Molecular insights into the coding region mutations of low‐density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia

Computational Molecular Phenotypic Analysis of PTPN22 (W620R), IL6R (D358A), and TYK2 (P1104A) Gene Mutations of Rheumatoid Arthritis

(2019) Noor Ahmad Shaik et al.   Frontiers in Genetics

Polygenic Hypercholesterolemia and Cardiovascular Disease Risk

(2019) Mahtab Sharifi et al.   Current Cardiology Reports

Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndrome

(2019) Noor A. Shaik et al.   JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS

Binding mechanism of spinosine and venenatine molecules with p300 HAT enzyme: Molecular screening, molecular dynamics and free‐energy analysis

(2019) Sivanandam Magudeeswaran et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

OUP accepted manuscript

(2018)   NUCLEIC ACIDS RESEARCH

Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia

(2018) Fahad Alnouri et al.   ATHEROSCLEROSIS

A computational method to characterize the missense mutations in the catalytic domain of GAA protein causing Pompe disease

(2018) D Thirumal Kumar et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

A Computational Protein Phenotype Prediction Approach to Analyze the Deleterious Mutations of Human MED12 Gene

(2016) Babajan Banaganapalli et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

(2016) Karthik A Jagadeesh et al.   NATURE GENETICS

The ExAC browser: displaying reference data information from over 60 000 exomes

(2016) Konrad J. Karczewski et al.   NUCLEIC ACIDS RESEARCH

The history of Autosomal Recessive Hypercholesterolemia (ARH). From clinical observations to gene identification

(2015) Renato Fellin et al.   GENE

The I-TASSER Suite: protein structure and function prediction

(2015) Jianyi Yang et al.   NATURE METHODS

Structural and Functional Characterization of Pathogenic Non- Synonymous Genetic Mutations of Human Insulin-Degrading Enzyme by In Silico Methods

(2014) Noor Shaik et al.   CNS & Neurological Disorders-Drug Targets

DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach

(2014) D. E. V. Pires et al.   NUCLEIC ACIDS RESEARCH

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

(2013) Peter D. Stenson et al.   HUMAN GENETICS

CABS-flex: server for fast simulation of protein structure fluctuations

(2013) Michal Jamroz et al.   NUCLEIC ACIDS RESEARCH

CDD: conserved domains and protein three-dimensional structure

(2012) Aron Marchler-Bauer et al.   NUCLEIC ACIDS RESEARCH

Hyperlipidemia as a Risk Factor for Cardiovascular Disease

(2012) Robert H. Nelson   PRIMARY CARE

Protein structure validation by generalized linear model root-mean-square deviation prediction

(2011) Anurag Bagaria et al.   PROTEIN SCIENCE

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Achieving reliability and high accuracy in automated protein docking: Cluspro, PIPER, SDU, and stability analysis in CAPRI rounds 13-19

(2010) Dima Kozakov et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

SNAP predicts effect of mutations on protein function

(2008) Yana Bromberg et al.   BIOINFORMATICS

Recent Progress and Future Directions in Protein-Protein Docking

(2008) David Ritchie   CURRENT PROTEIN & PEPTIDE SCIENCE