Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Asthma and MAF[original query] |
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| Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases. BMC medical genetics 2006 7 (): 20. Smyth Deborah J, Howson Joanna M M, Payne Felicity, Maier Lisa M, Bailey Rebecca, Holland Kieran, Lowe Christopher E, Cooper Jason D, Hulme John S, Vella Adrian, Dahlman Ingrid, Lam Alex C, Nutland Sarah, Walker Neil M, Twells Rebecca C J, Todd John |
| [TRPV1 UTR-3 polymorphism and susceptibility of childhood asthma of the Han Nationality in Beijing]. Wei sheng yan jiu = Journal of hygiene research 2009 Sep 38 (5): 516-21. Wang Qiang, Bai Xuetao, Xu Donggang, Xu Dongqun, Li Hong, Fang Jianlong, Zhu He, Fu Wenliang, Cai Xin, Wang Jinfeng, Jin Zhe, Wang Qin, Xu Chunyu, Chang Junr |
| A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31-32 region and asthma. Journal of human genetics 2010 Jun 55 (6): 358-65. Kim Jeong-Hyun, Cheong Hyun Sub, Park Byung-Lae, Bae Joon Seol, Jung Seok, Yoon Sang-Hyuk, Park Jong Sook, Jang An Soo, Park Sung Woo, Uh Soo-Taek, Kim Yong-Hoon, Hwang Hyeon-Kyu, Park Choon-Sik, Shin Hyoung D |
| Leukotriene B4 receptor locus gene characterisation and association studies in asthma. BMC medical genetics 2012 Nov 13 (1): 1. Tulah AS, Beghé B, Barton SJ, Holloway JW, Sayers I |
| Toll-like receptor 2 subfamily genotypes are not associated with severity of bronchiolitis or postbronchiolitis wheezing in infants. Acta paediatrica (Oslo, Norway : 1992) 2013 Dec 102 (12): 1160-4. Nuolivirta Kirsi, Vuononvirta Juho, Peltola Ville, Koponen Petri, Helminen Merja, He Qiushui, Korppi Mat |
| Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. Frontiers in genetics 2014 5 401. Namjou Bahram, Marsolo Keith, Caroll Robert J, Denny Joshua C, Ritchie Marylyn D, Verma Shefali S, Lingren Todd, Porollo Aleksey, Cobb Beth L, Perry Cassandra, Kottyan Leah C, Rothenberg Marc E, Thompson Susan D, Holm Ingrid A, Kohane Isaac S, Harley John |
| Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Nature communications 2015 6 5965. Igartua Catherine, Myers Rachel A, Mathias Rasika A, Pino-Yanes Maria, Eng Celeste, Graves Penelope E, Levin Albert M, Del-Rio-Navarro Blanca E, Jackson Daniel J, Livne Oren E, Rafaels Nicholas, Edlund Christopher K, Yang James J, Huntsman Scott, Salam Muhammad T, Romieu Isabelle, Mourad Raphael, Gern James E, Lemanske Robert F, Wyss Annah, Hoppin Jane A, Barnes Kathleen C, Burchard Esteban G, Gauderman W James, Martinez Fernando D, Raby Benjamin A, Weiss Scott T, Williams L Keoki, London Stephanie J, Gilliland Frank D, Nicolae Dan L, Ober Caro |
| Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases. G3 (Bethesda, Md.) 2016 May . Murk William, DeWan Andrew |
| Rare coding variants pinpoint genes that control human hematological traits. PLoS genetics 2017 Aug 13 (8): e1006925. Mousas Abdou, Ntritsos Georgios, Chen Ming-Huei, Song Ci, Huffman Jennifer E, Tzoulaki Ioanna, Elliott Paul, Psaty Bruce M, , Auer Paul L, Johnson Andrew D, Evangelou Evangelos, Lettre Guillaume, Reiner Alexander |
| A functional splice variant associated with decreased asthma risk abolishes the ability of gasdermin B to induce epithelial cell pyroptosis. The Journal of allergy and clinical immunology 2018 Jan . Panganiban Ronald A, Sun Maoyun, Dahlin Amber, Park Hae-Ryung, Kan Mengyuan, Himes Blanca E, Mitchel Jennifer A, Iribarren Carlos, Jorgenson Eric, Randell Scott H, Israel Elliot, Tantisira Kelan, Shore Stephanie, Park Jin-Ah, Weiss Scott T, Wu Ann Chen, Lu Qu |
| Metabolites downstream of predicted loss-of-function variants inform relationship to disease. Molecular genetics and metabolism 2019 11 128 (4): 476-482. Li Mengbo, Wang Andy, Quek Lake-Ee, Vernon Stephen, Figtree Gemma A, Yang Jean, O'Sullivan John |
| Associations between TMEM196 polymorphisms and NSAID-exacerbated respiratory disease in asthma. Pharmacogenetics and genomics 2019 Jan . Lee Jong-Uk, Chang Hun Soo, Baek Dong Gyu, Shin Hyoung Doo, Park Choon-Sik, Park Jong-So |
| A Novel Mutation in the IL6R Gene Identified in a Family with Asthma Patients. Genetic testing and molecular biomarkers 2020 9 24 (10): 658-664. Trueb Beat, Zhuang Lei, Villiger Peter |
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease.
American journal of physiology. Lung cellular and molecular physiology 2021 Apr . Moll Matthew, Jackson Victoria E, Yu Bing, Grove Megan L, London Stephanie J, Gharib Sina A, Bartz Traci M, Sitlani Colleen M, Dupuis Josée, O'Connor George T, Xu Hanfei, Cassano Patricia A, Patchen Bonnie Kaufmann, Kim Woo Jin, Park Jinkyeong, Kim Kun Hee, Han Buhm, Barr R Graham, Manichaikul Ani, Nguyen Jennifer N, Rich Stephen S, Lahousse Lies, Terzikhan Natalie, Brusselle Guy, Sakornsakolpat Phuwanat, Liu Jiangyuan, Benway Christopher J, Hall Ian P, Tobin Martin D, Wain Louise V, Silverman Edwin K, Cho Michael H, Hobbs Brian |
| Genome-wide association studies of exacerbations in children using long-acting beta2-agonists.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2021 Mar . Slob Elise M A, Richards Levi B, Vijverberg Susanne J H, Longo Cristina, Koppelman Gerard H, Pijnenburg Mariëlle W H, Bel Elisabeth H D, Neerincx Anne H, Herrera Luis Esther, Perez-Garcia Javier, Tim Chew Fook, Yie Sio Yang, Andiappan Anand K, Turner Steve W, Mukhopadhyay Somnath, Palmer Colin N A, Hawcutt Daniel, Jorgensen Andrea L, Burchard Esteban G, Hernandez-Pacheco Natalia, Pino-Yanes Maria, Maitland-van der Zee Anke |
| Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. medRxiv : the preprint server for health sciences 2023 7 . Frederik H Lassen, Samvida S Venkatesh, Nikolas Baya, Wei Zhou, Alex Bloemendal, Benjamin M Neale, Benedikt M Kessler, Nicola Whiffin, Cecilia M Lindgren, Duncan S Palm |
| Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. Cell genomics 2024 6 100602. Frederik H Lassen, Samvida S Venkatesh, Nikolas Baya, Barney Hill, Wei Zhou, Alex Bloemendal, Benjamin M Neale, Benedikt M Kessler, Nicola Whiffin, Cecilia M Lindgren, Duncan S Palm |
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