The genetics of human hematopoiesis and its disruption in disease-Reference-Cited by-同舟云学术

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The genetics of human hematopoiesis and its disruption in disease

Published:2019-07-17 Issue:8 Volume:11 Page:
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Bao Erik L¹²³⁴^ORCID,Cheng Aaron N¹²³,Sankaran Vijay G¹²³⁵^ORCID

Affiliation:

1. Division of Hematology/Oncology Boston Children's Hospital Harvard Medical School Boston MA USA

2. Department of Pediatric Oncology Dana‐Farber Cancer Institute Harvard Medical School Boston MA USA

3. Broad Institute of MIT and Harvard Cambridge MA USA

4. Harvard‐MIT Health Sciences and Technology Harvard Medical School Boston MA USA

5. Harvard Stem Cell Institute Cambridge MA USA

Funder

New York Stem Cell Foundation

National Institutes of Health

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201910316

Reference97 articles.

1. Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation

2. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

3. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

4. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

5. Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort

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