Louis M. Kunkel - Concepedia

Author

Louis M. Kunkel

Also Known As

Froehner, Stanley C., Kunkel, L. M., Kunkel, Louis, Kunkel, Louis M., Kyung-Ah Cho, L KUNKEL, L Kunkel, L M Kunkel, L. KUNKEL, L. Kunkel

355

Publications

46.7K

Citations

103

H-Index

216

Concepts

All Affiliations

Harvard University Boston Children's Hospital Howard Hughes Medical Institute Dana-Farber/Boston Children's Cancer and Blood Disorders Center Pediatrics and Genetics

About

Louis M. Kunkel is an author at Harvard University specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	71	137	25.5K
2	Natural Sciences	25	27	10.2K
3	Health Sciences	17	18	2.8K
4	Engineering	10	10	1.9K
5	Education	1	1	42

Louis M. Kunkel

241

Publications

42.5K

Citations

H-Index

Page 1

	Year	Citations
Dystrophin: The protein product of the duchenne muscular dystrophy locus Eric P. Hoffman, Robert H. Brown, Louis M. Kunkel Cell Protein FunctionBiochemistrySkeletal MuscleProtein FoldingNatural Sciences	1987	4.6K
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals Eric P. Hoffman, Corlee J. Bertelson, Anthony P. Monaco, Cell Mendelian DisorderDmd GeneDuchenne Muscular DystrophyGeneticsGenetic Disorder	1987	2.4K
Dystrophin expression in the mdx mouse restored by stem cell transplantation Emanuela Gussoni, Yuko Soneoka, Corinne D. Strickland, Nature Regenerative MedicineDevelopmental BiologyMedicineStem Cell TransplantationDystrophin Expression	1999	1.8K
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein Anthony P. Monaco, Louis M. Kunkel Cell Protein FunctionProtein FoldingNatural SciencesMolecular BiologyCell Motility	1988	1.5K
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Louis M. Kunkel, Kirby D. Smith, Samuel H. Boyer, Proceedings of the National Academy of Sciences Chromosome VariantsGenetic TestingCytogeneticsGenetic DisorderGenetics	1977	1.4K
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus Anthony P. Monaco, Corlee J. Bertelson, Sabina Liechti‐Gallati, Genomics Mendelian DisorderGenetic DisorderGeneticsClinical GeneticsPathology	1988	1.2K
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene Anthony P. Monaco, Rachael L. Neve, Chris Colletti-Feener, Nature Genetic DisorderNatural SciencesGeneticsMolecular BiologyDegenerative Disease	1986	1K
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Alan H. Beggs, Mary B. Moyer, S. Scherpf, PubMed	1989	961
Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular Dystrophy Eric P. Hoffman, Kenneth H. Fischbeck, Robert H. Brown, New England Journal of Medicine	1988	924
Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts T. Partridge, Jennifer E. Morgan, Gary R. Coulton, Nature Tissue EngineeringMechanobiologyRegenerative MedicineEngineeringPathology	1989	860

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