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Author Details

Menachem Fromer
1999
62
38
PMIDPaper TitleJournal TitlePublished Year
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
34383685Toward a Mobile Platform for Real-world Digital Measurement of Depression: User-Centered Design, Data Quality, and Behavioral and Clinical Modeling.JMIR Ment Health2021
32989243Correction: The AURORA Study: a longitudinal, multimodal library of brain biology and function after traumatic stress exposure.Mol Psychiatry2021
34383766A holistic approach for suppression of COVID-19 spread in workplaces and universities.PLoS One2021
32665711Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.Nat Neurosci2020
31745239The AURORA Study: a longitudinal, multimodal library of brain biology and function after traumatic stress exposure.Mol Psychiatry2020
31932770Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.Nat Neurosci2020
31767120Characterization of Single Gene Copy Number Variants in Schizophrenia.Biol Psychiatry2020
31086353Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.Nat Genet2019
31304319Transforming Psychiatry into Data-Driven Medicine with Digital Measurement Tools.NPJ Digit Med2018
30046039Unperturbed expression bias of imprinted genes in schizophrenia.Nat Commun2018
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
28714951Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.Nat Neurosci2017
29045836Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence.Cell Rep2017
29262854Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Genome Med2017
27113501Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue.Biol Psychiatry2017
27457813Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1-PAK3 signaling in neuroplasticity.Mol Psychiatry2017
27876817A framework for the detection of de novo mutations in family-based sequencing data.Eur J Hum Genet2017
27535533Analysis of protein-coding genetic variation in 60,706 humans.Nature2016
27065010Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.Nat Biotechnol2016
26605520Developmental Trajectories of Impaired Community Functioning in Schizophrenia.JAMA Psychiatry2016
26631610Genetic Effect of Chemotherapy Exposure in Children of Testicular Cancer Survivors.Clin Cancer Res2016
27533299Patterns of genic intolerance of rare copy number variation in 59,898 human exomes.Nat Genet2016
27694994Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.Nat Neurosci2016
27668389Gene expression elucidates functional impact of polygenic risk for schizophrenia.Nat Neurosci2016
26196440Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Transl Psychiatry2015
25626421Genomic aberrations in cervical adenocarcinomas in Hong Kong Chinese women.Int J Cancer2015
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
26605881The PsychENCODE project.Nat Neurosci2015
24776740Copy number variation in schizophrenia in Sweden.Mol Psychiatry2014
25453756A role for noncoding variation in schizophrenia.Cell Rep2014
25363760Synaptic, transcriptional and chromatin genes disrupted in autism.Nature2014
25426838Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.N Engl J Med2014
24463508A polygenic burden of rare disruptive mutations in schizophrenia.Nature2014
24463507De novo mutations in schizophrenia implicate synaptic networks.Nature2014
25205790Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.Circ Res2014
24763994Using XHMM Software to Detect Copy Number Variation in Whole-Exome Sequencing Data.Curr Protoc Hum Genet2014
23352160Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.Neuron2013
23938935Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.Mol Psychiatry2013
23974872Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Nat Genet2013
24094742Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.Am J Hum Genet2013
23040492Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.Am J Hum Genet2012
22843986zCall: a rare variant caller for array-based genotyping: genetics and population analysis.Bioinformatics2012
22344438A systematic survey of loss-of-function variants in human protein-coding genes.Science2012
22495311Patterns and rates of exonic de novo mutations in autism spectrum disorders.Nature2012
21258061Recovering key biological constituents through sparse representation of gene expression.Bioinformatics2011
20444873PANDORA: analysis of protein and peptide sets through the hierarchical integration of annotations.Nucleic Acids Res2010
20685957SPRINT: side-chain prediction inference toolbox for multistate protein design.Bioinformatics2010
20679332Exposing the co-adaptive potential of protein-protein interfaces through computational sequence design.Bioinformatics2010
19842166Design of multispecific protein sequences using probabilistic graphical modeling.Proteins2010
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