187 related articles for article (PubMed ID: 31826912)
21. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
Ross J; Badner J; Garrido H; Sheppard B; Chavira DA; Grados M; Woo JM; Doo P; Umaña P; Fournier E; Murray SS; Mathews CA
Hum Genet; 2011 Dec; 130(6):795-805. PubMed ID: 21691774
[TBL] [Abstract][Full Text] [Related]
22. Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.
Cicek MS; Cunningham JM; Fridley BL; Serie DJ; Bamlet WR; Diergaarde B; Haile RW; Le Marchand L; Krontiris TG; Younghusband HB; Gallinger S; Newcomb PA; Hopper JL; Jenkins MA; Casey G; Schumacher F; Chen Z; DeRycke MS; Templeton AS; Winship I; Green RC; Green JS; Macrae FA; Parry S; Young GP; Young JP; Buchanan D; Thomas DC; Bishop DT; Lindor NM; Thibodeau SN; Potter JD; Goode EL;
PLoS One; 2012; 7(5):e38175. PubMed ID: 22675446
[TBL] [Abstract][Full Text] [Related]
23. Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q.
MacDougall M; Jeffords LG; Gu TT; Knight CB; Frei G; Reus BE; Otterud B; Leppert M; Leach RJ
J Dent Res; 1999 Jun; 78(6):1277-82. PubMed ID: 10371253
[TBL] [Abstract][Full Text] [Related]
24. Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing.
Toma C; Díaz-Gay M; Soares de Lima Y; Arnau-Collell C; Franch-Expósito S; Muñoz J; Overs B; Bonjoch L; Carballal S; Ocaña T; Cuatrecasas M; Díaz de Bustamante A; Castells A; Bujanda L; Cubiella J; Balaguer F; Rodríguez-Alcalde D; Fullerton JM; Castellví-Bel S
Clin Transl Gastroenterol; 2019 Oct; 10(10):e00100. PubMed ID: 31663907
[TBL] [Abstract][Full Text] [Related]
25. TSC22D2 identified as a candidate susceptibility gene of multi-cancer pedigree using genome-wide linkage analysis and whole-exome sequencing.
Xiao L; Wei F; Liang F; Li Q; Deng H; Tan S; Chen S; Xiong F; Guo C; Liao Q; Li X; Zhang W; Wu M; Zhou Y; Xiang B; Zhou M; Li X; Xiong W; Zeng Z; Li G
Carcinogenesis; 2019 Jul; 40(7):819-827. PubMed ID: 31125406
[TBL] [Abstract][Full Text] [Related]
26. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
[TBL] [Abstract][Full Text] [Related]
27. Analysis of the RELN gene as a genetic risk factor for autism.
Skaar DA; Shao Y; Haines JL; Stenger JE; Jaworski J; Martin ER; DeLong GR; Moore JH; McCauley JL; Sutcliffe JS; Ashley-Koch AE; Cuccaro ML; Folstein SE; Gilbert JR; Pericak-Vance MA
Mol Psychiatry; 2005 Jun; 10(6):563-71. PubMed ID: 15558079
[TBL] [Abstract][Full Text] [Related]
28. Linkage analysis of high myopia susceptibility locus in 26 families.
Paget S; Julia S; Vitezica ZG; Soler V; Malecaze F; Calvas P
Mol Vis; 2008; 14():2566-74. PubMed ID: 19122830
[TBL] [Abstract][Full Text] [Related]
29. Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24.
Morissette J; Villeneuve A; Bordeleau L; Rochette D; Laberge C; Gagné B; Laprise C; Bouchard G; Plante M; Gobeil L; Shink E; Weissenbach J; Barden N
Am J Med Genet; 1999 Oct; 88(5):567-87. PubMed ID: 10490718
[TBL] [Abstract][Full Text] [Related]
30. Evidence that a locus for familial psoriasis maps to chromosome 4q.
Matthews D; Fry L; Powles A; Weber J; McCarthy M; Fisher E; Davies K; Williamson R
Nat Genet; 1996 Oct; 14(2):231-3. PubMed ID: 8841203
[TBL] [Abstract][Full Text] [Related]
31. High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.
Stamm DS; Rampersaud E; Slifer SH; Mehltretter L; Siegel DG; Xie J; Hu-Lince D; Craig DW; Stephan DA; George TM; Gilbert JR; Speer MC;
Birth Defects Res A Clin Mol Teratol; 2006 Jun; 76(6):499-505. PubMed ID: 16933213
[TBL] [Abstract][Full Text] [Related]
32. Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk.
Einarsdottir E; Koskinen LL; de Kauwe AL; Dukes E; Mustalahti K; Balogh M; Korponay-Szabo IR; Kaukinen K; Kurppa K; Adány R; Pocsai Z; Széles G; Mäki M; Kere J; Saavalainen P
Tissue Antigens; 2011 Dec; 78(6):428-37. PubMed ID: 22077623
[TBL] [Abstract][Full Text] [Related]
33. Haplotype phasing of a bipolar disorder pedigree revealed rare multiple mutations of SPOCD1 gene in the 1p36-35 susceptibility locus.
Takamatsu G; Yanagi K; Koganebuchi K; Yoshida F; Lee JS; Toyama K; Hattori K; Katagiri C; Kondo T; Kunugi H; Kimura R; Kaname T; Matsushita M
J Affect Disord; 2022 Aug; 310():96-105. PubMed ID: 35504398
[TBL] [Abstract][Full Text] [Related]
34. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3.
Ewald H; Flint T; Kruse TA; Mors O
Mol Psychiatry; 2002; 7(7):734-44. PubMed ID: 12192618
[TBL] [Abstract][Full Text] [Related]
35. Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1.
Wu LQ; Yang YF; Zheng D; Deng H; Pan Q; Zhao TL; Cai F; Feng Y; Long ZG; Dai HP; Tang BS; Yang YJ; Deng HX; Xia K; Xia JH
Br J Dermatol; 2004 May; 150(5):999-1004. PubMed ID: 15149516
[TBL] [Abstract][Full Text] [Related]
36. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
Cipriani V; Kalhoro A; Arno G; Silva RS; Pontikos N; Puech V; McClements ME; Hunt DM; van Heyningen V; Michaelides M; Webster AR; Moore AT; Puech B
Ophthalmic Genet; 2017 Dec; 38(6):511-519. PubMed ID: 28635424
[TBL] [Abstract][Full Text] [Related]
37. Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.
Desautels A; Turecki G; Montplaisir J; Xiong L; Walters AS; Ehrenberg BL; Brisebois K; Desautels AK; Gingras Y; Johnson WG; Lugaresi E; Coccagna G; Picchietti DL; Lazzarini A; Rouleau GA
Arch Neurol; 2005 Apr; 62(4):591-6. PubMed ID: 15824258
[TBL] [Abstract][Full Text] [Related]
38. First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q.
Devoto M; Shimoya K; Caminis J; Ott J; Tenenhouse A; Whyte MP; Sereda L; Hall S; Considine E; Williams CJ; Tromp G; Kuivaniemi H; Ala-Kokko L; Prockop DJ; Spotila LD
Eur J Hum Genet; 1998; 6(2):151-7. PubMed ID: 9781060
[TBL] [Abstract][Full Text] [Related]
39. No evidence for linkage at candidate type 2 diabetes susceptibility loci on chromosomes 12 and 20 in United Kingdom Caucasians.
Frayling TM; McCarthy MI; Walker M; Levy JC; O'Rahilly S; Hitman GA; Rao PV; Bennett AJ; Jones EC; Menzel S; Ellard S; Hattersley AT
J Clin Endocrinol Metab; 2000 Feb; 85(2):853-7. PubMed ID: 10690901
[TBL] [Abstract][Full Text] [Related]
40. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
Bayer Y; Neumann S; Meyer B; Rüschendorf F; Reske A; Brix T; Hegedüs L; Langer P; Nürnberg P; Paschke R
J Clin Endocrinol Metab; 2004 Aug; 89(8):4044-52. PubMed ID: 15292347
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
