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Personalized Human Papillomavirus Vaccination for Persistence of Immunity for Cervical Cancer Prevention: A Critical Review With Experts' Opinions

Frontiers in oncology, 2020-04, Vol.10, p.548-548

2020

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Genetic insights: High germline variant rate in an indigenous African cohort with early-onset colorectal cancer

Frontiers in oncology, 2023-10, Vol.13, p.1253867-1253867

2023

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Investigation of Cervical Tumor Biopsies for Chromosomal Loss of Heterozygosity (LOH) and Microsatellite Instability (MSI) at the HLA II Locus in HIV-1/HPV Co-infected Women

Frontiers in oncology, 2019-10, Vol.9, p.951-951

2019

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Apoptosis-Inducing Signal Sequence Mutation in Carbonic Anhydrase IV Identified in Patients with the RP17 Form of Retinitis Pigmentosa

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (17), p.6617-6622

2004

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Correspondence on “Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database” by Dominguez-Valentin et al

Genetics in medicine, 2022-05, Vol.24 (5), p.1148-1150

2022

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The impact of the c.5603A>T hypomorphic variant on founder mutation screening of ABCA4 for Stargardt disease in South Africa

Molecular vision, 2020-08, Vol.26, p.613-622

2020

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Update on Inherited Retinal Disease in South Africa: Encouraging Diversity in Molecular Genetics

Advances in experimental medicine and biology, 2019, Vol.1185, p.257-261

2019

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Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

American journal of human genetics, 2020-11, Vol.107 (5), p.802-814

2020

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De Novo Assembly-Based Analysis of RPGR Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline

Genes, 2020-07, Vol.11 (7), p.800

2020

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Human Leukocyte Antigen-Allelic Variations May Influence the Age at Cancer Diagnosis in Lynch Syndrome

Journal of personalized medicine, 2024-05, Vol.14 (6), p.575

2024

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Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B

Human mutation, 2020-11, Vol.41 (11), p.1871-1876

2020

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Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes

BMC medical genetics, 2006-03, Vol.7 (1), p.29-29, Article 29

2006

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Impact of Host Molecular Genetic Variations and HIV/HPV Co-infection on Cervical Cancer Progression: A Systematic review

Oncomedicine (Online), 2018, Vol.3, p.82-93

2018

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Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

European journal of obstetrics & gynecology and reproductive biology, 2008-09, Vol.140 (1), p.135-136

2008

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Management of a South African family with retinitis pigmentosa—should potential therapy influence translational research protocols?

Journal of ocular biology, diseases, and informatics, 2008-03, Vol.1 (1), p.55-58, Article 55

2008

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Analysis of RPGR in a South African family with X-linked retinitis pigmentosa: research and diagnostic implications

Clinical genetics, 2003-08, Vol.64 (2), p.137-141

2003

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Carbonic Anhydrase Inhibitors as a Possible Therapy for RP17, an Autosomal Dominant Retinitis Pigmentosa Associated With the R14W Mutation, Apoptosis, and the Unfolded Protein Response

Retinal Degenerations, p.455-458

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High‐Resolution Magnetic Resonance Imaging of Scalp Arteries for the Diagnosis of Giant Cell Arteritis: Results of a Prospective Cohort Study

Arthritis & rheumatology (Hoboken, N.J.), 2017-01, Vol.69 (1), p.161-168

2017

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Effects of endurance exercise training on left ventricular structure in healthy adults: a systematic review and meta-analysis

European journal of preventive cardiology, 2023-07, Vol.30 (9), p.772-793

2023

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Cohort Profile: Growing Up in Singapore Towards healthy Outcomes (GUSTO) birth cohort study

International journal of epidemiology, 2014-10, Vol.43 (5), p.1401-1409

2014

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Bioremediation of Endocrine Disrupting Chemicals- Advancements and Challenges

Environmental research, 2022-10, Vol.213, p.113509-113509, Article 113509

2022

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Dynamics of infant gut microbiota are influenced by delivery mode and gestational duration and are associated with subsequent adiposity

mBio, 2015-02, Vol.6 (1)

2015

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Device-associated infection rates, bacterial resistance, length of stay, and mortality in Kuwait: International Nosocomial Infection Consortium findings

American journal of infection control, 2016-04, Vol.44 (4), p.444-449

2016

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Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome

BMC medicine, 2017-03, Vol.15 (1), p.50, Article 50

2017

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Personalized Human Papillomavirus Vaccination for Persistence of Immunity for Cervical Cancer Prevention: A Critical Review With Experts' Opinions

Genetic insights: High germline variant rate in an indigenous African cohort with early-onset colorectal cancer

Investigation of Cervical Tumor Biopsies for Chromosomal Loss of Heterozygosity (LOH) and Microsatellite Instability (MSI) at the HLA II Locus in HIV-1/HPV Co-infected Women

Apoptosis-Inducing Signal Sequence Mutation in Carbonic Anhydrase IV Identified in Patients with the RP17 Form of Retinitis Pigmentosa

Correspondence on “Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database” by Dominguez-Valentin et al

The impact of the c.5603A>T hypomorphic variant on founder mutation screening of ABCA4 for Stargardt disease in South Africa

Update on Inherited Retinal Disease in South Africa: Encouraging Diversity in Molecular Genetics

Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

De Novo Assembly-Based Analysis of RPGR Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline

Human Leukocyte Antigen-Allelic Variations May Influence the Age at Cancer Diagnosis in Lynch Syndrome

Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B

Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes

Impact of Host Molecular Genetic Variations and HIV/HPV Co-infection on Cervical Cancer Progression: A Systematic review

Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

Management of a South African family with retinitis pigmentosa—should potential therapy influence translational research protocols?

Analysis of RPGR in a South African family with X-linked retinitis pigmentosa: research and diagnostic implications

Carbonic Anhydrase Inhibitors as a Possible Therapy for RP17, an Autosomal Dominant Retinitis Pigmentosa Associated With the R14W Mutation, Apoptosis, and the Unfolded Protein Response

High‐Resolution Magnetic Resonance Imaging of Scalp Arteries for the Diagnosis of Giant Cell Arteritis: Results of a Prospective Cohort Study

Effects of endurance exercise training on left ventricular structure in healthy adults: a systematic review and meta-analysis

Cohort Profile: Growing Up in Singapore Towards healthy Outcomes (GUSTO) birth cohort study

Bioremediation of Endocrine Disrupting Chemicals- Advancements and Challenges

Assessing sex differences in viral load suppression and reported deaths using routinely collected program data from PEPFAR-supported countries in sub-Saharan Africa

Dynamics of infant gut microbiota are influenced by delivery mode and gestational duration and are associated with subsequent adiposity

Device-associated infection rates, bacterial resistance, length of stay, and mortality in Kuwait: International Nosocomial Infection Consortium findings

Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome

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