Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and 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 |
| 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 |
| 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 |
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, |
| 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 |
| 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 |
| Joint genotype and ancestry analysis identify novel loci associated with atopic dermatitis in African American population. HGG advances 2024 9 100350. Yadu Gautam, Latha Satish, Stephen Ramirez, Brittany Grashel, Jocelyn M Biagini, Lisa J Martin, Marc E Rothenberg, Gurjit K Khurana Hershey, Tesfaye B Mers |
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