Publications by authors named "Robyn Kerr"

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A training program to extend the reach of the deciphering developmental disorders in Africa (DDD-Africa) study.
Aaliah Charles, Zané Lombard, Nadia Carstens, Zandisiwe Goliath, Aimé Lumaka, Robyn Kerr

Front Genet· October 2025

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Albinism research in a Southern African setting: unique findings.
Jennifer G R Kromberg, Robyn A Kerr

J Community Genet· April 2025

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A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.
Maria Mabyalwa Mudau, Heather Seymour, Patracia Nevondwe, Robyn Kerr, Careni Spencer

J Community Genet· February 2024

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Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.
Heather Seymour, Candice Feben, Patracia Nevondwe, Robyn Kerr, Careni Spencer

Mol Genet Genomic Med· January 2024

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Determining a Worldwide Prevalence of Oculocutaneous Albinism: A Systematic Review.
Jennifer G R Kromberg, Kaitlyn A Flynn, Robyn A Kerr

Invest Ophthalmol Vis Sci· July 2023

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Oculocutaneous albinism in southern Africa: Historical background, genetic, clinical and psychosocial issues.
Jennifer G R Kromberg, Robyn Kerr

Afr J Disabil· October 2022

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Correction: Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations.
Mahtaab Hayat, Robyn Kerr, Amy R Bentley, Charles N Rotimi, Frederick J Raal

PLoS One· March 2021

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Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations.
Mahtaab Hayat, Robyn Kerr, Amy R Bentley, Charles N Rotimi, Frederick J Raal

PLoS One· May 2020

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Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.
Wenlong C Chen, Hannah Bye, Marco Matejcic, Ariella Amar, Dhiren Govender, Robyn Kerr

Carcinogenesis· June 2019

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The Integrity and Yield of Genomic DNA Isolated from Whole Blood Following Long-Term Storage at -30°C.
Wenlong Carl Chen, Robyn Kerr, Andrew May, Babongile Ndlovu, Anelisa Sobalisa

Biopreserv Biobank· April 2018

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Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.
Tasha Wainstein, Robyn Kerr, Claire L Mitchell, Smita Madaree, Fahmida B Essop

S Afr Med J· October 2013

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Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa.
Robyn Kerr, Carol Robinson, Fahmida B Essop, Amanda Krause

S Afr Med J· October 2013

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Biology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa.
Prashiela Manga, Robyn Kerr, Michèle Ramsay, Jennifer G R Kromberg

S Afr Med J· July 2013

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