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PFRED: A computational platform for siRNA and antisense oligonucleotides design

PloS one, 2021-01, Vol.16 (1), p.e0238753-e0238753

2021

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Estimation of kinship coefficient in structured and admixed populations using sparse sequencing data

PLoS genetics, 2017-09, Vol.13 (9), p.e1007021-e1007021

2017

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Systematic determination of genetic network architecture

Nature genetics, 1999-07, Vol.22 (3), p.281-285

1999

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siRNA off-target effects can be reduced at concentrations that match their individual potency

PloS one, 2011-07, Vol.6 (7), p.e21503-e21503

2011

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Are protein–protein interfaces more conserved in sequence than the rest of the protein surface?

Protein science, 2004-01, Vol.13 (1), p.190-202

2004

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A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression

Nature genetics, 2000-10, Vol.26 (2), p.183-186

2000

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Magnesium Restores Activity to Peripheral Blood Cells in a Patient With Functionally Impaired Interleukin-2-Inducible T Cell Kinase

Frontiers in immunology, 2019-08, Vol.10, p.2000

2019

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Finding DNA regulatory motifs within unaligned noncoding sequences clustered by whole-genome mRNA quantitation

Nature biotechnology, 1998-10, Vol.16 (10), p.939-945

1998

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Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy

Science (American Association for the Advancement of Science), 2015-07, Vol.349 (6246), p.436-440

2015

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Physiochemical drug properties associated with in vivo toxicological outcomes

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (17), p.4872-4875

2008

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Measurement of ctDNA Tumor Fraction Identifies Informative Negative Liquid Biopsy Results and Informs Value of Tissue Confirmation

Clinical cancer research, 2024-06, Vol.30 (11), p.2452-OF9

2024

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Recurrent rhinovirus infections in a child with inherited MDA5 deficiency

The Journal of experimental medicine, 2017-07, Vol.214 (7), p.1949-1972

2017

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Analytical Validation of a Hybrid Capture–Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNA

The Journal of molecular diagnostics : JMD, 2018-09, Vol.20 (5), p.686-702

2018

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Autosomal recessive phosphoglucomutase 3 ( PGM3 ) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Journal of allergy and clinical immunology, 2014-05, Vol.133 (5), p.1400-1409.e5

2014

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Convergence of Clinical and Cellular Phenotypes Among Patients with STAT3 and ERBB2IP Mutations

Journal of allergy and clinical immunology, 2015-02, Vol.135 (2), p.AB152-AB152

2015

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Impaired Glycosylation Due To Autosomal Recessive PGM3 Mutations Results In Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment

Journal of allergy and clinical immunology, 2014-02, Vol.133 (2), p.AB161-AB161

2014

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Mutation Detection in an Antibody-Producing Chinese Hamster Ovary Cell Line by Targeted RNA Sequencing

BioMed research international, 2016-01, Vol.2016 (2016), p.1-8

2016

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Abstract 5455: Identifying somatic variants with defined confidence level in targeted sequencing of tumor DNA without a matched normal sample

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.5455-5455

2020

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Utility of ctDNA tumor fraction to inform negative liquid biopsy (LBx) results and need for tissue reflex in advanced non-small cell lung cancer (aNSCLC)

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.9076-9076

2023

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Computational identification of Cis-regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae

Journal of molecular biology, 2000-03, Vol.296 (5), p.1205-1214

2000

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MSI-H testing via hybrid capture based NGS sequencing of liquid biopsy samples

Journal of clinical oncology, 2019-02, Vol.37 (4_suppl), p.504-504

2019

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Conservation of DNA regulatory motifs and discovery of new motifs in microbial genomes

Genome research, 2000-06, Vol.10 (6), p.744-757

2000

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Autosomal recessive PGM3 mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Journal of allergy and clinical immunology, 2014-02, Vol.133 (5), p.1400-1409.e5

2014

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PFRED: A computational platform for siRNA and antisense oligonucleotides design

Estimation of kinship coefficient in structured and admixed populations using sparse sequencing data

Systematic determination of genetic network architecture

siRNA off-target effects can be reduced at concentrations that match their individual potency

Are protein–protein interfaces more conserved in sequence than the rest of the protein surface?

A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression

Magnesium Restores Activity to Peripheral Blood Cells in a Patient With Functionally Impaired Interleukin-2-Inducible T Cell Kinase

Finding DNA regulatory motifs within unaligned noncoding sequences clustered by whole-genome mRNA quantitation

Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy

Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number

Physiochemical drug properties associated with in vivo toxicological outcomes

Measurement of ctDNA Tumor Fraction Identifies Informative Negative Liquid Biopsy Results and Informs Value of Tissue Confirmation

BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency

Recurrent rhinovirus infections in a child with inherited MDA5 deficiency

Analytical Validation of a Hybrid Capture–Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNA

Autosomal recessive phosphoglucomutase 3 ( PGM3 ) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Convergence of Clinical and Cellular Phenotypes Among Patients with STAT3 and ERBB2IP Mutations

Impaired Glycosylation Due To Autosomal Recessive PGM3 Mutations Results In Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment

Mutation Detection in an Antibody-Producing Chinese Hamster Ovary Cell Line by Targeted RNA Sequencing

Abstract 5455: Identifying somatic variants with defined confidence level in targeted sequencing of tumor DNA without a matched normal sample

Utility of ctDNA tumor fraction to inform negative liquid biopsy (LBx) results and need for tissue reflex in advanced non-small cell lung cancer (aNSCLC)

Computational identification of Cis-regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae

MSI-H testing via hybrid capture based NGS sequencing of liquid biopsy samples

Conservation of DNA regulatory motifs and discovery of new motifs in microbial genomes

Autosomal recessive PGM3 mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

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