Sharon E Plon
Genetics · 2011–2022
A researcher in the Science corpus: 9 papers; trusts 20 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 98 citations into it; #5,094 of 6,854 by trust here, #1,264 by citations
- Molecular Biology — 88 citations into it; #13,928 of 17,773 by trust here, #6,817 by citations
Whom Sharon E Plon trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Pauline Crystal Ng
- Tal Galili
- Tom Fawcett
- Steven Henikoff
- Gregory M. Cooper
- Abel Gonzalez-Perez
- Ryota Suzuki
- Panagiotis Katsonis
- Xiaoming Liu
Who trusts Sharon E Plon overall
Papers from Sharon E Plon's perspective
Ordered by how strongly the researchers Sharon E Plon trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- Predicting the effects of amino acid substitutions on protein function.
- Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
- Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- Accounting for human polymorphisms predicted to affect protein function. (Genome Research)
- Prediction of Missense Mutation Functionality Depends on both the Algorithm and Sequence Alignment Employed
- Analysis of protein-coding genetic variation in 60,706 humans
- Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
Their papers
- Prediction of Missense Mutation Functionality Depends on both the Algorithm and Sequence Alignment Employed (2011) — 226 citations
- ClinGen--the Clinical Genome Resource. (2015) — 1,269 citations
- Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria (2022) — 419 citations
- Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework (2019) — 519 citations
- Pathogenic germline variants in 10,389 adult cancers (2018) — 734 citations
- Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines (2017) — 212 citations
- Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation (2016) — 676 citations
- Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing (2014) — 1,342 citations
- Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders (2013) — 1,887 citations