Krause A - Search Results

1

Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.

Asiimwe IG, Zhang EJ, Osanlou R, Krause A, Dillon C, Suarez-Kurtz G, Zhang H, Perini JA, Renta JY, Duconge J, Cavallari LH, Marcatto LR, Beasly MT, Perera MA, Limdi NA, Santos PCJL, Kimmel SE, Lubitz SA, Scott SA, Kawai VK, Jorgensen AL, Pirmohamed M. Asiimwe IG, et al. Among authors: krause a. Clin Pharmacol Ther. 2020 Jun;107(6):1420-1433. doi: 10.1002/cpt.1755. Epub 2020 Jan 28. Clin Pharmacol Ther. 2020. PMID: 31869433 Free PMC article.

2

Novel CYP2C9 and VKORC1 gene variants associated with warfarin dosage variability in the South African black population.

Mitchell C, Gregersen N, Krause A. Mitchell C, et al. Among authors: krause a. Pharmacogenomics. 2011 Jul;12(7):953-63. doi: 10.2217/pgs.11.36. Epub 2011 Jun 2. Pharmacogenomics. 2011. PMID: 21635147

3

Genetic factors influencing inhibitor development in a cohort of South African haemophilia A patients.

Lochan A, Macaulay S, Chen WC, Mahlangu JN, Krause A. Lochan A, et al. Among authors: krause a. Haemophilia. 2014 Sep;20(5):687-92. doi: 10.1111/hae.12436. Epub 2014 Jun 21. Haemophilia. 2014. PMID: 24953131

4

Huntington's disease confirmed by genetic testing in five African families.

Silber E, Kromberg J, Temlett JA, Krause A, Saffer D. Silber E, et al. Among authors: krause a. Mov Disord. 1998 Jul;13(4):726-30. doi: 10.1002/mds.870130420. Mov Disord. 1998. PMID: 9686782

5

The molecular basis of spinal muscular atrophy (SMA) in South African black patients.

Labrum R, Rodda J, Krause A. Labrum R, et al. Among authors: krause a. Neuromuscul Disord. 2007 Oct;17(9-10):684-92. doi: 10.1016/j.nmd.2007.05.005. Epub 2007 Jul 12. Neuromuscul Disord. 2007. PMID: 17627822

6

Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.

Baine FK, Kay C, Ketelaar ME, Collins JA, Semaka A, Doty CN, Krause A, Greenberg LJ, Hayden MR. Baine FK, et al. Among authors: krause a. Eur J Hum Genet. 2013 Oct;21(10):1120-7. doi: 10.1038/ejhg.2013.2. Epub 2013 Mar 6. Eur J Hum Genet. 2013. PMID: 23463025 Free PMC article.

7

Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.

Wainstein T, Kerr R, Mitchell CL, Madaree S, Essop FB, Vorster E, Wainwright R, Poole J, Krause A. Wainstein T, et al. Among authors: krause a. S Afr Med J. 2013 Oct 11;103(12 Suppl 1):970-3. doi: 10.7196/samj.7215. S Afr Med J. 2013. PMID: 24300640

8

The Frequency of Huntington Disease and Huntington Disease-Like 2 in the South African Population.

Baine FK, Krause A, Greenberg LJ. Baine FK, et al. Among authors: krause a. Neuroepidemiology. 2016;46(3):198-202. doi: 10.1159/000444020. Epub 2016 Feb 17. Neuroepidemiology. 2016. PMID: 26882115

9

Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations.

Krause A, Seymour H, Ramsay M. Krause A, et al. Annu Rev Genomics Hum Genet. 2018 Aug 31;19:149-175. doi: 10.1146/annurev-genom-083117-021256. Annu Rev Genomics Hum Genet. 2018. PMID: 30169122 Review.

10

Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients.

Dangerfield BT, Manga P, Field SP, Hartman E, Jenkins T, Krause A. Dangerfield BT, et al. Among authors: krause a. Br J Haematol. 1997 Jun;97(3):558-60. doi: 10.1046/j.1365-2141.1997.892905.x. Br J Haematol. 1997. PMID: 9207400 Free article.

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