A computational framework to empower probabilistic protein design

Por Fromer, Menachem, Yanover, Chen
Publicado em 2008

Tradeoff Between Stability and Multispecificity in the Design of Promiscuous Proteins

Por Fromer, Menachem, Shifman, Julia M.
Publicado em 2009

Using XHMM software to detect copy number variation in whole-exome sequencing data

Por Fromer, Menachem, Purcell, Shaun M.
Publicado em 2014

Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty?

Por Naamati, Guy, Fromer, Menachem, Linial, Michal
Publicado em 2009

A functional hierarchical organization of the protein sequence space

Por Fromer Menachem, Friedlich Moriah, Kaplan Noam, Linial Michal
Publicado em 2004-12-01

A functional hierarchical organization of the protein sequence space

Por Kaplan, Noam, Friedlich, Moriah, Fromer, Menachem, Linial, Michal
Publicado em 2004

Efficient algorithms for accurate hierarchical clustering of huge datasets: tackling the entire protein space

Por Loewenstein, Yaniv, Portugaly, Elon, Fromer, Menachem, Linial, Michal
Publicado em 2008

Viral adaptation to host: a proteome-based analysis of codon usage and amino acid preferences

Por Bahir, Iris, Fromer, Menachem, Prat, Yosef, Linial, Michal
Publicado em 2009

Codon usage is associated with the evolutionary age of genes in metazoan genomes

Por Prat, Yosef, Fromer, Menachem, Linial, Nathan, Linial, Michal
Publicado em 2009

PANDORA: analysis of protein and peptide sets through the hierarchical integration of annotations

Por Rappoport, Nadav, Fromer, Menachem, Schweiger, Regev, Linial, Michal
Publicado em 2010

Transforming Psychiatry into Data-Driven Medicine with Digital Measurement Tools

Por Hsin, Honor, Fromer, Menachem, Peterson, Bret, Walter, Collin, Fleck, Mathias, Campbell, Andrew, Varghese, Paul, Califf, Robert
Publicado no NPJ Digit Med (2018)

Unperturbed expression bias of imprinted genes in schizophrenia

Por Gulyás-Kovács, Attila, Keydar, Ifat, Xia, Eva, Fromer, Menachem, Hoffman, Gabriel, Ruderfer, Douglas, Sachidanandam, Ravi, Chess, Andrew
Publicado no Nat Commun (2018)

ProtoNet 4.0: A hierarchical classification of one million protein sequences

Por Kaplan, Noam, Sasson, Ori, Inbar, Uri, Friedlich, Moriah, Fromer, Menachem, Fleischer, Hillel, Portugaly, Elon, Linial, Nathan, Linial, Michal
Publicado em 2005

Patterns of genic intolerance of rare copy number variation in 59,898 human exomes

Por Ruderfer, Douglas M., Hamamsy, Tymor, Lek, Monkol, Karczewski, Konrad J., Kavanagh, David, Samocha, Kaitlin E., Daly, Mark J., MacArthur, Daniel G., Fromer, Menachem, Purcell, Shaun M.
Publicado no Nat Genet (2016)

Genetic effect of chemotherapy exposure in children of testicular cancer survivors

Por Kryukov, Gregory V., Bielski, Craig M., Samocha, Kaitlin, Fromer, Menachem, Seepo, Sara, Gentry, Carleen, Neale, Benjamin, Garraway, Levi A., Sweeney, Christopher, Taplin, Mary-Ellen, Van Allen, Eliezer M.
Publicado no Clin Cancer Res (2015)

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

Por Genovese, Giulio, Fromer, Menachem, Stahl, Eli A., Ruderfer, Douglas M., Chambert, Kimberly, Landén, Mikael, Moran, Jennifer L., Purcell, Shaun M., Sklar, Pamela, Sullivan, Patrick F., Hultman, Christina M., McCarroll, Steven A.
Publicado no Nat Neurosci (2016)

A framework for the detection of de novo mutations in family-based sequencing data

Por Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, Daly, Mark J, Banks, Eric, DePristo, Mark A, de Bakker, Paul IW
Publicado no Eur J Hum Genet (2017)

Identification of Small Exonic CNV from Whole-Exome Sequence Data and Application to Autism Spectrum Disorder

Por Poultney, Christopher S., Goldberg, Arthur P., Drapeau, Elodie, Kou, Yan, Harony-Nicolas, Hala, Kajiwara, Yuji, De Rubeis, Silvia, Durand, Simon, Stevens, Christine, Rehnström, Karola, Palotie, Aarno, Daly, Mark J., Ma’ayan, Avi, Fromer, Menachem, Buxbaum, Joseph D.
Publicado em 2013

Detecting Large Copy Number Variants Using Exome Genotyping Arrays In a Large Swedish Schizophrenia Sample

Por Szatkiewicz, Jin P., Neale, Benjamin M., O'Dushlaine, Colm, Fromer, Menachem, Goldstein, Jacqueline I., Moran, Jennifer L., Chambert, Kimberly, Kähler, Anna, Magnusson, Patrik KE, Hultman, Christina M., Sklar, Pamela, Purcell, Shaun, McCarroll, Steven A., Sullivan, Patrick F.
Publicado em 2013

Functional Analysis of Rare Variants Found in Schizophrenia Implicates a Critical Role for GIT1-PAK3 Signaling in Neuroplasticity

Por Kim, Myung Jong, Biag, Jonathan, Fass, Daniel M., Lewis, Michael C., Zhang, Qiangge, Fleishman, Morgan, Gangwar, Shanti Pal, Machius, Mischa, Fromer, Menachem, Purcell, Shaun M., McCarroll, Steven A., Rudenko, Gabby, Premont, Richard T., Scolnick, Edward M., Haggarty, Stephen J.
Publicado no Mol Psychiatry (2016)