Jawad Khoris - Concepedia

Author

Jawad Khoris

McGill University

Also Known As

J Khoris, J. Khoris, Jawad Khoris

Publications

671

Citations

H-Index

Concepts

All Affiliations

McGill University Montreal General Hospital Inserm Hôpital Gui de Chauliac Pitié-Salpêtrière Hospital

About

Jawad Khoris is an author at McGill University specializing in medicine, neurology, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	270
2	Neurology	4	4	270
3	Neuroscience	3	3	253
4	Genetic Medicine	1	1	34
5	Molecular Genetics	1	1	17

Jawad Khoris

Publications

532

Citations

H-Index

Page 1

	Year	Citations
A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q Collette K. Hand, Jawad Khoris, François Salachas, The American Journal of Human Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGenetic DisorderGenetics	2002	138
Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis Philippe Corcia, Véronique Mayeux‐Portas, Jawad Khoris, Annals of Neurology	2002	126
Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family Collette K. Hand, Véronique Mayeux‐Portas, Jawad Khoris, Annals of Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisD96n Sod1 MutationsNeurological DisorderGenetics	2001	81
Identification of Six Novel SOD1 Gene Mutations in Familial Amyotrophic Lateral Sclerosis Youssef Boukaftane, Jawad Khoris, Bruno Moulard, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques	1998	68
Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis Collette K. Hand, Rebecca S. Devon, François Gros‐Louis, Archives of Neurology	2003	43
Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country Jawad Khoris, Bruno Moulard, Valérie Briolotti, European Journal of Neurology NeurogenomicsNeurological DisorderGeneticsGenetic EpidemiologyPathology	2000	34
C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Hussein Daoud, Hamid Suhail, Mike Sabbagh, Archives of Neurology	2012	25
<i>SMN1</i> gene study in three families in which ALS and spinal muscular atrophy co-exist Philippe Corcia, Jawad Khoris, Philippe Couratier, Neurology Neurological DisorderGeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene Identification	2002	17

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