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Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction

BMC bioinformatics, 2012-06, Vol.13 (1), p.134-134, Article 134

2012

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Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers

Nature genetics, 2013-12, Vol.45 (12), p.1474-1478

2013

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Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Nature genetics, 2014-08, Vol.46 (8), p.877-880

2014

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Genome-wide mutational signatures of aristolochic acid and its application as a screening tool

Science translational medicine, 2013-08, Vol.5 (197), p.197ra101

2013

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GIGYF1 disruption associates with autism and impaired IGF-1R signaling

The Journal of clinical investigation, 2022-10, Vol.132 (19), p.1-15

2022

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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

Nature communications, 2022-07, Vol.13 (1), p.4112-4112, Article 4112

2022

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Exome-wide Sequencing Shows Low Mutation Rates and Identifies Novel Mutated Genes in Seminomas

European urology, 2015-07, Vol.68 (1), p.77-83

2015

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Genetic and Structural Variation in the Gastric Cancer Kinome Revealed through Targeted Deep Sequencing

Cancer research (Chicago, Ill.), 2011-01, Vol.71 (1), p.29-39

2011

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Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

Genome medicine, 2015-09, Vol.7 (1), p.98-98, Article 98

2015

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Abundant copy-number loss of CYCLOPS and STOP genes in gastric adenocarcinoma

Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2016-04, Vol.19 (2), p.453-465

2016

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Primer3--new capabilities and interfaces

Nucleic acids research, 2012-08, Vol.40 (15), p.e115

2012

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Towards realizing the vision of precision medicine: AI based prediction of clinical drug response

Brain (London, England : 1878), 2021-07, Vol.144 (6), p.1738-1750

2021

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Assessing matched normal and tumor pairs in next-generation sequencing studies

PloS one, 2011-03, Vol.6 (3), p.e17810-e17810

2011

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Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinants

Brain (London, England : 1878), 2021-10, Vol.144 (9), p.2879-2891

2021

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MSIseq: Software for Assessing Microsatellite Instability from Catalogs of Somatic Mutations

Scientific reports, 2015-08, Vol.5 (1), p.13321-13321, Article 13321

2015

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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.108-125

2020

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Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Nature communications, 2020-10, Vol.11 (1), p.5341-5341, Article 5341

2020

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Janus kinase 3-activating mutations identified in natural killer/T-cell lymphoma

Cancer discovery, 2012-07, Vol.2 (7), p.591-597

2012

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First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum

Genome biology, 2011-01, Vol.12 (9), p.R96-R96

2011

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Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Nature communications, 2020-12, Vol.11 (1)

2020

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Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Nature communications, 2020-10, Vol.11 (1)

2020

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Abstract 3874: Mutational landscapes of oral tongue squamous cell carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.3874-3874

2015

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Abstract 5168: Gastric adenocarcinomas show pervasive loss of heterozygosity and enrichment for “STOP” genes in regions of hemizygous deletion

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.5168-5168

2014

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Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction

Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers

Exome sequencing of liver fluke―associated cholangiocarcinoma

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Genome-wide mutational signatures of aristolochic acid and its application as a screening tool

GIGYF1 disruption associates with autism and impaired IGF-1R signaling

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

Exome-wide Sequencing Shows Low Mutation Rates and Identifies Novel Mutated Genes in Seminomas

Genetic and Structural Variation in the Gastric Cancer Kinome Revealed through Targeted Deep Sequencing

Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

Abundant copy-number loss of CYCLOPS and STOP genes in gastric adenocarcinoma

Primer3--new capabilities and interfaces

Towards realizing the vision of precision medicine: AI based prediction of clinical drug response

Assessing matched normal and tumor pairs in next-generation sequencing studies

Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinants

MSIseq: Software for Assessing Microsatellite Instability from Catalogs of Somatic Mutations

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes

Janus kinase 3-activating mutations identified in natural killer/T-cell lymphoma

First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Abstract 3874: Mutational landscapes of oral tongue squamous cell carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

Abstract 5168: Gastric adenocarcinomas show pervasive loss of heterozygosity and enrichment for “STOP” genes in regions of hemizygous deletion

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