H. Brent Clark - Concepedia

Author

H. Brent Clark

University of Minnesota ORCID

Also Known As

H B. Clark, H Brent Clark, H. B. Clark, H. Brent Clark, H.B. Clark, H.Brent Clark, H. Brent Clark, Harris Clark

Publications

6.8K

Citations

H-Index

Concepts

All Affiliations

University of Minnesota University of Minnesota Medical Center Howard Hughes Medical Institute Baylor College of Medicine Inserm

About

H. Brent Clark is an author at University of Minnesota specializing in medicine, cell biology, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	22	4K
2	Social Sciences	7	7	1.2K
3	Health Sciences	2	2	419
4	Allergy	2	2	326
5	Natural Sciences	1	1	78

H. Brent Clark

Publications

6.3K

Citations

H-Index

Page 1

	Year	Citations
Ataxin-1 Nuclear Localization and Aggregation Ivan A. Klement, Pamela J. Skinner, Michael D. Kaytor, Cell Nuclear OrganizationNuclear EngineeringMolecular BiologyAtaxin-1 Nuclear Localization	1998	959
Non-ATG–initiated translation directed by microsatellite expansions Tao Zu, Brian B. Gibbens, Noelle S. Doty, Proceedings of the National Academy of Sciences Trinucleotide ExpansionsNeurodegenerative DiseasesAllelic VariantGenetic DisorderMedicine	2010	896
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8 Melinda L. Moseley, Tao Zu, Yoshio Ikeda, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceCag Expansion TranscriptsBidirectional ExpressionNeuroscience	2006	419
Spectrin mutations cause spinocerebellar ataxia type 5 Yoshio Ikeda, Katherine A. Dick, Marcy R. Weatherspoon, Nature Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2006	382
Muscleblind-like 2-Mediated Alternative Splicing in the Developing Brain and Dysregulation in Myotonic Dystrophy Konstantinos Charizanis, Kuang-Yung Lee, Ranjan Batra, Neuron Developmental BiologyMolecular NeuroscienceSkeletal MuscleMedicineMyotonic Dystrophy	2012	341
Serine 776 of Ataxin-1 Is Critical for Polyglutamine-Induced Disease in SCA1 Transgenic Mice Effat S. Emamian, Michael D. Kaytor, Lisa Duvick, Neuron Knockout MouseNeurodegenerative DiseasesAllergyAutoimmune DiseaseDisease Mechanism	2003	306
Spinocerebellar ataxia type 6: Gaze‐evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset Christopher M. Gómez, Randall M. Thompson, Jason T. Gammack, Annals of Neurology	1997	280
Purkinje Cell Expression of a Mutant Allele of<i>SCA1</i>in Transgenic Mice Leads to Disparate Effects on Motor Behaviors, Followed by a Progressive Cerebellar Dysfunction and Histological Alterations H. Brent Clark, Eric N. Burright, Wael S. Yunis, Journal of Neuroscience Mutant AlleleMotor Control DisordersCellular NeurobiologySynaptic SignalingMutant Sca1 Mice	1997	273
Recovery from Polyglutamine-Induced Neurodegeneration in Conditional <i>SCA1</i> Transgenic Mice Tao Zu, Lisa Duvick, Michael D. Kaytor, Journal of Neuroscience	2004	264
RORα-Mediated Purkinje Cell Development Determines Disease Severity in Adult SCA1 Mice Heliane Guerra Serra, Lisa Duvick, Tao Zu, Cell Neurodegenerative DiseasesDevelopmental BiologyImmune Cell DevelopmentMedicineDegenerative Disease	2006	234

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