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Quantitative detection of ALK fusion breakpoints in plasma cell-free DNA from patients with non-small cell lung cancer using PCR-based target sequencing with a tiling primer set and two-step mapping/alignment

PloS one, 2019-09, Vol.14 (9), p.e0222233-e0222233

2019

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High‐throughput screening in colorectal cancer tissue‐originated spheroids

Cancer science, 2019-01, Vol.110 (1), p.345-355

2019

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Primary Epithelioid Rhabdomyosarcoma of the Liver: Case Report of an Unusual Histological Variant

International journal of surgical pathology, 2022-05, Vol.30 (3), p.331-334

2022

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Diagnostic Accuracy of Noninvasive Genotyping of EGFR in Lung Cancer Patients by Deep Sequencing of Plasma Cell-Free DNA

Clinical chemistry (Baltimore, Md.), 2015-09, Vol.61 (9), p.1191-1196

2015

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Monitoring of treatment responses and clonal evolution of tumor cells by circulating tumor DNA of heterogeneous mutant EGFR genes in lung cancer

Lung cancer (Amsterdam, Netherlands), 2016-04, Vol.94, p.68-73

2016

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HLA genotyping by next-generation sequencing of complementary DNA

BMC genomics, 2017-11, Vol.18 (1), p.914-914, Article 914

2017

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Selective identification of somatic mutations in pancreatic cancer cells through a combination of next-generation sequencing of plasma DNA using molecular barcodes and a bioinformatic variant filter

PloS one, 2018-02, Vol.13 (2), p.e0192611-e0192611

2018

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Dynamics of circulating tumor DNA represented by the activating and resistant mutations in epidermal growth factor receptor tyrosine kinase inhibitor treatment

Cancer science, 2016-03, Vol.107 (3), p.353-358

2016

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Quantitative identification of mutant alleles derived from lung cancer in plasma cell-free DNA via anomaly detection using deep sequencing data

PloS one, 2013-11, Vol.8 (11), p.e81468-e81468

2013

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Sweat-gland carcinoma with neuroendocrine differentiation (SCAND): a clinicopathologic study of 13 cases with genetic analysis

Modern pathology, 2022-01, Vol.35 (1), p.33-43

2022

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Lorlatinib for the Treatment of Inflammatory Myofibroblastic Tumor after Allogeneic Hematopoietic Stem Cell Transplantation: A Case Report

Internal medicine (Tokyo, 1992), 2024-07

2024

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Bcl‐2‐negative IGH‐BCL2 translocation‐negative follicular lymphoma of the thyroid differs genetically and epigenetically from Bcl‐2‐positive IGH‐BCL2 translocation‐positive follicular lymphoma

Histopathology, 2021-10, Vol.79 (4), p.521-532

2021

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Utility of Comprehensive Genomic Profiling Tests for Patients with Incurable Pancreatic Cancer in Clinical Practice

Cancers, 2023-02, Vol.15 (3), p.970

2023

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Numerical indices based on circulating tumor DNA for the evaluation of therapeutic response and disease progression in lung cancer patients

Scientific reports, 2016-07, Vol.6 (1), p.29093-29093, Article 29093

2016

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Analytical Performance of a Highly Sensitive System to Detect Gene Variants Using Next-Generation Sequencing for Lung Cancer Companion Diagnostics

Diagnostics (Basel), 2023-04, Vol.13 (8), p.1476

2023

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Early responses of EGFR circulating tumor DNA to EGFR tyrosine kinase inhibitors in lung cancer treatment

Oncotarget, 2016-11, Vol.7 (44), p.71782-71789

2016

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EML4-ALK fusion variant.3 and co-occurrent PIK3CA E542K mutation exhibiting primary resistance to three generations of ALK inhibitors

Cancer genetics, 2021-08, Vol.256-257, p.131-135

2021

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Clinical application of comprehensive genomic profiling panel to thoracic malignancies: A single‐center retrospective study

Thoracic cancer, 2022-11, Vol.13 (21), p.2970-2977

2022

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Prognostic prediction of glioblastoma by quantitative assessment of the methylation status of the entire MGMT promoter region

BMC cancer, 2014-08, Vol.14 (1), p.641-641, Article 641

2014

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Conversion Surgery for Advanced Thoracic SMARCA4-Deficient Undifferentiated Tumor With Atezolizumab in Combination With Bevacizumab, Paclitaxel, and Carboplatin Treatment: A Case Report

JTO clinical and research reports, 2021-11, Vol.2 (11), p.100235, Article 100235

2021

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Thoracic small round cell sarcoma with FGFR2::DCTN2 fusion

Histopathology, 2024-06

2024

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Evaluation of haplotype inference using definitive haplotype data obtained from complete hydatidiform moles, and its significance for the analyses of positively selected regions

PLoS genetics, 2009-05, Vol.5 (5), p.e1000468-e1000468

2009

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LC-SCRUM-Asiaでの再解析によりROS1融合遺伝子を検出し，治療につながった肺腺癌の1例

肺癌, 2021/08/20, Vol.61(4), pp.303-309

2021

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Malignant epithelioid soft‐tissue tumour with the NRID1–MAML1 fusion

Histopathology, 2021-12, Vol.79 (6), p.1112-1114

2021

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A novel EWSR1-HOXB13 rearrangement in a fibroblastic tumor from the abdomen of a young woman

Virchows Archiv : an international journal of pathology, 2022-09, Vol.481 (3), p.499-503

2022

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Quantitative detection of ALK fusion breakpoints in plasma cell-free DNA from patients with non-small cell lung cancer using PCR-based target sequencing with a tiling primer set and two-step mapping/alignment

High‐throughput screening in colorectal cancer tissue‐originated spheroids

Primary Epithelioid Rhabdomyosarcoma of the Liver: Case Report of an Unusual Histological Variant

Diagnostic Accuracy of Noninvasive Genotyping of EGFR in Lung Cancer Patients by Deep Sequencing of Plasma Cell-Free DNA

Monitoring of treatment responses and clonal evolution of tumor cells by circulating tumor DNA of heterogeneous mutant EGFR genes in lung cancer

HLA genotyping by next-generation sequencing of complementary DNA

Selective identification of somatic mutations in pancreatic cancer cells through a combination of next-generation sequencing of plasma DNA using molecular barcodes and a bioinformatic variant filter

Dynamics of circulating tumor DNA represented by the activating and resistant mutations in epidermal growth factor receptor tyrosine kinase inhibitor treatment

Quantitative identification of mutant alleles derived from lung cancer in plasma cell-free DNA via anomaly detection using deep sequencing data

Sweat-gland carcinoma with neuroendocrine differentiation (SCAND): a clinicopathologic study of 13 cases with genetic analysis

Lorlatinib for the Treatment of Inflammatory Myofibroblastic Tumor after Allogeneic Hematopoietic Stem Cell Transplantation: A Case Report

Bcl‐2‐negative IGH‐BCL2 translocation‐negative follicular lymphoma of the thyroid differs genetically and epigenetically from Bcl‐2‐positive IGH‐BCL2 translocation‐positive follicular lymphoma

Utility of Comprehensive Genomic Profiling Tests for Patients with Incurable Pancreatic Cancer in Clinical Practice

Numerical indices based on circulating tumor DNA for the evaluation of therapeutic response and disease progression in lung cancer patients

Analytical Performance of a Highly Sensitive System to Detect Gene Variants Using Next-Generation Sequencing for Lung Cancer Companion Diagnostics

Early responses of EGFR circulating tumor DNA to EGFR tyrosine kinase inhibitors in lung cancer treatment

EML4-ALK fusion variant.3 and co-occurrent PIK3CA E542K mutation exhibiting primary resistance to three generations of ALK inhibitors

Clinical application of comprehensive genomic profiling panel to thoracic malignancies: A single‐center retrospective study

Prognostic prediction of glioblastoma by quantitative assessment of the methylation status of the entire MGMT promoter region

Conversion Surgery for Advanced Thoracic SMARCA4-Deficient Undifferentiated Tumor With Atezolizumab in Combination With Bevacizumab, Paclitaxel, and Carboplatin Treatment: A Case Report

Thoracic small round cell sarcoma with FGFR2::DCTN2 fusion

Evaluation of haplotype inference using definitive haplotype data obtained from complete hydatidiform moles, and its significance for the analyses of positively selected regions

LC-SCRUM-Asiaでの再解析によりROS1融合遺伝子を検出し，治療につながった肺腺癌の1例

Malignant epithelioid soft‐tissue tumour with the NRID1–MAML1 fusion

A novel EWSR1-HOXB13 rearrangement in a fibroblastic tumor from the abdomen of a young woman

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