Cynthia C. Morton - Concepedia

Author

Cynthia C. Morton

Also Known As

Balasubramanian, Ravikumar, Bell, Scott C., C C Morton, C MORTON, C Morton, C. C Morton, C. C. Morton, C. Morton, C.C. Morton, CYNTHIA C. MORTON

440

Publications

32.5K

Citations

H-Index

264

Concepts

All Affiliations

Harvard University Brigham and Women's Hospital Massachusetts General Hospital Broad Institute Boston Children's Hospital

About

Cynthia C. Morton is an author at Harvard University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	70	158	18.4K
2	Health Sciences	14	15	1.4K
3	Arts	12	12	831
4	Engineering	3	3	93
5	Education	1	1	196

Cynthia C. Morton

249

Publications

28.4K

Citations

H-Index

Page 1

	Year	Citations
Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. Rebecca Taub, Ilan R. Kirsch, Cynthia C. Morton, Proceedings of the National Academy of Sciences Lymphoid NeoplasiaImmunogeneticsXenotransplantationSpecific TranslocationsMedicine	1982	1.4K
Replicating genotype–phenotype associations Stephen J. Chanock, Teri A. Manolio, Michael Boehnke, Nature Genome-wide Association StudyGenotype–phenotype AssociationsLinkage DisequilibriumPhenotypic VariationGenotype-phenotype Association	2007	1.3K
Derivation of Embryonic Stem-Cell Lines from Human Blastocysts Chad A. Cowan, Irina Klimanskaya, Jill A. McMahon, New England Journal of Medicine	2004	973
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson, Nature Genetics Renal FunctionMolecular PhysiologyBiochemistrySodium HomeostasisPhysiology	1999	681
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries Michael E. Talkowski, Jill A. Rosenfeld, Ian Blumenthal, Cell Developmental AnomalyConfer RiskDevelopmental BiologyMendelian DisorderGenetic Disorder	2012	586
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder Hyung‐Goo Kim, Shotaro Kishikawa, Anne W. Higgins, The American Journal of Human Genetics Syndromic AutismImmunologyAutismNeurexin 1Medicine	2008	579
Pleiotropic defects in ataxia-telangiectasia protein-deficient mice Ari Elson, Yaoqi Wang, Cathie Daugherty, Proceedings of the National Academy of Sciences Knockout MouseGenome InstabilityImmunogeneticsDevelopmental BiologyAtm Protein	1996	499
Tumor-Associated Endothelial Cells with Cytogenetic Abnormalities Kyoko Hida, Yasuhiro Hida, Dhara N. Amin, Cancer Research	2004	459
Association of Unconventional Myosin <i>MYO15</i> Mutations with Human Nonsyndromic Deafness <i>DFNB3</i> Aihui Wang, Yong Liang, Robert A. Fridell, Science	1998	439
Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains H.R. Asher, Marlena S. Fejzo, Alexey Tkachenko, Cell Transcriptional RegulationArchitectural FactorSignaling PathwayNatural SciencesMolecular Biology	1995	427

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