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Steven K. Reilly

Yale University · US
🔎 Find collaborators in Molecular Biology · Genetics →
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Area of research
Molecular Biology · Genetics
Research interest
Research interests include Genomics and Chromatin Dynamics, Genomics and Phylogenetic Studies, RNA Research and Splicing, and RNA and protein synthesis mechanisms.
h-index
39
citations
7,173
works
70
NIH funding
primary concept
email

Recent publications

Functional dissection of complex trait variants at single-nucleotide resolution
Nature 2026cited by 2position: middledoi
Machine-guided design of cell-type-targeting cis-regulatory elements
Nature 2024cited by 117position: middledoi
Deciphering the impact of genomic variation on function
Nature 2024cited by 77position: middledoi
Multicenter integrated analysis of noncoding CRISPRi screens
Nature Methods 2024cited by 49position: lastdoi
Vocal learning–associated convergent evolution in mammalian proteins and regulatory elements
Science 2024cited by 34position: middledoi
Functional dissection of complex and molecular trait variants at single nucleotide resolution
bioRxiv (Cold Spring Harbor Laboratory) 2024cited by 29position: middledoi
Somatic mosaicism in schizophrenia brains reveals prenatal mutational processes
Science 2024cited by 18position: middledoi
Genome-wide association study identifies human genetic variants associated with fatal outcome from Lassa fever
Nature Microbiology 2024cited by 10position: middledoi
Evolutionary constraint and innovation across hundreds of placental mammals
Science 2023cited by 261position: middledoi
Integrating gene annotation with orthology inference at scale
Science 2023cited by 196position: middledoi
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Science 2023cited by 116position: middledoi
Three-dimensional genome rewiring in loci with human accelerated regions
Science 2023cited by 111position: middledoi
The contribution of historical processes to contemporary extinction risk in placental mammals
Science 2023cited by 102position: middledoi
The functional and evolutionary impacts of human-specific deletions in conserved elements
Science 2023cited by 75position: middledoi
Evolutionary constraint and innovation across hundreds of placental mammals
bioRxiv (Cold Spring Harbor Laboratory) 2023cited by 24position: middledoi
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease
bioRxiv (Cold Spring Harbor Laboratory) 2023cited by 21position: middledoi
Comparative genomics of Balto, a famous historic dog, captures lost diversity of 1920s sled dogs
Science 2023cited by 13position: middledoi
Evolution of the ancestral mammalian karyotype and syntenic regions
Proceedings of the National Academy of Sciences 2022cited by 95position: middledoi
Genome-wide functional screen of 3′UTR variants uncovers causal variants for human disease and evolution
Cell 2021cited by 183position: middledoi
Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH
Nature Genetics 2021cited by 103position: firstdoi
Detection of Neanderthal Adaptively Introgressed Genetic Variants That Modulate Reporter Gene Expression in Human Immune Cells
Molecular Biology and Evolution 2021cited by 48position: middledoi
Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak
Cell 2021cited by 48position: middledoi
Synthetic DNA spike-ins (SDSIs) enable sample tracking and detection of inter-sample contamination in SARS-CoV-2 sequencing workflows
Nature Microbiology 2021cited by 17position: middledoi
Author Correction: Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH
Nature Genetics 2021cited by 3position: firstdoi
Phylogenetic analysis of SARS-CoV-2 in Boston highlights the impact of superspreading events
Science 2020cited by 318position: middledoi
Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features
Nature Communications 2020cited by 81position: middledoi
Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay
Cell 2016cited by 551position: middledoi
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Nature Communications 2015cited by 369position: middledoi
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
Cell 2013cited by 977position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Ryan Tewhey · Tufts University8 papers (2016–2024)Pardis C. Sabeti · Broad Institute8 papers (2016–2024)Masahiro Kanai · Broad Institute5 papers (2020–2024)Susan Kales · Jackson Laboratory5 papers (2021–2024)Hilary K. Finucane · Broad Institute5 papers (2020–2024)Jacob C. Ulirsch · Illumina (United States)5 papers (2020–2024)Kousuke Mouri · Jackson Laboratory4 papers (2021–2024)Daniel Berenzy · Jackson Laboratory4 papers (2021–2024)Sager J. Gosai · Broad Institute4 papers (2021–2024)Eric S. Lander · Broad Institute3 papers (2016–2024) · 3 papers (2024–2024)Adrianne Gladden-Young · Tufts University3 papers (2021–2021)Michael L. Stitzel · University of Connecticut2 papers (2021–2021)Rodrigo Castro · Jackson Laboratory2 papers (2024–2024) · 2 papers (2021–2021) · 2 papers (2021–2021)John C. Butts · Jackson Laboratory2 papers (2021–2024)Redwan M. Bhuiyan · University of Connecticut2 papers (2021–2021) · 2 papers (2021–2021)Hannah B. Dewey · Tufts University2 papers (2021–2024)
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