еНаука - преглед
Преглед према Аутор Werge, Thomas
Приказ резултата 1 до 3 од 3
Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
---|---|---|---|---|
2018 | Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection![]() | Pardiñas, Antonio F.; Holmans, Peter; Pocklington, Andrew J.; Escott-Price, Valentina; Ripke, Stephan; Carrera, Noa; Legge, Sophie E.; Bishop, Sophie; Cameron, Darren; Hamshere, Marian L.;
Han, Jun; Hubbard, Leon; Lynham, Amy; Mantripragada, Kiran; Rees, Elliott; MacCabe, James H.; McCarroll, Steven A.; Baune, Bernhard T.; Breen, Gerome; Byrne, Enda M.; Dannlowski, Udo; Eley, Thalia C.; Hayward, Caroline; Martin, Nicholas G.; McIntosh, Andrew M.; Plomin, Robert; Porteous, David J.; Wray, Naomi R.; Caballero, Armando; Geschwind, Daniel H.; Huckins, Laura M.; Ruderfer, Douglas M.; Santiago, Enrique; Sklar, Pamela; Stahl, Eli A.; Won, Hyejung; Agerbo, Esben; Als, Thomas D.; Andreassen, Ole A.; Bækvad-Hansen, Marie; Mortensen, Preben Bo; Pedersen, Carsten Bøcker; Børglum, Anders D.; Bybjerg-Grauholm, Jonas; Đurović, Srđan; Durmishi, Naser; Pedersen, Marianne Giørtz; Golimbet, Vera; Grove, Jakob; Hougaard, David M.; Mattheisen, Manuel; Molden, Espen; Mors, Ole; Nordentoft, Merete; Pejović-Milovančević, Milica
![]() ![]() | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2015 | Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness | Bigdeli, Tim B.; Ripke, Stephan; Bacanu, Silviu-Alin; Lee, Sang Hong; Wray, Naomi R.; Gejman, Pablo V.; Rietschel, Marcella; Cichon, Sven; St, Clair David; Corvin, Aiden;
Kirov, George; McQuillin, Andrew; Gurling, Hugh; Rujescu, Dan; Andreassen, Ole A.; Werge, Thomas; Blackwood, Douglas H. R.; Pato, Carlos N.; Pato, Michele T.; Malhotra, Anil K.; O'Donovan, Michael C.; Kendler, Kenneth S.; Fanous, Ayman H.;
| Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2017 | Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders | Weiner, Daniel J.; Wigdor, Emilie M.; Ripke, Stephan; Walters, Raymond K.; Kosmicki, Jack A.; Grove, Jakob; Samocha, Kaitlin E.; Goldstein, Jacqueline; Okbay, Aysu; Bybjerg-Gauholm, Jonas;
Werge, Thomas; Hougaard, David M.; Taylor, Jacob; Skuse, David; Devlin, Bernie; Anney, Richard; Sanders, Stephan; Bishop, Somer; Bo, Mortensen Preben; Børglum, Anders D.; Davey, Smith George; Daly, Mark J.; Robinson, Elise B.;
| Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |