# Menachem Fromer

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/menachem-fromer/

## Facts

| Field | Value |
| --- | --- |
| Citations | 56,184 |
| Field | Genetic Associations and Epidemiology |
| h-index | 57 |
| i10-index | 92 |
| OpenAlex ID | https://openalex.org/A5051946088 |
| ORCID iD | https://orcid.org/0000-0003-3749-4342 |
| Works | 140 |

## Researcher papers

Showing 12 of 14.

- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence](https://scholariq.org/papers/clonal-hematopoiesis-and-blood-cancer-risk-inferred-from-blood-dna-sequence/)
- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Mapping genomic loci implicates genes and synaptic biology in schizophrenia](https://scholariq.org/papers/mapping-genomic-loci-implicates-genes-and-synaptic-biology-in-schizophrenia/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)
- [A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes](https://scholariq.org/papers/a-systematic-survey-of-loss-of-function-variants-in-human-protein-coding-genes/)
- [Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects](https://scholariq.org/papers/contribution-of-copy-number-variants-to-schizophrenia-from-a-genome-wide-study/)
- [Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases](https://scholariq.org/papers/partitioning-heritability-of-regulatory-and-cell-type-specific-variants-across/)
- [The PsychENCODE project](https://scholariq.org/papers/the-psychencode-project/)
- [Effect of predicted protein-truncating genetic variants on the human transcriptome](https://scholariq.org/papers/effect-of-predicted-protein-truncating-genetic-variants-on-the-human/)
- [Copy number variation in schizophrenia in Sweden](https://scholariq.org/papers/copy-number-variation-in-schizophrenia-in-sweden/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [RNA and protein synthesis mechanisms](https://scholariq.org/topics/rna-and-protein-synthesis-mechanisms/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.