Craig L. Bennett - Concepedia

Author

Craig L. Bennett

Also Known As

C Bennett, C. BENNETT, C. Bennett, C. L. Bennett, C.L. Bennett, Craig Bennett, Craig C. Bennett, Craig L Bennett, Craig L. Bennett

Publications

Citations

H-Index

Concepts

All Affiliations

University of Washington University of California San Diego The University of Sydney Duke University University of California, Irvine

About

Craig L. Bennett is an author at University of Washington specializing in medicine, genetics, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	19	5.5K
2	Natural Sciences	2	2	904
3	Public Health	2	2	158
4	Education	1	1	11
5	Social Sciences	1	1	26

Craig L. Bennett

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 Craig L. Bennett, Jacinda R. Christie, Fred Ramsdell, Nature Genetics Autoimmune DiseaseDisease MechanismGenetic DisorderGeneticsPathogenesis	2001	3.3K
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4) Ying-Zhang Chen, Craig L. Bennett, Huy M. Huynh, The American Journal of Human Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderNatural SciencesGenetics	2004	810
The NPHP1 Gene Deletion Associated with Juvenile Nephronophthisis Is Present in a Subset of Individuals with Joubert Syndrome Melissa A. Parisi, Craig L. Bennett, Melissa Eckert, The American Journal of Human Genetics Developmental BiologyMendelian DisorderJoubert SyndromeGenetic DisorderGenetics	2004	255
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome Craig L. Bennett, Mary E. Brunkow, Fred Ramsdell, Immunogenetics Transcriptional RegulationMendelian DisorderGenetic DisorderGeneticsPathology	2001	243
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C V A Street, Craig L. Bennett, Jeff Goldy, Neurology	2003	196
INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES John Collinge, Jeremy M. Brown, John Hardy, Brain	1992	171
INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 1. GENEALOGICAL AND MOLECULAR STUDIES Mark Poulter, H. F. Baker, Chris Frith, Brain	1992	167
Cross-Sectional Analysis of Met235→Thr Variant of Angiotensinogen Gene in Severe, Familial Hypertension Craig L. Bennett, A. P. Schrader, Brian J. Morris Biochemical and Biophysical Research Communications HypertensionEpidemiologyCardiovascular DiseaseFamilial HypertensionGenetics	1993	118
X-Linked Syndrome of Polyendocrinopathy, Immune Dysfunction, and Diarrhea Maps to Xp11.23-Xq13.3 Craig L. Bennett, Ritsuko Yoshioka, Hidenori Kiyosawa, The American Journal of Human Genetics Diarrhea MapsDisease MechanismPathogenesisImmunologyGastroenterology	2000	112
Senataxin, the yeast Sen1p orthologue: Characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease Ying-Zhang Chen, Sayed Hossein Hashemi, Susan K. Anderson, Neurobiology of Disease Neurodegenerative DiseasesUnique ProteinMotor Neuron DiseaseYeast Sen1p OrthologueGenetic Disorder	2006	110

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