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Samia Ben Yahmed

LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
2008 · Mary M Hulihan, Lianna Ishihara-Paul, et al. · The Lancet Neurology · 191
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
2006 · Lianna Ishihara, Rachel A. Gibson, et al. · Movement Disorders · 93
PINK1 mutations and parkinsonism
2008 · L. Ishihara-Paul, M. M. Hulihan, et al. · Neurology · 64
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A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease
2009 · K. Nishioka, M. Kefi, et al. · Journal of Neurology Neurosurgery & Psychiatry · 51
ATP13A2variability in Parkinson disease
2008 · Carles Vilariño-Güell, Alexandra I. Soto, et al. · Human Mutation · 43
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Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa
2010 · Barbara Jasinska‐Myga, Jennifer Kachergus, et al. · Movement Disorders · 20
NR-WP-65 Neuro-anatomie fonctionnelle appliquee a l’IRM encephalique et medullaire dans l’exploration des troubles de la motricite
2008 · M. Jarraya, S. Ben Yahmed, et al. · Journal de Radiologie
2.116 Genetic characterization of ATP13A2 in Parkinson's disease
2007 · C. Vilarino-Guell, A.I. Soto, et al. · Parkinsonism & Related Disorders
Works count: 8
Citation count: 462
H-index: 6
I10-index: 6
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