المؤلفون: Consortium, Cross-Disorder Group of the Psychiatric Genomics, Lee, Phil H, Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A, Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M, Nivard, Michel G, Grotzinger, Andrew D, Posthuma, Danielle, Wang, Meg M-J, Yu, Dongmei, Stahl, Eli A, Walters, Raymond K, Anney, Richard JL, Duncan, Laramie E, Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H, Coppola, Giovanni, Derks, Eske M, Hoekstra, Pieter J, Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George, Kranzler, Henry R, Luykx, Jurjen J, Rohde, Luis A, Zai, Clement C, Agerbo, Esben, Arranz, MJ, Asherson, Philip, Bækvad-Hansen, Marie, Baldursson, Gísli, Bellgrove, Mark, Belliveau, Richard A, Buitelaar, Jan, Burton, Christie L, Bybjerg-Grauholm, Jonas, Casas, Miquel, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Cormand, Bru, Crosbie, Jennifer, Dalsgaard, Søren, Demontis, Ditte, Doyle, Alysa E, Dumont, Ashley, Elia, Josephine, Grove, Jakob, Gudmundsson, Olafur O, Haavik, Jan, Hakonarson, Hakon, Hansen, Christine S, Hartman, Catharina A, Hawi, Ziarih, Hervás, Amaia, Hougaard, David M, Howrigan, Daniel P, Huang, Hailiang, Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Leung, Patrick WL, Loo, Sandra K, Martin, Joanna, Martin, Alicia R, McGough, James J, Medland, Sarah E, Moran, Jennifer L, Mors, Ole, Mortensen, Preben B, Oades, Robert D, Palmer, Duncan S, Pedersen, Carsten B, Pedersen, Marianne G, Peters, Triinu, Poterba, Timothy, Poulsen, Jesper B, Ramos-Quiroga, Josep Antoni, Reif, Andreas, Ribasés, Marta, Rothenberger, Aribert, Rovira, Paula, Sánchez-Mora, Cristina, Satterstrom, F Kyle, Schachar, Russell, Artigas, Maria Soler, Steinberg, Stacy, Stefansson, Hreinn, Turley, Patrick, Walters, G Bragi, Team, 23andMe Research, Werge, Thomas, Zayats, Tetyana, Arking, Dan E

المصدر: Cell. 179(7)

مصطلحات موضوعية: Neurosciences, Serious Mental Illness, Human Genome, Schizophrenia, Intellectual and Developmental Disabilities (IDD), Brain Disorders, Genetics, Pediatric, Mental Health, Aetiology, 2.1 Biological and endogenous factors, Mental health, Genetic Pleiotropy, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Mental Disorders, Neurogenesis, Quantitative Trait Loci, Cross-Disorder Group of the Psychiatric Genomics Consortium. Electronic address: plee0@mgh.harvard.edu, Cross-Disorder Group of the Psychiatric Genomics Consortium, GWAS, Psychiatric genetics, cross-disorder genetics, functional genomics, gene expression, genetic architecture, genetic correlation, neurodevelopment, pleiotropy, psychiatric disorders, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/98t749xkTest

المؤلفون: Huckins, Laura M, Dobbyn, Amanda, Ruderfer, Douglas M, Hoffman, Gabriel, Wang, Weiqing, Pardiñas, Antonio F, Rajagopal, Veera M, Als, Thomas D, T. Nguyen, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R, Purcell, Shaun, Demontis, Ditte, Børglum, Anders D, Walters, James TR, O’Donovan, Michael C, Sullivan, Patrick, Owen, Michael J, Devlin, Bernie, Sieberts, Solveig K, Cox, Nancy J, Im, Hae Kyung, Sklar, Pamela, Stahl, Eli A

المصدر: Nature Genetics. 51(6)

مصطلحات موضوعية: Genetics, Neurosciences, Human Genome, Serious Mental Illness, Schizophrenia, Brain Disorders, Mental Health, Biotechnology, Mental health, CommonMind Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, iPSYCH-GEMS Schizophrenia Working Group, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/9t37j22rTest

المؤلفون: Huckins, Laura M, Dobbyn, Amanda, Ruderfer, Douglas M, Hoffman, Gabriel, Wang, Weiqing, Pardiñas, Antonio F, Rajagopal, Veera M, Als, Thomas D, T. Nguyen, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R, Purcell, Shaun, Demontis, Ditte, Børglum, Anders D, Walters, James TR, O’Donovan, Michael C, Sullivan, Patrick, Owen, Michael J, Devlin, Bernie, Sieberts, Solveig K, Cox, Nancy J, Im, Hae Kyung, Sklar, Pamela, Stahl, Eli A

المصدر: Nature Genetics. 51(4)

مصطلحات موضوعية: Biological Sciences, Genetics, Mental Health, Brain Disorders, Human Genome, Schizophrenia, 2.1 Biological and endogenous factors, Aetiology, Mental health, Brain, Case-Control Studies, Gene Expression, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Risk, Transcriptome, CommonMind Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, iPSYCH-GEMS Schizophrenia Working Group, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

الوصول الحر: https://escholarship.org/uc/item/3gm5c2wpTest

المؤلفون: Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H, Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L, Goldstein, Jacqueline I, Hansen, Christine S, Hauberg, Mads Engel, Hollegaard, Mads V, Hope, Sigrun, Howrigan, Daniel P, Huang, Hailiang, Hultman, Christina M, Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R, Moran, Jennifer L, Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S, Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B, Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R, Sullivan, Patrick F, Turley, Patrick, Walters, G Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M, Daly, Mark J, Børglum, Anders D

المصدر: Nature Genetics. 51(3)

مصطلحات موضوعية: Intellectual and Developmental Disabilities (IDD), Human Genome, Pediatric, Brain Disorders, Autism, Biotechnology, Genetics, Mental Health, Prevention, 2.3 Psychological, social and economic factors, Aetiology, 2.1 Biological and endogenous factors, Mental health, Adolescent, Autism Spectrum Disorder, Case-Control Studies, Child, Child, Preschool, Denmark, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Multifactorial Inheritance, Phenotype, Polymorphism, Single Nucleotide, Risk Factors, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4k2655gbTest

المؤلفون: Demontis, Ditte, Walters, Raymond K, Martin, Joanna, Mattheisen, Manuel, Als, Thomas D, Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I, Grasby, Katrina L, Grove, Jakob, Gudmundsson, Olafur O, Hansen, Christine S, Hauberg, Mads Engel, Hollegaard, Mads V, Howrigan, Daniel P, Huang, Hailiang, Maller, Julian B, Martin, Alicia R, Martin, Nicholas G, Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B, Satterstrom, F Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G Bragi, Won, Hyejung, Wright, Margaret J, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Andreassen, Ole A, Asherson, Philip, Burton, Christie L, Boomsma, Dorret I, Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R, Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund JS, Sullivan, Patrick F, Thapar, Anita, Tung, Joyce Y, Waldman, Irwin D, Medland, Sarah E, Stefansson, Kari, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J, Faraone, Stephen V, Børglum, Anders D, Neale, Benjamin M

المصدر: Nature genetics. 51(1)

مصطلحات موضوعية: ADHD Working Group of the Psychiatric Genomics Consortium, Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Brain, Humans, Genetic Predisposition to Disease, Risk, Cohort Studies, Attention Deficit Disorder with Hyperactivity, Gene Expression Regulation, Polymorphism, Single Nucleotide, Adolescent, Child, Child, Preschool, Female, Male, Genome-Wide Association Study, Genetic Loci, Clinical Research, Mental Health, Human Genome, Pediatric, Prevention, Genetics, Brain Disorders, Attention Deficit Hyperactivity Disorder (ADHD), Behavioral and Social Science, Aetiology, 2.1 Biological and endogenous factors, Mental health, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3bc6r12sTest

المؤلفون: Rajagopal, Veera M., Duan, Jinjie, Vilar-Ribo, Laura, Grove, Jakob, Zayats, Tetyana, Antoni Ramos-Quiroga, J., Satterstrom, F. Kyle, Soler Artigas, Maria, Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Als, Thomas D., Rosengren, Anders, Daly, Mark J., Neale, Benjamin M., Nordentoft, Merete, Werge, Thomas, Mors, Ole, Hougaard, David M., Mortensen, Preben B., Ribases, Marta, Borglum, Anders D., Demontis, Ditte

المساهمون: Institute for Molecular Medicine Finland, University of Helsinki

مصطلحات موضوعية: DEFICIT/HYPERACTIVITY DISORDER, ENVIRONMENTAL-INFLUENCES, GENOME, ADHD, ASSOCIATION, RISK, HERITABILITY, TRAJECTORIES, EVOLUTION, SEVERITY, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: D.D. was supported by the Novo Nordisk Foundation (NNF20OC0065561) and the Lundbeck Foundation (R344-2020-1060). The iPSYCH team was supported by grants from the Lundbeck Foundation (R102-A9118, R155-2014-1724 and R248-2017-2003), the EU FP7 Program (grant number 602805, 'Aggressotype') and H2020 Program (grant number 667302, 'CoCA'), National Institute of Mental Health (1U01MH109514-01 to A.D.B.) and the universities and university hospitals of Aarhus and Copenhagen. The Danish National Biobank resource was supported by the Novo Nordisk Foundation. High-performance computer capacity for handling and statistical analysis of iPSYCH data at the GenomeDK high-performance computer facility was provided by the Center for Genomics and Personalized Medicine and the Centre for Integrative Sequencing, iSEQ, Aarhus University, Denmark (grant to A.D.B.). M.S.A. is a recipient of a Juan de la Cierva Incorporacion contract from the Ministry of Science, Innovation and Universities, Spain (IJC2018-035346-I). The research leading to these results has received funding from the Instituto de Salud Carlos III (PI17/00289, PI18/01788, P19/01224 and PI20/00041) and from the Agencia de Gestio d'Ajuts Universitaris i de Recerca-AGAUR, Generalitat de Catalunya (2017SGR1461) and was cofinanced by the European Regional Development Fund. The Norwegian Mother, Father and Child Cohort Study is supported by the Norwegian Ministry of Health and Care Services and the Ministry of Education and Research. We are grateful to all the families in Norway who have taken part in this ongoing cohort study. L.V.R. is a recipient of a predoctoral fellowship from the Instituto de Salud Carlos III, Spain (FI18/00285). M.R. was a recipient of a Miguel de Servet contract from the Instituto de Salud Carlos III, Spain (CP09/00119 and CPII15/00023). T.Z. is funded by R37MH107649-07S1 and by the Research Council of Norway (grant number 288083).; Rajagopal , V M , Duan , J , Vilar-Ribo , L , Grove , J , Zayats , T , Antoni Ramos-Quiroga , J , Satterstrom , F K , Soler Artigas , M , Bybjerg-Grauholm , J , Baekvad-Hansen , M , Als , T D , Rosengren , A , Daly , M J , Neale , B M , Nordentoft , M , Werge , T , Mors , O , Hougaard , D M , Mortensen , P B , Ribases , M , Borglum , A D & Demontis , D 2022 , ' Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder ' , Nature Genetics , vol. 54 , no. 8 , pp. 1117-+ . https://doi.org/10.1038/s41588-022-01143-7Test; 6343cef8-41ec-4bc9-8dde-99cd7921e307; http://hdl.handle.net/10138/354126Test; 000836113900002

الإتاحة: http://hdl.handle.net/10138/354126Test

المؤلفون: Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagoz, Gokberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F. M., Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Borglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceronihh, Fabiola, Csepe, Valeria, Dale, Philip S., de Jong, Peter F., DeFries, John C., Demonet, Jean-Francois, Demontis, Ditte, Feng, Yu, Gordon, Scott D., Guger, Sharon L., Hayiou-Thomas, Marianna E., Hernandez-Cabrera, Juan A., Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N., Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T., Lovett, Maureen W., Lyytinen, Heikki, Martin, Nicholas G., Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J., Moll, Kristina, Monaco, Anthony P., Morgan, Angela T., Nothen, Markus M., Pausova, Zdenka, Pennell, Craig E., Pennington, Bruce F., Price, Kaitlyn M., Rajagopal, Veera M., Ramus, Franck, Richer, Louis, Simpson, Nuala H., Smith, Shelley D., Snowling, Margaret J., Stein, John, Struguuu, Lisa J., Talcott, Joel B., Tiemeier, Henning, van der Schroeff, Marc P., Verhoef, Ellen, Watkins, Kate E., Wilkinson, Margaret, Wright, Margaret J., Barr, Cathy L., Boomsma, Dorret, Carreiras, Manuel, Franken, Marie-Christine J., Gruen, Jeffrey R., Luciano, Michelle, Muller-Myhsok, Bertram, Newbury, Dianne F., Olson, Richard K., Paracchini, Silvia, Paus, Tomas, Plomin, Robert, Reilly, Sheena, Schulte-Korn, Gerd, Tomblin, J. Bruce, Bergen, Elsjevan, Whitehouse, Andrew J. O., Willcutt, Erik G., St Pourcain, Beate, Francks, Clyde, Fisher, Simon E.

المساهمون: STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Research Programs Unit, HUS Helsinki and Uusimaa Hospital District

مصطلحات موضوعية: Genome-wide association study, Language, Meta-analysis, Reading j, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: Eising , E , Mirza-Schreiber , N , de Zeeuw , E L , Wang , C A , Truong , D T , Allegrini , A G , Shapland , C Y , Zhu , G , Wigg , K G , Gerritse , M L , Molz , B , Alagoz , G , Gialluisi , A , Abbondanza , F , Rimfeld , K , van Donkelaar , M , Liao , Z , Jansen , P R , Andlauer , T F M , Bates , T C , Bernard , M , Blokland , K , Bonte , M , Borglum , A D , Bourgeron , T , Brandeis , D , Ceronihh , F , Csepe , V , Dale , P S , de Jong , P F , DeFries , J C , Demonet , J-F , Demontis , D , Feng , Y , Gordon , S D , Guger , S L , Hayiou-Thomas , M E , Hernandez-Cabrera , J A , Hottenga , J-J , Hulme , C , Kere , J , Kerr , E N , Koomar , T , Landerl , K , Leonard , G T , Lovett , M W , Lyytinen , H , Martin , N G , Martinelli , A , Maurer , U , Michaelson , J J , Moll , K , Monaco , A P , Morgan , A T , Nothen , M M , Pausova , Z , Pennell , C E , Pennington , B F , Price , K M , Rajagopal , V M , Ramus , F , Richer , L , Simpson , N H , Smith , S D , Snowling , M J , Stein , J , Struguuu , L J , Talcott , J B , Tiemeier , H , van der Schroeff , M P , Verhoef , E , Watkins , K E , Wilkinson , M , Wright , M J , Barr , C L , Boomsma , D , Carreiras , M , Franken , M-C J , Gruen , J R , Luciano , M , Muller-Myhsok , B , Newbury , D F , Olson , R K , Paracchini , S , Paus , T , Plomin , R , Reilly , S , Schulte-Korn , G , Tomblin , J B , Bergen , E , Whitehouse , A J O , Willcutt , E G , St Pourcain , B , Francks , C & Fisher , S E 2022 , ' Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people ' , Proceedings of the National Academy of Sciences of the United States of America , vol. 119 , no. 35 , e2202764119 . https://doi.org/10.1073/pnas.2202764119Test; 85136345356; d2c384c3-d52a-465e-93b5-f51c267642c9; http://hdl.handle.net/10138/354613Test; 000911585800009

الإتاحة: http://hdl.handle.net/10138/354613Test

المؤلفون: Rajagopal, Veera M., Ganna, Andrea, Coleman, Jonathan R., Allegrini, Andrea, Voloudakis, Georgios, Grove, Jakob, Als, Thomas D., Horsdal, Henriette T., Petersen, Liselotte, Appadurai, Vivek, Schork, Andrew, Buil, Alfonso, Bulik, Cynthia M., Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Hougaard, David M., Mors, Ole, Nordentoft, Merete, Werge, Thomas, Mortensen, Preben Bo, Breen, Gerome, Roussos, Panos, Plomin, Robert, Agerbo, Esben, Borglum, Anders D., Demontis, Ditte

المساهمون: Data Science Genetic Epidemiology Lab, Institute for Molecular Medicine Finland, University of Helsinki

مصطلحات موضوعية: Bipolar disorder, Genotype imputation, Whole-genome, Schizophrenia, Risk, Achievement, Biobank, Performance, Haplotypes, Depression, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: Rajagopal , V M , Ganna , A , Coleman , J R , Allegrini , A , Voloudakis , G , Grove , J , Als , T D , Horsdal , H T , Petersen , L , Appadurai , V , Schork , A , Buil , A , Bulik , C M , Bybjerg-Grauholm , J , Baekvad-Hansen , M , Hougaard , D M , Mors , O , Nordentoft , M , Werge , T , Mortensen , P B , Breen , G , Roussos , P , Plomin , R , Agerbo , E , Borglum , A D & Demontis , D 2023 , ' Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity ' , Scientific Reports , vol. 13 , no. 1 , 429 . https://doi.org/10.1038/s41598-022-26845-0Test; ORCID: /0000-0002-8147-240X/work/130152524; 116dbcba-9e39-4f7f-8c11-76acd630e7aa; http://hdl.handle.net/10138/355480Test; 000915457700014

الإتاحة: http://hdl.handle.net/10138/355480Test

المؤلفون: Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagoz, Gokberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F. M., Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Borglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceronihh, Fabiola, Csepe, Valeria, Dale, Philip S., de Jong, Peter F., DeFries, John C., Demonet, Jean-Francois, Demontis, Ditte, Feng, Yu, Gordon, Scott D., Guger, Sharon L., Hayiou-Thomas, Marianna E., Hernandez-Cabrera, Juan A., Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N., Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T., Lovett, Maureen W., Lyytinen, Heikki, Martin, Nicholas G., Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J., Moll, Kristina, Monaco, Anthony P., Morgan, Angela T., Nothen, Markus M., Pausova, Zdenka, Pennell, Craig E., Pennington, Bruce F., Price, Kaitlyn M., Rajagopal, Veera M., Ramus, Franck, Richer, Louis, Simpson, Nuala H., Smith, Shelley D., Snowling, Margaret J., Stein, John, Struguuu, Lisa J., Talcott, Joel B., Tiemeier, Henning, van der Schroeff, Marc P., Verhoef, Ellen, Watkins, Kate E., Wilkinson, Margaret, Wright, Margaret J., Barr, Cathy L., Boomsma, Dorret, Carreiras, Manuel, Franken, Marie-Christine J., Gruen, Jeffrey R., Luciano, Michelle, Muller-Myhsok, Bertram, Newbury, Dianne F., Olson, Richard K., Paracchini, Silvia, Paus, Tomas, Plomin, Robert, Reilly, Sheena, Schulte-Korn, Gerd, Tomblin, J. Bruce, Bergen, Elsjevan, Whitehouse, Andrew J. O., Willcutt, Erik G., St Pourcain, Beate, Francks, Clyde, Fisher, Simon E.

المساهمون: STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Research Programs Unit, University of Helsinki

مصطلحات موضوعية: Genome-wide association study, Language, Meta-analysis, Reading j, 1184 Genetics, developmental biology, physiology, psy, litt

العلاقة: http://hdl.handle.net/10138/354613Test

الإتاحة: http://hdl.handle.net/10138/354613Test

المؤلفون: Starnawska, Anna, Demontis, Ditte, McQuillin, Andrew, O’Brien, Niamh L., Staunstrup, Nicklas H., Mors, Ole, Nielsen, Anders L., Børglum, Anders D., Nyegaard, Mette

المساهمون: Lundbeckfonden (DK), Toyota Foundation (JP), Agnes og Poul Friis Fond

المصدر: Clinical Epigenetics ; volume 8, issue 1 ; ISSN 1868-7075 1868-7083

مصطلحات موضوعية: Genetics (clinical), Developmental Biology, Genetics, Molecular Biology

الإتاحة: https://doi.org/10.1186/s13148-016-0221-6Test