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K. Nakabayashi · SciRah

Researcher profile · Semantic Scholar

K. Nakabayashi

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K. Nakabayashi — researcher profile on SciRah

h-index: 49
Works: 295
Citations: 8,962

Most-cited papers

Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development
Masaki Yagi, Mio Kabata, A. Tanaka, Tomoyo Ukai +7 more
2020Nature Communications78 citations Open access
Semantic Scholar
Clonal expansion of second-hit cells with somatic recombinations or C>T transitions form porokeratosis in MVD or MVK mutant heterozygotes.
A. Kubo, T. Sasaki, Hisato Suzuki, A. Shiohama +12 more
2019Journal of Investigative Dermatology62 citations Open access
Semantic Scholar
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients
T. Inoue, Akie Nakamura, Megumi Iwahashi-Odano, Kanako Tanase-Nakao +16 more
2020Clinical Epigenetics39 citations Open access
Semantic Scholar
ZFAT binds to centromeres to control noncoding RNA transcription through the KAT2B–H4K8ac–BRD4 axis
S. Ishikura, K. Nakabayashi, Masayoshi Nagai, T. Tsunoda +1 more
2020Nucleic Acids Research27 citations Open access
Semantic Scholar
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance
M. Kagami, Kaori Hara-Isono, K. Matsubara, K. Nakabayashi +6 more
2021Clinical Epigenetics25 citations Open access
Semantic Scholar
Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis.
M. Miyado, M. Fukami, S. Takada, Miho Terao +11 more
2019Journal of the American Society of Nephrology23 citations Open access
Semantic Scholar
Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data
Kohei Kashima, T. Kawai, Riki Nishimura, Yuh Shiwa +19 more
2021Scientific Reports22 citations Open access
Semantic Scholar
Development of Human Gut Organoids With Resident Tissue Macrophages as a Model of Intestinal Immune Responses
S. Tsuruta, Tomoyuki Kawasaki, M. Machida, K. Iwatsuki +7 more
2022Cellular and Molecular Gastroenterology and Hepatology21 citations Open access
Semantic Scholar
Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome.
Yoko Narumi-Kishimoto, Naomi Araki, O. Migita, T. Kawai +7 more
2019European Journal of Medical Genetics21 citations Open access
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
Gene-specific somatic epigenetic mosaicism of FDFT1 underlies a non-hereditary localized form of porokeratosis.
S. Saito, Y. Saito, S. Sato, S. Aoki +15 more
2024American Journal of Human Genetics20 citations
Semantic Scholar
Reduced Representation Bisulfite Sequencing (RRBS).
K. Nakabayashi, M. Yamamura, Keita Haseagawa, K. Hata
2023Methods in molecular biology19 citations
Semantic Scholar
Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation
Harumi Fujita, T. Sasaki, Tatsuo Miyamoto, Silvia Natsuko Akutsu +10 more
2020Aging Cell18 citations Open access
Semantic Scholar
Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome
Kaori Hara-Isono, K. Matsubara, T. Fuke, K. Yamazawa +8 more
2020Clinical Epigenetics17 citations Open access
Semantic Scholar
Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency
Kenichi Kinjo, Keisuke Nagasaki, K. Muroya, E. Suzuki +10 more
2020Scientific Reports16 citations Open access
Semantic Scholar
Minimal residual disease detection by mutation-specific droplet digital PCR for leukemia/lymphoma
Ryota Shirai, T. Osumi, Dai Keino, K. Nakabayashi +15 more
2023International journal of hematology15 citations Open access
Semantic Scholar
Gene expression signatures associated with chronic endometritis revealed by RNA sequencing
K. Oshina, K. Kuroda, K. Nakabayashi, J. Tomikawa +4 more
2023Frontiers in Medicine15 citations Open access
Semantic Scholar
Direct platelet adhesion potentiates group 2 innate lymphoid cell functions
Keisuke Orimo, M. Tamari, Tomohiro Takeda, T. Kubo +23 more
2021Allergy. European Journal of Allergy and Clinical Immunology14 citations
Semantic Scholar
Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice
K. Nohara, K. Nakabayashi, Kazuyuki Okamura, Takehiro Suzuki +2 more
2020Epigenetics & Chromatin14 citations Open access
Semantic Scholar
Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles.
Ken Takahashi, O. Migita, Aiko Sasaki, Michiko Nasu +8 more
2019Clinical Chemistry14 citations
Semantic Scholar
Development of sexual dimorphism of skeletal muscles through the adrenal cortex, caused by androgen-induced global gene suppression.
Fumiya Takahashi, Takashi Baba, Antonius Christianto, Shogo Yanai +9 more
2024Cell Reports13 citations Open access
Semantic Scholar
Characteristics of genetic alterations of peripheral T‐cell lymphoma in childhood including identification of novel fusion genes: the Japan Children’s Cancer Group (JCCG)
K. Ohki, N. Kiyokawa, S. Watanabe, H. Iwafuchi +14 more
2021British Journal of Haematology12 citations Open access
Semantic Scholar
Quantitative assessment of copy number alterations by liquid biopsy for neuroblastoma
Ryota Shirai, T. Osumi, A. Sato-Otsubo, K. Nakabayashi +19 more
2022Genes, Chromosomes and Cancer11 citations
Semantic Scholar
Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia
Saori Aoki, K. Higashimoto, Hidenori Hidaka, Y. Ohtsuka +10 more
2022Clinical Epigenetics11 citations Open access
Semantic Scholar
Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions
K. Matsubara, M. Itoh, K. Shimizu, Shinji Saito +7 more
2019Clinical Epigenetics11 citations Open access
Semantic Scholar
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities
S. Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara +23 more
2024Nature Genetics10 citations Open access
Semantic Scholar
Myelodysplasia after clonal hematopoiesis with APOBEC3-mediated CYBB inactivation in retroviral gene therapy for X-CGD.
T. Uchiyama, T. Kawai, K. Nakabayashi, Y. Nakazawa +18 more
2023Molecular Therapy10 citations Open access
Semantic Scholar
Whole transcriptome sequencing reveals a KMT2A‐USP2 fusion in infant acute myeloid leukemia
Junji Ikeda, N. Shiba, Shin-ichi Tsujimoto, Masanori Yoshida +10 more
2019Genes, Chromosomes and Cancer10 citations
Semantic Scholar
Glucocorticoids increase the risk of preterm premature rupture of membranes possibly by inducing ITGA8 gene expression in the amnion.
Y. Okazaki, K. Taniguchi, Y. Miyamoto, Shiori Kinoshita +6 more
2022Placenta9 citations Open access
Semantic Scholar
CENP-B promotes the centromeric localization of ZFAT to control transcription of noncoding RNA
S. Ishikura, Kazumasa Yoshida, Sayuri Hashimoto, K. Nakabayashi +2 more
2021Journal of Biological Chemistry9 citations Open access
Semantic Scholar
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome
K. Yamazawa, T. Inoue, Yoshihiro Sakemi, T. Nakashima +12 more
2020Journal of Medical Genetics9 citations Open access
Semantic Scholar
Physical Properties of Ultrafine Bubbles Generated Using a Generator System
Shingo Miyamoto, Toyofumi Hirakawa, Yukiko Noguchi, D. Urushiyama +11 more
2023In Vivo8 citations Open access
Semantic Scholar
Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus
Sayaka Kawashima, Akiko Yuno, S. Sano, Akie Nakamura +10 more
2022Journal of Bone and Mineral Research8 citations
Semantic Scholar
NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia
Masanori Yoshida, K. Nakabayashi, Wentao Yang, A. Sato-Otsubo +43 more
2021Blood Advances8 citations Open access
Semantic Scholar
Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice
Shiori Kinoshita, Kazuaki Kojima, Eriko Ohnishi, Y. Takayama +5 more
2024Frontiers in Genetics6 citations Open access
Semantic Scholar
A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion
K. Hasegawa, K. Nakabayashi, Keisuke Ishiwata, Y. Kasuga +2 more
2023BMC Research Notes6 citations Open access
Semantic Scholar
Linear and disseminated porokeratosis in one family showing identical and independent second hits in MVD among skin lesions, respectively: a proof‐of‐concept study
C. Shiiya, S. Aoki, K. Nakabayashi, K. Hata +2 more
2021British Journal of Dermatology6 citations
Semantic Scholar
Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements
Sayaka Kawashima, Atsushi Hattori, E. Suzuki, K. Matsubara +6 more
2021Clinical Epigenetics6 citations Open access
Semantic Scholar
Genomic and Transcriptomic Analyses of Bioluminescence Genes in the Enope Squid Watasenia scintillans
M. Yoshida, Junichi Imoto, Yuri L Kawai, S. Funahashi +6 more
2020Marine Biotechnology6 citations Open access
Semantic Scholar
Approaches to Evaluate Whole Exome Sequencing Data That Incorporate Genetic Intolerance Scores for Congenital Anomalies, Including Intronic Regions Adjacent to Exons
K. Taniguchi, F. Hasegawa, Y. Okazaki, A. Hori +12 more
2025Molecular Genetics & Genomic Medicine5 citations Open access
Semantic Scholar
Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome
T. Kawai, Shiori Kinoshita, Y. Takayama, Eriko Ohnishi +22 more
2024Genetics in medicine open5 citations Open access
Semantic Scholar
Biallelic non-productive enhancer-promoter interactions precede imprinted expression of Kcnk9 during mouse neural commitment
Cecilia Rengifo Rojas, Jil Cercy, Sophie Perillous, Céline Gonthier-Guéret +12 more
2023bioRxiv5 citations Open access
Semantic Scholar
Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism
Y. Asahina, U. Tahara, S. Aoki, K. Nakabayashi +5 more
2023European Journal of Human Genetics5 citations Open access
Semantic Scholar
Exome‐based genome‐wide screening of rare variants associated with the risk of polycystic ovary syndrome
S. Tamaoka, Kazuki Saito, Tomoko Yoshida, K. Nakabayashi +8 more
2023Reproductive Medicine and Biology5 citations Open access
Semantic Scholar
Genome-wide association study of preterm birth and gestational age in a Japanese population
K. Hasegawa, N. Kumasaka, K. Nakabayashi, H. Kamura +4 more
2023Human Genome Variation5 citations Open access
Semantic Scholar
Genetic features of B‐cell lymphoblastic lymphoma with TCF3‐PBX1
Ryota Shirai, T. Osumi, A. Sato-Otsubo, K. Nakabayashi +17 more
2021Cancer Reports5 citations Open access
Semantic Scholar
Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing‐based non‐invasive genetic testing
N. Ito, Kazuhiro Tsukamoto, K. Taniguchi, Ken Takahashi +8 more
2021Reproductive Medicine and Biology5 citations Open access
Semantic Scholar
Gene expression and DNA methylation changes in BeWo cells dependent on tumor necrosis factor-α and insulin-like growth factor-I
Kei Tanaka, K. Nakabayashi, T. Kawai, Shinji Tanigaki +3 more
2019Human Cell5 citations
Semantic Scholar
Genome-wide association study on longitudinal and cross-sectional traits of child health and development in a Japanese population
N. Kumasaka, H. Mezawa, K. Sakamoto, T. Isobe +41 more
2025medRxiv4 citations
Semantic Scholar
Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis.
T. Kawai, Yuji Iwasaki, H. Ogata-Kawata, H. Kamura +4 more
2023European Journal of Medical Genetics4 citations
Semantic Scholar

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M. Fukami×11
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M. Fukami — researcher profile on SciRah
M. Kagami×10
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M. Kagami — researcher profile on SciRah
K. Hata×10
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