16 May 20251cites
First Insights Into the Phenotype and Genotype of Inherited Retinal Disorders in the Democratic Republic of Congo (DRC)Publisher siteAnnals of Human Genetics, Retinal Development and Disorders
Active, last published 2026
In genomics and rare diseases
Patrick
Fuanani
Scholar“Research focused on Genomics and Rare Diseases and adjacent fields.”
Université de Kinshasa (UNIKIN)
DR Congo
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01 · About the work
What I study
atrick Fuanani is a researcher working on Genomics and Rare Diseases. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Patrick's work has been cited 2 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Genomics and Rare Diseases×2
04 · Where I am
Affiliations
Affiliation on published researchUniversity of Kinshasa, DR CongoDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
3 works10 Dec 2024Open access
Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literaturePublisher siteClinical Dysmorphology, Hedgehog Signaling Pathway Studies
7 Jun 2022Open access1cites
<scp>PERCHING</scp> syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencingPublisher siteAmerican Journal of Medical Genetics Part A, Genomics and Rare Diseases
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