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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Disease and CNTN4[original query]
Contactin 4 as an autism susceptibility locus.
Autism research : official journal of the International Society for Autism Research 2011 Jun 4 (3): 189-99.
Cottrell Catherine E, Bir Natalie, Varga Elizabeth, Alvarez Carlos E, Bouyain Samuel, Zernzach Randall, Thrush Devon L, Evans Johnna, Trimarchi Michael, Butter Eric M, Cunningham David, Gastier-Foster Julie M, McBride Kim L, Herman Gail
Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis.
PloS one 2013 8 (7): e67776.
Zhao Zhongming, Webb Bradley T, Jia Peilin, Bigdeli T Bernard, Maher Brion S, van den Oord Edwin, Bergen Sarah E, Amdur Richard L, O'Neill Francis A, Walsh Dermot, Thiselton Dawn L, Chen Xiangning, Pato Carlos N, , Riley Brien P, Kendler Kenneth S, Fanous Ayman
Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins.
Investigative ophthalmology & visual science 2014 May 55 (5): 3258-64.
Kaurani Lalit, Vishal Mansi, Kumar Dhirendra, Sharma Anchal, Mehani Bharati, Sharma Charu, Chakraborty Subhadip, Jha Pankaj, Ray Jharna, Sen Abhijit, Dash Debasis, Ray Kunal, Mukhopadhyay Arij
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. GWAS Catalog
Neurobiology of aging 2014 Jul 35 (7): 1778.e9-1778.e23.
Xie Tong, Deng Libin, Mei Puming, Zhou Yiyi, Wang Bo, Zhang Jie, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens
GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
BMC genomics 2016 Apr 17 276.
Chittoor Geetha, Kent Jack W, Almeida Marcio, Puppala Sobha, Farook Vidya S, Cole Shelley A, Haack Karin, Göring Harald H H, MacCluer Jean W, Curran Joanne E, Carless Melanie A, Johnson Matthew P, Moses Eric K, Almasy Laura, Mahaney Michael C, Lehman Donna M, Duggirala Ravindranath, Comuzzie Anthony G, Blangero John, Voruganti Venkata Saro
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis. GWAS Catalog
Ophthalmology 2020 May .
Meguro Akira, Yamane Takahiro, Takeuchi Masaki, Miyake Masahiro, Fan Qiao, Zhao Wanting, Wang I-Jong, Mizuki Yuki, Yamada Norihiro, Nomura Naoko, Tsujikawa Akitaka, Matsuda Fumihiko, Hosoda Yoshikatsu, Saw Seang-Mei, Cheng Ching-Yu, Tsai Tzu-Hsun, Yoshida Masao, Iijima Yasuhito, Teshigawara Takeshi, Okada Eiichi, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhi
Effect of the Minor C Allele of CNTN4 rs2619566 on Medial Hypothalamic Connectivity in Early-Stage Patients of Chinese Han Ancestry with Sporadic Amyotrophic Lateral Sclerosis.
Neuropsychiatric disease and treatment 2022 3 18 437-448.
Wang Yao, He Yujie, Zhu Yanyan, He Ting, Xu Jie, Kuang Qinmei, Ji Yuqi, Xu Renshi, Li Fangjun, Zhou Fuqi
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
Journal of neurodevelopmental disorders 2023 4 15 (1): 14.
Joseph T Glessner, Munir E Khan, Xiao Chang, Yichuan Liu, F George Otieno, Maria Lemma, Isabella Slaby, Heather Hain, Frank Mentch, Jin Li, Charlly Kao, Patrick M A Sleiman, Michael E March, John Connolly, Hakon Hakonars
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