S.A. Latt - Concepedia

Author

S.A. Latt

Harvard University

Also Known As

J.D. Murken, S A Latt, S Latt, S. A. Latt, S. Latt, S.A. LATT, S.A. Latt, SM Latt, Samuel A. Latt, SamuelA. Latt

Publications

6.4K

Citations

H-Index

132

Concepts

All Affiliations

Harvard University Boston Children's Hospital Harvard University Press Howard Hughes Medical Institute Brigham and Women's Hospital

About

S.A. Latt is an author at Harvard University specializing in medicine, chromatin, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	43	4.4K
2	Natural Sciences	15	16	1.6K
3	Engineering	7	7	805
4	Health Sciences	5	5	531
5	Education	1	1	931

S.A. Latt

Publications

6.1K

Citations

H-Index

Page 1

	Year	Citations
Automatic measurement of sister chromatid exchange frequency. G W Zack, W E Rogers, S.A. Latt Journal of Histochemistry & Cytochemistry MeasurementCytogeneticsGeneticsEducationAutomatic System	1977	931
Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis, American Journal of Medical Genetics	1989	581
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Louis M. Kunkel, Anthony P. Monaco, William Middlesworth, Proceedings of the National Academy of Sciences CytogeneticsGeneticsDna AnalysisPathologyMolecular Biology	1985	453
Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Diana W. Bianchi, Alan F. Flint, M F Pizzimenti, Proceedings of the National Academy of Sciences ChromatinDevelopmental BiologyGeneticsHematologyFetal Medicine	1990	414
Spectral studies on 33258 Hoechst and related bisbenzimidazole dyes useful for fluorescent detection of deoxyribonucleic acid synthesis. S.A. Latt, Gail Stetten Journal of Histochemistry & Cytochemistry EngineeringMolecular BiologyOrganic ChemistryLess Intense FluorescencePhosphorescence Imaging	1976	356
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. S.A. Latt, Gail Stetten, L. Juergens, Proceedings of the National Academy of Sciences BiologyChromatinChromatid BreaksBone Marrow FailureCell Division	1975	265
Coamplification and coexpression of human tissue-type plasminogen activator and murine dihydrofolate reductase sequences in Chinese hamster ovary cells. Randal J. Kaufman, L C Wasley, Amelia J. Spiliotes, Molecular and Cellular Biology GeneticsCell ProliferationReproductive BiologyReproductive EndocrinologyProtein Expression	1985	204
A simplified technique for in vivo analysis of sister-chromatid exchanges using 5-bromodeoxyuridine tablets James W. Allen, Charles F. Shuler, Robert W. Mendes, Cytogenetic and Genome Research Brdu AdministrationImmunologySmall TabletDermatologyBioanalysis	1977	178
Energy Transfer. A System with Relatively Fixed Donor-Acceptor Separation S.A. Latt, H. T. Andrew Cheung, Elkan Blout Journal of the American Chemical Society EngineeringChemical AnalysisEnergy EfficiencyEnergy ConversionAltmetric Attention Score	1965	178
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Tim Donlon, M. Lalande, Arlene R. Wyman, Proceedings of the National Academy of Sciences CytogeneticsGeneticsPathologyMolecular GeneticsDisease Gene Identification	1986	159

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