# Shawn Levy

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/shawn-levy/

## Facts

| Field | Value |
| --- | --- |
| Citations | 69,995 |
| Field | Metabolomics and Mass Spectrometry Studies |
| h-index | 93 |
| i10-index | 210 |
| Last Known Institution | XCell Science (United States) |
| OpenAlex ID | https://openalex.org/A5034381224 |
| ORCID iD | https://orcid.org/0000-0002-1369-5740 |
| Works | 434 |

## Researcher papers

- [A reference panel of 64,976 haplotypes for genotype imputation](https://scholariq.org/papers/a-reference-panel-of-64-976-haplotypes-for-genotype-imputation/)
- [The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore](https://scholariq.org/papers/the-adp-atp-translocator-is-not-essential-for-the-mitochondrial-permeability/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [Experimentally Derived Metastasis Gene Expression Profile Predicts Recurrence and Death in Patients With Colon Cancer](https://scholariq.org/papers/experimentally-derived-metastasis-gene-expression-profile-predicts-recurrence/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [Proteome analysis of human colon cancer by two‐dimensional difference gel electrophoresis and mass spectrometry](https://scholariq.org/papers/proteome-analysis-of-human-colon-cancer-by-two-dimensional-difference-gel/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)
- [Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy](https://scholariq.org/papers/candidate-exome-capture-identifies-mutation-of-sdccag8-as-the-cause-of-a-retinal/)
- [ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling](https://scholariq.org/papers/arhgdia-mutations-cause-nephrotic-syndrome-via-defective-rho-gtpase-signaling/)
- [ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6](https://scholariq.org/papers/zmynd10-is-mutated-in-primary-ciliary-dyskinesia-and-interacts-with-lrrc6/)
- [KANK deficiency leads to podocyte dysfunction and nephrotic syndrome](https://scholariq.org/papers/kank-deficiency-leads-to-podocyte-dysfunction-and-nephrotic-syndrome/)

## Researcher topics

- [Metabolomics and Mass Spectrometry Studies](https://scholariq.org/topics/metabolomics-and-mass-spectrometry-studies/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Cancer-related molecular mechanisms research](https://scholariq.org/topics/cancer-related-molecular-mechanisms-research/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [XCell Science (United States)](https://scholariq.org/institutions/xcell-science-united-states/)

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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.