Anoop K Sendamarai
Overview
Explore the profile of Anoop K Sendamarai including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
18
Citations
593
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Gorman B, Ji S, Francis M, Sendamarai A, Shi Y, Devineni P, et al.
Nat Commun
. 2024 Oct;
15(1):8629.
PMID: 39366959
Lung cancer remains the leading cause of cancer mortality, despite declining smoking rates. Previous lung cancer GWAS have identified numerous loci, but separating the genetic risks of lung cancer and...
2.
Ducamp S, Sendamarai A, Campagna D, Chin D, Fujiwara Y, Schmidt P, et al.
Blood
. 2024 Jun;
144(13):1418-1432.
PMID: 38900972
X-linked sideroblastic anemia (XLSA) and X-linked protoporphyria (XLPP) are uncommon diseases caused by loss-of-function and gain-of-function mutations, respectively, in the erythroid form of 5-aminolevulinic acid synthetase (ALAS), ALAS2, which encodes...
3.
Klarin D, Devineni P, Sendamarai A, Angueira A, Graham S, Shen Y, et al.
Nat Genet
. 2023 Jun;
55(7):1106-1115.
PMID: 37308786
The current understanding of the genetic determinants of thoracic aortic aneurysms and dissections (TAAD) has largely been informed through studies of rare, Mendelian forms of disease. Here, we conducted a...
4.
Roychowdhury T, Lu H, Hornsby W, Crone B, Wang G, Guo D, et al.
Am J Hum Genet
. 2021 Jul;
108(9):1578-1589.
PMID: 34265237
Thoracic aortic aneurysm (TAA) is characterized by dilation of the aortic root or ascending/descending aorta. TAA is a heritable disease that can be potentially life threatening. While 10%-20% of TAA...
5.
Crispin A, Guo C, Chen C, Campagna D, Schmidt P, Lichtenstein D, et al.
J Clin Invest
. 2020 Jul;
130(10):5245-5256.
PMID: 32634119
The congenital sideroblastic anemias (CSAs) can be caused by primary defects in mitochondrial iron-sulfur (Fe-S) cluster biogenesis. HSCB (heat shock cognate B), which encodes a mitochondrial cochaperone, also known as...
6.
Lack of does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia
Guerra A, Oikonomidou P, Sinha S, Zhang J, Lo Presti V, Hamilton C, et al.
Blood
. 2019 Jun;
134(6):568-572.
PMID: 31151988
No abstract available.
7.
Chau K, Shannon M, Fame R, Fonseca E, Mullan H, Johnson M, et al.
Elife
. 2018 May;
7.
PMID: 29745900
Forebrain precursor cells are dynamic during early brain development, yet the underlying molecular changes remain elusive. We observed major differences in transcriptional signatures of precursor cells from mouse forebrain at...
8.
Nguyen A, Prado M, Schmidt P, Sendamarai A, Wilson-Grady J, Min M, et al.
Science
. 2017 Aug;
357(6350).
PMID: 28774900
During terminal differentiation, the global protein complement is remodeled, as epitomized by erythrocytes, whose cytosol is ~98% globin. The erythroid proteome undergoes a rapid transition at the reticulocyte stage; however,...
9.
Lichtenstein D, Crispin A, Sendamarai A, Campagna D, Schmitz-Abe K, Sousa C, et al.
Blood
. 2016 Aug;
128(15):1913-1917.
PMID: 27488349
The congenital sideroblastic anemias (CSAs) are a heterogeneous group of inherited blood disorders characterized by pathological mitochondrial iron deposition in erythroid precursors. Each known cause has been attributed to a...
10.
Mangum J, Hardee J, Fix D, Puppa M, Elkes J, Altomare D, et al.
Sci Rep
. 2016 May;
6:26202.
PMID: 27197761
Mitochondrial myopathy with lactic acidosis and sideroblastic anemia (MLASA) is an oxidative phosphorylation disorder, with primary clinical manifestations of myopathic exercise intolerance and a macrocytic sideroblastic anemia. One cause of...