Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
---|---|---|---|---|---|---|
2020 | Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations | Howrigan D.P.; Rose S.A.; Samocha K.E.; Fromer M.; Cerrato F.; WEI J. CHEN ; Churchhouse C.; Chambert K.; Chandler S.D.; Daly M.J.; Dumont A.; Genovese G.; HAI-GWO HWU ; Laird N.; Kosmicki J.A.; Moran J.L.; Roe C.; Singh T.; Wang S.-H.; Faraone S.V.; Glatt S.J.; McCarroll S.A.; Tsuang M.; Neale B.M. | Nature Neuroscience | 100 | 87 | |
2018 | Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia | Wang S.-H.; Hsiao P.-C.; Yeh L.-L.; CHIH-MIN LIU ; CHEN-CHUNG LIU ; TZUNG-JENG HWANG ; MING-HSIEN HSIEH ; YI-LING CHIEN ; YI-TING LIN ; Chandler S.D.; Faraone S.V.; Laird N.; Neale B.; McCarroll S.A.; Glatt S.J.; Tsuang M.T.; HAI-GWO HWU ; WEI J. CHEN | Genes, Brain and Behavior | 29 | 26 | |
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 | 37 | 28 | |
2016 | A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples | Cohen O.S.; Weickert T.W.; Hess J.L.; Paish L.M.; McCoy S.Y.; Rothmond D.A.; Galletly C.; Liu D.; Weinberg D.D.; Huang X.-F.; Xu Q.; Shen Y.; Zhang D.; Yue W.; Yan J.; Wang L.; Lu T.; He L.; Shi Y.; Xu M.; Che R.; Tang W.; Chen C.-H.; Chang W.-H.; HAI-GWO HWU ; CHIH-MIN LIU ; Liu Y.-L.; Wen C.-C.; Fann C.S.-J.; Chang C.-C.; Kanazawa T.; Middleton F.A.; Duncan T.M.; Faraone S.V.; Weickert C.S.; Tsuang M.T.; Glatt S.J. | Molecular Psychiatry | 25 | 18 |