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Risk factors for eight common cancers revealed from a phenome-wide Mendelian randomisation analysis of 378,142 cases and 485,715 controls.
Went M, Sud A, Mills C, Hyde A, Culliford R, Law P, Vijayakrishnan J, Gockel I, Maj C, Schumacher J, Palles C, Kaiser M, Houlston R. Went M, et al. Among authors: maj c. medRxiv [Preprint]. 2023 Apr 6:2023.02.15.23285952. doi: 10.1101/2023.02.15.23285952. medRxiv. 2023. Update in: Nat Commun. 2024 Mar 25;15(1):2637. doi: 10.1038/s41467-024-46927-z PMID: 37066289 Free PMC article. Updated. Preprint.
Risk factors for eight common cancers revealed from a phenome-wide Mendelian randomisation analysis of 378,142 cases and 485,715 controls.
Went M, Sud A, Mills C, Hyde A, Culliford R, Law P, Vijayakrishnan J, Gockel I, Maj C, Schumacher J, Palles C, Kaiser M, Houlston R. Went M, et al. Among authors: maj c. Res Sq [Preprint]. 2023 Mar 17:rs.3.rs-2587058. doi: 10.21203/rs.3.rs-2587058/v1. Res Sq. 2023. Update in: Nat Commun. 2024 Mar 25;15(1):2637. doi: 10.1038/s41467-024-46927-z PMID: 36993383 Free PMC article. Updated. Preprint.
The genetic regulation of the gastric transcriptome is associated with metabolic and obesity-related traits and diseases.
Koebbe LL, Hess T, Giel AS, Bigge J, Gehlen J, Schueller V, Geppert M, Dumoulin FL, Heller J, Schepke M, Plaßmann D, Vieth M, Venerito M, Schumacher J, Maj C. Koebbe LL, et al. Among authors: maj c. Physiol Genomics. 2024 May 1;56(5):384-396. doi: 10.1152/physiolgenomics.00120.2023. Epub 2024 Feb 26. Physiol Genomics. 2024. PMID: 38406838 Free PMC article.
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants.
Qiao L, Welch CL, Hernan R, Wynn J, Krishnan US, Zalieckas JM, Buchmiller T, Khlevner J, De A, Farkouh-Karoleski C, Wagner AJ, Heydweiller A, Mueller AC, de Klein A, Warner BW, Maj C, Chung D, McCulley DJ, Schindel D, Potoka D, Fialkowski E, Schulz F, Kipfmuller F, Lim FY, Magielsen F, Mychaliska GB, Aspelund G, Reutter HM, Needelman H, Schnater JM, Fisher JC, Azarow K, Elfiky M, Nöthen MM, Danko ME, Li M, Kosiński P, Wijnen RMH, Cusick RA, Soffer SZ, Cochius-Den Otter SCM, Schaible T, Crombleholme T, Duron VP, Donahoe PK, Sun X, High FA, Bendixen C, Brosens E, Shen Y, Chung WK. Qiao L, et al. Among authors: maj c. Am J Hum Genet. 2024 Nov 7;111(11):2362-2381. doi: 10.1016/j.ajhg.2024.08.024. Epub 2024 Sep 26. Am J Hum Genet. 2024. PMID: 39332409
A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney.
Groen In 't Woud S, Maj C, Renkema KY, Westland R, Galesloot T, van Rooij IALM, Vermeulen SH, Feitz WFJ, Roeleveld N, Schreuder MF, van der Zanden LFM; SOFIA Study Group. Groen In 't Woud S, et al. Among authors: maj c. Biomedicines. 2022 Nov 23;10(12):3023. doi: 10.3390/biomedicines10123023. Biomedicines. 2022. PMID: 36551779 Free PMC article.
Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS.
Yin X, Richardson M, Laner A, Shi X, Ognedal E, Vasta V, Hansen TVO, Pineda M, Ritter D, de Dunnen J, Hassanin E, Lin WL, Borras E, Krahn K, Nordling M, Martins A, Mahmood K, Nadeau E, Beshay V, Tops C, Genuardi M, Pesaran T, Frayling IM, Capellá G, Latchford A, Tavtigian SV, Maj C, Plon SE, Greenblatt MS, Macrae FA, Spier I, Aretz S. Yin X, et al. Among authors: maj c. Am J Hum Genet. 2024 Nov 7;111(11):2427-2443. doi: 10.1016/j.ajhg.2024.09.002. Epub 2024 Oct 1. Am J Hum Genet. 2024. PMID: 39357517 Free PMC article.
97 results