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American Journal of Human Genetics
|
May 11, 2020
Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
Dimitrios Vitsios, Slavé Petrovski
Epilepsy & Behavior : E&B
|
October 30, 2012
Unraveling the genetics of common epilepsies: approaches, platforms, and caveats
Slavé Petrovski, Patrick Kwan
Genome Biology
|
July 16, 2016
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine
Slavé Petrovski, David B Goldstein
Science Translational Medicine
|
September 19, 2014
Phenomics and the interpretation of personal genomes
Slavé Petrovski, David B Goldstein
Nature
|
December 6, 2023
An expanded genomic database for identifying disease-related variants
Ryan S Dhindsa, Slavé Petrovski
Nucleic Acids Research
|
June 7, 2019
MTR-Viewer: identifying regions within genes under purifying selection
Michael Silk, Slavé Petrovski, David B Ascher
The Lancet. Neurology
|
September 9, 2019
Epilepsy genetics: clinical impacts and biological insights
Colin A Ellis, Slavé Petrovski, Samuel F Berkovic
Nature Neuroscience
|
May 29, 2014
One gene, many neuropsychiatric disorders: lessons from Mendelian diseases
Xiaolin Zhu, Anna C Need, Slavé Petrovski, et al.
Neurology. Genetics
|
July 19, 2017
ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies
Caitlin A Bennett, Slavé Petrovski, Karen L Oliver, et al.
Journal of Medical Genetics
|
December 1, 2016
The importance of dynamic re-analysis in diagnostic whole exome sequencing
Anna C Need, Vandana Shashi, Kelly Schoch, et al.
Page
of 12
Search research articles
Search
Showing results (1-10 of 117) with videos related to
Sort By:
Page
of 12
American Journal of Human Genetics
|
May 11, 2020
Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
Dimitrios Vitsios, Slavé Petrovski
Epilepsy & Behavior : E&B
|
October 30, 2012
Unraveling the genetics of common epilepsies: approaches, platforms, and caveats
Slavé Petrovski, Patrick Kwan
Genome Biology
|
July 16, 2016
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine
Slavé Petrovski, David B Goldstein
Science Translational Medicine
|
September 19, 2014
Phenomics and the interpretation of personal genomes
Slavé Petrovski, David B Goldstein
Nature
|
December 6, 2023
An expanded genomic database for identifying disease-related variants
Ryan S Dhindsa, Slavé Petrovski
Nucleic Acids Research
|
June 7, 2019
MTR-Viewer: identifying regions within genes under purifying selection
Michael Silk, Slavé Petrovski, David B Ascher
The Lancet. Neurology
|
September 9, 2019
Epilepsy genetics: clinical impacts and biological insights
Colin A Ellis, Slavé Petrovski, Samuel F Berkovic
Nature Neuroscience
|
May 29, 2014
One gene, many neuropsychiatric disorders: lessons from Mendelian diseases
Xiaolin Zhu, Anna C Need, Slavé Petrovski, et al.
Neurology. Genetics
|
July 19, 2017
ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies
Caitlin A Bennett, Slavé Petrovski, Karen L Oliver, et al.
Journal of Medical Genetics
|
December 1, 2016
The importance of dynamic re-analysis in diagnostic whole exome sequencing
Anna C Need, Vandana Shashi, Kelly Schoch, et al.
Page
of 12