Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: GRID1[original query] |
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Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios. American journal of human genetics 2005 Dec 77 (6): 918-36. Fallin M Daniele, Lasseter Virginia K, Avramopoulos Dimitrios, Nicodemus Kristin K, Wolyniec Paula S, McGrath John A, Steel Gary, Nestadt Gerald, Liang Kung-Yee, Huganir Richard L, Valle David, Pulver Ann |
A case-control association study between the GRID1 gene and schizophrenia in the Chinese Northern Han population. Schizophrenia research 2007 Jul 93 (1-3): 385-90. Guo Sheng-Zhen, Huang Ke, Shi Yong-Yong, Tang Wei, Zhou Jian, Feng Guo-Yin, Zhu Shao-Min, Liu Hui-Jun, Chen Yi, Sun Xiao-Dong, He L |
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. Schizophrenia research 2009 Jun 111 (1-3): 123-30. Treutlein Jens, Mühleisen Thomas W, Frank Josef, Mattheisen Manuel, Herms Stefan, Ludwig Kerstin U, Treutlein Tsendsesmee, Schmael Christine, Strohmaier Jana, Bösshenz Katja Veronika, Breuer René, Paul Torsten, Witt Stephanie H, Schulze Thomas G, Schlösser Ralf G M, Nenadic Igor, Sauer Heinrich, Becker Tim, Maier Wolfgang, Cichon Sven, Nöthen Markus M, Rietschel Marcel |
Genome-wide association study of comorbid depressive syndrome and alcohol dependence.
Psychiatric genetics 2012 Feb 22 (1): 31-41. Edwards Alexis C, Aliev Fazil, Bierut Laura J, Bucholz Kathleen K, Edenberg Howard, Hesselbrock Victor, Kramer John, Kuperman Samuel, Nurnberger John I, Schuckit Marc A, Porjesz Bernice, Dick Danielle |
Glutamate receptor d 1 (GRID1) genetic variation and brain structure in schizophrenia. Journal of psychiatric research 2012 Dec 46 (12): 1531-9. Nenadic Igor, Maitra Raka, Scherpiet Sigrid, Gaser Christian, Schultz C Christoph, Schachtzabel Claudia, Smesny Stefan, Reichenbach Jürgen R, Treutlein Jens, Mühleisen Thomas W, Deufel Thomas, Cichon Sven, Rietschel Marcella, Nöthen Markus M, Sauer Heinrich, Schlösser Ralf G |
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human molecular genetics 2012 Aug 21 (15): 3513-23. Griswold Anthony J, Ma Deqiong, Cukier Holly N, Nations Laura D, Schmidt Mike A, Chung Ren-Hua, Jaworski James M, Salyakina Daria, Konidari Ioanna, Whitehead Patrice L, Wright Harry H, Abramson Ruth K, Williams Scott M, Menon Ramkumar, Martin Eden R, Haines Jonathan L, Gilbert John R, Cuccaro Michael L, Pericak-Vance Margaret |
Polymorphisms of PRLHR and HSPA12A and risk of gastric and colorectal cancer in the Chinese Han population. BMC gastroenterology 2015 15 (1): 107. Su Qinghua, Wang Yuan, Zhao Jun, Ma Cangjian, Wu Tao, Jin Tianbo, Xu Jink |
CREB-BDNF pathway influences alcohol cue-elicited activation in drinkers. Human brain mapping 2015 Aug 36 (8): 3007-19. Chen Jiayu, Hutchison Kent E, Calhoun Vince D, Claus Eric D, Turner Jessica A, Sui Jing, Liu Jing |
Physical activity, smoking, and genetic predisposition to obesity in people from Pakistan: the PROMIS study. BMC medical genetics 2015 16 (1): 114. Ahmad Shafqat, Zhao Wei, Renström Frida, Rasheed Asif, Samuel Maria, Zaidi Mozzam, Shah Nabi, Mallick Nadeem Hayyat, Zaman Khan Shah, Ishaq Mohammad, Rasheed Syed Zahed, Memon Fazal-Ur-Rheman, Hanif Bashir, Lakhani Muhammad Shakir, Ahmed Faisal, Kazmi Shahana Urooj, Frossard Philippe, Franks Paul W, Saleheen Dani |
Exome sequencing of a large family identifies potential candidate genes contributing risk to bipolar disorder. Gene 2018 Mar 645 119-123. Zhang Tianxiao, Hou Liping, Chen David T, McMahon Francis J, Wang Jen-Chyong, Rice John |
Two novel candidate genes identified in adults from the Newfoundland population with addictive tendencies towards food. Appetite 2017 1 115 71-79. Pedram Pardis, Zhai Guangju, Gulliver Wayne, Zhang Hongwei, Sun Gua |
Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.
Blood advances 2019 Nov 3 (22): 3579-3589. McGraw Kathy L, Cheng Chia-Ho, Chen Y Ann, Hou Hsin-An, Nilsson Björn, Genovese Giulio, Cluzeau Thomas, Pellagatti Andrea, Przychodzen Bartlomiej P, Mallo Mar, Arenillas Leonor, Mohamedali Azim, Adès Lionel, Sallman David A, Padron Eric, Sokol Lubomir, Moreilhon Chimene, Raynaud Sophie, Tien Hwei-Fang, Boultwood Jacqueline, Ebert Benjamin L, Sole Francesc, Fenaux Pierre, Mufti Ghulam J, Maciejewski Jaroslaw P, Kanetsky Peter A, List Alan |
Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies.
Atherosclerosis 2020 Feb 297 102-110. Feitosa Mary F, Lunetta Kathryn L, Wang Lihua, Wojczynski Mary K, Kammerer Candace M, Perls Thomas, Schupf Nicole, Christensen Kaare, Murabito Joanne M, Province Michael |
[Genetic testing and prenatal diagnosis for a family with 10q22.3q23.2 microdeletion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 Aug 38 (8): 768-770. Zeng Li'na, Zhang Yan, Lin Li, Dong Xian, Li Lij |
Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people.
Endokrynologia Polska 2022 8 . Lin Leweihua, Quan Huibiao, Fang Tuanyu, Lin Lu, Ou Qianying, Zhang Huachuan, Chen Kaining, Zhou Zhigua |
Association between 14 candidate genes, PM2.5, and affective disorders: a study of the Taiwan Biobank. BMC public health 2023 11 23 (1): 2346. Kai-Jie Ma, Yi-Ju Lin, Chiu-Shong Liu, Pei-Ying Tseng, Shi-Heng Wang, Chi-Yu Yao, Jong-Yi Wa |
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- Page last updated:Apr 16, 2024
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