Barr CL - Search Results

1

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.

Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL; Quantitative Trait Working Group of the GenLang Consortium; Fisher SE, Lovett MW, Strug LJ, Barr CL. Price KM, et al. Among authors: barr cl. Transl Psychiatry. 2022 Nov 29;12(1):495. doi: 10.1038/s41398-022-02250-z. Transl Psychiatry. 2022. PMID: 36446759 Free PMC article.

2

The norepinephrine transporter gene and attention-deficit hyperactivity disorder.

Barr CL, Kroft J, Feng Y, Wigg K, Roberts W, Malone M, Ickowicz A, Schachar R, Tannock R, Kennedy JL. Barr CL, et al. Am J Med Genet. 2002 Apr 8;114(3):255-9. doi: 10.1002/ajmg.10193. Am J Med Genet. 2002. PMID: 11920844

3

Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.

Wigg K, Zai G, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL, Barr CL. Wigg K, et al. Among authors: barr cl. Am J Psychiatry. 2002 Jun;159(6):1046-8. doi: 10.1176/appi.ajp.159.6.1046. Am J Psychiatry. 2002. PMID: 12042196

4

Evaluation of the genes for the adrenergic receptors alpha 2A and alpha 1C and Gilles de la Tourette Syndrome.

Xu C, Ozbay F, Wigg K, Shulman R, Tahir E, Yazgan Y, Sandor P, Barr CL; Tourette Syndrome Association Genetic Consortium. Xu C, et al. Among authors: barr cl. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):54-9. doi: 10.1002/ajmg.b.20001. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707939

5

Association study of neurotrophic tyrosine kinase receptor type 2 (NTRK2) and childhood-onset mood disorders.

Adams JH, Wigg KG, King N, Burcescu I, Vetró A, Kiss E, Baji I, George CJ, Kennedy JL, Kovacs M, Barr CL. Adams JH, et al. Among authors: barr cl. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):90-5. doi: 10.1002/ajmg.b.30084. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15389758

6

Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD).

Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL. Feng Y, et al. Among authors: barr cl. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):1-6. doi: 10.1002/ajmg.b.30190. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16082693

7

Gene for the serotonin transporter and ADHD: no association with two functional polymorphisms.

Wigg KG, Takhar A, Ickowicz A, Tannock R, Kennedy JL, Pathare T, Malone M, Schachar R, Barr CL. Wigg KG, et al. Among authors: barr cl. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):566-70. doi: 10.1002/ajmg.b.30247. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16856124

8

The gene for synapsin III and attention-deficit hyperactivity disorder.

Makkar R, Gomez L, Wigg KG, Ickowicz A, Pathare T, Tannock R, Malone M, Kennedy JL, Schachar R, Barr CL. Makkar R, et al. Among authors: barr cl. Psychiatr Genet. 2007 Apr;17(2):109-12. doi: 10.1097/YPG.0b013e328012a0c6. Psychiatr Genet. 2007. PMID: 17413450

9

Evidence of an association between the vasopressin V1b receptor gene (AVPR1B) and childhood-onset mood disorders.

Dempster EL, Burcescu I, Wigg K, Kiss E, Baji I, Gadoros J, Tamás Z, Kennedy JL, Vetró A, Kovacs M, Barr CL. Dempster EL, et al. Among authors: barr cl. Arch Gen Psychiatry. 2007 Oct;64(10):1189-95. doi: 10.1001/archpsyc.64.10.1189. Arch Gen Psychiatry. 2007. PMID: 17909131

10

GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families.

Feng Y, Wigg K, King N, Vetró A, Kiss E, Kapornai K, Mayer L, Gádoros J, Kennedy JL, Kovacs M, Barr CL; International Consortium for Childhood-Onset Mood Disorders. Feng Y, et al. Among authors: barr cl. Psychiatr Genet. 2007 Dec;17(6):347-50. doi: 10.1097/YPG.0b013e3281ac232f. Psychiatr Genet. 2007. PMID: 18075476

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