Julius Ob Jacobsen

20PUBLICATIONS
371CO-AUTHORS
Medical biotechnology diagnostics (incl. biosensors)Gene expression (incl. microarray and other genome-wide approaches)PharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)Computational linguistics
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Publications (20)

|Sep 09, 2026
Proteomics identify disease-associated variants in patients with rare diseases undiagnosed after genome sequencing.

|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

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Frequent Collaborators

21 joint publications

Peter Robinson

18 joint publications

Damian Smedley

11 joint publications

Melissa Haendel

11 joint publications

Christopher J Mungall