Concepedia

Author

Aimé Lumaka

University of KinshasaORCID

Also Known As

A Lumaka, A Zola, A. Lumaka, A. Zola, AIME LUMAKA, Aime Lumaka, Aimè Lumaka, Aimé LUMAKA, Aimé Lumaka, Aimé Lumaka Zola

120

Publications

682

Citations

15

H-Index

23

Concepts

All Affiliations

University of KinshasaUniversity of LiègeNational Institute of Biomedical ResearchKU LeuvenUniversidad Nacional Autónoma de México
AL

About

Aimé Lumaka is an author at University of Kinshasa specializing in medicine, psychiatry, and bioinformatics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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69

2

Public Health

1

1

22

3

Biostatistics

1

1

22

4

Critical Care Medicine

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1

25

5

Epidemiology

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22

Aimé Lumaka

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20

Publications

508

Citations

15

H-Index

YearCitations

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

Aimé Lumaka, Nele Cosemans, Aimée Lulebo Mampasi,

Clinical Genetics

2016

85

<scp><i>GREB1L</i></scp> variants in familial and sporadic hereditary urogenital adysplasia and <scp>Mayer‐Rokitansky‐Kuster‐Hauser</scp> syndrome

Adeline Jacquinet, Bouchra Boujemla, Corinne Fasquelle,

Clinical Genetics

2020

71

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,

Orphanet Journal of Rare Diseases

2022

46

Missense variants in <i>TAF1</i> and developmental phenotypes: Challenges of determining pathogenicity

Hanyin Cheng, Simona Capponi, Emma Wakeling,

Human Mutation

2019

28

Fragile X checklists: A meta‐analysis and development of a simplified universal clinical checklist

Toni Kasole Lubala, Aimé Lumaka, Gray Kanteng,

Molecular Genetics & Genomic Medicine

2018

25

Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours

Aimé Lumaka, Corinne Fasquelle, François‐Guillaume Debray,

International Journal of Molecular Sciences

2023

25

Variability in expression of a familial 2.79 Mb microdeletion in chromosome14q22.1–22.2

Aimé Lumaka, C. Van Hole, Ingele Casteels,

American Journal of Medical Genetics Part A

2012

22

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

Erin Rooney Riggs, Taylor I. Bingaman, Carrie-Ann Barry,

Genetics in Medicine

2022

22

Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International

Domenica Taruscio, Marco Salvatore, Aimé Lumaka,

Frontiers in Public Health

2023

22

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

Hellen Lesmann, Alexander Hustinx, Shahida Moosa,

2023

22

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