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Frontiers in Pharmacology
|
April 2, 2019
Actionable Pharmacogenetic Variation in the Slovenian Genomic Database
Keli Hočevar, Aleš Maver, Borut Peterlin
Life (Basel, Switzerland)
|
April 3, 2021
Whole-Genome Sequencing in Diagnostics of Selected Slovenian Undiagnosed Patients with Rare Disorders
Gaber Bergant, Aleš Maver, Borut Peterlin
Omics : a Journal of Integrative Biology
|
April 25, 2018
Sarcoidosis Related Novel Candidate Genes Identified by Multi-Omics Integrative Analyses
Keli Hočevar, Aleš Maver, Tanja Kunej, et al.
Scientific Reports
|
March 31, 2023
Assessment of pathogenic variation in gynecologic cancer genes in a national cohort
Urška Kotnik, Aleš Maver, Borut Peterlin, et al.
Journal of Community Genetics
|
January 16, 2021
Improving diagnostics of rare genetic diseases with NGS approaches
Mateja Vinkšel, Karin Writzl, Aleš Maver, et al.
Frontiers in Neurology
|
August 31, 2018
DNA Methylation Profiles in Whole Blood of Huntington's Disease Patients
Maja Zadel, Aleš Maver, Anja Kovanda, et al.
Omics : a Journal of Integrative Biology
|
April 14, 2018
Transcriptomic Biomarkers for Huntington's Disease: Are Gene Expression Signatures in Whole Blood Reliable Biomarkers?
Maja Zadel, Aleš Maver, Anja Kovanda, et al.
Metabolic Brain Disease
|
July 15, 2018
Contemporary scope of inborn errors of metabolism involving epilepsy or seizures
Birutė Tumienė, Borut Peterlin, Aleš Maver, et al.
European Journal of Medical Genetics
|
December 14, 2018
Rare missense TUBGCP5 gene variant in a patient with primary microcephaly
Aleš Maver, Goran Čuturilo, Anja Kovanda, et al.
Plos One
|
September 26, 2013
Expression signature as a biomarker for prenatal diagnosis of trisomy 21
Marija Volk, Aleš Maver, Luca Lovrečić, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 70) with videos related to
Sort By:
Page
of 7
Frontiers in Pharmacology
|
April 2, 2019
Actionable Pharmacogenetic Variation in the Slovenian Genomic Database
Keli Hočevar, Aleš Maver, Borut Peterlin
Life (Basel, Switzerland)
|
April 3, 2021
Whole-Genome Sequencing in Diagnostics of Selected Slovenian Undiagnosed Patients with Rare Disorders
Gaber Bergant, Aleš Maver, Borut Peterlin
Omics : a Journal of Integrative Biology
|
April 25, 2018
Sarcoidosis Related Novel Candidate Genes Identified by Multi-Omics Integrative Analyses
Keli Hočevar, Aleš Maver, Tanja Kunej, et al.
Scientific Reports
|
March 31, 2023
Assessment of pathogenic variation in gynecologic cancer genes in a national cohort
Urška Kotnik, Aleš Maver, Borut Peterlin, et al.
Journal of Community Genetics
|
January 16, 2021
Improving diagnostics of rare genetic diseases with NGS approaches
Mateja Vinkšel, Karin Writzl, Aleš Maver, et al.
Frontiers in Neurology
|
August 31, 2018
DNA Methylation Profiles in Whole Blood of Huntington's Disease Patients
Maja Zadel, Aleš Maver, Anja Kovanda, et al.
Omics : a Journal of Integrative Biology
|
April 14, 2018
Transcriptomic Biomarkers for Huntington's Disease: Are Gene Expression Signatures in Whole Blood Reliable Biomarkers?
Maja Zadel, Aleš Maver, Anja Kovanda, et al.
Metabolic Brain Disease
|
July 15, 2018
Contemporary scope of inborn errors of metabolism involving epilepsy or seizures
Birutė Tumienė, Borut Peterlin, Aleš Maver, et al.
European Journal of Medical Genetics
|
December 14, 2018
Rare missense TUBGCP5 gene variant in a patient with primary microcephaly
Aleš Maver, Goran Čuturilo, Anja Kovanda, et al.
Plos One
|
September 26, 2013
Expression signature as a biomarker for prenatal diagnosis of trisomy 21
Marija Volk, Aleš Maver, Luca Lovrečić, et al.
Page
of 7