Alan B Cantor
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Explore the profile of Alan B Cantor including associated specialties, affiliations and a list of published articles.
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74
Citations
3825
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Recent Articles
1.
Homan C, Drazer M, Yu K, Lawrence D, Feng J, Arriola-Martinez L, et al.
Blood Adv
. 2023 Jul;
7(20):6092-6107.
PMID: 37406166
Individuals with germ line variants associated with hereditary hematopoietic malignancies (HHMs) have a highly variable risk for leukemogenesis. Gaps in our understanding of premalignant states in HHMs have hampered efforts...
2.
Gorfinkel L, Wachter F, Luo H, Hansbury E, Williams D, Agarwal A, et al.
Pediatr Blood Cancer
. 2022 Oct;
70(1):e30067.
PMID: 36250986
Unstable gamma globin variants can cause transient neonatal hemolytic anemia. We have identified a novel variant in a newborn who presented with jaundice and anemia requiring phototherapy and red blood...
3.
Hasle H, Kline R, Kjeldsen E, Nik-Abdul-Rashid N, Bhojwani D, Verboon J, et al.
Blood
. 2021 Nov;
139(21):3159-3165.
PMID: 34758059
Individuals with Down syndrome are at increased risk of myeloid leukemia in early childhood, which is associated with acquisition of GATA1 mutations that generate a short GATA1 isoform called GATA1s....
4.
Samarakkody A, Cantor A
Genes Dev
. 2021 Nov;
35(21-22):1398-1400.
PMID: 34725127
Definitive long-term hematopoietic stem cells (LT-HSCs) arise during embryogenesis in a process termed endothelial-to-hematopoietic transition (EHT), in which specialized hemogenic endothelial cells (HECs) transform into hematopoietic cells. The transcription factor...
5.
Six K, Gerdemann U, Brown A, Place A, Cantor A, Kutny M, et al.
Blood Adv
. 2021 Aug;
5(16):3199-3202.
PMID: 34424323
Germline RUNX1 mutations underlie a syndrome, RUNX1-familial platelet disorder (RUNX1-FPD), characterized by bleeding symptoms that result from quantitative and/or qualitative defect in platelets and a significantly increased risk for developing...
6.
7.
Wahlster L, Verboon J, Ludwig L, Black S, Luo W, Garg K, et al.
J Exp Med
. 2021 Apr;
218(6).
PMID: 33857290
Advances in genome sequencing have resulted in the identification of the causes for numerous rare diseases. However, many cases remain unsolved with standard molecular analyses. We describe a family presenting...
8.
Choudhuri A, Trompouki E, Abraham B, Colli L, Kock K, Mallard W, et al.
Nat Genet
. 2020 Nov;
52(12):1333-1345.
PMID: 33230299
Genome-wide association studies identify genomic variants associated with human traits and diseases. Most trait-associated variants are located within cell-type-specific enhancers, but the molecular mechanisms governing phenotypic variation are less well...
9.
Hsu J, Huang H, Lee C, Choudhuri A, Wilson N, Abraham B, et al.
Proc Natl Acad Sci U S A
. 2020 Sep;
117(38):23626-23635.
PMID: 32883883
Hematopoietic stem and progenitor cell (HSPC) formation and lineage differentiation involve gene expression programs orchestrated by transcription factors and epigenetic regulators. Genetic disruption of the chromatin remodeler chromodomain-helicase-DNA-binding protein 7...
10.
Verboon J, Mahmut D, Kim A, Nakamura M, Abdulhay N, Nandakumar S, et al.
J Clin Immunol
. 2020 Apr;
40(4):554-566.
PMID: 32303876
Studies of genetic blood disorders have advanced our understanding of the intrinsic regulation of hematopoiesis. However, such genetic studies have only yielded limited insights into how interactions between hematopoietic cells...