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Gerrye Lumbono Mubungu

Observed names: G Mubungu, G Mubungu Lumbono, G. Mubungu, Gerrye Mubungu, Gerrye Mubungu Lumbono, Mubungu, Gerrye
ORCID: 0000-0002-8870-0575
Observed ORCID: 0000-0002-8870-0575
OpenAlex ID: A5049677201
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator
2016 · A. Lumaka, N. Cosemans, et al. · Clinical Genetics · 82
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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
2022 · Aimé Lumaka, Nadia Carstens, et al. · Orphanet Journal of Rare Diseases · 54
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The impact of clinical genome sequencing in a global population with suspected rare genetic disease
2024 · Erin Thorpe, Taylor Williams, et al. · The American Journal of Human Genetics · 25
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The status of emergency obstetric and newborn care in post-conflict eastern DRC: a facility-level cross-sectional study
2021 · Serge-André Mizerero, Calistus Wilunda, et al. · Conflict and Health · 17
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Clinical presentation and evolution of Xia‐Gibbs syndrome due to p.Gly375ArgfsTer3 variant in a patient from DR Congo (Central Africa)
2020 · Gerrye Mubungu, Prince Makay, et al. · American Journal of Medical Genetics Part A · 15
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
2020 · Gerrye Mubungu, Prince Makay, et al. · American Journal of Medical Genetics Part A · 15
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Williams–Beuren syndrome: pitfalls for diagnosis in limited resources setting
2016 · Aimé Lumaka, Rita Lukoo, et al. · Clinical Case Reports · 14
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A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family
2014 · Aimé Lumaka, Gerrye Mubungu, et al. · European Journal of Medical Genetics · 11
Enriching African genome representation through the AGenDA project
2026 · M. Ramsay, H. Etheredge, et al. · Nature · 9
A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo
2018 · Aimé Lumaka, Valerie Race, et al. · American Journal of Medical Genetics Part A · 8
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Skinfold over toenail is pathognomonic for the popliteal pterygium syndrome in a Congolese family with large intrafamilial variability
2014 · Gerrye Mubungu, Aimé Lumaka, et al. · Clinical Case Reports · 8
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X-linked adrenal hypoplasia congenita: a novel DAX1 missense mutation and challenges for clinical diagnosis in Africa
2011 · Aimé Lumaka, Gerrye Mubungu, et al. · European Journal of Pediatrics · 8
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Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease
2025 · Alka Malhotra, Erin Thorpe, et al. · Human Genetics and Genomics Advances · 7
Phenotype and growth in Sotos syndrome patient from DR Congo (Central Africa)
2020 · Gerrye Mubungu, Guy Lukute, et al. · American Journal of Medical Genetics Part A · 5
Morphological characterization of newborns in Kinshasa, DR Congo: Common variants, minor, and major anomalies
2020 · Gerrye Mubungu, Aimé Lumaka, et al. · American Journal of Medical Genetics Part A · 5
Usefulness of automated image analysis for recognition of the fragile X syndrome gestalt in Congolese subjects
2023 · Toni Kasole Lubala, Tony Kayembe-Kitenge, et al. · European Journal of Medical Genetics · 4
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Automated Evaluation of D‐Score for Facial Dysmorphism Analysis in Central African Children With Developmental Disorders
2025 · Prince Makay, Gerrye Mubungu, et al. · Annals of Human Genetics · 3
First Insights Into the Phenotype and Genotype of Inherited Retinal Disorders in the Democratic Republic of Congo (DRC)
2025 · Nadine Nsiangani Lusambo, Patrick Fuanani, et al. · Annals of Human Genetics · 2
Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population‐specific measurements
2022 · Gerrye Mubungu, Mathieu Roelants, et al. · American Journal of Medical Genetics Part A · 2
Editorial: Les gènes et la maladie
2022 · Gerrye Lumbono Mubungu · Annales Africaines de Medecine · 2
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PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing
2022 · Prince Makay, Gerrye Mubungu, et al. · American Journal of Medical Genetics Part A · 1
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Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders—the DDD-Africa study
2026 · Nadja Louw, Prince Makay, et al. · European Journal of Human Genetics
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A Novel Random Forest Algorithm-Based Prediction Model for in-Hospital Mortality Risk in Congolese Children with Severe Malaria
2026 · Ken Bisabu Kelu, Vicky Mayifuila Niangi, et al. · Research Square
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Clinical Validation of the Lambaréné Organ Dysfunction Score (LODS) and its influence on Survival in Congolese children presenting with Severe Malaria
2026 · Ken Bisabu Kelu, Vicky Niangi Mayifuila, et al. · Annales Africaines de Medecine
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P161: Impact and evolution of a philanthropic global network providing clinical genomic testing*
2025 · Erin Venti, Diane Masser-Frye, et al. · Genetics in Medicine Open
Works count: 45
Citation count: 297
H-index: 9
I10-index: 8
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