共 50 条
- [41] Development and validation of polygenic risk scores for prediction of breast cancer and breast cancer subtypes in Chinese womenBMC Cancer, 22Can HouBin XuYu HaoDaowen YangHuan SongJiayuan Li
- [42] Inherited and De Novo Genetic Risk for Autism Impacts Shared NetworksCELL, 2019, 178 (04) : 850 - +Ruzzo, Elizabeth K.Perez-Cano, LauraJung, Jae-YoonWang, Lee-kaiKashef-Haghighi, DornaHartl, ChrisSingh, ChanpreetXu, JinHoekstra, Jackson N.Leventhal, OliviaLeppa, Virpi M.Gandal, Michael J.Paskov, KelleyStockham, NatePolioudakis, DamonLowe, Jennifer K.Prober, David A.Geschwind, Daniel H.Wall, Dennis P.
- [43] POLYGENIC RISK SCORES REVEAL PATTERNS OF ASSORTATIVE MATING AND ANTICIPATION IN A LARGE PEDIGREE AFFECTED WITH MOOD DISORDERSEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S483 - S483de Jong, SimoneAbdalla Diniz, Mateus JoseSaloma Rodrigues, Andiara CaladoGadelha, ArySantoro, MarcosOta, VanessaNoto, ChristianoCurtis, CharlesPatel, HamelHall, LynseyO'Reilly, PaulBelangero, SintiaBressan, RodrigoBreen, Gerome
- [44] THE EMERGING LANDSCAPE OF SCHIZOPHRENIA RISK CONFERRED BY DE NOVO CODING MUTATIONSEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S346 - S347Howrtgan, DanielNeale, BenjaminSamocha, KaitlinMoran, JenniferChambert, KimberlyRose, SamuelFromer, MenachemChandler, SharonLaird, NanHwu, Hai-GwoChen, Wei J.Faraone, StephenGlatt, StephenTsuang, MingMcCarroll, Steven
- [45] DAMAGING MISSENSE DE NOVO CODING MUTATIONS CONTRIBUTE TO SCHIZOPHRENIA RISKEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S427 - S428Howrigan, DanielSamocha, KaitlinKosmicki, JackMoran, JenniferChambert, KimberlyFromer, MenachemChandler, SharonLaird, NanHwu, Hai-GwoChen, Wei J.Faraone, StephenGlatt, StephenTsuang, MingMcCarroll, StevenNeale, Benjamin
- [46] Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorderMolecular Psychiatry, 2022, 27 : 4680 - 4694Il Bin KimTaeyeop LeeJunehawk LeeJonghun KimSuho LeeIn Gyeong KohJae Hyun KimJoon-Yong AnHyunseong LeeWoo Kyeong KimYoung Seok JuYongseong ChoSeok Jong YuSoon Ae KimMiae OhDong Wook HanEunjoon KimJung Kyoon ChoiHee Jeong YooJeong Ho Lee
- [47] Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorderMOLECULAR PSYCHIATRY, 2022, 27 (11) : 4680 - 4694Kim, Il BinLee, TaeyeopLee, JunehawkKim, JonghunLee, SuhoKoh, In GyeongKim, Jae HyunAn, Joon-YongLee, HyunseongKim, Woo KyeongJu, Young SeokCho, YongseongYu, Seok JongKim, Soon AeOh, MiaeHan, Dong WookKim, EunjoonChoi, Jung KyoonYoo, Hee JeongLee, Jeong Ho
- [48] Associations Between MDD Neurovegetative Subtypes, Structural Brain Alterations and Polygenic Risk Scores in Enigma-MDDBIOLOGICAL PSYCHIATRY, 2023, 93 (09) : S14 - S14Toenders, YaraHan, LauraShen, XueyiPozzi, ElenaWhalley, HeatherMilaneschi, YuriSchmaal, Lianne
- [49] Multi-Ancestry Analysis Identifies Susceptibility Variants and Improves Polygenic Risk Scores for Breast Cancer SubtypesGENETIC EPIDEMIOLOGY, 2024, 48 (07) : 396 - 396Zhang, HaoyuWang, XiaoyuAhearn, Thomas U.Michailidou, KyriakiMilne, Roger L.Simard, JacquesPharoah, Paul D. P.Teo, Soo-HwangSchmidt, Marjanka K.Easton, Douglas F.Kraft, PeterHo, Weang KeeGarcia-Closas, Montserrat
- [50] Polygenic and transcriptional risk scores identify chronic obstructive pulmonary disease subtypes in the COPDGene and ECLIPSE cohort studiesEBIOMEDICINE, 2024, 110Moll, MatthewHecker, JulianPlatig, JohnZhang, JingzhouGhosh, Auyon J.Pratte, Katherine A.Wang, Rui-ShengHill, DavinKonigsberg, Iain R.Chiles, Joe W.Hersh, Craig P.Castaldi, Peter J.Glass, KimberlyDy, Jennifer G.Sin, Don D.Tal-Singer, RuthMouded, MajdRennard, Stephen I.Anderson, Gary P.Kinney, Gregory L.Bowler, Russell P.Curtis, Jeffrey L.Mcdonald, Merry-LynnSilverman, Edwin K.Hobbs, Brian D.Cho, Michael H.