167 related articles for article (PubMed ID: 22685595)
1. Genotype-based test in mapping cis-regulatory variants from allele-specific expression data.
Lefebvre JF; Vello E; Ge B; Montgomery SB; Dermitzakis ET; Pastinen T; Labuda D
PLoS One; 2012; 7(6):e38667. PubMed ID: 22685595
[TBL] [Abstract][Full Text] [Related]
2. Identification of a Cis-acting regulatory polymorphism in a Eucalypt COBRA-like gene affecting cellulose content.
Thumma BR; Matheson BA; Zhang D; Meeske C; Meder R; Downes GM; Southerton SG
Genetics; 2009 Nov; 183(3):1153-64. PubMed ID: 19737751
[TBL] [Abstract][Full Text] [Related]
3. The rs1024611 regulatory region polymorphism is associated with CCL2 allelic expression imbalance.
Pham MH; Bonello GB; Castiblanco J; Le T; Sigala J; He W; Mummidi S
PLoS One; 2012; 7(11):e49498. PubMed ID: 23166687
[TBL] [Abstract][Full Text] [Related]
4. Direct Testing for Allele-Specific Expression Differences Between Conditions.
León-Novelo L; Gerken AR; Graze RM; McIntyre LM; Marroni F
G3 (Bethesda); 2018 Feb; 8(2):447-460. PubMed ID: 29167272
[TBL] [Abstract][Full Text] [Related]
5. Detection of cis-acting regulatory SNPs using allelic expression data.
Xiao R; Scott LJ
Genet Epidemiol; 2011 Sep; 35(6):515-25. PubMed ID: 21769929
[TBL] [Abstract][Full Text] [Related]
6. Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.
Zhang K; Qin ZS; Liu JS; Chen T; Waterman MS; Sun F
Genome Res; 2004 May; 14(5):908-16. PubMed ID: 15078859
[TBL] [Abstract][Full Text] [Related]
7. Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation.
Hill MJ; Kenny E; Roche S; Morris DW; Corvin A; Hawi Z; Gill M; Anney RJ
Psychiatr Genet; 2011 Dec; 21(6):281-6. PubMed ID: 21642896
[TBL] [Abstract][Full Text] [Related]
8. Cis-acting regulatory variation in the human genome.
Pastinen T; Hudson TJ
Science; 2004 Oct; 306(5696):647-50. PubMed ID: 15499010
[TBL] [Abstract][Full Text] [Related]
9. Identification of cis-regulatory variations in the IL6R gene through the inheritance assessment of allelic transcription.
Oh SA; Byun H; Jang E; Jeong S
Biochim Biophys Acta; 2014 Jan; 1840(1):637-44. PubMed ID: 24482814
[TBL] [Abstract][Full Text] [Related]
10. Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.
Almlöf JC; Lundmark P; Lundmark A; Ge B; Maouche S; Göring HH; Liljedahl U; Enström C; Brocheton J; Proust C; Godefroy T; Sambrook JG; Jolley J; Crisp-Hihn A; Foad N; Lloyd-Jones H; Stephens J; Gwilliam R; Rice CM; Hengstenberg C; Samani NJ; Erdmann J; Schunkert H; Pastinen T; Deloukas P; Goodall AH; Ouwehand WH; Cambien F; Syvänen AC
PLoS One; 2012; 7(12):e52260. PubMed ID: 23300628
[TBL] [Abstract][Full Text] [Related]
11. Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?
Fish AE; Capra JA; Bush WS
Am J Hum Genet; 2016 Oct; 99(4):817-830. PubMed ID: 27640306
[TBL] [Abstract][Full Text] [Related]
12. RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method.
Hamazaki K; Iwata H
PLoS Comput Biol; 2020 Feb; 16(2):e1007663. PubMed ID: 32059004
[TBL] [Abstract][Full Text] [Related]
13. The causal element for the lactase persistence/non-persistence polymorphism is located in a 1 Mb region of linkage disequilibrium in Europeans.
Poulter M; Hollox E; Harvey CB; Mulcare C; Peuhkuri K; Kajander K; Sarner M; Korpela R; Swallow DM
Ann Hum Genet; 2003 Jul; 67(Pt 4):298-311. PubMed ID: 12914565
[TBL] [Abstract][Full Text] [Related]
14. Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15.
Sun C; Southard C; Witonsky DB; Olopade OI; Di Rienzo A
Hum Mutat; 2010 Jan; 31(1):99-107. PubMed ID: 19847790
[TBL] [Abstract][Full Text] [Related]
15. Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci.
Buchkovich ML; Eklund K; Duan Q; Li Y; Mohlke KL; Furey TS
BMC Med Genomics; 2015 Jul; 8():43. PubMed ID: 26210163
[TBL] [Abstract][Full Text] [Related]
16. Computational analysis of whole-genome differential allelic expression data in human.
Wagner JR; Ge B; Pokholok D; Gunderson KL; Pastinen T; Blanchette M
PLoS Comput Biol; 2010 Jul; 6(7):e1000849. PubMed ID: 20628616
[TBL] [Abstract][Full Text] [Related]
17. Haplotype and diplotype analyses of variation in ERCC5 transcription cis-regulation in normal bronchial epithelial cells.
Zhang X; Crawford EL; Blomquist TM; Khuder SA; Yeo J; Levin AM; Willey JC
Physiol Genomics; 2016 Jul; 48(7):537-43. PubMed ID: 27235448
[TBL] [Abstract][Full Text] [Related]
18. Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals.
Di Maio S; Grüneis R; Streiter G; Lamina C; Maglione M; Schoenherr S; Öfner D; Thorand B; Peters A; Eckardt KU; Köttgen A; Kronenberg F; Coassin S
Genome Med; 2020 Aug; 12(1):74. PubMed ID: 32825847
[TBL] [Abstract][Full Text] [Related]
19. Combined genetic influence of the nicotinic receptor gene cluster CHRNA5/A3/B4 on nicotine dependence.
Lee SH; Ahn WY; Seweryn M; Sadee W
BMC Genomics; 2018 Nov; 19(1):826. PubMed ID: 30453884
[TBL] [Abstract][Full Text] [Related]
20. Expression, SNV identification, linkage disequilibrium, and combined genotype association analysis of the muscle-specific gene CSRP3 in Chinese cattle.
He H; Zhang HL; Li ZX; Liu Y; Liu XL
Gene; 2014 Feb; 535(1):17-23. PubMed ID: 24279998
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
