Exposing the co-adaptive potential of protein-protein interfaces through computational sequence designFROMER, Menachem; LINIAL, Michal.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 18, pp 2266-2272, issn 1367-4803, 7 p.Article

Recovering key biological constituents through sparse representation of gene expressionPRAT, Yosef; FROMER, Menachem; LINIAL, Nathan et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 5, pp 655-661, issn 1367-4803, 7 p.Article

SPRINT: side-chain prediction inference toolbox for multistate protein designFROMER, Menachem; YANOVER, Chen; HAREL, Amir et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 19, pp 2466-2467, issn 1367-4803, 2 p.Article

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding GenesMACARTHUR, Daniel G; BALASUBRAMANIAN, Suganthi; ALBERS, Cornelis A et al.Science (Washington, D.C.). 2012, Vol 335, Num 6070, pp 823-828, issn 0036-8075, 6 p.Article

zCall: a rare variant caller for array-based genotypingGOLDSTEIN, Jacqueline I; CRENSHAW, Andrew; SCHIZOPHRENIA CONSORTIUM, Swedish et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 19, pp 2543-2545, issn 1367-4803, 3 p.Article

Patterns and rates of exonic de novo mutations in autism spectrum disordersNEALE, Benjamin M; YAN KOU; POLAK, Paz et al.Nature (London). 2012, Vol 485, Num 7397, pp 242-245, issn 0028-0836, 4 p.Article

Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA SequenceGENOVESE, Giulio; KÄHLER, Anna K; PURCELL, Shaun M et al.The New England journal of medicine. 2014, Vol 371, Num 26, pp 2477-2487, issn 0028-4793, 11 p.Article

Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing DepthFROMER, Menachem; MORAN, Jennifer L; KIROV, George et al.American journal of human genetics. 2012, Vol 91, Num 4, pp 597-607, issn 0002-9297, 11 p.Article