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 48 Citations 7,343 122 World Ranking 14250 National Ranking 5975

Overview

What is he best known for?

The fields of study he is best known for:

  • DNA
  • Gene
  • Enzyme

Samuel H. Wilson spends much of his time researching Base excision repair, DNA polymerase, Nucleotide excision repair, Molecular biology and AP site. In his works, Samuel H. Wilson performs multidisciplinary study on DNA polymerase and DNA polymerase delta. His biological study spans a wide range of topics, including DNA polymerase beta, DNA glycosylase and Oligonucleotide.

His research in Molecular biology intersects with topics in Polymerase, DNA and DNA synthesis. His AP site research focuses on AP endonuclease in particular. The concepts of his AP endonuclease study are interwoven with issues in DNA- lyase, DNA ligase and Class II AP Endonuclease.

His most cited work include:

  • Mammalian Abasic Site Base Excision Repair: IDENTIFICATION OF THE REACTION SEQUENCE AND RATE-DETERMINING STEPS * (331 citations)
  • A role for p53 in base excision repair. (286 citations)
  • Different DNA polymerases are involved in the short- and long-patch base excision repair in mammalian cells. (203 citations)

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

His primary areas of investigation include DNA polymerase, Molecular biology, Base excision repair, Biochemistry and DNA. His DNA polymerase study incorporates themes from Polymerase and Stereochemistry. His Polymerase research is multidisciplinary, incorporating elements of Biophysics, Base pair and Nucleic acid.

Samuel H. Wilson interconnects Promoter, Response element, Poly ADP ribose polymerase and Transcription in the investigation of issues within Molecular biology. His study in Base excision repair is interdisciplinary in nature, drawing from both Lyase activity, Nucleotide excision repair, DNA glycosylase and AP site. His DNA research includes elements of Lyase, Nucleotide and Mutagenesis.

He most often published in these fields:

  • DNA polymerase (68.57%)
  • Molecular biology (50.00%)
  • Base excision repair (45.71%)

What were the highlights of his more recent work (between 2014-2020)?

  • Base excision repair (45.71%)
  • DNA (37.14%)
  • DNA repair (27.14%)

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

Samuel H. Wilson focuses on Base excision repair, DNA, DNA repair, DNA polymerase and Molecular biology. His studies in Base excision repair integrate themes in fields like Nucleotide excision repair and AP site. DNA is a subfield of Biochemistry that Samuel H. Wilson investigates.

In the field of DNA repair, his study on DNA glycosylase and DNA- lyase overlaps with subjects such as Base and Lesion. Samuel H. Wilson undertakes multidisciplinary studies into DNA polymerase and Protein–DNA interaction in his work. His Molecular biology study frequently links to adjacent areas such as Polymerase.

Between 2014 and 2020, his most popular works were:

  • Mammalian Base Excision Repair: Functional Partnership between PARP-1 and APE1 in AP-Site Repair. (30 citations)
  • Unencumbered Pol β lyase activity in nucleosome core particles. (10 citations)
  • Molecular basis for the faithful replication of 5-methylcytosine and its oxidized forms by DNA polymerase β (6 citations)

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

  • DNA
  • Gene
  • Enzyme

His primary scientific interests are in Base excision repair, DNA, DNA repair, DNA polymerase and Stereochemistry. Samuel H. Wilson performs multidisciplinary study in Base excision repair and XRCC1 in his work. Samuel H. Wilson integrates many fields, such as XRCC1 and engineering, in his works.

His AP endonuclease study deals with the bigger picture of DNA glycosylase. His DNA polymerase research incorporates themes from Cytosine, 5-Methylcytosine, DNA methylation and Polymerase. Samuel H. Wilson combines subjects such as Lyase activity, Lyase, Nucleotide and DNA synthesis with his study of Histone.

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

Mammalian Abasic Site Base Excision Repair: IDENTIFICATION OF THE REACTION SEQUENCE AND RATE-DETERMINING STEPS *

Deepak K. Srivastava;Brian J. Vande Berg;Rajendra Prasad;James T. Molina.
Journal of Biological Chemistry (1998)

457 Citations

A role for p53 in base excision repair.

Jianmin Zhou;Jinwoo Ahn;Samuel H. Wilson;Carol Prives.
The EMBO Journal (2001)

425 Citations

Different DNA polymerases are involved in the short- and long-patch base excision repair in mammalian cells.

Paola Fortini;Barbara Pascucci;Eleonora Parlanti;Robert W. Sobol.
Biochemistry (1998)

326 Citations

Role of DNA polymerase beta in the excision step of long patch mammalian base excision repair.

Grigory L. Dianov;Rajendra Prasad;Samuel H. Wilson;Vilhelm A. Bohr.
Journal of Biological Chemistry (1999)

306 Citations

FEN1 stimulation of DNA polymerase beta mediates an excision step in mammalian long patch base excision repair.

Rajendra Prasad;Grigory L. Dianov;Vilhelm A. Bohr;Samuel H. Wilson.
Journal of Biological Chemistry (2000)

291 Citations

DNA Polymerase β-mediated Long Patch Base Excision Repair POLY(ADP-RIBOSE) POLYMERASE-1 STIMULATES STRAND DISPLACEMENT DNA SYNTHESIS

Rajendra Prasad;Olga I. Lavrik;Soon-Jong Kim;Padmini Kedar.
Journal of Biological Chemistry (2001)

258 Citations

Photoaffinity labeling of mouse fibroblast enzymes by a base excision repair intermediate. Evidence for the role of poly(ADP-ribose) polymerase-1 in DNA repair.

Olga I. Lavrik;Olga I. Lavrik;Rajendra Prasad;Robert W. Sobol;Julie K. Horton.
Journal of Biological Chemistry (2001)

225 Citations

DNA structure and aspartate 276 influence nucleotide binding to human DNA polymerase beta. Implication for the identity of the rate-limiting conformational change.

Brian J. Vande Berg;William A. Beard;Samuel H. Wilson.
Journal of Biological Chemistry (2001)

209 Citations

Protection against Methylation-induced Cytotoxicity by DNA Polymerase β-Dependent Long Patch Base Excision Repair

Julie K. Horton;Rajendra Prasad;Esther Hou;Samuel H. Wilson.
Journal of Biological Chemistry (2000)

203 Citations

Base Excision Repair Intermediates Induce p53-independent Cytotoxic and Genotoxic Responses

Robert W. Sobol;Maria Kartalou;Karen H. Almeida;Donna F. Joyce.
Journal of Biological Chemistry (2003)

200 Citations

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Samuel H. Wilson

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