Ambroise Wonkam
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Cameroonian academic
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Biology
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Genetics
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Biology
Ambroise Wonkam's Degrees
- PhD Human Genetics University of Cape Town
- Masters Genetic Epidemiology University of Cape Town
Why Is Ambroise Wonkam Influential?
(Suggest an Edit or Addition)According to Wikipedia, Ambroise Wonkam is a Cameroonian medical doctor and professor of medical genetics at Johns Hopkins School of Medicine. His research is in sickle cell disease, the genetics of congenital hearing impairment, and ethics in human genetics. He is the current president of the African Society of Human Genetics.
Ambroise Wonkam's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Enabling the genomic revolution in Africa (2014) (327)
- High-depth African genomes inform human migration and health (2020) (136)
- Sickle Cell Disease: New Opportunities and Challenges in Africa (2013) (123)
- The road ahead in genetics and genomics (2020) (88)
- The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival (2014) (87)
- The Role of Tumor Microenvironment in Chemoresistance: 3D Extracellular Matrices as Accomplices (2018) (85)
- Association of Variants at BCL11A and HBS1L-MYB with Hemoglobin F and Hospitalization Rates among Sickle Cell Patients in Cameroon (2014) (84)
- Pharmacogenomics Implications of Using Herbal Medicinal Plants on African Populations in Health Transition (2015) (80)
- Genomic newborn screening: public health policy considerations and recommendations (2017) (72)
- A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease (2015) (66)
- Noonan syndrome in diverse populations (2017) (61)
- Knowledge and attitudes concerning medical genetics amongst physicians and medical students in Cameroon (sub-Saharan Africa) (2006) (61)
- The epidemiology of stroke in sickle cell patients in Yaounde, Cameroon (2006) (60)
- Association between biological markers of sickle cell disease and cognitive functioning amongst Cameroonian children (2013) (59)
- Advances in Therapeutic Targeting of Cancer Stem Cells within the Tumor Microenvironment: An Updated Review (2020) (53)
- Williams–Beuren syndrome in diverse populations (2018) (50)
- Cytochrome P450 pharmacogenetics in African populations: implications for public health (2014) (48)
- Aetiology of childhood hearing loss in Cameroon (sub-Saharan Africa). (2013) (47)
- Beyond the Caster Semenya Controversy: The Case of the Use of Genetics for Gender Testing in Sport (2010) (46)
- Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa? (2015) (46)
- Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon (2017) (46)
- Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis (2018) (44)
- Initiation of a medical genetics service in sub-Saharan Africa: experience of prenatal diagnosis in Cameroon. (2011) (42)
- Ethics of human genetic studies in sub-saharan Africa: the case of Cameroon through a bibliometric analysis. (2011) (42)
- Management of neural tube defects in a Sub-Saharan African country: The situation in Yaounde, Cameroon (2008) (42)
- Psychosocial Burden of Sickle Cell Disease on Parents with an Affected Child in Cameroon (2014) (41)
- Pediatric Urolithiasis in Sub–Saharan Africa: A Comparative Study in Two Regions of Cameroon (2000) (39)
- Success stories in genomic medicine from resource-limited countries (2015) (37)
- Ready to put metadata on the post-2015 development agenda? Linking data publications to responsible innovation and science diplomacy. (2014) (37)
- Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease (2016) (36)
- CYP1A2, CYP2A6, CYP2B6, CYP3A4 and CYP3A5 Polymorphisms in Two Bantu-Speaking Populations from Cameroon and South Africa: Implications for Global Pharmacogenetics (2012) (35)
- Phenotypic and allelic distribution of the ABO and Rhesus (D) blood groups in the Cameroonian population (2014) (33)
- Capacity-Building in Human Genetics for Developing Countries: Initiatives and Perspectives in Sub-Saharan Africa (2010) (32)
- Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families (2016) (32)
- The role of CFTR and SPINK-1 mutations in pancreatic disorders in HIV-positive patients: a case–control study (2004) (31)
- Inhibition of CYP2B6 by Medicinal Plant Extracts: Implication for Use of Efavirenz and Nevirapine-Based Highly Active Anti-Retroviral Therapy (HAART) in Resource-Limited Settings (2016) (31)
- Frequency and clinical genetics of familial dilated cardiomyopathy in Cape Town: implications for the evaluation of patients with unexplained cardiomyopathy. (2011) (31)
- In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes. (2014) (30)
- Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon (2018) (30)
- High-grade intra-epithelial neoplasia and prostate cancer in Dibombari, Cameroon (2003) (30)
- Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans. (2014) (30)
- Cornelia de Lange syndrome in diverse populations (2019) (29)
- Returning incidental findings in African genomics research (2019) (29)
- Clinical characteristics and outcomes of familial and idiopathic dilated cardiomyopathy in Cape Town: a comparative study of 120 cases followed up over 14 years. (2011) (29)
- The burden of sickle cell disease in Cape Town. (2012) (28)
- Beta-cell crosstalk: a further dimension in the stimulus-secretion coupling of glucose-induced insulin release. (2002) (27)
- Sequence three million genomes across Africa (2021) (26)
- Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon (2013) (26)
- Genetics of hearing loss in Africans: use of next generation sequencing is the best way forward (2015) (26)
- A comprehensive survey of models for dissecting local ancestry deconvolution in human genome (2018) (25)
- GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana (2019) (25)
- Genomic medicine in Africa: promise, problems and prospects (2014) (25)
- In Vitro Reversible and Time-Dependent CYP450 Inhibition Profiles of Medicinal Herbal Plant Extracts Newbouldia laevis and Cassia abbreviata: Implications for Herb-Drug Interactions (2016) (25)
- Genomic Medicine Without Borders: Which Strategies Should Developing Countries Employ to Invest in Precision Medicine? A New "Fast-Second Winner" Strategy. (2017) (22)
- No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans. (2014) (22)
- Sickle cell disease in Africa: an urgent need for longitudinal cohort studies (2019) (20)
- Disease burden and the role of pharmacogenomics in African populations (2017) (20)
- Bush mint (Hyptis suaveolens) and spreading hogweed (Boerhavia diffusa) medicinal plant extracts differentially affect activities of CYP1A2, CYP2D6 and CYP3A4 enzymes. (2018) (20)
- Low hepatitis B vaccine uptake among surgical residents in Cameroon (2014) (20)
- Acceptance of abortion by doctors and medical students in Cameroon (2007) (19)
- Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions. (2015) (19)
- Psychosocial Stressors of Sickle Cell Disease on Adult Patients in Cameroon (2014) (19)
- Acceptability of Prenatal Diagnosis by a Sample of Parents of Sickle Cell Anemia Patients in Cameroon (Sub-Saharan Africa) (2011) (18)
- Current needs for human and medical genomics research infrastructure in low and middle income countries (2016) (18)
- A call for policy action in sub-Saharan Africa to rethink diagnostics for pregnancy affected by sickle cell disease: differential views of medical doctors, parents and adult patients predict value conflicts in Cameroon. (2014) (18)
- Evolutionary history of sickle-cell mutation: implications for global genetic medicine (2021) (18)
- Dissecting in silico Mutation Prediction of Variants in African Genomes: Challenges and Perspectives (2019) (18)
- Do solidarity and reciprocity obligations compel African researchers to feedback individual genetic results in genomics research? (2020) (17)
- Genetic modifiers of long‐term survival in sickle cell anemia (2020) (17)
- Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease (2016) (17)
- Coinheritance of sickle cell anemia and α‐thalassemia delays disease onset and could improve survival in cameroonian's patients (Sub‐Saharan Africa) (2014) (17)
- GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon (2019) (17)
- Implementing Artificial Intelligence and Digital Health in Resource-Limited Settings? Top 10 Lessons We Learned in Congenital Heart Defects and Cardiology. (2020) (17)
- Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa. (2018) (16)
- Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports from Cameroon (2014) (16)
- Personalized Herbal Medicine? A Roadmap for Convergence of Herbal and Precision Medicine Biomarker Innovations. (2018) (16)
- Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa (2019) (16)
- Letter to the editor regarding "GJB2, GJB6 or GJA1 genes should not be investigated in routine in non syndromic deafness in people of sub-Saharan African descent". (2015) (15)
- Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana (2018) (15)
- Post genome-wide association analysis: dissecting computational pathway/network-based approaches (2019) (14)
- Biomedical research, a tool to address the health issues that affect African populations (2013) (14)
- Association of Genetic Polymorphisms of TGF-β1, HMOX1, and APOL1 With CKD in Nigerian Patients With and Without HIV. (2020) (14)
- Stroke may appear to be rare in Saudi‐Arabian and Nigerian children with sickle cell disease, but not in Cameroonian sickle cell patients (2006) (14)
- Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden (2020) (13)
- Chemoresistance to Cancer Treatment: Benzo-α-Pyrene as Friend or Foe? (2018) (12)
- A Global Health Diagnostic for Personalized Medicine in Resource-Constrained World Settings: A Simple PCR-RFLP Method for Genotyping CYP2B6 g.15582C>T and Science and Policy Relevance for Optimal Use of Antiretroviral Drug Efavirenz. (2015) (12)
- Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harm (2020) (12)
- Turner syndrome in diverse populations (2019) (12)
- Hearing Impairment Overview in Africa: the Case of Cameroon (2020) (12)
- African Lettuce (Launaea taraxacifolia) Displays Possible Anticancer Effects and Herb-Drug Interaction Potential by CYP1A2, CYP2C9, and CYP2C19 Inhibition. (2016) (12)
- Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome (2013) (12)
- Establishing a Multi-Country Sickle Cell Disease Registry in Africa: Ethical Considerations (2019) (12)
- Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome (2012) (11)
- Noonan Syndrome in South Africa: Clinical and Molecular Profiles (2019) (11)
- Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients (2015) (11)
- SickleInAfrica. (2020) (11)
- 35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts. (1999) (11)
- Initiation of prenatal genetic diagnosis of sickle cell anaemia in Cameroon (sub‐Saharan Africa) (2011) (10)
- Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. (2013) (10)
- Sickle cell disease: tipping the balance of genomic research to catalyse discoveries in Africa (2017) (10)
- Features of Turner syndrome among a group of Cameroonian patients (2015) (10)
- Warfarin Dose and CYP2C Gene Cluster: An African Ancestral-Specific Variant Is a Strong Predictor of Dose in Black South African Patients. (2019) (9)
- A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing. (2017) (9)
- The Genetics of Warfarin Dose-Response Variability in Africans: An Expert Perspective on Past, Present, and Future. (2019) (9)
- UCT's contribution to medical genetics in Africa - from the past into the future. (2012) (9)
- Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation? (2014) (9)
- Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon (2015) (9)
- Discordant encephalocele in monozygotic twins (2006) (9)
- The University of Cape Town's contribution to medical genetics in Africa: from the past into the future (2012) (8)
- Profiling of warfarin pharmacokinetics‐associated genetic variants: Black Africans portray unique genetic markers important for an African specific warfarin pharmacogenetics‐dosing algorithm (2021) (8)
- Neurological Complications in Subjects With Sickle Cell Disease or Trait: Genetic Results From Mali. (2017) (8)
- Science must overcome its racist legacy: Nature’s guest editors speak (2022) (8)
- The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research (2019) (7)
- Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes (2022) (7)
- Public Health Burden of Hearing Impairment and the Promise of Genomics and Environmental Research: A Case Study in Ghana, Africa. (2017) (7)
- Waardenburg syndrome in childhood deafness in Cameroon (2014) (7)
- Frequency variation among sub-Saharan populations in virus restriction gene, BST-2 proximal promoter polymorphisms: implications for HIV-1 prevalence differences among African countries. (2014) (7)
- P1481: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES (2021) (7)
- Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana (2022) (7)
- The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon. (2017) (7)
- Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment (2020) (7)
- Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa) (2020) (7)
- Perceptions of parents of children with hearing loss of genetic origin in South Africa (2018) (6)
- Strengthening human genetics research in Africa: report of the 9th meeting of the African Society of Human Genetics in Dakar in May 2016 (2017) (6)
- Peripartum cardiomyopathy and familial dilated Cardiomyopathy: a tale of two cases. (2013) (6)
- Exploring the Role of Shared Decision Making in the Consent Process for Pediatric Genomics Research in Cameroon, Tanzania, and Ghana (2019) (6)
- Importance of Including Non-European Populations in Large Human Genetic Studies to Enhance Precision Medicine. (2022) (6)
- Urethral duplication in a 12-year-old child. (2011) (6)
- Translating biotechnology to knowledge-based innovation, peace, and development? Deploy a Science Peace Corps--an open letter to world leaders. (2014) (6)
- Frequencies of Single Nucleotide Polymorphisms in Cytochrome P450 Genes (CYP1A2, 2A6, 2B6, 3A4 and 3A5) in a Rwandan Population: Difference to Other African Populations (2013) (6)
- Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon (2020) (6)
- "Pain is Subjective": A Mixed-Method Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease across Three Countries. (2020) (6)
- Genetic variation in toll like receptors 2, 7, 9 and interleukin-6 is associated with cytomegalovirus infection in late pregnancy (2020) (6)
- Prenatal diagnosis may represent a point of entry of genetic science in sub‐Saharan Africa: a survey on the attitudes of medical students and physicians from Cameroon (2006) (6)
- The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications (2020) (5)
- Pyle metaphyseal dysplasia in an African child: Case report and review of the literature. (2016) (5)
- Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care. (2021) (5)
- Sickle cell disease is a global prototype for integrative research and healthcare (2020) (5)
- MECP2 duplication syndrome in a patient from Cameroon (2020) (5)
- Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations (2022) (5)
- Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon (2021) (5)
- Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana (2020) (5)
- The Sickle Cell Disease Ontology: enabling universal sickle cell-based knowledge representation (2019) (5)
- Beta-globin gene haplotypes and selected Malaria-associated variants among black Southern African populations (2017) (5)
- Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon. (2010) (4)
- Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment (2021) (4)
- Is there a role for pharmacogenetics in the treatment of sickle cell disease? (2017) (4)
- GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana (2020) (4)
- Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon (2016) (4)
- Introducing in AJMG Part A: Case reports in diverse populations (2018) (4)
- Polymorphism at BCL11A compared to HBS1L-MYB loci explains less of the variance in HbF in patients with sickle cell disease in Cameroon. (2015) (4)
- Systematic Review of the Economic Evaluation of Returning Incidental Findings in Genomic Research (2021) (4)
- Five Priorities of African Genomics Research: The Next Frontier. (2022) (3)
- Using the Drama of DNA approach to community engagement in genomic research in South Africa: experiences and lessons learnt (2020) (3)
- Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment (2020) (3)
- Considerations of Autonomy in Guiding Decisions around the Feedback of Individual Genetic Research Results from Genomics Research: Expectations of and Preferences from Researchers in Botswana (2022) (3)
- Effects of vaccines in patients with sickle cell disease: a systematic review protocol (2018) (3)
- A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family (2021) (3)
- Building Skills and Resources for Genomics, Epigenetics, and Bioinformatics Research for Africa: Report of the Joint 11th Conference of the African Society of Human Genetics and 12th H3Africa Consortium, 2018 (2020) (3)
- Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review (2022) (3)
- IHP-PING - generating integrated human protein-protein interaction networks on-the-fly (2020) (3)
- Hearing loss and brain disorders: A review of multiple pathologies (2021) (3)
- DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles (2020) (3)
- Participants’ Preferences and Reasons for Wanting Feedback of Individual Genetic Research Results From an HIV-TB Genomic Study: A Case Study From Botswana (2021) (3)
- Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa. (2016) (3)
- Ending racism is key to better science: a message from Nature’s guest editors (2022) (3)
- GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal (2022) (3)
- Genetic Determinants of Dyslipidemia in African-Based Populations: A Systematic Review. (2018) (3)
- A potential roadmap to overcome the current eastern DRC Ebola virus disease outbreak: From a computational perspective (2020) (3)
- Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali (2021) (3)
- Clinical Spectrum of congenital heart defects (CHD) detected at the child health Clinic in a Tertiary Health Facility in Ghana: a retrospective analysis (2020) (3)
- “Iron”ing out hemophagocytosis through PIEZO1 (2021) (2)
- Inauguration of the Cameroonian Society of Human Genetics (2009) (2)
- Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study. (2021) (2)
- Urinary Transforming Growth Factor-Beta 1 (uTGF-β1) and Prevalent CKD Risk in HIV-Positive Patients in West Africa (2019) (2)
- Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in SORBS2 and SCL11A1 Genes (2022) (2)
- A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family (2021) (2)
- SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon (2017) (2)
- Burden, genotype and phenotype profiles of adult patients with sickle cell disease in Cape Town, South Africa. (2017) (2)
- An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine. (2016) (2)
- Investigations of Kidney Dysfunction-Related Gene Variants in Sickle Cell Disease Patients in Cameroon (Sub-Saharan Africa) (2021) (2)
- GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali (2022) (2)
- Hearing loss in Africa: current genetic profile (2021) (2)
- Sickle Cell Disease. (2017) (2)
- Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana (2020) (2)
- Epistemic justice, African values and feedback of findings in African genomics research (2022) (2)
- Implementation science research for the scale-up of evidence-based interventions for sickle cell disease in africa: a commentary (2021) (2)
- Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies (2020) (2)
- Factors associated with blood pressure variation in sickle cell disease patients: a systematic review and meta-analyses (2022) (1)
- Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families (2022) (1)
- Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review. (2022) (1)
- Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example (2022) (1)
- Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening (2022) (1)
- Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment (2023) (1)
- Skills Capacity Building For Health Care Services and Research Through the Sickle Pan African Research Consortium (2022) (1)
- South African student protests, 2015 - 2016: The aftermath viewed through Medical Science Honours students at the University of Cape Town. (2017) (1)
- The Implementation of Laboratory Information Management System in Multi-Site Genetics Study in Africa: The Challenges and Up-Scaling Opportunities (2022) (1)
- Collect more data from Africa to improve gene therapy (2021) (1)
- Genomic newborn screening: public health policy considerations and recommendations (2017) (1)
- Birth Defects and Genetic Disease in Sub-Saharan Africa (2019) (1)
- Should institutions fund the feedback of individual findings in genomic research? (2022) (1)
- . The Burden of Birth Defects and Genetic Disease in Sub-Saharan Africa (2012) (1)
- “Black Lives Matter and Black Research Matters”: the African Society of Human Genetics’ call to halt racism in science (2022) (1)
- Investigating the missing heritability of fetal haemoglobin level in Africa (2020) (1)
- Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica (2021) (1)
- Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon (2012) (0)
- Comparative Analysis of Mobile Pain Management Applications in Developed versus Developing Countries (Preprint) (2021) (0)
- SUN-197 GENETIC POLYMORPHISMS OF TGF-beta-1 ARE NOT ASSOCIATED WITH CKD IN PATIENTS WITH HIV-RELATED NEPHROPATHIES IN EXTREME SOUTHERN NIGERIA (2019) (0)
- The future of sickle cell disease therapeutics rests in genomics (2023) (0)
- Participant views on practical considerations for feedback of individual genetic research results: a case study from Botswana (2023) (0)
- Genetic variation in toll like Receptor 2, 7, 9 and interleukin-6 influences risk of Cytomegalovirus infection in pregnancy (2020) (0)
- Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome (2012) (0)
- New mutations predict clinical manifestation of complex traits (2022) (0)
- Corrigendum to A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family (2021) (0)
- Modelling the mortality of sickle cell disease in Africa. (2021) (0)
- S125: THE ROLE OF THE MICROBIOME AS A SICKLE CELL DISEASE MODIFIER: AN EXPERT REVIEW (2022) (0)
- Cover Image, Volume 173A, Number 9, September 2017. (2017) (0)
- Are abdominal wall defects and external genitalia anomalies randomly expressed in some families? (2011) (0)
- Variants of LRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy (2023) (0)
- Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community (2021) (0)
- Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica (2023) (0)
- Clinical characteristics and outcome of familial and idiopathic dilated cardiomyopathy in South Africa : a case-comparison study (2011) (0)
- Contents Vol. 5, 2014 (2014) (0)
- Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. (2023) (0)
- Childhood Hearing Impairment in Senegal (2023) (0)
- PO01-MO-22 The risk of stroke in sickle cell subjects in Cameroon: the first report (2009) (0)
- Cystic fibrosis: the urgent need to report on mutations among patients of African descent (2016) (0)
- An Integrated Platform Supporting Semantic Similarity Score Calculation and Reproducibility (2021) (0)
- 5610131 A STANDARDISED LANGUAGE TAG PROTOCOL AND WORKFLOW FOR DEVELOPING AND MANAGING MULTILINGUAL ONTOLOGIES: SHOWCASING THE FRENCH SICKLE CELL DISEASE ONTOLOGY (SCDO) (2023) (0)
- P117: THE INTERNATIONAL HAEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HAEMOGLOBINOPATHIES (2022) (0)
- RETRACTED ARTICLE: Gender Testing in Sport: The Right of Genetic Diversity and the Right to Not Be Harmed (2011) (0)
- Preferences and expectations of feedback of individual genetic research results in African genomics: Views of South African parents of children with neurodevelopmental disorders [version 1; peer review: awaiting peer review] (2022) (0)
- L'expression forcée de la connexine 32 (Cx32) par les cellules β cause une augmentation post-natale du pancréas endocrine (2003) (0)
- Human slc11a1 Gene Polymorphism Has the Propensity to Confer Susceptibility to M. Africanum TB Disease in Ghana (2020) (0)
- Addressing exploitation and inequities in open science: A relational perspective. (2022) (0)
- The Sickle Cell Disease Ontology: recent development and expansion of the universal sickle cell knowledge representation (2022) (0)
- Leveraging our common African origins to understand human evolution and health (2023) (0)
- Should Feedback of Individual Results be Integrated into the Consent Process in African Genomics? Participants’ Views from an HIV-TB Genomics Research Project in Botswana (2021) (0)
- SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon (2017) (0)
- Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. (2022) (0)
- Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registry (2022) (0)
- WCN23-0839 CHRONIC KIDNEY DISEASE-RELATED SINGLE NUCLEOTIDE POLYMORPHISMS (SNPs) AMONG ADULT WEST AFRICANS WITH AND WITHOUT HIV (2023) (0)
- Genomic medicine in Africa: promise, problems and prospects (2014) (0)
- Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection (2021) (0)
- Knowledge and Challenges Associated With Hearing Impairment in Affected Individuals From Cameroon (Sub-Saharan Africa) (2021) (0)
- Preferences and Expectations of Feedback of Individual Genetic Research Results in African Genomics: Views of South African Parents of Children With Neurodevelopmental Conditions (2020) (0)
- Beyond Race: A Wake-up Call for Drug Therapy Informed by Genotyping (2022) (0)
- Hearing loss in Africa: current genetic profile (2021) (0)
- Hemoglobinopathies in Africa (2012) (0)
- Success stories in genomic medicine from resource-limited countries (2015) (0)
- Returning incidental findings in African genomics research (2019) (0)
- Development of the sickle Pan-African research consortium registry in Tanzania: opportunity to harness data science for sickle cell disease (2023) (0)
- 5612560 A MONITORING AND EVALUATION FRAMEWORK AND ASSOCIATED TOOLS FOR THE SICKLEINAFRICA CONSORTIUM (2023) (0)
- Biomarkers of sickle cell nephropathy in Senegal (2022) (0)
- Examining Experiences of Acute and Chronic Pain Among Individuals with Sickle Cell Disease (SCD) in Jamaica and Cameroon (2021) (0)
- Genomic Medicine in Developing Countries and Resource-Limited Environments (2017) (0)
- Unique Profile of Pharmacogenetics Variants Associated With Warfarin Response In Black Africans: Looking Beyond VKORC1 and CYP2C9 Polymorphisms (2018) (0)
- Perceptions of parents of children with hearing loss of genetic origin in South Africa (2018) (0)
- Craniofacial, dental, and molecular features of Pyle disease in a South African child (2022) (0)
- Clinical characteristics and risk factors of relative systemic hypertension and hypertension among sickle cell patients in Cameroon (2022) (0)
- Development and Implementation of the Sickle Cell Disease Ontology (2019) (0)
- Elucidating Biological Roles of Novel Murine Genes in Hearing Impairment in Africa (2019) (0)
- Competency-based Training Needs Assessment for Research Managers and Administrators in Africa and the United Kingdom to Strengthen Equitable Partnerships (2022) (0)
- High-depth African genomes inform human migration and health (2020) (0)
- Explanatory models for the cause of Fragile X Syndrome in rural Cameroon (2021) (0)
- Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection (2021) (0)
- A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family (2022) (0)
- An Open Letter in Support of Transformative Biotechnology and Social Innovation: SANKO University Innovation Summit in Medicine and Integrative Biology, Gaziantep, Turkey, May 5-7, 2016. (2016) (0)
- A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana (2022) (0)
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