Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: FBLN2[original query] |
---|
Genome-wide analysis of chromosomal alterations in patients with esophageal squamous cell carcinoma exposed to tobacco and betel quid from high-risk area in India. Mutation research 2010 Feb 696 (2): 130-8. Chattopadhyay Indranil, Singh Avninder, Phukan Rupkumar, Purkayastha Joydeep, Kataki Amal, Mahanta Jagadish, Saxena Sunita, Kapur Suja |
Two variants in the fibulin2 gene are associated with lower systolic blood pressure and decreased risk of hypertension. PloS one 2012 7 (8): e43051. Vallvé Joan-Carles, Serra Noemí, Zalba Guillermo, Fortuño Ana, Beloqui Oscar, Ferre Raimon, Ribalta Josep, Masana Llu |
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. American journal of human genetics 2012 Oct 91 (4): 646-59. Ackerman Christine, Locke Adam E, Feingold Eleanor, Reshey Benjamin, Espana Karina, Thusberg Janita, Mooney Sean, Bean Lora J H, Dooley Kenneth J, Cua Clifford L, Reeves Roger H, Sherman Stephanie L, Maslen Cheryl |
Exome-chip association analysis of intracranial aneurysms. Neurology 2019 Nov . van 't Hof Femke N G, Lai Dongbing, van Setten Jessica, Bots Michiel L, Vaartjes Ilonca, Broderick Joseph, Woo Daniel, Foroud Tatiana, Rinkel Gabriel J E, de Bakker Paul I W, Ruigrok Ynte |
Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing. Clinical and translational gastroenterology 2019 10 10 (10): e00100. Toma Claudio, Díaz-Gay Marcos, Soares de Lima Yasmin, Arnau-Collell Coral, Franch-Expósito Sebastià, Muñoz Jenifer, Overs Bronwyn, Bonjoch Laia, Carballal Sabela, Ocaña Teresa, Cuatrecasas Miriam, Díaz de Bustamante Aránzazu, Castells Antoni, Bujanda Luis, Cubiella Joaquín, Balaguer Francesc, Rodríguez-Alcalde Daniel, Fullerton Janice M, Castellví-Bel Ser |
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Communications biology 2020 03 3 (1): 133. Fan Qiao, Pozarickij Alfred, Tan Nicholas Y Q, Guo Xiaobo, Verhoeven Virginie J M, Vitart Veronique, Guggenheim Jeremy A, Miyake Masahiro, Tideman J Willem L, Khawaja Anthony P, Zhang Liang, MacGregor Stuart, Höhn René, Chen Peng, Biino Ginevra, Wedenoja Juho, Saffari Seyed Ehsan, Tedja Milly S, Xie Jing, Lanca Carla, Wang Ya Xing, Sahebjada Srujana, Mazur Johanna, Mirshahi Alireza, Martin Nicholas G, Yazar Seyhan, Pennell Craig E, Yap Maurice, Haarman Annechien E G, Enthoven Clair A, Polling JanRoelof, , , Hewitt Alex W, Jaddoe Vincent W V, van Duijn Cornelia M, Hayward Caroline, Polasek Ozren, Tai E-Shyong, Yoshikatsu Hosoda, Hysi Pirro G, Young Terri L, Tsujikawa Akitaka, Wang Jie Jing, Mitchell Paul, Pfeiffer Norbert, Pärssinen Olavi, Foster Paul J, Fossarello Maurizio, Yip Shea Ping, Williams Cathy, Hammond Christopher J, Jonas Jost B, He Mingguang, Mackey David A, Wong Tien-Yin, Klaver Caroline C W, Saw Seang-Mei, Baird Paul N, Cheng Ching- |
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH. Genome medicine 2021 May 13 (1): 80. Zhu Na, Swietlik Emilia M, Welch Carrie L, Pauciulo Michael W, Hagen Jacob J, Zhou Xueya, Guo Yicheng, Karten Johannes, Pandya Divya, Tilly Tobias, Lutz Katie A, Martin Jennifer M, Treacy Carmen M, Rosenzweig Erika B, Krishnan Usha, Coleman Anna W, Gonzaga-Jauregui Claudia, Lawrie Allan, Trembath Richard C, Wilkins Martin R, , , , , Morrell Nicholas W, Shen Yufeng, Gräf Stefan, Nichols William C, Chung Wendy |
Whole Exome Sequencing of Patients With Heritable and Idiopathic Pulmonary Arterial Hypertension in Central Taiwan. Frontiers in cardiovascular medicine 2022 9 911649. Liang Kae-Woei, Chang Sheng-Kai, Chen Yu-Wei, Lin Wei-Wen, Tsai Wan-Jane, Wang Kuo-Ya |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: