Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

Aimé Lumaka, Nele Cosemans, Aimée Lulebo Mampasi, +14

Clinical Genetics

Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group

Aimé Lumaka, Nadia Carstens, Koenraad Devriendt, +9

Orphanet Journal of Rare Diseases

Dysmorphism and major anomalies are a main predictor of survival in newborns admitted to the neonatal intensive care unit in the Democratic Republic of Congo

Gerrye Mubungu, Prince Makay, Aimé Lumaka, +7

American Journal of Medical Genetics Part A

The impact of clinical genome sequencing in a global population with suspected rare genetic disease

Erin Thorpe, Taylor Williams, Chad A. Shaw, +61

The American Journal of Human Genetics

Williams–Beuren syndrome: pitfalls for diagnosis in limited resources setting

Aimé Lumaka, Rita Lukoo, Gerrye Mubungu, +5

Clinical Case Reports

The status of emergency obstetric and newborn care in post-conflict eastern DRC: a facility-level cross-sectional study

Serge-André Uwunva MIZERERO, Calistus Wilunda, Patou Masika Musumari, +4

Conflict and Health