Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: GPR98[original query] |
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Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.
Molecular psychiatry 2011 Mar 16 (3): 321-32. Adkins D E, Aberg K, McClay J L, Bukszár J, Zhao Z, Jia P, Stroup T S, Perkins D, McEvoy J P, Lieberman J A, Sullivan P F, van den Oord E J C |
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Human molecular genetics 2011 Jun 20 (11): 2273-84. Fox Ervin R, Young J Hunter, Li Yali, Dreisbach Albert W, Keating Brendan J, Musani Solomon K, Liu Kiang, Morrison Alanna C, Ganesh Santhi, Kutlar Abdullah, Ramachandran Vasan S, Polak Josef F, Fabsitz Richard R, Dries Daniel L, Farlow Deborah N, Redline Susan, Adeyemo Adebowale, Hirschorn Joel N, Sun Yan V, Wyatt Sharon B, Penman Alan D, Palmas Walter, Rotter Jerome I, Townsend Raymond R, Doumatey Ayo P, Tayo Bamidele O, Mosley Thomas H, Lyon Helen N, Kang Sun J, Rotimi Charles N, Cooper Richard S, Franceschini Nora, Curb J David, Martin Lisa W, Eaton Charles B, Kardia Sharon L R, Taylor Herman A, Caulfield Mark J, Ehret Georg B, Johnson Toby, , Chakravarti Aravinda, Zhu Xiaofeng, Levy Dani |
GPR98/Gpr98 gene is involved in the regulation of human and mouse bone mineral density. The Journal of clinical endocrinology and metabolism 2012 Apr 97 (4): E565-74. Urano Tomohiko, Shiraki Masataka, Yagi Hideshi, Ito Masako, Sasaki Noriko, Sato Makoto, Ouchi Yasuyoshi, Inoue Satos |
Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations. Clinical genetics 2015 Jun 87 (6): 588-93. Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li |
Targeted next generation sequencing for molecular diagnosis of Usher syndrome. Orphanet journal of rare diseases 2014 9 168. Aparisi María J, Aller Elena, Fuster-García Carla, García-García Gema, Rodrigo Regina, Vázquez-Manrique Rafael P, Blanco-Kelly Fiona, Ayuso Carmen, Roux Anne-Françoise, Jaijo Teresa, Millán José |
Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. Orphanet journal of rare diseases 2015 10 (1): 110. Jiang Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui, Sui Ruifa |
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing. Molecular genetics & genomic medicine 2015 May 3 (3): 189-96. Ammar-Khodja Fatima, Bonnet Crystel, Dahmani Malika, Ouhab Sofiane, Lefèvre Gaelle M, Ibrahim Hassina, Hardelin Jean-Pierre, Weil Dominique, Louha Malek, Petit Christi |
Cone dystrophy in patient with homozygous RP1L1 mutation. BioMed research international 2015 2015 545243. Kikuchi Sachiko, Kameya Shuhei, Gocho Kiyoko, El Shamieh Said, Akeo Keiichiro, Sugawara Yuko, Yamaki Kunihiko, Zeitz Christina, Audo Isabelle, Takahashi Hiros |
[Genome-wide association study for Osteoporosis]. Clinical calcium 2016 Apr 26 (4): 537-43. Mori Seiji |
ADGRV1 is implicated in myoclonic epilepsy. Epilepsia 2017 Dec . Myers Kenneth A, Nasioulas Steven, Boys Amber, McMahon Jacinta M, Slater Howard, Lockhart Paul, Sart Desirée du, Scheffer Ingrid |
Genetic analysis of a Chinese family with members affected with Usher syndrome type II and Waardenburg syndrome type IV. International journal of pediatric otorhinolaryngology 2017 11 102 114-118. Wang Xueling, Lin Xiao-Jiang, Tang Xiangrong, Chai Yong-Chuan, Yu De-Hong, Chen Dong-Ye, Wu H |
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia. Oncotarget 2017 Sep 8 (38): 63324-63332. Wang Pu, Fan Xinmiao, Wang Yibei, Fan Yue, Liu Yaping, Zhang Shuyang, Chen Xiaow |
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular genetics 2017 Oct 10 (5): . Guo Tingwei, Repetto Gabriela M, McDonald McGinn Donna M, Chung Jonathan H, Nomaru Hiroko, Campbell Christopher L, Blonska Anna, Bassett Anne S, Chow Eva W C, Mlynarski Elisabeth E, Swillen Ann, Vermeesch Joris, Devriendt Koen, Gothelf Doron, Carmel Miri, Michaelovsky Elena, Schneider Maude, Eliez Stephan, Antonarakis Stylianos E, Coleman Karlene, Tomita-Mitchell Aoy, Mitchell Michael E, Digilio M Cristina, Dallapiccola Bruno, Marino Bruno, Philip Nicole, Busa Tiffany, Kushan-Wells Leila, Bearden Carrie E, Piotrowicz Ma?gorzata, Hawu?a Wanda, Roberts Amy E, Tassone Flora, Simon Tony J, van Duin Esther D A, van Amelsvoort Thérèse A, Kates Wendy R, Zackai Elaine, Johnston H Richard, Cutler David J, Agopian A J, Goldmuntz Elizabeth, Mitchell Laura E, Wang Tao, Emanuel Beverly S, Morrow Bernice E, |
Comprehensive Molecular Screening in Chinese Usher Syndrome Patients. Investigative ophthalmology & visual science 2018 Mar 59 (3): 1229-1237. Sun Tengyang, Xu Ke, Ren Yanfan, Xie Yue, Zhang Xiaohui, Tian Lu, Li Ya |
The Genetics of Usher Syndrome in the Israeli and Palestinian Populations. Investigative ophthalmology & visual science 2018 3 59 (2): 1095-1104. Khalaileh Ayat, Abu-Diab Alaa, Ben-Yosef Tamar, Raas-Rothschild Annick, Lerer Israela, Alswaiti Yahya, Chowers Itay, Banin Eyal, Sharon Dror, Khateb Sam |
Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes. Genes 2022 8 13 (8): . Feenstra Helena M, Al-Khuzaei Saoud, Shah Mital, Broadgate Suzanne, Shanks Morag, Kamath Archith, Yu Jing, Jolly Jasleen K, MacLaren Robert E, Clouston Penny, Halford Stephanie, Downes Susan |
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- Page last updated:Mar 25, 2024
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