Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and WNK1[original query] |
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| Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain : a journal of neurology 2009 Oct 132 (Pt 10): 2699-711. Rotthier Annelies, Baets Jonathan, De Vriendt Els, Jacobs An, Auer-Grumbach Michaela, Lévy Nicolas, Bonello-Palot Nathalie, Kilic Sara Sebnem, Weis Joachim, Nascimento Andrés, Swinkels Marielle, Kruyt Moyo C, Jordanova Albena, De Jonghe Peter, Timmerman Vince |
| Association of WNK1 exon 1 polymorphisms with essential hypertension in Hani and Yi minorities of China. Journal of genetics and genomics = Yi chuan xue bao 2011 Apr 38 (4): 165-71. Cun Yina, Li Jin, Tang Wenru, Sheng Xiaozhi, Yu Haijing, Zheng Bingrong, Xiao Chunj |
| Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation research 2012 Nov . Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freeman BI, Coresh J, Kao LW, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A |
| Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis. PLoS genetics 2014 Jul 10 (7): e1004376. LaRusch Jessica, Jung Jinsei, General Ignacio J, Lewis Michele D, Park Hyun Woo, Brand Randall E, Gelrud Andres, Anderson Michelle A, Banks Peter A, Conwell Darwin, Lawrence Christopher, Romagnuolo Joseph, Baillie John, Alkaade Samer, Cote Gregory, Gardner Timothy B, Amann Stephen T, Slivka Adam, Sandhu Bimaljit, Aloe Amy, Kienholz Michelle L, Yadav Dhiraj, Barmada M Michael, Bahar Ivet, Lee Min Goo, Whitcomb David C, |
| Interaction of Alu Polymorphisms and Novel Measures of Discrimination in Association with Blood Pressure in African Americans Living in Tallahassee, Florida. Human biology 2015 Oct 87 (4): 295-305. Boulter Alexis C, Quinlan Jacklyn, Miró-Herrans Aida T, Pearson Laurel N, Todd Nubiana L, , Gravlee Clarence C, Mulligan Connie |
| Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
| Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. Frontiers in genetics 2022 8 13 886038. Alaamery Manal, Alghamdi Jahad, Massadeh Salam, Alsawaji Mona, Aljawini Nora, Albesher Nour, Alghamdi Bader, Almutairi Mansour, Hejaili Fayez, Alfadhel Majid, Baz Batoul, Almuzzaini Bader, Almutairi Adel F, Abdullah Mubarak, Quintana Francisco J, Sayyari Abdull |
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