Michael T. Musser - Concepedia

Author

Michael T. Musser

University of Wisconsin–Madison

Also Known As

M. T. MUSSER, Michael Musser, Michael T. Musser, Michael Tuttle Musser

Publications

701

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison

About

Michael T. Musser is an author at University of Wisconsin–Madison specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	7	7	195
2	Natural Sciences	5	5	123
3	Medicine	3	3	433
4	Biochemistry	3	3	83
5	Social Sciences	1	1	168

Michael T. Musser

Publications

573

Citations

H-Index

Page 1

	Year	Citations
Deficits in human trisomy 21 iPSCs and neurons Jason P. Weick, Dustie L. Held, George F. Bonadurer, Proceedings of the National Academy of Sciences Down SyndromeCell LineageInduced Pluripotent Stem CellDevelopmental BiologyGenetic Disorder	2013	210
iPSC-Derived Forebrain Neurons from FXS Individuals Show Defects in Initial Neurite Outgrowth Matthew E. Doers, Michael T. Musser, Robert H. Nichol, Stem Cells and Development GeneticsNeurodevelopmentNeurotransmissionCellular NeurobiologyFxs Individuals Show	2014	168
Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (<i>FMR1</i>) Gene Reactivation in Human Neural Cells Meng Li, Huashan Zhao, Gene E. Ananiev, Stem Cells EngineeringGeneticsHigh ThroughputHigh Throughput AssaysGene Characterization	2016	55
New and Facile Substitution Reactions at Tertiary Carbon Nathan Kornblum, Thomas M. Davies, Gary W. Earl, Journal of the American Chemical Society Cross-coupling ReactionEngineeringTertiary CarbonnathanBiochemistryChemical Transformation	1967	44
New and facile substitution reactions at tertiary carbon. Displacement of a nitro group from a saturated carbon atom Nathan Kornblum, Thomas M. Davies, Gary W. Earl, Journal of the American Chemical Society EngineeringChemical TransformationChemical AnalysisOrganic ChemistryChemistry	1967	29
Substitution reactions which proceed via radical anion intermediates. 29. Electron-transfer substitution reactions: p-nitrocumyl system Nathan Kornblum, Leung Cheng, Thomas M. Davies, The Journal of Organic Chemistry Substitution ReactionsCross-coupling ReactionEngineeringChemical TransformationBiochemistry	1987	27
New and facile substitution reactions at tertiary carbon. The use of oxygen as a mechanistic probe Nathan Kornblum, Gary W. Earl, Norman L. Holy, Journal of the American Chemical Society Oxygen Reduction ReactionChemical EngineeringEngineeringChemical AnalysisTertiary Carbon	1968	17
New and facile substitution reactions at tertiary carbon. The m-nitrocumyl system Nathan Kornblum, Thomas M. Davies, Gary W. Earl, Journal of the American Chemical Society Chemical EngineeringM-nitrocumyl SystemEngineeringCross-coupling ReactionBiochemistry	1968	12
Electron-transfer substitution reactions: leaving groups Nathan Kornblum, Peter Ackermann, Joseph W. Manthey, The Journal of Organic Chemistry EngineeringChemical AnalysisProton-coupled Electron TransferAltmetric Attention ScoreOrganic Chemistry	1988	11

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