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Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Wang Y, Nudel R, Benros ME, Skogstrand K, Fishilevich S; iPSYCH-BROAD; Lancet D, Sun J, Hougaard DM, Andreassen OA, Mortensen PB, Buil A, Hansen TF, Thompson WK, Werge T. Wang Y, et al. Among authors: lancet d. PLoS Genet. 2020 Nov 23;16(11):e1009163. doi: 10.1371/journal.pgen.1009163. eCollection 2020 Nov. PLoS Genet. 2020. PMID: 33227023 Free PMC article.
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Stelzer G, Rosen N, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Stein TI, Nudel R, Lieder I, Mazor Y, Kaplan S, Dahary D, Warshawsky D, Guan-Golan Y, Kohn A, Rappaport N, Safran M, Lancet D. Stelzer G, et al. Among authors: lancet d. Curr Protoc Bioinformatics. 2016 Jun 20;54:1.30.1-1.30.33. doi: 10.1002/cpbi.5. Curr Protoc Bioinformatics. 2016. PMID: 27322403
VarElect: the phenotype-based variation prioritizer of the GeneCards Suite.
Stelzer G, Plaschkes I, Oz-Levi D, Alkelai A, Olender T, Zimmerman S, Twik M, Belinky F, Fishilevich S, Nudel R, Guan-Golan Y, Warshawsky D, Dahary D, Kohn A, Mazor Y, Kaplan S, Iny Stein T, Baris HN, Rappaport N, Safran M, Lancet D. Stelzer G, et al. Among authors: lancet d. BMC Genomics. 2016 Jun 23;17 Suppl 2(Suppl 2):444. doi: 10.1186/s12864-016-2722-2. BMC Genomics. 2016. PMID: 27357693 Free PMC article.
GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.
Fishilevich S, Nudel R, Rappaport N, Hadar R, Plaschkes I, Iny Stein T, Rosen N, Kohn A, Twik M, Safran M, Lancet D, Cohen D. Fishilevich S, et al. Among authors: lancet d. Database (Oxford). 2017 Jan 1;2017:bax028. doi: 10.1093/database/bax028. Database (Oxford). 2017. PMID: 28605766 Free PMC article.
Genome analysis and knowledge-driven variant interpretation with TGex.
Dahary D, Golan Y, Mazor Y, Zelig O, Barshir R, Twik M, Iny Stein T, Rosner G, Kariv R, Chen F, Zhang Q, Shen Y, Safran M, Lancet D, Fishilevich S. Dahary D, et al. Among authors: lancet d. BMC Med Genomics. 2019 Dec 30;12(1):200. doi: 10.1186/s12920-019-0647-8. BMC Med Genomics. 2019. PMID: 31888639 Free PMC article.
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene.
Cooper-Knock J, Zhang S, Kenna KP, Moll T, Franklin JP, Allen S, Nezhad HG, Iacoangeli A, Yacovzada NY, Eitan C, Hornstein E, Elhaik E, Celadova P, Bose D, Farhan S, Fishilevich S, Lancet D, Morrison KE, Shaw CE, Al-Chalabi A; Project MinE ALS Sequencing Consortium; Veldink JH, Kirby J, Snyder MP, Shaw PJ. Cooper-Knock J, et al. Among authors: lancet d. Cell Rep. 2020 Dec 1;33(9):108456. doi: 10.1016/j.celrep.2020.108456. Cell Rep. 2020. PMID: 33264630 Free PMC article.
Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y. Teltsh O, et al. Among authors: lancet d. Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15. doi: 10.1002/ajmg.b.30591. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17823922
250 results