SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations

Mapping proteome-wide interactions of reactive chemicals using chemoproteomic platforms

(2016) Jessica L Counihan et al.   CURRENT OPINION IN CHEMICAL BIOLOGY

Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding

(2016) Yunhui Peng et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

Editorial overview: Linking protein sequence and structural changes to function in the era of next-generation sequencing

(2015) Anna R Panchenko et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins

(2015) Tugba G Kucukkal et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

On Human Disease-Causing Amino Acid Variants: Statistical Study of Sequence and Structural Patterns

(2015) Marharyta Petukh et al.   HUMAN MUTATION

Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease

(2015) Yunhui Peng et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis

(2015) Lishou Pan et al.   NEUROLOGICAL SCIENCES

ClinVar: public archive of interpretations of clinically relevant variants

(2015) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Predicting Binding Free Energy Change Caused by Point Mutations with Knowledge-Modified MM/PBSA Method

(2015) Marharyta Petukh et al.   PLoS Computational Biology

Computational and Experimental Approaches to Reveal the Effects of Single Nucleotide Polymorphisms with Respect to Disease Diagnostics

(2014) Tugba Kucukkal et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Predicting the Impact of Missense Mutations on Protein–Protein Binding Affinity

(2014) Minghui Li et al.   Journal of Chemical Theory and Computation

Chronic Beryllium Disease: Revealing the Role of Beryllium Ion and Small Peptides Binding to HLA-DP2

(2014) Marharyta Petukh et al.   PLoS One

mCSM: predicting the effects of mutations in proteins using graph-based signatures

(2013) Douglas E. V. Pires et al.   BIOINFORMATICS

Scoring functions for protein–protein interactions

(2013) Iain H Moal et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Understanding Molecular Effects of Naturally Occurring Genetic Differences

(2013) Emil Alexov et al.   JOURNAL OF MOLECULAR BIOLOGY

Molecular Mechanisms of Disease-Causing Missense Mutations

(2013) Shannon Stefl et al.   JOURNAL OF MOLECULAR BIOLOGY

Immunohistochemical studies of angiogenin in the skin of patients with amyotrophic lateral sclerosis

(2013) Kazuhiro Higashida et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

BeAtMuSiC: prediction of changes in protein–protein binding affinity on mutations

(2013) Yves Dehouck et al.   NUCLEIC ACIDS RESEARCH

ClinVar: public archive of relationships among sequence variation and human phenotype

(2013) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Cancer Missense Mutations Alter Binding Properties of Proteins and Their Interaction Networks

(2013) Hafumi Nishi et al.   PLoS One

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort

(2012) Zhang-Yu Zou et al.   Amyotrophic Lateral Sclerosis

SKEMPI: a Structural Kinetic and Energetic database of Mutant Protein Interactions and its use in empirical models

(2012) Iain H. Moal et al.   BIOINFORMATICS

Analyzing Effects of Naturally Occurring Missense Mutations

(2012) Zhe Zhang et al.   Computational and Mathematical Methods in Medicine

An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity

(2012) Kyoko Takano et al.   HUMAN MOLECULAR GENETICS

Proteome-wide prediction of protein-protein interactions from high-throughput data

(2012) Zhi-Ping Liu et al.   Protein & Cell

Predicting protein-protein interactions on a proteome scale by matching evolutionary and structural similarities at interfaces using PRISM

(2011) Nurcan Tuncbag et al.   Nature Protocols

In Silico and In Vitro Investigations of the Mutability of Disease-Causing Missense Mutation Sites in Spermine Synthase

(2011) Zhe Zhang et al.   PLoS One

A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics

(2011) Shawn Witham et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

Computational analysis of missense mutations causing Snyder-Robinson syndrome

(2010) Zhe Zhang et al.   HUMAN MUTATION

Performance of protein stability predictors

(2010) Sofia Khan et al.   HUMAN MUTATION

Mutations in the promoter region of the aldolase B gene that cause hereditary fructose intolerance

(2010) Erin M. Coffee et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Modeling Effects of Human Single Nucleotide Polymorphisms on Protein-Protein Interactions

(2009) Shaolei Teng et al.   BIOPHYSICAL JOURNAL

Editorial [ Protein-Protein Interactions Guest Editor: Emil Alexov ]

(2008) Emil Alexov   CURRENT PHARMACEUTICAL BIOTECHNOLOGY

Approaches and Resources for Prediction of the Effects of Non-Synonymous Single Nucleotide Polymorphism on Protein Function and Interactions

(2008) S. Teng et al.   CURRENT PHARMACEUTICAL BIOTECHNOLOGY

Hereditary fructose intolerance: Frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France—Identification of eight new mutations

(2008) Anne Davit-Spraul et al.   MOLECULAR GENETICS AND METABOLISM