Annette Uwineza

1.2k total citations
28 papers, 195 citations indexed

About

Annette Uwineza is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Annette Uwineza has authored 28 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Annette Uwineza's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Annette Uwineza is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Annette Uwineza collaborates with scholars based in Rwanda, Belgium and United States. Annette Uwineza's co-authors include Léon Mutesa, Tafadzwa Dzinamarira, Tanjir Rashid Soron, Jean‐Hubert Caberg, Vincent Bours, Jean Mutabaruka, Eugène Rutembesa, Stefan Jansen, Segun Fatumo and Clarisse Musanabaganwa and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of Affective Disorders.

In The Last Decade

Annette Uwineza

26 papers receiving 185 citations

Peers

Annette Uwineza
Elisabeth Siti Herini Indonesia
Jalsi Tacon Arruda Brazil
Julianna Shinnick United States
Amy MacDougall United Kingdom
Davide Vecchio Italy
Veronica Fitzpatrick United States
Samet Özer Türkiye
Malissa Kay Shaw Taiwan
Lisa Hill United States
Laura Prescott United Kingdom
Elisabeth Siti Herini Indonesia
Annette Uwineza
Citations per year, relative to Annette Uwineza Annette Uwineza (= 1×) peers Elisabeth Siti Herini

Countries citing papers authored by Annette Uwineza

Since Specialization
Citations

This map shows the geographic impact of Annette Uwineza's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Annette Uwineza with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annette Uwineza more than expected).

Fields of papers citing papers by Annette Uwineza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annette Uwineza. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Annette Uwineza. The network helps show where Annette Uwineza may publish in the future.

Co-authorship network of co-authors of Annette Uwineza

This figure shows the co-authorship network connecting the top 25 collaborators of Annette Uwineza. A scholar is included among the top collaborators of Annette Uwineza based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Annette Uwineza. Annette Uwineza is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Uwineza, Annette, et al.. (2025). Environmental factors associated with microcephaly in Africa: A systematic review. Neurotoxicology and Teratology. 113. 107577–107577.
3.
Onohuean, Hope, et al.. (2024). Genetic etiology of autism spectrum disorder in the African population: a scoping review. Frontiers in Genetics. 15. 1431093–1431093. 1 indexed citations
4.
Yamada, Hidetaka, Yuji Iwashita, Belson Rugwizangoga, et al.. (2023). Clinicopathological Characteristics and Mutational Landscape of APC, HOXB13, and KRAS among Rwandan Patients with Colorectal Cancer. Current Issues in Molecular Biology. 45(5). 4359–4374. 2 indexed citations
5.
Uwineza, Annette, et al.. (2023). Precision medicine education for medical residents in Rwanda. Medical Education. 57(8). 775–776. 1 indexed citations
6.
7.
Musanabaganwa, Clarisse, Stefan Jansen, Agaz H. Wani, et al.. (2022). Community Engagement in Epigenomic and Neurocognitive Research on Post-Traumatic Stress Disorder in Rwandans Exposed to the 1994 Genocide against the Tutsi: Lessons Learned. Epigenomics. 14(15). 887–895. 2 indexed citations
8.
Musanabaganwa, Clarisse, Agaz H. Wani, Segun Fatumo, et al.. (2021). Leukocyte Methylomic Imprints of Exposure to the Genocide against the Tutsi in Rwanda: a Pilot Epigenome-Wide Analysis. Epigenomics. 14(1). 11–25. 14 indexed citations
9.
Rugwizangoga, Belson, et al.. (2021). Exploring Perceptions and Acceptance of Minimally Invasive Tissue Sampling among Bereaved Relatives and Health-Care Professionals in Rwanda. Journal of Multidisciplinary Healthcare. Volume 14. 3421–3427. 4 indexed citations
10.
Soron, Tanjir Rashid, et al.. (2021). Development of a Mobile App to Improve Numeracy Skills of Children With Autism Spectrum Disorder: Participatory Design and Usability Study. JMIR Pediatrics and Parenting. 4(3). e21471–e21471. 24 indexed citations
11.
Uwineza, Annette, et al.. (2020). Attendance to HIV Antiretroviral Collection Clinic Appointments During COVID-19 Lockdown. A Single Center Study in Kigali, Rwanda. AIDS and Behavior. 24(12). 3299–3301. 26 indexed citations
12.
Musanabaganwa, Clarisse, Stefan Jansen, Segun Fatumo, et al.. (2020). Burden of post-traumatic stress disorder in postgenocide Rwandan population following exposure to 1994 genocide against the Tutsi: A meta-analysis. Journal of Affective Disorders. 275. 7–13. 18 indexed citations
13.
Uwineza, Annette, Jean‐Hubert Caberg, Stéphane Wenric, et al.. (2019). VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report. European Journal of Medical Genetics. 62(8). 103704–103704. 14 indexed citations
14.
Uwineza, Annette, et al.. (2015). Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies. Journal of Tropical Pediatrics. 62(1). 38–45. 4 indexed citations
15.
Uwineza, Annette, Yvan Butera, Anne‐Cecile Hellin, et al.. (2014). Pattern of congenital heart diseases in Rwandan children with genetic defects. Pan African Medical Journal. 19. 85–85. 7 indexed citations
16.
Uwineza, Annette, et al.. (2013). Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients. Journal of Tropical Pediatrics. 60(2). 112–117. 8 indexed citations
17.
Uwineza, Annette, et al.. (2013). A Case of Rwandan Patient with Ring Chromosome 15 Syndrome. SHILAP Revista de lepidopterología. 2 indexed citations
18.
Uwineza, Annette, et al.. (2013). Patients With Noonan Syndrome Phenotype: Spectrum Of Clinical FeaturesAnd Congenital Heart Defect. TSpace. 1 indexed citations
19.
Mutimura, Eugene, Kathryn Anastos, Donald R. Hoover, et al.. (2011). Adherence to Highly Active Antiretroviral Treatment in HIV-Infected Rwandan Women. PLoS ONE. 6(11). e27832–e27832. 15 indexed citations
20.
Martin, Janet, et al.. (2009). Poland’s Syndrome: A Case Report. TSpace. 14(2). 112–114. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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