Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: SORCS3[original query] |
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Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational psychiatry 2013 3 e256. Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers R S, Conrad C, Haines J L, Pericak-Vance M A, Fallin M D, Foroud T, Farrer L A, Schellenberg G D, George-Hyslop P S, Mayeux R, |
Endurance Exercise Ability in the Horse: A Trait with Complex Polygenic Determinism. Frontiers in genetics 2017 8 89. Ricard Anne, Robert Céline, Blouin Christine, Baste Fanny, Torquet Gwendoline, Morgenthaler Caroline, Rivière Julie, Mach Nuria, Mata Xavier, Schibler Laurent, Barrey Er |
Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 9 17 (2): 215-225. Blue Elizabeth E, Thornton Timothy A, Kooperberg Charles, Liu Simin, Wactawski-Wende Jean, Manson JoAnn, Kuller Lew, Hayden Kathleen, Reiner Alexander |
Multi-trait analysis for genome-wide association study of five psychiatric disorders.
Translational psychiatry 2020 06 10 (1): 209. Wu Yulu, Cao Hongbao, Baranova Ancha, Huang Hailiang, Li Sheng, Cai Lei, Rao Shuquan, Dai Minhan, Xie Min, Dou Yikai, Hao Qinjian, Zhu Ling, Zhang Xiangrong, Yao Yin, Zhang Fuquan, Xu Mingqing, Wang Qia |
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Schizophrenia bulletin 2020 Nov . Bigdeli Tim B, Fanous Ayman H, Li Yuli, Rajeevan Nallakkandi, Sayward Frederick, Genovese Giulio, Gupta Rishab, Radhakrishnan Krishnan, Malhotra Anil K, Sun Ning, Lu Qiongshi, Hu Yiming, Li Boyang, Chen Quan, Mane Shrikant, Miller Perry, Cheung Kei-Hoi, Gur Raquel E, Greenwood Tiffany A, Braff David L, , Achtyes Eric D, Buckley Peter F, Escamilla Michael A, Lehrer Douglas, Malaspina Dolores P, McCarroll Steven A, Rapaport Mark H, Vawter Marquis P, Pato Michele T, Pato Carlos N, , Zhao Hongyu, Kosten Thomas R, Brophy Mary, Pyarajan Saiju, Shi Yunling, O'Leary Timothy J, Gleason Theresa, Przygodzki Ronald, Muralidhar Sumitra, Gaziano J Michael, , Huang Grant D, Concato John, Siever Larry J, Aslan Mihaela, Harvey Philip |
Genome-wide association study of brain arteriolosclerosis. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2022 Feb 271678X211066299. Shade Lincoln Mp, Katsumata Yuriko, Hohman Timothy J, Nho Kwangsik, Saykin Andrew J, Mukherjee Shubhabrata, Boehme Kevin L, Kauwe John Sk, Farrer Lindsay A, Schellenberg Gerard D, Haines Jonathan L, Mayeux Richard P, Schneider Julie A, Nelson Peter T, Fardo David |
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics 2023 1 55 (2): 198-208. Demontis Ditte, Walters G Bragi, Athanasiadis Georgios, Walters Raymond, Therrien Karen, Nielsen Trine Tollerup, Farajzadeh Leila, Voloudakis Georgios, Bendl Jaroslav, Zeng Biau, Zhang Wen, Grove Jakob, Als Thomas D, Duan Jinjie, Satterstrom F Kyle, Bybjerg-Grauholm Jonas, Bækved-Hansen Marie, Gudmundsson Olafur O, Magnusson Sigurdur H, Baldursson Gisli, Davidsdottir Katrin, Haraldsdottir Gyda S, Agerbo Esben, Hoffman Gabriel E, Dalsgaard Søren, Martin Joanna, Ribasés Marta, Boomsma Dorret I, Soler Artigas Maria, Roth Mota Nina, Howrigan Daniel, Medland Sarah E, Zayats Tetyana, Rajagopal Veera M, , , Nordentoft Merete, Mors Ole, Hougaard David M, Mortensen Preben Bo, Daly Mark J, Faraone Stephen V, Stefansson Hreinn, Roussos Panos, Franke Barbara, Werge Thomas, Neale Benjamin M, Stefansson Kari, Børglum Anders |
Replication of previous autism-GWAS hits suggests the association between NAA1, SORCS3, and GSDME and autism in the Han Chinese population. Heliyon 2024 1 10 (1): e23677. Fen Lin, Jun Li, Ziqi Wang, Tian Zhang, Tianlan Lu, Miaomiao Jiang, Kang Yang, Meixiang Jia, Dai Zhang, Lifang Wa |
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