Colin Fletcher - Concepedia

Author

Colin Fletcher

Also Known As

C F Fletcher, C Fletcher, C. F. Fletcher, C. Fletcher, C.F. Fletcher, COLIN F. FLETCHER, Colin F Fletcher, Colin F. Fletcher, Colin Fletcher, Craig Fletcher

Publications

11.7K

Citations

H-Index

110

Concepts

All Affiliations

Cancer Research Center Howard Hughes Medical Institute National Cancer Institute National Institutes of Health Genomics Institute of the Novartis Research Foundation

About

Colin Fletcher is an author at Cancer Research Center specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	30	7.7K
2	Natural Sciences	8	8	1.1K
3	Health Sciences	5	5	1.3K
4	Social Sciences	5	5	1.4K
5	Engineering	3	3	866

Colin Fletcher

Publications

9.9K

Citations

H-Index

Page 1

	Year	Citations
The Transcriptional Landscape of the Mammalian Genome Piero Carninci, Takeya Kasukawa, Shintaro Katayama, Science GeneticsGenomic MechanismGenomicsMammalian GenomeEpigenetics	2005	3.5K
Absence Epilepsy in Tottering Mutant Mice Is Associated with Calcium Channel Defects Colin Fletcher, Cathleen Lutz, T. Norene O’Sullivan, Cell Knockout MouseChannelopathiesMolecular NeuroscienceNeurophysiologyPhysiology	1996	776
Functional annotation of a full-length mouse cDNA collection Jun Kawai, Akira Shinagawa, Kazuhiro Shibata, Nature Knockout MouseFunctional GenomicsEngineeringMedicineComputational Biology	2001	669
Purification and characterization of OTF-1, a transcription factor regulating cell cycle expression of a human histone H2b gene Colin Fletcher, Nathaniel Heintz, Robert G. Roeder Cell Histone ModificationsChromatinCell Cycle ExpressionCell RegulationChromatin Remodeling	1987	514
The mammalian gene function resource: the international knockout mouse consortium Allan Bradley, Konstantinos Anastassiadis, A. Ayadi, Mammalian Genome	2012	317
Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease Scott M. Wilson, Bula J. Bhattacharyya, Rivka A. Rachel, Nature Genetics Neurodegenerative DiseasesProtein FunctionMolecular NeuroscienceMedicineNatural Sciences	2002	266
Familial hemiplegic migraine mutations increase Ca <sup>2+</sup> influx through single human Ca <sub>V</sub> 2.1 channels and decrease maximal Ca <sub>V</sub> 2.1 current density in neurons Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Proceedings of the National Academy of Sciences Current DensitySynaptic TransmissionFunctional Channel DensitiesNeurotransmissionCellular Neurobiology	2002	260
Mutations in <i>Mlph</i> , encoding a member of the Rab effector family, cause the melanosome transport defects observed in <i>leaden</i> mice Lydia E. Matesic, Richard Yip, Andreé E. Reuss, Proceedings of the National Academy of Sciences	2001	255
Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse Tim Wiltshire, Mathew T. Pletcher, Serge Batalov, Proceedings of the National Academy of Sciences BiologyDisease SusceptibilityPhenotypic VariationLinkage DisequilibriumGenotype-phenotype Association	2003	229
Dystonia and cerebellar atrophy in <i>Cacna1a</i> null mice lacking P/Q calcium channel activity Colin Fletcher, Angelita Tottene, Vanda A. Lennon, The FASEB Journal	2001	208

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