Anshuman Sewda
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Explore the profile of Anshuman Sewda including associated specialties, affiliations and a list of published articles.
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12
Citations
102
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Recent Articles
1.
Nicoletti P, Zafer S, Matok L, Irron I, Patrick M, Haklai R, et al.
Genet Med Open
. 2024 Sep;
2.
PMID: 39345948
Purpose: The etiopathogenesis of coronal nonsyndromic craniosynostosis (cNCS), a congenital condition defined by premature fusion of 1 or both coronal sutures, remains largely unknown. Methods: We conducted the largest genome-wide...
2.
Ganapathi M, Matsuoka L, March M, Li D, Brokamp E, Benito-Sanz S, et al.
Eur J Hum Genet
. 2023 Jul;
31(10):1117-1124.
PMID: 37500725
Nuclear receptor subfamily 2 group F member 2 (NR2F2 or COUP-TF2) encodes a transcription factor which is expressed at high levels during mammalian development. Rare heterozygous Mendelian variants in NR2F2...
3.
Cheng H, Sewda A, Marquez-Luna C, White S, Whitney B, Williams-Nguyen J, et al.
BMC Med
. 2021 May;
19(1):114.
PMID: 33947393
No abstract available.
4.
Cheng H, Sewda A, Marquez-Luna C, White S, Whitney B, Williams-Nguyen J, et al.
BMC Med
. 2020 Oct;
18(1):288.
PMID: 33109212
Background: Advances in antiretroviral therapies have greatly improved the survival of people living with human immunodeficiency virus (HIV) infection (PLWH); yet, PLWH have a higher risk of cardiovascular disease than...
5.
Sewda A, Agopian A, Goldmuntz E, Hakonarson H, Morrow B, Musfee F, et al.
PLoS One
. 2020 Jun;
15(6):e0234357.
PMID: 32516339
Congenital heart defects (CHDs) affect approximately 1% of newborns. Epidemiological studies have identified several genetically-mediated maternal phenotypes (e.g., pregestational diabetes, chronic hypertension) that are associated with the risk of CHDs...
6.
Hoang T, Manso P, Edman S, Mercer-Rosa L, Mitchell L, Sewda A, et al.
J Cardiovasc Magn Reson
. 2019 Aug;
21(1):51.
PMID: 31422771
Background: Studies suggest that right ventricular (RV) fibrosis is associated with RV remodeling and long-term outcomes in patients with tetralogy of Fallot (TOF). Pre-operative hypoxia may increase expression of hypoxia...
7.
Sewda A, Agopian A, Goldmuntz E, Hakonarson H, Morrow B, Taylor D, et al.
PLoS One
. 2019 Jul;
14(7):e0219926.
PMID: 31314787
Conotruncal heart defects (CTDs) are among the most common and severe groups of congenital heart defects. Despite evidence of an inherited genetic contribution to CTDs, little is known about the...
8.
Sewda A, White S, Erazo M, Hao K, Garcia-Fructuoso G, Fernandez-Rodriguez I, et al.
Pediatr Res
. 2019 Jan;
85(4):463-468.
PMID: 30651579
Background: Craniosynostosis (CS), the premature fusion of one or more neurocranial sutures, is associated with approximately 200 syndromes; however, about 65-85% of patients present with no additional major birth defects....
9.
Granot-Hershkovitz E, Karasik D, Friedlander Y, Rodriguez-Murillo L, Dorajoo R, Liu J, et al.
Eur J Hum Genet
. 2018 Aug;
26(12):1848-1858.
PMID: 30108283
Genetic studies in isolated populations often increase power for identifying loci associated with complex diseases and traits. We present here the Kibbutzim Family Study (KFS), aimed at investigating the genetic...
10.
Agopian A, Goldmuntz E, Hakonarson H, Sewda A, Taylor D, Mitchell L
Circ Cardiovasc Genet
. 2017 May;
10(3):e001449.
PMID: 28468790
Background: Maternal and inherited (ie, case) genetic factors likely contribute to the pathogenesis of congenital heart defects, but it is unclear whether individual common variants confer a large risk. Methods...