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Rosemary Ekong

Showing results (1-10 of 25) with videos related to

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Human Mutation|July 27, 2019
Checklist for gene/disease-specific variation database curators to enable ethical data managementRosemary Ekong, Mauno Vihinen
Annals of Human Genetics|August 6, 2025
The Centenary Special Issue of the Annals of Human GeneticsJohn Armour, Rosemary Ekong
Clinical Kidney Journal|March 18, 2016
Persistent severe polyuria after renal transplantTimothy Wong, Chris Laing, Rosemary Ekong, et al.
The Pharmacogenomics Journal|July 20, 2020
Group-based pharmacogenetic prediction: is it feasible and do current NHS England ethnic classifications provide appropriate data?Catherine J E Ingram, Rosemary Ekong, Naser Ansari-Pour, et al.
Pharmacogenetics and Genomics|May 4, 2016
Contrasting exome constancy and regulatory region variation in the gene encoding CYP3A4: an examination of the extent and potential implicationsOlivia J Creemer, Naser Ansari-Pour, Rosemary Ekong, et al.
European Journal of Human Genetics : EJHG|August 30, 2012
The frequency of an IL-18-associated haplotype in AfricansSimon R Thompson, Steve E Humphries, Mark G Thomas, et al.
Nature|April 15, 2020
Eugenics history: university geneticists respondAndrew Pomiankowski, Mark G Thomas, Steve Jones, et al.
Gene|June 13, 2023
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variantsLaura S Farach, Hope Northrup, Mark Nellist, et al.
Antiviral Therapy|February 2, 2012
Common inherited mitochondrial DNA mutations and nucleoside reverse transcriptase inhibitor-induced severe hyperlactataemia in HIV-infected adults: an exploratory studyAlejandro Arenas-Pinto, Ian Weller, Rosemary Ekong, et al.
Human Genetics|June 10, 2015
Diversity of lactase persistence in African milk drinkersBryony Leigh Jones, Tamiru Oljira, Anke Liebert, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Human Mutation|July 27, 2019
Checklist for gene/disease-specific variation database curators to enable ethical data managementRosemary Ekong, Mauno Vihinen
Annals of Human Genetics|August 6, 2025
The Centenary Special Issue of the Annals of Human GeneticsJohn Armour, Rosemary Ekong
Clinical Kidney Journal|March 18, 2016
Persistent severe polyuria after renal transplantTimothy Wong, Chris Laing, Rosemary Ekong, et al.
The Pharmacogenomics Journal|July 20, 2020
Group-based pharmacogenetic prediction: is it feasible and do current NHS England ethnic classifications provide appropriate data?Catherine J E Ingram, Rosemary Ekong, Naser Ansari-Pour, et al.
Pharmacogenetics and Genomics|May 4, 2016
Contrasting exome constancy and regulatory region variation in the gene encoding CYP3A4: an examination of the extent and potential implicationsOlivia J Creemer, Naser Ansari-Pour, Rosemary Ekong, et al.
European Journal of Human Genetics : EJHG|August 30, 2012
The frequency of an IL-18-associated haplotype in AfricansSimon R Thompson, Steve E Humphries, Mark G Thomas, et al.
Nature|April 15, 2020
Eugenics history: university geneticists respondAndrew Pomiankowski, Mark G Thomas, Steve Jones, et al.
Gene|June 13, 2023
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variantsLaura S Farach, Hope Northrup, Mark Nellist, et al.
Antiviral Therapy|February 2, 2012
Common inherited mitochondrial DNA mutations and nucleoside reverse transcriptase inhibitor-induced severe hyperlactataemia in HIV-infected adults: an exploratory studyAlejandro Arenas-Pinto, Ian Weller, Rosemary Ekong, et al.
Human Genetics|June 10, 2015
Diversity of lactase persistence in African milk drinkersBryony Leigh Jones, Tamiru Oljira, Anke Liebert, et al.
Pageof 3