Mahdi Ghani - Concepedia

Author

Mahdi Ghani

Also Known As

Allison Ann Dilliott, M Ghani, M Ghani-Kakhi, M. Ghani, M. Ghani-Kakhki, M. U. Ghani, Mahdi Ghani, Mehdi Ghani, Morris Freedman, Rob Hegele

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

University of Toronto Occupational Cancer Research Centre University of Cambridge Sunnybrook Health Science Centre Columbia University

About

Mahdi Ghani is an author at University of Toronto specializing in medicine, genetics, and alzheimer's disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	665
2	Public Health	3	3	123
3	Health Sciences	2	2	101
4	Engineering	1	1	42
5	Natural Sciences	1	1	18

Mahdi Ghani

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Coding mutations in <scp><i>SORL</i></scp><i>1</i> and <scp>A</scp>lzheimer disease Badri N. Vardarajan, Yalun Zhang, Joseph H. Lee, Annals of Neurology	2014	179
Rare coding mutations identified by sequencing of <scp>A</scp>lzheimer disease genome‐wide association studies loci Badri N. Vardarajan, Mahdi Ghani, A Kahn, Annals of Neurology	2015	151
Investigation of C9orf72 in 4 Neurodegenerative Disorders Zhengrui Xi, Lorne Zinman, Yakov Grinberg, Archives of Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisAlzheimer's DiseaseVariant InterpretationGenetics	2012	110
A clinical and molecular genetic study of 112 Iranian families with primary microcephaly Hossein Darvish, Sahar Esmaeeli-Nieh, Gholamreza Bahrami Monajemi, Journal of Medical Genetics	2010	93
Genetic association of CR1 with Alzheimer's disease: A tentative disease mechanism Lili‐Naz Hazrati, Caroline Van Cauwenberghe, Patricia L. Brooks, Neurobiology of Aging Alzheimer's DiseaseGeneticsDementiaTentative Disease MechanismNeurochemical Biomarkers	2012	83
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP) Christiane Reitz, Giuseppe Tosto, Badri N. Vardarajan, Translational Psychiatry	2013	82
The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? E Seemanová, Raymonda Varon, J Vejvalka, PLoS ONE FertilityGeneticsReproductive HealthGenetic EpidemiologyPathology	2016	67
Genome-Wide Survey of Large Rare Copy Number Variants in Alzheimer’s Disease Among Caribbean Hispanics Mahdi Ghani, Dalila Pinto, Joseph H. Lee, G3 Genes Genomes Genetics NeurogenomicsGeneticsGenetic EpidemiologyCnv RateDisease Gene Identification	2012	56
MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis Laura MacNair, Shangxi Xiao, Denise Miletic, Brain	2015	55
Establishment of a Mouse Model with Misregulated Chromosome Condensation due to Defective Mcph1 Function Marc Trimborn, Mahdi Ghani, Diego J. Walther, PLoS ONE	2010	52

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