학술논문
'학술논문'
에서 검색결과 399건 | 목록
1~10
Academic Journal
Satterstrom, FK; Kosmicki, JA; Wang, JB; Breen, MS; De Rubeis, S; An, JY; Peng, MS; Collins, R; Grove, J; Klei, L; Stevens, C; Reichert, J; Mulhern, MS; Artomov, M; Gerges, S; Sheppard, B; Xu, XY; Bhaduri, A; Norman, U; Brand, H; Schwartz, G; Nguyen, R; Guerrero, EE; Dias, C; Betancur, C; Cook, EH; Gallagher, L; Gill, M; Sutcliffe, JS; Thurm, A; Zwick, ME; Borglum, AD; State, MW; Cicek, AE; Talkowski, ME; Cutler, DJ; Devlin, B; Sanders, SJ; Roeder, K; Daly, MJ; Buxbaum, JD; Aleksic, B; Anney, R; Barbosa, M; Bishop, S; Brusco, A; Bybjerg-Grauholm, J; Carracedo, A; Chan, MCY; Chiocchetti, AG; Chung, BHY; Coon, H; Cuccaro, ML; Curro, A; Dalla Bernardina, B; Doan, R; Domenici, E; Dong, S; Fallerini, C; Fernandez-Prieto, M; Ferrero, GB; Freitag, CM; Fromer, M; Gargus, JJ; Geschwind, D; Giorgio, E; Gonzalez-Penas, J; Guter, S; Halpern, D; Hansen-Kiss, E; He, X; Herman, GE; Hertz-Picciotto, I; Hougaard, DM; Hultman, CM; Ionita-Laza, I; Jacob, S; Jamison, J; Jugessur, A; Kaartinen, M; Knudsen, GP; Kolevzon, A; Kushima, I; Lee, SL; Lehtimaki, T; Lim, ET; Lintas, C; Lipkin, WI; Lopergolo, D; Lopes, F; Ludena, Y; Maciel, P; Magnus, P; Mahjani, B; Maltman, N; Manoach, DS; Meiri, G; Menashe, I; Miller, J; Minshew, N; Montenegro, EMS; Moreira, D; Morrow, EM; Mors, O; Mortensen, PB; Mosconi, M; Muglia, P; Neale, BM; Nordentoft, M; Ozaki, N; Palotie, A; Parellada, M; Passos-Bueno, MR; Pericak-Vance, M; Persico, AM; Pessah, I; Puura, K; Reichenberg, A; Renieri, A; Riberi, E; Robinson, EB; Samocha, KE; Sandin, S; Santangelo, SL; Schellenberg, G; Scherer, SW; Schlitt, S; Schmidt, R; Schmitt, L; Silva, IMW; Singh, T; Siper, PM; Smith, M; Soares, G; Stoltenberg, C; Suren, P; Susser, E; Sweeney, J; Szatmari, P; Tang, L; Tassone, F; Teufel, K; Trabetti, E; Trelles, MD; Walsh, CA; Weiss, LA; Werge, T; Werling, DM; Wigdor, EM; Wilkinson, E; Willsey, AJ; Yu, TW; Yu, MH; Yuen, R; Zachi, E; Agerbo, E; Als, TD; Appadurai, V; Baekvad-Hansen, M; Belliveau, R; Buil, A; Carey, CE; Cerrato, F; Chambert, K; Churchhouse, C; Dalsgaard, S; Demontis, D; Dumont, A; Goldstein, J; Hansen, CS; Hauberg, ME; Hollegaard, MV; Howrigan, DP; Huang, HL; Maller, J; Martin, AR; Martin, J; Mattheisen, M; Moran, J; Pallesen, J; Palmer, DS; Pedersen, CB; Pedersen, MG; Poterba, T; Poulsen, JB; Ripke, S; Schork, AJ; Thompson, WK; Turley, P; Walters, RK
Cell. 180(3):568
Report
Karppa E; Tampere Center for Child, Adolescent and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Department of Children and Adolescents, Tampere University Hospital, Tampere, Finland.; Ostrobothnia Wellbeing Services County, Kuusamo Health Center, Kuusamo, Finland.; Puura K; Tampere Center for Child, Adolescent and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Department of Children and Adolescents, Tampere University Hospital, Tampere, Finland.; Jyskä I; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, Tampere, Finland.; Turunen M; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, Tampere, Finland.; Palmu S; Tampere Center for Child, Adolescent and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Department of Children and Adolescents, Tampere University Hospital, Tampere, Finland.
Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE
Academic Journal
Jyskä I; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Turunen M; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Chaychi Maleki A; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Karppa E; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Pediatrics, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.; Palmu S; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Pediatrics, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.; Viik J; Finnish Cardiovascular Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Mäkelä J; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Puura K; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Child Psychiatry, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.
Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101666525 Publication Model: Electronic Cited Medium: Print ISSN: 2227-9032 (Print) Linking ISSN: 22279032 NLM ISO Abbreviation: Healthcare (Basel) Subsets: PubMed not MEDLINE
Academic Journal
McCarthy, Shane E; Makarov, Vladimir; Kirov, George; Addington, Anjene M; McClellan, Jon; Yoon, Seungtai; Perkins, Diana O; Dickel, Diane E; Kusenda, Mary; Krastoshevsky, Olga; Krause, Verena; Kumar, Ravinesh A; Grozeva, Detelina; Malhotra, Dheeraj; Walsh, Tom; Zackai, Elaine H; Kaplan, Paige; Ganesh, Jaya; Krantz, Ian D; Spinner, Nancy B; Roccanova, Patricia; Bhandari, Abhishek; Pavon, Kevin; Lakshmi, B; Leotta, Anthony; Kendall, Jude; Lee, Yoon-ha; Vacic, Vladimir; Gary, Sydney; Iakoucheva, Lilia M; Crow, Timothy J; Christian, Susan L; Lieberman, Jeffrey A; Stroup, T Scott; Lehtimäki, Terho; Puura, Kaija; Haldeman-Englert, Chad; Pearl, Justin; Goodell, Meredith; Willour, Virginia L; DeRosse, Pamela; Steele, Jo; Kassem, Layla; Wolff, Jessica; Chitkara, Nisha; McMahon, Francis J; Malhotra, Anil K; Potash, James B; Schulze, Thomas G; Nöthen, Markus M; Cichon, Sven; Rietschel, Marcella; Leibenluft, Ellen; Kustanovich, Vlad; Lajonchere, Clara M; Sutcliffe, James S; Skuse, David; Gill, Michael; Gallagher, Louise; Mendell, Nancy R; Craddock, Nick; Owen, Michael J; O'Donovan, Michael C; Shaikh, Tamim H; Susser, Ezra; DeLisi, Lynn E; Sullivan, Patrick F; Deutsch, Curtis K; Rapoport, Judith; Levy, Deborah L; King, Mary-Claire; Sebat, Jonathan
Nature Genetics. 41(11)
Academic Journal
Jyskä I; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Turunen M; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Chaychi Maleki A; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Karppa E; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Pediatrics, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.; Palmu S; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Pediatrics, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.; Mäkelä J; TAUCHI Research Center, Faculty of Information Technology and Communication Sciences, Tampere University, FI-33014 Tampere, Finland.; Puura K; TamCAM Research Center, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.; Department of Child Psychiatry, Tampere University Hospital, Central Hospital, P.O. Box 2000, FI-33521 Tampere, Finland.
Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101666525 Publication Model: Electronic Cited Medium: Print ISSN: 2227-9032 (Print) Linking ISSN: 22279032 NLM ISO Abbreviation: Healthcare (Basel) Subsets: PubMed not MEDLINE
Academic Journal
Academic Journal
In: Substance Abuse: Treatment, Prevention, and Policy . (Substance Abuse: Treatment, Prevention, and Policy, December 2023, 18(1))
Academic Journal
Rots D; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands.; Jakub TE; Dalhousie University, Department of Biochemistry and Molecular Biology, Faculty of Medicine, Halifax, NS, Canada.; Keung C; Dalhousie University, Department of Biochemistry and Molecular Biology, Faculty of Medicine, Halifax, NS, Canada.; Jackson A; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Banka S; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Pfundt R; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands.; de Vries BBA; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands.; van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Hopman SMJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Valenzuela I; Hospital Universitari Vall D'Hebron, Clinical and Molecular Genetics Unit, Barcelona, Catalonia, Spain.; Hempel M; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Bierhals T; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Kortüm F; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Lecoquierre F; University Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Goldenberg A; University Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Hertz JM; Odense University Hospital, Department of Clinical Genetics, Odense, Denmark; University of Southern Denmark, Department of Clinical Research, Odense, Denmark.; Andersen CB; Odense University Hospital, Department of Clinical Genetics, Odense, Denmark.; Kibæk M; Department of Pediatrics, Odense University Hospital, Odense, Denmark.; Prijoles EJ; Greenwood Genetic Center, Greenwood, SC, USA.; Stevenson RE; Greenwood Genetic Center, Greenwood, SC, USA.; Everman DB; Greenwood Genetic Center, Greenwood, SC, USA.; Patterson WG; Greenwood Genetic Center, Greenwood, SC, USA.; Meng L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics Laboratories, Houston, TX 77021, USA.; Gijavanekar C; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics Laboratories, Houston, TX 77021, USA.; De Dios K; Division of Medical Genetics, Dayton Children's Hospital, Dayton, OH, USA.; Lakhani S; Center for Neurogenetics, Weill Cornell Medicine, Brain and Mind Research Institute, New York, NY, USA.; Levy T; Center for Neurogenetics, Weill Cornell Medicine, Brain and Mind Research Institute, New York, NY, USA.; Wagner M; Institute of Human Genetics, School of Medicine, Technical University Munich, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany; Division of Pediatric Neurology, Department of Pediatrics, Dr. von Hauner Children's Hospital, LMU University Hospital, Munich, Germany.; Wieczorek D; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.; Benke PJ; Division of Genetics, Joe DiMaggio Children's Hospital, Hollywood, FL, USA.; Lopez Garcia MS; Hospital Universitario Donostia, San Sebastián, Spain.; Perrier R; Department of Medical Genetics, Alberta Children's Hospital and Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Sousa SB; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.; Almeida PM; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.; Simões MJ; CBR Genomics, Cantanhede, Portugal; Genoinseq, Next-Generation Sequencing Unit, Biocant, Cantanhede, Portugal.; Isidor B; Service de Génétique Médicale, CHU Nantes, 44093 Nantes, France; Université de Nantes, CHU Nantes, CNRS, INSERM, l'Institut du Thorax, 44007 Nantes, France.; Deb W; Service de Génétique Médicale, CHU Nantes, 44093 Nantes, France; Université de Nantes, CHU Nantes, CNRS, INSERM, l'Institut du Thorax, 44007 Nantes, France.; Schmanski AA; Department of Genetic Medicine, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE, USA.; Abdul-Rahman O; Department of Genetic Medicine, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE, USA.; Philippe C; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Dijon, France; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France.; Bruel AL; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Dijon, France; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France.; Faivre L; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France; Centre de Référence Maladies Rares 'Anomalies du développement et syndromes malformatifs', Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU Dijon Bourgogne, Dijon, France.; Vitobello A; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Dijon, France; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France.; Thauvin C; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Dijon, France; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Smits JJ; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands.; Garavelli L; Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.; Caraffi SG; Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.; Peluso F; Medical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.; Davis-Keppen L; University of South Dakota Sanford School of Medicine and Sanford Children's Hospital, Sioux Falls, SD, USA.; Platt D; University of South Dakota Sanford School of Medicine and Sanford Children's Hospital, Sioux Falls, SD, USA.; Royer E; University of South Dakota Sanford School of Medicine and Sanford Children's Hospital, Sioux Falls, SD, USA.; Leeuwen L; University Medical Center Groningen, Department of Genetics, Groningen, the Netherlands.; Sinnema M; Maastricht University Medical Center, Department of Clinical Genetics, Maastricht, the Netherlands.; Stegmann APA; Maastricht University Medical Center, Department of Clinical Genetics, Maastricht, the Netherlands.; Stumpel CTRM; Maastricht University Medical Center, Department of Clinical Genetics, Maastricht, the Netherlands; Department of Clinical Genetics and GROW-School for Oncology and Reproduction, Maastricht, the Netherlands.; Tiller GE; Kaiser Permanente, Department of Genetics, Los Angeles, CA, USA.; Bosch DGM; Erasmus Medical Centre, Genetics Department, Rotterdam, the Netherlands.; Potgieter ST; Laurentius Hospital, Roermond, the Netherlands.; Joss S; West of Scotland Regional Genetics Service, Laboratory Medicine Building, Queen Elizabeth University Hospital, Glasgow, UK.; Splitt M; Northern Genetics Service, Institute of Genetic Medicine, International Centre for Life, Newcastle Upon Tyne NE1 3BZ, UK.; Holden S; Department of Clinical Genetics, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK.; Prapa M; Department of Clinical Genetics, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK.; Foulds N; Wessex Clinical Genetics Services, University Hospital Southampton NHS Foundation Trust, Southampton SO16 5YA, UK.; Douzgou S; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.; Puura K; Department of Child Psychiatry, Tampere University and Tampere University Hospital, Tampere, Finland.; Waltes R; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe-Universität, Frankfurt am Main, Germany.; Chiocchetti AG; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe-Universität, Frankfurt am Main, Germany.; Freitag CM; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe-Universität, Frankfurt am Main, Germany.; Satterstrom FK; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; De Rubeis S; Mindich Child Health and Development Institute and Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Buxbaum J; Mindich Child Health and Development Institute and Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Gelb BD; Mindich Child Health and Development Institute and Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Branko A; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Kushima I; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan; Medical Genomics Center, Nagoya University Hospital, Nagoya, Japan.; Howe J; The Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.; Scherer SW; The Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.; Arado A; Laboratory of Human Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Baldo C; Laboratory of Human Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Patat O; Service de Génétique Médicale, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.; Bénédicte D; Service de Génétique Clinique, Centre de référence maladies rares, CHU d'Amiens-site Sud, Amiens, France.; Lopergolo D; Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy; UOC Neurologia e Malattie Neurometaboliche, Azienda Ospedaliero Universitaria Senese, Policlinico Le Scotte, Viale Bracci, 2, 53100 Siena, Italy; IRCCS Stella Maris Foundation, Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, Pisa, Italy.; Santorelli FM; IRCCS Stella Maris Foundation, Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, Pisa, Italy.; Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Dufke A; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Bertrand M; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Falb RJ; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Rieß A; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Krieg P; Department of Pediatrics, Städtisches Klinikum Karlsruhe, Karlsruhe, Germany.; Spranger S; Practice of Human Genetics, Bremen, Germany.; Bedeschi MF; Medical Genetic Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.; Iascone M; Laboratory of Medical Genetics, Ospedale Papa Giovanni XXIII, Bergamo, Italy.; Josephi-Taylor S; Department of Clinical Genetics, The Children's Hospital at Westmead, Sydney, NSW, Australia; Discipline of Genomic Medicine, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.; Roscioli T; Neuroscience Research Australia, University of New South Wales, Sydney, NSW, Australia; New South Wales Health Pathology Randwick Genomics Laboratory, Sydney, NSW, Australia; Centre for Clinical Genetics, Sydney Children's Hospital, Sydney, NSW 2031, Australia; Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, NSW 2031, Australia.; Buckley MF; New South Wales Health Pathology Randwick Genomics Laboratory, Sydney, NSW, Australia.; Liebelt J; South Australian Clinical Genetics Service, Women's and Children's Hospital, Adelaide, SA, Australia.; Dagli AI; Orlando Health Arnold Palmer Hospital for Children, Division of Genetics, Orlando, FL, USA.; Aten E; Department of Clinical Genetics, Leiden University Medical Center, 2333 Leiden, the Netherlands.; Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.; Hicks A; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.; Suri M; Nottingham Clinical Genetics Service, City Hospital Campus, Nottingham, UK.; Aliu E; Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA, USA.; Naik S; Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA, USA.; Sidlow R; Valley Children's Hospital, Valley Children's Place, Madera, CA 93636, USA.; Coursimault J; University Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Nicolas G; University Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Küpper H; Neuropediatric Department, University Hospital Tübingen, Tübingen, Germany.; Petit F; Centre Hospitalier Universitaire de Lille, Clinique de Génétique Guy Fontaine, Lille, France.; Ibrahim V; Dalhousie University, Department of Biochemistry and Molecular Biology, Faculty of Medicine, Halifax, NS, Canada; Department of Pharmacology, Faculty of Medicine, Dalhousie University, Halifax, NS, Canada.; Top D; Dalhousie University, Department of Biochemistry and Molecular Biology, Faculty of Medicine, Halifax, NS, Canada; Department of Pharmacology, Faculty of Medicine, Dalhousie University, Halifax, NS, Canada.; Di Cara F; Department of Microbiology and Immunology, Faculty of Medicine, Dalhousie University, Halifax, NS, Canada.; Louie RJ; Greenwood Genetic Center, Greenwood, SC, USA.; Stolerman E; Greenwood Genetic Center, Greenwood, SC, USA.; Brunner HG; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands; Maastricht University Medical Center, Department of Clinical Genetics, Maastricht, the Netherlands.; Vissers LELM; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands.; Kramer JM; Dalhousie University, Department of Biochemistry and Molecular Biology, Faculty of Medicine, Halifax, NS, Canada. Electronic address: jkramer@dal.ca.; Kleefstra T; Radboudumc, Department of Human Genetics, Nijmegen, the Netherlands; Center for Neuropsychiatry, Vincent van Gogh, Venray, the Netherlands; Department of Clinical Genetics, ErasmusMC, Rotterdam, the Netherlands. Electronic address: t.kleefstra@erasmusmc.nl.
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
De Rubeis, S; He, X; Goldberg, AP; Poultney, CS; Samocha, K; Cicek, AE; Kou, Y; Liu, L; Fromer, M; Walker, S; Singh, T; Klei, L; Kosmicki, J; Fu, SC; Aleksic, B; Biscaldi, M; Bolton, PF; Brownfeld, JM; Cai, JL; Campbell, NG; Carracedo, A; Chahrour, MH; Chiocchetti, AG; Coon, H; Crawford, EL; Crooks, L; Curran, SR; Dawson, G; Duketis, E; Fernandez, BA; Gallagher, L; Geller, E; Guter, SJ; Hill, RS; Ionita-Laza, I; Gonzalez, PJ; Kilpinen, H; Klauck, SM; Kolevzon, A; Lee, I; Lei, J; Lehtimaki, T; Lin, CF; Ma'ayan, A; Marshall, CR; McInnes, AL; Neale, B; Owen, MJ; Ozaki, N; Parellada, M; Parr, JR; Purcell, S; Puura, K; Rajagopalan, D; Rehnstrom, K; Reichenberg, A; Sabo, A; Sachse, M; Sanders, SJ; Schafer, C; Schulte-Ruther, M; Skuse, D; Stevens, C; Szatmari, P; Tammimies, K; Valladares, O; Voran, A; Wang, LS; Weiss, LA; Willsey, AJ; Yu, TW; Yuen, RKC; Cook, EH; Freitag, CM; Gill, M; Hultman, CM; Lehner, T; Palotie, A; Schellenberg, GD; Skiar, P; State, MW; Sutcliffe, JS; Walsh, CA; Scherer, SW; Zwick, ME; Barrett, JC; Cutler, DJ; Roeder, K; Devlin, B; Daly, MJ; Buxbaum, JD
Nature. 515(7526):209
Academic Journal
Nordic Journal of Psychiatry. 60(5):379
검색 결과 제한하기
제한된 항목
[검색어] Puura, K.
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어