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Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels

PloS one, 2017-02, Vol.12 (2), p.e0170843-e0170843

2017

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Variant PADI3 in Central Centrifugal Cicatricial Alopecia

The New England journal of medicine, 2019-02, Vol.380 (9), p.833-841

2019

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Analysis of MicroRNA Regulation and Gene Expression Variability in Single Cell Data

Journal of personalized medicine, 2022-10, Vol.12 (10), p.1750

2022

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Determinants of targeting by endogenous and exogenous microRNAs and siRNAs

RNA (Cambridge), 2007-11, Vol.13 (11), p.1894-1910

2007

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Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

American journal of human genetics, 2012-07, Vol.91 (1), p.163-170

2012

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Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing

PloS one, 2013-05, Vol.8 (5), p.e64271

2013

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Noninvasive prenatal molecular karyotyping from maternal plasma

PloS one, 2013-04, Vol.8 (4), p.e60968

2013

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Phylogenetic and genome-wide deep-sequencing analyses of canine parvovirus reveal co-infection with field variants and emergence of a recent recombinant strain

PloS one, 2014-11, Vol.9 (11), p.e111779-e111779

2014

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Awareness and attitude of the public toward personalized medicine in Korea

PloS one, 2018-02, Vol.13 (2), p.e0192856-e0192856

2018

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Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic Elements

PLoS neglected tropical diseases, 2016-01, Vol.10 (1), p.e0004402-e0004402

2016

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MeDIP combined with in-solution targeted enrichment followed by NGS: Inter-individual methylation variability of fetal-specific biomarkers and their implementation in a proof of concept study for NIPT

PloS one, 2018-06, Vol.13 (6), p.e0199010-e0199010

2018

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Identification of hepatotropic viruses from plasma using deep sequencing: a next generation diagnostic tool

PloS one, 2013-04, Vol.8 (4), p.e60595-e60595

2013

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Pax6 regulates gene expression in the vertebrate lens through miR-204

PLoS genetics, 2013-03, Vol.9 (3), p.e1003357-e1003357

2013

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Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients

Viruses, 2023-11, Vol.15 (11), p.2227

2023

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SOLiD™ sequencing of genomes of clinical isolates of Leishmania donovani from India confirm leptomonas co-infection and raise some key questions

PloS one, 2013-02, Vol.8 (2), p.e55738-e55738

2013

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Risk for molecular contamination of tissue samples evaluated for targeted anti-cancer therapy

PloS one, 2017-03, Vol.12 (3), p.e0173760-e0173760

2017

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MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease Phenotypes

PloS one, 2016-08, Vol.11 (8), p.e0159956-e0159956

2016

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Comprehensive Genetic Analysis of Druze Provides Insights into Carrier Screening

Genes, 2023-04, Vol.14 (4), p.937

2023

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Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicine

PloS one, 2013-08, Vol.8 (8), p.e71554

2013

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Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients

PloS one, 2014-07, Vol.9 (7), p.e102556-e102556

2014

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Efficient and comprehensive representation of uniqueness for next-generation sequencing by minimum unique length analyses

PloS one, 2013-01, Vol.8 (1), p.e53822-e53822

2013

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Molecular Risk Factors for Schizophrenia

Trends in molecular medicine, 2016-03, Vol.22 (3), p.242-253

2016

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Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

PloS one, 2014-02, Vol.9 (2), p.e90391-e90391

2014

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MicroRNAs and pharmacogenomics

Pharmacogenomics, 2010-05, Vol.11 (5), p.629-632

Shomron, Noam

2010

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Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels

Variant PADI3 in Central Centrifugal Cicatricial Alopecia

Analysis of MicroRNA Regulation and Gene Expression Variability in Single Cell Data

Determinants of targeting by endogenous and exogenous microRNAs and siRNAs

Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing

Noninvasive prenatal molecular karyotyping from maternal plasma

Phylogenetic and genome-wide deep-sequencing analyses of canine parvovirus reveal co-infection with field variants and emergence of a recent recombinant strain

Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium

Awareness and attitude of the public toward personalized medicine in Korea

Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic Elements

MeDIP combined with in-solution targeted enrichment followed by NGS: Inter-individual methylation variability of fetal-specific biomarkers and their implementation in a proof of concept study for NIPT

Identification of hepatotropic viruses from plasma using deep sequencing: a next generation diagnostic tool

Pax6 regulates gene expression in the vertebrate lens through miR-204

Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients

SOLiD™ sequencing of genomes of clinical isolates of Leishmania donovani from India confirm leptomonas co-infection and raise some key questions

Risk for molecular contamination of tissue samples evaluated for targeted anti-cancer therapy

MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease Phenotypes

Comprehensive Genetic Analysis of Druze Provides Insights into Carrier Screening

Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicine

Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients

Efficient and comprehensive representation of uniqueness for next-generation sequencing by minimum unique length analyses

Molecular Risk Factors for Schizophrenia

Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

MicroRNAs and pharmacogenomics

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