Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Kidney Diseases and LARGE[original query] |
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A genome-wide association study of hypertension and blood pressure in African Americans.
PLoS genetics 2009 Jul 5 (7): e1000564. Adeyemo Adebowale, Gerry Norman, Chen Guanjie, Herbert Alan, Doumatey Ayo, Huang Hanxia, Zhou Jie, Lashley Kerrie, Chen Yuanxiu, Christman Michael, Rotimi Charl |
| Vascular endothelial growth factor gene polymorphisms in North Indian patients with end stage renal disease. Cytokine 2012 May 58 (2): 261-6. Prakash Swayam, Prasad Narayan, Sharma Raj K, Faridi Rehan M, Agrawal Suraks |
| Matrix metalloproteinase-9 gene polymorphisms and chronic kidney disease. American journal of nephrology 2012 Oct 36 (5): 5. Okada R, Kawai S, Naito M, Hishida A, Hamajima N, Shinchi K, Chowdhury Turin T, Suzuki S, Mantjoro EM, Toyomura K, Arisawa K, Kuriyama N, Hosono S, Mikami H, Kubo M, Tanaka H, Wakai K |
| APOL1 G1 genotype modifies the association between HDLC and kidney function in African Americans. BMC genomics 2015 16 421. Bentley Amy R, Divers Jasmin, Shriner Daniel, Doumatey Ayo P, Gutiérrez Orlando M, Adeyemo Adebowale A, Freedman Barry I, Rotimi Charles |
| Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies. Journal of medical genetics 2015 Dec . Schueler Markus, Halbritter Jan, Phelps Ian G, Braun Daniela A, Otto Edgar A, Porath Jonathan D, Gee Heon Yung, Shendure Jay, O'Roak Brian J, Lawson Jennifer A, Nabhan Marwa M, Soliman Neveen A, Nabhan Marwa M, Doherty Dan, Hildebrandt Friedhe |
| 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 |
| Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism. Journal of the Endocrine Society 2017 12 1 (5): 488-499. Guan Bin, Welch James M, Vemulapalli Meghana, Li Yulong, Ling Hua, Kebebew Electron, Simonds William F, Marx Stephen J, Agarwal Sunita |
| The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing. Annals of internal medicine 2018 11 170 (1): 11-21. Rasouly Hila Milo, Groopman Emily E, Heyman-Kantor Reuben, Fasel David A, Mitrotti Adele, Westland Rik, Bier Louise, Weng Chunhua, Ren Zhong, Copeland Brett, Krithivasan Priya, Chung Wendy K, Sanna-Cherchi Simone, Goldstein David B, Gharavi Ali |
| Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. Scientific reports 2021 6 11 (1): 11699. Kolifarhood Goodarz, Sabour Siamak, Akbarzadeh Mahdi, Sedaghati-Khayat Bahareh, Guity Kamran, Rasekhi Dehkordi Saeid, Amiri Roudbar Mahmoud, Hadaegh Farzad, Azizi Fereidoun, Daneshpour Maryam |
| Immune-Related Gene Polymorphisms and Pharmacogenetic Studies in Nephrology. Clinical therapeutics 2021 Nov . Tziastoudi Maria, Cholevas Christos, Stefanidis Ioannis, Theoharides Theoharis |
| The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. Frontiers in cardiovascular medicine 2021 11 8 647416. Natae Shewaye Fituma, Kósa Zsigmond, Sándor János, Merzah Mohammed Abdulridha, Bereczky Zsuzsanna, Pikó Péter, Ádány Róza, Fiatal Szilv |
| Medical Records-Based Genetic Studies of the Complement System.
Journal of the American Society of Nephrology : JASN 2021 5 32 (8): 2031-2047. Khan Atlas, Shang Ning, Petukhova Lynn, Zhang Jun, Shen Yufeng, Hebbring Scott J, Moncrieffe Halima, Kottyan Leah C, Namjou-Khales Bahram, Knevel Rachel, Raychaudhuri Soumya, Karlson Elizabeth W, Harley John B, Stanaway Ian B, Crosslin David, Denny Joshua C, Elkind Mitchell S V, Gharavi Ali G, Hripcsak George, Weng Chunhua, Kiryluk Krzyszt |
| An intermediate-effect size variant in UMOD confers risk for chronic kidney disease. Proceedings of the National Academy of Sciences of the United States of America 2022 8 119 (33): e2114734119. Olinger Eric, Schaeffer Céline, Kidd Kendrah, Elhassan Elhussein A E, Cheng Yurong, Dufour Inès, Schiano Guglielmo, Mabillard Holly, Pasqualetto Elena, Hofmann Patrick, Fuster Daniel G, Kistler Andreas D, Wilson Ian J, Kmoch Stanislav, Raymond Laure, Robert Thomas, , Eckardt Kai-Uwe, Bleyer Anthony J, Köttgen Anna, Conlon Peter J, Wiesener Michael, Sayer John A, Rampoldi Luca, Devuyst Olivi |
| Genetics of Kidney Disease: The Unexpected Role of Rare Disorders. Annual review of medicine 2022 11 74 353-367. Elliott Mark D, Rasouly Hila Milo, Gharavi Ali |
| Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families. Pediatric nephrology (Berlin, Germany) 2023 9 . Dalia Pantel, Nils D Mertens, Ronen Schneider, Selina Hölzel, Jameela A Kari, Sherif El Desoky, Mohamed A Shalaby, Tze Y Lim, Simone Sanna-Cherchi, Shirlee Shril, Friedhelm Hildebran |
| Molecular Diagnosis and Identification of Novel Pathogenic Variants in a Large Cohort of Italian Patients Affected by Polycystic Kidney Diseases. Genes 2023 6 14 (6): . Ersilia Nigro, Maria Amicone, Daniela D'Arco, Gina Sellitti, Oriana De Marco, Maria Guarino, Eleonora Riccio, Antonio Pisani, Aurora Danie |
| The causal relationship between immune cells and different kidney diseases: A Mendelian randomization study. Open medicine (Warsaw, Poland) 2023 12 18 (1): 20230877. Lei Pang, Zijun Ding, Hongqiang Chai, Weibing Shua |
| Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure. Kidney international reports 2023 10 8 (10): 2126-2135. Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin, Efrat Ben-Shalom, Hadas Shasha Lavsky, Oded Volovelsky, Shrikant Mane, Dror Ben-Ruby, Guy Chowers, Karl Skorecki, Yael Borovitz, Maayan Kagan, Nofar Mor, Yulia Khavkin, Shimrit Tzvi-Behr, Shirley Pollack, Moran Plonsky Toder, Michael Geylis, Aviad Schnapp, Rachel Becker-Cohen, Irith Weissman, Ruth Schreiber, Miriam Davidovits, Yaacov Frishberg, Daniella Magen, Ortal Barel, Asaf Vivan |
| Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions. Kidney international reports 2024 8 9 (8): 2514-2526. Bénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, Stefanie Weber, Jens König, Laurence Heidet, Nabila Moussaoui, Jeanne-Pierrette Vu, Stanislas Faguer, Audrey Casemayou, Richa Prakash, Véronique Baudouin, Julien Hogan, Demi Alexandrou, Detlef Bockenhauer, Justine Bacchetta, Bruno Ranchin, Stepanka Pruhova, Jakub Zieg, Annie Lahoche, Christine Okorn, Violetta Antal-Kónya, Denis Morin, Francesca Becherucci, Sandra Habbig, Max C Liebau, Mathilde Mauras, Tom Nijenhuis, Brigitte Llanas, Djalila Mekahli, Julia Thumfart, Burkhard Tönshoff, Laura Massella, Philippe Eckart, Sylvie Cloarec, Alejandro Cruz, Ludwig Patzer, Gwenaelle Roussey, Isabelle Vrillon, Olivier Dunand, Lucie Bessenay, Francesca Taroni, Marcin Zaniew, Ferielle Louillet, Carsten Bergmann, Franz Schaefer, Albertien M van Eerde, Joost P Schanstra, Stéphane Decramer, |
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