Ramsay M - Search Results

1

Complete androgen insensitivity syndrome in a black South African family: a clinical and molecular investigation.

Scott EC, Greenberg TS, Arndt S, Ramsay M, Shires R. Scott EC, et al. Among authors: ramsay m. Endocr Pract. 2006 Nov-Dec;12(6):664-9. doi: 10.4158/EP.12.6.664. Endocr Pract. 2006. PMID: 17229664

2

Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals.

Ramsay M, Greenberg T, Lombard Z, Labrum R, Lubbe S, Aron S, Marais AS, Terry S, Bercovitch L, Viljoen D. Ramsay M, et al. J Dermatol Sci. 2009 Jun;54(3):198-204. doi: 10.1016/j.jdermsci.2009.02.008. Epub 2009 Mar 31. J Dermatol Sci. 2009. PMID: 19339160

3

Glucocerebrosidase gene mutations in black South Africans with Gaucher disease.

Arndt S, Heitner R, Lane A, Ramsay M. Arndt S, et al. Among authors: ramsay m. Blood Cells Mol Dis. 2009 Jul-Aug;43(1):129-33. doi: 10.1016/j.bcmd.2009.02.008. Epub 2009 Apr 25. Blood Cells Mol Dis. 2009. PMID: 19394250

4

Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population.

Williams SE, Whigham BT, Liu Y, Carmichael TR, Qin X, Schmidt S, Ramsay M, Hauser MA, Allingham RR. Williams SE, et al. Among authors: ramsay m. Mol Vis. 2010 Apr 21;16:705-12. Mol Vis. 2010. PMID: 20431720 Free PMC article.

5

Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759.

Appel S, Filter M, Reis A, Hennies HC, Bergheim A, Ogilvie E, Arndt S, Simmons A, Lovett M, Hide W, Ramsay M, Reichwald K, Zimmermann W, Rosenthal A. Appel S, et al. Among authors: ramsay m. Eur J Hum Genet. 2002 Jan;10(1):17-25. doi: 10.1038/sj.ejhg.5200750. Eur J Hum Genet. 2002. PMID: 11896452

6

Interleukin-1 receptor antagonist gene polymorphisms are associated with disease severity in Black South Africans with rheumatoid arthritis.

Lubbe S, Tikly M, van der Merwe L, Hodkinson B, Ramsay M. Lubbe S, et al. Among authors: ramsay m. Joint Bone Spine. 2008 Jul;75(4):422-5. doi: 10.1016/j.jbspin.2007.09.015. Epub 2008 May 12. Joint Bone Spine. 2008. PMID: 18468936

7

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.

Kabahuma RI, Ouyang X, Du LL, Yan D, Hutchin T, Ramsay M, Penn C, Liu XZ. Kabahuma RI, et al. Among authors: ramsay m. Int J Pediatr Otorhinolaryngol. 2011 May;75(5):611-7. doi: 10.1016/j.ijporl.2011.01.029. Epub 2011 Mar 9. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21392827 Free PMC article.

8

Africa: the next frontier for human disease gene discovery?

Ramsay M, Tiemessen CT, Choudhury A, Soodyall H. Ramsay M, et al. Hum Mol Genet. 2011 Oct 15;20(R2):R214-20. doi: 10.1093/hmg/ddr401. Epub 2011 Sep 9. Hum Mol Genet. 2011. PMID: 21908518 Review.

9

Differential gene expression of MMP-1, TIMP-1 and HGF in clinically involved and uninvolved skin in South Africans with SSc.

Frost J, Ramsay M, Mia R, Moosa L, Musenge E, Tikly M. Frost J, et al. Among authors: ramsay m. Rheumatology (Oxford). 2012 Jun;51(6):1049-52. doi: 10.1093/rheumatology/ker367. Epub 2012 Jan 27. Rheumatology (Oxford). 2012. PMID: 22286923

10

Africa: continent of genome contrasts with implications for biomedical research and health.

Ramsay M. Ramsay M. FEBS Lett. 2012 Aug 31;586(18):2813-9. doi: 10.1016/j.febslet.2012.07.061. Epub 2012 Jul 31. FEBS Lett. 2012. PMID: 22858376 Free article. Review.

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