부산대학교 도서관

Gormley, P; Anttila, V; Winsvold, BS; Palta, P; Esko, T; Pers, TH; Farh, K-H; Cuenca-Leon, E; Muona, M; Furlotte, NA

NATURE GENETICS. 48(8):856-866

Savolainen, K.; Riihimäki, V.; Luukkonen, R.; Muona, O.

British Journal of Industrial Medicine, 1985 Nov 01. 42(11), 765-769.

Zilliacus, E.; Hathaway, J.; Huusko, J.; Cicerchia, M.; Ahonen, S.; Tommiska, J.; Gall, K.; Sluyters, A.; Lewis, A.; Liaquat, K.; Partack, E.; Howell, V.; Dodge, W.; Djupsjöbacka, J.; Muona, M.; Saarinen, I.; Seppälä, E.; Kangas-Kontio, T.; Koskinen, L.; Salmenperä, P.; Myllykangas, S.; Koskenvuo, J.

Heart, Lung and Circulation. 33:S120-S120

Bakker, Mark K.; Kanning, Jos P.; Abraham, Gad; Martinsen, Amy E.; Winsvold, Bendik S.; Zwart, John-Anker; Bourcier, Romain; Sawada, Tomonobu; Koido, Masaru; Kamatani, Yoichiro; Morel, Sandrine; Amouyel, Philippe; Debette, Stéphanie; Bijlenga, Philippe; Berrandou, Takiy; Ganesh, Santhi K.; Bouatia-Naji, Nabila; Jones, Gregory; Bown, Matthew; Rinkel, Gabriel J.E.; Veldink, Jan H.; Ruigrok, Ynte M.; Hege Aamodt, Anne; Heidi Skogholt, Anne; Brumpton, Ben M; Willer, Cristen J; Sandset, Else C; Kristoffersen, Espen S; Ellekjær, Hanne; Heuch, Ingrid; Nielsen, Jonas B; Hagen, Knut; Hveem, Kristian; Fritsche, Lars G; Thomas, Laurent F; Pedersen, Linda M; Gabrielsen, Maiken E; Holmen, Oddgeir L; Børte, Sigrid; Zhou, Wei; Abboud, Shérine; Pandolfo, Massimo; Thijs, Vincent; Leys, Didier; Bodenant, Marie; Louillet, Fabien; Touzé, Emmanuel; Mas, Jean-Louis; Samson, Yves; Leder, Sara; Léger, Anne; Deltour, Sandrine; Crozier, Sophie; Méresse, Isabelle; Canaple, Sandrine; Godefroy, Olivier; Giroud, 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Reinhold; Schmidt, Helena; Shrine, Nick; Siscovick, David; Smith, Albert V; Snieder, Harold; Sõber, Siim; Sorice, Rossella; Starr, John M; Stott, David J; Strachan, David P; Strawbridge, Rona J; Sundström, Johan; Swertz, Morris A; Taylor, Kent D; Teumer, Alexander; Tobin, Martin D; Tomaszewski, Maciej; Toniolo, Daniela; Traglia, Michela; Trompet, Stella; Tuomilehto, Jaakko; Tzourio, Christophe; Uitterlinden, André G; Vaez, Ahmad; van der Most, Peter J; van Duijn, Cornelia M; Verwoert, Germaine C; Vitart, Veronique; Völker, Uwe; Vollenweider, Peter; Vuckovic, Dragana; Watkins, Hugh; Wild, Sarah H; Willemsen, Gonneke; Wilson, James F; Wright, Alan F; Yao, Jie; Zemunik, Tatijana; Zhang, Weihua; Attia, John R; Butterworth, Adam S; Chasman, Daniel I; Conen, David; Cucca, Francesco; Danesh, John; Hayward, Caroline; Howson, Joanna MM; Laakso, Markku; Lakatta, Edward G; Langenberg, Claudia; Melander, Olle; Mook-Kanamori, Dennis O; Palmer, Colin NA; Risch, Lorenz; Scott, Robert A; Scott, Rodney J; Sever, Peter; Spector, Tim D; van der Harst, Pim; Wareham, Nicholas J; Zeggini, Eleftheria; Levy, Daniel; Munroe, Patricia B; Newton-Cheh, Christopher; Brown, Morris J; Metspalu, Andres; Psaty, Bruce M.; Wain, Louise V; Elliott, Paul; Caulfield, Mark J; Gormley, Padhraig; Anttila, Verneri; Palta, Priit; Esko, Tonu; Pers, Tune H; Farh, Kai-How; Cuenca-Leon, Ester; Muona, Mikko; Furlotte, Nicholas A; Kurth, Tobias; Ingason, Andres; McMahon, George; Ligthart, Lannie; Terwindt, Gisela M; Kallela, Mikko; Freilinger, Tobias M; Ran, Caroline; Gordon, Scott G; Stam, Anine H; Steinberg, Stacy; Borck, Guntram; Koiranen, Markku; Quaye, Lydia; Adams, Hieab H H; Lehtimäki, Terho; Sarin, Antti-Pekka; Wedenoja, Juho; Hinds, David A; Buring, Julie E; Schürks, Markus; Ridker, Paul M; Gudlaug Hrafnsdottir, Maria; Stefansson, Hreinn; Ring, Susan M; Hottenga, Jouke-Jan; Penninx, Brenda W J H; Färkkilä, Markus; Artto, Ville; Kaunisto, Mari; Vepsäläinen, Salli; Malik, Rainer; Heath, Andrew C; Madden, Pamela A F; Martin, Nicholas G; Montgomery, Grant W; Kurki, Mitja I; Kals, Mart; Mägi, Reedik; Pärn, Kalle; Hämäläinen, Eija; Huang, Hailiang; Byrnes, Andrea E; Franke, Lude; Huang, Jie; Stergiakouli, Evie; Lee, Phil H; Sandor, Cynthia; Webber, Caleb; Cader, Zameel; Muller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Eriksson, Johan G; Salomaa, Veikko; Heikkilä, Kauko; Loehrer, Elizabeth; Uitterlinden, Andre G; Hofman, Albert; van Duijn, Cornelia M; Cherkas, Lynn; Pedersen, Linda M; Stubhaug, Audun; Nielsen, Christopher S; Männikkö, Minna; Mihailov, Evelin; Milani, Lili; Göbel, Hartmut; Esserlind, Ann-Louise; Francke Christensen, Anne; Folkmann Hansen, Thomas; Werge, Thomas; Kaprio, Jaakko; Aromaa, Arpo J; Raitakari, Olli; Arfan Ikram, M; Spector, Tim; Järvelin, Marjo-Riitta; Metspalu, Andres; Kubisch, Christian; Strachan, David P; Ferrari, Michel D; Belin, Andrea C; Dichgans, Martin; Wessman, Maija; van den Maagdenberg, Arn M J M; Boomsma, Dorret I; Davey Smith, George; Stefansson, Kari; Eriksson, Nicholas; Daly, Mark J; Neale, Benjamin M; Olesen, Jes; Chasman, Daniel I; Nyholt, Dale R; Palotie, Aarno; Akiyama, Masato; Alg, Varinder S.; Børte, Sigrid; Broderick, Joseph P.; Brumpton, Ben M.; Dauvillier, Jérôme; Desal, Hubert; Dina, Christian; Friedrich, Christoph M.; Gaál-Paavola, Emília I.; Gentric, Jean-Christophe; Hirsch, Sven; Hostettler, Isabel C.; Houlden, Henry; Hveem, Kristian; Jääskeläinen, Juha E.; Johnsen, Marianne Bakke; Li, Liming; Lin, Kuang; Lindgren, Antti; Martin, Olivier; Matsuda, Koichi; Millwood, Iona Y.; Naggara, Olivier; Niemelä, Mika; Pera, Joanna; Redon, Richard; Rouleau, Guy A.; Sandvei, Marie Søfteland; Schilling, Sabine; Shotar, Eimad; Slowik, Agnieszka; Terao, Chikashi; Verschuren, W. M. Monique; Walters, Robin G.; Werring, David J.; Willer, Cristen J.; Woo, Daniel; Worrall, Bradford B.; Zhou, Sirui

Stroke. Mar 01, 2023 54(3):810-818

Zarate, Yuri A.; Uehara, Tomoko; Abe, Kota; Oginuma, Masayuki; Harako, Sora; Ishitani, Shizuka; Lehesjoki, Anna-Elina; Bierhals, Tatjana; Kloth, Katja; Ehmke, Nadja; Horn, Denise; Holtgrewe, Manuel; Anderson, Katherine; Viskochil, David; Edgar-Zarate, Courtney L.; Sacoto, Maria J. Guillen; Schnur, Rhonda E.; Morrow, Michelle M.; Sanchez-Valle, Amarilis; Pappas, John; Rabin, Rachel; Muona, Mikko; Anttonen, Anna-Kaisa; Platzer, Konrad; Luppe, Johannes; Gburek-Augustat, Janina; Kaname, Tadashi; Okamoto, Nobuhiko; Mizuno, Seiji; Kaido, Yusaku; Ohkuma, Yoshiaki; Hirose, Yutaka; Ishitani, Tohru; Kosaki, Kenjiro

Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 23(6):1050-1057

Keuters, Meike Hedwig; Keksa-Goldsteine, Velta; Dhungana, Hiramani; Huuskonen, Mikko T.; Pomeshchik, Yuriy; Savchenko, Ekaterina; Korhonen, Paula K.; Singh, Yajuvinder; Wojciechowski, Sara; Lehtonen, Šárka; Kanninen, Katja M.; Malm, Tarja; Sirviö, Jouni; Muona, Anu; Koistinaho, Milla; Goldsteins, Gundars; Koistinaho, Jari

Scientific Reports. 11(1)

Koskenvuo JW; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Saarinen I; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Ahonen S; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Tommiska J; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Weckström S; Heart and Lung Center, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.; Seppälä EH; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Tuupanen S; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Kangas-Kontio T; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Schleit J; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Heliö K; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Hathaway J; Blueprint Genetics Inc, a Quest Diagnostics Company, Seattle, Washington, United States of America.; Gummesson A; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.; Dahlberg P; Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.; Ojala TH; Department of Pediatric Cardiology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Vepsäläinen V; Heart Center, Kuopio University Hospital, Kuopio, Finland.; Kytölä V; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Muona M; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Sistonen J; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Salmenperä P; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Gentile M; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Paananen J; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Myllykangas S; Blueprint Genetics, a Quest Diagnostics Company, Espoo, Finland.; Alastalo TP; Blueprint Genetics Inc, a Quest Diagnostics Company, Seattle, Washington, United States of America.; Heliö T; Heart and Lung Center, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.

Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

van der Knoop MM; Department of Child Neurology, Sophia Children's Hospital, Erasmus University Medical Center, 3015 CN Rotterdam, The Netherlands.; Maroofian R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.; Fukata Y; Division of Membrane Physiology, Department of Molecular and Cellular Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan.; Department of Physiological Sciences, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Aichi 444-8585, Japan.; van Ierland Y; Department of Clinical Genetics, Erasmus University Medical Center, 3015 CN Rotterdam, The Netherlands.; Karimiani EG; Next Generation Genetic Polyclinic, Razavi International Hospital, Mashhad, Iran.; Genetics Research Centre, Molecular and Clinical Sciences Institute, St. George's University, London SW17 0RE, UK.; Lehesjoki AE; Folkhälsan Research Center, Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki 00290, Finland.; Muona M; Folkhälsan Research Center, Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki 00290, Finland.; Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Finland, 00100 Helsinki, Finland.; Blueprint Genetics, 02150 Espoo, Finland.; Paetau A; Department of Pathology, Medicum, University of Helsinki, 00100 Helsinki, Finland.; Miyazaki Y; Division of Membrane Physiology, Department of Molecular and Cellular Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan.; Department of Physiological Sciences, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Aichi 444-8585, Japan.; Hirano Y; Division of Membrane Physiology, Department of Molecular and Cellular Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan.; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Bunkyo, Tokyo 113-8655, Japan.; Selim L; Division of Neurology and Metabolism, Kasr Al Ainy School of Medicine, Cairo University Children Hospital, Cairo, Egypt.; de França M; Department of Morphology and Genetics, Clinical Center of Medical Genetics Federal, University of São Paulo, São Paulo, Brazil.; Fock RA; Department of Morphology and Genetics, Clinical Center of Medical Genetics Federal, University of São Paulo, São Paulo, Brazil.; Beetz C; Centogene GmbH, 18055 Rostock, Germany.; Ruivenkamp CAL; Department of Clinical Genetics, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.; Eaton AJ; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Morneau-Jacob FD; Division of Pediatric Neurology, University of Alberta, Edmonton, AB, Canada.; Sagi-Dain L; Affiliated to the Ruth and Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology, Genetics Institute, Carmel Medical Center, Haifa, Israel.; Shemer-Meiri L; Pediatric Neurology Unit, Carmel Medical Center, Haifa, Israel.; Peleg A; Affiliated to the Ruth and Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology, Genetics Institute, Carmel Medical Center, Haifa, Israel.; Haddad-Halloun J; Department of Biology, Technion-Israel Institute of Technology, Haifa 3200003, Israel.; Kamphuis DJ; Department of Neurology, Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands.; Peeters-Scholte CMPCD; Department of Neurology, Leiden University Medical Center, 2300 RA Leiden, The Netherlands.; Kurul SH; Izmir Biomedicine and Genome Center, Dokuz Eylul University Health Campus, Izmir, Turkey.; Izmir International Biomedicine and Genome Institute, Dokuz Eylul University, Izmir, Turkey.; Department of Paediatric Neurology, School of Medicine, Dokuz Eylul University, Izmir, Turkey.; Horvath R; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, School of Clinical Medicine, University of Cambridge, Cambridge, UK.; Lochmüller H; CNAG-CRG, Centre for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain.; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Department of Neuropediatrics and Muscle Disorders, Medical Center-University of Freiburg, Faculty of Medicine, Freiburg, Germany.; Division of Neurology, Department of Medicine, The Ottawa Hospital; and Brain and Mind Research Institute, University of Ottawa, Ottawa, Canada.; Murphy D; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.; Waldmüller S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen 72076, Germany.; Spranger S; Praxis für Humangenetik, Klinikum Bremen-Mitte, Bremen 28209, Germany.; Overberg D; Department of Pediatrics, Klinikum Bremen-Mitte, Bremen 28205, Germany.; Muir AM; Division of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, WA 98195, USA.; Rad A; Department of Otolaryngology - Head and Neck Surgery, Tübingen Hearing Research Centre, Eberhard Karls University Tübingen, Tübingen 72076, Germany.; Vona B; Department of Otolaryngology - Head and Neck Surgery, Tübingen Hearing Research Centre, Eberhard Karls University Tübingen, Tübingen 72076, Germany.; Abdulwahad F; Department of Translational Genomics, King Faisal Specialist Hospital and Research Center, Riyadh 11564, Saudi Arabia.; Maddirevula S; Department of Translational Genomics, King Faisal Specialist Hospital and Research Center, Riyadh 11564, Saudi Arabia.; Povolotskaya IS; Veltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University of the Russian Ministry of Health, Moscow, Russia.; Voinova VY; Veltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University of the Russian Ministry of Health, Moscow, Russia.; Mental Health Research Center, Moscow 107076, Russia.; Gowda VK; Department of Pediatric Neurology, Indira Gandhi Institute of Child Health, Bangalore, India.; Srinivasan VM; Department of Pediatric Neurology, Indira Gandhi Institute of Child Health, Bangalore, India.; Alkuraya FS; Department of Translational Genomics, King Faisal Specialist Hospital and Research Center, Riyadh 11564, Saudi Arabia.; Mefford HC; Division of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, WA 98195, USA.; Alfadhel M; Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital (KASCH), King Abdulaziz Medical City, Ministry of National Guard-Health Affairs (MNG-HA), Riyadh, Saudi Arabia.; Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences, King AbdulAziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.; Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen 72076, Germany.; Centre for Rare Diseases, University of Tübingen, Tübingen 72076, Germany.; Striano P; IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; Severino M; IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Fukata M; Division of Membrane Physiology, Department of Molecular and Cellular Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan.; Department of Physiological Sciences, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Aichi 444-8585, Japan.; Hilhorst-Hofstee Y; Department of Clinical Genetics, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.; Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.

Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Heliö K; Heart and Lung Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Mäyränpää MI; Department of Pathology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Saarinen I; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Ahonen S; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Junnila H; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Tommiska J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Weckström S; Heart and Lung Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Holmström M; Department of Radiology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Toivonen M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Nikus K; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Heart Center, Tampere University Hospital, Tampere, Finland.; Hathaway J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Siivonen P; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Muona M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Sistonen J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Salmenperä P; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Gentile M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Paananen J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Myllykangas S; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Alastalo TP; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Heliö T; Heart and Lung Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.; Koskenvuo J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.

Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

Bott LC; Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University, Evanston, IL 60208, USA.; Forouhan M; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.; Lieto M; Department of Physiology, Anatomy and Genetics, Oxford OX1 3QX, UK.; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples 80121, Italy.; Sala AJ; Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University, Evanston, IL 60208, USA.; Ellerington R; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.; Johnson JO; Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA.; Speciale AA; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.; Criscuolo C; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples 80121, Italy.; Filla A; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples 80121, Italy.; Chitayat D; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario M5G 1X8, Canada.; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario M5G 1X5, Canada.; Alkhunaizi E; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario M5G 1X8, Canada.; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario M5G 1X5, Canada.; Shannon P; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto, Toronto, Ontario M5G 1X5, Canada.; Nemeth AH; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK.; Angelucci F; Department of Life, Health and Environmental Sciences, University of L'Aquila, 67100 Coppito, L'Aquila, Italy.; Lim WF; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.; Striano P; Institute for Research, Hospitalization and Health Care (IRCCS) 'G. Gaslini' Institute, Genova 16147, Italy.; Zara F; Institute for Research, Hospitalization and Health Care (IRCCS) 'G. Gaslini' Institute, Genova 16147, Italy.; Helbig I; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA 19104, USA.; Muona M; Blueprint Genetics, 02150 Espoo, Finland.; Folkhälsan Research Center, Helsinki, Finland.; Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, 00290, Finland.; Courage C; Folkhälsan Research Center, Helsinki, Finland.; Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, 00290, Finland.; Lehesjoki AE; Folkhälsan Research Center, Helsinki, Finland.; Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, 00290, Finland.; Berkovic SF; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3010, Australia.; Fischbeck KH; Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, MD 20892, USA.; Brancati F; Department of Life, Health and Environmental Sciences, University of L'Aquila, 67100 Coppito, L'Aquila, Italy.; IRCCS San Raffaele Pisana, 00163 Roma, Italy.; Morimoto RI; Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University, Evanston, IL 60208, USA.; Wood MJA; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.; Oxford Harrington Rare Disease Centre, University of Oxford, Oxford OX1 3QX, UK.; Rinaldi C; Department of Paediatrics, University of Oxford, Oxford OX1 3QX, UK.

Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE

Gormley, P.; Anttila, V.; Winsvold, B.S.; Palta, P.; Esko, T.; Pers, T.H.; Farh, K.H.; Cuenca-Leon, E.; Muona, M.; Furlotte, N.A.; Kurth, T.; Ingason, A.; McMahon, G.; Ligthart, L.; Terwindt, G.M.; Kallela, M.; Freilinger, T.M.; Ran, C.; Gordon, S.G.; Stam, A.H.; Steinberg, S.; Borck, G.; Koiranen, M.; Quaye, L.; Adams, H.H.H.; Lehtimaki, T.; Sarin, A.P.; Wedenoja, J.; Hinds, D.A.; Buring, J.E.; Schurks, M.; Ridker, P.M.; Hrafnsdottir, M.G.; Stefansson, H.; Ring, S.M.; Hottenga, J.J.; Penninx, B.W.J.H.; Farkkila, M.; Artto, V.; Kaunisto, M.; Vepsalainen, S.; Malik, R.; Heath, A.C.; Madden, P.A.F.; Martin, N.G.; Montgomery, G.W.; Kurki, M.I.; Kals, M.; Magi, R.; Parn, K.; Hamalainen, E.; Huang, H.L.; Byrnes, A.E.; Franke, L.; Huang, J.; Stergiakouli, E.; Lee, P.H.; Sandor, C.; Webber, C.; Cader, Z.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Eriksson, J.G.; Salomaa, V.; Heikkila, K.; Loehrer, E.; Uitterlinden, A.G.; Hofman, A.; Duijn, C.M. van; Cherkas, L.; Pedersen, L.M.; Stubhaug, A.; Nielsen, C.S.; Mannikko, M.; Mihailov, E.; Milani, L.; Gobel, H.; Esserlind, A.L.; Christensen, A.F.; Hansen, T.F.; Werge, T.; Kaprio, J.; Aromaa, A.J.; Raitakari, O.; Ikram, M.A.; Spector, T.; Jarvelin, M.R.; Metspalu, A.; Kubisch, C.; Strachan, D.P.; Ferrari, M.D.; Belin, A.C.; Dichgans, M.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Zwart, J.A.; Boomsma, D.I.; Smith, G.D.; Stefansson, K.; Eriksson, N.; Daly, M.J.; Neale, B.M.; Olesen, J.; Chasman, D.I.; Nyholt, D.R.; Palotie, A.; Int Headache Genetics Consortium

Hedman, M; Muona, K; Hedman, A; Kivelä, A; Syvänne, M; Eränen, J; Rantala, A; Stjernvall, J; Nieminen, M S; Hartikainen, J; Ylä-Herttuala, S

Gene Therapy. 16(5):629-634

Gormley, P; Anttila, V; Winsvold, BS; Palta, P; Esko, T; Pers, TH; Farh, KH; Cuenca-Leon, E; Muona, M; Furlotte, NA; Kurth, T; Ingason, A; McMahon, G; Ligthart, L; Terwindt, GM; Kallela, M; Freilinger, TM; Ran, C; Gordon, SG; Stam, AH; Steinberg, S; Borck, G; Koiranen, M; Quaye, L; Adams, HHH; Lehtimäki, T; Sarin, AP; Wedenoja, J; Hinds, DA; Buring, JE; Schürks, M; Ridker, PM; Gudlaug Hrafnsdottir, M; Stefansson, H; Ring, SM; Hottenga, JJ; Penninx, BWJH; Färkkilä, M; Artto, V; Kaunisto, M; Vepsäläinen, S; Malik, R; Heath, AC; Madden, PAF; Martin, NG; Montgomery, GW; Kurki, MI; Kals, M; Mägi, R; Pärn, K; Hämäläinen, E; Huang, H; Byrnes, AE; Franke, L; Huang, J; Stergiakouli, E; Lee, PH; Sandor, C; Webber, C; Cader, Z; Muller-Myhsok, B; Schreiber, S; Meitinger, T; Eriksson, JG; Salomaa, V; Heikkilä, K; Loehrer, E; Uitterlinden, AG; Hofman, A; Van Duijn, CM; Cherkas, L; Pedersen, LM; Stubhaug, A; Nielsen, CS; Männikkö, M; Mihailov, E; Milani, L; Göbel, H; Esserlind, AL; Francke Christensen, A; Folkmann Hansen, T; Werge, T; Kaprio, J; Aromaa, AJ; Raitakari, O; Arfan Ikram, M; Spector, T; Järvelin, MR; Metspalu, A; Kubisch, C; Strachan, DP; Ferrari, MD; Belin, AC; Dichgans, M; Wessman, M; Van den Maagdenberg, AMJM; Zwart, JA; Boomsma, DI; Davey Smith, G

Gormley, P; Anttila, V; Winsvold, BS; Palta, P; Esko, T; Pers, TH; Farh, K-H; Cuenca-Leon, E; Muona, M; Furlotte, NA

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Mazzola L; Neurology Department, Saint-Étienne University Hospital Center, Saint-Étienne, France.; Lyon Neuroscience Research Center, Lyon, France.; Oliver KL; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Melbourne, Victoria, Australia.; Labalme A; Genetics Department, Lyon Civil Hospices, Lyon, France.; Baykan B; Departments of Neurology and Clinical Neurophysiology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.; Muona M; Folkhälsan Research Center, Helsinki, Finland.; Blueprint Genetics, Helsinki, Finland.; Joensuu TH; Folkhälsan Research Center, Helsinki, Finland.; Medicum, University of Helsinki, Helsinki, Finland.; Courage C; Folkhälsan Research Center, Helsinki, Finland.; Medicum, University of Helsinki, Helsinki, Finland.; Chatron N; Genetics Department, Lyon Civil Hospices, Lyon, France.; NeuroMyoGène Institute, University of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Borsani G; University of Brescia, Brescia, Italy.; Alix E; Genetics Department, Lyon Civil Hospices, Lyon, France.; Ramond F; Genetics Department, Saint-Étienne University Hospital Center, Saint-Étienne, France.; Touraine R; Genetics Department, Saint-Étienne University Hospital Center, Saint-Étienne, France.; Bahlo M; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Melbourne, Victoria, Australia.; Bebek N; Departments of Neurology and Clinical Neurophysiology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.; Berkovic SF; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Lehesjoki AE; Folkhälsan Research Center, Helsinki, Finland.; Medicum, University of Helsinki, Helsinki, Finland.; Lesca G; Genetics Department, Lyon Civil Hospices, Lyon, France.; NeuroMyoGène Institute, University of Lyon, Claude Bernard University Lyon 1, Lyon, France.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE

Heliö K; Heart and Lung Center, ERN GUARD-Heart Center, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.; Cicerchia M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Hathaway J; Blueprint Genetics, A Quest Diagnostics Company, Seattle, USA.; Tommiska J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Huusko J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Saarinen I; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Koskinen L; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Muona M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Kytölä V; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Djupsjöbacka J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Gentile M; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Salmenperä P; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Alastalo TP; Blueprint Genetics, A Quest Diagnostics Company, Seattle, USA.; Steinberg C; Quebec Heart and Lung Institute, Laval University, Quebec, Canada.; Heliö T; Heart and Lung Center, ERN GUARD-Heart Center, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.; Paananen J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Myllykangas S; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.; Koskenvuo J; Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.

Publisher: Frontiers Media S.A Country of Publication: Switzerland NLM ID: 101653388 Publication Model: eCollection Cited Medium: Print ISSN: 2297-055X (Print) Linking ISSN: 2297055X NLM ISO Abbreviation: Front Cardiovasc Med Subsets: PubMed not MEDLINE