H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 47 Citations 7,862 127 World Ranking 4147 National Ranking 192

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • DNA

Yann Herault mainly investigates Genetics, Gene, Trisomy, Neuroscience and Phenotype. His study involves Gene duplication, Retrotransposon, DNMT1, DNA methylation and DNA methyltransferase, a branch of Genetics. All of his Gene and Locus, Transposable element, Epigenetics, Transcriptome and DNMT3B investigations are sub-components of the entire Gene study.

His Trisomy research incorporates themes from Down syndrome and Chromosomal translocation. When carried out as part of a general Neuroscience research project, his work on Morris water navigation task and Neuron is frequently linked to work in Brain size and Gap-43 protein, therefore connecting diverse disciplines of study. Yann Herault interconnects Mutation, Mutant, Gene knockout, Induced pluripotent stem cell and Functional validation in the investigation of issues within Phenotype.

His most cited work include:

  • Distinct fibroblast lineages determine dermal architecture in skin development and repair (558 citations)
  • High-throughput discovery of novel developmental phenotypes (523 citations)
  • A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains (266 citations)

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

His primary areas of study are Genetics, Gene, Phenotype, Down syndrome and Neuroscience. His Gene duplication, Mutant, Copy-number variation, Trisomy and Locus study are his primary interests in Genetics. His Gene duplication study combines topics in areas such as Gene rearrangement and HOXD13.

His Copy-number variation research is multidisciplinary, incorporating elements of Gene dosage and Regulation of gene expression. The study of Gene is intertwined with the study of Computational biology in a number of ways. The study incorporates disciplines such as Endocrinology, Recognition memory, Cognition and Internal medicine in addition to Down syndrome.

He most often published in these fields:

  • Genetics (63.32%)
  • Gene (49.34%)
  • Phenotype (25.33%)

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

  • Gene (49.34%)
  • Genetics (63.32%)
  • Phenotype (25.33%)

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

Yann Herault spends much of his time researching Gene, Genetics, Phenotype, Computational biology and Gene duplication. Gene is frequently linked to Kinase in his study. His Genetics study is mostly concerned with Copy-number variation, Mutant and Genome-wide association study.

His study in Phenotype is interdisciplinary in nature, drawing from both DYRK1A, Down syndrome, Locus, Neuroscience and RHOA. The various areas that Yann Herault examines in his Computational biology study include Genome editing, Genome, CRISPR and Disease. His research investigates the connection between Gene duplication and topics such as Serum iron that intersect with problems in Red blood cell and Iron-deficiency anemia.

Between 2018 and 2021, his most popular works were:

  • BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr348 phosphorylation. (23 citations)
  • Human and mouse essentiality screens as a resource for disease gene discovery. (15 citations)
  • Cbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1a. (15 citations)

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

  • Gene
  • DNA
  • Genetics

His main research concerns Gene, Computational biology, Genetics, Phenotype and Gene duplication. Yann Herault performs multidisciplinary study in Gene and Actin cytoskeleton in his work. The various areas that Yann Herault examines in his Computational biology study include Genome editing, Disease, Inbred strain and Developmental disorder.

The Genetics study combines topics in areas such as Hemoglobin and Red blood cell. He has researched Phenotype in several fields, including Recognition memory, Zebrafish, Craniofacial and Copy-number variation. His Gene duplication research includes themes of Iron-deficiency anemia, Anemia, Microcytosis, Iron deficiency and Serum iron.

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

Distinct fibroblast lineages determine dermal architecture in skin development and repair

Ryan R. Driskell;Ryan R. Driskell;Beate M. Lichtenberger;Beate M. Lichtenberger;Esther Hoste;Kai Kretzschmar;Kai Kretzschmar.
Nature (2013)

701 Citations

High-throughput discovery of novel developmental phenotypes

Mary E. Dickinson;Ann M. Flenniken;Xiao Ji;Lydia Teboul.
Nature (2016)

561 Citations

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs.
Genome Biology (2013)

331 Citations

The mammalian gene function resource: the international knockout mouse consortium

Allan Bradley;Konstantinos Anastassiadis;Abdelkader Ayadi;James F. Battey.
Mammalian Genome (2012)

259 Citations

Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humans

Rafael De la Torre;Susana De Sola;Meritxell Pons;Arnaud Duchon.
Molecular Nutrition & Food Research (2014)

256 Citations

Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs

Marie Kmita;Nadine Fraudeau;Yann Hérault;Yann Hérault;Denis Duboule.
Nature (2002)

244 Citations

Domains of genome-wide gene expression dysregulation in Down/'s syndrome

Audrey Letourneau;Federico A. Santoni;Ximena Bonilla;M. Reza Sailani.
Nature (2014)

211 Citations

The DNA methyltransferase DNMT3C protects male germ cells from transposon activity.

Joan Barau;Aurélie Teissandier;Aurélie Teissandier;Natasha Zamudio;Stéphanie Roy.
Science (2016)

205 Citations

Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

Yann Hérault;Minoo Rassoulzadegan;François Cuzin;Denis Duboule..
Nature Genetics (1998)

198 Citations

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

Arnaud Duchon;Matthieu Raveau;Claire Chevalier;Valérie Nalesso.
Mammalian Genome (2011)

161 Citations

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