Kevin S. Smith - Concepedia

Author

Kevin S. Smith

Also Known As

Alyssa A. Tran, Ben Solomon, Carson A. Smith, Cecelia P. Tamburro, Chloe M. Reuter, Colleen E. Wahl, David A. Sweetser, Edward C Smith, Edward C. Smith, Edwin K Silverman

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine Columbia University Boston Children's Hospital Harvard University University of Utah

About

Kevin S. Smith is an author at Baylor College of Medicine specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	508
2	Neurology	4	4	288
3	Social Sciences	2	2	61
4	Genomic Medicine	1	1	39
5	Molecular Genetics	1	1	34

Kevin S. Smith

Publications

949

Citations

H-Index

Page 1

	Year	Citations
Antibody‐Functionalized Porous Silicon Nanoparticles for Vectorization of Hydrophobic Drugs Emilie Secret, Kevin S. Smith, Valentina Dubljevic, Advanced Healthcare Materials	2012	127
IRF2BPL Is Associated with Neurological Phenotypes Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann, The American Journal of Human Genetics NeurologyNeuroscienceMolecular NeurobiologyNeuropathologyMedicine	2018	108
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay Keren Machol, Justine Rousseau, Sophie Ehresmann, The American Journal of Human Genetics	2018	88
Loss of mouse Stmn2 function causes motor neuropathy Irune Guerra San Juan, Leslie A. Nash, Kevin S. Smith, Neuron Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMouse Stmn2 FunctionNeurologyNeuroscience	2022	78
Method of Biopsy and Incidence of Positive Margins in Primary Melanoma Virginia H. Stell, H. James Norton, Kevin S. Smith, Annals of Surgical Oncology Dermoscopic ImageSurgical OncologySurgical PathologyMelanomaPathology	2006	73
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia Oguz Kanca, Jonathan C. Andrews, Pei-Tseng Lee, The American Journal of Human Genetics Wdr37 Are AssociatedMendelian DisorderGenetic DisorderGeneticsDe Novo Variants	2019	55
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids Sacha Ferdinandusse, Kirsty McWalter, Heleen te Brinke, Genetics in Medicine	2020	49
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations Lance H. Rodan, Rebecca C. Spillmann, Harley T. Kurata, Genetics in Medicine Neurobiology Of DiseaseCorticobasal DegenerationNeurological DisorderIsolated Neurological ManifestationsPathology	2021	47
Regeneration of rat sciatic nerve across a LactoSorb bioresorbable conduit with interposed short-segment nerve grafts Paul C. Francel, Kevin S. Smith, Franklin A. Stevens, Journal of neurosurgery	2003	40
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science Kelly Schoch, Cecilia Esteves, Anna Bican, Genetics in Medicine Undiagnosed Diseases NetworkTranslational BioinformaticsMedicineGeneticsGenetic Epidemiology	2020	39

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