Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: NPNT[original query] |
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Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
Nature genetics 2010 Jan 42 (1): 45-52. Hancock Dana B, Eijgelsheim Mark, Wilk Jemma B, Gharib Sina A, Loehr Laura R, Marciante Kristin D, Franceschini Nora, van Durme Yannick M T A, Chen Ting-Hsu, Barr R Graham, Schabath Matthew B, Couper David J, Brusselle Guy G, Psaty Bruce M, van Duijn Cornelia M, Rotter Jerome I, Uitterlinden André G, Hofman Albert, Punjabi Naresh M, Rivadeneira Fernando, Morrison Alanna C, Enright Paul L, North Kari E, Heckbert Susan R, Lumley Thomas, Stricker Bruno H C, O'Connor George T, London Stephanie |
The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility. American journal of respiratory cell and molecular biology 2011 Dec 45 (6): 1147-53. Castaldi Peter J, Cho Michael H, Litonjua Augusto A, Bakke Per, Gulsvik Amund, Lomas David A, Anderson Wayne, Beaty Terri H, Hokanson John E, Crapo James D, Laird Nan, Silverman Edwin K, |
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
The Lancet. Respiratory medicine 2015 Oct 3 (10): 769-81. Wain Louise V, Shrine Nick, Miller Suzanne, Jackson Victoria E, Ntalla Ioanna, Soler Artigas María, Billington Charlotte K, Kheirallah Abdul Kader, Allen Richard, Cook James P, Probert Kelly, Obeidat Ma'en, Bossé Yohan, Hao Ke, Postma Dirkje S, Paré Peter D, Ramasamy Adaikalavan, , Mägi Reedik, Mihailov Evelin, Reinmaa Eva, Melén Erik, O'Connell Jared, Frangou Eleni, Delaneau Olivier, , Freeman Colin, Petkova Desislava, McCarthy Mark, Sayers Ian, Deloukas Panos, Hubbard Richard, Pavord Ian, Hansell Anna L, Thomson Neil C, Zeggini Eleftheria, Morris Andrew P, Marchini Jonathan, Strachan David P, Tobin Martin D, Hall Ian |
An Interleukin 13 Polymorphism Is Associated with Symptom Severity in Adult Subjects with Ever Asthma. PloS one 2016 11 (3): e0151292. Accordini Simone, Calciano Lucia, Bombieri Cristina, Malerba Giovanni, Belpinati Francesca, Lo Presti Anna Rita, Baldan Alessandro, Ferrari Marcello, Perbellini Luigi, de Marco Rober |
Characterization of a COPD-Associated NPNT Functional Splicing Genetic Variant in Human Lung Tissue via Long-Read Sequencing. medRxiv : the preprint server for health sciences 2020 11 . Saferali Aabida, Xu Zhonghui, Sheynkman Gloria M, Hersh Craig P, Cho Michael H, Silverman Edwin K, Laederach Alain, Vollmers Christopher, Castaldi Peter |
Identification of potential pathogenic mutations in Chinese children with first branchial cleft anomalies detected by whole-exome sequencing. Pediatric investigation 2021 9 5 (3): 211-216. Yang Yeran, Liu Wei, Jin Yaqiong, Chen Min, Lu Jie, Yu Yongbo, Ren Huimin, Han Shujing, Chu Ping, Guo Yongli, Zhang Jie, Ni X |
Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms. PloS one 2022 3 17 (3): e0265359. Maegawa Tatsuya, Akagawa Hiroyuki, Onda Hideaki, Kasuya Hidetos |
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