Ryan L Collins

21PUBLICATIONS

137CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Genome structure and regulation

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Publications (21)

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|Jun 03, 2026

Germline Whole-Genome Sequencing in Early-Onset Pediatric Solid Tumors Implicates Novel Risk Factors.

|May 25, 2026

Diverse mediators of cancer predisposition uncovered by germline whole genome sequencing of unexplained familial cancers.

|Jan 02, 2025

Rare germline structural variants increase risk for pediatric solid tumors.

Riaz Gillani, Ryan L Collins, Jett Crowdis

|May 15, 2024

Rare germline structural variants increase risk for pediatric solid tumors.

Riaz Gillani, Ryan L Collins, Jett Crowdis

|Jan 24, 2024

Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.

Mehrtash Babadi, Jack M Fu, Samuel K Lee

|Aug 21, 2023

GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.

Mehrtash Babadi, Jack M Fu, Samuel K Lee

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Frequent Collaborators

11 joint publications

Michael Talkowski

Benjamin M Neale

Konrad J Karczewski

Jessica Alföldi

Anne O'Donnell-Luria

Daniel G MacArthur

Laurent C Francioli

Xuefang Zhao

Mark J Daly

Christopher W Whelan

Frequent Collaborators

11 joint publications

Michael Talkowski

7 joint publications

Benjamin M Neale

7 joint publications

Konrad J Karczewski

5 joint publications

Jessica Alföldi