Azeez Butali

ORCID, self-asserted

ORCID 0000-0002-1229-5964

Publications

Citations

203

h-index

Computed over the works the graph holds, so it is a floor rather than a career figure.

i10-index

Publications

18 works in the graph, newest first.

Understanding and participation in genetics research among Nigerian mothers of children with orofacial cleft: a qualitative study of prior genetic study participants
2026BMC Oral HealthJournalOpen accessSenior authorCorresponding0 citations10.1186/s12903-026-09285-4
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
2025The American Journal of Human GeneticsJournalOpen access4 citations10.1016/j.ajhg.2025.08.008
Assessing the Psychosocial Impacts of Whole-Genome Sequencing Outcomes on Orofacial Cleft Caregivers in Nigeria: A Mixed-Methods Study
2025The Cleft Palate-Craniofacial JournalJournalSenior authorCorresponding3 citations10.1177/10556656251332351
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios
2025The American Journal of Human GeneticsJournalOpen access3 citations10.1016/j.ajhg.2025.09.009
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk
2025PLoS GeneticsJournalOpen access2 citations10.1371/journal.pgen.1011581
Pathogenic FANCC Variants Are Associated with Accessory Breasts in a Sub-Saharan African Multiplex Family
2025Current Issues in Molecular BiologyJournalOpen access2 citations10.3390/cimb47110875
Pharmacogenomics in Orofacial Clefts Care: Insights from Whole-Genome Sequencing of Case-Parents Trios
2025Journal of Personalized MedicineJournalOpen access1 citations10.3390/jpm15100456
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research
2024BMC Public HealthJournalOpen accessSenior authorCorresponding8 citations10.1186/s12889-024-17987-z
Rare variants analyses suggest novel cleft genes in the African population
2024Scientific ReportsJournalOpen accessSenior authorCorresponding7 citations10.1038/s41598-024-65151-9
Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa
2024AJOB Empirical BioethicsJournalOpen accessSenior authorCorresponding6 citations10.1080/23294515.2024.2302993
Shared genetic risk between major orofacial cleft phenotypes in an African population
2024Genetic EpidemiologyJournalOpen accessSenior author6 citations10.1002/gepi.22564
Genome-wide study of gene-by-sex interactions identifies risks for cleft palate
2024Human GeneticsJournalOpen access5 citations10.1007/s00439-024-02704-y
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate
2023Human Genetics and Genomics AdvancesJournalOpen access14 citations10.1016/j.xhgg.2023.100234
Clinically actionable secondary findings in 130 triads from sub‐Saharan African families with non‐syndromic orofacial clefts
2023Molecular Genetics & Genomic MedicineJournalOpen accessSenior authorCorresponding5 citations10.1002/mgg3.2237
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature
2023American Journal of Medical Genetics Part AJournalOpen access3 citations10.1002/ajmg.a.63130
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate
2022Scientific ReportsJournalOpen accessSenior authorCorresponding40 citations10.1038/s41598-022-15885-1
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate
2022The Cleft Palate-Craniofacial JournalJournalOpen accessSenior authorCorresponding6 citations10.1177/10556656221135926
Investigating the relationship between cancer and orofacial clefts using GWAS significant loci for cancers: A case-control and case-triad study
2022Frontiers in Oral HealthJournalOpen accessSenior author2 citations10.3389/froh.2022.915361