430 related articles for article (PubMed ID: 20637093)
1. 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]
2. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.
Kainu T; Juo SH; Desper R; Schaffer AA; Gillanders E; Rozenblum E; Freas-Lutz D; Weaver D; Stephan D; Bailey-Wilson J; Kallioniemi OP; Tirkkonen M; Syrjäkoski K; Kuukasjärvi T; Koivisto P; Karhu R; Holli K; Arason A; Johannesdottir G; Bergthorsson JT; Johannsdottir H; Egilsson V; Barkardottir RB; Johannsson O; Haraldsson K; Sandberg T; Holmberg E; Grönberg H; Olsson H; Borg A; Vehmanen P; Eerola H; Heikkila P; Pyrhönen S; Nevanlinna H
Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9603-8. PubMed ID: 10944226
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.
Oldenburg RA; Kroeze-Jansema KH; Houwing-Duistermaat JJ; Bayley JP; Dambrot C; van Asperen CJ; van den Ouweland AM; Bakker B; van Beers EH; Nederlof PM; Vasen H; Hoogerbrugge N; Cornelisse CJ; Meijers-Heijboer H; Devilee P
Genes Chromosomes Cancer; 2008 Nov; 47(11):947-56. PubMed ID: 18663745
[TBL] [Abstract][Full Text] [Related]
4. Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.
Marikkannu R; Aravidis C; Rantala J; Picelli S; Adamovic T; Keihas M; Liu T; Kontham V; Nilsson D; Lindblom A
Anticancer Res; 2015 Jun; 35(6):3155-65. PubMed ID: 26026075
[TBL] [Abstract][Full Text] [Related]
5. A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).
Andres EM; Hafeez H; Yousaf A; Riazuddin S; Rice ML; Basra MAR; Raza MH
Eur J Hum Genet; 2019 Aug; 27(8):1274-1285. PubMed ID: 30976110
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.
Rosa-Rosa JM; Pita G; Urioste M; Llort G; Brunet J; Lázaro C; Blanco I; Ramón y Cajal T; Díez O; de la Hoya M; Caldés T; Tejada MI; González-Neira A; Benítez J
Am J Hum Genet; 2009 Feb; 84(2):115-22. PubMed ID: 19147119
[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. Characterization of familial non-BRCA1/2 breast tumors by loss of heterozygosity and immunophenotyping.
Oldenburg RA; Kroeze-Jansema K; Meijers-Heijboer H; van Asperen CJ; Hoogerbrugge N; van Leeuwen I; Vasen HF; Cleton-Jansen AM; Kraan J; Houwing-Duistermaat JJ; Morreau H; Cornelisse CJ; Devilee P
Clin Cancer Res; 2006 Mar; 12(6):1693-700. PubMed ID: 16551851
[TBL] [Abstract][Full Text] [Related]
9. Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2.
Fitzpatrick E; Göring HH; Liu H; Borg A; Forrest S; Cooper DW; Brennecke SP; Moses EK
Hum Biol; 2004 Dec; 76(6):849-62. PubMed ID: 15974297
[TBL] [Abstract][Full Text] [Related]
10. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
11. CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.
Maguire P; Holmberg K; Kost-Alimova M; Imreh S; Skoog L; Lindblom A
Int J Mol Med; 2005 Jul; 16(1):135-41. PubMed ID: 15942690
[TBL] [Abstract][Full Text] [Related]
12. A second-generation genomic screen for multiple sclerosis.
Kenealy SJ; Babron MC; Bradford Y; Schnetz-Boutaud N; Haines JL; Rimmler JB; Schmidt S; Pericak-Vance MA; Barcellos LF; Lincoln RR; Oksenberg JR; Hauser SL; Clanet M; Brassat D; Edan G; Yaouanq J; Semana G; Cournu-Rebeix I; Lyon-Caen O; Fontaine B;
Am J Hum Genet; 2004 Dec; 75(6):1070-8. PubMed ID: 15494893
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
Gelernter J; Bonvicini K; Page G; Woods SW; Goddard AW; Kruger S; Pauls DL; Goodson S
Am J Med Genet; 2001 Aug; 105(6):548-57. PubMed ID: 11496373
[TBL] [Abstract][Full Text] [Related]
15. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
Scott WK; Gaskell PC; Lennon F; Wolpert CM; Menold MM; Aylsworth AS; Warner C; Farrell CD; Boustany RM; Albright SG; Boyd E; Kingston HM; Cumming WJ; Vance JM; Pericak-Vance MA
Neurogenetics; 1997 Sep; 1(2):95-102. PubMed ID: 10732810
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11.
Pato CN; Pato MT; Kirby A; Petryshen TL; Medeiros H; Carvalho C; Macedo A; Dourado A; Coelho I; Valente J; Soares MJ; Ferreira CP; Lei M; Verner A; Hudson TJ; Morley CP; Kennedy JL; Azevedo MH; Daly MJ; Sklar P
Am J Med Genet B Neuropsychiatr Genet; 2004 May; 127B(1):30-4. PubMed ID: 15108176
[TBL] [Abstract][Full Text] [Related]
17. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.
Djureinovic T; Skoglund J; Vandrovcova J; Zhou XL; Kalushkova A; Iselius L; Lindblom A
Gut; 2006 Mar; 55(3):362-6. PubMed ID: 16150854
[TBL] [Abstract][Full Text] [Related]
18. A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
Pillai SG; Chiano MN; White NJ; Speer M; Barnes KC; Carlsen K; Gerritsen J; Helms P; Lenney W; Silverman M; Sly P; Sundy J; Tsanakas J; von Berg A; Whyte M; Varsani S; Skelding P; Hauser M; Vance J; Pericak-Vance M; Burns DK; Middleton LT; Brewster SR; Anderson WH; Riley JH
Eur J Hum Genet; 2006 Mar; 14(3):307-16. PubMed ID: 16391567
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
