Point Mutations
Point Mutations is a type of genetic mutation characterized by the substitution, insertion, or deletion of a single nucleotide base in the DNA sequence, thereby altering the genetic code at a specific locus.
9.4K
Publications
691.1K
Citations
50.2K
Authors
6.3K
Institutions
Publications per year
2017–2026
1.3K
Variants
Point Mutation
Parents
9.4K
Mutational landscape and significance across 12 major cancer types
Cyriac Kandoth, Michael D. McLellan, Fabio Vandin et al. · Nature · 2013 · 4.5K citations · Full text
Core Signaling Pathways in Human Pancreatic Cancers Revealed by Global Genomic Analyses
Siân Jones, D. Williams Parsons, Jimmy Lin et al. · Science · 2008 · 4K citations · Full text
1–5 of 9.4K
50.2K
Massachusetts Institute of Technology, United States
20 publications · 1.4K citations
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13
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12
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12
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1–5 of 50.2K
6.3K
Harvard University
Cambridge, United States
88 h-index
717 publications
130.7K citations
Inserm
Paris, France
83 h-index
1.2K publications
125.6K citations

Howard Hughes Medical Institute
Chevy Chase, United States
76 h-index
408 publications
84.9K citations
National Institutes of Health
Bethesda, United States
72 h-index
597 publications
106.7K citations

Centre National de la Recherche Scientifique
Paris, France
70 h-index
880 publications
73.2K citations
National Cancer Institute
Bethesda, United States
63 h-index
424 publications
73.2K citations
University of Washington
Seattle, United States
57 h-index
420 publications
51.2K citations

Johns Hopkins University
Baltimore, United States
56 h-index
408 publications
222.4K citations
1–8 of 6.3K
PNAS · 384 publications · 60.3K citations
138
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JBC · 376 publications · 29.5K citations
93
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JVI · 280 publications · 23.5K citations
88
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Repository · 438 publications · 33.4K citations
88
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286 publications · 34.2K citations
80
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