# Marcin Imieliński

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/marcin-imielinski/

## Facts

| Field | Value |
| --- | --- |
| Citations | 69,037 |
| Field | Cancer Genomics and Diagnostics |
| h-index | 76 |
| i10-index | 134 |
| Last Known Institution | NYU Langone Health |
| OpenAlex ID | https://openalex.org/A5013992190 |
| ORCID iD | https://orcid.org/0000-0002-2211-4741 |
| Works | 267 |

## Researcher papers

- [Integrated genomic analyses of ovarian carcinoma](https://scholariq.org/papers/integrated-genomic-analyses-of-ovarian-carcinoma/)
- [Mapping the Hallmarks of Lung Adenocarcinoma with Massively Parallel Sequencing](https://scholariq.org/papers/mapping-the-hallmarks-of-lung-adenocarcinoma-with-massively-parallel-sequencing/)
- [Autism genome-wide copy number variation reveals ubiquitin and neuronal genes](https://scholariq.org/papers/autism-genome-wide-copy-number-variation-reveals-ubiquitin-and-neuronal-genes/)
- [Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47](https://scholariq.org/papers/meta-analysis-identifies-29-additional-ulcerative-colitis-risk-loci-increasing/)
- [The evolutionary history of 2,658 cancers](https://scholariq.org/papers/the-evolutionary-history-of-2-658-cancers/)
- [Patterns of somatic structural variation in human cancer genomes](https://scholariq.org/papers/patterns-of-somatic-structural-variation-in-human-cancer-genomes/)
- [Common genetic variants on 5p14.1 associate with autism spectrum disorders](https://scholariq.org/papers/common-genetic-variants-on-5p14-1-associate-with-autism-spectrum-disorders/)
- [Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing](https://scholariq.org/papers/comprehensive-analysis-of-chromothripsis-in-2-658-human-cancers-using-whole/)
- [Analyses of non-coding somatic drivers in 2,658 cancer whole genomes](https://scholariq.org/papers/analyses-of-non-coding-somatic-drivers-in-2-658-cancer-whole-genomes/)
- [Common variants at five new loci associated with early-onset inflammatory bowel disease](https://scholariq.org/papers/common-variants-at-five-new-loci-associated-with-early-onset-inflammatory-bowel/)
- [Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder](https://scholariq.org/papers/genome-wide-copy-number-variation-study-associates-metabotropic-glutamate/)
- [A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci](https://scholariq.org/papers/a-genome-wide-meta-analysis-of-six-type-1-diabetes-cohorts-identifies-multiple/)

## Researcher topics

- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)
- [Genetic factors in colorectal cancer](https://scholariq.org/topics/genetic-factors-in-colorectal-cancer/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Lymphoma Diagnosis and Treatment](https://scholariq.org/topics/lymphoma-diagnosis-and-treatment/)

## Researcher university

- [NYU Langone Health](https://scholariq.org/institutions/nyu-langone-health/)

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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.