269 related articles for article (PubMed ID: 26332131)
21. Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance.
Hayeck TJ; Stong N; Wolock CJ; Copeland B; Kamalakaran S; Goldstein DB; Allen AS
Am J Hum Genet; 2019 Feb; 104(2):299-309. PubMed ID: 30686509
[TBL] [Abstract][Full Text] [Related]
22. Deletions of chromosomal regulatory boundaries are associated with congenital disease.
Ibn-Salem J; Köhler S; Love MI; Chung HR; Huang N; Hurles ME; Haendel M; Washington NL; Smedley D; Mungall CJ; Lewis SE; Ott CE; Bauer S; Schofield PN; Mundlos S; Spielmann M; Robinson PN
Genome Biol; 2014 Sep; 15(9):423. PubMed ID: 25315429
[TBL] [Abstract][Full Text] [Related]
23. Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains.
Oeltjen JC; Malley TM; Muzny DM; Miller W; Gibbs RA; Belmont JW
Genome Res; 1997 Apr; 7(4):315-29. PubMed ID: 9110171
[TBL] [Abstract][Full Text] [Related]
24. Cis-regulatory variations: a study of SNPs around genes showing cis-linkage in segregating mouse populations.
GuhaThakurta D; Xie T; Anand M; Edwards SW; Li G; Wang SS; Schadt EE
BMC Genomics; 2006 Sep; 7():235. PubMed ID: 16978413
[TBL] [Abstract][Full Text] [Related]
25. Regulatory variation and evolution: implications for disease.
Dermitzakis ET
Adv Genet; 2008; 61():295-306. PubMed ID: 18282511
[TBL] [Abstract][Full Text] [Related]
26. Variance explained by whole genome sequence variants in coding and regulatory genome annotations for six dairy traits.
Koufariotis LT; Chen YP; Stothard P; Hayes BJ
BMC Genomics; 2018 Apr; 19(1):237. PubMed ID: 29618315
[TBL] [Abstract][Full Text] [Related]
27. Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics.
Gussow AB; Copeland BR; Dhindsa RS; Wang Q; Petrovski S; Majoros WH; Allen AS; Goldstein DB
PLoS One; 2017; 12(8):e0181604. PubMed ID: 28797091
[TBL] [Abstract][Full Text] [Related]
28. The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes.
Gussow AB; Petrovski S; Wang Q; Allen AS; Goldstein DB
Genome Biol; 2016 Jan; 17():9. PubMed ID: 26781712
[TBL] [Abstract][Full Text] [Related]
29. Effects of genome-wide copy number variation on expression in mammalian cells.
Wang RT; Ahn S; Park CC; Khan AH; Lange K; Smith DJ
BMC Genomics; 2011 Nov; 12():562. PubMed ID: 22085887
[TBL] [Abstract][Full Text] [Related]
30. Copy number variations in the genome of the Qatari population.
Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
[TBL] [Abstract][Full Text] [Related]
31. A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings.
Fusaro M; Coustal C; Barnabei L; Riller Q; Heller M; Ho Nhat D; Fourrage C; Rivière S; Rieux-Laucat F; Maria ATJ; Picard C
Clin Immunol; 2024 Apr; 261():110165. PubMed ID: 38423196
[TBL] [Abstract][Full Text] [Related]
32. Comparison of different functional prediction scores using a gene-based permutation model for identifying cancer driver genes.
Nono AD; Chen K; Liu X
BMC Med Genomics; 2019 Jan; 12(Suppl 1):22. PubMed ID: 30704472
[TBL] [Abstract][Full Text] [Related]
33. Identification of High-Impact cis-Regulatory Mutations Using Transcription Factor Specific Random Forest Models.
Svetlichnyy D; Imrichova H; Fiers M; Kalender Atak Z; Aerts S
PLoS Comput Biol; 2015 Nov; 11(11):e1004590. PubMed ID: 26562774
[TBL] [Abstract][Full Text] [Related]
34. Noncoding control region of naturally occurring BK virus variants: sequence comparison and functional analysis.
Moens U; Johansen T; Johnsen JI; Seternes OM; Traavik T
Virus Genes; 1995; 10(3):261-75. PubMed ID: 8560788
[TBL] [Abstract][Full Text] [Related]
35. Characterization of copy number-stable regions in the human genome.
Johansson AC; Feuk L
Hum Mutat; 2011 Aug; 32(8):947-55. PubMed ID: 21542059
[TBL] [Abstract][Full Text] [Related]
36. Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C.
Cornish AJ; Hoang PH; Dobbins SE; Law PJ; Chubb D; Orlando G; Houlston RS
Blood Adv; 2019 Jan; 3(1):21-32. PubMed ID: 30606723
[TBL] [Abstract][Full Text] [Related]
37. LARVA: an integrative framework for large-scale analysis of recurrent variants in noncoding annotations.
Lochovsky L; Zhang J; Fu Y; Khurana E; Gerstein M
Nucleic Acids Res; 2015 Sep; 43(17):8123-34. PubMed ID: 26304545
[TBL] [Abstract][Full Text] [Related]
38. Genome-wide analysis of somatic noncoding mutation patterns in cancer.
Dietlein F; Wang AB; Fagre C; Tang A; Besselink NJM; Cuppen E; Li C; Sunyaev SR; Neal JT; Van Allen EM
Science; 2022 Apr; 376(6589):eabg5601. PubMed ID: 35389777
[TBL] [Abstract][Full Text] [Related]
39. Dosage-sensitive genes in evolution and disease.
Rice AM; McLysaght A
BMC Biol; 2017 Sep; 15(1):78. PubMed ID: 28863777
[TBL] [Abstract][Full Text] [Related]
40. rVarBase: an updated database for regulatory features of human variants.
Guo L; Du Y; Qu S; Wang J
Nucleic Acids Res; 2016 Jan; 44(D1):D888-93. PubMed ID: 26503253
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
