Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: FOXA2[original query] |
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Evaluation of AGR2 and AGR3 as candidate genes for inflammatory bowel disease. Genes and immunity 2006 Jan 7 (1): 11-8. Zheng W, Rosenstiel P, Huse K, Sina C, Valentonyte R, Mah N, Zeitlmann L, Grosse J, Ruf N, Nürnberg P, Costello C M, Onnie C, Mathew C, Platzer M, Schreiber S, Hampe |
Genetic variants of FOXA2: risk of type 2 diabetes and effect on metabolic traits in North Indians. Journal of human genetics 2008 53 (11-12): 957-65. Tabassum Rubina, Chavali Sreenivas, Dwivedi Om Prakash, Tandon Nikhil, Bharadwaj Dwaipay |
A single-nucleotide polymorphism in a methylatable Foxa2 binding site of the G6PC2 promoter is associated with insulin secretion in vivo and increased promoter activity in vitro. Diabetes 2009 Feb 58 (2): 489-92. Dos Santos Christine, Bougnères Pierre, Fradin Delphi |
Genetic predictors of interindividual variability in hepatic CYP3A4 expression. The Journal of pharmacology and experimental therapeutics 2010 Mar 332 (3): 1088-99. Lamba Vishal, Panetta John C, Strom Stephen, Schuetz Erin |
Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels. Diabetes 2010 Oct 59 (10): 2662-71. Bouatia-Naji Nabila, Bonnefond Amélie, Baerenwald Devin A, Marchand Marion, Bugliani Marco, Marchetti Piero, Pattou François, Printz Richard L, Flemming Brian P, Umunakwe Obi C, Conley Nicholas L, Vaxillaire Martine, Lantieri Olivier, Balkau Beverley, Marre Michel, Lévy-Marchal Claire, Elliott Paul, Jarvelin Marjo-Riitta, Meyre David, Dina Christian, Oeser James K, Froguel Philippe, O'Brien Richard |
A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels.
American journal of human genetics 2010 Mar 86 (3): 440-6. Xing Chao, Cohen Jonathan C, Boerwinkle Er |
Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE. Human genetics 2010 1 127 (4): 421-40. Rosenfeld Jill A, Ballif Blake C, Martin Donna M, Aylsworth Arthur S, Bejjani Bassem A, Torchia Beth S, Shaffer Lisa |
High levels of protein C are determined by PROCR haplotype 3. Journal of thrombosis and haemostasis : JTH 2011 May 9 (5): 969-76. Pintao M C, Roshani S, de Visser M C H, Tieken C, Tanck M W T, Wichers I M, Meijers J C M, Rosendaal F R, Middeldorp S, Reitsma P |
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.
The British journal of dermatology 2011 Dec 165 (6): 1293-302. Brockschmidt F F, Heilmann S, Ellis J A, Eigelshoven S, Hanneken S, Herold C, Moebus S, Alblas M A, Lippke B, Kluck N, Priebe L, Degenhardt F A, Jamra R A, Meesters C, Jöckel K-H, Erbel R, Harrap S, Schumacher J, Fröhlich H, Kruse R, Hillmer A M, Becker T, Nöthen M |
Potential role of upstream stimulatory factor 1 gene variant in familial combined hyperlipidemia and related disorders. Arteriosclerosis, thrombosis, and vascular biology 2012 Jun 32 (6): 1535-44. Auer Simon, Hahne Penelope, Soyal Selma M, Felder Thomas, Miller Karl, Paulmichl Markus, Krempler Franz, Oberkofler Hannes, Patsch Wolfga |
The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals. BMC medical genetics 2012 Feb 13 (1): 1. Banasik K, Hollensted M, Andersson E, Sparso T, Sandbaek A, Lauritzen T, Jorgensen T, Witte DR, Pedersen O, Hansen T |
Allele-specific transactivation of matrix metalloproteinase 7 by FOXA2 and correlation with plasma levels in idiopathic pulmonary fibrosis. American journal of physiology. Lung cellular and molecular physiology 2012 Apr 302 (8): L746-54. Richards Thomas J, Park Chunghyun, Chen Yiliang, Gibson Kevin F, Peter Di Y, Pardo Annie, Watkins Simon C, Choi Augustine M K, Selman Moises, Pilewski Joseph, Kaminski Naftali, Zhang Ying |
Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels. Diabetologia 2013 Jun 56 (6): 1306-16. Baerenwald D A, Bonnefond A, Bouatia-Naji N, Flemming B P, Umunakwe O C, Oeser J K, Pound L D, Conley N L, Cauchi S, Lobbens S, Eury E, Balkau B, Lantieri O, , Dadi P K, Jacobson D A, Froguel P, O'Brien R |
Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. International journal of molecular epidemiology and genetics 2013 4 (4): 193-206. Luong Hien Tt, Painter Jodie N, Shakhbazov Konstantin, Chapman Brett, Henders Anjali K, Powell Joseph E, Nyholt Dale R, Montgomery Grant |
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. PloS one 2013 8 (1): e53944. Gupta Vipin, Vinay Donipadi Guru, Sovio Ulla, Rafiq Sajjad, Kranthi Kumar Madamchetty Venkata, Janipalli Charles Spurgeon, Evans David, Mani Kulathu Radha, Sandeep Madana Narasimha, Taylor Amy, Kinra Sanjay, Sullivan Ruth, Bowen Liza, Timpson Nicholas, Smith George Davey, Dudbridge Frank, Prabhakaran Dorairaj, Ben-Shlomo Yoav, Reddy Kolli Srinath, Ebrahim Shah, Chandak Giriraj Ratan, |
Integrative genomic analysis identifies that SERPINA6-rs1998056 regulated by FOXA/ERa is associated with female hepatocellular carcinoma. PloS one 2014 9 (9): e107246. Shen Na, Gong Jing, Wang Ying, Tian Jing, Qian Jiaming, Zou Li, Chen Wei, Zhu Beibei, Lu Xinghua, Zhong Rong, Guo Anyuan, Wang Li, Miao Xiaopi |
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk. Scientific reports 2015 5 8922. Figlioli Gisella, Chen Bowang, Elisei Rossella, Romei Cristina, Campo Chiara, Cipollini Monica, Cristaudo Alfonso, Bambi Franco, Paolicchi Elisa, Hoffmann Per, Herms Stefan, Kalemba Micha?, Kula Dorota, Pastor Susana, Marcos Ricard, Velázquez Antonia, Jarz?b Barbara, Landi Stefano, Hemminki Kari, Gemignani Federica, Försti As |
Pulmonary expression of CYP2A13 and ABCB1 is regulated by FOXA2, and their genetic interaction is associated with lung cancer. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2015 May 29 (5): 1986-98. Xiang Chan, Wang Jiucun, Kou Xiaochen, Chen Xiabin, Qin Zhaoyu, Jiang Yan, Sun Chang, Xu Jibin, Tan Wen, Jin Li, Lin Dongxin, He Fuchu, Wang Haiji |
Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study.
The Journal of steroid biochemistry and molecular biology 2015 Dec . Sapkota Bishwa R, Hopkins Ruth, Bjonnes Andrew, Ralhan Sarju, Wander Gurpreet S, Mehra Narinder K, Singh Jai Rup, Blackett Piers R, Saxena Richa, Sanghera Dharambir |
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature genetics 2015 Nov . Gaulton Kyle J, Ferreira Teresa, Lee Yeji, Raimondo Anne, Mägi Reedik, Reschen Michael E, Mahajan Anubha, Locke Adam, William Rayner N, Robertson Neil, Scott Robert A, Prokopenko Inga, Scott Laura J, Green Todd, Sparso Thomas, Thuillier Dorothee, Yengo Loic, Grallert Harald, Wahl Simone, Frånberg Mattias, Strawbridge Rona J, Kestler Hans, Chheda Himanshu, Eisele Lewin, Gustafsson Stefan, Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Qi Lu, Karssen Lennart C, van Leeuwen Elisabeth M, Willems Sara M, Li Man, Chen Han, Fuchsberger Christian, Kwan Phoenix, Ma Clement, Linderman Michael, Lu Yingchang, Thomsen Soren K, Rundle Jana K, Beer Nicola L, van de Bunt Martijn, Chalisey Anil, Kang Hyun Min, Voight Benjamin F, Abecasis Gonçalo R, Almgren Peter, Baldassarre Damiano, Balkau Beverley, Benediktsson Rafn, Blüher Matthias, Boeing Heiner, Bonnycastle Lori L, Bottinger Erwin P, Burtt Noël P, Carey Jason, Charpentier Guillaume, Chines Peter S, Cornelis Marilyn C, Couper David J, Crenshaw Andrew T, van Dam Rob M, Doney Alex S F, Dorkhan Mozhgan, Edkins Sarah, Eriksson Johan G, Esko Tonu, Eury Elodie, Fadista João, Flannick Jason, Fontanillas Pierre, Fox Caroline, Franks Paul W, Gertow Karl, Gieger Christian, Gigante Bruna, Gottesman Omri, Grant George B, Grarup Niels, Groves Christopher J, Hassinen Maija, Have Christian T, Herder Christian, Holmen Oddgeir L, Hreidarsson Astradur B, Humphries Steve E, Hunter David J, Jackson Anne U, Jonsson Anna, Jørgensen Marit E, Jørgensen Torben, Kao Wen-Hong L, Kerrison Nicola D, Kinnunen Leena, Klopp Norman, Kong Augustine, Kovacs Peter, Kraft Peter, Kravic Jasmina, Langford Cordelia, Leander Karin, Liang Liming, Lichtner Peter, Lindgren Cecilia M, Lindholm Eero, Linneberg Allan, Liu Ching-Ti, Lobbens Stéphane, Luan Jian'an, Lyssenko Valeriya, Männistö Satu, McLeod Olga, Meyer Julia, Mihailov Evelin, Mirza Ghazala, Mühleisen Thomas W, Müller-Nurasyid Martina, Navarro Carmen, Nöthen Markus M, Oskolkov Nikolay N, Owen Katharine R, Palli Domenico, Pechlivanis Sonali, Peltonen Leena, Perry John R B, Platou Carl G P, Roden Michael, Ruderfer Douglas, Rybin Denis, van der Schouw Yvonne T, Sennblad Bengt, Sigurðsson Gunnar, Stan?áková Alena, Steinbach Gerald, Storm Petter, Strauch Konstantin, Stringham Heather M, Sun Qi, Thorand Barbara, Tikkanen Emmi, Tonjes Anke, Trakalo Joseph, Tremoli Elena, Tuomi Tiinamaija, Wennauer Roman, Wiltshire Steven, Wood Andrew R, Zeggini Eleftheria, Dunham Ian, Birney Ewan, Pasquali Lorenzo, Ferrer Jorge, Loos Ruth J F, Dupuis Josée, Florez Jose C, Boerwinkle Eric, Pankow James S, van Duijn Cornelia, Sijbrands Eric, Meigs James B, Hu Frank B, Thorsteinsdottir Unnur, Stefansson Kari, Lakka Timo A, Rauramaa Rainer, Stumvoll Michael, Pedersen Nancy L, Lind Lars, Keinanen-Kiukaanniemi Sirkka M, Korpi-Hyövälti Eeva, Saaristo Timo E, Saltevo Juha, Kuusisto Johanna, Laakso Markku, Metspalu Andres, Erbel Raimund, Jöcke Karl-Heinz, Moebus Susanne, Ripatti Samuli, Salomaa Veikko, Ingelsson Erik, Boehm Bernhard O, Bergman Richard N, Collins Francis S, Mohlke Karen L, Koistinen Heikki, Tuomilehto Jaakko, Hveem Kristian, Njølstad Inger, Deloukas Panagiotis, Donnelly Peter J, Frayling Timothy M, Hattersley Andrew T, de Faire Ulf, Hamsten Anders, Illig Thomas, Peters Annette, Cauchi Stephane, Sladek Rob, Froguel Philippe, Hansen Torben, Pedersen Oluf, Morris Andrew D, Palmer Collin N A, Kathiresan Sekar, Melander Olle, Nilsson Peter M, Groop Leif C, Barroso Inês, Langenberg Claudia, Wareham Nicholas J, O'Callaghan Christopher A, Gloyn Anna L, Altshuler David, Boehnke Michael, Teslovich Tanya M, McCarthy Mark I, Morris Andrew P, |
The FOXA2 transcription factor is frequently somatically mutated in uterine carcinosarcomas and carcinomas. Cancer 2017 9 124 (1): 65-73. Le Gallo Matthieu, Rudd Meghan L, Urick Mary Ellen, Hansen Nancy F, , Merino Maria J, Mutch David G, Goodfellow Paul J, Mullikin James C, Bell Daphne |
Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers. Epigenetics & chromatin 2019 02 12 (1): 10. Mordaunt Charles E, Kieffer Dorothy A, Shibata Noreene M, Cz?onkowska Anna, Litwin Tomasz, Weiss Karl-Heinz, Zhu Yihui, Bowlus Christopher L, Sarkar Souvik, Cooper Stewart, Wan Yu-Jui Yvonne, Ali Mohamed R, LaSalle Janine M, Medici Valenti |
Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response. Journal for immunotherapy of cancer 2020 5 8 (1): . Roelands Jessica, Hendrickx Wouter, Zoppoli Gabriele, Mall Raghvendra, Saad Mohamad, Halliwill Kyle, Curigliano Giuseppe, Rinchai Darawan, Decock Julie, Delogu Lucia G, Turan Tolga, Samayoa Josue, Chouchane Lotfi, Ballestrero Alberto, Wang Ena, Finetti Pascal, Bertucci Francois, Miller Lance D, Galon Jerome, Marincola Francesco M, Kuppen Peter J K, Ceccarelli Michele, Bedognetti Davi |
Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort. Frontiers in genetics 2021 12 12 746082. Xiang Huifen, Wang Chunyan, Pan Hong, Hu Qian, Wang Ruyi, Xu Zuying, Li Tengyan, Su Yezhou, Ma Xu, Cao Yunxia, Wang Binb |
Genetic variants for prediction of gestational diabetes mellitus and modulation of susceptibility by a nutritional intervention based on a Mediterranean diet. Frontiers in endocrinology 2022 10 13 1036088. Ramos-Levi Ana, Barabash Ana, Valerio Johanna, García de la Torre Nuria, Mendizabal Leire, Zulueta Mirella, de Miguel Maria Paz, Diaz Angel, Duran Alejandra, Familiar Cristina, Jimenez Inés, Del Valle Laura, Melero Veronica, Moraga Inmaculada, Herraiz Miguel A, Torrejon María José, Arregi Maddi, Simón Laureano, Rubio Miguel A, Calle-Pascual Alfonso |
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.
Communications biology 2022 7 5 (1): 756. DiCorpo Daniel, Gaynor Sheila M, Russell Emily M, Westerman Kenneth E, Raffield Laura M, Majarian Timothy D, Wu Peitao, Sarnowski Chloé, Highland Heather M, Jackson Anne, Hasbani Natalie R, de Vries Paul S, Brody Jennifer A, Hidalgo Bertha, Guo Xiuqing, Perry James A, O'Connell Jeffrey R, Lent Samantha, Montasser May E, Cade Brian E, Jain Deepti, Wang Heming, D'Oliveira Albanus Ricardo, Varshney Arushi, Yanek Lisa R, Lange Leslie, Palmer Nicholette D, Almeida Marcio, Peralta Juan M, Aslibekyan Stella, Baldridge Abigail S, Bertoni Alain G, Bielak Lawrence F, Chen Chung-Shiuan, Chen Yii-Der Ida, Choi Won Jung, Goodarzi Mark O, Floyd James S, Irvin Marguerite R, Kalyani Rita R, Kelly Tanika N, Lee Seonwook, Liu Ching-Ti, Loesch Douglas, Manson JoAnn E, Minster Ryan L, Naseri Take, Pankow James S, Rasmussen-Torvik Laura J, Reiner Alexander P, Reupena Muagututi'a Sefuiva, Selvin Elizabeth, Smith Jennifer A, Weeks Daniel E, Xu Huichun, Yao Jie, Zhao Wei, Parker Stephen, Alonso Alvaro, Arnett Donna K, Blangero John, Boerwinkle Eric, Correa Adolfo, Cupples L Adrienne, Curran Joanne E, Duggirala Ravindranath, He Jiang, Heckbert Susan R, Kardia Sharon L R, Kim Ryan W, Kooperberg Charles, Liu Simin, Mathias Rasika A, McGarvey Stephen T, Mitchell Braxton D, Morrison Alanna C, Peyser Patricia A, Psaty Bruce M, Redline Susan, Shuldiner Alan R, Taylor Kent D, Vasan Ramachandran S, Viaud-Martinez Karine A, Florez Jose C, Wilson James G, Sladek Robert, Rich Stephen S, Rotter Jerome I, Lin Xihong, Dupuis Josée, Meigs James B, Wessel Jennifer, Manning Alisa |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
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