Prasanth Potluri - Concepedia

Author

Prasanth Potluri

Children's Hospital of Philadelphia

Also Known As

P Potluri, P. Potluri, Prasanth Potluri

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Children's Hospital of Philadelphia University of Pennsylvania University of California San Diego University of California, Irvine Columbia University Irving Medical Center

About

Prasanth Potluri is an author at Children's Hospital of Philadelphia specializing in medicine, mitochondrial function, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	922
2	Natural Sciences	7	7	550
3	Biochemistry	2	2	76
4	Public Health	1	1	30
5	Social Sciences	1	1	84

Prasanth Potluri

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming Martin Picard, Jiangwen Zhang, Saege Hancock, Proceedings of the National Academy of Sciences	2014	296
The ADP/ATP translocase drives mitophagy independent of nucleotide exchange Atsushi Hoshino, Weijia Wang, Shogo Wada, Nature MitophagyMitochondrial FunctionNatural SciencesAdp/atp Translocase DrivesAutophagy	2019	250
Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy Piotr Kopiński, Kevin A. Janssen, Patrick M. Schaefer, Proceedings of the National Academy of Sciences	2019	155
Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome Mariella Simon, Élodie M. Richard, Xinjian Wang, PLoS Genetics Neurodegenerative DiseasesMendelian DisorderMitochondrial BiogenesisMitochondrial FunctionGenetic Disorder	2015	113
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease Prasanth Potluri, Antonio Dávila, Eduardo Ruiz‐Pesini, Molecular Genetics and Metabolism Neurodegenerative DiseasesAlzheimer's DiseaseMitochondrial FunctionDegenerative DiseaseDegenerative Pathology	2009	99
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome Hailing Su, Weiwei Fan, Pınar Coşkun, Neuroscience Letters Molecular NeuroscienceMitochondrial FunctionSynaptic SignalingMitochondrial DysfunctionAngelman Syndrome	2009	84
Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy Meagan J. McManus, Martin Picard, Hsiao‐Wen Chen, Cell Metabolism Cardiac MuscleCardiomyopathyMitochondrial FunctionNatural SciencesGenetics	2018	79
Cyanide Detoxification by the Cobalamin Precursor Cobinamide Kate E. Broderick, Prasanth Potluri, Shunhui Zhuang, Experimental Biology and Medicine	2006	74
Development and Characterization of a Conditional Mitochondrial Complex I Assembly System Nagendra Yadava, Toby Houchens, Prasanth Potluri, Journal of Biological Chemistry GeneticsMolecular BiologyMitochondrial BiogenesisProtein FoldingMitochondrial Structure	2004	68
Species-specific and Mutant MWFE Proteins Nagendra Yadava, Prasanth Potluri, Erin N. Smith, Journal of Biological Chemistry	2002	64

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