Suchergebnisse - Sunyaev, Shamil

Biocomputing enters its adolescence von Sunyaev, Shamil

Volltext Volltext Volltext

Inferring causality and functional significance of human coding DNA variants von Sunyaev, Shamil R.

Volltext Volltext Volltext

Human non-synonymous SNPs: server and survey von Ramensky, Vasily, Bork, Peer, Sunyaev, Shamil

Volltext Volltext

Systems biology and the analysis of genetic variation von Sunyaev, Shamil R, Roth, Frederick P

Volltext Volltext Volltext

Maintenance of Complex Trait Variation: Classic Theory and Modern Data von Koch, Evan M., Sunyaev, Shamil R.

Volltext Volltext Volltext

Dobzhansky–Muller incompatibilities in protein evolution von Kondrashov, Alexey S., Sunyaev, Shamil, Kondrashov, Fyodor A.

Volltext Volltext Volltext

Computational and statistical approaches to analyzing variants identified by exome sequencing von Stitziel, Nathan O, Kiezun, Adam, Sunyaev, Shamil

Volltext Volltext Volltext

Indel-Based Evolutionary Distance and Mouse–Human Divergence von Ogurtsov, Aleksey Y., Sunyaev, Shamil, Kondrashov, Alexey S.

Volltext Volltext Volltext

Analysis of Sequence Conservation at Nucleotide Resolution von Asthana, Saurabh, Roytberg, Mikhail, Stamatoyannopoulos, John, Sunyaev, Shamil

Volltext Volltext Volltext

The mystery of missing heritability: Genetic interactions create phantom heritability von Zuk, Or, Hechter, Eliana, Sunyaev, Shamil R., Lander, Eric S.

Volltext Volltext Volltext

Evaluating empirical bounds on complex disease genetic architecture von Agarwala, Vineeta, Flannick, Jason, Sunyaev, Shamil, Altshuler, David

Volltext Volltext Volltext

Predicting Functional Effect of Human Missense Mutations Using PolyPhen-2 von Adzhubei, Ivan, Jordan, Daniel M., Sunyaev, Shamil R.

Volltext Volltext Volltext

Most Rare Missense Alleles Are Deleterious in Humans: Implications for Complex Disease and Association Studies von Kryukov, Gregory V., Pennacchio, Len A., Sunyaev, Shamil R.

Volltext Volltext

Adaptive Mutations in the JC Virus Protein Capsid Are Associated with Progressive Multifocal Leukoencephalopathy (PML) von Sunyaev, Shamil R., Lugovskoy, Alexey, Simon, Kenneth, Gorelik, Leonid

Volltext Volltext Volltext

Human allelic variation: perspective from protein function, structure, and evolution von Jordan, Daniel M., Ramensky, Vasily E., Sunyaev, Shamil R.

Volltext Volltext Volltext

Shared associations identify causal relationships between gene expression and immune cell phenotypes von Gasperi, Christiane, Chun, Sung, Sunyaev, Shamil R., Cotsapas, Chris

Volltext Volltext Volltext

Triplet repeat length bias and variation in the human transcriptome von Molla, Michael, Delcher, Arthur, Sunyaev, Shamil, Cantor, Charles, Kasif, Simon

Volltext Volltext Volltext

A literature review at genome scale: improving clinical variant assessment von Cassa, Christopher A., Jordan, Daniel M., Adzhubei, Ivan, Sunyaev, Shamil

Volltext Volltext Volltext

Overcoming constraints on the detection of recessive selection in human genes from population frequency data von Balick, Daniel J., Jordan, Daniel M., Sunyaev, Shamil, Do, Ron

Volltext Volltext Volltext

Power of deep, all-exon resequencing for discovery of human trait genes von Kryukov, Gregory V., Shpunt, Alexander, Stamatoyannopoulos, John A., Sunyaev, Shamil R.

Volltext Volltext Volltext