Naïma Bouslam

2.6k total citations
29 papers, 550 citations indexed

About

Naïma Bouslam is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Naïma Bouslam has authored 29 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Naïma Bouslam's work include Neurological diseases and metabolism (11 papers), Hereditary Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Naïma Bouslam is often cited by papers focused on Neurological diseases and metabolism (11 papers), Hereditary Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Naïma Bouslam collaborates with scholars based in Morocco, France and Israel. Naïma Bouslam's co-authors include Alexis Brice, Ahmed Bouhouche, Ali Benomar, Giovanni Stévanin, Alexandra Dürr, Mohamed Yahyaoui, Stephan Klebe, Hamid Azzedine, Réda Ouazzani and Merle Ruberg and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Naïma Bouslam

29 papers receiving 539 citations

Peers

Countries citing papers authored by Naïma Bouslam

Since Specialization

Citations

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

Fields of papers citing papers by Naïma Bouslam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naïma Bouslam

This figure shows the co-authorship network connecting the top 25 collaborators of Naïma Bouslam. A scholar is included among the top collaborators of Naïma Bouslam 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 Naïma Bouslam. Naïma Bouslam is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome 2024 ·Genetic Testing and Molecular Biomarkers ·Ahmed Bouhouche, (unknown), Hicham Charoute, Houyam Tibar, Naïma Bouslam, (unknown), (unknown), Ali Benomar, (unknown), (unknown)	1
2	Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease 2020 ·Journal of Molecular Neuroscience ·(unknown), Christelle Tesson, Wafa Regragui, Hélène Bertrand, (unknown), Naïma Bouslam, Ali Benomar, Alexis Brice, Suzanne Lesage, Ahmed Bouhouche	2
3	Association of vitamin D status with multiple sclerosis in a case-control study from Morocco 2018 ·Revue Neurologique ·(unknown), (unknown), Rachid El Jaoudi, Rachid Razıne, (unknown), Houyam Tibar, Elmostafa El Fahime, Naïma Bouslam, (unknown), Ali Benomar, (unknown), M. Yahyaoui, Ahmed Bouhouche	14
4	Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel 2017 ·Frontiers in Neurology ·Ahmed Bouhouche, Christelle Tesson, (unknown), (unknown), Valérie Drouet, Houyam Tibar, Zouhayr Souirti, Rafiqua Ben El Haj, Naïma Bouslam, Mohamed Yahyaoui, Alexis Brice, Ali Benomar, Suzanne Lesage	14
5	Evidence for prehistoric origins of the G2019S mutation in the North African Berber population 2017 ·PLoS ONE ·Rafiqua Ben El Haj, (unknown), Wafa Regragui, Ahmed Moussa, Naïma Bouslam, Houyam Tibar, Ali Benomar, Mohamed Yahyaoui, Ahmed Bouhouche	11
6	LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease 2017 ·Parkinson s Disease ·Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, (unknown), Rachid Razıne, (unknown), (unknown), Naïma Bouslam, (unknown), Ali Benomar, (unknown), Wafa Regragui	33
7	Clinical and genetic data of Huntington disease in Moroccan patients 2016 ·African Health Sciences ·Ahmed Bouhouche, (unknown), (unknown), (unknown), Nazha Birouk, (unknown), (unknown), Yamna Kriouile, Naïma Bouslam, (unknown), (unknown), Ali Benomar, Mohamed Yahyaoui	4
8	A Novel Homozygous p.L539F Mutation Identified inPINK1Gene in a Moroccan Patient with Parkinsonism 2016 ·BioMed Research International ·Rafiqua Ben El Haj, (unknown), Rachid Tazi‐Ahnini, (unknown), Naïma Bouslam, Ali Benomar, Mohamed Yahyaoui, Ahmed Bouhouche	9
9	An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3 2012 ·BMC Medical Genetics ·Ahmed Bouhouche, Ali Benomar, (unknown), (unknown), Naïma Bouslam, (unknown), (unknown), (unknown), Elmostafa El Fahime, (unknown), Mohamed Jiddane, Mohamed Yahyaoui	2
10	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Stephan Klebe, Alexandra Dürr, Naïma Bouslam, Djamel Grid, Caroline Paternotte, Christel Depienne, Sylvain Hanein, Ahmed Bouhouche, Nizar Elleuch, Hamid Azzedine, Sandrine Poëa‐Guyon, Sylvie Forlani, (unknown), Céline Charon, Jamïlé Hazan, Alexis Brice, Giovanni Stévanin	14
11	Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families 2007 ·Neurogenetics ·Nizar Elleuch, Naïma Bouslam, Sylvain Hanein, Alexander Lossos, Abdelmadjid Hamri, Stephan Klebe, Vardiella Meiner, (unknown), Israela Lerer, Djamel Grid, Delphine Bacq, Mériem Tazir, Diana Zélénika, Zohar Argov, Alexandra Dürr, Mohamed Yahyaoui, Ali Benomar, Alexis Brice, Giovanni Stévanin	15
12	A novel locus for autosomal recessive spastic ataxia on chromosome 17p 2007 ·Human Genetics ·Naïma Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Stephan Klebe, Hamid Azzedine, Silvia Di Giandomenico, Anne Boland, Filippo M. Santorelli, Alexandra Dürr, Alexis Brice, Mohamed Yahyaoui, Giovanni Stévanin	21
13	A new phenotype linked to SPG27 and refinement of the critical region on chromosome 2006 ·Journal of Neurology ·Pascale Ribaı̈, Giovanni Stévanin, Naïma Bouslam, (unknown), Isabelle Nelson, Bertrand Fontaine, (unknown), Céline Charon, Alexandra Dürr, Alexis Brice	14
14	Hereditary Spastic Paraplegia With Thin Corpus Callosum 2006 ·Archives of Neurology ·Alexander Lossos, Giovanni Stévanin, Vardiella Meiner, Zohar Argov, Naïma Bouslam, J. P. Newman, John M. Gomori, Stephan Klebe, Israela Lerer, Nizar Elleuch, (unknown), Alexandra Dürr, Oded Abramsky, (unknown), Alexis Brice	25
15	Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1 2005 ·European Journal of Human Genetics ·Ahmed Bouhouche, Ali Benomar, Naïma Bouslam, Réda Ouazzani, T. Chkili, Mohamed Yahyaoui	26
16	Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) 2005 ·Annals of Neurology ·Naïma Bouslam, Ali Benomar, Hamid Azzedine, Ahmed Bouhouche, Michito Namekawa, Stephan Klebe, Céline Charon, Alexandra Dürr, Merle Ruberg, Alexis Brice, Mohamed Yahyaoui, Giovanni Stévanin	43
17	Mutation in the Catalytic Domain of Protein Kinase C γ and Extension of the Phenotype Associated With Spinocerebellar Ataxia Type 14 2004 ·Archives of Neurology ·Giovanni Stévanin, (unknown), (unknown), Naïma Bouslam, (unknown), (unknown), Marie‐Laure Welter, Elisabeth Ollagnon‐Roman, Arnaud Lemainque, Merle Ruberg, Alexis Brice, Alexandra Dürr	66
18	Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p 2003 ·Annals of Neurology ·Giovanni Stévanin, Naïma Bouslam, Stéphane Thobois, Hamid Azzedine, (unknown), Anne Boland, Martin Schalling, Emmanuel Broussolle, Alexandra Dürr, Alexis Brice	54
19	Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families 2002 ·Journal of the Neurological Sciences ·Ali Benomar, (unknown), Farid Meggouh, Ahmed Bouhouche, (unknown), Naïma Bouslam, (unknown), M. Schmitt, (unknown), Réda Ouazzani, (unknown), Michel Kœnig	40
20	Vitamin E deficiency ataxia associated with adenoma 1999 ·Journal of the Neurological Sciences ·Ali Benomar, (unknown), (unknown), (unknown), Naïma Bouslam, (unknown), Afaf Amarti, Réda Ouazzani, T. Chkili	7

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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