Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: PCDHA[original query] |
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Protocadherin a (PCDHA) as a novel susceptibility gene for autism. Journal of psychiatry & neuroscience : JPN 2012 Oct 37 (6): 6. Anitha A, Thanseem I, Nakamura K, Yamada K, Iwayama Y, Toyota T, Iwata Y, Suzuki K, Sugiyama T, Tsujii M, Yoshikawa T, Mori N |
Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. PloS one 2013 8 (2): 2. Ukkola-Vuoti L, Kanduri C, Oikkonen J, Buck G, Blancher C, Raijas P, Karma K, Lähdesmäki H, Järvelä I |
Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder. Behavioural neurology 2021 7 2021 4150926. Fang Fang, Ge Minxia, Liu Jun, Zhang Zengyu, Yu Hong, Zhu Shuilong, Xu Liwei, Shao Li |
Common deletion variants causing protocadherin-? deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG advances 2021 12 2 (3): . Teekakirikul Polakit, Zhu Wenjuan, Gabriel George C, Young Cullen B, Williams Kylia, Martin Lisa J, Hill Jennifer C, Richards Tara, Billaud Marie, Phillippi Julie A, Wang Jianbin, Wu Yijen, Tan Tuantuan, Devine William, Lin Jiuann-Huey, Bais Abha S, Klonowski Jonathan, Moreau de Bellaing Anne, Saini Ankur, Wang Michael X, Emerel Leonid, Salamacha Nathan, Wyman Samuel K, Lee Carrie, Sing Li Hung, Miron Anastasia, Zhang Jingyu, Xing Jianhua, McNamara Dennis M, Fung Erik, Kirshbom Paul, Mahle William, Kochilas Lazaros K, He Yihua, Garg Vidu, White Peter, McBride Kim L, Benson D Woodrow, Gleason Thomas G, Mital Seema, Lo Cecilia |
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta. Genes 2022 4 13 (4): . Zhu Wenjuan, Williams Kylia, Young Cullen, Lin Jiaunn-Huey, Teekakirikul Polakit, Lo Cecilia |
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