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 46 Citations 10,533 137 World Ranking 15031 National Ranking 424

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Mutation

His primary scientific interests are in Genetics, Cell biology, Gene, X chromosome and Missense mutation. Genetics is often connected to Epilepsy in his work. His work carried out in the field of Cell biology brings together such families of science as Corticotropic cell, Cell type and Cellular differentiation.

His work on RNA-binding protein, Messenger RNA and Phenotype as part of his general Gene study is frequently connected to Nonsense-mediated decay, thereby bridging the divide between different branches of science. His X chromosome research incorporates elements of Molecular biology, Cell nucleus, Zinc finger and Gene mutation. His work in Mutation addresses subjects such as Bone morphogenetic protein 4, which are connected to disciplines such as Internal medicine and Endocrinology.

His most cited work include:

  • Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse (636 citations)
  • Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo (490 citations)
  • Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors (473 citations)

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

His primary areas of study are Genetics, Cell biology, Gene, Endocrinology and Internal medicine. In most of his Genetics studies, his work intersects topics such as Epilepsy. His study in Cell biology is interdisciplinary in nature, drawing from both Embryonic stem cell, Regulation of gene expression, Cellular differentiation and Anatomy.

Paul Q. Thomas works mostly in the field of Cellular differentiation, limiting it down to concerns involving Progenitor cell and, occasionally, Pituitary gland and Cell type. The Anatomy study combines topics in areas such as Gastrulation and Endoderm. His studies deal with areas such as Homing and Bioinformatics as well as Gene.

He most often published in these fields:

  • Genetics (40.58%)
  • Cell biology (34.78%)
  • Gene (23.19%)

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

  • CRISPR (13.04%)
  • Gene (23.19%)
  • Genetics (40.58%)

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

Paul Q. Thomas mainly focuses on CRISPR, Gene, Genetics, Gene drive and Allele. His work on Cas9 and Genome editing as part of general CRISPR research is frequently linked to Synthetic gene, thereby connecting diverse disciplines of science. He has researched Gene in several fields, including Precision medicine and Bioinformatics.

His research ties Epilepsy and Genetics together. His work is dedicated to discovering how Disorders of sex development, Regulation of gene expression are connected with Testis determining factor and Mutation and other disciplines. His Conditional gene knockout research focuses on Embryonic stem cell and how it relates to Cell biology.

Between 2017 and 2021, his most popular works were:

  • Large deletions induced by Cas9 cleavage. (97 citations)
  • Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy (45 citations)
  • Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation (25 citations)

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

  • Gene
  • Genetics
  • Mutation

Paul Q. Thomas spends much of his time researching Gene drive, Allele, CRISPR, Genetics and Cas9. His study explores the link between Allele and topics such as Computational biology that cross with problems in Human genetics and Mutagenesis. His CRISPR study is related to the wider topic of Gene.

His Genetics study frequently links to adjacent areas such as Epilepsy. His work deals with themes such as Cleavage, Transgene, Subgenomic mRNA, Stereochemistry and Genome editing, which intersect with Cas9. His study looks at the relationship between Protocadherin and topics such as Mutation, which overlap with Cell biology.

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

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Mehul T. Dattani;Juan-Pedro Martinez-Barbera;Paul Q. Thomas;Joshua M. Brickman.
Nature Genetics (1998)

862 Citations

Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo

Paul Thomas;Rosa Beddington.
Current Biology (1996)

620 Citations

Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors

Paul Thomas;A. Brown;R. S.P. Beddington.
Development (1998)

599 Citations

The homeobox gene Hex is required in definitive endodermal tissues for normal forebrain, liver and thyroid formation.

J.P. Martinez Barbera;M. Clements;P. Thomas;T. Rodriguez.
Development (2000)

504 Citations

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.

Sabina Benko;Judy A. Fantes;Jeanne Amiel;Dirk Jan Kleinjan.
Nature Genetics (2009)

419 Citations

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.

Leanne M. Dibbens;Leanne M. Dibbens;Patrick S. Tarpey;Kim Hynes;Kim Hynes;Marta A. Bayly.
Nature Genetics (2008)

417 Citations

GDNF is a chemoattractant for enteric neural cells

H. M. Young;C. J. Hearn;P. G. Farlie;A. J. Canty.
Developmental Biology (2001)

349 Citations

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

Paul Q. Thomas;Mehul T. Dattani;Mehul T. Dattani;Joshua M. Brickman;David McNay.
Human Molecular Genetics (2001)

338 Citations

Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency

Frederic Laumonnier;Nathalie Ronce;Ben C.J. Hamel;Paul Thomas.
American Journal of Human Genetics (2002)

324 Citations

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism

Kathryn S. Woods;Maria Cundall;James Turton;Karine Rizotti.
American Journal of Human Genetics (2005)

316 Citations

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