المؤلفون: Inês Barroso, Gail Davies, H.-Erich Wichmann, Bjarke Feenstra, Peter Vollenweider, Nicholas J. Timpson, Alan F. Wright, Frank Geller, Gérard Waeber, John M. Starr, Benjamin M. Neale, George Davey Smith, Tõnu Esko, Ruth J. F. Loos, Andrew A. Hicks, Pedro Marques-Vidal, Dorret I. Boomsma, Harry Campbell, Zoltán Kutalik, David M. Evans, Scott D. Gordon, Eva Albrecht, Peter P. Pramstaller, Leena Peltonen, Jing Hua Zhao, Lavinia Paternoster, Thomas Hansen, Massimo Mangino, Fazil Aliev, Beate St Pourcain, Panos Deloukas, Heather A. Boyd, Guillaume Paré, Marco P. Boks, Monique M.B. Breteler, Jouke-Jan Hottenga, Xin Li, Kari Stefansson, Ian J. Deary, Jari Lahti, Inga Prokopenko, Nicholas Eriksson, Lili Milani, Nicholas J. Wareham, Jordan W. Smoller, Norman Klopp, Lynn Cherkas, Reedik Mägi, Margaret J. Wright, Peter Kraft, Jacques S. Beckmann, Brenda W.J.H. Penninx, Gabriel Cuellar-Partida, André G. Uitterlinden, Fernando Rivadeneira, Wendy L. McArdle, Johan G. Eriksson, Jiali Han, Jennifer E. Huffman, Andres Metspalu, J.M. Vink, Frank J. A. van Rooij, Christian Gieger, M. Arfan Ikram, Cecilia M. Lindgren, Aarno Palotie, Daniel I. Chasman, Joyce Y. Tung, Liang-Dar Hwang, David A. Hinds, Elisabeth Widen, Caroline Hayward, Michelle Luciano, Johannes H. Smit, Gonneke Willemsen, Dale R. Nyholt, Carolina Medina-Gomez, Nicole M. Warrington, Teemu Palviainen, Stacy Steinberg, Kay-Tee Khaw, Kevin S. O’Connell, Bettina Konte, Gudmar Thorleifsson, Eco J. C. de Geus, John P. Kemp, Mads Melbye, Mark I. McCarthy, Sarah E. Medland, Jaakko Kaprio, Cameron D. Palmer, Joel N. Hirschhorn, Ina Giegling, Scott Melville, Thomas Werge, Nicole Soranzo, Sigurdur H. Magnusson, Maris Teder-Laving, Hreinn Stefansson, Kauko Heikkilä, Cornelia M. van Duijn, David L. Duffy, Samuli Ripatti, Igor Rudan, Annette M. Hartmann, Ole A. Andreassen, Mari Nelis, Ozren Polasek, Vincent Mooser, Mousheng Xu, Eero Vuoksimaa, Katri Räikkönen, Nicholas G. Martin, Dan Rujescu, Tim D. Spector, Dawn M. Waterworth, Danielle M. Dick, Roel A. Ophoff

المساهمون: Epidemiology, Internal Medicine, Psychiatry, Biological Psychology, APH - Mental Health, APH - Methodology, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Epidemiology and Data Science, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Pediatric surgery, APH - Digital Health

المصدر: Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkila, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O'Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefansson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Partida, G C, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M MB, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E JC, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R JF, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B WJH, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, St Pourcain, B, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F JA, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour . https://doi.org/10.1038/s41562-020-00956-y
Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J J, Huffman, J E, Hwang, L D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefánsson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Mägi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, no. 1, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Nature Human Behaviour, 5, 1, pp. 59-70
Nature Human Behaviour, 5(1), 59-70. Nature Publishing Group
Nat Hum Behav
Nature Human Behaviour, 5(1), 59-70. Springer Nature
Nature Human Behaviour
Nat. Hum. Behav. 5, 59–70 (2021)
Nature Human Behaviour, 5, 59-70
Nature human behaviour 5(1), 59-70 (2021). doi:10.1038/s41562-020-00956-y
Cuellar-Partida, G, Deloukas, P, Kemp, J P, McArdle, W L, Paternoster, L, Davey Smith, G, Timpson, N J, Medland, S E & al., E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59–70 . https://doi.org/10.1038/s41562-020-00956-y

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Linkage disequilibrium, Genome-wide association study, LANGUAGE DOMINANCE, Functional Laterality, Linkage Disequilibrium, Behavioral Neuroscience, 0302 clinical medicine, ddc:150, Gene Frequency, SCHIZOPHRENIA, Genetics, 0303 health sciences, Middle Aged, genetics [Genetic Variation], genetics [Functional Laterality], Schizophrenia, ASYMMETRY, genetics [Polymorphism, Single Nucleotide], Female, Adult, Social Psychology, LATERALIZATION, Experimental and Cognitive Psychology, genetics [Genetic Loci], Biology, Quantitative trait locus, Genetic correlation, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, LINKAGE ANALYSIS, METAANALYSIS, MICROTUBULE, AUTISM, ORIGINS, SCREEN, Quantitative Trait, Heritable, Sex Factors, Genetic linkage, medicine, Humans, Bipolar disorder, 030304 developmental biology, Genetic association study, Aged, Genetic Variation, medicine.disease, Genetic Loci, Autism, genetics [Gene Frequency], Developmental Psychopathology, 030217 neurology & neurosurgery, Neuroscience, Genome-Wide Association Study

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986a1504a38fc87e9588fa425872923b
https://curis.ku.dk/portal/da/publications/genomewide-association-study-identifies-48-common-genetic-variants-associated-with-handedness(3aa476e7-e13d-48f1-af0d-544a2ee787fd).html

المؤلفون: Guiyan Ni, Gerhard Moser, Naomi R. Wray, S. Hong Lee, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James T.R. Walters, Kai-How Farh, Peter A. Holmans, Phil Lee, Brendan Bulik-Sullivan, David A. Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu A. Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C.K. Chan, Ronald Y.L. Chen, Eric Y.H. Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del Favero, Ditte Demontis, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan Eriksson, Valentina Escott-Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti-Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Vera Golimbet, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Mads V. Hollegaard, David M. Hougaard, Masashi Ikeda, Inge Joa, Antonio Juliá, René S. Kahn, Luba Kalaydjieva, Sena Karachanak-Yankova, Juha Karjalainen, David Kavanagh, Matthew C. Keller, James L. Kennedy, Andrey Khrunin, Yunjung Kim, Janis Klovins, James A. Knowles, Bettina Konte, Vaidutis Kucinskas, Zita Ausrele Kucinskiene, Hana Kuzelova-Ptackova, Anna K. Kähler, Claudine Laurent, Jimmy Lee Chee Keong, Sophie E. Legge, Bernard Lerer, Miaoxin Li, Tao Li, Kung-Yee Liang, Jeffrey Lieberman, Svetlana Limborska, Carmel M. Loughland, Jan Lubinski, Jouko Lönnqvist, Milan Macek, Patrik K.E. Magnusson, Brion S. Maher, Wolfgang Maier, Jacques Mallet, Sara Marsal, Manuel Mattheisen, Morten Mattingsda, Robert W. McCarley, Colm McDonald, Andrew M. McIntosh, Sandra Meier, Carin J. Meijer, Bela Melegh, Ingrid Melle, Raquelle I. Mesholam-Gately, Andres Metspalu, Patricia T. Michie, Lili Milani, Vihra Milanova, Younes Mokrab, Derek W. Morris, Ole Mors, Kieran C. Murphy, Robin M. Murray, Inez Myin-Germeys, Bertram Müller-Myhsok, Mari Nelis, Igor Nenadic, Deborah A. Nertney, Gerald Nestadt, Kristin K. Nicodemus, Liene Nikitina-Zake, Laura Nisenbaum, Annelie Nordin, Eadbhard O’Callaghan, Colm O’Dushlaine, F. Anthony O’Neill, Sang-Yun Oh, Ann Olinc, Line Olsen, Jim Van Os, Christos Pantelis, George N. Papadimitriou, Sergi Papio, Elena Parkhomenko, Michele T. Pato, Tiina Paunio, Milica Pejovic-Milovancevic, Diana O. Perkins, Olli Pietiläinenl, Jonathan Pimm, Andrew J. Pocklington, John Powell, Alkes Price, Ann E. Pulver, Shaun M. Purcell, Digby Quested, Henrik B. Rasmussen, Abraham Reichenberg, Mark A. Reimers, Alexander L. Richards, Joshua L. Roffman, Panos Roussos, Douglas M. Ruderfer, Veikko Salomaa, Alan R. Sanders, Ulrich Schall, Christian R. Schubert, Thomas G. Schulze, Sibylle G. Schwab, Edward M. Scolnick, Rodney J. Scott, Larry J. Seidman, Jianxin Shi, Engilbert Sigurdsson, Teimuraz Silagadze, Jeremy M. Silverman, Kang Sim, Petr Slominsky, Jordan W. Smoller, Hon-Cheong So, Chris C.A. Spencer, Eli A. Stah, Hreinn Stefansson, Stacy Steinberg, Elisabeth Stogmann, Richard E. Straub, Eric Strengman, Jana Strohmaier, T. Scott Stroup, Mythily Subramaniam, Jaana Suvisaari, Dragan M. Svrakic, Jin P. Szatkiewicz, Erik Söderman, Srinivas Thirumalai, Draga Toncheva, Sarah Tosato, Juha Veijola, John Waddington, Dermot Walsh, Dai Wang, Qiang Wang, Bradley T. Webb, Mark Weiser, Dieter B. Wildenauer, Nigel M. Williams, Stephanie Williams, Stephanie H. Witt, Aaron R. Wolen, Emily H.M. Wong, Brandon K. Wormley, Hualin Simon Xi, Clement C. Zai, Xuebin Zheng, Fritz Zimprich, Kari Stefansson, Peter M. Visscher, Rolf Adolfsson, Ole A. Andreassen, Douglas H.R. Blackwood, Elvira Bramon, Joseph D. Buxbaum, Anders D. Børglum, Sven Cichon, Ariel Darvasi, Enrico Domenici, Hannelore Ehrenreich, Tõnu Esko, Pablo V. Gejman, Michael Gill, Hugh Gurling, Christina M. Hultman, Nakao Iwata, Assen V. Jablensky, Erik G. Jönsson, Kenneth S. Kendler, George Kirov, Jo Knight, Todd Lencz, Douglas F. Levinson, Qingqin S. Li, Jianjun Liu, Anil K. Malhotra, Steven A. McCarrol, Andrew McQuillin, Jennifer L. Moran, Preben B. Mortensen, Bryan J. Mowry, Markus M. Nöthen, Roel A. Ophoff, Michael J. Owen, Aarno Palotie, Carlos N. Pato, Tracey L. Petryshen, Danielle Posthuma, Marcella Rietsche, Brien P. Riley, Dan Rujescu, Pak C. Sham, Pamela Sklar, David St Clair, Daniel R. Weinberger, Jens R. Wendland, Thomas Werge, Mark J. Daly, Patrick F. Sullivan, Michael C. O’Donovan

المساهمون: APH - Mental Health, ANS - Complex Trait Genetics, Adult Psychiatry, Ni, Guiyan, Moser, Gerhard, Wray, Naomi R, Lee, S Hong, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Amsterdam Neuroscience - Complex Trait Genetics, Complex Trait Genetics, Clinicum, Department of Psychiatry, HUS Psychiatry

المصدر: American journal of human genetics, 102(6), 1185-1194. Cell Press
The American Journal of Human Genetics
Agerbo, E & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018, ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ', American Journal of Human Genetics, vol. 102, no. 6, pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021
Posthuma, D & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018, ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ', American Journal of Human Genetics, vol. 102, no. 6, pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021
American Journal of Human Genetics, 102(6), 1185-1194. Cell Press
American Journal of Human Genetics, 102(6), 1185. Cell Press
American journal of human genetics, vol 102, iss 6
American journal of human genetics
The American journal of human genetics 102(6), 1185-1194 (2018). doi:10.1016/j.ajhg.2018.03.021

مصطلحات موضوعية: 0301 basic medicine, Linkage disequilibrium, Schizophrenia/genetics, INFORMATION, Restricted maximum likelihood, Inheritance Patterns, linkage disequilibrium score regression, Bioinformatics, Medical and Health Sciences, 3124 Neurology and psychiatry, Linkage Disequilibrium, biasedness, 0302 clinical medicine, Statistics, Databases, Genetic, WIDE ASSOCIATION, Genetics(clinical), PARTITIONING HERITABILITY, Genetics (clinical), Genetics & Heredity, education.field_of_study, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Likelihood Functions, Genome, Body Height/genetics, accuracy, Regression analysis, Single Nucleotide, Biological Sciences, Polymorphism, Single Nucleotide/genetics, genetic correlation, Regression, STATISTICS, genomic restricted maximum likelihood, Mental Health, Phenotype, Regression Analysis, COMPLEX HUMAN TRAITS, Single Nucleotide/genetics, Human, Adult, SUSCEPTIBILITY LOCI, Genotype, SNP heritability, body mass index, genome-wide SNPs, height, schizophrenia, Population, Haplotypes/genetics, Biology, Genetic correlation, Polymorphism, Single Nucleotide, 03 medical and health sciences, Databases, Genetic, ddc:570, Report, Genetics, Humans, Linkage Disequilibrium/genetics, Computer Simulation, Polymorphism, education, linkage disequilibrium score regression (LDSC), Genome, Human, Human Genome, genetic architecture, Genetic architecture, Body Height, Brain Disorders, Inheritance Patterns/genetics, BODY-MASS INDEX, 030104 developmental biology, Haplotypes, Sample size determination, Schizophrenia, 3111 Biomedicine, HUMAN HEIGHT, 030217 neurology & neurosurgery

وصف الملف: application/pdf; image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7da58790da12a5d173c787aa331767e
https://pubmed.ncbi.nlm.nih.gov/29754766

المؤلفون: Fritz Zimprich, Manuel Mattheisen, Edward M. Scolnick, Ayman H. Fanous, Henrik B. Rasmussen, Steven A. McCarroll, Ingrid Agartz, Carmel M. Loughland, Aiden Corvin, Ann Olincy, Anders D. Børglum, F. Anthony O'Neill, T. Scott Stroup, Elizabeth Bevilacqua, Sandra Meier, Ulrich Schall, Jouko Lönnqvist, Jianxin Shi, C. Robert Cloninger, Judit Bene, Veikko Salomaa, George N. Papadimitriou, Milica Pejovic-Milovancevic, Béla Melegh, Kari Stefansson, Brendan Bulik-Sullivan, Janis Klovins, Enrico Domenici, Sibylle G. Schwab, Dai Wang, Assen Jablensky, Mari Nelis, Sang Yun Oh, Peter Holmans, Aaron R. Wolen, Hualin Simon Xi, Eric Strengman, Bryan J. Mowry, Michael Gill, Kung Yee Liang, William Byerley, Rolf Adolfsson, Hugh Gurling, Joseph I. Friedman, Andrew Pocklington, Brien P. Riley, Engilbert Sigurdsson, Benjamin M. Neale, Miaoxin Li, Michael Davidson, Bernard Lerer, Michele T. Pato, Xuebin Zheng, Patrick F. Sullivan, Frans Henskens, Madeline Alexander, Andrew M. McIntosh, Inez Myin-Germeys, Draga Toncheva, Liene Nikitina-Zake, Kenneth S. Kendler, Carin J. Meijer, Robin M. Murray, Richard E. Straub, Ann E. Pulver, Menachem Fromer, Derek W. Morris, Douglas M. Ruderfer, Mythily Subramaniam, Paul Cormican, Lyudmila Georgieva, Giulio Genovese, Brion S. Maher, Stanley V. Catts, David St Clair, Robert W. McCarley, David Cohen, Nancy G. Buccola, Dan Rujescu, Carlos N. Pato, Kristin K. Nicodemus, Josef Frank, Claudine Laurent, Dominique Campion, Guiyan Ni, James L. Kennedy, Sena Karachanak-Yankova, Nicholas John Craddock, Peter M. Visscher, Valentina Escott-Price, Jeffrey A. Lieberman, Deborah A. Nertney, Bertram Müller-Myhsok, Marcella Rietschel, Dimitris Dikeos, Stephanie Godard, Stephanie Williams, Andres Metspalu, John L. Waddington, Sophie E. Legge, Roel A. Ophoff, Jonathan Pimm, Richard Bruggeman, Tim B. Bigdeli, Gerald Nestadt, Mark Weiser, Kieran C. Murphy, Eric F.C. Cheung, Kang Sim, Jordan W. Smoller, David J. Kavanagh, Inge Joa, Jens R. Wendland, Thomas G. Schulze, Richard A. Belliveau, Sarah E. Bergen, Ditte Demontis, David Curtis, Todd Lencz, Danielle Posthuma, René S. Kahn, Lili Milani, Randy L. Buckner, Jianjun Liu, Petr Slominsky, Wiepke Cahn, Hana Kuzelova-Ptackova, Sergi Papiol, Tune H. Pers, Stephan Ripke, Rita M. Cantor, Ariel Darvasi, Christina M. Hultman, Larry J. Seidman, Eli A. Stahl, David A. Collier, Michael Conlon O'Donovan, Svetlana A. Limborska, James T.R. Walters, Farooq Amin, Noa Carrera, Ronald Y.L. Chen, Pablo V. Gejman, Joel N. Hirschhorn, Zita Ausrele Kucinskiene, Michael John Owen, Ina Giegling, Stephanie H. Witt, Timothy G. Dinan, Margot Albus, Wei Cheng, Marian L. Hamshere, Markus M. Nöthen, Thomas Werge, Guiqing Cai, Raquelle I. Mesholam-Gately, Annette M. Hartmann, Ingrid Melle, Ole A. Andreassen, Preben Bo Mortensen, Hannelore Ehrenreich, Tiina Paunio, James A. Knowles, Pak C. Sham, Marion Friedl, Teimuraz Silagadze, Dermot Walsh, Emily H. M. Wong, Igor Nenadic, Matthew C. Keller, John Powell, Naomi R. Wray, Patricia T. Michie, Bradley T. Webb, Lude Franke, Mark Hansen, Masashi Ikeda, Sven Cichon, Elvira Bramon, Frank Dudbridge, Erik G. Jönsson, Annelie Nordin, Wolfgang Maier, Peter Eichhammer, Christian R. Schubert, J. Mallet, Jacob Gratten, Andrey Khrunin, Jacqueline I. Goldstein, Panos Roussos, Pamela Sklar, Diana O. Perkins, Srdjan Djurovic, Phil Lee, Elodie Drapeau, Douglas F. Levinson, Nadine Cohen, Luba Kalaydjieva, Brandon Wormley, Tao Li, Tõnu Esko, Alexander Richards, Srihari Gopal, Jubao Duan, Anil K. Malhotra, Elisabeth Stögmann, Gary Donohoe, Kimberly Chambert, Sara Marsal, Hreinn Stefansson, Jo Knight, Ole Mors, Per Hoffmann, Dieter B. Wildenauer, James J. Crowley, Srinivas Thirumalai, Vahram Haroutunian, A. Hofman, Hailiang Huang, Thomas Hansen, Daniel R. Weinberger, Andrew McQuillin, Vaughan J. Carr, Vaidutis Kučinskas, Jimmy Lee Chee Keong, Digby Quested, Aarno Palotie, Robert Freedman, Hon-Cheong So, Jennifer L. Moran, Donald W. Black, Mark Reimers, Abraham Reichenberg, Jurgen Del Favero, Paola Giusti-Rodríguez, Tracey L. Petryshen, Olli Pietiläinen, Franziska Degenhardt, Laurent Essioux, Esben Agerbo, Qiang Wang, Jana Strohmaier, Siow Ann Chong, Johan G. Eriksson, Martin Begemann, Younes Mokrab, Colm McDonald, Silviu Alin Bacanu, Martilias S. Farrell, Christos Pantelis, Kai How Farh, Line Olsen, Naser Durmishi, Antonio Julià, Stefan Herms, Qingqin S. Li, Bettina Konte, George Kirov, Rodney J. Scott, Nelson B. Freimer, Mads V. Hollegaard, Shaun Purcell, Erik Söderman, Dragan M. Svrakic, Patrik K. E. Magnusson, Douglas Blackwood, Jin P. Szatkiewicz, Sang Hong Lee, Yunjung Kim, Colm O'Dushlaine, Morten Mattingsdal, Jim van Os, Sarah Tosato, Milan Macek, Joshua L. Roffman, Jan Lubinski, Eadbhard O'Callaghan, Juha Karjalainen, Vera Golimbet, Anna K. Kähler, Clement C. Zai, Nigel Williams, Joseph D. Buxbaum, Laura Nisenbaum, Eric Y.H. Chen, David M. Hougaard, Jaana Suvisaari, Chris C. A. Spencer, Alan R. Sanders, Alkes L. Price, Vihra Milanova, Juha Veijola, Christian Hammer, Raymond C.K. Chan, Stacy Steinberg, Nakao Iwata, Jeremy M. Silverman, Mark J. Daly, Elena Parkhomenko, Kenneth L. Davis, Lieuwe de Haan

المساهمون: Schizophrenia Working Group of the Psychiatric Genomics Consortium, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Kučinskas, Vaidutis, Kučinskienė, Zita Aušrelė, Ni, Guiyan, Gratten, Jacob, Wray, Naomi R, Lee, Sang Hong, Germeys, Inez, Complex Trait Genetics, Háskóli Íslands, University of Iceland, Child and Adolescent Psychiatry / Psychology, Research Programs Unit, Diabetes and Obesity Research Program, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, University Management, Department of Psychiatry, Center for Population, Health and Society, Department of Public Health, Centre of Excellence in Complex Disease Genetics, Research Programme of Molecular Medicine, Aarno Palotie / Principal Investigator, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders

المصدر: Scientific reports
Mortensen, P B & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018, ' Age at first birth in women is genetically associated with increased risk of schizophrenia ', Scientific Reports, vol. 8, no. 1, 10168 . https://doi.org/10.1038/s41598-018-28160-z
Scientific Reports, 8(1):10168. Nature Publishing Group
Scientific reports, London, Nature publishing group, 2018, vol. 8, iss. 1, art. no. 10168, p. [1-14]
Ni, G, Gratten, J, Wray, N R, Lee, S H, Ripke, S, Neale, B M, Corvin, A, Walters, J T R, Farh, K H, Holmans, P A, Lee, P, Bulik-Sullivan, B, Collier, D A, Huang, H, Pers, T H, Agartz, I, Agerbo, E, Albus, M, Alexander, M, Amin, F, Bacanu, S A, Begemann, M, Belliveau, R A, Bene, J, Bergen, S E, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Chan, R C K, Chen, R Y L, Chen, E Y H, Cheng, W, Cheung, E F C, Chong, S A, Cloninger, C R, Cohen, D, Cohen, N, Cormican, P, Craddock, N, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Durmishi, N, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedl, M, Friedman, J I, Fromer, M, Genovese, G, Georgieva, L, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Golimbet, V, Gopal, S, Haan, L D, Hammer, C, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Hollegaard, M V, Hougaard, D M, Ikeda, M, Joa, I, Juliá, A, Kahn, R S, Kalaydjieva, L, Karachanak-Yankova, S, Karjalainen, J, Kavanagh, D, Keller, M C, Kennedy, J L, Khrunin, A, Kim, Y, Klovins, J, Knowles, J A, Konte, B, Kucinskas, V, Kucinskiene, Z A, Kuzelova-Ptackova, H, Kähler, A K, Laurent, C, Keong, J L C, Legge, S E, Lerer, B, Li, M, Li, T, Liang, K Y, Lieberman, J, Limborska, S, Loughland, C M, Lubinski, J, Lönnqvist, J, Macek, M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Marsal, S, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melegh, B, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Mors, O, Murphy, K C, Murray, R M, Myin-Germeys, I, Müller-Myhsok, B, Nelis, M, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nikitina-Zake, L, Nisenbaum, L, Nordin, A, O'callaghan, E, O'dushlaine, C, O'neill, F A, Oh, S Y, Olincy, A, Olsen, L, Os, J V, Pantelis, C, Papadimitriou, G N, Papiol, S, Parkhomenko, E, Pato, M T, Paunio, T, Pejovic-Milovancevic, M, Perkins, D O, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Schall, U, Schubert, C R, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Sigurdsson, E, Silagadze, T, Silverman, J M, Sim, K, Slominsky, P, Smoller, J W, So, H C, Spencer, C C A, Stahl, E A, Stefansson, H, Steinberg, S, Stogmann, E, Straub, R E, Strengman, E, Strohmaier, J, Stroup, T S, Subramaniam, M, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Söderman, E, Thirumalai, S, Toncheva, D, Tosato, S, Veijola, J, Waddington, J, Walsh, D, Wang, D, Wang, Q, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wong, E H M, Wormley, B K, Xi, H S, Zai, C C, Zheng, X, Zimprich, F, Stefansson, K, Visscher, P M, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Børglum, A D, Cichon, S, Darvasi, A, Domenici, E, Ehrenreich, H, Esko, T, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Lencz, T, Levinson, D F, Li, Q S, Liu, J, Malhotra, A K, McCarroll, S A, McQuillin, A, Moran, J L, Mortensen, P B, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sham, P C, Sklar, P, Clair, D S, Weinberger, D R, Wendland, J R, Werge, T, Daly, M J, Sullivan, P F & O'donovan, M C 2018, ' Age at first birth in women is genetically associated with increased risk of schizophrenia ', Scientific Reports, vol. 8, 10168, pp. 1-14 . https://doi.org/10.1038/s41598-018-28160-z
Scientific reports, vol 8, iss 1
Scientific Reports
Scientific Reports, 8:10168, 1-14. Nature Publishing Group
Scientific reports 8(1), 10168 (2018). doi:10.1038/s41598-018-28160-z
Schizophrenia Working Group of the Psychiatric Genomics Consortium, Ni, G, Gratten, J, Wray, N R, Lee, S H, Agerbo, E, Demontis, D, Hansen, T, Hollegaard, M V, Hougaard, D M, Mattheisen, M, Mors, O, Olsen, L, Rasmussen, H B, Børglum, A D, Mortensen, P B, Werge, T & Pers, T H 2018, ' Age at first birth in women is genetically associated with increased risk of schizophrenia ', Scientific Reports, vol. 8, 10168 . https://doi.org/10.1038/s41598-018-28160-z
Ni, Guiyan; Gratten, Jacob; Wray, Naomi R; Lee, Sang Hong; & Schizophrenia Working Group of the Psychiatric Genomics Consortium,. (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia.. Scientific reports, 8(1), 10168. doi: 10.1038/s41598-018-28160-z. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/724855t4
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Ni, G, Gratten, J, Wray, N R, Lee, S H, Ripke, S, Neale, B M, Corvin, A, Walters, J T R, Farh, K H, Holmans, P A, Lee, P, Bulik-Sullivan, B, Collier, D A, Huang, H, Pers, T H, Agartz, I, Agerbo, E, Albus, M, Alexander, M, Amin, F, Bacanu, S A, Begemann, M, Belliveau, R A, Bene, J, Bergen, S E, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Chan, R C K, Chen, R Y L, Chen, E Y H, Cheng, W, Cheung, E F C, Chong, S A, Cloninger, C R, Cohen, D, Cohen, N, Cormican, P, Craddock, N, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Durmishi, N, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedl, M, Friedman, J I, Fromer, M, Genovese, G, Georgieva, L, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Golimbet, V, Gopal, S, Haan, L D, Hammer, C, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Hollegaard, M V, Hougaard, D M, Ikeda, M, Joa, I, Juliá, A, Kahn, R S, Kalaydjieva, L, Karachanak-Yankova, S, Karjalainen, J, Kavanagh, D, Keller, M C, Kennedy, J L, Khrunin, A, Kim, Y, Klovins, J, Knowles, J A, Konte, B, Kucinskas, V, Kucinskiene, Z A, Kuzelova-Ptackova, H, Kähler, A K, Laurent, C, Keong, J L C, Legge, S E, Lerer, B, Li, M, Li, T, Liang, K Y, Lieberman, J, Limborska, S, Loughland, C M, Lubinski, J, Lönnqvist, J, Macek, M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Marsal, S, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melegh, B, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Mors, O, Murphy, K C, Murray, R M, Myin-Germeys, I, Müller-Myhsok, B, Nelis, M, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nikitina-Zake, L, Nisenbaum, L, Nordin, A, O'callaghan, E, O'dushlaine, C, O'neill, F A, Oh, S Y, Olincy, A, Olsen, L, Os, J V, Pantelis, C, Papadimitriou, G N, Papiol, S, Parkhomenko, E, Pato, M T, Paunio, T, Pejovic-Milovancevic, M, Perkins, D O, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Schall, U, Schubert, C R, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Sigurdsson, E, Silagadze, T, Silverman, J M, Sim, K, Slominsky, P, Smoller, J W, So, H C, Spencer, C C A, Stahl, E A, Stefansson, H, Steinberg, S, Stogmann, E, Straub, R E, Strengman, E, Strohmaier, J, Stroup, T S, Subramaniam, M, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Söderman, E, Thirumalai, S, Toncheva, D, Tosato, S, Veijola, J, Waddington, J, Walsh, D, Wang, D, Wang, Q, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wong, E H M, Wormley, B K, Xi, H S, Zai, C C, Zheng, X, Zimprich, F, Stefansson, K, Visscher, P M, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Børglum, A D, Cichon, S, Darvasi, A, Domenici, E, Ehrenreich, H, Esko, T, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Lencz, T, Levinson, D F, Li, Q S, Liu, J, Malhotra, A K, McCarroll, S A, McQuillin, A, Moran, J L, Mortensen, P B, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sham, P C, Sklar, P, Clair, D S, Weinberger, D R, Wendland, J R, Werge, T, Daly, M J, Sullivan, P F & O'donovan, M C 2018, ' Age at first birth in women is genetically associated with increased risk of schizophrenia ', Scientific Reports, vol. 8, no. 1, 10168, pp. 1-14 . https://doi.org/10.1038/s41598-018-28160-z
Scientific Reports, 8(1). Nature Publishing Group
Ni, G, Gratten, J, Wray, N R, Lee, S H, Ripke, S, Neale, B M, Corvin, A, Walters, J T R, Farh, K-H, Holmans, P A, Lee, P, Bulik-Sullivan, B, Collier, D A, Huang, H, Pers, T H, Agartz, I, Agerbo, E, Albus, M, Alexander, M, Amin, F, Bacanu, S A, Begemann, M, Belliveau, R A, Bene, J, Bergen, S E, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Chan, R C K, Chen, R Y L, Chen, E Y H, Cheng, W, Cheung, E F C, Chong, S A, Cloninger, C R, Cohen, D, Cohen, N, Cormican, P, Craddock, N, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Durmishi, N, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedl, M, Friedman, J I, Fromer, M, Genovese, G, Georgieva, L, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Golimbet, V, Gopal, S, Haan, L D, Hammer, C, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Hollegaard, M V, Hougaard, D M, Ikeda, M, Joa, I, Juliá, A, Kahn, R S, Kalaydjieva, L, Karachanak-Yankova, S, Karjalainen, J, Kavanagh, D, Keller, M C, Kennedy, J L, Khrunin, A, Kim, Y, Klovins, J, Knowles, J A, Konte, B, Kucinskas, V, Kucinskiene, Z A, Kuzelova-Ptackova, H, Kähler, A K, Laurent, C, Keong, J L C, Legge, S E, Lerer, B, Li, M, Li, T, Liang, K-Y, Lieberman, J, Limborska, S, Loughland, C M, Lubinski, J, Lönnqvist, J, Macek, M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Marsal, S, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melegh, B, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Mors, O, Murphy, K C, Murray, R M, Myin-Germeys, I, Müller-Myhsok, B, Nelis, M, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nikitina-Zake, L, Nisenbaum, L, Nordin, A, O'callaghan, E, O'dushlaine, C, O'neill, F A, Oh, S-Y, Olincy, A, Olsen, L, Os, J V, Pantelis, C, Papadimitriou, G N, Papiol, S, Parkhomenko, E, Pato, M T, Paunio, T, Pejovic-Milovancevic, M, Perkins, D O, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Schall, U, Schubert, C R, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Sigurdsson, E, Silagadze, T, Silverman, J M, Sim, K, Slominsky, P, Smoller, J W, So, H-C, Spencer, C C A, Stahl, E A, Stefansson, H, Steinberg, S, Stogmann, E, Straub, R E, Strengman, E, Strohmaier, J, Stroup, T S, Subramaniam, M, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Söderman, E, Thirumalai, S, Toncheva, D, Tosato, S, Veijola, J, Waddington, J, Walsh, D, Wang, D, Wang, Q, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wong, E H M, Wormley, B K, Xi, H S, Zai, C C, Zheng, X, Zimprich, F, Stefansson, K, Visscher, P M, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Børglum, A D, Cichon, S, Darvasi, A, Domenici, E, Ehrenreich, H, Esko, T N, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Lencz, T, Levinson, D F, Li, Q S, Liu, J, Malhotra, A K, McCarroll, S A, McQuillin, A, Moran, J L, Mortensen, P B, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sham, P C, Sklar, P, Clair, D S, Weinberger, D R, Wendland, J R, Werge, T, Daly, M J, Sullivan, P F & O'donovan, M C 2018, ' Age at first birth in women is genetically associated with increased risk of schizophrenia ', Scientific Reports, vol. 8, no. 1, 10168 . https://doi.org/10.1038/s41598-018-28160-z

مصطلحات موضوعية: 0301 basic medicine, Multifactorial Inheritance, PATERNAL-AGE, 3124 Neurology and psychiatry, COMMON SNPS, fluids and secretions, 0302 clinical medicine, CHILD, Risk Factors, Pregnancy, 2.1 Biological and endogenous factors, Medicine, Aetiology, Pediatric, PROPORTION, Schizophrenia Working Group of the Psychiatric Genomics Consortium, 0303 health sciences, Multidisciplinary, PSYCHIATRIC-DISORDERS, BIPOLAR DISORDER, Biobank, 3. Good health, AFB, Mental Health, Schizophrenia, Female, Erfðarannsóknir, Psychosocial, TRAITS, schizophrenia, age at birth, AFB, Maternal Age, Adult, age at first birth in women, genetic association, Offspring, Science, Genetic correlation, Article, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Geðklofi, Genetics, age at birth, Humans, Genetic Predisposition to Disease, Bipolar disorder, General, Biology, Genetic association study, 030304 developmental biology, Genetic association, business.industry, Genetic heterogeneity, Prevention, average aged parents, Parturition, SCORE REGRESSION, bacterial infections and mycoses, medicine.disease, Mental health, Brain Disorders, respiratory tract diseases, schizophrenia, Good Health and Well Being, 030104 developmental biology, younger and older parents, DE-NOVO MUTATIONS, ddc:000, Human medicine, business, 030217 neurology & neurosurgery, Demography

وصف الملف: pdf; application/pdf; Electronic; image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::436254c35466d6765dfc11f141722ecb
https://doi.org/10.1101/194076

المؤلفون: Paul Korrovits, Ruth Mikelsaar, Ants Kurg, Ranno Rätsep, Mari Nelis, Olga Žilina, Maie Väli

المصدر: Journal of Applied Genetics. 53:93-97

مصطلحات موضوعية: Adult, Male, Infertility, TUBA3C Gene, Inheritance Patterns, Abnormal Karyotype, Chromosomal translocation, Haploinsufficiency, Biology, Polymorphism, Single Nucleotide, Genomic Instability, Translocation, Genetic, Male infertility, Abnormal sperm morphology, Tubulin, Chromosome Duplication, Gene duplication, Genetics, medicine, Humans, Infertility, Male, Sperm motility, Chromosomes, Human, Pair 13, Sperm Count, Rhinitis, Allergic, Seasonal, General Medicine, medicine.disease, Spermatozoa, Sperm Motility, Chromosomes, Human, Pair 5, Chromosomes, Human, Pair 9

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94573be3965c8fcb6841092f3c22a88e
https://doi.org/10.1007/s13353-011-0078-5

المؤلفون: Vilmundur Gudnason, Robert J. Weyant, Robert C. Kaplan, Jeffrey R. O'Connell, Panos Deloukas, Barbara McKnight, Alessandro De Grandi, Gert-Jan B. van Ommen, Eric Boerwinkle, Liming Liang, Douglas F. Levinson, Richard B. Hayes, Mark I. McCarthy, Andrew P. Morris, Joel N. Hirschhorn, Jaakko Kaprio, Nilesh J. Samani, Inke R. König, Frank B. Hu, Nicholas J. Wareham, Ozren Polasek, Michael C. Turchin, Daniel F. Gudbjartsson, Wilmar Igl, Vincent Mooser, Aki S. Havulinna, Themistocles L. Assimes, Cameron D. Palmer, Lachlan J. M. Coin, Eva Albrecht, Hana Lango Allen, Inês Barroso, Eco J. C. de Geus, H.-Erich Wichmann, Michael A. Province, Sarah H. Wild, Patricia B. Munroe, Jeanette Erdmann, Mattias Lorentzon, Michael Preuss, Nelson B. Freimer, Mika Kähönen, Tushar Bhangale, Nicole L. Glazer, Markku S. Nieminen, Andrew A. Hicks, Jonathan Tyrer, Grant W. Montgomery, Ruth J. F. Loos, Shaun Purcell, Manfred Kayser, Marjo-Riitta Järvelin, Guillaume Paré, Terho Lehtimäki, Irene Pichler, Ida Surakka, Tõnu Esko, Peter Kraft, Talin Haritunians, Juha Sinisalo, Mari Nelis, Veronique Vitart, Alan R. Sanders, Alistair S. Hall, Carlos Iribarren, Mark E. Cooper, André G. Uitterlinden, Peter Kovacs, David Schlessinger, Florian Ernst, Marja-Liisa Lokki, M. Juhani Junttila, Martin Ridderstråle, Jorma Viikari, Inga Prokopenko, Christopher J. O'Donnell, Jennie Hui, Aila Rissanen, Gonçalo R. Abecasis, Jouke-Jan Hottenga, Tomi Pastinen, Kevin B. Jacobs, Jan Smit, Kristin G. Ardlie, Niina Pellikka, Neil R. Robertson, Martina Müller, John F. Peden, Mary F. Feitosa, Thomas W. Winkler, Kari Stefansson, Jianjun Liu, Jaana Laitinen, Shen Haiqing, Martin Farrall, Nilanjan Chatterjee, Eleanor Wheeler, Tamara B. Harris, Åsa Johansson, Anders Hamsten, Elizabeth K. Speliotes, Larry D. Atwood, Valgerdur Steinthorsdottir, Elin Grundberg, Nicole Soranzo, Anna-Liisa Hartikainen, Devin Absher, Cecilia M. Lindgren, Rany M. Salem, Lorena Citterio, Karol Estrada, Sven Bergmann, Tony Kwan, Thomas Meitinger, Alan F. Wright, Richard N. Bergman, Sailaja Vedantam, Kirsi H. Pietiläinen, Lina Zgaga, Anne U. Jackson, Stefan Schreiber, Ju-Hyun Park, Nicola Glorioso, Jianxin Shi, Najaf Amin, Dale R. Nyholt, Lenore J. Launer, Heribert Schunkert, Thomas Quertermous, Mari Liis Tammesoo, Dorret I. Boomsma, Harry Campbell, Albert V. Smith, Andrew R. Wood, Caroline S. Fox, Paavo Zitting, Gabrielle Boucher, Alex N. Parker, Jennifer G. Sambrook, Joyce B. J. van Meurs, Heather M. Stringham, Marjolein J. Peters, Sekar Kathiresan, Elisabeth Widen, Caroline Hayward, Tim D. Spector, Dawn M. Waterworth, Carlo Rivolta, Antti Jula, Albert Hofman, Hugh Watkins, Wendy L. McArdle, Roberto Elosua, Markku Koiranen, Paul M. Ridker, Iris M. Heid, Lee M. Kaplan, Brenda W.J.H. Penninx, Peter M. Visscher, Claes Ohlsson, Per Hall, Benjamin F. Voight, Ben A. Oostra, Anna F. Dominiczak, Martin den Heijer, Andrea Maschio, Quince Gibson, Peter P. Pramstaller, Nigel W. Rayner, Carsten Oliver Schmidt, Toby Johnson, Henrik Grönberg, M. Carola Zillikens, Alan R. Shuldiner, Cornelia M. van Duijn, Samuli Ripatti, Erik Ingelsson, John R. Thompson, Stephen J. Chanock, Johannes Kettunen, David J. Hunter, Lyle J. Palmer, Ulf Gyllensten, Jianfeng Xu, Astrid Petersmann, Johan G. Eriksson, Guillaume Lettre, Teresa Ferreira, Fredrik Wiklund, Andreas Ziegler, Andres Metspalu, Jerome I. Rotter, Suzanne Rafelt, Julius S. Ngwa, Francis S. Collins, Michael N. Weedon, Thomas Illig, Wolfgang Hoffman, Nancy L. Heard-Costa, Anke Tönjes, Daniel I. Chasman, Alice M. Arnold, Olli T. Raitakari, Anna L. Dixon, Lu Qi, Michael E. Goddard, Anneli Pouta, Mark J. Caulfield, Liesbeth Vandenput, Christian Gieger, L. Adrienne Cupples, Veikko Salomaa, Elizabeth L. Altmaier, Nicholas G. Martin, Thomas D. Kocher, Jubao Duan, David S. Siscovick, Heikki V. Huikuri, Willem H. Ouwehand, Kari E. North, Christian Hengstenberg, Jacques S. Beckmann, Constance Chen, John Perry, Ana Marušić, Olle Melander, John D. Rioux, Erika Salvi, Andrew T. Hattersley, Paul Elliott, Leif Groop, Cristen J. Willer, Manuela Uda, Gudmar Thorleifsson, Eric E. Schadt, Charles C. White, Pablo V. Gejman, Serena Sanna, Ulla Sovio, Robert W. Lawrence, Unnur Thorsteinsdottir, Ayellet V. Segrè, Daniele Cusi, G. Bragi Walters, Ken Sin Lo, Ivana Kolcic, Igor Rudan, Sonja I. Berndt, Keri L. Monda, Soumya Raychaudhuri, Jian'an Luan, Joshua C. Randall, Anthony J. Balmforth, Yurii S. Aulchenko, Peter Almgren, Karen L. Mohlke, Timothy M. Frayling, Shamika Ketkar, Thomas H. Mosley, Markus Perola, Henry Völzke, Laura Zagato, Leena Peltonen, Seppo Koskinen, Massimo Mangino, Ke Hao, Tsegaselassie Workalemahu, Lambertus A. Kiemeney, Helene Alavere, Jaakko Tuomilehto, Reedik Mägi, James F. Wilson, Ingrid B. Borecki, Zoltán Kutalik, Michael Stumvoll, Dominique J. Verlaan, Arthur W. Musk, Eero Kajantie, Jian Yang, Joshua W. Knowles, Tuomas O. Kilpeläinen, Michael Boehnke, G. Mark Lathrop, John Beilby, Fernando Rivadeneira, Gudny Eiriksdottir, Gonneke Willemsen, Andrew C. Heath, Antonella Mulas, Katja K.H. Aben, David P. Strachan, Thor Aspelund, Jing Hua Zhao

المساهمون: Psychiatry, NCA - Anxiety & Depression, EMGO - Mental health, Internal Medicine, Epidemiology, Intensive Care, Clinical Genetics, Genetic Identification, Medical Research Council (MRC), Biological Psychology, Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Mental Health, Genetics of Complex Traits, University of Exeter, Department of Epidemiology, Erasmus Medical Centre, Netherlands Genomics Initiative (NGI), Netherlands Genomics Initiative, Department of Medicine, Montreal, National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH), Department of Biostatistics, University of Michigan [Ann Arbor], University of Michigan System-University of Michigan System, deCODE Genetics, deCODE genetics [Reykjavik], Divisions of Genetics and Endocrinology and Program in Genomics, Boston Children's Hospital, Metabolism Initiative and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston]-Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Institut de Génomique d'Evry (IG), Institut de Biologie François JACOB (JACOB), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, the Genetic Investigation of ANthropocentric Traits (GIANT) Consortium, Université Paris-Saclay-Institut de Biologie François JACOB (JACOB), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)

المصدر: Nature
Nature; Vol 467
Nature, 467, 7317, pp. 832-8
Nature, 467, 832-8
Nature, 467(7317), 832-838. Nature Publishing Group
Lango Allen, H, Estrada, K, Lettre, G, Berndt, S I, Weedon, M N, Rivadeneira, F, Hottenga, J J, de Geus, E J C, Willemsen, G, van Ommen, G J B, Martin, N G, Montgomery, GW, Boomsma, D I, Penninx, B W J H, van Duijn, C M, Peltonen, L, Visscher, P M, Uitterlinden, A G, Abecasis, G R, Stefansson, H, Frayling, T M & Hirschhorn, J N 2010, ' Hundreds of variants clustered in genomic loci and biological pathways affect human height ', Nature, vol. 467, no. 7317, pp. 832-838 . https://doi.org/10.1038/nature09410
Nature, 467(7317), 832-838
Nature, Nature Publishing Group, 2010, 467 (7317), pp.832-838. ⟨10.1038/nature09410⟩
Nature, 2010, 467 (7317), pp.832-838. ⟨10.1038/nature09410⟩

مصطلحات موضوعية: Netherlands Twin Register (NTR), Multifactorial Inheritance, [SDV]Life Sciences [q-bio], Genome-wide association study, Aetiology, screening and detection [ONCOL 5], 0302 clinical medicine, POPULATION, SNPS, Genetics, 0303 health sciences, Multidisciplinary, HERITABILITY, COMMON VARIANTS, Phenotype, DISEASES, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Science & Technology - Other Topics, GROWTH, Allelic heterogeneity, Chromosomes, Human, Pair 3, Metabolic Networks and Pathways, TRAITS, Common disease-common variant, General Science & Technology, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Molecular epidemiology [NCEBP 1], 03 medical and health sciences, SDG 3 - Good Health and Well-being, ADULT, STRATIFICATION, MD Multidisciplinary, Humans, Genetic Predisposition to Disease, Genetic variability, 030304 developmental biology, Science & Technology, MULTIDISCIPLINARY SCIENCES, Genome, Human, Hormonal regulation [IGMD 6], Body Height, Genetic architecture, wide association analysis common variants heritability population adult stratification diseases traits growth snps, WIDE ASSOCIATION ANALYSIS, Genetic Loci, Evaluation of complex medical interventions [NCEBP 2], Polygene, Expression quantitative trait loci, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d493384b4f86f521131ee5b11d9b22c
https://doi.org/10.1038/nature09410

المؤلفون: Gerhard Steinbeck, John Barnard, Dan M. Roden, Tamara B. Harris, Calum A. MacRae, Moritz F. Sinner, David R. Van Wagoner, Lenore J. Launer, Seiko Makino, Eric J. Topol, Siegfried Perz, Thomas J. Wang, Aravinda Chakravarti, Ke Wang, Kathryn L. Lunetta, Markus M. Nöthen, Mina K. Chung, Elsayed Z. Soliman, Stefan Kääb, David J. Milan, Mari Nelis, Stanley L. Hazen, Arne Pfeufer, Thomas Meitinger, Daniel Levy, Dawood Darbar, Susanne Moebus, Andres Metspalu, Jacqueline C.M. Witteman, Vilmundur Gudnason, Jonathan D. Smith, Albert Hofman, Anna Köttgen, Susan R. Heckbert, Paul I.W. de Bakker, Emelia J. Benjamin, Kenneth Rice, Britt-M. Beckmann, Ramachandran S. Vasan, Charlotte van Noord, Eric Boerwinkle, Stefan Möhlenkamp, Martina Mueller, Bruce M. Psaty, Alvaro Alonso, Dan E. Arking, H.-Erich Wichmann, Christopher Newton-Cheh, Man Li, Nicole L. Glazer, André G. Uitterlinden, Georg Ehret, Tõnu Esko, Bruno H. Stricker, Nicholas L. Smith, W. H. Linda Kao, Albert V. Smith, Steven A. Lubitz, Jerome I. Rotter, Patrick T. Ellinor, Renate B. Schnabel, Ervin R. Fox

المساهمون: Epidemiology, Internal Medicine

المصدر: Nature genetics
Nature Genetics, 42(3), 240-U36. Nature Publishing Group

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Heart disease, Small-Conductance Calcium-Activated Potassium Channels, Medizin, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Article, Cohort Studies, Young Adult, Meta-Analysis as Topic, Polymorphism (computer science), Internal medicine, Atrial Fibrillation, Genetics, medicine, Humans, Aged, Genetic association, Case-control study, Atrial fibrillation, Odds ratio, Middle Aged, medicine.disease, Introns, Endocrinology, Case-Control Studies, Cardiology, Female, Genome-Wide Association Study, Cohort study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91baa4deeb9a00a9d45d45cefa9ed171
https://doi.org/10.1038/ng.537

المؤلفون: Kristina Kjærheim, Patricia A. McKinney, Simone Benhamou, Franco Merletti, Antonio Agudo, Cristina Canova, Alena Slamova, B. E. McCartan, Xavier Castellsagué, Gary J. Macfarlane, Renato Talamini, Paul Brennan, Miriam Schejbalova, Pagona Lagiou, Lorenzo Richiardi, Ray Lowry, Christina Georgila, Andres Metspalu, Luigi Barzan, Lorenzo Simonato, Wolfgang Ahrens, Hermann Pohlabeln, Mari Nelis, P. Minaki, David I. Conway, Claire M. Healy, Tatiana V. Macfarlane, Manuela Marron, Mia Hashibe, Christine Bouchardy, Ariana Znaor

المصدر: European Journal of Cancer Prevention, Vol. 18, No 1 (2009) pp. 76-84

مصطلحات موضوعية: Adult, Male, Oncology, Cancer Research, medicine.medical_specialty, Pathology, Alcohol Drinking, Epidemiology, Single-nucleotide polymorphism, Head and Neck Neoplasms/etiology/genetics, Internal medicine, Genetic variation, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Esophagus, Life Style, ddc:613, Aged, Aged, 80 and over, business.industry, Data Collection, Pharynx, Public Health, Environmental and Occupational Health, Case-control study, Cancer, upper aerodigestive cancers, case-control study, Middle Aged, Esophageal cancer, Alcohol Drinking/adverse effects/genetics, medicine.disease, Europe, stomatognathic diseases, medicine.anatomical_structure, Head and Neck Neoplasms, Case-Control Studies, Carcinoma, Squamous Cell/etiology/genetics, Carcinoma, Squamous Cell, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ceda645f49b3d495bff063f30cecf47
https://doi.org/10.1097/cej.0b013e32830c8dca

المؤلفون: Konstantinos Aliferis, David Neil Cooper, Stefania Gimelli, E. Kanavakis, Lorraine Gwanmesia, Sofia Kitsiou-Tzeli, Abdelaziz Sefiani, Frédérique Béna, Habiba Chaabouni Bouhamed, Helen Fryssira, Samia A. Temtamy, Stavroula Psoni, Nasir A. S. Al-Allawi, Hanan Hamamy, Georgios Stamoulis, Nadine Jalkh, André Mégarbané, Ebtesam M. Abdalla, Stylianos E. Antonarakis, Mari Nelis, Siham Chafai Elalaoui, Periklis Makrythanasis, Amira Masri, Siv Fokstuen, Lihadh Al-Gazali, Sana' Al Hait, Mariana Bustamante Eduardo, Michel Guipponi, Anne Vannier, Armand Bottani, Maha S. Zaki, Fatma Al-Jasmi, Federico Santoni, Mona Aglan, Elisavet Stathaki

المصدر: Human Mutation, Vol. 35, No 10 (2014) pp. 1203-10
HUMAN MUTATION

مصطلحات موضوعية: Adult, Male, Adolescent, Genes, Recessive, Consanguinity, Biology, DNA sequencing, Young Adult, 03 medical and health sciences, Rare Diseases, Genotype, Genetics, Humans, Exome, ddc:576.5, Child, Genetics (clinical), Exome sequencing, 030304 developmental biology, 0303 health sciences, 030305 genetics & heredity, Infant, Sequence Analysis, DNA, Disease gene identification, Arabs, Pedigree, 3. Good health, Child, Preschool, Female, SNP array, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe6dc06e32afdde6c2e01a74f3d03145
https://archive-ouverte.unige.ch/unige:42302

المؤلفون: Keri L. Monda, Caroline S. Fox, David P. Strachan, Henri Wallaschofski, M. Carola Zillikens, Andres Metspalu, Tit Nikopensius, Sabine Schipf, Zhaoming Wang, Cornelia M. van Duijn, Richard B. Hayes, Audrey C. Choh, Mariaelisa Graff, Henry Völzke, Xiangjun Xiao, Cucca Francesco, Ellen W. Demerath, Carlo Sidore, Mary L. Marazita, Julius S. Ngwa, John R. Shaffer, Richard J. Crout, Penny Gordon-Larsen, Rob M. van Dam, Ben A. Oostra, Tsegaselassie Workalemahu, David Schlessinger, Lakatta Edward, Stefan A. Czerwinski, L. Adrienne Cupples, Thomas D. Dyer, Larry D. Atwood, Najaf Amin, Paul Scheet, Georg Homuth, Bradford Towne, Charles S. White, Frank B. Hu, Sonja I. Berndt, Stephen J. Chanock, Gonçalo R. Abecasis, Kari E. North, Nancy L. Heard-Costa, Lu Qi, Alexander Teumer, Serena Sanna, Mari Nelis, Tõnu Esko, Kevin B. Jacobs

المساهمون: Epidemiology, Clinical Genetics, Internal Medicine

المصدر: Human Molecular Genetics
Human Molecular Genetics, 22(17), 3597-3607. Oxford University Press
Hum. Mol. Genet. 22, 3597-3607 (2013)

مصطلحات موضوعية: Adult, Adolescent, 030209 endocrinology & metabolism, Locus (genetics), Genome-wide association study, Single-nucleotide polymorphism, Biology, Weight Gain, Polymorphism, Single Nucleotide, White People, Body Mass Index, Cohort Studies, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Genetic variation, Genetics, medicine, Humans, Young adult, 10. No inequality, Molecular Biology, Genetics (clinical), 030304 developmental biology, Genetic association, Aged, Aged, 80 and over, 0303 health sciences, Association Studies Articles, Age Factors, General Medicine, Middle Aged, medicine.disease, Obesity, Genetic Loci, Body mass index, Demography, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3548a6f08c702a527f96d56aa6e3c4bb
https://pubmed.ncbi.nlm.nih.gov/23669352

المؤلفون: Peter Vollenweider, Leena Peltonen, Audrey Labalme, Jessica L. Buxton, Alessandra Ferrarini, Dawn M. Waterworth, Sven Bergmann, Gérard Waeber, Marie Pigeyre, Sébastien Jacquemont, Vincent Mooser, Audrey Guilmatre, C. Lecoeur, Muriel Holder-Espinasse, Bettina Blaumeiser, Elena G. Bochukova, Ni Huang, Andrew Walley, Danielle Martinet, Peter Jacobson, B. Leheup, Marie-Pierre Lemaitre, A. Brioschi, Julia M. Keogh, Damien Sanlaville, Stephen O'Rahilly, Robert Sladek, Bruno Delobel, Fanny Stutzmann, Sophie Dupuis-Girod, Philippe Froguel, Muriel Gaillard, Anne Philippe, Katrin Männik, Jean-Marie Cuisset, M. Béri-Dexheimer, Lachlan J. M. Coin, Fei Chen, François Pattou, Katrin Õunap, Mari Nelis, A.-L. Hartikainen, Jean-Claude Chèvre, Philippe Jonveaux, Alice Goldenberg, Kay D. MacDermot, Elana Henning, Odile Boute, Sonia Bouquillon, Armand Valsesia, Valérie Malan, Stéphane Lobbens, R. F. Kooy, Alexandra I. F. Blakemore, Marie-Pierre Cordier, Lena M. S. Carlsson, Marjo-Riitta Järvelin, Lars Sjöström, Paul Elliott, C Le Caignec, Florence Fellmann, Nadège Calmels, Dominique Campion, M. M. van Haelst, Vincent Vatin, B. Balkau, Jacques S. Beckmann, Mark I. McCarthy, Robert Caiazzo, Jean-Louis Mandel, Joris Andrieux, Nouchine Hadjikhani, Catherine Vincent-Delorme, David Meyre, Ants Kurg, J. S. El-Sayed Moustafa, Johanna C. Andersson, Jean Chiesa, Michèle Mathieu-Dramard, R. Touraine, Tõnu Esko, Albert David, Alexandre Reymond, Priit Palta, Ghislaine Plessis, Andres Metspalu, Robin G. Walters, Vittorio Giusti, Richard J. Ellis, Bertrand Isidor, Anne-Emmanuelle Ambresin, A J de Smith, I. S. Farooqi, Matthew E. Hurles, Mario Falchi

المساهمون: Medical Research Council (MRC), Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Other departments

المصدر: Nature, 463(7281), 671-5. Nature Publishing Group
Nature
Nature, vol. 463, no. 7281, pp. 671-675
Nature; Vol 463
Walters, R G, Jacquemont, S, Valsesia, A, de Smith, A J, Martinet, D, Andersson, J, Falchi, M, Chen, F, Andrieux, J, Lobbens, S, Delobel, B, Stutzmann, F, El-Sayed Moustafa, J S, Chèvre, J-C, Lecoeur, C, Vatin, V, Bouquillon, S, Buxton, J L, Boute, O, Holder-Espinasse, M, Cuisset, J-M, Lemaitre, M-P, Ambresin, A-E, Brioschi, A, Gaillard, M, Giusti, V, Fellmann, F, Ferrarini, A, Hadjikhani, N, Campion, D, Guilmatre, A, Goldenberg, A, Calmels, N, Mandel, J-L, Le Caignec, C, David, A, Isidor, B, Cordier, M-P, Dupuis-Girod, S, Labalme, A, Sanlaville, D, Béri-Dexheimer, M, Jonveaux, P, Leheup, B, Ounap, K, Bochukova, E G, Henning, E, Keogh, J, Ellis, R J, Macdermot, K D, van Haelst, M M, Vincent-Delorme, C, Plessis, G, Touraine, R, Philippe, A, Malan, V, Mathieu-Dramard, M, Chiesa, J, Blaumeiser, B, Kooy, R F, Caiazzo, R, Pigeyre, M, Balkau, B, Sladek, R, Bergmann, S, Mooser, V, Waterworth, D, Reymond, A, Vollenweider, P, Waeber, G, Kurg, A, Palta, P, Esko, T, Metspalu, A, Nelis, M, Elliott, P, Hartikainen, A-L, McCarthy, M I, Peltonen, L, Carlsson, L, Jacobson, P, Sjöström, L, Huang, N, Hurles, M E, O'Rahilly, S, Farooqi, I S, Männik, K, Jarvelin, M-R, Pattou, F, Meyre, D, Walley, A J, Coin, L J M, Blakemore, A I F, Froguel, P & Beckmann, J S 2010, ' A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 ', Nature, vol. 463, no. 7281, pp. 671-5 . https://doi.org/10.1038/nature08727
Nature, 463(7281), 671-U104. Nature Publishing Group

مصطلحات موضوعية: Male, Aging, SAMPLE, Inheritance Patterns, Genome-wide association study, Penetrance, MC4R, Body Mass Index, Cohort Studies, 0302 clinical medicine, SH2B1, Missing heritability problem, Age of Onset, Child, 2. Zero hunger, Genetics, 0303 health sciences, education.field_of_study, Sex Characteristics, Multidisciplinary, Mental-Retardation, Adolescent Adult Age of Onset Aging Body Mass Index Case-Control Studies Child *Chromosome Deletion Chromosomes, Human, Pair 16/*genetics Cognition Disorders/complications/genetics Cohort Studies Europe Female Genome-Wide Association Study Heterozygote Humans Inheritance Patterns/genetics Male Mutation/genetics Obesity/complications/*genetics/*physiopathology *Penetrance Reproducibility of Results Sex Characteristics Young Adult, 3. Good health, Multidisciplinary Sciences, Europe, Adolescent, Adult, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 16/genetics, Cognition Disorders/complications, Cognition Disorders/genetics, Female, Genome-Wide Association Study, Heterozygote, Humans, Inheritance Patterns/genetics, Mutation/genetics, Obesity/complications, Obesity/genetics, Obesity/physiopathology, Reproducibility of Results, Young Adult, Medical genetics, Science & Technology - Other Topics, CHILDHOOD OBESITY, medicine.medical_specialty, Childhood Obesity, BIRTH, General Science & Technology, Population, Single-nucleotide polymorphism, Biology, Article, Childhood obesity, 03 medical and health sciences, medicine, MICRODELETION, Obesity, GENOME-WIDE ASSOCIATION, AUTISM, education, 030304 developmental biology, COPY NUMBER VARIATION, Science & Technology, MULTIDISCIPLINARY SCIENCES, FRAMESHIFT MUTATION, Individuals, medicine.disease, RISK LOCI, INDIVIDUALS, CIRCULAR BINARY SEGMENTATION, Mutation, Human medicine, Cognition Disorders, MENTAL-RETARDATION, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 16

وصف الملف: application/pdf; pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35a49847e321d4ca01f15aef737ad7d
http://ora.ox.ac.uk/objects/uuid:f0001a16-0ea7-4f93-a4a3-7fe79cafe6ed