Peter Robinson

98PUBLICATIONS

679CO-AUTHORS

Genomics and transcriptomicsDeep learningGene expression (incl. microarray and other genome-wide approaches)Computational linguisticsFoetal development and medicine

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Publications (98)

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|Jul 07, 2026

FABIAN-variant 2026: improved prediction of the effects of DNA variants on transcription factor binding.

|Jun 16, 2026

In-depth Human Phenotype Ontology Curation Boosts Prioritization Performance for Netherton Syndrome.

|May 07, 2026

Data-driven prioritization of mouse strains for improved preclinical modeling of rare and common disease.

|Feb 24, 2026

Systematic benchmarking demonstrates large language models have not reached the diagnostic accuracy of traditional rare-disease decision support tools.

Justin T Reese, Leonardo Chimirri, Yasemin Bridges

|Feb 06, 2026

A Phenotypic Paradigm for Cerebral Palsy Genetics.

Adam S Arterbery, Michael A Gargano, Anita Bagley

|Dec 08, 2025

Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections.

Natalie B Gulrajani, John Boscardin, Billie R Lianoglou

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Frequent Collaborators

22 joint publications

Christopher Mungall

22 joint publications

Melissa Haendel

21 joint publications

Damian Smedley

20 joint publications

Julius Ob Jacobsen

20 joint publications

Justin T Reese

17 joint publications

Daniel Danis

16 joint publications

Elena Casiraghi

16 joint publications

Giorgio Valentini

13 joint publications

J Harry Caufield

11 joint publications

Leigh Carmody

Frequent Collaborators

22 joint publications

Christopher Mungall

22 joint publications

Melissa Haendel

21 joint publications

Damian Smedley

20 joint publications

Julius Ob Jacobsen