M.K., H.O.H.).; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Finland (J.S.W., J.R., H.O.H.).; Krafft M; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Germany (J.S.W., M.K., H.O.H.).; Niiranen T; Population Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland (T.N.).; Department of Internal Medicine, Turku University Hospital and University of Turku, Finland (T.N.).; Zimmerman DS; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam UMC, University of Amsterdam, the Netherlands (D.S.Z., S.J.J.).; FinnGen; Ellinor PT; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (P.T.E., S.J.J., J.R.).; Division of Cardiology, Heart and Vascular Institute, Mass General Brigham, Boston, MA (P.T.E., S.J.J., J.R).; Nadkarni G; Hasso Plattner Institute for Digital Health at Mount Sinai, Mount Sinai School of Medicine, New York, NY (G.N., H.O.H.).; Jurgens SJ; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (P.T.E., S.J.J., J.R.).; Division of Cardiology, Heart and Vascular Institute, Mass General Brigham, Boston, MA (P.T.E., S.J.J., J.R).; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam UMC, University of Amsterdam, the Netherlands (D.S.Z., S.J.J.).; Rämö J; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Finland (J.S.W., J.R., H.O.H.).; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (P.T.E., S.J.J., J.R.).; Division of Cardiology, Heart and Vascular Institute, Mass General Brigham, Boston, MA (P.T.E., S.J.J., J.R).; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Germany (J.S.W., M.K., H.O.H.).; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Finland (J.S.W., J.R., H.O.H.).; Hasso Plattner Institute for Digital Health at Mount Sinai, Mount Sinai School of Medicine, New York, NY (G.N., H.O.H.).
Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0147763 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1524-4539 (Electronic) Linking ISSN: 00097322 NLM ISO Abbreviation: Circulation Subsets: MEDLINE
Academic Journal
Kurki, Mitja I; Karjalainen, Juha; Palta, Priit; Sipilä, Timo P; Kristiansson, Kati; Donner, Kati M; Reeve, Mary P; Laivuori, Hannele; Aavikko, Mervi; Kaunisto, Mari A; Loukola, Anu; Lahtela, Elisa; Mattsson, Hannele; Laiho, Päivi; Della Briotta Parolo, Pietro; Lehisto, Arto A; Kanai, Masahiro; Mars, Nina; Rämö, Joel; Kiiskinen, Tuomo; Heyne, Henrike O; Veerapen, Kumar; Rüeger, Sina; Lemmelä, Susanna; Zhou, Wei; Ruotsalainen, Sanni; Pärn, Kalle; Hiekkalinna, Tero; Koskelainen, Sami; Paajanen, Teemu; Llorens, Vincent; Gracia-Tabuenca, Javier; Siirtola, Harri; Reis, Kadri; Elnahas, Abdelrahman G; Sun, Benjamin; Foley, Christopher N; Aalto-Setälä, Katriina; Alasoo, Kaur; Arvas, Mikko; Auro, Kirsi; Biswas, Shameek; Bizaki-Vallaskangas, Argyro; Carpen, Olli; Chen, Chia-Yen; Dada, Oluwaseun A; Ding, Zhihao; Ehm, Margaret G; Eklund, Kari; Färkkilä, Martti; Finucane, Hilary; Ganna, Andrea; Ghazal, Awaisa; Graham, Robert R; Green, Eric M; Hakanen, Antti; Hautalahti, Marco; Hedman, Åsa K; Hiltunen, Mikko; Hinttala, Reetta; Hovatta, Iiris; Hu, Xinli; Huertas-Vazquez, Adriana; Huilaja, Laura; Hunkapiller, Julie; Jacob, Howard; Jensen, Jan-Nygaard; Joensuu, Heikki; John, Sally; Julkunen, Valtteri; Jung, Marc; Junttila, Juhani; Kaarniranta, Kai; Kähönen, Mika; Kajanne, Risto; Kallio, Lila; Kälviäinen, Reetta; Kaprio, Jaakko; FinnGen; Kerimov, Nurlan; Kettunen, Johannes; Kilpeläinen, Elina; Kilpi, Terhi; Klinger, Katherine; Kosma, Veli-Matti; Kuopio, Teijo; Kurra, Venla; Laisk, Triin; Laukkanen, Jari; Lawless, Nathan; Liu, Aoxing; Longerich, Simonne; Mägi, Reedik; Mäkelä, Johanna; Mäkitie, Antti; Malarstig, Anders; Mannermaa, Arto; Maranville, Joseph; Matakidou, Athena; Meretoja, Tuomo; Mozaffari, Sahar V; Niemi, Mari EK; Niemi, Marianna; Niiranen, Teemu; O Donnell, Christopher J; Obeidat, Ma En; Okafo, George; Ollila, Hanna M; Palomäki, Antti; Palotie, Tuula; Partanen, Jukka; Paul, Dirk S; Pelkonen, Margit; Pendergrass, Rion K; Petrovski, Slavé; Pitkäranta, Anne; Platt, Adam; Pulford, David; Punkka, Eero; Pussinen, Pirkko; Raghavan, Neha; Rahimov, Fedik; Rajpal, Deepak; Renaud, Nicole A; Riley-Gillis, Bridget; Rodosthenous, Rodosthenis; Saarentaus, Elmo; Salminen, Aino; Salminen, Eveliina; Salomaa, Veikko; Schleutker, Johanna; Serpi, Raisa; Shen, Huei-Yi; Siegel, Richard; Silander, Kaisa; Siltanen, Sanna; Soini, Sirpa; Soininen, Hilkka; Sul, Jae Hoon; Tachmazidou, Ioanna; Tasanen, Kaisa; Tienari, Pentti; Toppila-Salmi, Sanna; Tukiainen, Taru; Tuomi, Tiinamaija; Turunen, Joni A; Ulirsch, Jacob C; Vaura, Felix; Virolainen, Petri; Waring, Jeffrey; Waterworth, Dawn; Yang, Robert; Nelis, Mari; Reigo, Anu; Metspalu, Andres; Milani, Lili; Esko, Tõnu; Fox, Caroline; Havulinna, Aki S; Perola, Markus; Ripatti, Samuli; Jalanko, Anu; Laitinen, Tarja; Mäkelä, Tomi P; Plenge, Robert; McCarthy, Mark; Runz, Heiko; Daly, Mark J; Palotie, Aarno
Nature
Academic Journal
Heyne HO; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Potsdam, Germany. henrike.heyne@hpi.de.; Hasso Plattner Institute, Mount Sinai School of Medicine, New York, NY, US. henrike.heyne@hpi.de.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. henrike.heyne@hpi.de.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. henrike.heyne@hpi.de.; Pajuste FD; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.; Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.; Wanner J; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Potsdam, Germany.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Daniel Onwuchekwa JI; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Potsdam, Germany.; Faculty of Life Sciences, University of Siegen, Siegen, Germany.; Mägi R; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.; Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.; Palotie A; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Kälviainen R; Kuopio Epilepsy Center, Neurocenter, Kuopio University Hospital, Member of ERN EpiCARE, Kuopio, Finland.; Institute of Clinical Medicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.; Daly MJ; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
German J; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Eric and Wendy Schmidt Center, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Cordioli M; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Tozzo V; Department of Computational Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Urbut S; Division of Cardiovascular Medicine, Massachusetts General Hospital, Boston, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.; Arumäe K; Institute of Psychology, University of Tartu, Tartu, Estonia.; Smit RAJ; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.; Novo Nordisk Foundation Center for Genomic Mechanisms of Disease, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Lee J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Li JH; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Diabetes Unit, Massachusetts General Hospital, Boston, MA, USA.; Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.; Harvard Medical School, Boston, MA, USA.; Janucik A; Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.; Center for Digital Medicine, Medical University of Bialystok, Bialystok, Poland.; Ding Y; Department of Computational Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Akinkuolie A; Department of Computational Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Heyne HO; Hasso Plattner Institute, University of Potsdam, Potsdam, Germany.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Eoli A; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Saad C; Qatar Genome Program, Qatar Precision Health Institute, Qatar Foundation, Doha, Qatar.; Al-Sarraj Y; Qatar Genome Program, Qatar Precision Health Institute, Qatar Foundation, Doha, Qatar.; Abdel-Latif R; Qatar Genome Program, Qatar Precision Health Institute, Qatar Foundation, Doha, Qatar.; Mohammed S; Department of Pharmacy, Hamad Medical Corporation, Doha, Qatar.; Hail MA; Department of Pharmacy, Hamad Medical Corporation, Doha, Qatar.; Barry A; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.; Harvard T.H. Chan School of Public Health, Boston, MA, USA.; Wang Z; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.; Cajuso T; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Department of Pathology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.; Corbetta A; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Health Data Science Centre, Human Technopole, Milan, Italy.; MOX - Laboratory for Modeling and Scientific Computing, Department of Mathematics, Politecnico di Milano, Milan, Italy.; Natarajan P; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.; Personalized Medicine, Mass General Brigham, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA.; Ripatti S; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.; Department of Public Health, Clinicum, University of Helsinki, Helsinki, Finland.; Analytic & Translational Genetics Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.; Philippakis A; Eric and Wendy Schmidt Center, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Szczerbinski L; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Diabetes Unit, Massachusetts General Hospital, Boston, MA, USA.; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland.; Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.; Pasaniuc B; Department of Computational Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Pennsylvania, USA.; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Institute of Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Kutalik Z; University Center for Primary Care and Public Health, Lausanne, Switzerland.; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.; Swiss Institute of Bioinformatics, Lausanne, Switzerland.; Mbarek H; Qatar Genome Program, Qatar Precision Health Institute, Qatar Foundation, Doha, Qatar.; Loos RJF; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.; Novo Nordisk Foundation Center for Genomic Mechanisms of Disease, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Vainik U; Institute of Psychology, University of Tartu, Tartu, Estonia.; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.; Ganna A; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. andrea.ganna@helsinki.fi.; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. andrea.ganna@helsinki.fi.
Publisher: Nature Publishing Company Country of Publication: United States NLM ID: 9502015 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-170X (Electronic) Linking ISSN: 10788956 NLM ISO Abbreviation: Nat Med Subsets: MEDLINE
Academic Journal
Johannesen, Katrine M; Liu, Yuanyuan; Koko, Mahmoud; Gjerulfsen, Cathrine E; Sonnenberg, Lukas; Schubert, Julian; Fenger, Christina D; Eltokhi, Ahmed; Rannap, Maert; Koch, Nils A; Lauxmann, Stephan; Krüger, Johanna; Kegele, Josua; Canafoglia, Laura; Franceschetti, Silvana; Mayer, Thomas; Rebstock, Johannes; Zacher, Pia; Ruf, Susanne; Alber, Michael; Sterbova, Katalin; Lassuthová, Petra; Vlckova, Marketa; Lemke, Johannes R; Platzer, Konrad; Krey, Ilona; Heine, Constanze; Wieczorek, Dagmar; Kroell-Seger, Judith; Lund, Caroline; Klein, Karl Martin; Au, P Y Billie; Rho, Jong M; Ho, Alice W; Masnada, Silvia; Veggiotti, Pierangelo; Giordano, Lucio; Accorsi, Patrizia; Hoei-Hansen, Christina E; Striano, Pasquale; Zara, Federico; Verhelst, Helene; Verhoeven, Judith S; Braakman, Hilde M H; van der Zwaag, Bert; Harder, Aster V E; Brilstra, Eva; Pendziwiat, Manuela; Lebon, Sebastian; Vaccarezza, Maria; Le, Ngoc Minh; Christensen, Jakob; Grønborg, Sabine; Scherer, Stephen W; Howe, Jennifer; Fazeli, Walid; Howell, Katherine B; Leventer, Richard; Stutterd, Chloe; Walsh, Sonja; Gerard, Marion; Gerard, Bénédicte; Matricardi, Sara; Bonardi, Claudia M; Sartori, Stefano; Berger, Andrea; Hoffman-Zacharska, Dorota; Mastrangelo, Massimo; Darra, Francesca; Vøllo, Arve; Motazacker, M Mahdi; Lakeman, Phillis; Nizon, Mathilde; Betzler, Cornelia; Altuzarra, Cecilia; Caume, Roseline; Roubertie, Agathe; Gélisse, Philippe; Marini, Carla; Guerrini, Renzo; Bilan, Frederic; Tibussek, Daniel; Koch-Hogrebe, Margarete; Perry, M Scott; Ichikawa, Shoji; Dadali, Elena; Sharkov, Artem; Mishina, Irina; Abramov, Mikhail; Kanivets, Ilya; Korostelev, Sergey; Kutsev, Sergey; Wain, Karen E; Eisenhauer, Nancy; Wagner, Monisa; Savatt, Juliann M; Müller-Schlüter, Karen; Bassan, Haim; Borovikov, Artem; Nassogne, Marie Cecile; Destrée, Anne; Schoonjans, An Sofie; Meuwissen, Marije; Buzatu, Marga; Jansen, Anna; Scalais, Emmanuel; Srivastava, Siddharth; Tan, Wen Hann; Olson, Heather E; Loddenkemper, Tobias; Poduri, Annapurna; Helbig, Katherine L; Helbig, Ingo; Fitzgerald, Mark P; Goldberg, Ethan M; Roser, Timo; Borggraefe, Ingo; Brünger, Tobias; May, Patrick; Lal, Dennis; Lederer, Damien; Rubboli, Guido; Heyne, Henrike O; Lesca, Gaetan; Hedrich, Ulrike B S; Benda, Jan; Gardella, Elena; Lerche, Holger; Møller, Rikke S
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B N, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, 'Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications', Brain, vol. 145, no. 9, pp. 2991-3009. https://doi.org/10.1093/brain/awab321
Brain, Vol. 145, no.9, p. 2991-3009 (2022)
Brain
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Brain, vol. 145, no. 9, pp. 2991-3009 . https://doi.org/10.1093/brain/awab321
Johannesen, K M, Liu, Y, Gjerulfsen, C E, Koko, M, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N, Lauxmann, S, Krueger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthova, P, Vlckova, M, Lemke, J, Krey, I, Heine, C, Wieczorek, D, Kroell, J, Lund, C, Klein, K M, Au, P B, Rho, J, Ho, A, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoi-Hansen, C, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, van der Zwaag, B, Harder, A, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Schmidt-Petersen, M, Gronborg, S, Scherer, S, Howe, J, Fazeli, W, Howell, K, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vollo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caumes, R, Roubertie, A, Gelisse, P, Marini, C, Guerrini, R, Bilan, F, Koch-Hogrebe, M, Perry, S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J, Mueller-Schlueter, K, Bassan, H, Borovikov, A, Nassogne, M-C, Destree, A, Schoonjans, A-S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W-H, Olson, H, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M, Goldberg, E M, Roser, T, Borggrafe, I, Brunger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Lesca, G, Hedrich, U, Benda, J, Gardella, E, Lerche, H & Moeller, R S 2021, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Epilepsia, vol. 62, no. Suppl. 3, 80, pp. 34-36 . https://doi.org/10.1111/epi.17079
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, 'Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications', Brain, vol. 145, no. 9, pp. 2991-3009. https://doi.org/10.1093/brain/awab321
Brain, Vol. 145, no.9, p. 2991-3009 (2022)
Brain
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Brain, vol. 145, no. 9, pp. 2991-3009 . https://doi.org/10.1093/brain/awab321
Johannesen, K M, Liu, Y, Gjerulfsen, C E, Koko, M, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N, Lauxmann, S, Krueger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthova, P, Vlckova, M, Lemke, J, Krey, I, Heine, C, Wieczorek, D, Kroell, J, Lund, C, Klein, K M, Au, P B, Rho, J, Ho, A, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoi-Hansen, C, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, van der Zwaag, B, Harder, A, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Schmidt-Petersen, M, Gronborg, S, Scherer, S, Howe, J, Fazeli, W, Howell, K, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vollo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caumes, R, Roubertie, A, Gelisse, P, Marini, C, Guerrini, R, Bilan, F, Koch-Hogrebe, M, Perry, S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J, Mueller-Schlueter, K, Bassan, H, Borovikov, A, Nassogne, M-C, Destree, A, Schoonjans, A-S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W-H, Olson, H, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M, Goldberg, E M, Roser, T, Borggrafe, I, Brunger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Lesca, G, Hedrich, U, Benda, J, Gardella, E, Lerche, H & Moeller, R S 2021, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Epilepsia, vol. 62, no. Suppl. 3, 80, pp. 34-36 . https://doi.org/10.1111/epi.17079
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Academic Journal
Bonardi, Claudia M; Heyne, Henrike O; Fiannacca, Martina; Fitzgerald, Mark P; Gardella, Elena; Gunning, Boudewijn; Olofsson, Kern; Lesca, Gaétan; Verbeek, Nienke; Stamberger, Hannah; Striano, Pasquale; Zara, Federico; Mancardi, Maria M; Nava, Caroline; Syrbe, Steffen; Buono, Salvatore; Baulac, Stephanie; Coppola, Antonietta; Weckhuysen, Sarah; Schoonjans, An-Sofie
Academic Journal
Rohrlach AB; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany. adam_ben_rohrlach@eva.mpg.de.; School of Computer and Mathematical Sciences, University of Adelaide, Adelaide, SA, Australia. adam_ben_rohrlach@eva.mpg.de.; Rivollat M; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; ArcheOs lab, Department of Archaeology, Ghent University, Sint-Pietersnieuwstraat 35, 9000, Gent, Belgium.; Archaeo-DNA lab, Department of Archaeology, Durham University, Lower Mount Joy, South Road, Durham, DH1 3LE, UK.; De la Préhistoire à l'Actuel, Culture, Environnement, Anthropologie - UMR 5199, Bordeaux University, Bât. B8, Allée Geoffroy Saint Hilaire, CS50023, 33615, Pessac cedex, France.; de-Miguel-Ibáñez P; Department of Prehistory, Archaeology, Ancient History and Greek and Latin Philology, INAPH, University of Alicante, San Vicente del Raspeig, Spain.; Sociedad de Ciencias Aranzadi, Donosti, Spain.; Hospital Verge dels Lliris, Alcoi, Alicante, Spain.; Nordfors U; Department of Biology, University of Turku, Turku, Finland.; Liira AM; Department of Archaeology, University of Turku, Turku, Finland.; Teixeira JC; Evolution of Cultural Diversity Initiative, Australian National University, Canberra, ACT, Australia.; Australian Centre for Ancient DNA, School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.; Centre of Excellence for Australian Biodiversity and Heritage, University of Adelaide, Adelaide, SA, Australia.; CEIS.20 Centro de Estudos Interdisciplinares, Universidade de Coimbra, Coimbra, Portugal.; Roca-Rada X; Australian Centre for Ancient DNA, School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.; Armendáriz-Martija J; Departamento de Ciencias Humanas y de la Educación, Universidad Pública de Navarra, Pamplona, Spain.; Boyadzhiev K; National Archaeological Institute with Museum at the Bulgarian Academy of Sciences, Saborna str. 2, Sofia, Bulgaria.; Boyadzhiev Y; National Archaeological Institute with Museum at the Bulgarian Academy of Sciences, Saborna str. 2, Sofia, Bulgaria.; Llamas B; Australian Centre for Ancient DNA, School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.; Centre of Excellence for Australian Biodiversity and Heritage, University of Adelaide, Adelaide, SA, Australia.; National Centre for Indigenous Genomics, Australian National University, Canberra, ACT, Australia.; Telethon Kids Institute, Indigenous Genomics Research Group, Adelaide, SA, Australia.; Tiliakou A; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Mötsch A; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Max Planck-Harvard Research Center for the Archaeoscience of the Ancient Mediterranean (MHAAM), Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, Leipzig, Germany.; Tuke J; School of Computer and Mathematical Sciences, University of Adelaide, Adelaide, SA, Australia.; Prevedorou EA; Hellenic Center for Bioarchaeology, Athens, Greece.; Polychronakou-Sgouritsa N; Department of History and Archaeology, National and Kapodistrian University of Athens, Athens, Greece.; Buikstra J; Department of Anthropology, Arizona State University, Tempe, AZ, USA.; Onkamo P; Department of Biology, University of Turku, Turku, Finland.; Department of Biosciences, University of Helsinki, Helsinki, Finland.; Stockhammer PW; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Max Planck-Harvard Research Center for the Archaeoscience of the Ancient Mediterranean (MHAAM), Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, Leipzig, Germany.; Institute for Pre- and Protohistoric Archaeology and Archaeology of the Roman Provinces, Ludwig Maximilian University, Geschwister-Scholl-Platz 1, München, Germany.; Heyne HO; Hasso-Plattner-Institute, University of Potsdam, Potsdam, Germany.; Hasso Plattner Institute, Mount Sinai School of Medicine, New York, USA.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.; Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Risch R; Departament de Prehistòria, Universitat Autònoma de Barcelona, Bellaterra, Spain.; Schiffels S; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Krause J; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Haak W; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.; Prüfer K; Department of Archaeogenetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany. pruefer@eva.mpg.de.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
Heng TH; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK. Electronic address: teng-hiang.heng@sanger.ac.uk.; Walter K; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.; Huang QQ; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.; Karjalainen J; Broad Institute, 415 Main Street, Cambridge, MA 02142, USA.; Daly MJ; Broad Institute, 415 Main Street, Cambridge, MA 02142, USA.; Heyne HO; Broad Institute, 415 Main Street, Cambridge, MA 02142, USA; Hasso Plattner Institute, 14482 Potsdam, Germany.; Malawsky DS; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.; Kalantzis G; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.; Finer S; Wolfson Institute for Population Health, Queen Mary University of London, London E1 4NS, UK.; van Heel DA; Blizard Institute, Queen Mary University of London, London E1 2AT, UK.; Martin HC; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK. Electronic address: hilary.martin@sanger.ac.uk.
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Academic Journal
Iqbal, Sumaiya; Hoksza, David; Pérez-Palma, Eduardo; May, Patrick; Jespersen, Jakob B; Ahmed, Shehab S; Rifat, Zaara T; Heyne, Henrike O; Rahman, M Sohel; Cottrell, Jeffrey R; Wagner, Florence F; Daly, Mark J; Campbell, Arthur J; Lal, Dennis
Nucleic Acids Research; 7/2/2020, Vol. 48 Issue W1, pW132-W139, 8p
Academic Journal
Slosarek T; Digital Health Center, Hasso Plattner Institute, University of Potsdam, Prof.-Dr.-Helmert-Str. 2-3, 14482, Potsdam, Germany.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USA.; Ibing S; Digital Health Center, Hasso Plattner Institute, University of Potsdam, Prof.-Dr.-Helmert-Str. 2-3, 14482, Potsdam, Germany.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USA.; Schormair B; Institute of Neurogenomics, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Neuherberg, Germany.; Institute of Human Genetics, Klinikum Rechts der isar, School of Medicine, Technical University of Munich, Munich, Germany.; Heyne HO; Digital Health Center, Hasso Plattner Institute, University of Potsdam, Prof.-Dr.-Helmert-Str. 2-3, 14482, Potsdam, Germany.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USA.; Böttinger EP; Digital Health Center, Hasso Plattner Institute, University of Potsdam, Prof.-Dr.-Helmert-Str. 2-3, 14482, Potsdam, Germany.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USA.; Andlauer TFM; Department of Neurology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.; Schurmann C; Digital Health Center, Hasso Plattner Institute, University of Potsdam, Prof.-Dr.-Helmert-Str. 2-3, 14482, Potsdam, Germany. claudia.schurmann2@gmail.com.; Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, 10029, USA. claudia.schurmann2@gmail.com.
Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE
Academic Journal
Strehlow, Vincent; Heyne, Henrike O; Vlaskamp, Danique R M; Marwick, Katie F M; Rudolf, Gabrielle; Bellescize, Julitta de; Biskup, Saskia; Brilstra, Eva H; Brouwer, Oebele F; Callenbach, Petra M C; Hentschel, Julia; Hirsch, Edouard; Kind, Peter C; Mignot, Cyril; Platzer, Konrad; Rump, Patrick; Skehel, Paul A; Wyllie, David J A; Hardingham, Giles E; Ravenswaaij-Arts, Conny M A van
Academic Journal
Cosimo Posth; Valentina Zaro; Maria A. Spyrou; Stefania Vai; Guido A. Gnecchi-Ruscone; Alessandra Modi; Alexander Peltzer; Angela Mötsch; Kathrin Nägele; Åshild J. Vågene; Elizabeth A. Nelson; Rita Radzevičiūtė; Cäcilia Freund; Lorenzo M. Bondioli; Luca Cappuccini; Hannah Frenzel; Elsa Pacciani; Francesco Boschin; Giulia Capecchi; Ivan Martini; Adriana Moroni; Stefano Ricci; Alessandra Sperduti; Maria Angela Turchetti; Alessandro Riga; Monica Zavattaro; Andrea Zifferero; Henrike O. Heyne; Eva Fernández-Domínguez; Guus J. Kroonen; Michael McCormick; Wolfgang Haak; Martina Lari; Guido Barbujani; Luca Bondioli; Kirsten I. Bos; David Caramelli; Johannes Krause
Sci Adv
Science Advances
Posth, C, Zaro, V, Spyrou, M A, Vai, S, Gnecchi-Ruscone, G A, Modi, A, Peltzer, A, Mötsch, A, Nägele, K, Vågene, Å J, Nelson, E A, Radzeviciute, R, Freund, C, Bondioli, L M, Cappuccini, L, Frenzel, H, Pacciani, E, Boschin, F, Capecchi, G, Martini, I, Moroni, A, Ricci, S, Sperduti, A, Turchetti, M A, Riga, A, Zavattaro, M, Zifferero, A, Heyne, H O, Fernández-Domínguez, E, Kroonen, G J, McCormick, M, Haak, W, Lari, M, Barbujani, G, Bondioli, L, Bos, K I, Caramelli, D & Krause, J 2021, ' The origin and legacy of the Etruscans through a 2000-year archeogenomic time transect ', Science Advances, vol. 7, no. 39, eabi7673 . https://doi.org/10.1126/sciadv.abi7673
Science advances, 2021, Vol.7(39) [Peer Reviewed Journal]
Science Advances
Posth, C, Zaro, V, Spyrou, M A, Vai, S, Gnecchi-Ruscone, G A, Modi, A, Peltzer, A, Mötsch, A, Nägele, K, Vågene, Å J, Nelson, E A, Radzeviciute, R, Freund, C, Bondioli, L M, Cappuccini, L, Frenzel, H, Pacciani, E, Boschin, F, Capecchi, G, Martini, I, Moroni, A, Ricci, S, Sperduti, A, Turchetti, M A, Riga, A, Zavattaro, M, Zifferero, A, Heyne, H O, Fernández-Domínguez, E, Kroonen, G J, McCormick, M, Haak, W, Lari, M, Barbujani, G, Bondioli, L, Bos, K I, Caramelli, D & Krause, J 2021, ' The origin and legacy of the Etruscans through a 2000-year archeogenomic time transect ', Science Advances, vol. 7, no. 39, eabi7673 . https://doi.org/10.1126/sciadv.abi7673
Science advances, 2021, Vol.7(39) [Peer Reviewed Journal]
Academic Journal
Lemke, Johannes R; Geider, Kirsten; Helbig, Katherine L; Heyne, Henrike O; Schütz, Hannah; Hentschel, Julia; Courage, Carolina; Depienne, Christel; Nava, Caroline; Heron, Delphine; Møller, Rikke S; Hjalgrim, Helle; Lal, Dennis; Neubauer, Bernd A; Nürnberg, Peter; Thiele, Holger; Kurlemann, Gerhard; Arnold, Georgianne L; Bhambhani, Vikas; Bartholdi, Deborah
Academic Journal
Heyne HO; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Germany.; Hasso Plattner Institute, Mount Sinai School of Medicine, NY, US.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Pajuste FD; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.; Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.; Wanner J; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Germany.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.; Onwuchekwa JID; Hasso Plattner Institute for Digital Engineering, University of Potsdam, Germany.; Faculty of Life Sciences, University of Siegen, Germany.; Mägi R; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.; Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.; Palotie A; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Kälviainen R; Kuopio Epilepsy Center, Neurocenter, Kuopio University Hospital, Member of ERN EpiCARE, Kuopio, Finland.; Institute of Clinical Medicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.; Daly MJ; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland.; Program for Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Academic Journal
Heyne HO; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA. hheyne@broadinstitute.org mark.daly@helsinki.fi.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, 5WR36M Helsinki, Finland.; Baez-Nieto D; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Iqbal S; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Center for Development of Therapeutics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Palmer DS; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Brunklaus A; Paediatric Neurosciences Research Group, Royal Hospital for Sick Children, Glasgow G51 4TF, UK.; School of Medicine, University of Glasgow, Glasgow G12 8QQ, UK.; May P; Luxembourg Centre for Systems Biomedicine, Belvaux, University of Luxembourg, 4365 Esch-sur-Alzette, Luxembourg.; Johannesen KM; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Centre, 4293 Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, 5230 Odense, Denmark.; Lauxmann S; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, 72076 Tuebingen, Germany.; Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.; Møller RS; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Centre, 4293 Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, 5230 Odense, Denmark.; Pérez-Palma E; Cologne Center for Genomics (CCG), University of Cologne, 50923, Germany.; Genomic Medicine Institute, Lemer Research Institute Cleveland Clinic, OH G92J47, USA.; Scholl UI; Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Nephrology and Medical Intensive Care and BIH Center for Regenerative Therapies, 10178 Berlin, Germany.; Berlin Institute of Health (BIH), 10178 Berlin, Germany.; Syrbe S; Division of Pediatric Epileptology, Center for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, 69120 Heidelberg, Germany.; Lerche H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, 72076 Tuebingen, Germany.; Lal D; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Cologne Center for Genomics (CCG), University of Cologne, 50923, Germany.; Genomic Medicine Institute, Lemer Research Institute Cleveland Clinic, OH G92J47, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH G92J47, USA.; Campbell AJ; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Center for Development of Therapeutics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Wang HR; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Pan J; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Daly MJ; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA. hheyne@broadinstitute.org mark.daly@helsinki.fi.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, 5WR36M Helsinki, Finland.
Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 101505086 Publication Model: Print Cited Medium: Internet ISSN: 1946-6242 (Electronic) Linking ISSN: 19466234 NLM ISO Abbreviation: Sci Transl Med Subsets: MEDLINE
Academic Journal
Bundalian L; Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany. Electronic address: linnaeusbundalian@gmail.com.; Su YY; Institute of Biomedical Informatics, National Yang Ming Chiao Tung University, Taipei, Taiwan.; Chen S; Analytic and Translational Genetics Unit, Department of Medicine, Boston, MA, USA; Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Velluva A; Division of General Biochemistry, Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, 04103 Leipzig, Germany; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany.; Kirstein AS; Pediatric Research Center, University Hospital for Children and Adolescents, Leipzig University, 04103 Leipzig, Germany.; Garten A; Pediatric Research Center, University Hospital for Children and Adolescents, Leipzig University, 04103 Leipzig, Germany.; Biskup S; CeGaT GmbH, 72076 Tuebingen, Germany; Hertie-Institute for Clinical Brain Research, 72070 Tubingen, Germany.; Battke F; CeGaT GmbH, 72076 Tuebingen, Germany.; Lal D; Analytic and Translational Genetics Unit, Department of Medicine, Boston, MA, USA; Massachusetts General Hospital, Boston, MA 02114, USA; Cologne Center for Genomics, University of Cologne, 50937 Cologne, Germany.; Heyne HO; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Hasso-Plattner-Institut for Digital Engineering, University of Potsdam, Potsdam, Germany; Hasso Plattner Institute at Mount Sinai, Mount Sinai School of Medicine, New York, NY, USA; Institute for Molecular Medicine Finland: FIMM, University of Helsinki, Helsinki, Finland.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.; Lin CC; Institute of Biomedical Informatics, National Yang Ming Chiao Tung University, Taipei, Taiwan.; Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany; Center for Rare Diseases, University of Leipzig Medical Center, 04103 Leipzig, Germany.; Le Duc D; Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany. Electronic address: diana_leduc@eva.mpg.de.
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Academic Journal
Taylor JL; Department of Psychiatry, Brigham and Woman's Hospital, Boston, MA, 02115, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Debost JPG; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8210, Denmark.; Aarhus University Hospital, Risskov, Department P, Aarhus, 8200, Denmark.; Morton SU; Division of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA, 02115, USA.; Wigdor EM; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Heyne HO; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Lal D; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Cologne Center for Genomics, University of Cologne, Cologne, 50923, Germany.; Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, 02114, USA.; Howrigan DP; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Bloemendal A; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Larsen JT; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8210, Denmark.; Kosmicki JA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Program in Genetics and Genomics, Biological and Biomedical Sciences, Harvard Medical School, Boston, MA, 02115, USA.; Weiner DJ; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Homsy J; Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA.; Seidman JG; Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA.; Seidman CE; Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA.; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, 02115, USA.; Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, 02115, USA.; Agerbo E; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8210, Denmark.; Centre for Integrated Register-based Research, CIRRAU, Aarhus University, Aarhus, 8210, Denmark.; McGrath JJ; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; Queensland Brain Institute, The University of Queensland, Brisbane, 4072, Queensland, Australia.; Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Richlands, 4076, Queensland, Australia.; Mortensen PB; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8210, Denmark.; Centre for Integrated Register-based Research, CIRRAU, Aarhus University, Aarhus, 8210, Denmark.; Department of Biomedicine and iSEQ, Centre for Integrative Sequencing, Aarhus University, Aarhus, 08210, Denmark.; Petersen L; National Centre for Register-based Research, Department of Economics and Business, Aarhus University, Aarhus, 8210, Denmark.; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8210, Denmark.; Daly MJ; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.; Robinson EB; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA. erobinso@hsph.harvard.edu.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02412, USA. erobinso@hsph.harvard.edu.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA. erobinso@hsph.harvard.edu.; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA. erobinso@hsph.harvard.edu.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
Heyne, Henrike O; Lautenschläger, Susann; Nelson, Ronald; Besnier, François; Rotival, Maxime; Cagan, Alexander; Kozhemyakina, Rimma; Plyusnina, Irina Z; Trut, Lyudmila; Carlborg, Örjan; Petretto, Enrico; Kruglyak, Leonid; Pääbo, Svante; Schöneberg, Torsten; Albert, Frank W
Genetics, vol 198, iss 3
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