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 54 Citations 10,412 123 World Ranking 11023 National Ranking 124

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Gene expression

The scientist’s investigation covers issues in Genetics, Cell biology, Cellular differentiation, Progenitor cell and Cancer research. His work on Regulation of gene expression, Alternative splicing and PRC2 as part of general Genetics study is frequently linked to Polycomb-group proteins, bridging the gap between disciplines. The various areas that he examines in his PRC2 study include Transcription factor and BMI1.

In Cellular differentiation, Bo T. Porse works on issues like Haematopoiesis, which are connected to Wnt signaling pathway. His work carried out in the field of Progenitor cell brings together such families of science as Carboxyfluorescein succinimidyl ester, Myeloid, Myeloid leukemia, Growth factor and Leukemia. His studies deal with areas such as Carcinogenesis and Mutation as well as Cancer research.

His most cited work include:

  • The Polycomb group proteins bind throughout the INK4A-ARF locus and are disassociated in senescent cells (697 citations)
  • Bone Marrow-Derived Macrophages (BMM): Isolation and Applications (551 citations)
  • Activation of the canonical Wnt pathway leads to loss of hematopoietic stem cell repopulation and multilineage differentiation block (390 citations)

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

Bo T. Porse mostly deals with Cell biology, Haematopoiesis, Cancer research, Myeloid leukemia and Leukemia. His Cell biology research is multidisciplinary, incorporating elements of Genetics, Transcription factor and Cellular differentiation. Bo T. Porse has included themes like Phenotype, Gene and Hematology in his Haematopoiesis study.

In his research on the topic of Cancer research, Ubiquitin is strongly related with Mutation. His work deals with themes such as Myeloid, Epigenetics, CEBPA and Gene expression profiling, which intersect with Myeloid leukemia. Bo T. Porse studied Myeloid and Progenitor cell that intersect with Cell.

He most often published in these fields:

  • Cell biology (31.45%)
  • Haematopoiesis (29.84%)
  • Cancer research (29.84%)

What were the highlights of his more recent work (between 2017-2021)?

  • Cell biology (31.45%)
  • Cancer research (29.84%)
  • CEBPA (18.55%)

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

Bo T. Porse mainly focuses on Cell biology, Cancer research, CEBPA, Transcription factor and Myeloid leukemia. His research in Cell biology is mostly focused on CD34. He combines subjects such as Haematopoiesis, Apoptosis, Protein kinase B, DNA damage and Chemotherapy with his study of Cancer research.

Bo T. Porse focuses mostly in the field of CEBPA, narrowing it down to matters related to Myeloid and, in some cases, Splicing factor, RNA splicing, Leukemia, Gene knockdown and Regulator. His Transcription factor research is multidisciplinary, relying on both Progenitor cell and Corepressor. Bo T. Porse works mostly in the field of Myeloid leukemia, limiting it down to topics relating to Mutant and, in certain cases, Gene isoform and Gene expression profiling, as a part of the same area of interest.

Between 2017 and 2021, his most popular works were:

  • Leukemogenic nucleophosmin mutation disrupts the transcription factor hub that regulates granulomonocytic fates (49 citations)
  • Testosterone is an endogenous regulator of BAFF and splenic B cell number (25 citations)
  • Differences in Cell Cycle Status Underlie Transcriptional Heterogeneity in the HSC Compartment (21 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • DNA
  • Gene expression

Cell biology, Progenitor cell, Cell, Myeloid leukemia and CEBPA are his primary areas of study. His study in Progenitor cell is interdisciplinary in nature, drawing from both Myeloid, Enhancer, Gene expression and Function. His Cell research incorporates themes from Computational biology, Stem cell, Retinoic acid and Proteomics.

His biological study focuses on Haematopoiesis. His Myeloid leukemia study incorporates themes from Nuclear export signal, Protein level, RUNX1 and Single-cell analysis. His CEBPA research is classified as research in Transcription factor.

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

The Polycomb group proteins bind throughout the INK4A-ARF locus and are disassociated in senescent cells

Adrian P. Bracken;Daniela Kleine-Kohlbrecher;Nikolaj Dietrich;Diego Pasini.
Genes & Development (2007)

942 Citations

Bone Marrow-Derived Macrophages (BMM): Isolation and Applications

Joachim Weischenfeldt;Bo Porse.
CSH Protocols (2008)

717 Citations

Activation of the canonical Wnt pathway leads to loss of hematopoietic stem cell repopulation and multilineage differentiation block

Peggy Kirstetter;Kristina Anderson;Bo T Porse;Sten Eirik W Jacobsen.
Nature Immunology (2006)

556 Citations

E2F Repression by C/EBPα Is Required for Adipogenesis and Granulopoiesis In Vivo

Bo T. Porse;Thomas Å. Pedersen;Xiufeng Xu;Bo Lindberg.
Cell (2001)

376 Citations

BLUEPRINT to decode the epigenetic signature written in blood

David Adams;Lucia Altucci;Stylionos E. Antonarakis;Juan Ballesteros.
Nature Biotechnology (2012)

341 Citations

Characterization of an antagonistic switch between histone H3 lysine 27 methylation and acetylation in the transcriptional regulation of Polycomb group target genes

Diego Pasini;Martina Malatesta;Hye Ryung Jung;Julian Walfridsson.
Nucleic Acids Research (2010)

318 Citations

Modeling of C/EBPalpha mutant acute myeloid leukemia reveals a common expression signature of committed myeloid leukemia-initiating cells.

Peggy Kirstetter;Mikkel B Schuster;Oksana Bereshchenko;Susan Moore.
Cancer Cell (2008)

285 Citations

NMD is essential for hematopoietic stem and progenitor cells and for eliminating by-products of programmed DNA rearrangements

Joachim Weischenfeldt;Inge Damgaard;David Bryder;Kim Theilgaard-Mönch.
Genes & Development (2008)

266 Citations

EZH2 is a potential therapeutic target for H3K27M-mutant pediatric gliomas

Faizaan Mohammad;Simon Weissmann;Benjamin Leblanc;Deo P Pandey.
Nature Medicine (2017)

260 Citations

BloodSpot: a database of gene expression profiles and transcriptional programs for healthy and malignant haematopoiesis.

Frederik Otzen Bagger;Damir Sasivarevic;Sina Hadi Sohi;Linea Gøricke Laursen.
Nucleic Acids Research (2016)

234 Citations

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