|
| 36384317 | Damaging Mutations in <b><i>AFDN</i></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate. | Cleft Palate Craniofac J | 2024 |
| 36384317 | Damaging Mutations in <b><i>AFDN</i></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate. | Cleft Palate Craniofac J | 2024 |
| 38009642 | Sickle cell allele HBB-rs334(T) is associated with decreased risk of childhood Burkitt lymphoma in East Africa. | Am J Hematol | 2024 |
| 38009642 | Sickle cell allele HBB-rs334(T) is associated with decreased risk of childhood Burkitt lymphoma in East Africa. | Am J Hematol | 2024 |
| 36112944 | Paediatric paranasal sinus fibrous dysplasia. | Trop Doct | 2023 |
| 36112944 | Paediatric paranasal sinus fibrous dysplasia. | Trop Doct | 2023 |
| 36301051 | Hajdu-Cheney syndrome with atypical cardiovascular abnormalities. | Am J Med Genet A | 2023 |
| 37598069 | Genes, environment, and African ancestry in cardiometabolic disorders. | Trends Endocrinol Metab | 2023 |
| 37653728 | Universal genome-wide association studies: Powerful joint ancestry and association testing. | HGG Adv | 2023 |
| 38049854 | Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of β-cell function and insulin sensitivity in Africans without type 2 diabetes. | Genome Med | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 36649705 | Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI. | Am J Hum Genet | 2023 |
| 36950382 | Leveraging our common African origins to understand human evolution and health. | Cell Genom | 2023 |
| 37004336 | Ancestral and environmental patterns in the association between triglycerides and other cardiometabolic risk factors. | EBioMedicine | 2023 |
| 37313780 | Ambiguous genitalia, giant congenital melanocytic nevus and subpulmonic outlet ventricular septal defect in an African child with Neurofibromatosis 1. | Am J Med Genet A | 2023 |
| 36791658 | Epigenome-wide association study of plasma lipids in West Africans: the RODAM study. | EBioMedicine | 2023 |
| 37496383 | Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts. | Mol Genet Genomic Med | 2023 |
| 37598069 | Genes, environment, and African ancestry in cardiometabolic disorders. | Trends Endocrinol Metab | 2023 |
| 37653728 | Universal genome-wide association studies: Powerful joint ancestry and association testing. | HGG Adv | 2023 |
| 38049854 | Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of β-cell function and insulin sensitivity in Africans without type 2 diabetes. | Genome Med | 2023 |
| 37496383 | Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts. | Mol Genet Genomic Med | 2023 |
| 36950382 | Leveraging our common African origins to understand human evolution and health. | Cell Genom | 2023 |
| 37313780 | Ambiguous genitalia, giant congenital melanocytic nevus and subpulmonic outlet ventricular septal defect in an African child with Neurofibromatosis 1. | Am J Med Genet A | 2023 |
| 37004336 | Ancestral and environmental patterns in the association between triglycerides and other cardiometabolic risk factors. | EBioMedicine | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 36649705 | Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI. | Am J Hum Genet | 2023 |
| 36791658 | Epigenome-wide association study of plasma lipids in West Africans: the RODAM study. | EBioMedicine | 2023 |
| 36301051 | Hajdu-Cheney syndrome with atypical cardiovascular abnormalities. | Am J Med Genet A | 2023 |
| 34061439 | Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. | Oral Dis | 2022 |
| 35657990 | Additive genetic effect of GCKR, G6PC2, and SLC30A8 variants on fasting glucose levels and risk of type 2 diabetes. | PLoS One | 2022 |
| 35836279 | An epigenome-wide association study of insulin resistance in African Americans. | Clin Epigenetics | 2022 |
| 35513726 | Polygenic risk scores for CARDINAL study. | Nat Genet | 2022 |
| 36347891 | Mendelian randomization study reveals a causal relationship between adiponectin and LDL cholesterol in Africans. | Sci Rep | 2022 |
| 35817949 | Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate. | Sci Rep | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35405984 | Vitamin D Deficiency and Its Association with Iron Deficiency in African Children. | Nutrients | 2022 |
| 36938080 | Cardiovascular Risk Factor Burden and Association With CKD in Ghana and Nigeria. | Kidney Int Rep | 2022 |
| 34061439 | Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. | Oral Dis | 2022 |
| 35210285 | Beta-cell dysfunction and insulin resistance in relation to abnormal glucose tolerance in African populations: can we afford to ignore the diversity within African populations? | BMJ Open Diabetes Res Care | 2022 |
| 34382870 | Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P). | Cleft Palate Craniofac J | 2022 |
| 35015074 | Polygenic Prediction of Type 2 Diabetes in Africa. | Diabetes Care | 2022 |
| 35303470 | The Lancet Nigeria Commission: investing in health and the future of the nation. | Lancet | 2022 |
| 34689653 | Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. | J Dent Res | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35405984 | Vitamin D Deficiency and Its Association with Iron Deficiency in African Children. | Nutrients | 2022 |
| 35836279 | An epigenome-wide association study of insulin resistance in African Americans. | Clin Epigenetics | 2022 |
| 35817949 | Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate. | Sci Rep | 2022 |
| 35657990 | Additive genetic effect of GCKR, G6PC2, and SLC30A8 variants on fasting glucose levels and risk of type 2 diabetes. | PLoS One | 2022 |
| 35513726 | Polygenic risk scores for CARDINAL study. | Nat Genet | 2022 |
| 36938080 | Cardiovascular Risk Factor Burden and Association With CKD in Ghana and Nigeria. | Kidney Int Rep | 2022 |