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 61 Citations 12,723 281 World Ranking 7456 National Ranking 3416

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • DNA

His scientific interests lie mostly in Biochemistry, Cancer research, Methyltransferase, Signal transduction and Histone H3. His Cancer research research includes themes of Haematopoiesis, Leukemia, Immunology, Kinase and Genomic imprinting. His research investigates the connection between Methyltransferase and topics such as Transferase that intersect with issues in Arginine and Chromatin remodeling.

His Signal transduction study which covers Receptor that intersects with Neuroscience and Optogenetics. Jian Jin combines subjects such as EZH2 and Gene knockdown with his study of Histone H3. Jian Jin has included themes like Stereochemistry and Small molecule in his Structure–activity relationship study.

His most cited work include:

  • Dynamic Reprogramming of the Kinome in Response to Targeted MEK Inhibition in Triple-Negative Breast Cancer (509 citations)
  • The promise and peril of chemical probes. (443 citations)
  • A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells (375 citations)

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

Jian Jin focuses on Biochemistry, Cancer research, Methyltransferase, Epigenetics and Pharmacology. His study in Structure–activity relationship, Lysine, Small molecule, Enzyme and Drug discovery is carried out as part of his studies in Biochemistry. Jian Jin focuses mostly in the field of Cancer research, narrowing it down to matters related to EZH2 and, in some cases, Multiple myeloma and Histone H3.

The various areas that Jian Jin examines in his Methyltransferase study include Arginine, Stereochemistry and Transferase. His Epigenetics research is multidisciplinary, incorporating perspectives in Histone, Cellular differentiation and Cell biology. His Pharmacology study integrates concerns from other disciplines, such as Agonist, Receptor, Muscarinic acetylcholine receptor M1, Muscarinic acetylcholine receptor and In vivo.

He most often published in these fields:

  • Biochemistry (21.76%)
  • Cancer research (19.08%)
  • Methyltransferase (15.65%)

What were the highlights of his more recent work (between 2018-2021)?

  • Cancer research (19.08%)
  • Cell biology (11.83%)
  • Epigenetics (14.50%)

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

Jian Jin spends much of his time researching Cancer research, Cell biology, Epigenetics, Methylation and Methyltransferase. His work deals with themes such as Cancer, Cell culture, EZH2, Cyclin-dependent kinase 6 and Multiple myeloma, which intersect with Cancer research. His Cell biology research also works with subjects such as

  • Regulation of gene expression, Carcinogenesis and Small molecule most often made with reference to Chromatin,
  • Ubiquitin ligase which connect with Proteolysis, In vivo and Kinase,
  • Gene which connect with Neuroblastoma,
  • Acetylation that connect with fields like Tyrosine phosphorylation.

He interconnects Wnt signaling pathway, Epigenomics, Downregulation and upregulation and Cellular differentiation in the investigation of issues within Epigenetics. His research integrates issues of RNA Splicing Factors, RNA splicing, Histone and Leukemia in his study of Methylation. Biochemistry and DNA are closely tied to his Methyltransferase research.

Between 2018 and 2021, his most popular works were:

  • Therapeutic Targeting of RNA Splicing Catalysis through Inhibition of Protein Arginine Methylation. (64 citations)
  • A chemical biology toolbox to study protein methyltransferases and epigenetic signaling (60 citations)
  • Light-induced control of protein destruction by opto-PROTAC. (32 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

Dynamic Reprogramming of the Kinome in Response to Targeted MEK Inhibition in Triple-Negative Breast Cancer

James S. Duncan;Martin C. Whittle;Kazuhiro Nakamura;Amy N. Abell.
Cell (2012)

767 Citations

The promise and peril of chemical probes.

Cheryl H. Arrowsmith;James E. Audia;Christopher Austin;Jonathan Baell.
Nature Chemical Biology (2015)

674 Citations

A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells

Masoud Vedadi;Dalia Barsyte-Lovejoy;Feng Liu;Sylvie Rival-Gervier.
Nature Chemical Biology (2011)

546 Citations

An orally bioavailable chemical probe of the Lysine Methyltransferases EZH2 and EZH1.

Kyle D. Konze;Anqi Ma;Fengling Li;Dalia Barsyte-Lovejoy.
ACS Chemical Biology (2013)

417 Citations

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons.

Hsien Sung Huang;John A. Allen;Angela M. Mabb;Ian F. King.
Nature (2012)

351 Citations

Discovery of β-Arrestin–Biased Dopamine D2 Ligands for Probing Signal Transduction Pathways Essential for Antipsychotic Efficacy

John A. Allen;Julianne M. Yost;Vincent Setola;Xin Chen.
Proceedings of the National Academy of Sciences of the United States of America (2011)

342 Citations

Inhibition of Lapatinib-Induced Kinome Reprogramming in ERBB2-Positive Breast Cancer by Targeting BET Family Bromodomains

Timothy J. Stuhlmiller;Samantha M. Miller;Jon S. Zawistowski;Kazuhiro Nakamura.
Cell Reports (2015)

283 Citations

First chelated chiral N-heterocyclic bis-carbene complexes

Dean S. Clyne;Jian Jin;Evan Genest;and Judith C. Gallucci.
Organic Letters (2000)

242 Citations

Discovery of a 2,4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a.

Feng Liu;Xin Chen;Abdellah Allali-Hassani;Amy M. Quinn.
Journal of Medicinal Chemistry (2009)

214 Citations

Discovery of an in vivo chemical probe of the lysine methyltransferases G9a and GLP.

Feng Liu;Dalia Barsyte-Lovejoy;Fengling Li;Yan Xiong.
Journal of Medicinal Chemistry (2013)

210 Citations

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Best Scientists Citing Jian Jin

Cheryl H. Arrowsmith

Cheryl H. Arrowsmith

Structural Genomics Consortium

Publications: 103

Masoud Vedadi

Masoud Vedadi

Structural Genomics Consortium

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Bryan L. Roth

Bryan L. Roth

University of North Carolina at Chapel Hill

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Stefan Knapp

Stefan Knapp

Goethe University Frankfurt

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Matthieu Schapira

Matthieu Schapira

University of Toronto

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Gary L. Johnson

Gary L. Johnson

University of North Carolina at Chapel Hill

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Peter Brown

Peter Brown

University of Oxford

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Stephen V. Frye

Stephen V. Frye

University of North Carolina at Chapel Hill

Publications: 28

Susanne Müller

Susanne Müller

Structural Genomics Consortium

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Paul Brennan

Paul Brennan

International Agency For Research On Cancer

Publications: 27

Lee M. Graves

Lee M. Graves

University of North Carolina at Chapel Hill

Publications: 26

Nathanael S. Gray

Nathanael S. Gray

Stanford University

Publications: 26

Mark T. Bedford

Mark T. Bedford

The University of Texas MD Anderson Cancer Center

Publications: 25

Dalia Barsyte-Lovejoy

Dalia Barsyte-Lovejoy

Structural Genomics Consortium

Publications: 23

Robert A. Copeland

Robert A. Copeland

Accent Therapeutics (United States)

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Arthur Christopoulos

Arthur Christopoulos

Monash University

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