D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 40 Citations 8,928 95 World Ranking 17785 National Ranking 1307

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Gene expression

His primary scientific interests are in Molecular biology, Genetics, Telomerase, Cell biology and EZH2. In the subject of general Genetics, his work in Histone code and Histone is often linked to Chromodomain, thereby combining diverse domains of study. His Telomerase study integrates concerns from other disciplines, such as Carcinogenesis and Cancer cell.

His Cell biology study combines topics from a wide range of disciplines, such as Heterochromatin, Heterochromatin protein 1 and Histone H3, Epigenetics. His biological study spans a wide range of topics, including Histone methyltransferase and Epigenetics of physical exercise, DNA methylation. His Histone methyltransferase research includes themes of Epigenomics and Histone methylation.

His most cited work include:

  • Role of Histone H3 Lysine 9 Methylation in Epigenetic Control of Heterochromatin Assembly (1421 citations)
  • Telomerase activation by hTRT in human normal fibroblasts and hepatocellular carcinomas. (553 citations)
  • Maintenance of self‐renewal ability of mouse embryonic stem cells in the absence of DNA methyltransferases Dnmt1, Dnmt3a and Dnmt3b (421 citations)

What are the main themes of his work throughout his whole career to date?

Jun-ichi Nakayama focuses on Cell biology, Heterochromatin, Chromatin, Genetics and Molecular biology. His Cell biology research is multidisciplinary, incorporating elements of Histone H3, Histone, Nucleosome, HDAC11 and Histone methylation. His Histone methylation research is multidisciplinary, incorporating perspectives in Histone methyltransferase, Histone code, Histone H2A, Histone H1 and Methyltransferase complex.

His work carried out in the field of Heterochromatin brings together such families of science as RNA interference and Gene silencing. His Molecular biology study combines topics in areas such as Gene expression, RNA, Gene, Telomerase and Telomerase reverse transcriptase. His research in Heterochromatin protein 1 tackles topics such as EZH2 which are related to areas like DNA methylation.

He most often published in these fields:

  • Cell biology (55.14%)
  • Heterochromatin (43.93%)
  • Chromatin (48.60%)

What were the highlights of his more recent work (between 2016-2020)?

  • Cell biology (55.14%)
  • Chromatin (48.60%)
  • Heterochromatin (43.93%)

In recent papers he was focusing on the following fields of study:

His primary scientific interests are in Cell biology, Chromatin, Heterochromatin, Chromodomain and Heterochromatin protein 1. His Cell biology research incorporates themes from Histone H3, Epigenetics, Histone, Nucleosome and Histone methylation. His work in Histone methylation addresses issues such as Methyltransferase complex, which are connected to fields such as Chromatin immunoprecipitation.

His work deals with themes such as RNA, Nuclear protein and Proteomics, which intersect with Chromatin. Heterochromatin is a subfield of Genetics that Jun-ichi Nakayama explores. Jun-ichi Nakayama works mostly in the field of Euchromatin, limiting it down to topics relating to EZH2 and, in certain cases, Non-histone protein, RNA-induced transcriptional silencing and SUV39H1, as a part of the same area of interest.

Between 2016 and 2020, his most popular works were:

  • Structural Basis of Heterochromatin Formation by Human HP1 (97 citations)
  • Impact of nucleic acid and methylated H3K9 binding activities of Suv39h1 on its heterochromatin assembly. (42 citations)
  • Impact of nucleic acid and methylated H3K9 binding activities of Suv39h1 on its heterochromatin assembly. (42 citations)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Role of Histone H3 Lysine 9 Methylation in Epigenetic Control of Heterochromatin Assembly

Jun-ichi Nakayama;Judd C. Rice;Brian D. Strahl;C. David Allis.
Science (2001)

2018 Citations

Telomerase activation by hTRT in human normal fibroblasts and hepatocellular carcinomas.

J.-I. Nakayama;H. Tahara;E. Tahara;M. Saito.
Nature Genetics (1998)

834 Citations

Maintenance of self-renewal ability of mouse embryonic stem cells in the absence of DNA methyltransferases Dnmt1, Dnmt3a and Dnmt3b.

Akiko Tsumura;Tomohiro Hayakawa;Yuichi Kumaki;Shin-ichiro Takebayashi.
Genes to Cells (2006)

559 Citations

TLP1: A Gene Encoding a Protein Component of Mammalian Telomerase Is a Novel Member of WD Repeats Family

Jun-ichi Nakayama;Motoki Saito;Hideo Nakamura;Akira Matsuura.
Cell (1997)

547 Citations

Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassa.

Hisashi Tamaru;Xing Zhang;Debra McMillen;Prim B. Singh.
Nature Genetics (2003)

441 Citations

Immuno-histochemical detection of human telomerase catalytic component, hTERT, in human colorectal tumor and non-tumor tissue sections.

Hidetoshi Tahara;Wataru Yasui;Eiji Tahara;Junya Fujimoto.
Oncogene (1999)

228 Citations

A chromodomain protein, Chp1, is required for the establishment of heterochromatin in fission yeast

Mahito Sadaie;Tetsushi Iida;Takeshi Urano;Jun-ichi Nakayama.
The EMBO Journal (2004)

224 Citations

A chromodomain protein, Swi6, performs imprinting functions in fission yeast during mitosis and meiosis.

Jun-ichi Nakayama;Amar J.S Klar;Shiv I.S Grewal.
Cell (2000)

205 Citations

Physiological Roles of Class I HDAC Complex and Histone Demethylase

Tomohiro Hayakawa;Jun-ichi Nakayama.
BioMed Research International (2011)

187 Citations

A novel quantitative 'stretch PCR assay', that detects a dramatic increase in telomerase activity during the progression of myeloid leukemias.

K.-I. Tatematsu;J.-I. Nakayama;M. Danbara;S. Shionoya.
Oncogene (1996)

184 Citations

If you think any of the details on this page are incorrect, let us know.

Contact us

Best Scientists Citing Jun-ichi Nakayama

Shiv I. S. Grewal

Shiv I. S. Grewal

National Institutes of Health

Publications: 51

Danesh Moazed

Danesh Moazed

Harvard University

Publications: 49

Robin C. Allshire

Robin C. Allshire

University of Edinburgh

Publications: 46

Eric U. Selker

Eric U. Selker

University of Oregon

Publications: 37

Marc Bühler

Marc Bühler

Friedrich Miescher Institute

Publications: 35

Robert A. Martienssen

Robert A. Martienssen

Howard Hughes Medical Institute

Publications: 35

Fuyuki Ishikawa

Fuyuki Ishikawa

Kyoto University

Publications: 31

C. David Allis

C. David Allis

Rockefeller University

Publications: 30

Karl Ekwall

Karl Ekwall

Karolinska Institute

Publications: 29

Toshiyoshi Fujiwara

Toshiyoshi Fujiwara

Okayama University

Publications: 28

Thomas R. Cech

Thomas R. Cech

University of Colorado Boulder

Publications: 27

Thomas Jenuwein

Thomas Jenuwein

Max Planck Society

Publications: 26

Yasushi Hiraoka

Yasushi Hiraoka

Osaka University

Publications: 26

Prim B. Singh

Prim B. Singh

Nazarbayev University

Publications: 26

Xiaodong Cheng

Xiaodong Cheng

The University of Texas MD Anderson Cancer Center

Publications: 25

Michael Freitag

Michael Freitag

Oregon State University

Publications: 24

Trending Scientists

Xun Yi

Xun Yi

RMIT University

Robert E. Kearney

Robert E. Kearney

McGill University

Werner Herz

Werner Herz

Florida State University

Richard Inger

Richard Inger

University of Exeter

Adalgisa Caccone

Adalgisa Caccone

Yale University

Paul N. Newton

Paul N. Newton

University of Oxford

Gerald C. Nanson

Gerald C. Nanson

University of Wollongong

Ignatius Rigor

Ignatius Rigor

University of Washington

Liesbet Goubert

Liesbet Goubert

Ghent University

Matthew R. Pearson

Matthew R. Pearson

University of New Mexico

Walter P. Maksymowych

Walter P. Maksymowych

University of Alberta

Hope S. Rugo

Hope S. Rugo

University of California, San Francisco

Richard C. Semelka

Richard C. Semelka

University of North Carolina at Chapel Hill

Larry Dwyer

Larry Dwyer

University of Technology Sydney

Elizabeth Fennema

Elizabeth Fennema

University of Wisconsin–Madison

David Pion-Berlin

David Pion-Berlin

University of California, Riverside

Something went wrong. Please try again later.