Ramesar RS - Search Results

1

Personality: is it a viable endophenotype for genetic studies of bipolar affective disorder?

Savitz JB, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. Bipolar Disord. 2006 Aug;8(4):322-37. doi: 10.1111/j.1399-5618.2006.00309.x. Bipolar Disord. 2006. PMID: 16879133 Review.

2

Genetic variants implicated in personality: a review of the more promising candidates.

Savitz JB, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):20-32. doi: 10.1002/ajmg.b.20155. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389772 Review.

3

Neurocognitive function as an endophenotype for genetic studies of bipolar affective disorder.

Savitz JB, Solms M, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. Neuromolecular Med. 2005;7(4):275-86. doi: 10.1385/NMM:7:4:275. Neuromolecular Med. 2005. PMID: 16391385 Review.

4

Trends in suicidology: personality as an endophenotype for molecular genetic investigations.

Savitz JB, Cupido CL, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. PLoS Med. 2006 May;3(5):e107. doi: 10.1371/journal.pmed.0030107. Epub 2006 May 9. PLoS Med. 2006. PMID: 16646633 Free PMC article. Review.

5

The relationship between childhood abuse and dissociation. Is it influenced by catechol-O-methyltransferase (COMT) activity?

Savitz JB, van der Merwe L, Newman TK, Solms M, Stein DJ, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. Int J Neuropsychopharmacol. 2008 Mar;11(2):149-61. doi: 10.1017/S1461145707007900. Epub 2007 Jul 3. Int J Neuropsychopharmacol. 2008. PMID: 17608961 Free article.

6

Neuropsychological task performance in bipolar spectrum illness: genetics, alcohol abuse, medication and childhood trauma.

Savitz JB, van der Merwe L, Stein DJ, Solms M, Ramesar RS. Savitz JB, et al. Among authors: ramesar rs. Bipolar Disord. 2008 Jun;10(4):479-94. doi: 10.1111/j.1399-5618.2008.00591.x. Bipolar Disord. 2008. PMID: 18452444

7

Stargardt disease: towards developing a model to predict phenotype.

Heathfield L, Lacerda M, Nossek C, Roberts L, Ramesar RS. Heathfield L, et al. Among authors: ramesar rs. Eur J Hum Genet. 2013 Oct;21(10):1173-6. doi: 10.1038/ejhg.2013.92. Epub 2013 May 22. Eur J Hum Genet. 2013. PMID: 23695285 Free PMC article.

8

GSTM1 and GSTT1 polymorphisms as modifiers of age at diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) in a homogeneous cohort of individuals carrying a single predisposing mutation.

Felix R, Bodmer W, Fearnhead NS, van der Merwe L, Goldberg P, Ramesar RS. Felix R, et al. Among authors: ramesar rs. Mutat Res. 2006 Dec 1;602(1-2):175-81. doi: 10.1016/j.mrfmmm.2006.09.004. Mutat Res. 2006. PMID: 17087981

9

Analysis of RPGR in a South African family with X-linked retinitis pigmentosa: research and diagnostic implications.

Rebello G, Vorster A, Greenberg J, Coutts N, Roberts L, Ehrenreich L, Gama D, Ramesar R. Rebello G, et al. Clin Genet. 2003 Aug;64(2):137-41. doi: 10.1034/j.1399-0004.2003.00090.x. Clin Genet. 2003. PMID: 12859409

10

Clinical utility of the ABCR400 microarray: basing a genetic service on a commercial gene chip.

Roberts LJ, Ramesar RS, Greenberg J. Roberts LJ, et al. Among authors: ramesar rs. Arch Ophthalmol. 2009 Apr;127(4):549-54. doi: 10.1001/archophthalmol.2009.47. Arch Ophthalmol. 2009. PMID: 19365039

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