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Journal of Multidisciplinary Healthcare|December 23, 2021
Exploring Perceptions and Acceptance of Minimally Invasive Tissue Sampling among Bereaved Relatives and Health-Care Professionals in RwandaBelson Rugwizangoga, Jean Berchmans Niyibizi, Marie Claire Ndayisaba, et al.
Genes|May 4, 2026
The First Case of Kleefstra Syndrome in a Rwandan Patient with Global Developmental DelayNorbert Dukuze, Janvier Hitayezu, Jeanne Primitive Uyisenga, et al.
Journal of Affective Disorders|July 14, 2020
Burden of post-traumatic stress disorder in postgenocide Rwandan population following exposure to 1994 genocide against the Tutsi: A meta-analysisClarisse Musanabaganwa, Stefan Jansen, Segun Fatumo, et al.
Plos One|November 25, 2011
Adherence to highly active antiretroviral treatment in HIV-infected Rwandan womenStephenson Musiime, Fred Muhairwe, Alfred Rutagengwa, et al.
European Journal of Medical Genetics|June 18, 2019
VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory reportAnnette Uwineza, Jean-Hubert Caberg, Janvier Hitayezu, et al.
Current Issues in Molecular Biology|May 26, 2023
Clinicopathological Characteristics and Mutational Landscape of APC, HOXB13, and KRAS among Rwandan Patients with Colorectal CancerFelix Manirakiza, Eric Rutaganda, Hidetaka Yamada, et al.
Epigenomics|December 8, 2021
Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysisClarisse Musanabaganwa, Agaz H Wani, Janelle Donglasan, et al.
The Pan African Medical Journal|February 28, 2015
Pattern of congenital heart diseases in Rwandan children with genetic defectsRaissa Teteli, Annette Uwineza, Yvan Butera, et al.
Epigenomics|August 25, 2022
Community engagement in epigenomic and neurocognitive research on post-traumatic stress disorder in Rwandans exposed to the 1994 genocide against the Tutsi: lessons learnedClarisse Musanabaganwa, Stefan Jansen, Agaz Wani, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Limb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)?Paul Kruszka, Annette Uwineza, Leon Mutesa, et al.
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