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Author Details
Full Name
Julius O B Jacobsen
Affiliation
William Harvey Research Institute, Queen Mary University of London
ORCID
Career Start Year
2012
Papers
35
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38000386
The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species.
Nucleic Acids Res
2024
37953324
The Human Phenotype Ontology in 2024: phenotypes around the world.
Nucleic Acids Res
2024
37196000
Phenopacket-tools: Building and validating GA4GH Phenopackets.
PLoS One
2023
36910590
GA4GH Phenopackets: A Practical Introduction.
Adv Genet (Hoboken)
2022
35442193
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice.
Genet Med
2022
35705716
The GA4GH Phenopacket schema defines a computable representation of clinical data.
Nat Biotechnol
2022
35391505
Phenotype-driven approaches to enhance variant prioritization and diagnosis of rare disease.
Hum Mutat
2022
35595299
Evaluation of phenotype-driven gene prioritization methods for Mendelian diseases.
Brief Bioinform
2022
35484572
SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing.
Genome Med
2022
34289339
Interpretable prioritization of splice variants in diagnostic next-generation sequencing.
Am J Hum Genet
2021
35072136
GA4GH: International policies and standards for data sharing across genomic research and healthcare.
Cell Genom
2021
34758253
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
N Engl J Med
2021
34739835
Interpretable prioritization of splice variants in diagnostic next-generation sequencing.
Am J Hum Genet
2021
32340307
An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data.
Genes (Basel)
2020
32755546
Interpretable Clinical Genomics with a Likelihood Ratio Paradigm.
Am J Hum Genet
2020
30476213
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.
Nucleic Acids Res
2019
31479590
Encoding Clinical Data with the Human Phenotype Ontology for Computational Differential Diagnostics.
Curr Protoc Hum Genet
2019
30240502
matchbox: An open-source tool for patient matching via the Matchmaker Exchange.
Hum Mutat
2018
27899602
The Human Phenotype Ontology in 2017.
Nucleic Acids Res
2017
28334266
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data.
Bioinformatics
2017
29044468
Matchmaker Exchange.
Curr Protoc Hum Genet
2017
28650483
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
2017
27899636
The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.
Nucleic Acids Res
2017
27569544
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.
Am J Hum Genet
2016
26562225
Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.
Genet Med
2016
27516611
Navigating the Phenotype Frontier: The Monarch Initiative.
Genetics
2016
25992600
Applying the ARRIVE Guidelines to an In Vivo Database.
PLoS Biol
2015
26562621
Next-generation diagnostics and disease-gene discovery with the Exomiser.
Nat Protoc
2015
26314589
A mouse informatics platform for phenotypic and translational discovery.
Mamm Genome
2015
26092691
Disease insights through cross-species phenotype comparisons.
Mamm Genome
2015
24319146
The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes.
Nucleic Acids Res
2014
24932005
Using association rule mining to determine promising secondary phenotyping hypotheses.
Bioinformatics
2014
23203869
SIFTS: Structure Integration with Function, Taxonomy and Sequences resource.
Nucleic Acids Res
2013
23175605
The EBI enzyme portal.
Nucleic Acids Res
2013
22877863
BioJava: an open-source framework for bioinformatics in 2012.
Bioinformatics
2012
1 - 35 of 35
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Valentina Cipriani
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Orion J Buske
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Leigh C Carmody
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