319 related articles for article (PubMed ID: 17634434)
1. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
Paterson AD; Liu XQ; Wang K; Magistroni R; Song X; Kappel J; Klassen J; Cattran D; St George-Hyslop P; Pei Y
J Am Soc Nephrol; 2007 Aug; 18(8):2408-15. PubMed ID: 17634434
[TBL] [Abstract][Full Text] [Related]
2. Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci.
Bisceglia L; Cerullo G; Forabosco P; Torres DD; Scolari F; Di Perna M; Foramitti M; Amoroso A; Bertok S; Floege J; Mertens PR; Zerres K; Alexopoulos E; Kirmizis D; Ermelinda M; Zelante L; Schena FP;
Am J Hum Genet; 2006 Dec; 79(6):1130-4. PubMed ID: 17186473
[TBL] [Abstract][Full Text] [Related]
3. Characterization of a large Lebanese family segregating IgA nephropathy.
Karnib HH; Sanna-Cherchi S; Zalloua PA; Medawar W; D'Agati VD; Lifton RP; Badr K; Gharavi AG
Nephrol Dial Transplant; 2007 Mar; 22(3):772-7. PubMed ID: 17172253
[TBL] [Abstract][Full Text] [Related]
4. Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.
Tang YG; Rabinowitz YS; Taylor KD; Li X; Hu M; Picornell Y; Yang H
Genet Med; 2005; 7(6):397-405. PubMed ID: 16024971
[TBL] [Abstract][Full Text] [Related]
5. Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
Hocking LJ; Herbert CA; Nicholls RK; Williams F; Bennett ST; Cundy T; Nicholson GC; Wuyts W; Van Hul W; Ralston SH
Am J Hum Genet; 2001 Nov; 69(5):1055-61. PubMed ID: 11555792
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
Arason A; Gunnarsson H; Johannesdottir G; Jonasson K; Bendahl PO; Gillanders EM; Agnarsson BA; Jönsson G; Pylkäs K; Mustonen A; Heikkinen T; Aittomäki K; Blomqvist C; Melin B; Johannsson OT; Møller P; Winqvist R; Nevanlinna H; Borg A; Barkardottir RB
Breast Cancer Res; 2010; 12(4):R50. PubMed ID: 20637093
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Advances in molecular genetics research of IgA nephropathy].
Li X; Xiao L; Sun L; Liu F
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Nov; 36(11):1120-4. PubMed ID: 22169725
[TBL] [Abstract][Full Text] [Related]
9. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
Lucas GJ; Riches PL; Hocking LJ; Cundy T; Nicholson GC; Walsh JP; Ralston SH
J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
[TBL] [Abstract][Full Text] [Related]
10. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
[TBL] [Abstract][Full Text] [Related]
11. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
Chen S; Ondo WG; Rao S; Li L; Chen Q; Wang Q
Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200
[TBL] [Abstract][Full Text] [Related]
12. IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.
Gharavi AG; Yan Y; Scolari F; Schena FP; Frasca GM; Ghiggeri GM; Cooper K; Amoroso A; Viola BF; Battini G; Caridi G; Canova C; Farhi A; Subramanian V; Nelson-Williams C; Woodford S; Julian BA; Wyatt RJ; Lifton RP
Nat Genet; 2000 Nov; 26(3):354-7. PubMed ID: 11062479
[TBL] [Abstract][Full Text] [Related]
13. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.
Jalali A; Aldinger KA; Chary A; McLone DG; Bowman RM; Le LC; Jardine P; Newbury-Ecob R; Mallick A; Jafari N; Russell EJ; Curran J; Nguyen P; Ouahchi K; Lee C; Dobyns WB; Millen KJ; Pina-Neto JM; Kessler JA; Bassuk AG
Hum Genet; 2008 Apr; 123(3):237-45. PubMed ID: 18204864
[TBL] [Abstract][Full Text] [Related]
14. Mapping a new familial thyroid epithelial neoplasia susceptibility locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis.
Cavaco BM; Batista PF; Sobrinho LG; Leite V
J Clin Endocrinol Metab; 2008 Nov; 93(11):4426-30. PubMed ID: 18765515
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
Silverman EK; Mosley JD; Palmer LJ; Barth M; Senter JM; Brown A; Drazen JM; Kwiatkowski DJ; Chapman HA; Campbell EJ; Province MA; Rao DC; Reilly JJ; Ginns LC; Speizer FE; Weiss ST
Hum Mol Genet; 2002 Mar; 11(6):623-32. PubMed ID: 11912177
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide scan in a novel IgA nephropathy model identifies a susceptibility locus on murine chromosome 10, in a region syntenic to human IGAN1 on chromosome 6q22-23.
Suzuki H; Suzuki Y; Yamanaka T; Hirose S; Nishimura H; Toei J; Horikoshi S; Tomino Y
J Am Soc Nephrol; 2005 May; 16(5):1289-99. PubMed ID: 15772254
[TBL] [Abstract][Full Text] [Related]
17. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
[TBL] [Abstract][Full Text] [Related]
18. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
Hoffmann K; Mattheisen M; Dahm S; Nürnberg P; Roe C; Johnson J; Cox NJ; Wichmann HE; Wienker TF; Schulze J; Schwarz PE; Lindner TH
Diabetologia; 2007 Jul; 50(7):1418-22. PubMed ID: 17464498
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20.
Ross J; Berrettini W; Coryell W; Gershon ES; Badner JA; Kelsoe JR; McInnis MG; McMahon FJ; Murphy DL; Nurnberger JI; Foroud T; Rice JP; Scheftner WB; Zandi P; Edenberg H; Byerley W
Psychiatr Genet; 2008 Aug; 18(4):191-8. PubMed ID: 18628681
[TBL] [Abstract][Full Text] [Related]
20. Evidence for a nonallelic heterogeneity of epidermodysplasia verruciformis with two susceptibility loci mapped to chromosome regions 2p21-p24 and 17q25.
Ramoz N; Taïeb A; Rueda LA; Montoya LS; Bouadjar B; Favre M; Orth G
J Invest Dermatol; 2000 Jun; 114(6):1148-53. PubMed ID: 10844558
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
