List of works - Oliver D King

A global analysis of IFT-A function reveals specialization for transport of membrane-associated proteins into cilia

scientific article published on 11 February 2019

A mass formula for unimodular lattices with no roots

scientific article (publication date: 25 June 2002)

A new approach for the study of lung smooth muscle phenotypes and its application in a murine model of allergic airway inflammation

scientific article

A non-parametric model for transcription factor binding sites ⬇️

scientific article published on October 1, 2003

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

scientific article

A yeast functional screen predicts new candidate ALS disease genes

scientific article published on 7 November 2011

An open system for automatic home-cage behavioral analysis and its application to male and female mouse models of Huntington's disease.

scientific article published on 13 January 2012

Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy

scientific article published on 01 March 2020

Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity

scientific article

Characterizing gene sets with FuncAssociate

scientific article published on December 2003

Combining biological networks to predict genetic interactions

scholarly article

Combining guilt-by-association and guilt-by-profiling to predict Saccharomyces cerevisiae gene function

scientific article published on 27 June 2008

Comment on "Subgraphs in random networks".

scientific article published on 18 November 2004

Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo

scientific article published on November 2007

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

scientific article

Exome sequencing to identify de novo mutations in sporadic ALS trios

scientific article published on 26 May 2013

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

scientific article

Free-Wilson Analysis of Comprehensive Data on Phosphoinositide-3-kinase (PI3K) Inhibitors Reveals Importance of N-Methylation for PI3Kδ Activity

scientific article published on 06 November 2019

Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor

scientific article

GoFish finds genes with combinations of Gene Ontology attributes

scientific article

Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease

scientific article

Human skeletal muscle xenograft as a new preclinical model for muscle disorders

scientific article

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

scientific article

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

scientific article published on 29 March 2015

Inhibiting GPI anchor biosynthesis in fungi stresses the endoplasmic reticulum and enhances immunogenicity

scientific article

Intensity-based protein identification by machine learning from a library of tandem mass spectra.

scientific article

Knocking out multigene redundancies via cycles of sexual assortment and fluorescence selection

scientific article

Ly6a Differential Expression in Blood-Brain Barrier Is Responsible for Strain Specific Central Nervous System Transduction Profile of AAV-PHP.B.

scientific article published on 13 December 2019

Morpholino-mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics

scientific article published on 05 July 2016

Motifs, themes and thematic maps of an integrated Saccharomyces cerevisiae interaction network

scientific article

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

scientific article

Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains

scientific article published on 01 April 2018

Opposing effects of glutamine and asparagine govern prion formation by intrinsically disordered proteins

scientific article

PLAAC: a web and command-line application to identify proteins with prion-like amino acid composition

scientific article

Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

article

Predicting co-complexed protein pairs using genomic and proteomic data integration

scientific article

Predicting gene function from patterns of annotation

scientific article published on 14 April 2003

Predicting phenotype from patterns of annotation

scientific article published on January 2003

Predicting protein complex membership using probabilistic network reliability

scientific article

Prion-like disorders: blurring the divide between transmissibility and infectivity

scientific article published on April 2010

Prion-like domains as epigenetic regulators, scaffolds for subcellular organization, and drivers of neurodegenerative disease

scientific article

Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases

scientific article

Salivary metabolite levels in perinatally HIV-infected youth with periodontal disease

scientific article published on 11 September 2020

Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice

scientific article

Stress granules as crucibles of ALS pathogenesis.

scientific article published on April 2013

The Cryptosporidium parvum Kinome ⬇️

scientific article

The evolution of bet-hedging adaptations to rare scenarios

scientific article

The loss of adaptive plasticity during long periods of environmental stasis

scientific article

The power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

scientific article

The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease.

scientific article

Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.

scientific article

List of works by Oliver D King

A global analysis of IFT-A function reveals specialization for transport of membrane-associated proteins into cilia

A mass formula for unimodular lattices with no roots

A new approach for the study of lung smooth muscle phenotypes and its application in a murine model of allergic airway inflammation

A non-parametric model for transcription factor binding sites ⬇️

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

A yeast functional screen predicts new candidate ALS disease genes

An open system for automatic home-cage behavioral analysis and its application to male and female mouse models of Huntington's disease.

Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy

Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity

Characterizing gene sets with FuncAssociate

Combining biological networks to predict genetic interactions

Combining guilt-by-association and guilt-by-profiling to predict Saccharomyces cerevisiae gene function

Comment on "Subgraphs in random networks".

Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

Exome sequencing to identify de novo mutations in sporadic ALS trios

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Free-Wilson Analysis of Comprehensive Data on Phosphoinositide-3-kinase (PI3K) Inhibitors Reveals Importance of N-Methylation for PI3Kδ Activity

Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor

GoFish finds genes with combinations of Gene Ontology attributes

Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease

Human skeletal muscle xenograft as a new preclinical model for muscle disorders

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

Inhibiting GPI anchor biosynthesis in fungi stresses the endoplasmic reticulum and enhances immunogenicity

Intensity-based protein identification by machine learning from a library of tandem mass spectra.

Knocking out multigene redundancies via cycles of sexual assortment and fluorescence selection

Ly6a Differential Expression in Blood-Brain Barrier Is Responsible for Strain Specific Central Nervous System Transduction Profile of AAV-PHP.B.

Morpholino-mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics

Motifs, themes and thematic maps of an integrated Saccharomyces cerevisiae interaction network

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains

Opposing effects of glutamine and asparagine govern prion formation by intrinsically disordered proteins

PLAAC: a web and command-line application to identify proteins with prion-like amino acid composition

Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

Predicting co-complexed protein pairs using genomic and proteomic data integration

Predicting gene function from patterns of annotation

Predicting phenotype from patterns of annotation

Predicting protein complex membership using probabilistic network reliability

Prion-like disorders: blurring the divide between transmissibility and infectivity

Prion-like domains as epigenetic regulators, scaffolds for subcellular organization, and drivers of neurodegenerative disease

Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases

Salivary metabolite levels in perinatally HIV-infected youth with periodontal disease

Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice

Stress granules as crucibles of ALS pathogenesis.

The Cryptosporidium parvum Kinome ⬇️

The evolution of bet-hedging adaptations to rare scenarios

The loss of adaptive plasticity during long periods of environmental stasis

The power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease.

Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.