Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: FOXF1[original query] |
---|
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
Nature genetics 2012 Oct 44 (10): 1131-6. Su Zhan, Gay Laura J, Strange Amy, Palles Claire, Band Gavin, Whiteman David C, Lescai Francesco, Langford Cordelia, Nanji Manoj, Edkins Sarah, van der Winkel Anouk, Levine David, Sasieni Peter, Bellenguez Céline, Howarth Kimberley, Freeman Colin, Trudgill Nigel, Tucker Art T, Pirinen Matti, Peppelenbosch Maikel P, van der Laan Luc J W, Kuipers Ernst J, Drenth Joost P H, Peters Wilbert H, Reynolds John V, Kelleher Dermot P, McManus Ross, Grabsch Heike, Prenen Hans, Bisschops Raf, Krishnadath Kausila, Siersema Peter D, van Baal Jantine W P M, Middleton Mark, Petty Russell, Gillies Richard, Burch Nicola, Bhandari Pradeep, Paterson Stuart, Edwards Cathryn, Penman Ian, Vaidya Kishor, Ang Yeng, Murray Iain, Patel Praful, Ye Weimin, Mullins Paul, Wu Anna H, Bird Nigel C, Dallal Helen, Shaheen Nicholas J, Murray Liam J, Koss Konrad, Bernstein Leslie, Romero Yvonne, Hardie Laura J, Zhang Rui, Winter Helen, Corley Douglas A, Panter Simon, Risch Harvey A, Reid Brian J, Sargeant Ian, Gammon Marilie D, Smart Howard, Dhar Anjan, McMurtry Hugh, Ali Haythem, Liu Geoffrey, Casson Alan G, Chow Wong-Ho, Rutter Matt, Tawil Ashref, Morris Danielle, Nwokolo Chuka, Isaacs Peter, Rodgers Colin, Ragunath Krish, MacDonald Chris, Haigh Chris, Monk David, Davies Gareth, Wajed Saj, Johnston David, Gibbons Michael, Cullen Sue, Church Nicholas, Langley Ruth, Griffin Michael, Alderson Derek, Deloukas Panos, Hunt Sarah E, Gray Emma, Dronov Serge, Potter Simon C, Tashakkori-Ghanbaria Avazeh, Anderson Mark, Brooks Claire, Blackwell Jenefer M, Bramon Elvira, Brown Matthew A, Casas Juan P, Corvin Aiden, Duncanson Audrey, Markus Hugh S, Mathew Christopher G, Palmer Colin N A, Plomin Robert, Rautanen Anna, Sawcer Stephen J, Trembath Richard C, Viswanathan Ananth C, Wood Nicholas, Trynka Gosia, Wijmenga Cisca, Cazier Jean-Baptiste, Atherfold Paul, Nicholson Anna M, Gellatly Nichola L, Glancy Deborah, Cooper Sheldon C, Cunningham David, Lind Tore, Hapeshi Julie, Ferry David, Rathbone Barrie, Brown Julia, Love Sharon, Attwood Stephen, MacGregor Stuart, Watson Peter, Sanders Scott, Ek Weronica, Harrison Rebecca F, Moayyedi Paul, de Caestecker John, Barr Hugh, Stupka Elia, Vaughan Thomas L, Peltonen Leena, Spencer Chris C A, Tomlinson Ian, Donnelly Peter, Jankowski Janusz A Z, , |
Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk. International journal of cancer. Journal international du cancer 2013 Oct 133 (7): 1751-5. Dura Polat, van Veen Elke M, Salomon Jody, te Morsche Rene H M, Roelofs Hennie M J, Kristinsson Jon O, Wobbes Theo, Witteman Ben J M, Tan Adriaan C I T L, Drenth Joost P H, Peters Wilbert H |
A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
Nature genetics 2013 Dec 45 (12): 1487-93. Levine David M, Ek Weronica E, Zhang Rui, Liu Xinxue, Onstad Lynn, Sather Cassandra, Lao-Sirieix Pierre, Gammon Marilie D, Corley Douglas A, Shaheen Nicholas J, Bird Nigel C, Hardie Laura J, Murray Liam J, Reid Brian J, Chow Wong-Ho, Risch Harvey A, Nyrén Olof, Ye Weimin, Liu Geoffrey, Romero Yvonne, Bernstein Leslie, Wu Anna H, Casson Alan G, Chanock Stephen J, Harrington Patricia, Caldas Isabel, Debiram-Beecham Irene, Caldas Carlos, Hayward Nicholas K, Pharoah Paul D, Fitzgerald Rebecca C, Macgregor Stuart, Whiteman David C, Vaughan Thomas |
The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death. Medical science monitor : international medical journal of experimental and clinical research 2014 20 1531-8. Lozi? Bernarda, Krželj Vjekoslav, Kuzmi?-Prusac Ivana, Kuzmani?-Šamija Radenka, ?apkun Vesna, Lasan Ružica, Zemunik Tatija |
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus. Gastroenterology 2015 Feb 148 (2): 367-78. Palles Claire, Chegwidden Laura, Li Xinzhong, Findlay John M, Farnham Garry, Castro Giner Francesc, Peppelenbosch Maikel P, Kovac Michal, Adams Claire L, Prenen Hans, Briggs Sarah, Harrison Rebecca, Sanders Scott, MacDonald David, Haigh Chris, Tucker Art, Love Sharon, Nanji Manoj, deCaestecker John, Ferry David, Rathbone Barrie, Hapeshi Julie, Barr Hugh, Moayyedi Paul, Watson Peter, Zietek Barbara, Maroo Neera, Gay Laura, Underwood Tim, Boulter Lisa, McMurtry Hugh, Monk David, Patel Praful, Ragunath Krish, Al Dulaimi David, Murray Iain, Koss Konrad, Veitch Andrew, Trudgill Nigel, Nwokolo Chuka, Rembacken Bjorn, Atherfold Paul, Green Elaine, Ang Yeng, Kuipers Ernst J, Chow Wu, Paterson Stuart, Kadri Sudarshan, Beales Ian, Grimley Charles, Mullins Paul, Beckett Conrad, Farrant Mark, Dixon Andrew, Kelly Sean, Johnson Matthew, Wajed Shahjehan, Dhar Anjan, Sawyer Elinor, Roylance Rebecca, Onstad Lynn, Gammon Marilie D, Corley Douglas A, Shaheen Nicholas J, Bird Nigel C, Hardie Laura J, Reid Brian J, Ye Weimin, Liu Geoffrey, Romero Yvonne, Bernstein Leslie, Wu Anna H, Casson Alan G, Fitzgerald Rebecca, Whiteman David C, Risch Harvey A, Levine David M, Vaughan Tom L, Verhaar Auke P, van den Brande Jan, Toxopeus Eelke L, Spaander Manon C, Wijnhoven Bas P L, van der Laan Luc J W, Krishnadath Kausilia, Wijmenga Cisca, Trynka Gosia, McManus Ross, Reynolds John V, O'Sullivan Jacintha, MacMathuna Padraic, McGarrigle Sarah A, Kelleher Dermot, Vermeire Severine, Cleynen Isabelle, Bisschops Raf, Tomlinson Ian, Jankowski Janu |
A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis.
PloS one 2014 9 (12): e101488. Rafiq Sajjad, Khan Sofia, Tapper William, Collins Andrew, Upstill-Goddard Rosanna, Gerty Susan, Blomqvist Carl, Aittomäki Kristiina, Couch Fergus J, Liu Jianjun, Nevanlinna Heli, Eccles Dia |
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Human mutation 2015 Aug . Hilger Alina C, Halbritter Jan, Pennimpede Tracie, van der Ven Amelie, Sarma Georgia, Braun Daniela A, Porath Jonathan D, Kohl Stefan, Hwang Daw-Yang, Dworschak Gabriel C, Hermann Bernhard G, Pavlova Anna, El-Maarri Osman, Nöthen Markus M, Ludwig Michael, Reutter Heiko, Hildebrandt Friedhe |
Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma. Journal of carcinogenesis 2015 14 5. van Nistelrooij Anna M J, van der Korput Hetty A G M, Broer Linda, van Marion Ronald, van Berge Henegouwen Mark I, van Noesel Carel J, Biermann Katharina, Spaander Manon C W, Tilanus Hugo W, van Lanschot J Jan B, Hofman Albert, Uitterlinden André G, Wijnhoven Bas P L, Dinjens Winand N |
Polymorphisms of the FOXF1 and MHC locus genes in individuals undergoing esophageal acid reflux assessments. Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus 2017 02 30 (2): 1-7. Lam C, Liu W F, Bel R D, Chan K, Miller L, Brown M C, Chen Z, Cheng D, Patel D, Xu W, Darling G E, Liu |
Genetic polymorphisms are associated with the risk of gastric and colorectal cancers in a Han Chinese population. Oncotarget 2017 Feb . Wang Nan, Qiao Qing, Bao Guoqiang, Wu Tao, Li Yizhou, Li Jingjie, Lu Jianguo, He Xian |
Prognostic impact of FOXF1 polymorphisms in gastric cancer patients. The pharmacogenomics journal 2018 04 18 (2): 262-269. Matsusaka S, Wu A H, Cao S, Hanna D L, Chin K, Yang D, Zhang W, Ning Y, Stintzing S, Sebio A, Sunakawa Y, Stremitzer S, Yamauchi S, Okazaki S, Berger M D, Parekh A, Miyamoto Y, Mizunuma N, Lenz H |
Risk factors for gastroesophageal reflux disease and analysis of genetic contributors. World journal of clinical cases 2018 8 6 (8): 176-182. Argyrou Alexandra, Legaki Evangelia, Koutserimpas Christos, Gazouli Maria, Papaconstantinou Ioannis, Gkiokas George, Karamanolis Geor |
Genetic variants of FOXP1 and FOXF1 are associated with the susceptibility of oesophageal adenocarcinoma in Chinese population. Journal of genetics 2018 Mar 97 (1): 213-218. Zhang Jie, Chen Jiebin, Ma Tianheng, Guo Huimin, Yang B |
Genetic basis for childhood interstitial lung disease among Japanese infants and children. Pediatric research 2018 3 83 (2): 477-483. Hayasaka Itaru, Cho Kazutoshi, Akimoto Takuma, Ikeda Masahiko, Uzuki Yutaka, Yamada Masafumi, Nakata Koh, Furuta Itsuko, Ariga Tadashi, Minakami Hisano |
GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12.
Carcinogenesis 2018 May 39 (5): 652-660. Tanikawa Chizu, Kamatani Yoichiro, Takahashi Atsushi, Momozawa Yukihide, Leveque Karine, Nagayama Satoshi, Mimori Koshi, Mori Masaki, Ishii Hideshi, Inazawa Johji, Yasuda Jun, Tsuboi Akito, Shimizu Atsushi, Sasaki Makoto, Yamaji Taiki, Sawada Norie, Iwasaki Motoki, Tsugane Shoichiro, Naito Mariko, Wakai Kenji, Koyama Teruhide, Takezaki Toshiro, Yuji Koichiro, Murakami Yoshinori, Nakamura Yusuke, Kubo Michiaki, Matsuda Koic |
A functional CNVR_3425.1 damping lincRNA FENDRR increases lifetime risk of lung cancer and COPD in Chinese. Carcinogenesis 2018 1 39 (3): 347-359. Yang Lei, Wu Di, Chen Jinbin, Chen Jiansong, Qiu Fuman, Li Yinyan, Liu Li, Cao Yi, Yang Binyao, Zhou Yifeng, Lu Jiach |
Bioinformatic analysis of the prognostic value and potential regulatory network of FOXF1 in papillary thyroid cancer. BioFactors (Oxford, England) 2019 9 45 (6): 902-911. Gu Yi, Hu Chunm |
Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1. American journal of medical genetics. Part A 2019 5 179 (7): 1325-1329. Bourque Danielle K, Fonseca Inara Chacon, Staines Andrea, Teitelbaum Ronni, Axford Michelle M, Jobling Rebekah, Chiasson David, Chitayat Dav |
Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation. Molecular genetics & genomic medicine 2019 Jan e549. Salehi Karlslätt Karin, Pettersson Maria, Jäntti Nina, Szafranski Przemyslaw, Wester Tomas, Husberg Britt, Ullberg Ulla, Stankiewicz Pawel, Nordgren Ann, Lundin Johanna, Lindstrand Anna, Nordenskjöld Agne |
Incidence of alveolar capillary dysplasia with misalignment of pulmonary veins in infants with unexplained severe pulmonary hypertension: The roles of clinical, pathological, and genetic testing. Early human development 2021 Jan 155 105323. Onda Tetsuo, Akimoto Takuma, Hayasaka Itaru, Ikeda Masahiko, Furuse Yuta, Ando Akiko, Nakamura Yuichi, Honjo Ryota, Manabe Atsushi, Furuta Itsuko, Cho Kazutos |
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. Birth defects research 2022 4 114 (10): 478-486. Thiem Corina E, Stegmann Jil D, Hilger Alina C, Waffenschmidt Lea, Bendixen Charlotte, Köllges Ricarda, Schmiedeke Eberhard, Schäfer Frank-Mattias, Lacher Martin, Kosch Ferdinand, Grasshoff-Derr Sabine, Kabs Carmen, Neser Jörg, Jenetzky Ekkehart, Fazaal Julia, Schumacher Johannes, Hoefele Julia, Ludwig Kerstin U, Reutter Hei |
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
HGG advances 2022 2 3 (2): 100093. Gehlen Jan, Giel Ann-Sophie, Köllges Ricarda, Haas Stephan L, Zhang Rong, Trcka Jiri, Sungur Ayse Ö, Renziehausen Florian, Bornholdt Dorothea, Jung Daphne, Hoyer Paul D, Nordenskjöld Agneta, Tibboel Dick, Vlot John, Spaander Manon C W, Smigiel Robert, Patkowski Dariusz, Roeleveld Nel, van Rooij Iris Alm, de Blaauw Ivo, Hölscher Alice, Pauly Marcus, Leutner Andreas, Fuchs Joerg, Niethammer Joel, Melissari Maria-Theodora, Jenetzky Ekkehart, Zwink Nadine, Thiele Holger, Hilger Alina Christine, Hess Timo, Trautmann Jessica, Marks Matthias, Baumgarten Martin, Bläss Gaby, Landén Mikael, Fundin Bengt, Bulik Cynthia M, Pennimpede Tracie, Ludwig Michael, Ludwig Kerstin U, Mangold Elisabeth, Heilmann-Heimbach Stefanie, Moebus Susanne, Herrmann Bernhard G, Alsabeah Kristina, Burgos Carmen M, Lilja Helene E, Azodi Sahar, Stenström Pernilla, Arnbjörnsson Einar, Frybova Barbora, Lebensztejn Dariusz M, Debek Wojciech, Kolodziejczyk Elwira, Kozera Katarzyna, Kierkus Jaroslaw, Kalici?ski Piotr, Stefanowicz Marek, Socha-Banasiak Anna, Kolejwa Michal, Piaseczna-Piotrowska Anna, Czkwianianc Elzbieta, Nöthen Markus M, Grote Phillip, Rygl Michal, Reinshagen Konrad, Spychalski Nicole, Ludwikowski Barbara, Hubertus Jochen, Heydweiller Andreas, Ure Benno, Muensterer Oliver J, Aubert Ophelia, Gosemann Jan-Hendrik, Lacher Martin, Degenhardt Petra, Boemers Thomas M, Mokrowiecka Anna, Ma?ecka-Panas Ewa, Wöhr Markus, Knapp Michael, Seitz Guido, de Klein Annelies, Oracz Grzegorz, Brosens Erwin, Reutter Heiko, Schumacher Johann |
Exome sequencing findings in children with annular pancreas. Molecular genetics & genomic medicine 2023 8 e2233. Georgia Pitsava, Nathan Pankratz, John Lane, Wei Yang, Shannon Rigler, Gary M Shaw, James L Mil |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: