Teepu Siddique - Concepedia

Author

Teepu Siddique

Also Known As

B. N. Smith, Guy Rouleau, Nailah Siddique, Siddique Teepu, T SIDDIQUE, T Siddique, T. Siddique, T.S. Siddique, Tahir Saeed Siddique, Tayyaba Zareen Siddique

242

Publications

30.4K

Citations

H-Index

157

Concepts

All Affiliations

Northwestern University Duke Medical Center Duke University University of Chicago Massachusetts General Hospital

About

Teepu Siddique is an author at Northwestern University specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	68	16.7K
2	Health Sciences	6	6	585
3	Natural Sciences	6	6	2.9K
4	Public Health	5	5	336
5	Engineering	1	1	38

Teepu Siddique

110

Publications

25.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis D.R. Rosen, Teepu Siddique, David T. Patterson, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsMolecular Biology	1993	7K
Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation Mark E. Gurney, Haifeng Pu, Arlene Y. Chiu, Science	1994	4.1K
Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc, Science Neurodegenerative DiseasesAmyotrophic Lateral SclerosisSomatic VariantMendelian DisorderGenetic Disorder	2009	2.5K
Pathological TDP‐43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with <i>SOD1</i> mutations Ian R. Mackenzie, Eileen H. Bigio, Paul G. Ince, Annals of Neurology	2007	975
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis Yi Yang, Afif Hentati, Han‐Xiang Deng, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsProtein MisfoldingNeuroscience	2001	731
Presence of dendritic cells, MCP‐1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue Jenny S. Henkel, J. Engelhardt, László Siklós, Annals of Neurology ImmunologyImmune RegulationAls Spinal CordImmune SystemSocial Sciences	2003	535
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria Han‐Xiang Deng, Yong Shi, Yoshiaki Furukawa, Proceedings of the National Academy of Sciences Amyotrophic Lateral SclerosisMolecular NeuroscienceDevelopmental BiologyMedicineMolecular Biology	2006	418
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3 Caroline Vance, Ammar Al‐Chalabi, Deborah Ruddy, Brain Neurological DisorderGeneticsGenetic EpidemiologyMolecular BiologyDisease Gene Identification	2006	382
Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity Teepu Siddique, Denise A. Figlewigz, Margaret A. Pericak‐Vance, New England Journal of Medicine	1991	379
FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis Han‐Xiang Deng, Hong Zhai, Eileen H. Bigio, Annals of Neurology	2010	346

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