Menachem Fromer

Molecular Biology · 2007–2022

A researcher in the Science corpus: 20 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 316 citations into it
• Artificial Intelligence — 9 citations into it

Whom Menachem Fromer trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Patrik D'haeseleer
2. John J. McGrath
3. Shaun Purcell
4. Jarupon Fah Sathirapongsasuti

Who trusts Menachem Fromer overall

1. Daniel C. Koboldt
2. R. Brody
3. Min Zhao
4. Alexander M. Sevy
5. Patrick F. Sullivan
6. Naomi R. Wray

Papers from Menachem Fromer's perspective

Ordered by how strongly the researchers Menachem Fromer trusts endorse each paper. Same corpus, a different order for every researcher.

1. Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
2. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
3. The endophenotype concept in psychiatry: etymology and strategic intentions. (American Journal of Psychiatry)
4. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
5. Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
6. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
7. A Copy Number Variation Morbidity Map of Developmental Delay (Nature Genetics)
8. The support of human genetic evidence for approved drug indications (Nature Genetics)
9. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
10. Detection of large-scale variation in the human genome (Nature Genetics)

Their papers

• A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
• Efficient algorithms for accurate hierarchical clustering of huge datasets: tackling the entire protein space (2008) — 160 citations
• Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) — 1,080 citations
• De novo mutations in schizophrenia implicate synaptic networks (2014) — 1,622 citations
• A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 citations
• A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
• Dead‐end elimination for multistate protein design (2007) — 48 citations
• Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
• Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) — 577 citations
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
• Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
• Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) — 444 citations
• Patterns of genic intolerance of rare copy number variation in 59,898 human exomes (2016) — 182 citations
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) — 996 citations
• Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations
• Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) — 7,422 citations
• Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence (2014) — 3,098 citations
• Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) — 816 citations
• Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) — 740 citations
• Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations