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Preattentive dysfunction in bipolar disorder: A MEG study using auditory mismatch negativity

Progress in neuro-psychopharmacology & biological psychiatry, 2010-08, Vol.34 (6), p.903-912

2010

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Incidence and risk factors for postpartum hemorrhage among transvaginal deliveries at a tertiary perinatal medical facility in Japan

PloS one, 2019-01, Vol.14 (1), p.e0208873-e0208873

2019

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Impact of sleep on the microbiome of oral biofilms

PloS one, 2021-12, Vol.16 (12), p.e0259850-e0259850

2021

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Simple prediction model for homologous recombination deficiency in breast cancers in adolescents and young adults

Breast cancer research and treatment, 2020-07, Vol.182 (2), p.491-502

2020

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Trends in nutritional intake and coronary risk factors over 60 years among Japanese men in Tanushimaru

Heart and vessels, 2020-07, Vol.35 (7), p.901-908

2020

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HTLV-1 bZIP factor impairs DNA mismatch repair system

Biochemical and biophysical research communications, 2023-05, Vol.657, p.43-49

2023

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Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism

Fertility and sterility, 2014-10, Vol.102 (4), p.1130-1136.e3

2014

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The global DNA methylation surrogate LINE-1 methylation is correlated with MGMT promoter methylation and is a better prognostic factor for glioma

PloS one, 2011-08, Vol.6 (8), p.e23332-e23332

2011

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TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia

PloS one, 2014-03, Vol.9 (3), p.e91598-e91598

2014

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Clinical significance of soluble CADM1 as a novel marker for adult T-cell leukemia/lymphoma

Haematologica (Roma), 2021-02, Vol.106 (2), p.532

2021

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Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT

Prenatal diagnosis, 2019-01, Vol.39 (2), p.100-106

2019

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Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure

Journal of human genetics, 2013-05, Vol.58 (5), p.259-266

2013

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Predictors of short-term repetition of self-harm among patients admitted to an emergency room following self-harm: A retrospective one-year cohort study

Psychiatry research, 2017-12, Vol.258, p.421-426

2017

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Low-dose aspirin for primary prevention of atherosclerotic events in patients with type 2 diabetes: a randomized controlled trial

JAMA : the journal of the American Medical Association, 2008-11, Vol.300 (18), p.2134

2008

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Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations

Journal of human genetics, 2012-10, Vol.57 (10), p.654-659

2012

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Growth hormone receptor gene variant and three-dimensional mandibular morphology

The Angle orthodontist, 2017-01, Vol.87 (1), p.68-73

2017

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Alternate-day Treatment with Crizotinib for Drug-induced Esophagitis and Liver Damage in a Patient with EML4-ALK Fusion Gene-positive Lung Adenocarcinoma

Internal Medicine, 2015, Vol.54(24), pp.3185-3188

2015

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Further evidence for an association between mandibular height and the growth hormone receptor gene in a Japanese population

American journal of orthodontics and dentofacial orthopedics, 2009-10, Vol.136 (4), p.536-541

2009

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A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan

Journal of human genetics, 2016-12, Vol.61 (12), p.995-1001

2016

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A novel 8.57‐kb deletion of the upstream region of PRKAR1A in a family with Carney complex

Molecular genetics & genomic medicine, 2022-03, Vol.10 (3), p.e1884-n/a

2022

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GNE myopathy associated with congenital thrombocytopenia: A report of two siblings

Neuromuscular disorders : NMD, 2014-12, Vol.24 (12), p.1068-1072

2014

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Factors associated with health service utilization in Ulaanbaatar, Mongolia: a population-based survey

Journal of epidemiology, 2013-09, Vol.23 (5), p.320-328

2013

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An Autopsy Case of Injuries Caused by Automobile Dragging for a Distance of 3.4 km Without Thoracoabdominal Organ Injuries

The American journal of forensic medicine and pathology, 2018-12, Vol.39 (4), p.348-350

2018

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Recurrent cerebral infarction synchronous with menorrhagia caused by endometrial stromal sarcoma

Journal of the neurological sciences, 2015-11, Vol.358 (1), p.509-511

2015

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Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy

Journal of human genetics, 2016-07, Vol.61 (7), p.647-652

2016

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Preattentive dysfunction in bipolar disorder: A MEG study using auditory mismatch negativity

Incidence and risk factors for postpartum hemorrhage among transvaginal deliveries at a tertiary perinatal medical facility in Japan

Impact of sleep on the microbiome of oral biofilms

Simple prediction model for homologous recombination deficiency in breast cancers in adolescents and young adults

Trends in nutritional intake and coronary risk factors over 60 years among Japanese men in Tanushimaru

HTLV-1 bZIP factor impairs DNA mismatch repair system

Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism

The global DNA methylation surrogate LINE-1 methylation is correlated with MGMT promoter methylation and is a better prognostic factor for glioma

TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia

Clinical significance of soluble CADM1 as a novel marker for adult T-cell leukemia/lymphoma

Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT

Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure

Predictors of short-term repetition of self-harm among patients admitted to an emergency room following self-harm: A retrospective one-year cohort study

Low-dose aspirin for primary prevention of atherosclerotic events in patients with type 2 diabetes: a randomized controlled trial

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations

Growth hormone receptor gene variant and three-dimensional mandibular morphology

Alternate-day Treatment with Crizotinib for Drug-induced Esophagitis and Liver Damage in a Patient with EML4-ALK Fusion Gene-positive Lung Adenocarcinoma

Further evidence for an association between mandibular height and the growth hormone receptor gene in a Japanese population

A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan

A novel 8.57‐kb deletion of the upstream region of PRKAR1A in a family with Carney complex

GNE myopathy associated with congenital thrombocytopenia: A report of two siblings

Factors associated with health service utilization in Ulaanbaatar, Mongolia: a population-based survey

An Autopsy Case of Injuries Caused by Automobile Dragging for a Distance of 3.4 km Without Thoracoabdominal Organ Injuries

Recurrent cerebral infarction synchronous with menorrhagia caused by endometrial stromal sarcoma

Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy

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