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Items: 1 to 20 of 287

1.

Toward localizing genes underlying cerebral asymmetry and mental health.

Smalley SL, Loo SK, Yang MH, Cantor RM.

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):79-84. Erratum in: Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136(1):107.

PMID:
15806584
2.

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.

Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL.

Mol Psychiatry. 2004 May;9(5):485-93.

PMID:
14625563
3.

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ, van 't Slot R, Minderaa RB, Gunning WB, Pearson PL, Sinke RJ.

Am J Hum Genet. 2003 May;72(5):1251-60. Epub 2003 Apr 4.

4.

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M.

Am J Hum Genet. 2004 Dec;75(6):998-1014. Epub 2004 Oct 20.

5.

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

Ogdie MN, Fisher SE, Yang M, Ishii J, Francks C, Loo SK, Cantor RM, McCracken JT, McGough JJ, Smalley SL, Nelson SF.

Am J Hum Genet. 2004 Oct;75(4):661-8. Epub 2004 Aug 3.

6.

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.

7.

Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23.

Cantor RM, Yuan J, Napier S, Kono N, Grossman JM, Hahn BH, Tsao BP.

Arthritis Rheum. 2004 Oct;50(10):3203-10.

8.

Genome-wide scan of bipolar disorder and investigation of population stratification effects on linkage: support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13.

Cassidy F, Zhao C, Badger J, Claffey E, Dobrin S, Roche S, McKeon P.

Am J Med Genet B Neuropsychiatr Genet. 2007 Sep 5;144B(6):791-801.

PMID:
17455214
9.

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.

Asherson P, Zhou K, Anney RJ, Franke B, Buitelaar J, Ebstein R, Gill M, Altink M, Arnold R, Boer F, Brookes K, Buschgens C, Butler L, Cambell D, Chen W, Christiansen H, Feldman L, Fleischman K, Fliers E, Howe-Forbes R, Goldfarb A, Heise A, Gabriëls I, Johansson L, Lubetzki I, Marco R, Medad S, Minderaa R, Mulas F, Müller U, Mulligan A, Neale B, Rijsdijk F, Rabin K, Rommelse N, Sethna V, Sorohan J, Uebel H, Psychogiou L, Weeks A, Barrett R, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV.

Mol Psychiatry. 2008 May;13(5):514-21. doi: 10.1038/sj.mp.4002140. Epub 2008 Jan 8.

PMID:
18180756
10.

Evidence for multiple loci from a genome scan of autism kindreds.

Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.

Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. Epub 2006 Aug 1.

11.

Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.

Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS; Type 1 Diabetes Genetics Consortium.

Diabetes. 2005 Oct;54(10):2995-3001.

12.

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

Auranen M, Nieminen T, Majuri S, Vanhala R, Peltonen L, Järvelä I.

Mol Psychiatry. 2000 May;5(3):320-2.

PMID:
10889536
13.

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.

Kaminen N, Hannula-Jouppi K, Kestilä M, Lahermo P, Muller K, Kaaranen M, Myllyluoma B, Voutilainen A, Lyytinen H, Nopola-Hemmi J, Kere J.

J Med Genet. 2003 May;40(5):340-5.

14.

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
15.

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
16.

Autism and mental retardation: the genetic relationship and contribution.

el-Hazmi MA.

East Mediterr Health J. 2001 May;7(3):536-43. Review.

PMID:
12690777
17.

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.

Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC.

J Child Psychol Psychiatry. 2005 Oct;46(10):1045-56.

PMID:
16178928
18.

[Hereditary factors in attention deficit hyperactivity disorder].

Fliers EA, Franke B, Buitelaar JK.

Ned Tijdschr Geneeskd. 2005 Jul 30;149(31):1726-9. Review. Dutch.

PMID:
16114287
19.

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism.

Am J Med Genet. 2001 Dec 8;105(8):609-15.

PMID:
11811142
20.

Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.

Pinto D, Westland B, de Haan GJ, Rudolf G, da Silva BM, Hirsch E, Lindhout D, Trenité DG, Koeleman BP.

Hum Mol Genet. 2005 Jan 1;14(1):171-8. Epub 2004 Nov 17.

PMID:
15548544

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