Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Disease and EBF1[original query] |
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Early B-cell Factor gene association with multiple sclerosis in the Spanish population. BMC neurology 2005 5 (): 19. Martínez Alfonso, Mas Ana, de las Heras Virginia, Arroyo Rafael, Fernández-Arquero Miguel, de la Concha Emilio G, Urcelay Ele |
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5. BMC genetics 2012 13 12. Nolan Daniel K, Sutton Beth, Haynes Carol, Johnson Jessica, Sebek Jacqueline, Dowdy Elaine, Crosslin David, Crossman David, Sketch Michael H, Granger Christopher B, Seo David, Goldschmidt-Clermont Pascal, Kraus William E, Gregory Simon G, Hauser Elizabeth R, Shah Svati |
A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians. BMC medical genetics 2012 13 (1): 5. Png Eileen, Alisjahbana Bachti, Sahiratmadja Edhyana, Marzuki Sangkot, Nelwan Ron, Balabanova Yanina, Nikolayevskyy Vladyslav, Drobniewski Francis, Nejentsev Sergey, Adnan Iskandar, van de Vosse Esther, Hibberd Martin L, van Crevel Reinout, Ottenhoff Tom H M, Seielstad Ma |
Novel gene targets detected by genomic profiling in a consecutive series of 126 adults with acute lymphoblastic leukemia. Haematologica 2015 Jan 100 (1): 55-61. Safavi Setareh, Hansson Markus, Karlsson Karin, Biloglav Andrea, Johansson Bertil, Paulsson Kaj |
Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.
European journal of human genetics : EJHG 2015 Jun 23 (6): 854-62. Singh Abanish, Babyak Michael A, Nolan Daniel K, Brummett Beverly H, Jiang Rong, Siegler Ilene C, Kraus William E, Shah Svati H, Williams Redford B, Hauser Elizabeth |
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Nature genetics 2017 Jan 49 (1): 125-130. Chu Audrey Y, Deng Xuan, Fisher Virginia A, Drong Alexander, Zhang Yang, Feitosa Mary F, Liu Ching-Ti, Weeks Olivia, Choh Audrey C, Duan Qing, Dyer Thomas D, Eicher John D, Guo Xiuqing, Heard-Costa Nancy L, Kacprowski Tim, Kent Jack W, Lange Leslie A, Liu Xinggang, Lohman Kurt, Lu Lingyi, Mahajan Anubha, O'Connell Jeffrey R, Parihar Ankita, Peralta Juan M, Smith Albert V, Zhang Yi, Homuth Georg, Kissebah Ahmed H, Kullberg Joel, Laqua René, Launer Lenore J, Nauck Matthias, Olivier Michael, Peyser Patricia A, Terry James G, Wojczynski Mary K, Yao Jie, Bielak Lawrence F, Blangero John, Borecki Ingrid B, Bowden Donald W, Carr John Jeffrey, Czerwinski Stefan A, Ding Jingzhong, Friedrich Nele, Gudnason Vilmunder, Harris Tamara B, Ingelsson Erik, Johnson Andrew D, Kardia Sharon L R, Langefeld Carl D, Lind Lars, Liu Yongmei, Mitchell Braxton D, Morris Andrew P, Mosley Thomas H, Rotter Jerome I, Shuldiner Alan R, Towne Bradford, Völzke Henry, Wallaschofski Henri, Wilson James G, Allison Matthew, Lindgren Cecilia M, Goessling Wolfram, Cupples L Adrienne, Steinhauser Matthew L, Fox Caroline |
Replication of Early B-cell Factor 1 (EBF1) Gene-by-psychosocial Stress Interaction Effects on Central Adiposity in a Korean Population. Journal of preventive medicine and public health = Yebang Uihakhoe chi 2016 Sep 49 (5): 253-259. Kim Hyun-Jin, Min Jin-Young, Min Kyoung-B |
The correlation between Pax5 deletion and patients survival in Iranian children with precursor B-cell acute lymphocytic leukemia. Cellular and molecular biology (Noisy-le-Grand, France) 2017 9 63 (8): 19-22. Moafi A, Zojaji A, Salehi R, Najafi Dorcheh S, Rahgozar |
Clinical significance of recurrent copy number aberrations in B-lineage acute lymphoblastic leukaemia without recurrent fusion genes across age cohorts. British journal of haematology 2017 Apr . Messina Monica, Chiaretti Sabina, Fedullo Anna Lucia, Piciocchi Alfonso, Puzzolo Maria Cristina, Lauretti Alessia, Gianfelici Valentina, Apicella Valerio, Fazi Paola, Te Kronnie Geertruy, Testi Anna Maria, Vitale Antonella, Guarini Anna, Foà Rob |
Genomic analysis of adult B-ALL identifies potential markers of shorter survival. Leukemia research 2017 Feb 56 44-51. Patel Shiven, Mason Clinton C, Glenn Martha J, Paxton Christian N, South Sara T, Cessna Melissa H, Asch Julie, Cobain Erin F, Bixby Dale L, Smith Lauren B, Reshmi Shalini, Gastier-Foster Julie M, Schiffman Joshua D, Miles Rodney |
Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease. BMC cardiovascular disorders 2017 Feb 17 (1): 57. Li Yafei, Xie Zhiyong, Chen Lei, Yan Jianjun, Ma Yao, Wang Liansheng, Chen Zho |
Association of genetic variation with blood pressure traits among East Africans. Clinical genetics 2017 Jan . Kayima James, Liang Jingjing, Natanzon Yanina, Nankabirwa Joaniter, Ssinabulya Isaac, Nakibuuka Jane, Katamba Achilles, Mayanja-Kizza Harriet, Miron Alexander, Li Chun, Zhu Xiaofe |
EBF1 gene polymorphism and its interaction with smoking and drinking on the risk of coronary artery disease for Chinese patients. Bioscience reports 2018 May . Ying Yongjun, Luo Yuxuan, Peng H |
High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction. Leukemia research 2018 2 66 79-84. Singh Minu, Bhatia Prateek, Trehan Amita, Varma Neelam, Sachdeva Manupdesh Singh, Bansal Deepak, Jain Richa, Naseem Sha |
Genomic CDKN2A/2B deletions in adult Ph ALL are adverse despite allogeneic stem cell transplantation. Blood 2018 Jan . Pfeifer Heike, Raum Katharina, Markovic Sandra, Nowak Verena, Fey Stephanie, Obländer Julia, Pressler Jovita, Böhm Verena, Brüggemann Monika, Wunderle Lydia, Hüttmann Andreas, Wäsch Ralph, Beck Joachim, Stelljes Matthias, Viardot Andreas, Lang Fabian, Hoelzer Dieter, Hofmann Wolf-Karsten, Serve Hubert, Weiss Christel, Goekbuget Nicola, Ottmann Oliver G, Nowak Dani |
Varicose veins of lower extremities: Insights from the first large-scale genetic study.
PLoS genetics 2019 Apr 15 (4): e1008110. Shadrina Alexandra S, Sharapov Sodbo Z, Shashkova Tatiana I, Tsepilov Yakov |
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
eLife 2019 01 8 . Timmers Paul Rhj, Mounier Ninon, Lall Kristi, Fischer Krista, Ning Zheng, Feng Xiao, Bretherick Andrew D, Clark David W, , Shen Xia, Esko Tõnu, Kutalik Zoltán, Wilson James F, Joshi Peter |
Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms.
Annals of the rheumatic diseases 2020 Oct . López-Isac Elena, Smith Samantha L, Marion Miranda C, Wood Abigail, Sudman Marc, Yarwood Annie, Shi Chenfu, Gaddi Vasanthi Priyadarshini, Martin Paul, Prahalad Sampath, Eyre Stephen, Orozco Gisela, Morris Andrew P, Langefeld Carl D, Thompson Susan D, Thomson Wendy, Bowes Jo |
Evaluating the precision of EBF1 SNP x stress interaction association: sex, race, and age differences in a big harmonized data set of 28,026 participants. Translational psychiatry 2020 10 10 (1): 351. Singh Abanish, Babyak Michael A, Sims Mario, Musani Solomon K, Brummett Beverly H, Jiang Rong, Kraus William E, Shah Svati H, Siegler Ilene C, Hauser Elizabeth R, Williams Redford |
Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.
Genes 2022 12 13 (12): . Changalidis Anton I, Maksiutenko Evgeniia M, Barbitoff Yury A, Tkachenko Alexander A, Vashukova Elena S, Pachuliia Olga V, Nasykhova Yulia A, Glotov Andrey |
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