Julius Ob Jacobsen
19PUBLICATIONS
357CO-AUTHORS
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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
