Gill Bejerano

Affiliations: 
Stanford University, Palo Alto, CA 
Area:
Developmental Biology, Computer Science
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"Gill Bejerano"
Mean distance: 106866
 

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Chen HI, Turakhia Y, Bejerano G, et al. (2023) Whole-genome Comparisons Identify Repeated Regulatory Changes Underlying Convergent Appendage Evolution in Diverse Fish Lineages. Molecular Biology and Evolution. 40
Chen HI, Turakhia Y, Bejerano G, et al. (2023) Whole-genome comparisons identify repeated regulatory changes underlying convergent appendage evolution in diverse fish lineages. Biorxiv : the Preprint Server For Biology
Schull JK, Turakhia Y, Hemker JA, et al. (2022) Champagne: Automated whole-genome phylogenomic character matrix method using large genomic indels for homoplasy-free inference. Genome Biology and Evolution
Yoo B, Birgmeier J, Bernstein JA, et al. (2021) InpherNet accelerates monogenic disease diagnosis using patients' candidate genes' neighbors. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Heavner WE, Ji S, Notwell JH, et al. (2020) Transcription factor expression defines subclasses of developing projection neurons highly similar to single-cell RNA-seq subtypes. Proceedings of the National Academy of Sciences of the United States of America
Turakhia Y, Chen HI, Marcovitz A, et al. (2020) A fully-automated method discovers loss of mouse-lethal and human-monogenic disease genes in 58 mammals. Nucleic Acids Research
Birgmeier J, Haeussler M, Deisseroth CA, et al. (2020) AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature. Science Translational Medicine. 12
Marcovitz A, Turakhia Y, Chen HI, et al. (2019) A functional enrichment test for molecular convergent evolution finds a clear protein-coding signal in echolocating bats and whales. Proceedings of the National Academy of Sciences of the United States of America
Tanigawa Y, Li J, Justesen JM, et al. (2019) Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology. Nature Communications. 10: 4064
Birgmeier J, Deisseroth CA, Hayward LE, et al. (2019) 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
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