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Results: 1 to 20 of 94

1.

Genome-wide linkage in Utah autism pedigrees.

Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon H.

Mol Psychiatry. 2010 Oct;15(10):1006-15. doi: 10.1038/mp.2009.42. Epub 2009 May 19.

PMID:
19455147
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees.

Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM.

Mol Autism. 2010 Apr 8;1(1):8. doi: 10.1186/2040-2392-1-8.

PMID:
20678250
[PubMed]
Free PMC Article
3.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.

Mol Psychiatry. 2007 Apr;12(4):376-84. Epub 2006 Dec 19.

PMID:
17179998
[PubMed - indexed for MEDLINE]
4.

Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage.

Stanford JL, FitzGerald LM, McDonnell SK, Carlson EE, McIntosh LM, Deutsch K, Hood L, Ostrander EA, Schaid DJ.

Hum Mol Genet. 2009 May 15;18(10):1839-48. doi: 10.1093/hmg/ddp100. Epub 2009 Feb 27.

PMID:
19251732
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees.

Christensen GB, Camp NJ, Farnham JM, Cannon-Albright LA.

Prostate. 2007 May 1;67(6):605-13.

PMID:
17299800
[PubMed - indexed for MEDLINE]
6.

Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

Fitzgerald LM, McDonnell SK, Carlson EE, Langeberg W, McIntosh LM, Deutsch K, Ostrander EA, Schaid DJ, Stanford JL.

Eur J Hum Genet. 2010 Oct;18(10):1141-7. doi: 10.1038/ejhg.2010.49. Epub 2010 Apr 21.

PMID:
20407467
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
8.

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium.

Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16.

PMID:
18632090
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders.

Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H.

Mol Autism. 2010 Feb 22;1(1):3. doi: 10.1186/2040-2392-1-3.

PMID:
20678246
[PubMed]
Free PMC Article
10.

Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.

Camp NJ, Lowry MR, Richards RL, Plenk AM, Carter C, Hensel CH, Abkevich V, Skolnick MH, Shattuck D, Rowe KG, Hughes DC, Cannon-Albright LA.

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):85-93.

PMID:
15806581
[PubMed - indexed for MEDLINE]
11.

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS.

BMC Med Genet. 2005 Jan 12;6:1.

PMID:
15647115
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Chromosome 2p14 is linked to susceptibility to leprosy.

Yang Q, Liu H, Low HQ, Wang H, Yu Y, Fu X, Yu G, Chen M, Yan X, Chen S, Huang W, Liu J, Zhang F.

PLoS One. 2012;7(1):e29747. doi: 10.1371/journal.pone.0029747. Epub 2012 Jan 6.

PMID:
22238647
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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; Colon CFR.

PLoS One. 2012;7(5):e38175. doi: 10.1371/journal.pone.0038175. Epub 2012 May 31. Erratum in: PLoS One. 2012;7(11). doi:10.1371/annotation/1ba2f5e3-8aef-4a12-909b-23f95a889325.

PMID:
22675446
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.

Lu L, Cancel-Tassin G, Valeri A, Cussenot O, Lange EM, Cooney KA, Farnham JM, Camp NJ, Cannon-Albright LA, Tammela TL, Schleutker J, Hoegel J, Herkommer K, Maier C, Vogel W, Wiklund F, Emanuelsson M, Grönberg H, Wiley KE, Isaacs SD, Walsh PC, Helfand BT, Kan D, Catalona WJ, Stanford JL, FitzGerald LM, Johanneson B, Deutsch K, McIntosh L, Ostrander EA, Thibodeau SN, McDonnell SK, Hebbring S, Schaid DJ, Whittemore AS, Oakley-Girvan I, Hsieh CL, Powell I, Bailey-Wilson JE, Cropp CD, Simpson C, Carpten JD, Seminara D, Zheng SL, Xu J, Giles GG, Severi G, Hopper JL, English DR, Foulkes WD, Maehle L, Moller P, Badzioch MD, Edwards S, Guy M, Eeles R, Easton D, Isaacs WB; International Consortium for Prostate Cancer Genetics.

Prostate. 2012 Mar;72(4):410-26. doi: 10.1002/pros.21443. Epub 2011 Jul 11.

PMID:
21748754
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data.

Holliday E, Mowry B, Chant D, Nyholt D.

Hum Genet. 2005 Jul;117(2-3):160-7. Epub 2005 Apr 21.

PMID:
15843988
[PubMed - indexed for MEDLINE]
16.

Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.

Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.

Genes Brain Behav. 2013 Feb;12(1):56-69. doi: 10.1111/gbb.12003. Epub 2012 Dec 7.

PMID:
23190410
[PubMed - indexed for MEDLINE]
17.

Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36.

Mathews CA, Badner JA, Andresen JM, Sheppard B, Himle JA, Grant JE, Williams KA, Chavira DA, Azzam A, Schwartz M, Reus VI, Kim SW, Cook EH, Hanna GL.

Biol Psychiatry. 2012 Oct 15;72(8):629-36. doi: 10.1016/j.biopsych.2012.03.037. Epub 2012 May 25.

PMID:
22633946
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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. doi: 10.1007/s00439-011-1033-6. Epub 2011 Jun 21.

PMID:
21691774
[PubMed - indexed for MEDLINE]
19.

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF.

Hum Mol Genet. 2006 Jan 15;15(2):251-8. Epub 2005 Dec 5.

PMID:
16330481
[PubMed - indexed for MEDLINE]
Free Article
20.

Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.

Fradin D, Cheslack-Postava K, Ladd-Acosta C, Newschaffer C, Chakravarti A, Arking DE, Feinberg A, Fallin MD.

PLoS One. 2010 Sep 2;5(9). pii: e12513. doi: 10.1371/journal.pone.0012513.

PMID:
20824079
[PubMed - indexed for MEDLINE]
Free PMC Article

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