Wigg KG - 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: wigg kg. Transl Psychiatry. 2022 Nov 29;12(1):495. doi: 10.1038/s41398-022-02250-z. Transl Psychiatry. 2022. PMID: 36446759 Free PMC article.

2

No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families.

Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. Barr CL, et al. Among authors: wigg kg. Am J Med Genet. 1996 May 31;67(3):301-5. doi: 10.1002/(SICI)1096-8628(19960531)67:3<301::AID-AJMG6>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8725747

3

Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome.

Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. Barr CL, et al. Among authors: wigg kg. Am J Med Genet. 1997 Feb 21;74(1):58-61. Am J Med Genet. 1997. PMID: 9034008

4

Genome scan for linkage to Gilles de la Tourette syndrome.

Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls D, Kidd KK, Tsui LC, Sandor P. Barr CL, et al. Among authors: wigg kg. Am J Med Genet. 1999 Aug 20;88(4):437-45. doi: 10.1002/(sici)1096-8628(19990820)88:4<437::aid-ajmg24>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10402514

5

Catechol-O-methyltransferase and Gilles de la Tourette syndrome.

Barr CL, Wigg KG, Sandor P. Barr CL, et al. Among authors: wigg kg. Mol Psychiatry. 1999 Sep;4(5):492-5. doi: 10.1038/sj.mp.4000549. Mol Psychiatry. 1999. PMID: 10523824

6

Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.

Barr CL, Wigg K, Malone M, Schachar R, Tannock R, Roberts W, Kennedy JL. Barr CL, et al. Am J Med Genet. 1999 Dec 15;88(6):710-3. doi: 10.1002/(sici)1096-8628(19991215)88:6<710::aid-ajmg23>3.0.co;2-q. Am J Med Genet. 1999. PMID: 10581494

7

Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder.

Barr CL, Wigg KG, Wu J, Zai C, Bloom S, Tannock R, Roberts W, Malone M, Schachar R, Kennedy JL. Barr CL, et al. Among authors: wigg kg. Am J Med Genet. 2000 Feb 7;96(1):114-7. Am J Med Genet. 2000. PMID: 10686563

8

Genetics and sleep disorders.

Zai C, Wigg KG, Barr CL. Zai C, et al. Among authors: wigg kg. Semin Clin Neuropsychiatry. 2000 Jan;5(1):33-43. doi: 10.153/SCNP00500033. Semin Clin Neuropsychiatry. 2000. PMID: 10704536 Review.

9

Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder.

Barr CL, Feng Y, Wigg K, Bloom S, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Barr CL, et al. Mol Psychiatry. 2000 Jul;5(4):405-9. doi: 10.1038/sj.mp.4000733. Mol Psychiatry. 2000. PMID: 10889551

10

Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.

Barr CL, Wigg KG, Bloom S, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Barr CL, et al. Among authors: wigg kg. Am J Med Genet. 2000 Jun 12;96(3):262-7. doi: 10.1002/1096-8628(20000612)96:3<262::aid-ajmg5>3.0.co;2-8. Am J Med Genet. 2000. PMID: 10898896

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