Charlene J. Williams

Author

Also Known As

C J C Williams, C J Williams, C Williams, C. J. Williams, C. Williams, C.J. Williams, CHARLENE J. WILLIAMS, Charlene J Williams, Charlene J. Williams, Charlene Williams

Publications

4.1K

Citations

H-Index

124

Concepts

All Affiliations

Thomas Jefferson University Rutgers, The State University of New Jersey Jefferson Institute Cooper Medical School of Rowan University Center for Molecular Medicine and Immunology

About

Charlene J. Williams is an author at Thomas Jefferson University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	24	2.3K
2	Natural Sciences	5	5	481
3	Engineering	3	3	167
4	Health Sciences	2	2	247
5	Education	1	1	29

Charlene J. Williams

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Rat brain preproenkephalin mRNA. cDNA cloning, primary structure, and distribution in the central nervous system. Kenichi Yoshikawa, Charlene J. Williams, Steven L. Sabol Journal of Biological Chemistry Synaptic TransmissionCdna CloningMolecular BiologyTotal RnaCellular Neurobiology	1984	544
Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition Tsuyoshi Tanabe, Mathias Chamaillard, Yasunori Ogura, The EMBO Journal Molecular CharacterizationMuramyl Dipeptide RecognitionBiochemistryNatural SciencesBiomolecular Analysis	2004	358
Identification of Incidental Sequence Polymorphisms and Absence of the <i>db/db</i> Mouse and <i>fa/fa</i> Rat Mutations Robert V. Considine, F. José, Eileen L. Considine, Diabetes Human GrowthGeneticsMolecular GeneticsDisease Gene IdentificationAdipokines	1996	234
Mutations in ANKH Cause Chondrocalcinosis Adrian Pendleton, Michelle D. Johnson, Anne E. Hughes, The American Journal of Human Genetics GeneticsSurgical PathologyHistopathologyPathologyMolecular Pathology	2002	216
Human proα1(I) collagen gene structure reveals evolutionary conservation of a pattern of introns and exons Mon‐Li Chu, Wouter de Wet, Michael P. Bernard, Nature Cell LineageDevelopmental BiologyHuman Proα1Developmental GeneticsGenetics	1984	208
Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta Mon‐Li Chu, Charlene J. Williams, Gugliemina Pepe, Nature Developmental BiologyBone Morphogenic ProteinBone RepairFracture HealingOsteogenesis	1983	178
<i>CARD15</i> mutations in familial granulomatosis syndromes: A study of the original Blau syndrome kindred and other families with large‐vessel arteritis and cranial neuropathy Xiaoju Wang, Helena Kuivaniemi, Gina Bonavita, Arthritis & Rheumatism	2002	139
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16. Gerard Tromp, Helena Kuivaniemi, Steven Raphael, PubMed	1996	132
Synthesis and processing of a type I procollagen containing shortened pro-alpha 1(I) chains by fibroblasts from a patient with osteogenesis imperfecta. Charlene J. Williams, Darwin J. Prockop Journal of Biological Chemistry	1983	119
Autosomal Dominant Familial Calcium Pyrophosphate Dihydrate Deposition Disease Is Caused by Mutation in the Transmembrane Protein ANKH Charlene J. Williams, Yun Zhang, Andrew E. Timms, The American Journal of Human Genetics Molecular PhysiologyMendelian DisorderTransmembrane Protein AnkhGenetic DisorderGenetics	2002	114

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