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Masayo Kagami

National Research Institute for Child Health and Development

33H指数
189论文数
4.6K被引数
收录论文 63
发表时间
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Author Correction: Diagnosis and management of Silver–Russell syndrome: second international consensus statement作者更正：Silver–Russell综合征的诊断与管理：第二份国际共识声明
errNature Reviews Endocrinology
IF40
err2026-09-30
err0
PREAI
errEmma Wakeling; Justin H. Davies; Eloïse Giabicani; Susan M. O’Connell; Madeleine D. Harbison; Amélie Perriere; Jennifer B. Salem; Matthias Begemann; Gerhard Binder; Frédéric Brioude; Dayna Morris-Carney; Jovanna Dahlgren; Bea Dickinson; Bruno Donadille; Beatrice Dubern; Katja Eggermann; Gabriella Gazdagh; Karen Grønskov; Anita C. Hokken Koelega; Youn Hee Jee; Alicia Jurians; Masayo Kagami; Satomi Koyama; Emilie Kulak; Asmahane Ladjouze; Paola Lombardi; Mohamad Maghnie; Louise McClelland; Veronica Mericq; Giuseppa Patti; Klaudia Raabe; Andrea Riccio; Silvia Russo; Helen L. Storr; I. Karen Temple; Zeynep Tümer; Thomas Eggermann; Deborah J. G. Mackay; Irene Netchine
err分享
err收藏
Diagnosis and management of Silver–Russell syndrome: second international consensus statement银- Russell 综合征的诊断与管理：第二届国际共识声明
errNature Reviews Endocrinology
IF40
err2026-09-23
err0
PREAI
errEmma Wakeling; Justin H. Davies; Eloïse Giabicani; Susan M. O’Connell; Madeleine D. Harbison; Amélie Perriere; Jennifer B. Salem; Matthias Begemann; Gerhard Binder; Frédéric Brioude; Dayna Morris-Carney; Jovanna Dahlgren; Bea Dickinson; Bruno Donadille; Beatrice Dubern; Katja Eggermann; Gabriella Gazdagh; Karen Grønskov; Anita C. Hokken Koelega; Youn Hee Jee; Alicia Jurians; Masayo Kagami; Satomi Koyama; Emilie Kulak; Asmahane Ladjouze; Paola Lombardi; Mohamad Maghnie; Louise McClelland; Veronica Mericq; Guiseppa Patti; Klaudia Raabe; Andrea Riccio; Silvia Russo; Helen L. Storr; I. Karen Temple; Zeynep Tümer; Thomas Eggermann; Deborah J. G. Mackay; Irene Netchine
err分享
err收藏
A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genes一种综合的长读长测序系统，用于评估差异甲基化区域和印记障碍相关基因的DNA甲基化
errGenome Medicine
IF11.2
err2025-11-19
err0
errOAAI
errTatsuki Urakawa; Atsushi Hattori; Yasuko Ogiwara; Hayate Masubuchi; Mizuho Igarashi; Sayuri Nakamura; Kaori Hara-Isono; Keisuke Ishiwata; Hiroko Ogata-Kawata; Hiromi Kamura; Yoko Kuroki; Kazuhiko Nakabayashi; Maki Fukami; Masayo Kagami
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Prenatal suspicion of Kagami-Ogata syndrome based on Robertsonian translocation (14;22)基于罗伯逊易位（14;22）的Kagami-Ogata综合征产前怀疑
errPEDIATRICS INTERNATIONAL
IF0.9
err2025-11-17
err0
PREAI
errOdagiri, Shizuka; Tamura, Kentaro; Nagaoka, Mitsuhide; Sasamoto, Kyota; Arai, Eri N.; Kagami, Masayo; Yoshida, Taketoshi
err分享
err收藏
Investigation of methylation profiles in Silver–Russell syndrome to explore episignatures对Silver–Russell综合征中甲基化谱的研究，以探索表观遗传签名。
errClinical Epigenetics
IF4.4
err2025-11-09
err0
errOAAI
errKaori Hara-Isono; Takanobu Inoue; Akie Nakamura; Tomoko Fuke; Kazuki Yamazawa; Keiko Matsubara; Maki Fukami; Tsutomu Ogata; Tomoko Kawai; Masayo Kagami
err分享
err收藏
Chromosomal and hormonal factors involved in human sexual dimorphism涉及人类性别二态性的染色体和激素因素
errENDOCRINE JOURNAL
IF2.1
err2025-11-01
err0
PREAI
errFukami, Maki; Okamura, Kohji; Sasaki, Shoko; Kagami, Masayo; Dateki, Sumito
err分享
err收藏
Association between imprinting disorders and assisted reproductive technologies
errEPIGENOMICS
IF2.6
err2025-03-01
err0
errOAAI
errKagami, Masayo; Hara-Isono, Kaori; Sasaki, Aiko; Amita, Mitsuyoshi
err分享
err收藏
An unstable variant of GAP43 leads to neurodevelopmental deficiency
errSCIENTIFIC REPORTS
IF3.9
err2024-12-30
err0
errOAAI
errNoda, Mariko; Matsumoto, Ayumi; Ito, Hidenori; Kagami, Masayo; Tajima, Toshihiro; Matsumura, Takayoshi; Yamagata, Takanori; Nagata, Koh-ichi
err分享
err收藏
Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese PatientsTemple综合征: 60例经遗传证实的日本患者的综合临床研究
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2024-12-18
err0
errOAAI
errOgawa, Tomoe; Narusawa, Hiromune; Nagasaki, Keisuke; Kosaki, Rika; Naiki, Yasuhiro; Aramaki, Michihiko; Matsubara, Keiko; Nakamura, Akie; Fukami, Maki; Ogata, Tsutomu; Kagami, Masayo
err分享
err收藏
Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
errCLINICAL EPIGENETICS
IF4.4
err2024-10-05
err0
errOAAI
errUrakawa, Tatsuki; Soejima, Hidenobu; Yamoto, Kaori; Hara-Isono, Kaori; Nakamura, Akie; Kawashima, Sayaka; Narusawa, Hiromune; Kosaki, Rika; Nishimura, Yutaka; Yamazawa, Kazuki; Hattori, Tetsuo; Muramatsu, Yukako; Inoue, Takanobu; Matsubara, Keiko; Fukami, Maki; Saitoh, Shinji; Ogata, Tsutomu; Kagami, Masayo
err分享
err收藏
Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 Patients
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2024-09-26
err2
errOAAI
errNarusawa, Hiromune; Ogawa, Tomoe; Yagasaki, Hideaki; Nagasaki, Keisuke; Urakawa, Tatsuki; Saito, Tomohiro; Soneda, Shun; Kinjo, Saori; Sano, Shinichiro; Mamada, Mitsukazu; Terashita, Shintaro; Dateki, Sumito; Narumi, Satoshi; Naiki, Yasuhiro; Horikawa, Reiko; Ogata, Tsutomu; Fukami, Maki; Kagami, Masayo
err分享
err收藏
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
errCLINICAL EPIGENETICS
IF4.4
err2024-08-01
err1
errOAAI
errMackay, Deborah J. G.; Gazdagh, Gabriella; Monk, David; Brioude, Frederic; Giabicani, Eloise; Krzyzewska, Izabela M.; Kalish, Jennifer M.; Maas, Saskia M.; Kagami, Masayo; Beygo, Jasmin; Kahre, Tiina; Tenorio-Castano, Jair; Ambrozaityte, Laima; Burnyte, Birute; Cerrato, Flavia; Davies, Justin H.; Ferrero, Giovanni Battista; Fjodorova, Olga; Manero-Azua, Africa; Pereda, Arrate; Russo, Silvia; Tannorella, Pierpaola; Temple, Karen I.; Ounap, Katrin; Riccio, Andrea; de Nanclares, Guiomar Perez; Maher, Eamonn R.; Lapunzina, Pablo; Netchine, Irene; Eggermann, Thomas; Bliek, Jet; Tumer, Zeynep
err分享
err收藏
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review
errCLINICAL EPIGENETICS
IF4.4
err2024-06-05
err0
errOAAI
errYamoto, Kaori; Saitsu, Hirotomo; Ohkubo, Yumiko; Kagami, Masayo; Ogata, Tsutomu
err分享
err收藏
Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes
errSCIENTIFIC REPORTS
IF3.9
err2024-04-05
err1
errOAAI
errHattori, Atsushi; Seki, Atsuhito; Inaba, Naoto; Nakabayashi, Kazuhiko; Takeda, Kazue; Tatsusmi, Kuniko; Naiki, Yasuhiro; Nakamura, Akie; Ishiwata, Keisuke; Matsumoto, Kenji; Nasu, Michiyo; Okamura, Kohji; Michigami, Toshimi; Katoh-Fukui, Yuko; Umezawa, Akihiro; Ogata, Tsutomu; Kagami, Masayo; Fukami, Maki
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err收藏
(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B
errEUROPEAN JOURNAL OF ENDOCRINOLOGY
IF5.2
err2023-12-01
err0
PREAI
errUrakawa, Tatsuki; Sano, Shinichiro; Kawashima, Sayaka; Nakamura, Akie; Shima, Hirohito; Ohta, Motoki; Yamada, Yuki; Nishida, Ai; Narusawa, Hiromune; Ohtsu, Yoshiaki; Matsubara, Keiko; Dateki, Sumito; Maruo, Yoshihiro; Fukami, Maki; Ogata, Tsutomu; Kagami, Masayo
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err收藏
Imprinting disorders
errNATURE REVIEWS DISEASE PRIMERS
IF60.6
err2023-06-29
err22
PREAI
errEggermann, Thomas; Monk, David; de Nanclares, Guiomar Perez; Kagami, Masayo; Giabicani, Eloise; Riccio, Andrea; Tumer, Zeynep; Kalish, Jennifer M.; Tauber, Maithe; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R.; Begemann, Matthias; Elbracht, Miriam
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Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes
errCLINICAL EPIGENETICS
IF4.4
err2023-05-06
err2
errOAAI
errHara-Isono, Kaori; Matsubara, Keiko; Nakamura, Akie; Sano, Shinichiro; Inoue, Takanobu; Kawashima, Sayaka; Fuke, Tomoko; Yamazawa, Kazuki; Fukami, Maki; Ogata, Tsutomu; Kagami, Masayo
err分享
err收藏
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
errCLINICAL EPIGENETICS
IF4.4
err2022-11-07
err20
errOAAI
errMackay, Deborah; Bliek, Jet; Kagami, Masayo; Tenorio-Castano, Jair; Pereda, Arrate; Brioude, Frederic; Netchine, Irene; Papingi, Dzhoy; de Franco, Elisa; Lever, Margaret; Sillibourne, Julie; Lombardi, Paola; Gaston, Veronique; Tauber, Maithe; Diene, Gwenaelle; Bieth, Eric; Fernandez, Luis; Nevado, Julian; Tumer, Zeynep; Riccio, Andrea; Maher, Eamonn R.; Beygo, Jasmin; Tannorella, Pierpaola; Russo, Silvia; de Nanclares, Guiomar Perez; Temple, I. Karen; Ogata, Tsutomu; Lapunzina, Pablo; Eggermann, Thomas
err分享
err收藏
CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2022-07-29
err0
PREAI
errHara-Isono, Kaori; Yamazawa, Kazuki; Tanaka, Satsuki; Nishi, Eriko; Fukami, Maki; Kagami, Masayo
err分享
err收藏
Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus
errJOURNAL OF BONE AND MINERAL RESEARCH
IF5.9
err2022-07-20
err6
PREAI
errKawashima, Sayaka; Yuno, Akiko; Sano, Shinichiro; Nakamura, Akie; Ishiwata, Keisuke; Kawasaki, Tomoyuki; Hosomichi, Kazuyoshi; Nakabayashi, Kazuhiko; Akustu, Hidenori; Saitsu, Hirotomo; Fukami, Maki; Usui, Takeshi; Ogata, Tsutomu; Kagami, Masayo
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研究方向

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