Rim Amouri - Concepedia

Author

Rim Amouri

National Institute of Neurology Mongi-Ben Hamida ORCID

Also Known As

Amouri Rim, R Amouri, R. Amouri, Rauan Kaiyrzhanov, Rim Amouri, Rim EL Amouri, Serena Wu, Yih-Ru Wu, Yihru Wu

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurology Mongi-Ben Hamida Institut National de Santé Publique Inserm Centre National de la Recherche Scientifique Tunis El Manar University

About

Rim Amouri is an author at National Institute of Neurology Mongi-Ben Hamida specializing in medicine, genetics, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	28	1.4K
2	Social Sciences	3	3	85
3	Public Health	2	2	36
4	Engineering	1	1	20
5	Health Sciences	1	1	11

Rim Amouri

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study Mary Hulihan, L. Ishihara-Paul, Jennifer M. Kachergus, The Lancet Neurology Genetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyLrrk2 Gly2019ser Penetrance	2008	189
Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity Monia Hammer, Ghada Eleuch-Fayache, Lucía Schottlaender, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderDegenerative DiseaseNeuroscienceNeurology	2013	116
Clinicogenetic study of mutations in <i>LRRK2</i> exon 41 in Parkinson's disease patients from 18 countries Hiroyuki Tomiyama, Yuanzhe Li, Manabu Funayama, Movement Disorders	2006	111
Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia Ghada El Euch-Fayache, Irfan Lalani, Rim Amouri, Archives of Neurology	2003	107
Clinical Features of Parkinson Disease Patients With Homozygous Leucine-Rich Repeat Kinase 2 G2019S Mutations Lianna Ishihara, Liling Warren, Rachel A. Gibson, Archives of Neurology	2006	101
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans Yubin Wang, Joshua Hersheson, Dulce Lopez, Cell Reports Knockout MouseDevelopmental BiologySynaptic SignalingGenetic DisorderGenetics	2016	98
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency Ghada El Euch-Fayache, Yosr Bouhlal, Rim Amouri, Brain Neurological DisorderGeneticsGenetic EpidemiologySerum Vitamin E.Disease Gene Identification	2013	97
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses Emil K. Gustavsson, Jordan Follett, Joanne Trinh, The Lancet Neurology	2024	96
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study N. Gouider‐Khouja, A. Larnaout, Rim Amouri, Parkinsonism & Related Disorders Neurodegenerative DiseasesGenetic DisorderGeneticsParkinson DiseaseAutosomal Recessive Parkinsonism	2003	92
A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism Joanne Trinh, Rim Amouri, John E. Duda, Neurobiology of Aging MedicineParkinson DiseaseDegenerative DiseaseDegenerative PathologyNeurology	2013	91

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