Nailah Siddique - Concepedia

Author

Nailah Siddique

Northwestern University

Also Known As

Christopher E Shaw, Nailah A. Siddique, Nailah Siddique, Stephen Scelsa

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Northwestern University Duke University Massachusetts General Hospital Harvard University Howard Hughes Medical Institute

About

Nailah Siddique is an author at Northwestern University specializing in medicine, neuroscience, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	784
2	Public Health	2	2	44
3	Health Sciences	1	1	43
4	Family Medicine	1	1	13
5	Immunology	1	1	271

Nailah Siddique

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
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
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4 Han‐Xiang Deng, Christopher J. Klein, Jianhua Yan, Nature Genetics Rare DiseasesAllelic DisordersMedicineImmunologyPathology	2009	271
Identification of TMEM230 mutations in familial Parkinson's disease Han‐Xiang Deng, Yi Yang, Kreshnik Ahmeti, Nature Genetics Neurodegenerative DiseasesGenetic DisorderMedicineParkinson DiseaseGenetics	2016	171
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy Senda Ajroud‐Driss, Faisal Fecto, Kaouther Ajroud, Neurogenetics Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderGenetics	2014	126
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis Rebecca Schüle, Teepu Siddique, Han‐Xiang Deng, Journal of Lipid Research	2009	114
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis Yi‐Ju Li, Margaret A. Pericak‐Vance, Jonathan L. Haines, Neurogenetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisApolipoprotein EAgingNeurochemical Biomarkers	2004	76
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration Sarah Opie-Martin, Alfredo Iacoangeli, Simon Topp, Nature Communications	2022	54
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis Teepu Siddique, Margaret A. Pericak‐Vance, Janice Caliendo, Neurogenetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderMedicineGenetics	1998	53
Neuronal Ubiquitinated Intranuclear Inclusions in Familial and Non-Familial Frontotemporal Dementia of the Motor Neuron Disease Type Associated with Amyotrophic Lateral Sclerosis Eileen H. Bigio, Nancy Johnson, Alfred Rademaker, Journal of Neuropathology & Experimental Neurology Neurological DisorderIntranuclear InclusionsCytoplasmic InclusionsAlzheimer's DiseaseNeurology	2004	43
A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy Kourosh Rezania, Jianhua Yan, Lisa Dellefave, Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders	2003	43

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