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Results: 16

1.

Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis.

Davis LK, Maltman N, Mosconi MW, Macmillan C, Schmitt L, Moore K, Francis SM, Jacob S, Sweeney JA, Cook EH.

Am J Med Genet A. 2012 Jul;158A(7):1654-61. doi: 10.1002/ajmg.a.35396. Epub 2012 Jun 7.

2.

Identifying a distinctive familial frequency band in reaction time fluctuations in ADHD.

Helps SK, Broyd SJ, Bitsakou P, Sonuga-Barke EJ.

Neuropsychology. 2011 Nov;25(6):711-9. doi: 10.1037/a0024479.

PMID:
21728424
3.

Findings from bipolar offspring studies: methodology matters.

Duffy A, Doucette S, Lewitzka U, Alda M, Hajek T, Grof P.

Early Interv Psychiatry. 2011 Aug;5(3):181-91. doi: 10.1111/j.1751-7893.2011.00276.x. Epub 2011 Jul 1. Review.

PMID:
21718461
4.

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.

Lichtenstein P, Carlström E, Råstam M, Gillberg C, Anckarsäter H.

Am J Psychiatry. 2010 Nov;167(11):1357-63. doi: 10.1176/appi.ajp.2010.10020223. Epub 2010 Aug 4.

PMID:
20686188
5.

Attention deficit hyperactivity disorder in obese melanocortin-4-receptor (MC4R) deficient subjects: a newly described expression of MC4R deficiency.

Agranat-Meged A, Ghanadri Y, Eisenberg I, Ben Neriah Z, Kieselstein-Gross E, Mitrani-Rosenbaum S.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1547-53. doi: 10.1002/ajmg.b.30842.

PMID:
18777518
6.

Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder.

Willcutt EG, Pennington BF, Olson RK, DeFries JC.

Am J Med Genet B Neuropsychiatr Genet. 2007 Sep 5;144B(6):709-14.

PMID:
17440942
7.

No support for association between the dopamine transporter (DAT1) gene and ADHD.

Langley K, Turic D, Peirce TR, Mills S, Van Den Bree MB, Owen MJ, O'Donovan MC, Thapar A.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):7-10.

PMID:
16082688
8.

ADHD and dyscalculia: Evidence for independent familial transmission.

Monuteaux MC, Faraone SV, Herzig K, Navsaria N, Biederman J.

J Learn Disabil. 2005 Jan-Feb;38(1):86-93.

PMID:
15727331
9.

Inherited ring chromosome 8 without loss of subtelomeric sequences.

Le Caignec C, Boceno M, Jacquemont S, Nguyen The Tich S, Rival JM, David A.

Ann Genet. 2004 Jul-Sep;47(3):289-96. Review.

PMID:
15337475
10.
11.

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
12.
13.

Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor.

Barr CL, Wigg KG, Feng Y, Zai G, Malone M, Roberts W, Schachar R, Tannock R, Kennedy JL.

Mol Psychiatry. 2000 Sep;5(5):548-51.

PMID:
11032390
14.

Attention-deficit disorder and conduct disorder in girls: evidence for a familial subtype.

Faraone SV, Biederman J, Monuteaux MC.

Biol Psychiatry. 2000 Jul 1;48(1):21-9.

PMID:
10913504
15.

Etiology of inattention and hyperactivity/impulsivity in a community sample of twins with learning difficulties.

Willcutt EG, Pennington BF, DeFries JC.

J Abnorm Child Psychol. 2000 Apr;28(2):149-59.

PMID:
10834767
16.
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