Ambroise Wonkam universitaire camerounais
Wonkam, Ambroise, 19..-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 94157340593309920586 ( Personal )
Permalink: http://viaf.org/viaf/94157340593309920586
Preferred Forms
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
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| Drépanocytose et polymorphismes génétiques : épidémiologie, prédiction de gravité et stress-oxydant |
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| Features of Turner syndrome among a group of Cameroonian patients. |
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| Frequencies of Single Nucleotide Polymorphisms in Cytochrome P450 Genes (CYP1A2, 2A6, 2B6, 3A4 and 3A5) in a Rwandan Population: Difference to Other African Populations |
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| Frequency and clinical genetics of familial dilated cardiomyopathy in Cape Town: implications for the evaluation of patients with unexplained cardiomyopathy |
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| Genetic Determinants of Dyslipidemia in African-Based Populations: A Systematic Review |
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| Genetic modifiers of long-term survival in sickle cell anemia |
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| Genetic variation in toll like receptors 2, 7, 9 and interleukin-6 is associated with cytomegalovirus infection in late pregnancy |
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| Genetics of hearing loss in Africans: use of next generation sequencing is the best way forward |
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| The Genetics of Warfarin Dose-Response Variability in Africans: An Expert Perspective on Past, Present, and Future |
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| Genomic medicine in Africa: promise, problems and prospects |
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| Genomic Medicine Without Borders: Which Strategies Should Developing Countries Employ to Invest in Precision Medicine? A New "Fast-Second Winner" Strategy. |
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| Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa |
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| GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon |
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| Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review |
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| The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research |
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| Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome |
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| Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa. |
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| IHP-PING-generating integrated human protein-protein interaction networks on-the-fly |
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| Implementing Artificial Intelligence and Digital Health in Resource-Limited Settings? Top 10 Lessons We Learned in Congenital Heart Defects and Cardiology |
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| In Vitro Reversible and Time-Dependent CYP450 Inhibition Profiles of Medicinal Herbal Plant Extracts Newbouldia laevis and Cassia abbreviata: Implications for Herb-Drug Interactions. |
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| 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. |
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| Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon. |
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| Introducing in AJMG Part A: Case reports in diverse populations |
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| Investigating the missing heritability of foetal haemoglobin level in Africa |
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| Is there a role for pharmacogenetics in the treatment of sickle cell disease? |
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| 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". |
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| Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies |
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| Low hepatitis B vaccine uptake among surgical residents in Cameroon |
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| Management of neural tube defects in a Sub-Saharan African country: the situation in Yaounde, Cameroon. |
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| MECP2 duplication syndrome in a patient from Cameroon |
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| Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community |
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| Neurological Complications in Subjects With Sickle Cell Disease or Trait: Genetic Results From Mali. |
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| New mutations predict clinical manifestation of complex traits |
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| Noonan Syndrome in South Africa: Clinical and Molecular Profiles |
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| A novel variant in <i>DMXL2</i> gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family |
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| 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. |
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| Perceptions of parents of children with hearing loss of genetic origin in South Africa |
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| Personalized Herbal Medicine? A Roadmap for Convergence of Herbal and Precision Medicine Biomarker Innovations |
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| Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon |
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| Pharmacogenomics Implications of Using Herbal Medicinal Plants on African Populations in Health Transition |
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| Polymorphism at BCL11A compared to HBS1L-MYB loci explains less of the variance in HbF in patients with sickle cell disease in Cameroon. |
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| Post genome-wide association analysis: dissecting computational pathway/network-based approaches. |
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| Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome |
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| 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 |
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| Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease |
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| Public Health Burden of Hearing Impairment and the Promise of Genomics and Environmental Research: A Case Study in Ghana, Africa. |
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| Ready to put metadata on the post-2015 development agenda? Linking data publications to responsible innovation and science diplomacy |
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| Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon |
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| Research capacity. Enabling the genomic revolution in Africa |
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| The road ahead in genetics and genomics |
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| The role of CFTR and SPINK-1 mutations in pancreatic disorders in HIV-positive patients: a case-control study. |
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| The Role of Tumor Microenvironment in Chemoresistance: 3D Extracellular Matrices as Accomplices |
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| Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana |
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| 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 |
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| Sickle cell disease and genetic polymorphisms : epidemiology, prediction of severity and oxidative stress. |
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| Sickle cell disease in Africa: an urgent need for longitudinal cohort studies |
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| The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications |
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| The Sickle Cell Disease Ontology: recent development and expansion of the universal sickle cell knowledge representation |
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| Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis |
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| Sickle cell disease: tipping the balance of genomic research to catalyse discoveries in Africa |
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| SickleInAfrica |
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| Stakeholder Perspectives on Public Health Genomics Applications for Sickle Cell Disease: A Methodology for a Human Heredity and Health in Africa (H3Africa) Qualitative Research Study. |
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| Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harm |
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| Stroke may appear to be rare in Saudi-Arabian and Nigerian children with sickle cell disease, but not in Cameroonian sickle cell patients. |
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| Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon. |
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| Success stories in genomic medicine from resource-limited countries |
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| Systematic Review of the Economic Evaluation of Returning Incidental Findings in Genomic Research |
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| Translating biotechnology to knowledge-based innovation, peace, and development? Deploy a Science Peace Corps--an open letter to world leaders |
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| Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation? |
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| UCT's contribution to medical genetics in Africa - from the past into the future |
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| Urethral duplication in a 12-year-old child. |
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| Urinary Transforming Growth Factor-Beta 1 (uTGF-β1) and Prevalent CKD Risk in HIV-Positive Patients in West Africa |
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| Warfarin Dose and CYP2C Gene Cluster: An African Ancestral-Specific Variant Is a Strong Predictor of Dose in Black South African Patients |
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| Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment |
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| 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 |
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| Williams–Beuren syndrome in diverse populations |
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| Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon |
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