Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease-Reference-Cited by-同舟云学术

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

Published:2018-03-28 Issue:3 Volume:14 Page:e1007293
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Raffield Laura M.,Ulirsch Jacob C.,Naik Rakhi P.^ORCID,Lessard Samuel,Handsaker Robert E.,Jain Deepti^ORCID,Kang Hyun M.,Pankratz Nathan^ORCID,Auer Paul L.,Bao Erik L.^ORCID,Smith Joshua D.,Lange Leslie A.,Lange Ethan M.,Li Yun,Thornton Timothy A.,Young Bessie A.,Abecasis Goncalo R.,Laurie Cathy C.,Nickerson Deborah A.,McCarroll Steven A.,Correa Adolfo,Wilson James G.,Lettre Guillaume^ORCID,Sankaran Vijay G.,Reiner Alex P.,

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference71 articles.

1. Sickle-cell trait: novel clinical significance;NS Key;Hematology Am Soc Hematol Educ Program,2010

2. Alpha-thalassaemia;CL Harteveld;Orphanet J Rare Dis,2010

3. Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos;CJ Hodonsky;PLoS Genet,2017

4. Hematologic differences between African-Americans and whites: the roles of iron deficiency and alpha-thalassemia on hemoglobin levels and mean corpuscular volume;E Beutler;Blood,2005

5. alpha-Thalassemia: prevalence and hematologic findings in American Blacks;CS Johnson;Arch Intern Med,1982

Cited by 48 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Parallel Evolution at the Regulatory Base-Pair Level Contributes to Mammalian Interspecific Differences in Polygenic Traits;Molecular Biology and Evolution;2024-07-29

2. Association of clonal hematopoiesis and mosaic chromosomal alterations with solid malignancy incidence and mortality;Cancer;2024-07-16

3. Genetic Modifiers of Stroke in Patients with Sickle Cell Disease—A Scoping Review;International Journal of Molecular Sciences;2024-06-07

4. Interplay between α‐thalassemia and β‐hemoglobinopathies: Translating genotype–phenotype relationships into therapies;HemaSphere;2024-05

5. Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis;Hemoglobin;2024-03-03