Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and TNS1[original query] |
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Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Ophthalmology science 2023 5 3 (3): 100288. Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv |
| Genome-wide association study identifies five loci associated with lung function.
Nature genetics 2010 Jan 42 (1): 36-44. Repapi Emmanouela, Sayers Ian, Wain Louise V, Burton Paul R, Johnson Toby, Obeidat Ma'en, Zhao Jing Hua, Ramasamy Adaikalavan, Zhai Guangju, Vitart Veronique, Huffman Jennifer E, Igl Wilmar, Albrecht Eva, Deloukas Panos, Henderson John, Granell Raquel, McArdle Wendy L, Rudnicka Alicja R, , Barroso Inês, Loos Ruth J F, Wareham Nicholas J, Mustelin Linda, Rantanen Taina, Surakka Ida, Imboden Medea, Wichmann H Erich, Grkovic Ivica, Jankovic Stipan, Zgaga Lina, Hartikainen Anna-Liisa, Peltonen Leena, Gyllensten Ulf, Johansson Asa, Zaboli Ghazal, Campbell Harry, Wild Sarah H, Wilson James F, Gläser Sven, Homuth Georg, Völzke Henry, Mangino Massimo, Soranzo Nicole, Spector Tim D, Polasek Ozren, Rudan Igor, Wright Alan F, Heliövaara Markku, Ripatti Samuli, Pouta Anneli, Naluai Asa Torinsson, Olin Anna-Carin, Torén Kjell, Cooper Matthew N, James Alan L, Palmer Lyle J, Hingorani Aroon D, Wannamethee S Goya, Whincup Peter H, Smith George Davey, Ebrahim Shah, McKeever Tricia M, Pavord Ian D, MacLeod Andrew K, Morris Andrew D, Porteous David J, Cooper Cyrus, Dennison Elaine, Shaheen Seif, Karrasch Stefan, Schnabel Eva, Schulz Holger, Grallert Harald, Bouatia-Naji Nabila, Delplanque Jérôme, Froguel Philippe, Blakey John D, , Britton John R, Morris Richard W, Holloway John W, Lawlor Debbie A, Hui Jennie, Nyberg Fredrik, Jarvelin Marjo-Riitta, Jackson Cathy, Kähönen Mika, Kaprio Jaakko, Probst-Hensch Nicole M, Koch Beate, Hayward Caroline, Evans David M, Elliott Paul, Strachan David P, Hall Ian P, Tobin Martin |
| Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. American journal of respiratory and critical care medicine 2011 Oct 184 (7): 786-95. Soler Artigas María, Wain Louise V, Repapi Emmanouela, Obeidat Ma'en, Sayers Ian, Burton Paul R, Johnson Toby, Zhao Jing Hua, Albrecht Eva, Dominiczak Anna F, Kerr Shona M, Smith Blair H, Cadby Gemma, Hui Jennie, Palmer Lyle J, Hingorani Aroon D, Wannamethee S Goya, Whincup Peter H, Ebrahim Shah, Smith George Davey, Barroso Inês, Loos Ruth J F, Wareham Nicholas J, Cooper Cyrus, Dennison Elaine, Shaheen Seif O, Liu Jason Z, Marchini Jonathan, , Dahgam Santosh, Naluai Asa Torinsson, Olin Anna-Carin, Karrasch Stefan, Heinrich Joachim, Schulz Holger, McKeever Tricia M, Pavord Ian D, Heliövaara Markku, Ripatti Samuli, Surakka Ida, Blakey John D, Kähönen Mika, Britton John R, Nyberg Fredrik, Holloway John W, Lawlor Debbie A, Morris Richard W, James Alan L, Jackson Cathy M, Hall Ian P, Tobin Martin D, |
| Transient early wheeze and lung function in early childhood associated with chronic obstructive pulmonary disease genes. The Journal of allergy and clinical immunology 2014 Jan 133 (1): 68-76.e1-4. Kerkhof Marjan, Boezen H Marike, Granell Raquel, Wijga Alet H, Brunekreef Bert, Smit Henriëtte A, de Jongste Johan C, Thijs Carel, Mommers Monique, Penders John, Henderson John, Koppelman Gerard H, Postma Dirkje |
| Association of five genetic variants with chronic obstructive pulmonary disease susceptibility and spirometric phenotypes in a Chinese Han population. Respirology (Carlton, Vic.) 2014 Feb 19 (2): 262-8. Yang Jing, Zhou Haixia, Liang Binmiao, Xiao Jun, Su Zhiguang, Chen Hong, Ma Chunlan, Li Dengxue, Feng Yulin, Ou Xuem |
| Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.
The Journal of allergy and clinical immunology 2014 Jun 133 (6): 1564-71. Ferreira Manuel A R, Matheson Melanie C, Tang Clara S, Granell Raquel, Ang Wei, Hui Jennie, Kiefer Amy K, Duffy David L, Baltic Svetlana, Danoy Patrick, Bui Minh, Price Loren, Sly Peter D, Eriksson Nicholas, Madden Pamela A, Abramson Michael J, Holt Patrick G, Heath Andrew C, Hunter Michael, Musk Bill, Robertson Colin F, Le Souëf Peter, Montgomery Grant W, Henderson A John, Tung Joyce Y, Dharmage Shyamali C, Brown Matthew A, James Alan, Thompson Philip J, Pennell Craig, Martin Nicholas G, Evans David M, Hinds David A, Hopper John L, |
| Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease. American journal of respiratory cell and molecular biology 2018 Jun . Prokopenko Dmitry, Sakornsakolpat Phuwanat, Fier Heide Loehlein, Qiao Dandi, Parker Margaret M, McDonald Merry-Lynn N, Manichaikul Ani, Rich Stephen S, Barr R Graham, Williams Christopher J, Brantly Mark L, Lange Christoph, Beaty Terri H, Crapo James D, Silverman Edwin K, Cho Michael |
| Coding Variants Coupled With Rapid Modeling in Zebrafish Implicate Dynein Genes, dnaaf1 and zmynd10, as Adolescent Idiopathic Scoliosis Candidate Genes. Frontiers in cell and developmental biology 2020 8 582255. Wang Yunjia, Liu Zhenhao, Yang Guanteng, Gao Qile, Xiao Lige, Li Jiong, Guo Chaofeng, Troutwine Benjamin R, Gray Ryan S, Xie Lu, Zhang Hong |
| Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.
Circulation. Genomic and precision medicine 2021 9 14 (5): e003148. Yu Mengyao, Kyryachenko Sergiy, Debette Stephanie, Amouyel Philippe, Schott Jean-Jacques, Le Tourneau Thierry, Dina Christian, Norris Russell A, Hagège Albert A, Jeunemaitre Xavier, Bouatia-Naji Nabi |
| Tensin 1 (TNS1) is a modifier gene for low body mass index (BMI) in homozygous [F508del]CFTR patients. Physiological reports 2021 Jun 9 (11): e14886. Walton Nathan I, Zhang Xijun, Soltis Anthony R, Starr Joshua, Dalgard Clifton L, Wilkerson Matthew D, Conrad Douglas, Pollard Harvey |
| Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
| Across-breed genetic investigation of canine hip dysplasia, elbow dysplasia, and anterior cruciate ligament rupture using whole-genome sequencing. Frontiers in genetics 2022 12 13 913354. Binversie Emily E, Momen Mehdi, Rosa Guilherme J M, Davis Brian W, Muir Pet |
| TNS1 and NRXN1 Genes Interacting With Early-Life Smoking Exposure in Asthma-Plus-Eczema Susceptibility. Allergy, asthma & immunology research 2023 11 15 (6): 779-794. Patricia Margaritte-Jeannin, Raphaël Vernet, Ashley Budu-Aggrey, Markus Ege, Anne-Marie Madore, Christophe Linhard, Hamida Mohamdi, Erika von Mutius, Raquell Granell, Florence Demenais, Cathrine Laprise, Emmanuelle Bouzigon, Marie-Hélène Dizi |
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