Pathare T - Search Results

1

Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder.

Dorval KM, Wigg KG, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Pathare T, Malone M, Schachar R, Barr CL. Dorval KM, et al. Among authors: pathare t. Genes Brain Behav. 2007 Jul;6(5):444-52. doi: 10.1111/j.1601-183X.2006.00273.x. Epub 2006 Sep 8. Genes Brain Behav. 2007. PMID: 17010153 Free PMC article.

2

The serotonin receptor HTR1B: gene polymorphisms in attention deficit hyperactivity disorder.

Ickowicz A, Feng Y, Wigg K, Quist J, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL. Ickowicz A, et al. Among authors: pathare t. Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):121-5. doi: 10.1002/ajmg.b.30398. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 16958036

3

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: pathare t. Mol Psychiatry. 2004 May;9(5):494-9. doi: 10.1038/sj.mp.4001455. Mol Psychiatry. 2004. PMID: 14699423

4

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.

Feng Y, Crosbie J, Wigg K, Pathare T, Ickowicz A, Schachar R, Tannock R, Roberts W, Malone M, Swanson J, Kennedy JL, Barr CL. Feng Y, et al. Among authors: pathare t. Mol Psychiatry. 2005 Nov;10(11):998-1005, 973. doi: 10.1038/sj.mp.4001722. Mol Psychiatry. 2005. PMID: 16088329

5

Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder.

Laurin N, Misener VL, Crosbie J, Ickowicz A, Pathare T, Roberts W, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Laurin N, et al. Among authors: pathare t. Mol Psychiatry. 2005 Dec;10(12):1117-25. doi: 10.1038/sj.mp.4001737. Mol Psychiatry. 2005. PMID: 16172615 Clinical Trial.

6

Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder.

Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Kennedy JL, Tannock R, Schachar R, Barr CL. Lee J, et al. Among authors: pathare t. Genes Brain Behav. 2008 Feb;7(1):53-60. doi: 10.1111/j.1601-183X.2007.00325.x. Epub 2007 May 14. Genes Brain Behav. 2008. PMID: 17504247 Free PMC article.

7

No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder.

Laurin N, Feng Y, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Laurin N, et al. Among authors: pathare t. Mol Psychiatry. 2007 Mar;12(3):226-9. doi: 10.1038/sj.mp.4001936. Mol Psychiatry. 2007. PMID: 17325714 No abstract available.

8

Mapping the genetic landscape of treatable inherited metabolic disorders in a large Middle Eastern biobank.

Devadoss Gandhi G, Aliyev E, Syed N, Vempalli FR, Saad C, Mbarek H, Al-Saei O, Al-Maraghi A, Abdi M, Krishnamoorthy N, Badii R; Qatar Genome Program Research Consortium; Akil AA, Ben-Omran T, Fakhro KA. Devadoss Gandhi G, et al. Genet Med. 2024 Sep 14;26(12):101268. doi: 10.1016/j.gim.2024.101268. Online ahead of print. Genet Med. 2024. PMID: 39286960 Free article.

9

Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants.

Elfatih A, Saad C; Qatar Genome Program Research Consortium; Mifsud B, Mbarek H. Elfatih A, et al. Eur J Hum Genet. 2024 Nov;32(11):1465-1473. doi: 10.1038/s41431-024-01656-1. Epub 2024 Jul 17. Eur J Hum Genet. 2024. PMID: 39020067 Free PMC article.

10

Burden of Mendelian disorders in a large Middle Eastern biobank.

Aamer W, Al-Maraghi A, Syed N, Gandhi GD, Aliyev E, Al-Kurbi AA, Al-Saei O, Kohailan M, Krishnamoorthy N, Palaniswamy S, Al-Malki K, Abbasi S, Agrebi N, Abbaszadeh F, Akil ASA, Badii R, Ben-Omran T, Lo B; Qatar Genome Program Research Consortium; Mokrab Y, Fakhro KA. Aamer W, et al. Genome Med. 2024 Apr 8;16(1):46. doi: 10.1186/s13073-024-01307-6. Genome Med. 2024. PMID: 38584274 Free PMC article.

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