|
| 37889387 | Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries. | Qual Life Res | 2024 |
| 36256961 | Addressing exploitation and inequities in open science: A relational perspective. | Dev World Bioeth | 2023 |
| 37501718 | Editorial: Building capacity for sickle cell disease research and healthcare. | Front Genet | 2023 |
| 36950382 | Leveraging our common African origins to understand human evolution and health. | Cell Genom | 2023 |
| 36980833 | Childhood Hearing Impairment in Senegal. | Genes (Basel) | 2023 |
| 37270597 | Feeding back of individual genetic results in Botswana: mapping opportunities and challenges. | BMC Med Ethics | 2023 |
| 37063478 | Participant views on practical considerations for feedback of individual genetic research results: a case study from Botswana. | Glob Bioeth | 2023 |
| 36752565 | Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. | Hum Mol Genet | 2023 |
| 36815490 | The future of sickle cell disease therapeutics rests in genomics. | Dis Model Mech | 2023 |
| 36807241 | Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy. | Clin Genet | 2023 |
| 36712852 | Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica. | Front Genet | 2023 |
| 36833326 | Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment. | Genes (Basel) | 2023 |
| 34197280 | 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. | AJOB Empir Bioeth | 2022 |
| 35710317 | Should institutions fund the feedback of individual findings in genomic research? | J Med Ethics | 2022 |
| 35383424 | GJB1 variants in Charcot-Marie-Tooth disease X-linked type 1 in Mali. | J Peripher Nerv Syst | 2022 |
| 35383421 | Current profile of Charcot-Marie-Tooth disease in Africa: A systematic review. | J Peripher Nerv Syst | 2022 |
| 35676434 | Science must overcome its racist legacy: Nature's guest editors speak. | Nature | 2022 |
| 35441036 | 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. | Glob Health Epidemiol Genom | 2022 |
| 35440622 | Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes. | Commun Biol | 2022 |
| 35611053 | Effects of Senegal haplotype (<i>Xmn1</i>-rs7412844), alpha-thalassemia (3.7kb <i>HBA1/HBA2</i> deletion), <i>NPRL3</i>-rs11248850 and <i>BCL11A</i>-rs4671393 variants on sickle cell nephropathy. | Int J Biochem Mol Biol | 2022 |
| 35538368 | Variability exposes hidden buffering in the network specifying intestinal cell fate. | Nat Rev Genet | 2022 |
| 35698919 | A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family. | Mol Genet Genomic Med | 2022 |
| 35576571 | Five Priorities of African Genomics Research: The Next Frontier. | Annu Rev Genomics Hum Genet | 2022 |
| 35576557 | Importance of Including Non-European Populations in Large Human Genetic Studies to Enhance Precision Medicine. | Annu Rev Biomed Data Sci | 2022 |
| 35463879 | Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening. | Front Pediatr | 2022 |
| 35724383 | Beyond Race: A Wake-up Call for Drug Therapy Informed by Genotyping. | Ann Intern Med | 2022 |
| 35422501 | New mutations predict clinical manifestation of complex traits. | Nat Rev Genet | 2022 |
| 35363306 | The Sickle Cell Disease Ontology: recent development and expansion of the universal sickle cell knowledge representation. | Database (Oxford) | 2022 |
| 35783259 | Skills Capacity Building For Health Care Services and Research Through the Sickle Pan African Research Consortium. | Front Genet | 2022 |
| 35625523 | <i>GJB2</i> Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal. | Biology (Basel) | 2022 |
| 35862495 | "Black Lives Matter and Black Research Matters": the African Society of Human Genetics' call to halt racism in science. | Mol Biol Cell | 2022 |
| 36409722 | Biomarkers of sickle cell nephropathy in Senegal. | PLoS One | 2022 |
| 36406113 | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example. | Front Genet | 2022 |
| 36420448 | Competency-based Training Needs Assessment for Research Managers and Administrators in Africa and the United Kingdom to Strengthen Equitable Partnerships. | AAS Open Res | 2022 |
| 36138002 | Craniofacial, dental, and molecular features of Pyle disease in a South African child. | BDJ Open | 2022 |
| 36035115 | Cell-based analysis of <i>CLIC5A</i> and <i>SLC12A2</i> variants associated with hearing impairment in two African families. | Front Genet | 2022 |
| 36357908 | A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana. | BMC Med Genomics | 2022 |
| 35928290 | Clinical characteristics and risk factors of relative systemic hypertension and hypertension among sickle cell patients in Cameroon. | Front Med (Lausanne) | 2022 |
| 36261556 | Ending racism is key to better science: a message from Nature's guest editors. | Nature | 2022 |
| 36185769 | Epistemic justice, African values and feedback of findings in African genomics research. | Glob Bioeth | 2022 |
| 35041532 | Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review. | OMICS | 2022 |
| 35281803 | Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana. | Front Genet | 2022 |
| 35242163 | Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in <i>SORBS2</i> and <i>SCL11A1</i> Genes. | Front Genet | 2022 |
| 35209795 | Factors associated with blood pressure variation in sickle cell disease patients: a systematic review and meta-analyses. | Expert Rev Hematol | 2022 |
| 35336849 | Age Estimate of <i>GJB2</i>-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations. | Biology (Basel) | 2022 |
| 34609590 | Hearing loss in Africa: current genetic profile. | Hum Genet | 2022 |
| 32996353 | Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment. | Exp Biol Med (Maywood) | 2021 |
| 36618444 | Sickle cell disease is a global prototype for integrative research and healthcare. | Adv Genet (Hoboken) | 2021 |
| 36188771 | Knowledge and Challenges Associated With Hearing Impairment in Affected Individuals From Cameroon (Sub-Saharan Africa). | Front Rehabil Sci | 2021 |
| 33715530 | A novel variant in <i>DMXL2</i> gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. | Exp Biol Med (Maywood) | 2021 |