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Julius Ob Jacobsen

19PUBLICATIONS

357CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)PharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)Computational linguisticsBioinformatic methods development

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Publications (19)

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|Apr 03, 2026

Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Jenny Lord, Alistair T Pagnamenta, Letizia Vestito

|Feb 06, 2026

A Phenotypic Paradigm for Cerebral Palsy Genetics.

Adam S Arterbery, Michael A Gargano, Anita Bagley

|Mar 27, 2025

Pharmacogenetics and adverse drug reports: Insights from a United Kingdom national pharmacovigilance database.

Emma F Magavern, Maia Megase, Jack Thompson

|Mar 17, 2025

GA4GH Phenopacket-Driven Characterization of Genotype-Phenotype Correlations in Mendelian Disorders.

Lauren Rekerle, Daniel Danis, Filip Rehburg

|Feb 26, 2025

Rare disease gene association discovery in the 100,000 Genomes Project.

Valentina Cipriani, Letizia Vestito, Emma F Magavern

|Dec 18, 2024

Efficient reinterpretation of rare disease cases using Exomiser.

Letizia Vestito, Julius O B Jacobsen, Susan Walker

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Frequent Collaborators

20 joint publications

Peter Robinson

17 joint publications

Damian Smedley

11 joint publications

Melissa Haendel

11 joint publications

Christopher J Mungall

7 joint publications

Daniel Danis

7 joint publications

Justin T Reese

6 joint publications

Nomi L Harris

6 joint publications

Julie A McMurry

5 joint publications

J Harry Caufield

5 joint publications

Nicole Vasilevsky

Frequent Collaborators

20 joint publications

Peter Robinson

17 joint publications

Damian Smedley

11 joint publications

Melissa Haendel

11 joint publications

Christopher J Mungall

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