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Role of the Embodied Cognition Process in Perspective‐Taking Ability During Childhood

Child development, 2020-01, Vol.91 (1), p.214-235

2020

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Developmental changes in orienting towards faces: A behavioral and eye-tracking study

International journal of behavioral development, 2020-03, Vol.44 (2), p.157-165

2020

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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

Journal of human genetics, 2022-06, Vol.67 (6), p.363-368

2022

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Establishment of in-hospital clinical network for patients with neurofibromatosis type 1 in Nagoya University Hospital

Scientific reports, 2021-06, Vol.11 (1), p.11933-11933, Article 11933

2021

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A case report of rare ZC4H2‐associated disorders associated with three large hernias

Pediatrics international, 2020-08, Vol.62 (8), p.985-986

2020

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Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy

Brain & development (Tokyo. 1979), 2019-09, Vol.41 (8), p.721-725

2019

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Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

Scientific reports, 2022-08, Vol.12 (1), p.14589-14589, Article 14589

2022

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Prognosis of conventional vs. high-frequency ventilation for congenital diaphragmatic hernia: a retrospective cohort study

Journal of perinatology, 2021-04, Vol.41 (4), p.814-823

2021

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Factors related to survival discharge in trisomy 18: A retrospective multicenter study

American journal of medical genetics. Part A, 2019-07, Vol.179 (7), p.1253-1259

2019

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Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature

Journal of medical case reports, 2022-12, Vol.16 (1), p.481-481, Article 481

2022

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Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23

Brain & development (Tokyo. 1979), 2017-02, Vol.39 (2), p.145-153

2017

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Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome

Journal of neurodevelopmental disorders, 2016-10, Vol.8 (1), p.38-38, Article 38

2016

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The impact of noninvasive prenatal testing on clinical factors related to chromosome analysis using amniotic fluid in a tertiary perinatal center

Journal of Japan Society of Perinatal and Neonatal Medicine, 2021, Vol.57(3), pp.452-456

2021

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Factors related to home health‐care transition in trisomy 13

American journal of medical genetics. Part A, 2017-10, Vol.173 (10), p.2635-2640

2017

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Prenatal diagnosis of X‐linked recessive Lenz microphthalmia syndrome

The journal of obstetrics and gynaecology research, 2013-11, Vol.39 (11), p.1545-1547

2013

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Hydrogen-rich water ameliorates bronchopulmonary dysplasia (BPD) in newborn rats

Pediatric pulmonology, 2016-09, Vol.51 (9), p.928-935

2016

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Biallelic loss-of-function variants in the centriolar protein CCP110 leads to a ciliopathy-like phenotype

European journal of medical genetics, 2024-08, Vol.70, p.104955, Article 104955

2024

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Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm

Human genetics, 2023-10, Vol.142 (10), p.1451-1460

2023

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The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications

Human genetics, 2020-11, Vol.139 (11), p.1417-1427

2020

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Hydrogen-rich water ameliorates bronchopulmonary dysplasia (BPD) in newborn rats: Hydrogen-Rich Water for BPD

Pediatric pulmonology, 2016-09, Vol.51 (9), p.928-935

2016

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Phenotype–genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties

Human mutation, 2017-07, Vol.38 (7), p.805-815

2017

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Cognitive and linguistic abilities of a boy with PVL showing relatively higher VIQ compared to PIQ

No to hattatsu, 2015-09, Vol.47 (5), p.363

2015

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Preserved search asymmetry in the detection of fearful faces among neutral faces in individuals with Williams syndrome revealed by measurement of both manual responses and eye tracking

Journal of neurodevelopmental disorders, 2017-03, Vol.9 (1), p.8-8, Article 8

2017

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Phenotype-genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties: TANIGAWA et al

Human mutation, 2017-07, Vol.38 (7), p.805-815

2017

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Cover Image, Volume 38, Issue 7

Human mutation, 2017-07, Vol.38 (7), p.i-i

2017

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Role of the Embodied Cognition Process in Perspective‐Taking Ability During Childhood

Developmental changes in orienting towards faces: A behavioral and eye-tracking study

Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

Establishment of in-hospital clinical network for patients with neurofibromatosis type 1 in Nagoya University Hospital

A case report of rare ZC4H2‐associated disorders associated with three large hernias

Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

Prognosis of conventional vs. high-frequency ventilation for congenital diaphragmatic hernia: a retrospective cohort study

Factors related to survival discharge in trisomy 18: A retrospective multicenter study

Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature

Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23

Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome

The impact of noninvasive prenatal testing on clinical factors related to chromosome analysis using amniotic fluid in a tertiary perinatal center

Factors related to home health‐care transition in trisomy 13

Prenatal diagnosis of X‐linked recessive Lenz microphthalmia syndrome

Hydrogen-rich water ameliorates bronchopulmonary dysplasia (BPD) in newborn rats

Biallelic loss-of-function variants in the centriolar protein CCP110 leads to a ciliopathy-like phenotype

Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm

The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications

Hydrogen-rich water ameliorates bronchopulmonary dysplasia (BPD) in newborn rats: Hydrogen-Rich Water for BPD

Phenotype–genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties

Cognitive and linguistic abilities of a boy with PVL showing relatively higher VIQ compared to PIQ

Preserved search asymmetry in the detection of fearful faces among neutral faces in individuals with Williams syndrome revealed by measurement of both manual responses and eye tracking

Phenotype-genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties: TANIGAWA et al

Cover Image, Volume 38, Issue 7

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