Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 55 Records) |
| Query Trace: Disease and MYH9[original query] |
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| Genetic contribution and associated pathophysiology in end-stage renal disease. The application of clinical genetics 2013 6 3 65-84. Agrawal Suraksha, Agarwal Ss, Naik Si |
| Pilot study of an association between a common variant in the non-muscle myosin heavy chain 9 (MYH9) gene and type 2 diabetic nephropathy in a Taiwanese population. The application of clinical genetics 2013 6 3 17-22. Hsieh Chang-Hsun, Hung Yi-Jen, Pei Dee, Kuo Shi-Wen, Lin Euge |
| Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. Medicina oral, patología oral y cirugía bucal 2013 May 18 (3): e414-20. Paranaíba Lívia-Máris-Ribeiro, de Aquino Sibele-Nascimento, Bufalino Andreia, Martelli-Júnior Hercílio, Graner Edgard, Brito Luciano-Abreu, e Passos-Bueno Maria-Rita dos Santos, Coletta Ricardo-D, Swerts Mário-Sérgio-Olivei |
| Epistatic role of the MYH9/APOL1 region on familial hematuria genes. PloS one 2013 8 (3): e57925. Voskarides Konstantinos, Demosthenous Panayiota, Papazachariou Louiza, Arsali Maria, Athanasiou Yiannis, Zavros Michalis, Stylianou Kostas, Xydakis Dimitris, Daphnis Eugenios, Gale Daniel P, Maxwell Patrick H, Elia Avraam, Pattaro Cristian, Pierides Alkis, Deltas Constantin |
| MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population. PloS one 2014 9 (3): e87716. Colares Vinícius Sardão, Titan Silvia Maria de Oliveira, Pereira Alexandre da Costa, Malafronte Patrícia, Cardena Mari M, Santos Sidney, Santos Paulo C, Fridman Cíntia, Barros Rui Toledo, Woronik Viktór |
| Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease. PloS one 2014 9 (2): e88273. Palmer Nicholette D, Ng Maggie C Y, Hicks Pamela J, Mudgal Poorva, Langefeld Carl D, Freedman Barry I, Bowden Donald |
| Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression. American journal of nephrology 2015 Sep 42 (2): 99-106. Hawkins Gregory A, Friedman David J, Lu Lingyi, McWilliams David R, Chou Jeff W, Sajuthi Satria, Divers Jasmin, Parekh Rulan S, Li Man, Genovese Giulio, Pollack Martin R, Hicks Pamela J, Bowden Donald W, Ma Lijun, Freedman Barry I, Langefeld Carl |
| Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease. Ear and hearing 2015 Jul . Verver Eva J J, Topsakal Vedat, Kunst Henricus P M, Huygen Patrick L M, Heller Paula G, Pujol-Moix Nuria, Savoia Anna, Benazzo Marco, Fierro Tiziana, Grolman Wilko, Gresele Paolo, Pecci Alessand |
| In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress. PLoS genetics 2015 Jul 11 (7): e1005349. Anderson Blair R, Howell David N, Soldano Karen, Garrett Melanie E, Katsanis Nicholas, Telen Marilyn J, Davis Erica E, Ashley-Koch Allison |
| Copy Number Variation at the APOL1 Locus. PloS one 2015 10 (5): e0125410. Ruchi Rupam, Genovese Giulio, Lee Jessica, Charoonratana Victoria T, Bernhardy Andrea J, Alper Seth L, Kopp Jeffrey B, Thadhani Ravi, Friedman David J, Pollak Martin |
| MYH9 gene polymorphisms may be associated with cerebrovascular blood flow in patients with type 2 diabetes. Genetics and molecular research : GMR 2015 14 (1): 1008-16. Ling C, Cai C Y, Chang B C, Shi W T, Wei F J, Yu P, Chen L M, Li W |
| Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis. Transplantation proceedings 2016 Jun 48 (5): 1561-5. Pazik J, Lewandowski Z, Oldak M, Ozieblo D, Perkowska Ptasinska A, Sadowska A, Nowacka-Cieciura E, Nowaczyk M, Malejczyk J, Kwiatkowski A, Durlik |
| Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China. Kidney & blood pressure research 2016 41 (6): 956-965. Liu Liping, Wang Caili, Mi Yan, Liu Dan, Li Li, Fan Junying, Nan Lei, Jia Niya, Du |
| KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2016 21 285-96. Bailey Jessica N Cooke, Wilson Sarah, Brown-Gentry Kristin, Goodloe Robert, Crawford Dana |
| Progressive macrothrombocytopenia and hearing loss in a large family with DIAPH1 related disease. American journal of medical genetics. Part A 2017 8 173 (10): 2826-2830. Ganaha Akira, Kaname Tadashi, Shinjou Ayano, Chinen Yasutsugu, Yanagi Kumiko, Higa Teruyuki, Kondo Shunsuke, Suzuki Mik |
| Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD). Journal of human genetics 2018 Aug . Wang Kun, Zhao Sen, Zhang Qianqian, Yuan Jian, Liu Jiaqi, Ding Xinghuan, Song Xiaofei, Lin Jiachen, Du Renqian, Zhou Yangzhong, Sugimoto Michihiko, Chen Weisheng, Yuan Bo, Liu Jian, Yan Zihui, Liu Bowen, Zhang Yisen, Li Xiaoxin, Niu Yuchen, Long Bo, Shen Yiping, Zhang Shuyang, Abe Kuniya, Su Jianzhong, Wu Zhihong, Wu Nan, Liu Pengfei, Yang Xinjian, |
| Association between MYH9 and APOL1 Gene Polymorphisms and the Risk of Diabetic Kidney Disease in Patients with Type 2 Diabetes in a Chinese Han Population. Journal of diabetes research 2018 2018 5068578. Zhao Hailing, Ma Liang, Yan Meihua, Wang Yan, Zhao Tingting, Zhang Haojun, Liu Peng, Liu Yanzhen, Li Pi |
| 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 |
| An African perspective on the genetic risk of chronic kidney disease: a systematic review. BMC medical genetics 2018 10 19 (1): 187. George Cindy, Yako Yandiswa Y, Okpechi Ikechi G, Matsha Tandi E, Kaze Folefack Francois J, Kengne Andre |
| 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 |
| Association between polymorphism rs2032487 in the non-muscle myosin heavy chain IIA gene (MHY9) and chronic kidney disease secondary to type 2 diabetes mellitus in a population of the Canary Islands. Endocrinologia, diabetes y nutricion 2019 Apr . Boronat Mauro, Tugores Antonio, Saavedra Pedro, Garay Paloma, Bosch Elvira, Lorenzo Dionisio, García-Cantón Cés |
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A.
Annals of neurology 2019 Mar 85 (3): 316-330. Tao Feifei, Beecham Gary W, Rebelo Adriana P, Svaren John, Blanton Susan H, Moran John J, Lopez-Anido Camila, Morrow Jasper M, Abreu Lisa, Rizzo Devon, Kirk Callyn A, Wu Xingyao, Feely Shawna, Verhamme Camiel, Saporta Mario A, Herrmann David N, Day John W, Sumner Charlotte J, Lloyd Thomas E, Li Jun, Yum Sabrina W, Taroni Franco, Baas Frank, Choi Byung-Ok, Pareyson Davide, Scherer Steven S, Reilly Mary M, Shy Michael E, Züchner Stephan, |
| Effect of donor non-muscle myosin heavy chain (MYH9) gene polymorphisms on clinically relevant kidney allograft dysfunction. BMC nephrology 2020 Sep 21 (1): 380. Pazik Joanna, Oldak Monika, Ozi?b?o Dominika, Materkowska Dominika D?borska, Sadowska Anna, Malejczyk Jacek, Durlik Magdale |
| Association of MYH9-rs3752462 polymorphisms with chronic kidney disease among clinically diagnosed hypertensive patients: a case-control study in a Ghanaian population. Clinical hypertension 2020 26 15. Owiredu William K B A, Appiah Michael, Obirikorang Christian, Adu Evans Asamoah, Boima Vincent, Amos-Abanyie Ernestine Kubi, Akyaw Priscilla Abena, Owiredu Eddie-Williams, Acheampong Emmanu |
| Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene. Medicine 2020 Jan 99 (3): e18722. Adam Khalid Mohamed, Mohammed Ali Mahmoud, Elamin Abubakr A |
| A Custom Target Next-Generation Sequencing 70-Gene Panel and Replication Study to Identify Genetic Markers of Diabetic Kidney Disease. Genes 2021 12 12 (12): . Mota-Zamorano Sonia, González Luz María, Robles Nicolás Roberto, Valdivielso José Manuel, Cancho Bárbara, López-Gómez Juan, Gervasini Guiller |
| Association of the myosin heavy chain 9 gene single nucleotide polymorphism with inflammatory bowel disease. Biochemistry and biophysics reports 2021 Dec 28 101113. Abd Al-Aliem Ahmed Ezz El-Arab, Badr Eman A E, El-Shayeb Elsayed Ibrahem, Taman Ahmed Megahed Ahmed, Gadallah Abd El-Naser Abd El-At |
| [Unexpected diagnosis of nephronopthisis in the genetic study of hypertension due to histological diagnosis of benign nephroangioesclerosis evolved in a young caucasian patient]. Hipertension y riesgo vascular 2023 3 . Heras Benito M, Pérez García M L, Antúnez Plaza P, Montero Mateos |
| Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
| Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
- Page last reviewed:Feb 1, 2024
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