118 related articles for article (PubMed ID: 26188062)
1. Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.
Li J; Fung I; Glessner JT; Pandey R; Wei Z; Bakay M; Mentch FD; Pellegrino R; Wang T; Kim C; Hou C; Wang F; Chiavacci RM; Thomas KA; Spergel JM; Hakonarson H; Sleiman PM
J Immunol; 2015 Aug; 195(4):1599-607. PubMed ID: 26188062
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.
Asai Y; Eslami A; van Ginkel CD; Akhabir L; Wan M; Ellis G; Ben-Shoshan M; Martino D; Ferreira MA; Allen K; Mazer B; de Groot H; de Jong NW; Gerth van Wijk RN; Dubois AEJ; Chin R; Cheuk S; Hoffman J; Jorgensen E; Witte JS; Melles RB; Hong X; Wang X; Hui J; Musk AWB; Hunter M; James AL; Koppelman GH; Sandford AJ; Clarke AE; Daley D
J Allergy Clin Immunol; 2018 Mar; 141(3):991-1001. PubMed ID: 29030101
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
[TBL] [Abstract][Full Text] [Related]
5. Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.
White PS; Xie HM; Werner P; Glessner J; Latney B; Hakonarson H; Goldmuntz E
Birth Defects Res A Clin Mol Teratol; 2014 Dec; 100(12):951-64. PubMed ID: 25066379
[TBL] [Abstract][Full Text] [Related]
6. CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies.
McGeachie MJ; Wu AC; Tse SM; Clemmer GL; Sordillo J; Himes BE; Lasky-Su J; Chase RP; Martinez FD; Weeke P; Shaffer CM; Xu H; Denny JC; Roden DM; Panettieri RA; Raby BA; Weiss ST; Tantisira KG
J Allergy Clin Immunol; 2015 Dec; 136(6):1503-1510. PubMed ID: 26073756
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide association study of copy number variations (CNVs) with opioid dependence.
Li D; Zhao H; Kranzler HR; Li MD; Jensen KP; Zayats T; Farrer LA; Gelernter J
Neuropsychopharmacology; 2015 Mar; 40(4):1016-26. PubMed ID: 25345593
[TBL] [Abstract][Full Text] [Related]
8. Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.
Ramos-Quiroga JA; Sánchez-Mora C; Casas M; Garcia-Martínez I; Bosch R; Nogueira M; Corrales M; Palomar G; Vidal R; Coll-Tané M; Bayés M; Cormand B; Ribasés M
J Psychiatr Res; 2014 Feb; 49():60-7. PubMed ID: 24269040
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide copy number analysis in a family with p.G533C RET mutation and medullary thyroid carcinoma identified regions potentially associated with a higher predisposition to lymph node metastasis.
Araujo AN; Moraes L; França MI; Hakonarson H; Li J; Pellegrino R; Maciel RM; Cerutti JM
J Clin Endocrinol Metab; 2014 Jun; 99(6):E1104-12. PubMed ID: 24601688
[TBL] [Abstract][Full Text] [Related]
10. A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.
Moon S; Keam B; Hwang MY; Lee Y; Park S; Oh JH; Kim YJ; Lee HS; Kim NH; Kim YJ; Kim DH; Han BG; Kim BJ; Lee J
BMC Musculoskelet Disord; 2015 Apr; 16():76. PubMed ID: 25880085
[TBL] [Abstract][Full Text] [Related]
11. Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.
Mosca SJ; Langevin LM; Dewey D; Innes AM; Lionel AC; Marshall CC; Scherer SW; Parboosingh JS; Bernier FP
J Med Genet; 2016 Dec; 53(12):812-819. PubMed ID: 27489308
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
Costain G; Lionel AC; Ogura L; Marshall CR; Scherer SW; Silversides CK; Bassett AS
Int J Cardiol; 2016 Feb; 204():115-21. PubMed ID: 26655555
[TBL] [Abstract][Full Text] [Related]
13. A genome-wide assessment of rare copy number variants in colorectal cancer.
Li Z; Yu D; Gan M; Shan Q; Yin X; Tang S; Zhang S; Shi Y; Zhu Y; Lai M; Zhang D
Oncotarget; 2015 Sep; 6(28):26411-23. PubMed ID: 26315111
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.
Jacob CP; Weber H; Retz W; Kittel-Schneider S; Heupel J; Renner T; Lesch KP; Reif A
J Psychiatr Res; 2013 Dec; 47(12):1902-8. PubMed ID: 24041656
[TBL] [Abstract][Full Text] [Related]
16. Genetic determinants of paediatric food allergy: A systematic review.
Suaini NHA; Wang Y; Soriano VX; Martino DJ; Allen KJ; Ellis JA; Koplin JJ
Allergy; 2019 Sep; 74(9):1631-1648. PubMed ID: 30835860
[TBL] [Abstract][Full Text] [Related]
17. Large germline copy number variations as predisposing factor in childhood neoplasms.
Krepischi AC; Capelli LP; Silva AG; de Araújo ÉS; Pearson PL; Heck B; da Costa CM; de Camargo B; Rosenberg C
Future Oncol; 2014; 10(9):1627-33. PubMed ID: 25145432
[TBL] [Abstract][Full Text] [Related]
18. Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis.
Kim SH; Cho BY; Park CS; Shin ES; Cho EY; Yang EM; Kim CW; Hong CS; Lee JE; Park HS
Clin Exp Allergy; 2009 Feb; 39(2):203-12. PubMed ID: 19187332
[TBL] [Abstract][Full Text] [Related]
19. Are genetic tests informative in predicting food allergy?
Li J; Maggadottir SM; Hakonarson H
Curr Opin Allergy Clin Immunol; 2016 Jun; 16(3):257-64. PubMed ID: 27070332
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.
Molin AM; Berglund J; Webster MT; Lindblad-Toh K
BMC Genomics; 2014 Mar; 15():210. PubMed ID: 24640994
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
