Ahmed Bouhouche

2.6k total citations
44 papers, 1.0k citations indexed

About

Ahmed Bouhouche is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Ahmed Bouhouche has authored 44 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cellular and Molecular Neuroscience, 16 papers in Molecular Biology and 12 papers in Neurology. Recurrent topics in Ahmed Bouhouche's work include Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (12 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Ahmed Bouhouche is often cited by papers focused on Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (12 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Ahmed Bouhouche collaborates with scholars based in Morocco, France and Algeria. Ahmed Bouhouche's co-authors include Ali Benomar, Alexis Brice, Mohamed Yahyaoui, Nazha Birouk, Éric Leguern, Hamid Azzedine, Naïma Bouslam, T. Chkili, Riadh Gouider and Houyam Tibar and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Ahmed Bouhouche

43 papers receiving 1.0k citations

Peers

Countries citing papers authored by Ahmed Bouhouche

Since Specialization

Citations

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

Fields of papers citing papers by Ahmed Bouhouche

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ahmed Bouhouche

This figure shows the co-authorship network connecting the top 25 collaborators of Ahmed Bouhouche. A scholar is included among the top collaborators of Ahmed Bouhouche 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 Ahmed Bouhouche. Ahmed Bouhouche 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	Association study of the JAK/STAT signaling pathway with susceptibility to COVID-19 in moroccan patient and in-silico analysis of rare variants 2024 ·Virus Research ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Idriss Lahlou Amine, (unknown), Rabii Ameziane El Hassani, (unknown), Rédouane Abouqal, Khalid Ennibi, Ahmed Bouhouche, Jamila El Baghdadi	2
2	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
3	Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection 2024 ·Archives of Virology ·(unknown), (unknown), (unknown), Jihane Belayachi, (unknown), Elmostafa El Fahime, (unknown), Khalid Ennibi, Rédouane Abouqal, Rachid Razıne, Ahmed Bouhouche	2
4	Implication of IL-12A, IL-12B, IL-6, and TNF single-nucleotide polymorphisms in severity and susceptibility to COVID-19 2024 ·International Journal of Immunopathology and Pharmacology ·(unknown), (unknown), (unknown), Hicham Oumzil, (unknown), (unknown), Nawal Doghmi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Nadia Touil, Khalid Ennibi, Ahmed Bouhouche	2
5	Association of Renin–Angiotensin Pathway Gene Polymorphisms with COVID-19 Susceptibility and Severity in Moroccans: A Case–Control Study 2024 ·Biochemical Genetics ·(unknown), (unknown), Jihane Belayachi, Khalid Ennibi, Rachid Razıne, Rédouane Abouqal, Ahmed Bouhouche	0
6	Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome 2021 ·Experimental Eye Research ·Ahmed Bouhouche, (unknown), (unknown), (unknown), (unknown), (unknown), Hinde Iraqi, Elmostafa El Fahime, Mohammed Belmekki	7
7	Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing 2020 ·BMC Genetics ·Lucy Crooks, Johnathan Cooper‐Knock, Paul R. Heath, Ahmed Bouhouche, (unknown), Mimoun Azzouz, Youssef Bakri, M. Adnaoui, Azeddine Ibrahimi, Saaïd Amzazi, Rachid Tazi‐Ahnini	3
8	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
9	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
10	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
11	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
12	Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family 2013 ·European Journal of Medical Genetics ·Imane Cherkaoui Jaouad, Mustapha El Alloussi, (unknown), Ahmed Bouhouche, (unknown), Abdelaziz Sefiani	10
13	A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22 2008 ·Neurogenetics ·(unknown), Stéphanie Baulac, (unknown), Ahmed Bouhouche, Philippe Couarch, (unknown), (unknown), Stéphane Lehéricy, Merle Ruberg, Ali Benomar, Simon Heath, (unknown), Mohamed Yahyaoui, Mohamed Jiddane, Réda Ouazzani, Éric Leguern	6
14	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
15	A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families 2007 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Ahmed Bouhouche, Nazha Birouk, Ali Benomar, Réda Ouazzani, T. Chkili, Mohamed Yahyaoui	10
16	Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease 2006 ·NeuroMolecular Medicine ·O. Dubourg, Hamid Azzedine, Christophe Verny, (unknown), Nazha Birouk, Riadh Gouider, Mustafa A. Salih, Ahmed Bouhouche, (unknown), (unknown), M Mayer, Merle Ruberg, Mériem Tazir, Alexis Brice, Éric Leguern	66
17	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
18	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
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	A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 1999 ·The American Journal of Human Genetics ·Ahmed Bouhouche, Ali Benomar, Nazha Birouk, (unknown), Farid Meggouh, Jean‐Pol Tassin, (unknown), Antoon Vandenberghe, Mohamed Yahyaoui, T. Chkili, Alexis Brice, Éric Leguern	68

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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