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Germline and somatic mutations of homologous recombination-associated genes in Japanese ovarian cancer patients

Scientific reports, 2019-11, Vol.9 (1), p.17808-9, Article 17808

2019

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Applying Machine Learning to Kinematic and Eye Movement Features of a Movement Imitation Task to Predict Autism Diagnosis

Scientific reports, 2020-05, Vol.10 (1), p.8346-8346, Article 8346

2020

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Vascular risk profile and changes of arterial hypertension after surgical revascularization in adult Moyamoya patients

Scientific reports, 2024-05, Vol.14 (1), p.12364-8, Article 12364

2024

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Association of predicted pathogenic mutations in mitochondrial ND genes with distant metastasis in NSCLC and colon cancer

Scientific reports, 2017-11, Vol.7 (1), p.15535-11, Article 15535

2017

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Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants

Scientific reports, 2024-05, Vol.14 (1), p.10596-10596, Article 10596

2024

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Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand

Scientific reports, 2024-04, Vol.14 (1), p.9255-9255, Article 9255

2024

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Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19

Scientific reports, 2022-03, Vol.12 (1), p.3854-3854, Article 3854

2022

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Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency

Scientific reports, 2020-03, Vol.10 (1), p.5497-5497, Article 5497

2020

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Killer cell immunoglobulin-like receptors (KIR) and human leukocyte antigen-C (HLA-C) allorecognition patterns in women with endometriosis

Scientific reports, 2020-03, Vol.10 (1), p.4897-4897, Article 4897

2020

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Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis

Scientific reports, 2022-12, Vol.12 (1), p.20709-20709, Article 20709

2022

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Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis

Scientific reports, 2023-01, Vol.13 (1), p.805-805, Article 805

2023

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Sequence variations, flanking region mutations, and allele frequency at 31 autosomal STRs in the central Indian population by next generation sequencing (NGS)

Scientific reports, 2021-12, Vol.11 (1), p.23238-23238, Article 23238

2021

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Tryptophan-enriched diet or 5-hydroxytryptophan supplementation given in a randomized controlled trial impacts social cognition on a neural and behavioral level

Scientific reports, 2021-11, Vol.11 (1), p.21637-21637, Article 21637

2021

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Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

Scientific reports, 2020-09, Vol.10 (1), p.15156-15156, Article 15156

2020

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Simulated proximity enhances perceptual and physiological responses to emotional facial expressions

Scientific reports, 2022-01, Vol.12 (1), p.109-109, Article 109

2022

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Replication of FTO Gene associated with lean mass in a Meta-Analysis of Genome-Wide Association Studies

Scientific reports, 2020-03, Vol.10 (1), p.5057-5057, Article 5057

2020

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Serotonin transporter functional polymorphisms potentially increase risk of schizophrenia separately and as a haplotype

Scientific reports, 2022-01, Vol.12 (1), p.1336-1336, Article 1336

2022

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Common genetic variation in obesity, lipid transfer genes and risk of Metabolic Syndrome: Results from IDEFICS/I.Family study and meta-analysis

Scientific reports, 2020-04, Vol.10 (1), p.7189-7189, Article 7189

2020

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Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses

Scientific reports, 2016-02, Vol.6 (1), p.19798-19798, Article 19798

2016

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The rs1256328 (ALPL) and rs12654812 (RGS14) Polymorphisms are Associated with Susceptibility to Calcium Nephrolithiasis in a Taiwanese population

Scientific reports, 2019-11, Vol.9 (1), p.17296-9, Article 17296

2019

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Depression, Neuroticism and 2D:4D Ratio: Evidence from a Large, Representative Sample

Scientific reports, 2020-07, Vol.10 (1), p.11136-11136, Article 11136

2020

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Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss

Scientific reports, 2021-11, Vol.11 (1), p.22488-11, Article 22488

2021

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T-cell receptor repertoire of cytomegalovirus-specific cytotoxic T-cells after allogeneic stem cell transplantation

Scientific reports, 2020-12, Vol.10 (1), p.22218-22218, Article 22218

2020

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An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations

Scientific reports, 2020-06, Vol.10 (1), p.10236-10236, Article 10236

2020

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Decreased grey matter volumes in unaffected mothers of individuals with autism spectrum disorder reflect the broader autism endophenotype

Scientific reports, 2021-05, Vol.11 (1), p.10001-10001, Article 10001

2021

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Germline and somatic mutations of homologous recombination-associated genes in Japanese ovarian cancer patients

Applying Machine Learning to Kinematic and Eye Movement Features of a Movement Imitation Task to Predict Autism Diagnosis

Vascular risk profile and changes of arterial hypertension after surgical revascularization in adult Moyamoya patients

Association of predicted pathogenic mutations in mitochondrial ND genes with distant metastasis in NSCLC and colon cancer

Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants

Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand

Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19

Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency

Killer cell immunoglobulin-like receptors (KIR) and human leukocyte antigen-C (HLA-C) allorecognition patterns in women with endometriosis

Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis

Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis

Sequence variations, flanking region mutations, and allele frequency at 31 autosomal STRs in the central Indian population by next generation sequencing (NGS)

Tryptophan-enriched diet or 5-hydroxytryptophan supplementation given in a randomized controlled trial impacts social cognition on a neural and behavioral level

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

Simulated proximity enhances perceptual and physiological responses to emotional facial expressions

Replication of FTO Gene associated with lean mass in a Meta-Analysis of Genome-Wide Association Studies

Serotonin transporter functional polymorphisms potentially increase risk of schizophrenia separately and as a haplotype

Common genetic variation in obesity, lipid transfer genes and risk of Metabolic Syndrome: Results from IDEFICS/I.Family study and meta-analysis

Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses

The rs1256328 (ALPL) and rs12654812 (RGS14) Polymorphisms are Associated with Susceptibility to Calcium Nephrolithiasis in a Taiwanese population

Depression, Neuroticism and 2D:4D Ratio: Evidence from a Large, Representative Sample

Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss

T-cell receptor repertoire of cytomegalovirus-specific cytotoxic T-cells after allogeneic stem cell transplantation

An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations

Decreased grey matter volumes in unaffected mothers of individuals with autism spectrum disorder reflect the broader autism endophenotype

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