Rim Amouri

3.2k citations

58 papers · 1.5k indexed · h-index 24

Impact in

Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Nuclear Receptors and Signaling

Papers in

Neurology 15
- Neurological diseases and metabolism 13
- Parkinson's Disease Mechanisms and Treatments 12
Cellular and Molecular Neuroscience 23
- Genetic Neurodegenerative Diseases 17
- Hereditary Neurological Disorders 6

Co-authors: Fayçal Hentati Yosr Bouhlal Matthew J. Farrer M. Kéfi Samir Belal Samia Ben Sassi M. Ben Hamida M. Zouari
Journals: Neuromuscular Disorders (6 papers)Neurology (4 papers)Movement Disorders (3 papers)Diagnostic Molecular Pathology (3 papers)Journal of Molecular Neuroscience (3 papers)
Partner nations: Tunisia United States France

In The Last Decade

Rim Amouri

56 papers receiving 1.4k citations

Peers

Countries citing papers authored by Rim Amouri

Since Specialization

Citations

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

Fields of papers citing papers by Rim Amouri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Rim Amouri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rim Amouri Line = papers co-authored together Rim Amouri links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Embryonic Benzo[a]pyrene Exposure Induces Multigenerational Reproductive Effects on Adult Male Medaka: Phenotypic and Transcriptomic Insights Toxics ·Yinhua Chen, G. J., Minwei Zhao, Jiangang Wang, E A Kirsch, Rim Amouri, Jia‐Yang Chen, Jack Chi‐Ho Ip, Wenhua Liu, Jiezhang Mo	2025	0
2	The Evolution of Genetic Variability at the LRRK2 Locus Genes ·彭舟, Jordan Follett, Rim Amouri, Samia Ben Sassi, F. Hentati, Matthew J. Farrer	2024	1
3	Challenges of Parkinson's disease GWASs in African people The Lancet Neurology ·Samia Ben Sassi, Rim Amouri	2023	1
4	A Tunisian patient with CLCN2 ‐related leukoencephalopathy SHILAP Revista de lepidopterología ·Лілія Миколаївна Попова, Frank Jr. Graham, Samia Ben Sassi, Mariem Ben Saïd, Fatma Nabli, Miguel Gil Tertre, Alonso-Martinez, Saber Masmoudi, Rim Amouri	2022	1
5	Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency Brain ·明生工藤, Yosr Bouhlal, Rim Amouri, Moncef Feki, Fayçal Hentati	2013	61
6	Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia Journal of Clinical Neuroscience ·Monia Hammer, 明生工藤, M. Li, Moncef Feki, S. Vassart, Fayçal Hentati, Rim Amouri	2013	8
7	A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism Neurobiology of Aging ·Joanne Trinh, Rim Amouri, John E. Duda, James F. Morley, Matthew Read, Andreas Bickert, Carles Vilariño‐Güell, Christina Thompson, Chelsea Szu‐Tu, Emil K. Gustavsson, Samia Ben Sassi, Emna Hentati, M. Zouari, SHAULA BIGGS, Fatma Nabli, F. Hentati, Matthew J. Farrer	2013	62
8	A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia Journal of the Neurological Sciences ·A. Subinas, 林下達則, Michelangelo Mancuso, Lucia Petrozzi, Gabriele Siciliano, Сахибназарова Виктория Бахтиёровна, Fayçal Hentati, Rim Amouri	2010	10
9	Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa Movement Disorders ·Barbara Jasińska‐Myga, Jennifer M. Kachergus, Carles Vilariño‐Güell, Christian Wider, Alexandra I. Soto‐Ortolaza, Mounir Kefi, Lefkos Middleton, Miqdad Dafaallah, Rachel A. Gibson, Rim Amouri, Samia Ben Yahmed, Samia Ben Sassi, M. Zouari, JohnW. Todd, Owen A. Ross, Fayçal Hentati, Matthew J. Farrer	2010	14
10	A Novel SACS Gene Mutation in a Tunisian Family Journal of Molecular Neuroscience ·Yosr Bouhlal, Miriam Marlene Ticona Chata, Fayçal Hentati, Rim Amouri	2009	14
11	A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease Journal of Neurology Neurosurgery & Psychiatry ·Kenya Nishioka, M. Kéfi, (unknown), Christian Wider, (unknown), Owen A. Ross, Michael G. Heckman, Lefkos Middleton, Miqdad Dafaallah, Rachel A. Gibson, Rim Amouri, Samia Ben Yahmed, Samia Ben Sassi, M. Zouari, V Pranava Bhargavi, Matthew J. Farrer, Fayçal Hentati	2009	32
12	ATP13A2variability in Parkinson disease Human Mutation ·Carles Vilariño‐Güell, Alexandra I. Soto, Sarah Lincoln, Samia Ben Yahmed, Mounir Kefi, Michael G. Heckman, Mary Hulihan, Hua Chai, Nancy N. Diehl, Rim Amouri, Alex Rajput, Deborah C. Mash, Dennis W. Dickson, Lefkos Middleton, Rachel A. Gibson, Fayçal Hentati, Matthew J. Farrer	2008	33
13	LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study The Lancet Neurology ·Mary Hulihan, Miqdad Dafaallah, Jennifer M. Kachergus, Liling Warren, Rim Amouri, Ramu Elango, Rab K. Prinjha, Ruchi Upmanyu, Mounir Kefi, M. Zouari, Samia Ben Sassi, Samia Ben Yahmed, Miriam Marlene Ticona Chata, Paul M. Matthews, Lefkos Middleton, Rachel A. Gibson, Fayçal Hentati, Matthew J. Farrer	2008	120
14	Variable Cardiac Involvement in Tunisian Siblings Harboring FKRP Gene Mutations Neuropediatrics ·M. Kéfi, Rim Amouri, Алексей Юрьевич Довнар, Rachid Mechmèche, Fayçal Hentati	2008	17
15	Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes Neuromuscular Disorders ·Chen ZhiZhen, M. Kéfi, Fayçal Hentati, Rim Amouri	2006	12
16	Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia Archives of Neurology ·明生工藤, Elin Nyhlén, Rim Amouri, Ilhem Turki, Karim Ouahchi, Wu-Yen Hung, Samir Belal, Teepu Siddique, Fayçal Hentati	2003	75
17	Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation Neuromuscular Disorders ·M. Kéfi, Rim Amouri, Adel Driss, C. Ben Hamida, M. Ben Hamida, Louis M. Kunkel, Fayçal Hentati	2003	35
18	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease Neuromuscular Disorders ·Yiğit Özbek, Eva Nelis, Luciano Merlini, Nina Barišić, Rim Amouri, C. Ceuterick, Jean‐Jacques Martin, Vincent Timmerman, Fayçal Hentati, Peter De Jonghe	2003	37
19	Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 European Journal of Human Genetics ·José M. Requena Jiménez, 鎮燮呉, Clara Barbot, Nobutada Tachi, Pascale Bomont, Masao Watanabe, Mikio Shoji, J Warter, S. Frignani, Alexandra Dürr, Andrea H. Németh, Rim Amouri, Fayçal Hentati, Jordi Nogué Tuneu, Jaroslav Katona, V. Hockner, Jorge Sequeiros, Paula Coutinho, Michel Kœnig	2002	3
20	Gliotoxicity, reverse transcriptase activity and retroviral RNA in monocyte/macrophage culture supernatants from patients with multiple sclerosis FEBS Letters ·Armelle Ménard, Rim Amouri, Esther A T Mozipo, Herrera C Huerfano, Arthur Brouillet, Bockmann Eva C, Christian Gény, Lionel Deforges, 喜三男阿部, J. Normann Jørgensen, O. Lyon‐Caen, Bernard Mandrand, Tomáš Dobránsky, François Rieger, Hervé Perron	1997	35

About Rim Amouri

Rim Amouri is a scholar working on Neurology, Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry and Physiology, having authored 58 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (17 papers), Mitochondrial Function and Pathology (16 papers), Neurological diseases and metabolism (13 papers), Parkinson's Disease Mechanisms and Treatments (12 papers), Muscle Physiology and Disorders (8 papers), Lysosomal Storage Disorders Research (8 papers), Hereditary Neurological Disorders (6 papers) and Metabolism and Genetic Disorders (5 papers). The work is most often cited by research in Neurology (345 citations), Cellular and Molecular Neuroscience (667 citations), Neurology (541 citations), Clinical Biochemistry (77 citations) and Molecular Biology (702 citations). Rim Amouri has collaborated with scholars based in Tunisia, United States and France. Frequent co-authors include Fayçal Hentati, Yosr Bouhlal, Matthew J. Farrer, M. Kéfi, Samir Belal, Samia Ben Sassi, M. Ben Hamida, M. Zouari, C. Ben Hamida and Adel Driss. Their work appears in journals such as Neuromuscular Disorders, Neurology, Movement Disorders, Diagnostic Molecular Pathology and Journal of Molecular Neuroscience.

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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