Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

K. Matsuoka · SciRah

Researcher profile · Semantic Scholar

K. Matsuoka

Share profile

K. Matsuoka — researcher profile on SciRah

h-index: 24
Works: 122
Citations: 2,733

Most-cited papers

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
M. Kagami, Y. Sekita, G. Nishimura, Masahito Irie +20 more
2008Nature Genetics303 citations
Semantic Scholar
The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers
M. Kagami, M. O'Sullivan, A. Green, Y. Watabe +8 more
2010PLoS Genetics217 citations Open access
Semantic Scholar
Clinical Features and Prognosis of Generalized Lymphatic Anomaly, Kaposiform Lymphangiomatosis, and Gorham–Stout Disease
M. Ozeki, Akihiro Fujino, K. Matsuoka, S. Nosaka +2 more
2016Pediatric Blood & Cancer124 citations
Semantic Scholar
Rituximab for refractory focal segmental glomerulosclerosis
Makiko Nakayama, Koichi Kamei, K. Nozu, K. Matsuoka +3 more
2008Pediatric nephrology (Berlin, West)102 citations
Semantic Scholar
Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami–Ogata syndrome)
M. Kagami, K. Kurosawa, O. Miyazaki, F. Ishino +2 more
2015European Journal of Human Genetics98 citations Open access
Semantic Scholar
Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosis
M. Ozeki, Y. Aoki, Akifumi Nozawa, Shiho Yasue +8 more
2019Orphanet Journal of Rare Diseases64 citations Open access
Semantic Scholar
Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas
K. Yamazawa, M. Kagami, T. Nagai, T. Kondoh +11 more
2008Journal of molecular medicine64 citations
Semantic Scholar
Atypical Pneumocystis jiroveci pneumonia with multiple nodular granulomas after rituximab for refractory nephrotic syndrome
Mai Sato, S. Ito, M. Ogura, Koichi Kamei +4 more
2012Pediatric nephrology (Berlin, West)52 citations
Semantic Scholar
Efficacy and safety of sirolimus treatment for intractable lymphatic anomalies: A study protocol for an open-label, single-arm, multicenter, prospective study (SILA)
M. Ozeki, R. Asada, A. Saito, H. Hashimoto +17 more
2019Regenerative Therapy41 citations Open access
Semantic Scholar
Paternal uniparental disomy 14 and related disorders
M. Kagami, K. Matsuoka, T. Nagai, Michiko Yamanaka +9 more
2012Epigenetics39 citations Open access
Semantic Scholar
Sacrococcygeal yolk sac tumor developing after teratoma: a clinicopathological study of pediatric sacrococcygeal germ cell tumors and a proposal of the pathogenesis of sacrococcygeal yolk sac tumors.
Mariko Yoshida, K. Matsuoka, A. Nakazawa, Makiko Yoshida +16 more
2013Journal of Pediatric Surgery38 citations
Semantic Scholar
Pathological characterization of pachydermia in pachydermoperiostosis
K. Tanese, H. Niizeki, A. Seki, A. Otsuka +12 more
2015Journal of dermatology (Print)33 citations Open access
Semantic Scholar
Analysis of mTOR pathway expression in lymphatic malformation and related diseases
Y. Hori, M. Ozeki, Katsutoshi Hirose, K. Matsuoka +6 more
2020Pathology international (Print)32 citations
Semantic Scholar
The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.
H. Niizeki, Aiko Shiohama, T. Sasaki, A. Seki +15 more
2014Journal of dermatological science (Amsterdam)32 citations
Semantic Scholar
Gorham–Stout Disease of the Skull Base With Hearing Loss: Dramatic Recovery and Antiangiogenic Therapy
Akifumi Nozawa, M. Ozeki, Bunya Kuze, T. Asano +2 more
2016Pediatric Blood & Cancer30 citations
Semantic Scholar
Prognostic significance of circulating tumor cells and bone marrow micrometastasis in advanced neuroblastoma.
T. Kuroda, N. Morikawa, K. Matsuoka, Akihiro Fujino +5 more
2008Journal of Pediatric Surgery29 citations
Semantic Scholar
Japanese clinical practice guidelines for vascular anomalies 2017
H. Mimura, S. Akita, Akihiro Fujino, M. Jinnin +43 more
2020Pediatrics International28 citations Open access
Semantic Scholar
Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd(14)pat-like phenotypes
K. Yamazawa, K. Nakabayashi, K. Matsuoka, Keiko Masubara +3 more
2011Journal of Human Genetics28 citations
Semantic Scholar
Apparent diffusion coefficient of intracranial germ cell tumors
Hideki Ogiwara, Y. Tsutsumi, K. Matsuoka, C. Kiyotani +2 more
2015Journal of Neuro-Oncology27 citations
Semantic Scholar
Clinical Features of Congenital Cystic Lung Diseases: A Report on a Nationwide Multicenter Study in Japan
T. Kuroda, E. Nishijima, K. Maeda, Y. Fuchimoto +5 more
2015European journal of pediatric surgery25 citations
Semantic Scholar
Successful treatment of collapsing focal segmental glomerulosclerosis with a combination of rituximab, steroids and ciclosporin
H. Kaito, Koichi Kamei, Eriko Kikuchi, M. Ogura +4 more
2010Pediatric nephrology (Berlin, West)24 citations
Semantic Scholar
Japanese clinical practice guidelines for vascular anomalies 2017
H. Mimura, S. Akita, Akihiro Fujino, M. Jinnin +43 more
2020Japanese Journal of Radiology23 citations Open access
Semantic Scholar
Congenital cutaneous fistula at the sternoclavicular joint - Not a dermoid fistula but the remnant of the fourth branchial (pharyngeal) cleft ?
Michinobu Ohno, Y. Kanamori, Kotaro Tomonaga, T. Yamashita +5 more
2015International Journal of Pediatric Otorhinolaryngology23 citations
Semantic Scholar
Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2
Y. Yamaguchi, Chiharu Tayama, J. Tomikawa, R. Akaishi +8 more
2019Clinical Epigenetics22 citations Open access
Semantic Scholar
Use of serial assessment of disease severity and liver biopsy for indication for liver transplantation in pediatric Epstein‐Barr virus–induced fulminant hepatic failure
A. Nakazawa, Natsuko Nakano, A. Fukuda, S. Sakamoto +4 more
2015Liver transplantation22 citations
Semantic Scholar
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR
M. Kagami, Atsuhiro Yanagisawa, Miyuki Ota, K. Matsuoka +6 more
2019Clinical Epigenetics21 citations Open access
Semantic Scholar
Significant improvement in Fabry disease podocytopathy after 3 years of treatment with agalsidase beta
S. Ito, M. Ogura, Koichi Kamei, K. Matsuoka +1 more
2016Pediatric nephrology (Berlin, West)21 citations
Semantic Scholar
A novel association of duodenal atresia, malrotation, segmental dilatation of the colon, and anorectal malformation
N. Morikawa, T. Kuroda, T. Honna, Y. Kitano +7 more
2009Pediatric surgery international (Print)21 citations
Semantic Scholar
Neoadjuvant chemotherapy for brain tumors in infants and young children.
J. Iwama, Hideki Ogiwara, C. Kiyotani, K. Terashima +3 more
2015Journal of Neurosurgery: Pediatrics19 citations Open access
Semantic Scholar
Twin Anemia-Polycythemia Sequence after Laser Surgery for Twin-Twin Transfusion Syndrome and Maternal Morbidity
K. Taniguchi, M. Sumie, R. Sugibayashi, S. Wada +2 more
2015Fetal Diagnosis and Therapy18 citations
Semantic Scholar
Long survival of congenital alveolar capillary dysplasia patient with NO inhalation and epoprostenol: Effect of sildenafil, beraprost and bosentan
Y. Kodama, Ka-Tsuo Tao, F. Ishida, Tadashi Kawakami +6 more
2012Pediatrics International18 citations
Semantic Scholar
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole
Yuki Ito, K. Maehara, E. Kaneki, K. Matsuoka +15 more
2015Gynecologic and Obstetric Investigation17 citations
Semantic Scholar
Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation
K. Iijima, K. Nozu, Koichi Kamei, Makiko Nakayama +6 more
2010Pediatric nephrology (Berlin, West)17 citations Open access
Semantic Scholar
Central venous catheter infection-related glomerulonephritis under long-term parenteral nutrition: a report of two cases
M. Okada, Mai Sato, M. Ogura, Koichi Kamei +2 more
2016BMC Research Notes16 citations Open access
Semantic Scholar
Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis
C. Nagano, S. Hara, N. Yoshikawa, A. Takeda +24 more
2022Kidney36015 citations Open access
Semantic Scholar
SRY-Positive 46, XX Testicular Disorder of Sexual Development With Leydig Cell Tumor
A. Osaka, H. Ide, K. Matsuoka, T. Iwahata +4 more
2020American Journal of Men's Health15 citations Open access
Semantic Scholar
Placenta accreta following uterine artery embolization.
Hironori Takahashi, S. Hayashi, K. Matsuoka, M. Kitagawa
2010Taiwanese Journal of Obstetrics & Gynecology15 citations Open access
Semantic Scholar
Japanese Clinical Practice Guidelines for Vascular Anomalies 2017
H. Mimura, S. Akita, Akihiro Fujino, M. Jinnin +43 more
2020Journal of dermatology (Print)14 citations Open access
Semantic Scholar
Indications for tracheostomy in children with head and neck lymphatic malformation: analysis of a nationwide survey in Japan
S. Ueno, Akihiro Fujino, Y. Morikawa, T. Iwanaka +5 more
2019Surgery today (Print)14 citations
Semantic Scholar
Treatment of mediastinal lymphatic malformation in children: an analysis of a nationwide survey in Japan
S. Ueno, Akihiro Fujino, Y. Morikawa, T. Iwanaka +5 more
2018Surgery today (Print)14 citations
Semantic Scholar
Chronic histiocytic intervillositis in three consecutive pregnancies in a single patient: Differing clinical results and pathology according to treatment used
N. Ozawa, K. Yamaguchi, Megumi Shibata, R. Sugibayashi +3 more
2017The journal of obstetrics and gynaecology research14 citations
Semantic Scholar
Thrombotic microangiopathy due to multiple autoantibodies related to antiphospholipid syndrome
Shunsuke Noda, M. Ogura, Akiko Tsutsumi, T. Udagawa +5 more
2012Pediatric nephrology (Berlin, West)14 citations
Semantic Scholar
Endoscopic Fetal Urethrotomy for Anterior Urethral Valves: A Preliminary Report
H. Sago, S. Hayashi, T. Chiba, K. Ueoka +3 more
2008Fetal Diagnosis and Therapy14 citations
Semantic Scholar
Focal Segmental Glomerulosclerosis in Patients With Complete Deletion of One WT1 Allele
K. Iijima, Tomonosuke Someya, S. Ito, K. Nozu +6 more
2012Pediatrics13 citations
Semantic Scholar
Sequential liver–kidney transplantation in a boy with congenital hepatic fibrosis and nephronophthisis from a living donor
T. Udagawa, Koichi Kamei, M. Ogura, Akiko Tsutsumi +12 more
2012Pediatric Transplantation13 citations
Semantic Scholar
Vincristine, actinomycin D, cyclophosphamide chemotherapy resolves Kasabach–Merritt syndrome resistant to conventional therapies
Y. Fuchimoto, N. Morikawa, T. Kuroda, S. Hirobe +4 more
2012Pediatrics International13 citations
Semantic Scholar
Vaginal yolk sac (endodermal sinus) tumors in infancy presenting persistent vaginal bleeding
N. Watanabe, H. Okita, K. Matsuoka, C. Kiyotani +3 more
2010The journal of obstetrics and gynaecology research12 citations
Semantic Scholar
Clinical and histological features in pediatric and adolescent/young adult patients with renal disease: a cross-sectional analysis of the Japan Renal Biopsy Registry (J-RBR)
Maki Urushihara, Hiroshi Sato, Akira Shimizu, H. Sugiyama +14 more
2021Clinical and Experimental Nephrology11 citations
Semantic Scholar
A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease
Ken Saida, Koichi Kamei, N. Morisada, M. Ogura +5 more
2019CEN Case Reports11 citations Open access
Semantic Scholar
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.
J. M. Rumbajan, Y. Yamaguchi, K. Nakabayashi, K. Higashimoto +11 more
2016Gene11 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Koichi Kamei×11
Invite
Koichi Kamei — researcher profile on SciRah
M. Ozeki×10
Invite
M. Ozeki — researcher profile on SciRah
T. Kuroda×10
Invite
T. Kuroda — researcher profile on SciRah
S. Ito×10
Invite
S. Ito — researcher profile on SciRah

×8

Invite

T. Ogata — researcher profile on SciRah

Akihiro Fujino×8

Invite

Akihiro Fujino — researcher profile on SciRah

Invite

S. Nosaka — researcher profile on SciRah

Invite

M. Ogura — researcher profile on SciRah

Invite

M. Kagami — researcher profile on SciRah

Invite

K. Iijima — researcher profile on SciRah

Invite

S. Ueno — researcher profile on SciRah

Yoshiaki Kinoshita×6

Invite

Yoshiaki Kinoshita — researcher profile on SciRah