Search Results

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

by Huckins, L. M. (Laura M.), Dobbyn, A. (Amanda), Ruderfer, D. M. (Douglas M.), Hoffman, G. (Gabriel), Wang, W. (Weiqing), Pardiñas, A. (Antonio), Rajagopal, V. M. (Veera M.), Als, T. D. (Thomas D.), Nguyen, H. (Hoang), Girdhar, K. (Kiran), Boocock, J. (James), Roussos, P. (Panos), Fromer, M. (Menachem), Kramer, R. (Robin), Domencini, E. (Enrico), Gamazon, E. (Eric), Purcell, S. (Shaun), C. C. (CommonMind Consortium), T. S. (The Schizophrenia Working Group of the Psychiatric Genomics Consortium), i. S. (iPSYCH-GEMS Schizophrenia Working Group), Demontis, D. (Ditte), Børglum, A. D. (Anders D.), Walters, J. T. (James T. R.), O'Donovan, M. C. (Michael C.), Sullivan, P. (Patrick), Owen, M. J. (Michael J.), Devlin, B. (Bernie), Sieberts, S. K. (Solveig K.), Cox, N. J. (Nancy J.), Im, H. K. (Hae Kyung), Sklar, P. (Pamela), Stahl, E. A. (Eli A.)
Published 2019

Age at first birth in women is genetically associated with increased risk of schizophrenia

by Ni, G. (Guiyan), Gratten, J. (Jacob), Wray, N. R. (Naomi R.), Lee, S. H. (Sang Hong), S. W. (Schizophrenia Working Group of the Psychiatric Genomics Consortium)
Published 2018

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Mathieu, Alexandre, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Mathieu, Alexandre, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Alexandre, Mathieu, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Alexandre, Mathieu, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Alexandre, Mathieu, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Alexandre, Mathieu, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Alexandre, Mathieu, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

Hair cortisol in twins:heritability and genetic overlap with psychological variables and stress-system genes

by Rietschel, L. (Liz), Streit, F. (Fabian), Zhu, G. (Gu), McAlone, K. (Kerrie), Frank, J. (Josef), Couvy-Duchesne, B. (Baptiste), Witt, S. H. (Stephanie H.), Binz, T. M. (Tina M.), McGrath, J. (John), Hickie, I. B. (Ian B.), Hansel, N. K. (Narelle K.), Wright, M. J. (Margaret J.), Gillespie, N. A. (Nathan A.), Forstner, A. J. (Andreas J.), Schulze, T. G. (Thomas G.), Wüst, S. (Stefan), Nöthen, M. M. (Markus M.), Baumgartner, M. R. (Markus R.), Walker, B. R. (Brian R.), Crawford, A. A. (Andrew A.), Colodro-Conde, L. (Lucía), Medland, S. E. (Sarah E.), Martin, N. G. (Nicholas G.), Rietschel, M. (Marcella)
Published 2017