Wigg K - Search Results

1

Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.

Adams J, Crosbie J, Wigg K, Ickowicz A, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL. Adams J, et al. Among authors: wigg k. Mol Psychiatry. 2004 May;9(5):494-9. doi: 10.1038/sj.mp.4001455. Mol Psychiatry. 2004. PMID: 14699423

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

Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy.

Minassian BA, Sainz J, Serratosa JM, Gee M, Sakamoto LM, Bohlega S, Geoffroy G, Barr C, Scherer SW, Tomiyasu U, Carpenter S, Wigg K, Sanghvi AV, Delgado-Escueta AV. Minassian BA, et al. Among authors: wigg k. Ann Neurol. 1999 Feb;45(2):262-5. doi: 10.1002/1531-8249(199902)45:2<262::aid-ana20>3.0.co;2-9. Ann Neurol. 1999. PMID: 9989632

5

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

6

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

7

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. Among authors: wigg k. 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

8

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

9

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.

10

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. Among authors: wigg k. Mol Psychiatry. 2000 Jul;5(4):405-9. doi: 10.1038/sj.mp.4000733. Mol Psychiatry. 2000. PMID: 10889551

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

71 results

Search Page

Filters