Pauls D - Search Results

1

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection.

de Kovel CG, Franke B, Hol FA, Lebrec JJ, Maassen B, Brunner H, Padberg GW, Platko J, Pauls D. de Kovel CG, et al. Among authors: pauls d. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):294-300. doi: 10.1002/ajmg.b.30598. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17886254

2

Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.

Stewart SE, Fagerness JA, Platko J, Smoller JW, Scharf JM, Illmann C, Jenike E, Chabane N, Leboyer M, Delorme R, Jenike MA, Pauls DL. Stewart SE, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1027-33. doi: 10.1002/ajmg.b.30533. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17894418

3

Association of reading disability on chromosome 6p22 in the Afrikaner population.

Platko JV, Wood FB, Pelser I, Meyer M, Gericke GS, O'Rourke J, Birns J, Purcell S, Pauls DL. Platko JV, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1278-87. doi: 10.1002/ajmg.b.30774. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18452150

4

The familial association of tourette's disorder and ADHD: the impact of OCD symptoms.

O'Rourke JA, Scharf JM, Platko J, Stewart SE, Illmann C, Geller DA, King RA, Leckman JF, Pauls DL. O'Rourke JA, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):553-60. doi: 10.1002/ajmg.b.31195. Epub 2011 May 6. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21557467 Free PMC article.

5

Family-based genetic association study of DLGAP3 in Tourette Syndrome.

Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM; Tourette Syndrome International Consortium for Genetics (TSAICG). Crane J, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):108-14. doi: 10.1002/ajmg.b.31134. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184590 Free PMC article.

6

Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder.

Poelmans G, Pauls DL, Buitelaar JK, Franke B. Poelmans G, et al. Am J Psychiatry. 2011 Apr;168(4):365-77. doi: 10.1176/appi.ajp.2010.10070948. Epub 2011 Feb 15. Am J Psychiatry. 2011. PMID: 21324949 Review.

7

Continuing the search for dyslexia genes on 6p.

Grigorenko EL, Wood FB, Golovyan L, Meyer M, Romano C, Pauls D. Grigorenko EL, et al. Among authors: pauls d. Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):89-98. doi: 10.1002/ajmg.b.10032. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12627473

8

An integrated molecular landscape implicates the regulation of dendritic spine formation through insulin-related signalling in obsessive-compulsive disorder.

van de Vondervoort I, Poelmans G, Aschrafi A, Pauls DL, Buitelaar JK, Glennon JC, Franke B. van de Vondervoort I, et al. J Psychiatry Neurosci. 2016 Jun;41(4):280-5. doi: 10.1503/jpn.140327. J Psychiatry Neurosci. 2016. PMID: 26854754 Free PMC article. Review.

9

A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.

Stewart SE, Platko J, Fagerness J, Birns J, Jenike E, Smoller JW, Perlis R, Leboyer M, Delorme R, Chabane N, Rauch SL, Jenike MA, Pauls DL. Stewart SE, et al. Arch Gen Psychiatry. 2007 Feb;64(2):209-14. doi: 10.1001/archpsyc.64.2.209. Arch Gen Psychiatry. 2007. PMID: 17283288

10

Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.

Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL; Tourette Syndrome International Consortium for Genetics. Scharf JM, et al. Among authors: pauls dl. Neurology. 2008 Apr 15;70(16 Pt 2):1495-6. doi: 10.1212/01.wnl.0000296833.25484.bb. Neurology. 2008. PMID: 18413575 Free PMC article. No abstract available.

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