Atsushi Watanabe

发表

A method for quantification of serum tenascin-X by nano-LC/MS/MS.

Ken-ichi Matsumoto, H. Takeshita, Kazuo Yamada, 2016, Clinica chimica acta; international journal of clinical chemistry.

RNF213 c.14576G>A Is Associated with Intracranial Internal Carotid Artery Saccular Aneurysms

T. Sekine, Y. Murai, Fumihiro Matano, 2021, Genes.

Role of RNF213 polymorphism in defining quasi-moyamoya disease and definitive moyamoya disease.

A. Morita, Y. Murai, Fumihiro Matano, 2021, Neurosurgical focus.

Institutional and Social Issues Surrounding Genetic Counselors in Japan: Current Challenges and Implications for the Global Community

Kazuto Kato, Atsushi Watanabe, Yayoi Aizawa, 2021, Frontiers in Genetics.

First report of inherited protein S deficiency caused by paternal PROS1 mosaicism

K. Kokame, Makiko Meguro-Horike, Atsushi Watanabe, 2021, Haematologica.

Association of ALPL variants with serum alkaline phosphatase and bone traits in the general Japanese population: The Nagahama Study

T. Kawaguchi, F. Matsuda, K. Higasa, 2019, Journal of Human Genetics.

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

K. Haino, F. Hirahara, H. Masuyama, 2019, Prenatal diagnosis.

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

T. Okai, T. Yoshizato, K. Haino, 2016, Journal of Human Genetics.

Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome Patients.

N. Matsumoto, N. Miyake, Ken-ichi Matsumoto, 2019, Biological & pharmaceutical bulletin.

Prevalence of Germline Variants in a Large Cohort of Japanese Patients with Pheochromocytoma and/or Paraganglioma

Katsutoshi Takahashi, T. Matsuda, H. Nishiyama, 2021, Cancers.

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan

K. Kurosawa, H. Yoshihashi, Junko Yotsumoto, 2020, Journal of Human Genetics.

Parental serum alkaline phosphatase activity as an auxiliary tool for prenatal diagnosis of hypophosphatasia

G. Nishimura, Takahiro Yamada, J. Murotsuki, 2017, Prenatal diagnosis.

Prenatal diagnosis facilitated prompt enzyme replacement therapy for prenatal benign hypophosphatasia

Y. Niida, H. Fujiwara, R. Yamazaki, 2020, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Current status of non‐invasive prenatal testing in Japan

T. Okai, K. Haino, F. Hirahara, 2017, The journal of obstetrics and gynaecology research.

Proteomic analysis for the identification of serum diagnostic markers for joint hypermobility syndrome.

Ken-ichi Matsumoto, Atsushi Watanabe, Kazumi Satoh, 2016, International journal of molecular medicine.

Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.

T. Ichinohe, Makiko Meguro-Horike, H. Asakura, 2020, Thrombosis research.

Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

Y. Fukushima, T. Morio, H. Kurahashi, 2022, Journal of Human Genetics.

Qualitative investigation of the factors that generate ambivalent feelings in women who give birth after receiving negative results from non-invasive prenatal testing

K. Haino, H. Masuyama, T. Ohba, 2019, BMC Pregnancy and Childbirth.

Fetal cell-free DNA fraction in maternal plasma for the prediction of hypertensive disorders of pregnancy.

T. Okai, K. Haino, F. Hirahara, 2018, European journal of obstetrics, gynecology, and reproductive biology.

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan

I. Imoto, F. Nomura, A. Hirasawa, 2020, Journal of Human Genetics.

Safety and efficacy of treatment with asfotase alfa in patients with hypophosphatasia: Results from a Japanese clinical trial

T. Ogata, K. Ozono, S. Okada, 2017, Clinical endocrinology.

Japanese nationwide survey of hypophosphatasia reveals prominent differences in genetic and dental findings between odonto and non-odonto types

T. Taketani, K. Ozono, T. Kubota, 2019, PloS one.

Marked motor function improvement in a 32-year-old woman with childhood-onset hypophosphatasia by asfotase alfa therapy: Evaluation based on standardized testing batteries used in Duchenne muscular dystrophy clinical trials

T. Akiyama, Kyoko Takano, T. Kosho, 2020, Molecular genetics and metabolism reports.

Ring finger protein 213 c.14576G>A mutation is not involved in internal carotid artery and middle cerebral artery dysplasia

T. Sekine, Y. Murai, Fumihiro Matano, 2021, Scientific Reports.

Pancreatic developmental defect evaluated by celiac artery angiography in a patient with MODY5

Kayoko Saito, N. Iwasaki, M. Ogata, 2016, Human Genome Variation.

A new mouse model of Ehlers-Danlos syndrome generated using CRISPR/Cas9-mediated genomic editing

Guillermo Posadas-Herrera, Y. Inoue, Takayoshi Inoue, 2021, Disease models & mechanisms.

Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency

Makiko Meguro-Horike, Eiichi Sato, Atsushi Watanabe, 2022, International Journal of Hematology.