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Results: 1 to 20 of 87

Similar articles for PubMed (Select 12596796)

1.

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.

Francks C, DeLisi LE, Fisher SE, Laval SH, Rue JE, Stein JF, Monaco AP.

Am J Hum Genet. 2003 Feb;72(2):499-502. No abstract available.

2.

A genomewide linkage screen for relative hand skill in sibling pairs.

Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP.

Am J Hum Genet. 2002 Mar;70(3):800-5. Epub 2002 Jan 3. Erratum in: Am J Hum Genet 2002 Apr;70(4):1075.

3.

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

Francks C, DeLisi LE, Shaw SH, Fisher SE, Richardson AJ, Stein JF, Monaco AP.

Hum Mol Genet. 2003 Dec 15;12(24):3225-30. Epub 2003 Oct 28.

4.

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

Luciano M, Wright MJ, Duffy DL, Wainwright MA, Zhu G, Evans DM, Geffen GM, Montgomery GW, Martin NG.

Behav Genet. 2006 Jan;36(1):45-55. Epub 2005 Dec 9.

PMID:
16341610
5.

Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.

Tourette Syndrome Association International Consortium for Genetics.

Am J Hum Genet. 2007 Feb;80(2):265-72.

6.

A discordant sib-pair linkage analysis of age-related macular degeneration.

Santangelo SL, Yen CH, Haddad S, Fagerness J, Huang C, Seddon JM.

Ophthalmic Genet. 2005 Jun;26(2):61-7.

PMID:
16020308
7.

Familial and genetic effects on motor coordination, laterality, and reading-related cognition.

Francks C, Fisher SE, Marlow AJ, MacPhie IL, Taylor KE, Richardson AJ, Stein JF, Monaco AP.

Am J Psychiatry. 2003 Nov;160(11):1970-7. Erratum in: Am J Psychiatry. 2004 Jan;161(1):185.

PMID:
14594743
8.

Genome-wide linkage scan for prostate cancer aggressiveness loci using families from the University of Michigan Prostate Cancer Genetics Project.

Slager SL, Zarfas KE, Brown WM, Lange EM, McDonnell SK, Wojno KJ, Cooney KA.

Prostate. 2006 Feb 1;66(2):173-9.

PMID:
16173044
9.

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12.

McInnis MG, Lan TH, Willour VL, McMahon FJ, Simpson SG, Addington AM, MacKinnon DF, Potash JB, Mahoney AT, Chellis J, Huo Y, Swift-Scanlan T, Chen H, Koskela R, Stine OC, Jamison KR, Holmans P, Folstein SE, Ranade K, Friddle C, Botstein D, Marr T, Beaty TH, Zandi P, DePaulo JR.

Mol Psychiatry. 2003 Mar;8(3):288-98.

PMID:
12660801
10.

A genome-wide search for quantitative trait Loci that influence antisocial drug dependence in adolescence.

Stallings MC, Corley RP, Dennehey B, Hewitt JK, Krauter KS, Lessem JM, Mikulich-Gilbertson SK, Rhee SH, Smolen A, Young SE, Crowley TJ.

Arch Gen Psychiatry. 2005 Sep;62(9):1042-51.

PMID:
16143736
11.

A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study.

Schick JH, Iyengar SK, Klein BE, Klein R, Reading K, Liptak R, Millard C, Lee KE, Tomany SC, Moore EL, Fijal BA, Elston RC.

Am J Hum Genet. 2003 Jun;72(6):1412-24. Epub 2003 Apr 24.

12.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, Ayadi H.

Hum Genet. 2009 Oct;126(4):575-87. doi: 10.1007/s00439-009-0688-8. Epub 2009 Jun 14.

PMID:
19526372
13.

An affected pedigree member analysis of linkage between the dopamine D2 receptor gene TaqI polymorphism and obesity and hypertension.

Fang YJ, Thomas GN, Xu ZL, Fang JQ, Critchley JA, Tomlinson B.

Int J Cardiol. 2005 Jun 22;102(1):111-6.

PMID:
15939106
14.

Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.

Flex E, Mangino M, Mazzoli M, Martini A, Migliosi V, Colosimo A, Mingarelli R, Pizzuti A, Dallapiccola B.

J Med Genet. 2003 Apr;40(4):278-81.

15.
16.

Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.

Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes T, Ciner E, Bailey-Wilson JE.

Am J Hum Genet. 2004 Sep;75(3):448-59. Epub 2004 Jul 23.

17.

Genetic linkage and association analysis of COPD-related traits on chromosome 8p.

Hersh CP, DeMeo DL, Raby BA, Litonjua AA, Sylvia JS, Sparrow D, Reilly JJ, Silverman EK.

COPD. 2006 Dec;3(4):189-94.

PMID:
17361499
18.

Linkage analysis of cross-sectional and longitudinally derived phenotypic measures to identify loci influencing blood pressure.

Shephard N, Falcaro M, Zeggini E, Chapman P, Hinks A, Barton A, Worthington J, Pickles A, John S.

BMC Genet. 2003 Dec 31;4 Suppl 1:S26.

19.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44.

PMID:
15892143
20.

A genome-wide linkage scan for homocysteine levels suggests three regions of interest.

Vermeulen SH, van der Vleuten GM, de Graaf J, Hermus AR, Blom HJ, Stalenhoef AF, den Heijer M.

J Thromb Haemost. 2006 Jun;4(6):1303-7.

PMID:
16706975
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