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Human Mutation
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April 17, 2012
Deep phenotyping for precision medicine
Peter N Robinson
The New England Journal of Medicine
|
October 22, 2025
A Rare-in-Common Paradigm for Precision Genomic Medicine
Peter N Robinson
Human Mutation
|
April 21, 2017
Once doesn't count: Phenotype-driven gene hunting in cohorts
Peter N Robinson
Genome Medicine
|
December 5, 2014
Genomic data sharing for translational research and diagnostics
Peter N Robinson
Human Mutation
|
November 15, 2013
A systematic large-scale phenotypic analysis of de novo and inherited copy number variation
Peter N Robinson
Genome Biology
|
December 22, 2010
Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
Peter N Robinson
BMC Bioinformatics
|
February 14, 2006
HotSwap for bioinformatics: a STRAP tutorial
Christoph Gille, Peter N Robinson
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology
|
October 27, 2023
Computing Minimal Boolean Models of Gene Regulatory Networks
Guy Karlebach, Peter N Robinson
Plos Genetics
|
April 5, 2014
Phenotype ontologies and cross-species analysis for translational research
Peter N Robinson, Caleb Webber
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 23, 2022
[Rare-disease data standards]
Peter N Robinson, Holm Graessner
Page
of 35
Search research articles
Search
Showing results (1-10 of 347) with videos related to
Sort By:
Page
of 35
Human Mutation
|
April 17, 2012
Deep phenotyping for precision medicine
Peter N Robinson
The New England Journal of Medicine
|
October 22, 2025
A Rare-in-Common Paradigm for Precision Genomic Medicine
Peter N Robinson
Human Mutation
|
April 21, 2017
Once doesn't count: Phenotype-driven gene hunting in cohorts
Peter N Robinson
Genome Medicine
|
December 5, 2014
Genomic data sharing for translational research and diagnostics
Peter N Robinson
Human Mutation
|
November 15, 2013
A systematic large-scale phenotypic analysis of de novo and inherited copy number variation
Peter N Robinson
Genome Biology
|
December 22, 2010
Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
Peter N Robinson
BMC Bioinformatics
|
February 14, 2006
HotSwap for bioinformatics: a STRAP tutorial
Christoph Gille, Peter N Robinson
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology
|
October 27, 2023
Computing Minimal Boolean Models of Gene Regulatory Networks
Guy Karlebach, Peter N Robinson
Plos Genetics
|
April 5, 2014
Phenotype ontologies and cross-species analysis for translational research
Peter N Robinson, Caleb Webber
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 23, 2022
[Rare-disease data standards]
Peter N Robinson, Holm Graessner
Page
of 35