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Teepu Siddique

Affiliations: 
Northwestern University, Evanston, IL 
Area:
ALS, Neurogenetics, Neurobiology of disease
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"Teepu Siddique"
Mean distance: 21.97 (cluster 32)
 
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Parents

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William King Engel research scientist
Allen  D. Roses research scientist Duke

Children

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Y. Taylan Esengul research assistant 2010- Northwestern School of Medicine
Faisal Fecto grad student 2006-2012 Northwestern
Faisal Fecto post-doc 2012- Northwestern
Y. Taylan Esengul post-doc 2016- Northwestern School of Medicine
Kreshnik B. Ahmeti research scientist Northwestern

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Publications

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Opie-Martin S, Iacoangeli A, Topp SD, et al. (2022) The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. Nature Communications. 13: 6901
Silani V, Corcia P, Harms MB, et al. (2020) Genetics of primary lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 21: 28-34
Lowry JL, Ryan ÉB, Esengul YT, et al. (2020) Intricacies of aetiology in intrafamilial degenerative disease. Brain Communications. 2: fcaa120
Pytte J, Flynn LL, Anderton RS, et al. (2020) Disease-modifying effects of an structural variant in a predominantly ALS cohort. Neurology. Genetics. 6: e470
Wu JJ, Cai A, Greenslade JE, et al. (2020) ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of function. Proceedings of the National Academy of Sciences of the United States of America
Pytte J, Anderton RS, Flynn LL, et al. (2020) Association of a structural variant within the gene with amyotrophic lateral sclerosis. Neurology. Genetics. 6: e406
Ortega JA, Daley EL, Kour S, et al. (2020) Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 Toxicity. Neuron
Deng S, Feely SME, Shi Y, et al. (2019) Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2. Neuromolecular Medicine
Deng HX, Pericak-Vance MA, Siddique T. (2019) Reply to 'TMEM230 variants in Parkinson's disease' and 'Doubts about TMEM230 as a gene for parkinsonism'. Nature Genetics
Edens BM, Yan J, Deng HX, et al. (2017) A novel ALS-associated variant in UBQLN4 regulates motor axon morphogenesis. Elife. 6
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