About: Hiroyuki Mishima

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researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Hiroyuki Mishima (en) Hiroyuki Mishima (es) Hiroyuki Mishima (nl) Hiroyuki Mishima (sl) Hiroyuki Mishima (ast)
skos:prefLabel	Hiroyuki Mishima (en) Hiroyuki Mishima (es) Hiroyuki Mishima (nl) Hiroyuki Mishima (sl) Hiroyuki Mishima (ast)
name	Hiroyuki Mishima (en) Hiroyuki Mishima (es) Hiroyuki Mishima (nl) Hiroyuki Mishima (sl) Hiroyuki Mishima (ast)
LinkedIn personal profile ID	wds:Q42237537-0CD9F8DB-75FC-49CB-8360-C736AC871C57
LinkedIn personal profile ID	hiroyuki-mishima
Scopus author ID	wds:Q42237537-B9F5B377-AA0D-422F-8688-3EDF57EB682F
Scopus author ID	25935713800
given name	wds:Q42237537-23EFE506-61D5-469F-AF40-5ADD85C68FC5
given name	Hiroyuki
instance of	wds:Q42237537-BA6407B2-D4AE-498A-87CB-9182D69C0EA4
instance of	Homo sapiens
occupation	wds:Q42237537-7161B7E8-4853-495E-9F31-5A83CEFF515B
employer	wds:Q42237537-510BB5E0-72C3-4171-8023-05C5B6397E09
X username	wds:Q42237537-F612C851-1DC7-4D42-AF25-CE3CB40FE741
Facebook username	wds:Q42237537-EE22189F-783E-4495-A39B-84EAC9F645E0
GitHub username	wds:Q42237537-E1DDE4ED-5978-4263-86EB-B4A473F181A2
sex or gender	wds:Q42237537-2251AF6E-EB1B-4542-92BA-56B555336243
date of birth	wds:Q42237537-5B5FB6AC-CEE3-4DF2-9991-CB0C8FE2190E
educated at	wds:Q42237537-5F003C2B-AE2B-4D7F-BCEF-71CC45137D19
family name	wds:Q42237537-0937DB89-F716-4E32-9C86-68CE8C2A4E4B
occupation	researcher
employer	Nagasaki University
X username	mishima_eng
Facebook username	hiroyuki.mishima.718
GitHub username	misshie
sex or gender	male
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
educated at	Hokkaido University
family name	Mishima
ORCID iD	wds:Q42237537-CC1EEA6F-5C31-41DF-9F24-1ED12A537673
Dimensions author ID	wds:Q42237537-2776E453-DEB3-4E96-947D-A43C51AD670A
ORCID iD	https://orcid.org/0000-0001-5050-2509
ORCID iD	0000-0001-5050-2509
Dimensions author ID	0643355356.48
ResearcherID	wds:Q42237537-7631C175-AF20-4F70-890C-C03F69045A3A
Publons author ID	wds:Q42237537-A060A0CE-60D8-4F2C-AAFC-0F7E31894604
ResearcherID	Y-2638-2019
Publons author ID	3111527
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42237537
is author of	Identification of novel schizophrenia loci by homozygosity mapping using DNA microarray analysis Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome. Biogem: an effective tool-based approach for scaling up open source software development in bioinformatics Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair Application of the Linux cluster for exhaustive window haplotype analysis using the FBAT and Unphased programs Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populations. Identification of endometrioid endometrial carcinoma-associated microRNAs in tissue and plasma. Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancer Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease Genome-wide association study of HPV-associated cervical cancer in Japanese women A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese population Identification of a variant-associated with early-onset diabetes in the intron of INS gene with exome sequencing Clinical applications of analysis of plasma circulating complete hydatidiform mole pregnancy-associated miRNAs in gestational trophoblastic neoplasia: a preliminary investigation Germline mutations causing familial lung cancer Ultra-sensitive droplet digital PCR for detecting a low-prevalence somatic GNAQ mutation in Sturge-Weber syndrome Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities Genome analysis of myelodysplastic syndromes among atomic bomb survivors in Nagasaki Heterogenous nature of gene expression patterns in BRAF-like papillary thyroid carcinomas with BRAFV600E Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population KAT6B-related disorder in a patient with a novel frameshift variant (c.3925dup) Metabolic autopsy with next generation sequencing in sudden unexpected death in infancy: Postmortem diagnosis of fatty acid oxidation disorders Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome. Predominantly placenta-expressed mRNAs in maternal plasma as predictive markers for twin-twin transfusion syndrome Detection of de novo single nucleotide variants in offspring of atomic-bomb survivors close to the hypocenter by whole-genome sequencing. Circulating levels of maternal plasma cell-free pregnancy-associated placenta-specific microRNAs are associated with placental weight. Pregnancy-associated microRNAs in plasma as potential molecular markers of ectopic pregnancy. Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan Targeting Adaptive IRE1α Signaling and PLK2 in Multiple Myeloma: Possible Anti-Tumor Mechanisms of KIRA8 and Nilotinib Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction. Single human papillomavirus 16 or 52 infection and later cytological findings in Japanese women with NILM or ASC-US. A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency BioHackathon 2015: Semantics of data for life sciences and reproducible research

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