Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: DAB1[original query] |
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The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.
Human genetics 2012 Mar 131 (3): 365-72. Ahn Myung-Ju, Won Hong-Hee, Lee Jeeyun, Lee Seung-Tae, Sun Jong-Mu, Park Yeon Hee, Ahn Jin Seok, Kwon O Jung, Kim Hojoong, Shim Young Mog, Kim Jhingook, Kim Kwhanmien, Kim Yeul Hong, Park Jae Yong, Kim Jong-Won, Park Keunch |
Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jun 159B (4): 392-404. Verbrugghe Phebe, Bouwer Sonja, Wiltshire Steven, Carter Kim, Chandler David, Cooper Matthew, Morar Bharti, Razif Muhammad F M, Henders Anjali, Badcock Johanna C, Dragovic Milan, Carr Vaughan, Almeida Osvaldo P, Flicker Leon, Montgomery Grant, Jablensky Assen, Kalaydjieva Lu |
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes. Parkinsonism & related disorders 2014 Jan 20 (1): 93-8. Wan Jia Y, Edwards Karen L, Hutter Carolyn M, Mata Ignacio F, Samii Ali, Roberts John W, Agarwal Pinky, Checkoway Harvey, Farin Federico M, Yearout Dora, Zabetian Cyrus |
Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population. Progress in neuro-psychopharmacology & biological psychiatry 2013 Jul 44 226-32. Li Jun, Liu Jing, Zhao Linnan, Ma Yuanlin, Jia Meixiang, Lu Tianlan, Ruan Yanyan, Li Qizhai, Yue Weihua, Zhang Dai, Wang Lifa |
Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population. Autism research : official journal of the International Society for Autism Research 2015 Aug . Shen Yidong, Xun Guanglei, Guo Hui, He Yiqun, Ou Jianjun, Dong Huixi, Xia Kun, Zhao Jingpi |
Functional enrichment analysis of three Alzheimer's disease genome-wide association studies identities DAB1 as a novel candidate liability/protective gene. Biochemical and biophysical research communications 2015 Aug 463 (4): 490-5. Gao Hui, Tao Yu, He Qin, Song Fan, Saffen Dav |
Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies. American journal of medical genetics. Part A 2015 Oct 167 (10): 2406-10. Kehrer Martin, Schäferhoff Karin, Bonin Michael, Jauch Anna, Bevot Andrea, Tzschach Andre |
Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study.
The Journal of steroid biochemistry and molecular biology 2015 Dec . Sapkota Bishwa R, Hopkins Ruth, Bjonnes Andrew, Ralhan Sarju, Wander Gurpreet S, Mehra Narinder K, Singh Jai Rup, Blackett Piers R, Saxena Richa, Sanghera Dharambir |
Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity).
Circulation. Cardiovascular genetics 2017 Dec 10 (6): . Li Changwei, He Jiang, Chen Jing, Zhao Jinying, Gu Dongfeng, Hixson James E, Rao Dabeeru C, Jaquish Cashell E, Rice Treva K, Sung Yun Ju, Kelly Tanika |
A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN. Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
Genome-Wide Association and Functional Studies Identify SCML4 and THSD7A as Novel Susceptibility Genes for Coronary Artery Disease.
Arteriosclerosis, thrombosis, and vascular biology 2018 Apr 38 (4): 964-975. Li Yang, Wang Dao Wen, Chen Yundai, Chen Can, Guo Jian, Zhang Shu, Sun Zhijun, Ding Hu, Yao Yan, Zhou Lei, Xu Ke, Song Chun, Yang Fan, Zhao Bin, Yan Han, Wang Wen-Jing, Wu Chong, Lu Xiangfeng, Yang Xueli, Dong Jie, Zheng Guyan, Tian Shuhan, Cui Yanjun, Jin Lijuan, Liu Gangqiong, Cui Hanbin, Wang Shenghuang, Jiang Feng, Wang Changhua, Erdmann Jeanette, Zeng Linyao, Huang Shian, Zhong Jianfeng, Ma Yuehua, Chen Wenjiang, Sun Jianli, Lei Wei, Chen Shenghan, Rao Shaoqi, Gu Dongfeng, Schunkert Heribert, Tian Xiao- |
Prevalence of RFC1-mediated spinocerebellar ataxia in a North American ataxia cohort. Neurology. Genetics 2020 6 6 (3): e440. Aboud Syriani Dona, Wong Darice, Andani Sameer, De Gusmao Claudio M, Mao Yuanming, Sanyoura May, Glotzer Giacomo, Lockhart Paul J, Hassin-Baer Sharon, Khurana Vikram, Gomez Christopher M, Perlman Susan, Das Soma, Fogel Brent |
Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility. Human genome variation 2020 Nov 7 (1): 37. Nawa Yoshihiro, Kimura Hiroki, Mori Daisuke, Kato Hidekazu, Toyama Miho, Furuta Sho, Yu Yanjie, Ishizuka Kanako, Kushima Itaru, Aleksic Branko, Arioka Yuko, Morikawa Mako, Okada Takashi, Inada Toshiya, Kaibuchi Kozo, Ikeda Masashi, Iwata Nakao, Suzuki Michio, Okahisa Yuko, Egawa Jun, Someya Toshiyuki, Nishimura Fumichika, Sasaki Tsukasa, Ozaki Nor |
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer. Journal of personalized medicine 2021 8 11 (7): . Slater Emily P, Wilke Lisa M, Böhm Lutz Benedikt, Strauch Konstantin, Lutz Manuel, Gercke Norman, Matthäi Elvira, Hemminki Kari, Försti Asta, Schlesner Matthias, Paramasivam Nagarajan, Bartsch Detlef |
Potential Common Genetic Risks of Sporadic Parkinson's Disease and Amyotrophic Lateral Sclerosis in the Han Population of Mainland China. Frontiers in neuroscience 2021 15 753870. Lu Yi, Chen Wenzhi, Wei Caihui, Zhu Yu, Xu Rens |
Relationship between RELN signaling pathway genes and language development of autism based on a cluster model. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2022 8 47 (7): 858-864. Shen Yidong, Dong Huixi, Zhao Jingping, Xia Kun, Ou Jianj |
Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis.
Neurobiology of aging 2022 8 119 67-76. Bracher-Smith Matthew, Leonenko Ganna, Baker Emily, Crawford Karen, Graham Andrew C, Salih Dervis A, Howell Brian W, Hardy John, Escott-Price Valenti |
Resilience to autosomal dominant Alzheimer's disease in a Reelin-COLBOS heterozygous man. Nature medicine 2023 5 29 (5): 1243-1252. Francisco Lopera, Claudia Marino, Anita S Chandrahas, Michael O'Hare, Nelson David Villalba-Moreno, David Aguillon, Ana Baena, Justin S Sanchez, Clara Vila-Castelar, Liliana Ramirez Gomez, Natalia Chmielewska, Gabriel M Oliveira, Jessica Lisa Littau, Kristin Hartmann, Kyungeun Park, Susanne Krasemann, Markus Glatzel, Dorothee Schoemaker, Lucia Gonzalez-Buendia, Santiago Delgado-Tirado, Said Arevalo-Alquichire, Kahira L Saez-Torres, Dhanesh Amarnani, Leo A Kim, Randall C Mazzarino, Harper Gordon, Yamile Bocanegra, Andres Villegas, Xiaowu Gai, Moiz Bootwalla, Jianling Ji, Lishuang Shen, Kenneth S Kosik, Yi Su, Yinghua Chen, Aaron Schultz, Reisa A Sperling, Keith Johnson, Eric M Reiman, Diego Sepulveda-Falla, Joseph F Arboleda-Velasquez, Yakeel T Quir |
A Genome-Wide Interaction Study of Erythrocyte ?3 Polyunsaturated Fatty Acid Species and Memory in The Framingham Heart Study Offspring Cohort. The Journal of nutrition 2023 12 . Carmen E Annevelink, Jason Westra, Aleix Sala-Vila, William S Harris, Nathan L Tintle, Gregory C Shear |
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