sameAs
Genetic and epigenetic insights into fetal alcohol spectrum disordersEvidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populationsRufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 geneThe H3Africa policy framework: negotiating fairness in genomicsAppetite regulation genes are associated with body mass index in black South African adolescents: a genetic association studyComputational selection and prioritization of candidate genes for fetal alcohol syndrome.Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevanceUnderstanding the rise in cardiovascular diseases in Africa: harmonising H3Africa genomic epidemiological teams and toolsResearch capacity. Enabling the genomic revolution in Africa.Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759.Immunochip identifies novel, and replicates known, genetic risk loci for rheumatoid arthritis in black South AfricansBiology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa.The African Genome Variation Project shapes medical genetics in Africa.Genetic diversity in black South Africans from SowetoThe genetics of POAG in black South Africans: a candidate gene association study.A computational approach to candidate gene prioritization for X-linked mental retardation using annotation-based binary filtering and motif-based linear discriminatory analysis.Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort studyAn arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4.Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutationA new marker on chromosome 15, D15S74, detects three RFLPsAn anonymous single copy probe, D3S153, detects an SstI RFLPAfrican origins and chronic kidney disease susceptibility in the human immunodeficiency virus era.Ethical issues in genomic research on the African continent: experiences and challenges to ethics review committees.The effect of preconception paternal alcohol exposure on epigenetic remodeling of the h19 and rasgrf1 imprinting control regions in mouse offspring.Exploring genetic markers of adult obesity risk in black adolescent South Africans-the Birth to Twenty Cohort.No Evidence for a Parent-of-Origin Specific Differentially Methylated Region Linked to RASGRF1.Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family.Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.APOL1 Risk Variants Are Strongly Associated with HIV-Associated Nephropathy in Black South AfricansYeast artificial chromosome cloning.Does the sun play a role in the aetiology of malignant melanoma? A review.Building a Platform to Enable NCD Research to Address Population Health in Africa: CVD Working Group Discussion at the Sixth H3Africa Consortium Meeting in Zambia.Genetic factors influencing bone mineral content in a black South African population.Population Stratification and Underrepresentation of Indian Subcontinent Genetic Diversity in the 1000 Genomes Project Dataset.Africa: the next frontier for human disease gene discovery?Africa: continent of genome contrasts with implications for biomedical research and health.Epigenetics and the burden of noncommunicable disease: a paucity of research in Africa.Establishing an academic biobank in a resource-challenged environment.Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
P50
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P50
description
South African professor of human genetics
@en
Zuid-Afrikaans onderzoekster
@nl
name
Michele Ramsay
@sq
Michèle Ramsay
@ast
Michèle Ramsay
@en
Michèle Ramsay
@es
Michèle Ramsay
@fr
Michèle Ramsay
@ga
Michèle Ramsay
@nl
Michèle Ramsay
@sl
Michèle Ramsay
@vi
type
label
Michele Ramsay
@sq
Michèle Ramsay
@ast
Michèle Ramsay
@en
Michèle Ramsay
@es
Michèle Ramsay
@fr
Michèle Ramsay
@ga
Michèle Ramsay
@nl
Michèle Ramsay
@sl
Michèle Ramsay
@vi
altLabel
Michele Ramsay
@ast
Michele Ramsay
@en
Michele Ramsay
@es
Michele Ramsay
@nl
prefLabel
Michele Ramsay
@sq
Michèle Ramsay
@ast
Michèle Ramsay
@en
Michèle Ramsay
@es
Michèle Ramsay
@fr
Michèle Ramsay
@ga
Michèle Ramsay
@nl
Michèle Ramsay
@sl
Michèle Ramsay
@vi
P106
P101
P1153
7102729474
P21
P31
P496
0000-0002-4156-4801