Shamil R. Sunyaev

发表

novoCaller: a Bayesian network approach for de novo variant calling from pedigree and population sequence data

Anwoy Kumar Mohanty, Dana Vuzman, Laurent Francioli, 2018, Bioinform..

Analysis of Sequence Conservation at Nucleotide Resolution

Mikhail A. Roytberg, John A. Stamatoyannopoulos, Shamil R. Sunyaev, 2007, PLoS Comput. Biol..

Analysis of the position dependent amino acid probabilities and its application to the search for remote homologues

Frank Eisenhaber, Shamil R. Sunyaev, Igor V. Rodchenkov, 1998, RECOMB '98.

Assigning spectrum-specific P-values to protein identifications by mass spectrometry

Shamil R. Sunyaev, Victor Spirin, Alexander Shpunt, 2011, Bioinform..

Session Introduction: Inferring SNP Function Using Evolutionary, Structural and Computational Methods

Matthew W. Dimmic, Shamil R. Sunyaev, Carlos D. Bustamante, 2005, Pacific Symposium on Biocomputing.

Bioinformatics: Bits and Bytes

Peer Bork, Jens G. Reich, Shamil R. Sunyaev, 1999 .

Non-parametric polygenic risk prediction using partitioned GWAS summary statistics

Benjamin M. Neale, Shamil R. Sunyaev, Sekar Kathiresan, 2018, bioRxiv.

Interpreting Population Sequencing Data

Shamil R. Sunyaev, 2009, ISBRA.

Network-based inference from complex proteomic mixtures using SNIPE

Adam Kiezun, Shamil R. Sunyaev, Steven Gygi, 2012, Bioinform..

Cell-of-origin chromatin organization shapes the mutational landscape of cancer

Paz Polak, John A. Stamatoyannopoulos, Shamil R. Sunyaev, 2015, Nature.

Quantifying the unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects

Gregory Valiant, Paul Valiant, Daniel G. MacArthur, 2015 .

Phenotype-specific information improves prediction of functional impact for noncoding variants

Shamil R. Sunyaev, Corneliu A. Bodea, Alex Bloemendal, 2016, bioRxiv.

Genome-wide patterns and properties of de novo mutations in humans

Morris Swertz, Victor Guryev, Dorret I. Boomsma, 2015, Nature Genetics.

Impact of deleterious passenger mutations on cancer progression

Shamil R. Sunyaev, Leonid A. Mirny, Christopher D. McFarland, 2012, Proceedings of the National Academy of Sciences.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

David M. Herrington, Adam Kiezun, Peter Donnelly, 2014, Nature.

Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection

Alkes L. Price, Shamil R. Sunyaev, Po-Ru Loh, 2019, Nature Communications.

Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency

Adam Kiezun, Morris Swertz, Dorret I. Boomsma, 2013, PLoS genetics.

Inferring SNP function using evolutionary, structural, and computational methods.

Carlos Bustamante, Shamil R. Sunyaev, C. Bustamante, 2005 .

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Genome analysis reveals insights into physiology and longevity of the Brandt’s bat Myotis brandtii

Anders Krogh, Vadim N. Gladyshev, Yue Feng, 2013, Nature Communications.