Guida Landouré

Biographic Data

ID2396640
NAMEGuida Landouré
GIVEN NAMESGuida
FAMILY NAMELandouré
SIGNATURELANDOURÉ G
AFFILIATIONSUniversité des Sciences, des Techniques et des Technologies de Bamako
ORCID0000-0002-5921-7832
VERIFIEDYes
TOTAL WORKS6
TOTAL CITATIONS3
WORKS AS AUTHOR6
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2011
LATEST PUBLICATION YEAR2025
H-INDEX1

  • A global survey about undiagnosed rare diseases

    Open AccessSimone Baldovino, Savino Sciascia et al.ARTICLEFrontiers in Public Health2025

    Background: Undiagnosed rare diseases (URDs) are a complex and multifaceted challenge, especially in low-and medium-income countries. They affect individuals with unique clinical features and lack a clear diagnostic label. Although the Undiagnosed Diseases Network International (UDNI) definition of URDs is not universally accepted, it is widely recognized. Methods: We surveyed UDNI members and participants from other countries to explore the chal…

  • Undiagnosed diseases

    Open AccessDomenica Taruscio, Marco Salvatore et al.ARTICLEFrontiers in Public Health2023

    Introduction: Rare diseases (RD) are a health priority worldwide, overall affecting hundreds of millions of people globally. Early and accurate diagnosis is essential to support clinical care but remains challenging in many countries, especially the low- and medium-income ones. Hence, undiagnosed RD (URD) account for a significant portion of the overall RD burden. Methods: In October 2020, the Developing Nations Working Group of the Undiagnosed D…

  • Unmet needs in countries participating in the undiagnosed diseases network international

    Open AccessSavino Sciascia, Dario Roccatello et al.ARTICLEFrontiers in Public Health2023

    Background Patients, families, the healthcare system, and society as a whole are all significantly impacted by rare diseases (RDs). According to various classifications, there are currently up to 9,000 different rare diseases that have been recognized, and new diseases are discovered every month. Although very few people are affected by each uncommon disease individually, millions of people are thought to be impacted globally when all these condi…

  • Stigma in African genomics research

    Open AccessJantina De Vries, Guida Landouré et al.ARTICLESocial Science & Medicine2020Cited by: 3References: 35

    A recurring concern in genomics research is the possibility that it could lead to stigma for participants, their families and the population groups they belong to. Little evidence exists to explain how and when this ought to be a concern in genomics research in Africa whilst there is growing international evidence drawing into question the direct link between stigma and genetics. In this paper, we interrogate practical instances from African geno…

  • Implementation of genomics research in Africa

    Open AccessSally N Adebamowo, Veronica Francis et al.ARTICLEGlobal Health Action2018

    BACKGROUND: There is exponential growth in the interest and implementation of genomics research in Africa. This growth has been facilitated by the Human Hereditary and Health in Africa (H3Africa) initiative, which aims to promote a contemporary research approach to the study of genomics and environmental determinants of common diseases in African populations. OBJECTIVE: The purpose of this article is to describe important challenges affecting gen…

  • Genetic testing and counseling for hereditary neurological diseases in Mali

    Open AccessKatherine G Meilleur, Sidiki Coulibaly et al.ARTICLEJournal of Community Genetics2011