Author

Clif Duhn

Broad InstituteORCID 0000-0002-5693-0165Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Matthew W. StateiD· 2 shared A. Jeremy Willsey· 1 shared Aaron R. QuinlaniD· 1 shared Andrew FarrelliD· 1 shared Anita ThapariD· 1 shared Arnold R. KriegsteiniD· 1 shared Arthur Jeremy WillseyiD· 1 shared Belinda Lei WangiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Matthew W. StateORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 22, 2022

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

Sheng Wang, Belinda Lei Wang, Vanessa Drury…·Arthur Jeremy Willsey

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsEuropean NeuropsychopharmacologyPeer-reviewedJan 1, 2019

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Donna M. Werling, Harrison Brand, Joon‐Yong An…·Stephan Sanders

This study examines the role of noncoding variation in autism spectrum disorder using whole genome sequencing of 2,076 genomes, finding no significant association after correction for multiple testing.

20 citations

humanwhole-genome sequencing

𝕏 PostBluesky