Nakamura Y

No ORCID on file · 31 papers in corpus · active 1991-2026

Study types

  • article 8
  • case-report 3
  • other 2
  • review 2

Condition tags

  • endometriosis 14
  • adenomyosis 3
  • infertility 2
  • bowel_endometriosis 1
  • endometrioma 1
2026
Women's health (London, England) ·doi:10.1177/17455057261440253

BackgroundMenstrual-related symptoms and menstrual cycle abnormalities linked to low energy availability can have detrimental long-term health consequences. However, longitudinal data regarding the prevalence trends of these conditions in e…

2024
Mammalian genome : official journal of the International Mammalian Genome Society ·doi:10.1007/s00335-024-10063-2

Mammalian genome research has conventionally involved mice and rats as model organisms for humans. Given the recent advances in life science research, to understand complex and higher-order biological phenomena and to elucidate pathologies …

2024
BMC cancer ·doi:10.1186/s12885-024-12827-0

BackgroundEndometrial cancer is the most common gynecological malignancy; however, there is no useful blood diagnostic biomarker. This study aimed to determine the utility of tissue factor pathway inhibitor 2 (TFPI2), a biomarker of ovarian…

2021
Proceedings of the Japan Academy. Series B, Physical and biological sciences ·doi:10.2183/pjab.97.018

As we look so different, our genomic sequences vary enormously. The differences in our genome, genetic variations, have played very significant roles in medical research and have contributed to improvement of medical managements in the last…

2020
Nature genetics ·doi:10.1038/s41588-020-0640-3

The overwhelming majority of participants in current genetic studies are of European ancestry. To elucidate disease biology in the East Asian population, we conducted a genome-wide association study (GWAS) with 212,453 Japanese individuals …

2019
International journal of molecular sciences ·doi:10.3390/ijms20040899

Background: Vanin-1 is a novel acute kidney injury (AKI) biomarker that has not been clinically investigated as a biomarker for obstructive nephropathy. This study investigated the diagnostic value of vanin-1 as a biomarker for adult obstru…

case-report 2019
Medicine ·doi:10.1097/MD.0000000000015427

RATIONALE: Myotonic dystrophy is a progressive multisystem genetic heterogeneous disorder. General anesthesia with opioids increases the risk of prolonged postanesthetic respiratory recovery in myotonic dystrophy patients. PATIENT CONCERNS…

2018
Journal of epidemiology ·doi:10.2188/jea.je20170032

BackgroundGlobally, few published studies have tracked the temporal trend of dioxin levels in the human body since 2000. This study describes the annual trend of dioxin levels in human breast milk in Japanese mothers from 1998 through 2015.…

article 2018
Journal of surgical case reports ·doi:10.1093/jscr/rjy034

A 43-year-old female noticed hematochezia and lower-right abdominal pain during menstruation. Her family doctor detected a mass by computed tomography at the ileocecum. She was referred to our hospital and colonoscopy was performed. We obse…

2017
JAMA oncology ·doi:10.1001/jamaoncol.2016.5945

ImportanceThe causal direction and magnitude of the association between telomere length and incidence of cancer and non-neoplastic diseases is uncertain owing to the susceptibility of observational studies to confounding and reverse causati…

2017
Journal of epidemiology ·doi:10.1016/j.je.2016.12.003

BackgroundTo implement personalized medicine, we established a large-scale patient cohort, BioBank Japan, in 2003. BioBank Japan contains DNA, serum, and clinical information derived from approximately 200,000 patients with 47 diseases. Ser…

2017
Journal of epidemiology ·doi:10.1016/j.je.2016.12.005

BackgroundThe BioBank Japan (BBJ) Project was launched in 2003 with the aim of providing evidence for the implementation of personalized medicine by constructing a large, patient-based biobank (BBJ). This report describes the study design a…

article 2014
PloS one ·doi:10.1371/journal.pone.0115618

Although endometriosis is suspected to be a cause of premature ovarian insufficiency (POI), the mechanism(s) underlying this process have not been elucidated. Recently, androgens were shown to promote oocyte maturation and to play a role in…

other 2014
Journal of assisted reproduction and genetics ·doi:10.1007/s10815-013-0134-7

PURPOSE: We performed TaqMan genotyping assays of anti-Mullerian hormone (AMH) and anti-Mullerian hormone receptor type II (AMHRII) single nucleotide polymorphisms (SNPs) in order to investigate how their frequency and distribution affect i…

article 2014
Journal of ovarian research ·doi:10.1186/s13048-014-0100-8

BACKGROUND: Additional treatment with a gonadotropin-releasing hormone (GnRH) agonist (GnRHa) before IVF-ET (ultralong GnRHa therapy) has been reported to improve the outcome of IVF-ET in endometriosis patients. However, the mechanism of ul…

2014
Journal of assisted reproduction and genetics ·doi:10.1007/s10815-014-0323-z

PurposeTo examine the impact on development of derived embryos from smooth endoplasmic reticulum clusters (SERC) in human metaphase II (MII) oocytes.MethodsRetrospective analysis at Kyono ART Clinic. Comparison of embryological development,…

article 2014
Pathology international ·doi:10.1111/pin.12148

Adenomyosis is characterized by extension of endometrial glands and stromal cells into the myometrium. Here we proved that 'moesin' is a unique biomarker of adenomyosis. We selected two cases of adenomyosis that had been surgically resected…

2013
PloS one ·doi:10.1371/journal.pone.0080359

Ovarian clear cell adenocarcinoma (CCC) is the second most common subtype of ovarian cancer after high-grade serous adenocarcinomas. CCC tends to develop resistance to the standard platinum-based chemotherapy, and has a poor prognosis when …

2013
PloS one ·doi:10.1371/journal.pone.0063821

Age at menarche (AAM) is a complex trait involving both genetic and environmental factors. To identify the genetic factors associated with AAM, we conducted a large-scale meta-analysis of genome-wide association studies using more than 15,0…

2013
PloS one ·doi:10.1371/journal.pone.0063698

Peptic ulcer is one of the most common gastrointestinal disorders with complex etiology. Recently we conducted the genome wide association study for duodenal ulcer and identified disease susceptibility variations at two genetic loci corresp…

2013
British journal of cancer ·doi:10.1038/bjc.2013.51

BackgroundNY-ESO-1 antibodies are specifically observed in patients with NY-ESO-1-expressing tumours. We analysed whether the NY-ESO-1 humoral immune response is a useful tumour marker of gastric cancer.MethodsSera from 363 gastric cancer p…

review 2012
Nature genetics ·doi:10.1038/ng.2445

We conducted a genome-wide association meta-analysis of 4,604 endometriosis cases and 9,393 controls of Japanese and European ancestry. We show that rs12700667 on chromosome 7p15.2, previously found to associate with disease in Europeans, r…

2012
Cancer science ·doi:10.1111/j.1349-7006.2012.02224.x

Numerous studies have suggested that the different histological subtypes of ovarian carcinoma (i.e. clear cell, endometrioid, mucinous, and serous) have distinct clinical histories and characteristics; however, most studies that have aimed …

article 2010
Nature genetics ·doi:10.1038/ng.612

Although the pathogenesis of endometriosis is not well understood, genetic factors have been considered to have critical roles in its etiology. Through a genome-wide association study and a replication study using a total of 1,907 Japanese …

case-report 2009
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists ·doi:10.1097/PGP.0b013e318192924d

A rare case of a clear cell adenocarcinoma and an adenosarcoma coexisting with a heterologous rhabdomyosarcoma in an endometriotic cyst of the ovary is reported. The tumor was composed of a cystic area and a solid area arising from the cyst…