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Year | Number of Results |
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2019 | 1 |
2023 | 2 |
2024 | 2 |
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Page 1
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
N Engl J Med. 2023 Apr 27;388(17):1559-1571. doi: 10.1056/NEJMoa2209046. Epub 2023 Apr 12.
N Engl J Med. 2023.
PMID: 37043637
Free PMC article.
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference.
Meng X, Navoly G, Giannakopoulou O, Levey DF, Koller D, Pathak GA, Koen N, Lin K, Adams MJ, Rentería ME, Feng Y, Gaziano JM, Stein DJ, Zar HJ, Campbell ML, van Heel DA, Trivedi B, Finer S, McQuillin A, Bass N, Chundru VK, Martin HC, Huang QQ, Valkovskaya M, Chu CY, Kanjira S, Kuo PH, Chen HC, Tsai SJ, Liu YL, Kendler KS, Peterson RE, Cai N, Fang Y, Sen S, Scott LJ, Burmeister M, Loos RJF, Preuss MH, Actkins KV, Davis LK, Uddin M, Wani AH, Wildman DE, Aiello AE, Ursano RJ, Kessler RC, Kanai M, Okada Y, Sakaue S, Rabinowitz JA, Maher BS, Uhl G, Eaton W, Cruz-Fuentes CS, Martinez-Levy GA, Campos AI, Millwood IY, Chen Z, Li L, Wassertheil-Smoller S, Jiang Y, Tian C, Martin NG, Mitchell BL, Byrne EM, Awasthi S, Coleman JRI, Ripke S; PGC-MDD Working Group; China Kadoorie Biobank Collaborative Group; 23andMe Research Team; Genes and Health Research Team; BioBank Japan Project; Sofer T, Walters RG, McIntosh AM, Polimanti R, Dunn EC, Stein MB, Gelernter J, Lewis CM, Kuchenbaecker K.
Meng X, et al. Among authors: chundru vk.
Nat Genet. 2024 Feb;56(2):222-233. doi: 10.1038/s41588-023-01596-4. Epub 2024 Jan 4.
Nat Genet. 2024.
PMID: 38177345
Free PMC article.
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Rare genetic variants underlie outlying levels of DNA methylation and gene-expression.
Chundru VK, Marioni RE, Prendergast JGD, Lin T, Beveridge AJ, Martin NG, Montgomery GW, Hume DA, Deary IJ, Visscher PM, Wray NR, McRae AF.
Chundru VK, et al.
Hum Mol Genet. 2023 May 18;32(11):1912-1921. doi: 10.1093/hmg/ddad028.
Hum Mol Genet. 2023.
PMID: 36790133
Free PMC article.
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Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait.
Chundru VK, Marioni RE, Prendergast JGD, Vallerga CL, Lin T, Beveridge AJ; SGPD Consortium; Gratten J, Hume DA, Deary IJ, Wray NR, Visscher PM, McRae AF.
Chundru VK, et al.
Genetics. 2019 Jul;212(3):577-586. doi: 10.1534/genetics.118.301861. Epub 2019 Apr 30.
Genetics. 2019.
PMID: 31040117
Free PMC article.
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Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders.
Wigdor EM, Samocha KE, Eberhardt RY, Chundru VK, Firth HV, Wright CF, Hurles ME, Martin HC.
Wigdor EM, et al. Among authors: chundru vk.
Sci Rep. 2024 Apr 15;14(1):8708. doi: 10.1038/s41598-024-58894-y.
Sci Rep. 2024.
PMID: 38622173
Free PMC article.
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