Global Genetic Architecture of an Erythroid Quantitative Trait Locus,HMIP-2-Reference-Cited by-同舟云学术

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Global Genetic Architecture of an Erythroid Quantitative Trait Locus,HMIP-2

Published:2014-07-29 Issue:6 Volume:78 Page:434-451
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Menzel Stephan¹,Rooks Helen¹,Zelenika Diana²,Mtatiro Siana N.¹³,Gnanakulasekaran Akshala¹,Drasar Emma¹⁴,Cox Sharon³,Liu Li⁵,Masood Mariam¹,Silver Nicholas¹,Garner Chad⁶,Vasavda Nisha¹,Howard Jo¹⁷,Makani Julie³,Adekile Adekunle⁸,Pace Betty⁹,Spector Tim¹,Farrall Martin¹⁰,Lathrop Mark¹¹,Thein Swee Lay¹⁴

Affiliation:

1. King's College London; London UK

2. Centre National de Génotypage; Evry France

3. Muhimbili University; Dar es Salaam Tanzania

4. King's College Hospital NHS Foundation Trust; London UK

5. University of Texas at Dallas; Richardson TX USA

6. University of California Irvine School of Medicine; Irvine CA USA

7. Guy's and St Thomas’ Hospital NHS Foundation Trust; London UK

8. Faculty of Medicine; Kuwait University; Kuwait

9. Georgia Regents University; Augusta GA USA

10. Division of Cardiovascular Medicine; Radcliffe Department of Medicine; Wellcome Trust Centre for Human Genetics; University of Oxford; Oxford UK

11. McGill University; Montreal Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12077/fullpdf

Reference70 articles.

1. A map of human genome variation from population-scale sequencing;Abecasis;Nature,2010

2. An integrated map of genetic variation from 1,092 human genomes;Abecasis;Nature,2012

3. Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels;Adekile;Ann Hematol,1992

4. The southern route “out of Africa”: evidence for an early expansion of modern humans into Arabia;Armitage;Science,2011

5. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans;Bae;Blood,2012

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1. The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria;Human Molecular Genetics;2024-02-10

2. The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria;2023-05-18

3. Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia;Journal of Human Genetics;2022-09-27

4. Pharmacogenomics of hydroxyurea therapy and fetal hemoglobin levels in sickle cell anemia;Pharmacogenomics;2022-05

5. F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease;British Journal of Haematology;2020-10-19

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