Aimé Z Lumaka

24PUBLICATIONS
139CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiovascular medicine and haematology not elsewhere classifiedGenomicsNeurology and neuromuscular diseasesInfant and child health
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Publications (24)

|Feb 12, 2026
Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders - the DDD-Africa study.

Nadja Louw, Prince Makay, Phelelani T Mpangase

|Oct 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

|Sep 09, 2024
Defining and pursuing diversity in human genetic studies.

Maili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

|Nov 13, 2023
My Bantu vision of genomic medicine in Africa.

Aimé Lumaka

|Sep 05, 2023
Valuable insights into hereditary spinocerebellar degeneration from clusters of homozygosity in Africa.

Aimé Lumaka

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Frequent Collaborators

7 joint publications

Gerrye Mubungu

4 joint publications

Gloire Mbayabo

3 joint publications

Alain Verloes

3 joint publications

Prosper Tshilobo Lukusa