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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Disease and GATA1[original query]
Analysis of GATA1 mutations and leukemogenesis in newborns with Down syndrome.
Genetics and molecular research : GMR 2013 12 (4): 4630-8.
Queiroz L B, Lima B D, Mazzeu J F, Camargo R, Córdoba M S, Q Magalhães I, Martins-de-Sá C, Ferrari
Implications of mutational spectrum in myelodysplastic syndromes based on targeted next-generation sequencing.
Oncotarget 2017 Oct 8 (47): 82475-82490.
Xu Yuanyuan, Li Yan, Xu Qingyu, Chen Yuelong, Lv Na, Jing Yu, Dou Liping, Bo Jian, Hou Guangyuan, Guo Jing, Wang Xiuli, Wang Lili, Li Yonghui, Chen Chongjian, Yu
Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data.
Transfusion 2018 12 59 (2): 768-778.
Schoeman Elizna M, Roulis Eileen V, Perry Maree A, Flower Robert L, Hyland Catherine
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling. GWAS Catalog
American journal of human genetics 2020 Jul .
Rodriguez Benjamin A T, Bhan Arunoday, Beswick Andrew, Elwood Peter C, Niiranen Teemu J, Salomaa Veikko, , Trégouët David-Alexandre, Morange Pierre-Emmanuel, Civelek Mete, Ben-Shlomo Yoav, Schlaeger Thorsten, Chen Ming-Huei, Johnson Andrew
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling.
Neuroscience letters 2021 04 750 135802.
Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum
G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. GWAS Catalog
Blood advances 2021 9 6 (7): 2319-2330.
Downes Kate, Zhao Xuefei, Gleadall Nicholas S, McKinney Harriet, Kempster Carly, Batista Joana, Thomas Patrick L, Cooper Matthew, Michael James V, Kreuzhuber Roman, Wedderburn Katherine, Waller Kathryn, Varney Bianca, Verdier Hippolyte, Kriek Neline, Ashford Sofie E, Stirrups Kathleen E, Dunster Joanne L, McKenzie Steven E, Ouwehand Willem H, Gibbins Jonathan M, Yang Jing, Astle William J, Ma Peiso
Accelerated epigenetic aging in newborns with Down syndrome.
Aging cell 2022 6 21 (7): e13652.
Xu Keren, Li Shaobo, Muskens Ivo S, Elliott Natalina, Myint Swe Swe, Pandey Priyatama, Hansen Helen M, Morimoto Libby M, Kang Alice Y, Ma Xiaomei, Metayer Catherine, Mueller Beth A, Roberts Irene, Walsh Kyle M, Horvath Steve, Wiemels Joseph L, de Smith Adam
Novel Candidate loci and Pathogenic Germline Variants Involved in Familial Hematological Malignancies Revealed by Whole-Exome Sequencing.
Cancers 2023 2 15 (3): .
Andrés-Zayas Cristina, Suárez-González Julia, Chicano-Lavilla María, Bastos Oreiro Mariana, Rodríguez-Macías Gabriela, Font López Patricia, Osorio Prendes Santiago, Oarbeascoa Royuela Gillen, García Ramírez Patricia, Nieves Salgado Rocío, Gómez-Centurión Ignacio, Carbonell Muñoz Diego, Muñiz Paula, Kwon Mi, Díez-Martín José Luis, Buño Ismael, Martínez-Laperche Caroli
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