Peter C. Sapp - Concepedia

Author

Peter C. Sapp

Also Known As

Jacqueline de Belleroche, P Sapp, P. C. Sapp, P. Sapp, P.C. Sapp, Peter C Sapp, Peter C. Sapp, Peter Sapp, Peter C. Sapp, Tea B. Cau

Publications

17.5K

Citations

H-Index

Concepts

All Affiliations

Massachusetts General Hospital Massachusetts Institute of Technology Howard Hughes Medical Institute University of Massachusetts Chan Medical School Emory University

About

Peter C. Sapp is an author at Massachusetts General Hospital specializing in medicine, neurodegenerative diseases, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	19	13K
2	Cell Biology	5	5	4.3K
3	Natural Sciences	2	2	3K
4	Engineering	1	1	972
5	Social Sciences	1	1	75

Peter C. Sapp

Publications

15.3K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis D.R. Rosen, Teepu Siddique, David T. Patterson, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsMolecular Biology	1993	7K
Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc, Science Neurodegenerative DiseasesAmyotrophic Lateral SclerosisSomatic VariantMendelian DisorderGenetic Disorder	2009	2.5K
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Science EngineeringExome SequencingGeneticsImmunologyDisease Gene Identification	2015	972
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisDevelopmental BiologyProfilin 1Genetic Disorder	2012	594
Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules Daryl A. Bosco, Nathan Lemay, Hae Kyung Ko, Human Molecular Genetics Rna-binding Protein FusMutant FusNeurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular Neuroscience	2010	511
Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity Teepu Siddique, Denise A. Figlewigz, Margaret A. Pericak‐Vance, New England Journal of Medicine	1991	379
Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration Claire L. Simpson, Robin Lemmens, Katarzyna Miśkiewicz, Human Molecular Genetics	2008	290
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis Kevin P. Kenna, Perry T.C. van Doormaal, Annelot M. Dekker, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderNeurologyNeuroscience	2016	278
Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice Owen M. Peters, Gabriela Toro Cabrera, Hélène Tran, Neuron Knockout MouseBac Transgenic MiceNeurodegenerative DiseasesMolecular NeuroscienceGenetics	2015	252
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis Bradley Smith, Simon Topp, Claudia Fallini, Science Translational Medicine	2017	243

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