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Results: 1 to 20 of 103

1.

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J.

Mol Psychiatry. 2003 Feb;8(2):176-85.

PMID:
12610650
[PubMed - indexed for MEDLINE]
2.

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia.

Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL.

Am J Med Genet. 2001 Aug 8;105(6):507-17.

PMID:
11496366
[PubMed - indexed for MEDLINE]
3.

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.

Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, Hopkin E, Pound K, Fernando S, Easton M, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J.

Hum Mol Genet. 2000 Mar 22;9(5):843-8.

PMID:
10749993
[PubMed - indexed for MEDLINE]
Free Article
4.

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, Smith SD.

Hum Genet. 2004 Jul;115(2):128-38. Epub 2004 May 11.

PMID:
15138886
[PubMed - indexed for MEDLINE]
5.

Evidence for linkage and association with reading disability on 6p21.3-22.

Kaplan DE, Gayán J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR.

Am J Hum Genet. 2002 May;70(5):1287-98. Epub 2002 Apr 10.

PMID:
11951179
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Continuing the search for dyslexia genes on 6p.

Grigorenko EL, Wood FB, Golovyan L, Meyer M, Romano C, Pauls D.

Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):89-98.

PMID:
12627473
[PubMed - indexed for MEDLINE]
7.

Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene.

Smith SD, Kelley PM, Askew JW, Hoover DM, Deffenbacher KE, Gayán J, Brower AM, Olson RK.

J Learn Disabil. 2001 Nov-Dec;34(6):512-9.

PMID:
15503566
[PubMed - indexed for MEDLINE]
8.

Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, Remschmidt H.

Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:56-9.

PMID:
10638372
[PubMed - indexed for MEDLINE]
9.

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.

Wigg KG, Feng Y, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Malone M, Schachar R, Barr CL.

Genes Brain Behav. 2008 Nov;7(8):877-86. doi: 10.1111/j.1601-183X.2008.00425.x.

PMID:
19076634
[PubMed - indexed for MEDLINE]
10.

Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.

Schumacher J, König IR, Schröder T, Duell M, Plume E, Propping P, Warnke A, Libertus C, Ziegler A, Müller-Myhsok B, Schulte-Körne G, Nöthen MM.

Psychiatr Genet. 2008 Jun;18(3):137-42. doi: 10.1097/YPG.0b013e3282fb7fc6.

PMID:
18496212
[PubMed - indexed for MEDLINE]
11.

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J.

Am J Hum Genet. 2005 Apr;76(4):581-91. Epub 2005 Feb 16. Erratum in: Am J Hum Genet. 2005 Nov;77(5):898.

PMID:
15717286
[PubMed - indexed for MEDLINE]
Free PMC Article
12.
13.

Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.

Barr CL, Shulman R, Wigg K, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL.

Am J Med Genet. 2001 Apr 8;105(3):250-4.

PMID:
11353444
[PubMed - indexed for MEDLINE]
14.

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.

Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP.

Am J Hum Genet. 1999 Jan;64(1):146-56.

PMID:
9915953
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21.

Herr M, Dudbridge F, Zavattari P, Cucca F, Guja C, March R, Campbell RD, Barnett AH, Bain SC, Todd JA, Koeleman BP.

Hum Mol Genet. 2000 May 22;9(9):1291-301.

PMID:
10814711
[PubMed - indexed for MEDLINE]
Free Article
16.

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.

Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, Pauls DL.

Am J Hum Genet. 1997 Jan;60(1):27-39.

PMID:
8981944
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.

Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL.

Biol Psychiatry. 2009 Aug 15;66(4):368-75. doi: 10.1016/j.biopsych.2009.02.016. Epub 2009 Apr 11.

PMID:
19362708
[PubMed - indexed for MEDLINE]
18.

Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability.

Davis CJ, Gayán J, Knopik VS, Smith SD, Cardon LR, Pennington BF, Olson RK, DeFries JC.

Behav Genet. 2001 Nov;31(6):625-35.

PMID:
11838539
[PubMed - indexed for MEDLINE]
19.

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.

Stein CM, Schick JH, Gerry Taylor H, Shriberg LD, Millard C, Kundtz-Kluge A, Russo K, Minich N, Hansen A, Freebairn LA, Elston RC, Lewis BA, Iyengar SK.

Am J Hum Genet. 2004 Feb;74(2):283-97. Epub 2004 Jan 20.

PMID:
14740317
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP.

Am J Hum Genet. 2004 Dec;75(6):1046-58. Epub 2004 Oct 22.

PMID:
15514892
[PubMed - indexed for MEDLINE]
Free PMC Article

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