Guida Landouré

2.4k total citations
54 papers, 715 citations indexed

About

Guida Landouré is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Guida Landouré has authored 54 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 16 papers in Genetics and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Guida Landouré's work include Hereditary Neurological Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Genetic Neurodegenerative Diseases (7 papers). Guida Landouré is often cited by papers focused on Hereditary Neurological Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Genetic Neurodegenerative Diseases (7 papers). Guida Landouré collaborates with scholars based in Mali, United States and South Africa. Guida Landouré's co-authors include Kenneth H. Fischbeck, Barrington G. Burnett, Yijun Shi, Rachelle Gaudet, Clare H. Munns, Christy L. Ludlow, Robert Kleta, Ambroise Wonkam, Charlotte J. Sumner and Horia Stanescu and has published in prestigious journals such as Nature, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Guida Landouré

49 papers receiving 698 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Guida Landouré Mali 13 304 204 160 153 87 54 715
Anita Y. Bahar Australia 11 160 0.5× 211 1.0× 195 1.2× 63 0.4× 162 1.9× 13 763
Kate M. Brody Australia 14 318 1.0× 74 0.4× 151 0.9× 135 0.9× 66 0.8× 20 734
Yijun Shi United States 9 198 0.7× 150 0.7× 146 0.9× 42 0.3× 39 0.4× 10 453
Nancy D. Merner United States 13 267 0.9× 97 0.5× 42 0.3× 139 0.9× 36 0.4× 25 854
Ratneswary Sutharsan Australia 15 202 0.7× 221 1.1× 36 0.2× 25 0.2× 88 1.0× 20 636
Antonio Garcı́a-Merino Spain 17 209 0.7× 163 0.8× 30 0.2× 30 0.2× 94 1.1× 31 811
T.C. Theoharides United States 15 170 0.6× 73 0.4× 78 0.5× 30 0.2× 23 0.3× 29 1.0k
Fred A. Martinson United States 12 447 1.5× 72 0.4× 38 0.2× 447 2.9× 17 0.2× 15 899
Dianna Armstrong Canada 9 138 0.5× 431 2.1× 28 0.2× 28 0.2× 263 3.0× 10 840
Cristina Tinti Italy 14 394 1.3× 249 1.2× 28 0.2× 83 0.5× 24 0.3× 23 702

Countries citing papers authored by Guida Landouré

Since Specialization
Citations

This map shows the geographic impact of Guida Landouré'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 Guida Landouré with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Guida Landouré more than expected).

Fields of papers citing papers by Guida Landouré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guida Landouré. 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 Guida Landouré. The network helps show where Guida Landouré may publish in the future.

Co-authorship network of co-authors of Guida Landouré

This figure shows the co-authorship network connecting the top 25 collaborators of Guida Landouré. A scholar is included among the top collaborators of Guida Landouré 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 Guida Landouré. Guida Landouré 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.
Gahl, William A., et al.. (2024). Rare Disease Day: Amplifying voices, advocating hope. Med. 5(2). 103–105. 1 indexed citations
2.
Cissoko, Mamadou, et al.. (2024). A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young Malian. SHILAP Revista de lepidopterología. 12(2). e8527–e8527. 1 indexed citations
3.
Cissé, Lassana, et al.. (2024). The First Case of Huntington’s Disease like 2 in Mali, West Africa. Tremor and Other Hyperkinetic Movements. 14(1). 15–15. 1 indexed citations
4.
Cissé, Lassana, et al.. (2024). A novel variant in the GNE gene in a Malian patient presenting with distal myopathy. Neurogenetics. 25(4). 487–492. 1 indexed citations
5.
6.
Yeetong, Patra, Monnat Pongpanich, Lassana Cissé, et al.. (2023). Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8. Movement Disorders. 39(1). 164–172. 10 indexed citations
7.
Rebelo, Adriana, Lassana Cissé, Lynette Rives, et al.. (2023). Novel variant in CADM3 causes Charcot–Marie–Tooth disease. Brain Communications. 5(5). fcad227–fcad227. 2 indexed citations
8.
Lombard, Zané & Guida Landouré. (2023). Could Africa be the future for genomics research?. Nature. 614(7946). 30–33. 6 indexed citations
9.
Landouré, Guida, et al.. (2022). An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient. SHILAP Revista de lepidopterología. 10(10). e6428–e6428. 2 indexed citations
10.
Cissé, Lassana, Oumar Samassékou, Salimata Diarra, et al.. (2021). Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family. SHILAP Revista de lepidopterología. 9(5). e04065–e04065. 3 indexed citations
11.
El‐Kamah, Ghada, Yehia Z. Gad, Sonia Abdelhak, et al.. (2020). Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt. American Journal of Tropical Medicine and Hygiene. 102(4). 719–723. 7 indexed citations
12.
Vries, Jantina de, Guida Landouré, & Ambroise Wonkam. (2020). Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harm. Social Science & Medicine. 258. 113091–113091. 20 indexed citations
13.
Adebamowo, Sally N., Veronica Francis, Guida Landouré, et al.. (2018). Implementation of genomics research in Africa: challenges and recommendations. Global Health Action. 11(1). 1419033–1419033. 45 indexed citations
14.
Maïga, Boubacar, Guida Landouré, Modibo Sangaré, et al.. (2016). Non-motor signs in patients with Parkinson's disease at the University Hospital of Point “G”, Mali. eNeurologicalSci. 3. 35–36. 6 indexed citations
15.
Guinto, Cheick O., Boubacar Maïga, Lassana Cissé, et al.. (2016). Socio-cultural adaptation and standardization of Dubois' five words testing in a population of normal subject in Mali, West Africa. eNeurologicalSci. 3. 60–63. 1 indexed citations
16.
Rinaldi, Carlo, Christopher Grunseich, Irina F. Sevrioukova, et al.. (2012). Cowchock Syndrome Is Associated with a Mutation in Apoptosis-Inducing Factor. The American Journal of Human Genetics. 91(6). 1095–1102. 113 indexed citations
17.
Meilleur, Katherine G., Alison La Pean, Modibo Sangaré, et al.. (2011). Clinical and genetic analysis of spinocerebellar ataxia in Mali. European Journal of Neurology. 18(10). 1269–1271. 9 indexed citations
18.
Meilleur, Katherine G., Mamadou Traoré, Modibo Sangaré, et al.. (2009). Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19. Neurogenetics. 11(3). 313–318. 15 indexed citations
19.
Landouré, Guida, Anselm A. Zdebik, Tara Martinez, et al.. (2009). Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C. Nature Genetics. 42(2). 170–174. 236 indexed citations
20.
Kane, Madeleine, et al.. (2007). [Using CT to diagnose brain tumors at the Point G Hospital in Mali].. PubMed. 22(2). 14–8. 1 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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