Priyanka Nandakumar
Overview
Explore the profile of Priyanka Nandakumar including associated specialties, affiliations and a list of published articles.
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24
Citations
1372
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Recent Articles
1.
Schormair B, Zhao C, Bell S, Didriksen M, Nawaz M, Schandra N, et al.
Nat Genet
. 2024 Jun;
56(6):1090-1099.
PMID: 38839884
Restless legs syndrome (RLS) affects up to 10% of older adults. Their healthcare is impeded by delayed diagnosis and insufficient treatment. To advance disease prediction and find new entry points...
2.
Watanabe K, Jansen P, Savage J, Nandakumar P, Wang X, Hinds D, et al.
Nat Genet
. 2022 Jul;
54(8):1125-1132.
PMID: 35835914
Insomnia is a heritable, highly prevalent sleep disorder for which no sufficient treatment currently exists. Previous genome-wide association studies with up to 1.3 million subjects identified over 200 associated loci....
3.
Choquet H, Li W, Yin J, Bradley R, Hoffmann T, Nandakumar P, et al.
Hum Mol Genet
. 2022 Jan;
31(13):2279-2293.
PMID: 35022708
Inguinal hernias are some of the most frequently diagnosed conditions in clinical practice and inguinal hernia repair is the most common procedure performed by general surgeons. Studies of inguinal hernias...
4.
Ong J, An J, Han X, Law M, Nandakumar P, Schumacher J, et al.
Gut
. 2021 Jun;
71(6):1053-1061.
PMID: 34187846
Objective: Gastro-oesophageal reflux disease (GERD) has heterogeneous aetiology primarily attributable to its symptom-based definitions. GERD genome-wide association studies (GWASs) have shown strong genetic overlaps with established risk factors such as...
5.
Kapoor A, Nandakumar P, Auer D, Sosa M, Ross H, Bollinger J, et al.
J Pediatr Surg
. 2021 May;
56(12):2286-2294.
PMID: 34006365
Purpose: Hirschsprung disease (HSCR) is a developmental disorder of the enteric nervous system (ENS) characterized by congenital aganglionosis arising from coding variants in ENS genes causing partial or total loss-of-function....
6.
Pirastu N, Cordioli M, Nandakumar P, Mignogna G, Abdellaoui A, Hollis B, et al.
Nat Genet
. 2021 Apr;
53(5):663-671.
PMID: 33888908
Genetic association results are often interpreted with the assumption that study participation does not affect downstream analyses. Understanding the genetic basis of participation bias is challenging since it requires the...
7.
Nandakumar P, Tian C, OConnell J, Hinds D, Paterson A, Sondheimer N
Sci Adv
. 2021 Mar;
7(12).
PMID: 33731350
The role of the nuclear genome in maintaining the stability of the mitochondrial genome (mtDNA) is incompletely known. mtDNA sequence variants can exist in a state of heteroplasmy, which denotes...
8.
Nandakumar P, Lee D, Hoffmann T, Ehret G, Arking D, Ranatunga D, et al.
Hum Mol Genet
. 2020 May;
29(11):1922-1932.
PMID: 32436959
Hundreds of loci have been associated with blood pressure (BP) traits from many genome-wide association studies. We identified an enrichment of these loci in aorta and tibial artery expression quantitative...
9.
Chatterjee S, Nandakumar P, Auer D, Gabriel S, Chakravarti A
Proc Natl Acad Sci U S A
. 2019 Dec;
116(52):26697-26708.
PMID: 31818953
The development of the gut from endodermal tissue to an organ with multiple distinct structures and functions occurs over a prolonged time during embryonic days E10.5-E14.5 in the mouse. During...
10.
Boutin T, Charteris D, Chandra A, Campbell S, Hayward C, Campbell A, et al.
Hum Mol Genet
. 2019 Dec;
29(4):689-702.
PMID: 31816047
Retinal detachment (RD) is a serious and common condition, but genetic studies to date have been hampered by the small size of the assembled cohorts. In the UK Biobank data...