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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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Immunosuppression as a Hub for SARS-CoV-2 Mutational Drift

Viruses, 2023-03, Vol.15 (4), p.855

2023

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Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

PloS one, 2012-03, Vol.7 (3), p.e33251-e33251

2012

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Heterozygous APC germline mutations impart predisposition to colorectal cancer

Scientific reports, 2021-03, Vol.11 (1), p.5113-5113, Article 5113

2021

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A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)

Human mutation, 2020-01, Vol.41 (1), p.140-149

2020

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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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Transcriptomic Analysis of Human Fragile X Syndrome Neurons Reveals Neurite Outgrowth Modulation by the TGFβ/BMP Pathway

International journal of molecular sciences, 2022-08, Vol.23 (16), p.9278

2022

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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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Analysis of microRNAs in familial Mediterranean fever

PloS one, 2018-05, Vol.13 (5), p.e0197829-e0197829

2018

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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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Downregulation of miR-31, miR-155, and miR-564 in chronic myeloid leukemia cells

PloS one, 2012-04, Vol.7 (4), p.e35501-e35501

2012

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Group Selection and Contribution of Minority Variants during Virus Adaptation Determines Virus Fitness and Phenotype

PLoS pathogens, 2015-05, Vol.11 (5), p.e1004838-e1004838

2015

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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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Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel

PloS one, 2013-01, Vol.8 (1), p.e53083-e53083

2013

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MicroRNA-15a-5p acts as a tumor suppressor in histiocytosis by mediating CXCL10-ERK-LIN28a-let-7 axis

Leukemia, 2022-04, Vol.36 (4), p.1139-1149

2022

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Blood RNA Sequencing Indicates Upregulated BATF2 and LY6E and Downregulated ISG15 and MT2A Expression in Children with Autism Spectrum Disorder

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9843

2022

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miRviewer: a multispecies microRNA homologous viewer

BMC research notes, 2012-02, Vol.5 (1), p.92-92, Article 92

2012

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Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis

PLoS genetics, 2016-10, Vol.12 (10), p.e1006369-e1006369

2016

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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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Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis

Journal of investigative dermatology, 2017-02, Vol.137 (2), p.385-393

2017

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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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HIV-1 quasispecies delineation by tag linkage deep sequencing

PloS one, 2014-05, Vol.9 (5), p.e97505-e97505

2014

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Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

Experimental dermatology, 2021-09, Vol.30 (9), p.1290-1297

2021

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

Variant PADI3 in Central Centrifugal Cicatricial Alopecia

Immunosuppression as a Hub for SARS-CoV-2 Mutational Drift

Transient cell-in-cell formation underlies tumor relapse and resistance to immunotherapy

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

Heterozygous APC germline mutations impart predisposition to colorectal cancer

A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)

Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

Transcriptomic Analysis of Human Fragile X Syndrome Neurons Reveals Neurite Outgrowth Modulation by the TGFβ/BMP Pathway

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

Analysis of microRNAs in familial Mediterranean fever

Noninvasive prenatal molecular karyotyping from maternal plasma

Downregulation of miR-31, miR-155, and miR-564 in chronic myeloid leukemia cells

Group Selection and Contribution of Minority Variants during Virus Adaptation Determines Virus Fitness and Phenotype

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

Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel

MicroRNA-15a-5p acts as a tumor suppressor in histiocytosis by mediating CXCL10-ERK-LIN28a-let-7 axis

Blood RNA Sequencing Indicates Upregulated BATF2 and LY6E and Downregulated ISG15 and MT2A Expression in Children with Autism Spectrum Disorder

miRviewer: a multispecies microRNA homologous viewer

Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis

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

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis

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

HIV-1 quasispecies delineation by tag linkage deep sequencing

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

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