Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: GFI1[original query] |
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Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia. British journal of haematology 2009 Nov 147 (4): 535-42. Xia Jun, Bolyard Audrey A, Rodger Elin, Stein Steve, Aprikyan Andrew A, Dale David C, Link Daniel |
Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis. European journal of human genetics : EJHG 2010 Jul 18 (7): 827-31. Alcina Antonio, Fernández Oscar, Gonzalez Juan Ramón, Catalá-Rabasa Antonio, Fedetz María, Ndagire Dorothy, Leyva Laura, Guerrero Miguel, Arnal Carmen, Delgado Concepción, Lucas Miguel, Izquierdo Guillermo, Matesanz Fuencis |
A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia. Blood 2010 Mar 115 (12): 2462-72. Khandanpour Cyrus, Thiede Christian, Valk Peter J M, Sharif-Askari Ehssan, Nückel Holger, Lohmann Dietmar, Horsthemke Bernhard, Siffert Winfried, Neubauer Andreas, Grzeschik Karl-Heinz, Bloomfield Clara D, Marcucci Guido, Maharry Kati, Slovak Marilyn L, van der Reijden Bert A, Jansen Joop H, Schackert Hans K, Afshar Khashayar, Schnittger Susanne, Peeters Justine K, Kroschinsky Frank, Ehninger Gerhard, Lowenberg Bob, Dührsen Ulrich, Möröy Tar |
Characterization of the colorectal cancer-associated enhancer MYC-335 at 8q24: the role of rs67491583. Cancer genetics 0 205 (1-2): 25-33. Tuupanen Sari, Yan Jian, Turunen Mikko, Gylfe Alexandra E, Kaasinen Eevi, Li Li, Eng Charis, Culver Daniel A, Kalady Matthew F, Pennison Michael J, Pasche Boris, Manne Upender, de la Chapelle Albert, Hampel Heather, Henderson Brian E, Le Marchand Loic, Hautaniemi Sampsa, Askhtorab Hassan, Smoot Duane, Sandler Robert S, Keku Temitope, Kupfer Sonia S, Ellis Nathan A, Haiman Christopher A, Taipale Jussi, Aaltonen Lauri |
Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates. Epigenetics 2016 Jul 0. Gonseth Semira, de Smith Adam J, Roy Ritu, Zhou Mi, Lee Seung-Tae, Shao Xiaorong, Ohja Juhi, Wrensch Margaret R, Walsh Kyle M, Metayer Catherine, Wiemels Joseph |
GFI1(36N) as a therapeutic and prognostic marker for myelodysplastic syndrome. Experimental hematology 2016 Apr . Botezatu Lacramioara, Michel Lars C, Makishima Hideki, Schroeder Thomas, Germing Ulrich, Haas Rainer, van der Reijden Bert, Marneth Anna E, Bergevoet Saskia M, Jansen Joop H, Przychodzen Bartlomiej, Wlodarski Marcin, Niemeyer Charlotte, Platzbecker Uwe, Ehninger Gerhard, Unnikrishnan Ashwin, Beck Dominik, Pimanda John, Hellström-Lindberg Eva, Cazzola Mario, Malcovati Luca, Boultwood Jacqueline, Pellagatti Andrea, Papaemmanuil Elli, Le Coutre Philipp, Kaeda Jaspal, Opalka Bertram, Möröy Tarik, Dührsen Ulrich, Maciejewski Jaroslaw, Khandanpour Cyr |
Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.
Experimental biology and medicine (Maywood, N.J.) 2016 04 241 (7): 706-18. Liu Li, Pertsemlidis Alexander, Ding Liang-Hao, Story Michael D, Steinberg Martin H, Sebastiani Paola, Hoppe Carolyn, Ballas Samir K, Pace Betty |
Prognostic significance of high GFI1 expression in AML of normal karyotype and its association with a FLT3-ITD signature. Scientific reports 2017 9 7 (1): 11148. Volpe Giacomo, Walton David S, Grainger David E, Ward Carl, Cauchy Pierre, Blakemore Daniel, Coleman Daniel J L, Cockerill Peter N, Garcia Paloma, Frampton J |
Analyzing a putative enhancer of optic disc morphology. BMC genetics 2020 10 21 (Suppl 1): 73. Babenko Vladimir, Babenko Roman, Orlov Yu |
Prevalence of the GFI1-36N SNP in Multiple Myeloma Patients and Its Impact on the Prognosis. Frontiers in oncology 2021 11 757664. Khandanpour Cyrus, Eisfeld Christine, Nimmagadda Subbaiah Chary, Raab Marc S, Weinhold Niels, Seckinger Anja, Hose Dirk, Jauch Anna, Försti Asta, Hemminki Kari, Hielscher Thomas, Hummel Manuela, Lenz Georg, Goldschmidt Hartmut, Huhn Stefan |
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- Page last updated:Apr 22, 2024
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