Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI

Variation Interpretation Predictors: Principles, Types, Performance, and Choice

(2016) Abhishek Niroula et al.   HUMAN MUTATION

VHLdb: A database of von Hippel-Lindau protein interactors and mutations

(2016) Francesco Tabaro et al.   Scientific Reports

Correct machine learning on protein sequences: a peer-reviewing perspective

(2015) Ian Walsh et al.   BRIEFINGS IN BIOINFORMATICS

Genetics of familial melanoma: 20 years afterCDKN2A

(2015) Lauren G. Aoude et al.   Pigment Cell & Melanoma Research

TheCDKN2A/p16INK4a5′UTR sequence and translational regulation: impact of novel variants predisposing to melanoma

(2015) Virginia Andreotti et al.   Pigment Cell & Melanoma Research

DBGC: A Database of Human Gastric Cancer

(2015) Chao Wang et al.   PLoS One

CDKN2AUnclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment

(2014) Maria Chiara Scaini et al.   HUMAN MUTATION

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

(2014) Simon A. Forbes et al.   NUCLEIC ACIDS RESEARCH

WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation

(2013) Emidio Capriotti et al.   BMC GENOMICS

When a "Disease-Causing Mutation" Is Not a Pathogenic Variant

(2013) J. Wang et al.   CLINICAL CHEMISTRY

Alternative Protein-Protein Interfaces Are Frequent Exceptions

(2012) Tobias Hamp et al.   PLoS Computational Biology

Identification and In Silico Analysis of Novel von Hippel-Lindau (VHL) Gene Variants from a Large Population

(2011) Emanuela Leonardi et al.   ANNALS OF HUMAN GENETICS

Classifying variants of CDKN2A using computational and laboratory studies

(2011) Peter J. Miller et al.   HUMAN MUTATION

Modeling Symmetric Macromolecular Structures in Rosetta3

(2011) Frank DiMaio et al.   PLoS One

Genomewide Association Studies and Assessment of the Risk of Disease

(2010) Teri A. Manolio   NEW ENGLAND JOURNAL OF MEDICINE

Functional, structural, and genetic evaluation of 20CDKN2Agerm line mutations identified in melanoma-prone families or patients

(2009) Caroline Kannengiesser et al.   HUMAN MUTATION

Functional annotations improve the predictive score of human disease-related mutations in proteins

(2009) Remo Calabrese et al.   HUMAN MUTATION

Functional impairment of p16INK4A due to CDKN2A p.Gly23Asp missense mutation

(2009) Maria Chiara Scaini et al.   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS

Distance-scaled, finite ideal-gas reference state improves structure-derived potentials of mean force for structure selection and stability prediction

(2002) Hongyi Zhou et al.   PROTEIN SCIENCE