Gill Bejerano

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 15

Top Topics

Gene Expression

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

bioRxiv : the preprint server for biology

Genome medicine

Genome biology and evolution

This page only lists publications with an associated author ORCID identifier.

Publications

Heidi I Chen, Yatish Turakhia, Gill Bejerano, David M Kingsley
Whole-genome comparisons identify repeated regulatory changes underlying convergent appendage evolution in diverse fish lineages. bioRxiv : the preprint server for biology (2023)
Heidi I Chen, Yatish Turakhia, Gill Bejerano, David M Kingsley
Whole-genome comparisons identify repeated regulatory changes underlying convergent appendage evolution in diverse fish lineages. bioRxiv : the preprint server for biology (2023)
Heidi I Chen, Yatish Turakhia, Gill Bejerano, David M Kingsley
Whole-genome Comparisons Identify Repeated Regulatory Changes Underlying Convergent Appendage Evolution in Diverse Fish Lineages. Molecular biology and evolution 40 (9) (2023)
Ruchir Rastogi, Peter D Stenson, David N Cooper, Gill Bejerano
X-CAP improves pathogenicity prediction of stopgain variants. Genome medicine 14 (1) (2022)
James K Schull, Yatish Turakhia, James A Hemker, William J Dally, Gill Bejerano
Champagne: Automated Whole-Genome Phylogenomic Character Matrix Method Using Large Genomic Indels for Homoplasy-Free Inference. Genome biology and evolution 14 (3) (2022)
Boyoung Yoo, Johannes Birgmeier, Jonathan A Bernstein, Gill Bejerano
InpherNet accelerates monogenic disease diagnosis using patients' candidate genes' neighbors. Genetics in medicine : official journal of the American College of Medical Genetics 23 (10) (2021)
Johannes Birgmeier, Maximilian Haeussler, Cole A Deisseroth, Ethan H Steinberg, Karthik A Jagadeesh, Alexander J Ratner, Harendra Guturu, Aaron M Wenger, Mark E Diekhans, Peter D Stenson, David N Cooper, Christopher Ré, Alan H Beggs, Jonathan A Bernstein, Gill Bejerano
AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature. Science translational medicine 12 (544) (2021)
Jacob A Blindenbach, Karthik A Jagadeesh, Gill Bejerano, David J Wu
Avoiding genetic racial profiling in criminal DNA profile databases. Nature computational science 1 (4) (2021)
Raphaël Aguillon, Romain Madelaine, Marion Aguirrebengoa, Harendra Guturu, Sandra Link, Pascale Dufourcq, Virginie Lecaudey, Gill Bejerano, Patrick Blader, Julie Batut
Morphogenesis is transcriptionally coupled to neurogenesis during peripheral olfactory organ development. Development (Cambridge, England) 147 (24) (2020)
Karthik A Jagadeesh, Joseph M Paggi, James S Ye, Peter D Stenson, David N Cooper, Jonathan A Bernstein, Gill Bejerano
S-CAP extends pathogenicity prediction to genetic variants that affect RNA splicing. Nature genetics 51 (4) (2019)
Johannes Birgmeier, Cole A Deisseroth, Laura E Hayward, Luisa M T Galhardo, Andrew P Tierno, Karthik A Jagadeesh, Peter D Stenson, David N Cooper, Jonathan A Bernstein, Maximilian Haeussler, Gill Bejerano
AVADA: toward automated pathogenic variant evidence retrieval directly from the full-text literature. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Yosuke Tanigawa, Jiehan Li, Johanne M Justesen, Heiko Horn, Matthew Aguirre, Christopher DeBoever, Chris Chang, Balasubramanian Narasimhan, Kasper Lage, Trevor Hastie, Chong Y Park, Gill Bejerano, Erik Ingelsson, Manuel A Rivas
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology. Nature communications 10 (1) (2019)
Johannes Birgmeier, Edward D Esplin, Karthik A Jagadeesh, Harendra Guturu, Aaron M Wenger, Hassan Chaib, Julia A Buckingham, Gill Bejerano, Jonathan A Bernstein
Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome. American journal of medical genetics. Part A 176 (4) (2019)
Heidi I Chen, Karthik A Jagadeesh, Johannes Birgmeier, Aaron M Wenger, Harendra Guturu, Susan Schelley, Jonathan A Bernstein, Gill Bejerano
An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease. European journal of human genetics : EJHG 26 (12) (2018)
Karthik A Jagadeesh, David J Wu, Johannes A Birgmeier, Dan Boneh, Gill Bejerano
Deriving genomic diagnoses without revealing patient genomes. Science (New York, N.Y.) 357 (6352) (2017)