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2
Rare coding variants in ten genes confer substantial risk for schizophrenia. 미리보기

학술저널

issue
Nature. 604(7906)
Author
Singh, Tarjinder
Poterba, Timothy
Curtis, David
Akil, Huda
Al Eissa, Mariam
Barchas, Jack D
Bass, Nicholas
Bigdeli, Tim B
Breen, Gerome
Bromet, Evelyn J
Buckley, Peter F
Bunney, William E
Bybjerg-Grauholm, Jonas
Byerley, William F
Chapman, Sinéad B
Chen, Wei J
Churchhouse, Claire
Craddock, Nicholas
Cusick, Caroline M
DeLisi, Lynn
Dodge, Sheila
Escamilla, Michael A
Eskelinen, Saana
Fanous, Ayman H
Faraone, Stephen V
Fiorentino, Alessia
Francioli, Laurent
Gabriel, Stacey B
Gage, Diane
Gagliano Taliun, Sarah A
Ganna, Andrea
Genovese, Giulio
Glahn, David C
Grove, Jakob
Hall, Mei-Hua
Hämäläinen, Eija
Heyne, Henrike O
Holi, Matti
Hougaard, David M
Howrigan, Daniel P
Huang, Hailiang
Hwu, Hai-Gwo
Kahn, René S
Kang, Hyun Min
Karczewski, Konrad J
Kirov, George
Knowles, James A
Lee, Francis S
Lehrer, Douglas S
Lescai, Francesco
Malaspina, Dolores
Marder, Stephen R
McCarroll, Steven A
McIntosh, Andrew M
Medeiros, Helena
Milani, Lili
Morley, Christopher P
Morris, Derek W
Mortensen, Preben Bo
Myers, Richard M
Nordentoft, Merete
O'Brien, Niamh L
Olivares, Ana Maria
Ongur, Dost
Ouwehand, Willem H
Palmer, Duncan S
Paunio, Tiina
Quested, Digby
Rapaport, Mark H
Rees, Elliott
Rollins, Brandi
Satterstrom, F Kyle
Schatzberg, Alan
Scolnick, Edward
Scott, Laura J
Sharp, Sally I
Sklar, Pamela
Smoller, Jordan W
Sobell, Janet L
Solomonson, Matthew
Stahl, Eli A
Stevens, Christine R
Suvisaari, Jaana
Tiao, Grace
Watson, Stanley J
Watts, Nicholas A
Blackwood, Douglas H
Børglum, Anders D
Cohen, Bruce M
Corvin, Aiden P
Esko, Tõnu
Freimer, Nelson B
Glatt, Stephen J
Hultman, Christina M
McQuillin, Andrew
Palotie, Aarno
Pato, Carlos N
Pato, Michele T
Pulver, Ann E
St Clair, David
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
4
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders 미리보기

학술저널

issue
Cell. 179(7)
Author
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
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
5
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals 미리보기

학술저널

issue
American Journal of Human Genetics. 105(2)
Author
Collaborative, Epi25
Feng, Yen-Chen Anne
Howrigan, Daniel P
Abbott, Liam E
Tashman, Katherine
Cerrato, Felecia
Singh, Tarjinder
Heyne, Henrike
Byrnes, Andrea
Churchhouse, Claire
Watts, Nick
Solomonson, Matthew
Lal, Dennis
Heinzen, Erin L
Dhindsa, Ryan S
Stanley, Kate E
Cavalleri, Gianpiero L
Hakonarson, Hakon
Helbig, Ingo
Krause, Roland
May, Patrick
Weckhuysen, Sarah
Petrovski, Slavé
Kamalakaran, Sitharthan
Sisodiya, Sanjay M
Cossette, Patrick
Cotsapas, Chris
De Jonghe, Peter
Dixon-Salazar, Tracy
Guerrini, Renzo
Kwan, Patrick
Marson, Anthony G
Stewart, Randy
Depondt, Chantal
Dlugos, Dennis J
Scheffer, Ingrid E
Striano, Pasquale
Freyer, Catharine
McKenna, Kevin
Regan, Brigid M
Bellows, Susannah T
Leu, Costin
Bennett, Caitlin A
Johns, Esther MC
Macdonald, Alexandra
Shilling, Hannah
Burgess, Rosemary
Weckhuysen, Dorien
Bahlo, Melanie
O’Brien, Terence J
Todaro, Marian
Stamberger, Hannah
Andrade, Danielle M
Sadoway, Tara R
Mo, Kelly
Krestel, Heinz
Gallati, Sabina
Papacostas, Savvas S
Kousiappa, Ioanna
Tanteles, George A
Štěrbová, Katalin
Vlčková, Markéta
Sedláčková, Lucie
Laššuthová, Petra
Klein, Karl Martin
Rosenow, Felix
Reif, Philipp S
Knake, Susanne
Kunz, Wolfram S
Zsurka, Gábor
Elger, Christian E
Bauer, Jürgen
Rademacher, Michael
Pendziwiat, Manuela
Muhle, Hiltrud
Rademacher, Annika
van Baalen, Andreas
von Spiczak, Sarah
Stephani, Ulrich
Afawi, Zaid
Korczyn, Amos D
Kanaan, Moien
Canavati, Christina
Kurlemann, Gerhard
Müller-Schlüter, Karen
Kluger, Gerhard
Häusler, Martin
Blatt, Ilan
Lemke, Johannes R
Krey, Ilona
Weber, Yvonne G
Wolking, Stefan
Becker, Felicitas
Hengsbach, Christian
Rau, Sarah
Maisch, Ana F
Steinhoff, Bernhard J
Schulze-Bonhage, Andreas
Schubert-Bast, Susanne
Schreiber, Herbert
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
6
Genome-wide association study identifies 30 loci associated with bipolar disorder 미리보기

학술저널

issue
Nature Genetics. 51(5)
Author
Stahl, Eli A
Breen, Gerome
Forstner, Andreas J
McQuillin, Andrew
Ripke, Stephan
Trubetskoy, Vassily
Mattheisen, Manuel
Wang, Yunpeng
Coleman, Jonathan RI
Gaspar, Héléna A
de Leeuw, Christiaan A
Steinberg, Stacy
Pavlides, Jennifer M Whitehead
Trzaskowski, Maciej
Byrne, Enda M
Pers, Tune H
Holmans, Peter A
Richards, Alexander L
Abbott, Liam
Agerbo, Esben
Akil, Huda
Albani, Diego
Alliey-Rodriguez, Ney
Als, Thomas D
Anjorin, Adebayo
Antilla, Verneri
Awasthi, Swapnil
Badner, Judith A
Bækvad-Hansen, Marie
Barchas, Jack D
Bass, Nicholas
Bauer, Michael
Belliveau, Richard
Bergen, Sarah E
Pedersen, Carsten Bøcker
Bøen, Erlend
Boks, Marco P
Boocock, James
Budde, Monika
Bunney, William
Burmeister, Margit
Bybjerg-Grauholm, Jonas
Byerley, William
Casas, Miquel
Cerrato, Felecia
Cervantes, Pablo
Chambert, Kimberly
Charney, Alexander W
Chen, Danfeng
Churchhouse, Claire
Clarke, Toni-Kim
Coryell, William
Craig, David W
Cruceanu, Cristiana
Curtis, David
Czerski, Piotr M
Dale, Anders M
de Jong, Simone
Degenhardt, Franziska
Del-Favero, Jurgen
DePaulo, J Raymond
Djurovic, Srdjan
Dobbyn, Amanda L
Dumont, Ashley
Elvsåshagen, Torbjørn
Escott-Price, Valentina
Fan, Chun Chieh
Fischer, Sascha B
Flickinger, Matthew
Foroud, Tatiana M
Forty, Liz
Frank, Josef
Fraser, Christine
Freimer, Nelson B
Frisén, Louise
Gade, Katrin
Gage, Diane
Garnham, Julie
Giambartolomei, Claudia
Pedersen, Marianne Giørtz
Goldstein, Jaqueline
Gordon, Scott D
Gordon-Smith, Katherine
Green, Elaine K
Green, Melissa J
Greenwood, Tiffany A
Grove, Jakob
Guan, Weihua
Guzman-Parra, José
Hamshere, Marian L
Hautzinger, Martin
Heilbronner, Urs
Herms, Stefan
Hipolito, Maria
Hoffmann, Per
Holland, Dominic
Huckins, Laura
Jamain, Stéphane
Johnson, Jessica S
Juréus, Anders
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
8
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. 미리보기

학술저널

issue
Nature genetics. 51(1)
Author
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
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
10
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap 미리보기

학술저널

issue
Science. 359(6376)
Author
Gandal, Michael J
Haney, Jillian R
Parikshak, Neelroop N
Leppa, Virpi
Ramaswami, Gokul
Hartl, Chris
Schork, Andrew J
Appadurai, Vivek
Buil, Alfonso
Werge, Thomas M
Liu, Chunyu
White, Kevin P
Horvath, Steve
Geschwind, Daniel H
Sestan, Nenad
Vaccarino, Flora
Gerstein, Mark
Weissman, Sherman
Pochareddy, Sirisha
State, Matthew
Knowles, James
Farnham, Peggy
Akbarian, Schahram
Pinto, Dalila
Van Baekl, Harm
Dracheva, Stella
Jaffe, Andrew
Hyde, Thomas
Zandi, Peter
Crawford, Gregory
Sullivan, Pat
Thompson, Wesley Kurt
Mortensen, Preben Bo
Agerbo, Esben
Pedersen, Marianne Giørtz
Pedersen, Carsten Bøcker
Mors, Ole
Børglum, Anders D
Nordentoft, Merete
Hougaard, David M
Bybjerg-Grauholm, Jonas
Bækvad-Hansen, Marie
Martin, Alicia R
Dumont, Ashley
Stevens, Christine
Churchhouse, Claire
Howrigan, Daniel P
Palmer, Duncan S
Robinson, Elise B
Satterstrom, Kyle F
Cerrato, Felecia
Huang, Hailiang
Goldstein, Jacqueline
Moran, Jennifer
Julian, Joanna Martin
Kimberly, Maller
Patrick, Chambert
Turley, Patrick
Walters, Raymond
Belliveau, Rich
Ripke, Stephan
Poterba, Timothy
Daly, Mark J
Neale, Benjamin
Fromer, Menachem
Roussos, Panos
Johnson, Jessica S
Shah, Hardik R
Mahajan, Milind C
Schadt, Eric
Haroutunian, Vahram
Ruderfer, Douglas M
Buxbaum, Joseph D
Sieberts, Solveig K
Dang, Kristen
Logsdon, Ben
Mangravite, Lara M
Peters, Mette
Gur, Raquel E
Hahn, Chang-Gyu
Devlin, Bernie
Klei, Lambertus L
Lewis, David
Lipska, Barbara
Hirai, Keisuke
Toyoshiba, Hiroyoshi
Domenici, Enrico
DB Label
Database : eScholarship
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Open Access (eScholarship) 
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