公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2011 | ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure | Chen J.; Brunzell D.H.; Jackson K.; van der Vaart A.; Ma J.Z.; Payne T.J.; Sherva R.; Farrer L.A.; Gejman P.; Levinson D.F.; Holmans P.; Aggen S.H.; Damaj I.; PO-HSIU KUO ; Webb B.T.; Anton R.; Kranzler H.R.; Gelernter J.; Li M.D.; Kendler K.S.; HSIU-PO KUO | PLoS ONE | 11 | 10 | |
2015 | Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia | WEI J. CHEN ; Kirov G.; Walters J.T.; Richards A.L.; Howrigan D.; Kavanagh D.H.; Pocklington A.J.; Fromer M.; Ruderfer D.M.; Georgieva L.; Carrera N.; Gormley P.; Palta P.; Williams H.; Dwyer S.; Johnson J.S.; Roussos P.; Barker D.D.; Banks E.; Milanova V.; Rose S.A.; Chambert K.; Mahajan M.; Scolnick E.M.; Moran J.L.; Tsuang M.T.; Glatt S.J.; Chen W.J.; HAI-GWO HWU ; Taiwanese Trios Exome Sequencing Consortium, Neale B.M.; Palotie A.; Sklar P.; Purcell S.M.; McCarroll S.A.; Holmans P.; Owen M.J.; O'Donovan M.C. | Translational psychiatry | 32 | 28 | |
2019 | Comparative genetic architectures of schizophrenia in East Asian and European populations | WEI J. CHEN ; Chen C.-Y.; Li Z.; Martin A.R.; Bryois J.; Ma X.; Gaspar H.; Ikeda M.; Benyamin B.; Brown B.C.; Liu R.; Zhou W.; Guan L.; Kamatani Y.; Kim S.-W.; Kubo M.; Kusumawardhani A.A.A.A.; CHIH-MIN LIU ; Ma H.; Periyasamy S.; Takahashi A.; Xu Z.; Yu H.; Zhu F.; Chen W.J.; Faraone S.; Glatt S.J.; He L.; Hyman S.E.; HAI-GWO HWU ; McCarroll S.A.; Neale B.M.; Sklar P.; Wildenauer D.B.; Yu X.; Zhang D.; Mowry B.J.; Lee J.; Holmans P.; Xu S.; Sullivan P.F.; Ripke S.; O’Donovan M.C.; Daly M.J.; Qin S.; Sham P.; Iwata N.; Hong K.S.; Schwab S.G.; Yue W.; Tsuang M.; Liu J.; Ma X.; Kahn R.S.; Shi Y.; Huang H.; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Indonesia Schizophrenia Consortium, Genetic REsearch on schizophreniA neTwork-China and the Netherlands (GREAT-CN) | Nature Genetics | 351 | 294 | |
2021 | Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations | Rees E.; Creeth H.D.J.; Hwu H.-G.; WEI J. CHEN ; Tsuang M.; Glatt S.J.; Rey R.; Kirov G.; Walters J.T.R.; Holmans P.; Owen M.J.; O’Donovan M.C. | Nature Communications | 35 | 28 | |