Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: SHROOM3[original query] |
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Multiple loci associated with indices of renal function and chronic kidney disease.
Nature genetics 2009 Jun 41 (6): 712-7. Köttgen Anna, Glazer Nicole L, Dehghan Abbas, Hwang Shih-Jen, Katz Ronit, Li Man, Yang Qiong, Gudnason Vilmundur, Launer Lenore J, Harris Tamara B, Smith Albert V, Arking Dan E, Astor Brad C, Boerwinkle Eric, Ehret Georg B, Ruczinski Ingo, Scharpf Robert B, Chen Yii-Der Ida, de Boer Ian H, Haritunians Talin, Lumley Thomas, Sarnak Mark, Siscovick David, Benjamin Emelia J, Levy Daniel, Upadhyay Ashish, Aulchenko Yurii S, Hofman Albert, Rivadeneira Fernando, Uitterlinden André G, van Duijn Cornelia M, Chasman Daniel I, Paré Guillaume, Ridker Paul M, Kao W H Linda, Witteman Jacqueline C, Coresh Josef, Shlipak Michael G, Fox Caroline |
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
PLoS genetics 2010 Aug 6 (8): 8. Meyer Tamra E, Verwoert Germaine C, Hwang Shih-Jen, Glazer Nicole L, Smith Albert V, van Rooij Frank J A, Ehret Georg B, Boerwinkle Eric, Felix Janine F, Leak Tennille S, Harris Tamara B, Yang Qiong, Dehghan Abbas, Aspelund Thor, Katz Ronit, Homuth Georg, Kocher Thomas, Rettig Rainer, Ried Janina S, Gieger Christian, Prucha Hanna, Pfeufer Arne, Meitinger Thomas, Coresh Josef, Hofman Albert, Sarnak Mark J, Chen Yii-Der Ida, Uitterlinden André G, Chakravarti Aravinda, Psaty Bruce M, van Duijn Cornelia M, Kao W H Linda, Witteman Jacqueline C M, Gudnason Vilmundur, Siscovick David S, Fox Caroline S, Köttgen Anna, , |
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. PLoS genetics 2011 Sep 7 (9): e1002292. Böger Carsten A, Gorski Mathias, Li Man, Hoffmann Michael M, Huang Chunmei, Yang Qiong, Teumer Alexander, Krane Vera, O'Seaghdha Conall M, Kutalik Zoltán, Wichmann H-Erich, Haak Thomas, Boes Eva, Coassin Stefan, Coresh Josef, Kollerits Barbara, Haun Margot, Paulweber Bernhard, Köttgen Anna, Li Guo, Shlipak Michael G, Powe Neil, Hwang Shih-Jen, Dehghan Abbas, Rivadeneira Fernando, Uitterlinden André, Hofman Albert, Beckmann Jacques S, Krämer Bernhard K, Witteman Jacqueline, Bochud Murielle, Siscovick David, Rettig Rainer, Kronenberg Florian, Wanner Christoph, Thadhani Ravi I, Heid Iris M, Fox Caroline S, Kao W H, |
Validated SNPs for eGFR and their associations with albuminuria. Human molecular genetics 2012 Jul 21 (14): 3293-8. Ellis Jaclyn W, Chen Ming-Huei, Foster Meredith C, Liu Ching-Ti, Larson Martin G, de Boer Ian, Köttgen Anna, Parsa Afshin, Bochud Murielle, Böger Carsten A, Kao Linda, Fox Caroline S, O'Seaghdha Conall M, , |
Investigation of known estimated glomerular filtration rate loci in patients with type 2 diabetes. Diabetic medicine : a journal of the British Diabetic Association 2013 Oct 30 (10): 1230-5. Deshmukh H A, Palmer C N A, Morris A D, Colhoun H |
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study.
BMC genetics 2015 May 16 56. Tin Adrienne, Köttgen Anna, Folsom Aaron R, Maruthur Nisa M, Tajuddin Salman M, Nalls Mike A, Evans Michele K, Zonderman Alan B, Friedrich Christopher A, Boerwinkle Eric, Coresh Josef, Kao Wen Hong Lin |
Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans. Human genetics 2016 Jul . Guan Meijian, Ma Jun, Keaton Jacob M, Dimitrov Latchezar, Mudgal Poorva, Stromberg Mary, Bonomo Jason A, Hicks Pamela J, Freedman Barry I, Bowden Donald W, Ng Maggie C |
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits. Nature genetics 2016 08 48 (8): 867-76. Authors are not available |
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
Nature communications 2016 7 10605. Zhang Yong-Biao, Hu Jintian, Zhang Jiao, Zhou Xu, Li Xin, Gu Chaohao, Liu Tun, Xie Yangchun, Liu Jiqiang, Gu Mingliang, Wang Panpan, Wu Tingting, Qian Jin, Wang Yue, Dong Xiaoqun, Yu Jun, Zhang Qingg |
The influence of living donor SHROOM3 and ABCB1 genetic variants on renal function after kidney transplantation. Pharmacogenetics and genomics 2016 Oct . Yan Lin, Li Yi, Tang Jiang-Tao, An Yun-Fei, Luo Li-Mei, Dai Bo, Shi Yun-Ying, Wang Lan-L |
Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers. PloS one 2017 12 (10): e0185476. Kubo Yoko, Imaizumi Takahiro, Ando Masahiko, Nakatochi Masahiro, Yasuda Yoshinari, Honda Hiroyuki, Kuwatsuka Yachiyo, Kato Sawako, Kikuchi Kyoko, Kondo Takaaki, Iwata Masamitsu, Nakashima Toru, Yasui Hiroshi, Takamatsu Hideki, Okajima Hiroshi, Yoshida Yasuko, Maruyama Shoic |
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Human genetics 2017 Mar 136 (3): 275-286. Leslie Elizabeth J, Carlson Jenna C, Shaffer John R, Butali Azeez, Buxó Carmen J, Castilla Eduardo E, Christensen Kaare, Deleyiannis Fred W B, Leigh Field L, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Feingold Eleanor, Weinberg Seth M, Murray Jeffrey C, Beaty Terri H, Marazita Mary |
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations. BMC nephrology 2018 Apr 19 (1): 88. Cyrus Cyril, Al-Mueilo Samir, Vatte Chittibabu, Chathoth Shahanas, Li Yun R, Qutub Hatem, Al Ali Rudaynah, Al-Muhanna Fahad, Lanktree Matthew B, Alkharsah Khaled Riyad, Al-Rubaish Abdullah, Kim-Mozeleski Brian, Keating Brendan, Al Ali Ame |
Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD. Journal of the American Society of Nephrology : JASN 2018 2 29 (5): 1525-1535. Prokop Jeremy W, Yeo Nan Cher, Ottmann Christian, Chhetri Surya B, Florus Kacie L, Ross Emily J, Sosonkina Nadiya, Link Brian A, Freedman Barry I, Coppola Candice J, McDermott-Roe Chris, Leysen Seppe, Milroy Lech-Gustav, Meijer Femke A, Geurts Aron M, Rauscher Frank J, Ramaker Ryne, Flister Michael J, Jacob Howard J, Mendenhall Eric M, Lazar Joz |
Genetic and functional analysis of SHROOM1-4 in a Chinese neural tube defect cohort. Human genetics 2018 Feb . Chen Zhongzhong, Kuang Lele, Finnell Richard H, Wang Hongy |
Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study. BMJ open 2018 12 8 (12): e020759. Osman Wael M, Jelinek Herbert F, Tay Guan K, Khandoker Ahsan H, Khalaf Kinda, Almahmeed Wael, Hassan Mohamed H, Alsafar Habiba |
Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients. International journal of nephrology 2019 9 2019 1095215. Cyrus Cyril, Chathoth Shahanas, Vatte Chittibabu, Alrubaish Nafie, Almuhanna Othman, Borgio J Francis, Al-Mueilo Samir, Al Muhanna Fahd, Al Ali Amein |
Genetic Susceptibility to Chronic Kidney Disease - Some More Pieces for the Heritability Puzzle. Frontiers in genetics 2019 10 453. Cañadas-Garre Marisa, Anderson Kerry, Cappa Ruaidhri, Skelly Ryan, Smyth Laura Jane, McKnight Amy Jayne, Maxwell Alexander Pet |
Loci associated with genomic damage levels in chronic kidney disease patients and controls. Mutation research 2020 04 852 503167. Corredor Zuray, da Silva Filho Miguel Inácio, Rodríguez-Ribera Lara, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José Aurelio, Henández Alba, Försti Asta, Marcos Ricard, Pastor Susa |
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific reports 2020 Jan 10 (1): 144. Corredor Zuray, Filho Miguel Inácio da Silva, Rodríguez-Ribera Lara, Velázquez Antonia, Hernández Alba, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José, Vallés Prats Martí, Calabia Martínez Jordi, Försti Asta, Marcos Ricard, Pastor Susa |
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PloS one 2022 17 (8): e0273280. Przyby?a Weronika, Gjersvoll Paulsen Kirsti Marie, Mishra Charitra Kumar, Nygård Ståle, Engebretsen Solveig, Ruud Ellen, Trøen Gunhild, Beiske Klaus, Baumbusch Lars Oliv |
Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors.
Scientific reports 2022 4 12 (1): 6662. Aggarwal Puja, Hutcheson Katherine A, Yu Robert, Wang Jian, Fuller Clifton D, Garden Adam S, Goepfert Ryan P, Rigert Jillian, Mott Frank E, Lu Charles, Lai Stephen Y, Gunn G Brandon, Chambers Mark S, Li Guojun, Wu Chih-Chieh, Hanna Ehab Y, Sturgis Erich M, Shete Sanj |
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