C. Thomas Caskey - Concepedia

Author

C. Thomas Caskey

Also Known As

C CASKEY, C Caskey, C T Caskey, C THOMAS CASKEY, C Thomas Caskey, C. Caskey, C. T. CASKEY, C. T. Caskey, C. THOMAS CASKEY, C. Thomas Caskey

214

Publications

24.7K

Citations

H-Index

146

Concepts

All Affiliations

Baylor College of Medicine Howard Hughes Medical Institute Baylor Genetics United States Military Academy The University of Texas Health Science Center at Houston

About

C. Thomas Caskey is an author at Baylor College of Medicine specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	49	75	18.6K
2	Natural Sciences	24	27	3K
3	Engineering	4	4	615
4	Public Health	4	4	306
5	Health Sciences	1	1	405

C. Thomas Caskey

115

Publications

23K

Citations

H-Index

Page 1

	Year	Citations
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe, Cell Breakpoint Cluster RegionFragile X SyndromeMendelian DisorderGenetic DisorderGenetics	1991	3.5K
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox Ying‐Hui Fu, Derek P.A. Kuhl, Antonio Pizzuti, Cell Sherman ParadoxGenome InstabilityGenetic InstabilityGenetic DisorderMedicine	1991	2.1K
Absence of expression of the FMR-1 gene in fragile X syndrome Maura Pieretti, F Zhang, Ying‐Hui Fu, Cell Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1991	1.5K
An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy Ying‐Hui Fu, Antonio Pizzuti, Raymond G. Fenwick, Science Rare DiseasesGene RelatedMendelian DisorderGenetic DisorderMedicine	1992	1.5K
Characterization of the human cysteinyl leukotriene CysLT1 receptor Kevin R. Lynch, Gary P. O’Neill, Qingyun Liu, Nature InflammationCytokineG Protein-coupled ReceptorMedicineImmunology	1999	967
Identification of the gene responsible for Best macular dystrophy Konstantin Petrukhin, Markus J. Koisti, Benjamin Bakall, Nature Genetics Ocular DiseaseOphthalmologyGeneticsBest Macular DystrophyMedicine	1998	679
Two independent mutational events in the loss of urate oxidase during hominoid evolution Xiangwei Wu, Donna M. Muzny, Cheng Chi Lee, Journal of Molecular Evolution BiologyHeme DegradationGeneticsHominoid EvolutionBiochemical Genetics	1992	536
Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites Tao Long, Michael Hicks, Hung‐Chun Yu, Nature Genetics Allelic VariantSequencingEngineeringMedicineGenetics	2017	478
Identification of a (CUG)n Triplet Repeat RNA-Binding Protein and Its Expression in Myotonic Dystrophy Lubov Timchenko, J. W. Miller, Nikolai A. Timchenko, Nucleic Acids Research	1996	457
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Catherine A. Brownstein, Alan H. Beggs, Nils Homer, Genome biology	2014	432

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