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
Genetics D-index 63 Citations 10,997 146 World Ranking 2108 National Ranking 944

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Mutation
  • Genetics

Vijaya Ramesh mainly focuses on Genetics, Tumor suppressor gene, Molecular biology, Carcinogenesis and Gene. Her research integrates issues of Merlin, Mutation, Ectoderm, Mesoderm and Gene targeting in her study of Tumor suppressor gene. The various areas that she examines in her Merlin study include Moesin, COS cells and Filopodia.

Her Carcinogenesis research includes themes of Cancer research and Neurofibromatosis. Her work is dedicated to discovering how Cancer research, TSC2 are connected with Cell cycle and other disciplines. Vijaya Ramesh has researched Exon in several fields, including Locus and Loss of heterozygosity.

Her most cited work include:

  • Reversal of learning deficits in a Tsc2 +/− mouse model of tuberous sclerosis (675 citations)
  • The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane (461 citations)
  • NHE-RF, a Regulatory Cofactor for Na+-H+Exchange, Is a Common Interactor for Merlin and ERM (MERM) Proteins (235 citations)

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

Her main research concerns Genetics, Merlin, Molecular biology, Cell biology and Gene. Her Merlin research also works with subjects such as

  • Pathology that connect with fields like TSC1 and Human brain,
  • Stop codon most often made with reference to Frameshift mutation. Vijaya Ramesh combines subjects such as genomic DNA, Protein subunit, RNA and Coding region with her study of Molecular biology.

Her Cell biology research incorporates themes from Moesin, Actin-binding protein, Actin cytoskeleton, Immunoprecipitation and Radixin. Her studies examine the connections between Moesin and genetics, as well as such issues in Actin, with regards to PDZ domain. Her Neurofibromatosis study combines topics from a wide range of disciplines, such as Carcinogenesis, Cancer research and Meningioma.

She most often published in these fields:

  • Genetics (35.04%)
  • Merlin (23.08%)
  • Molecular biology (24.79%)

What were the highlights of her more recent work (between 2012-2021)?

  • Cancer research (19.66%)
  • Schwannomatosis (6.84%)
  • mTORC1 (8.55%)

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

Cancer research, Schwannomatosis, mTORC1, Neurofibromatosis and Kinome are her primary areas of study. The concepts of her Cancer research study are interwoven with issues in Tuberous sclerosis, Genetic enhancement, Tumor suppressor gene and TSC2, PI3K/AKT/mTOR pathway. Her TSC2 study is concerned with the larger field of Genetics.

Particularly relevant to TSC1 is her body of work in Genetics. Her Neurofibromatosis type 2 study, which is part of a larger body of work in Neurofibromatosis, is frequently linked to Foundation, bridging the gap between disciplines. Her Neurofibromatosis type 2 research includes elements of Merlin and Clinical trial, Bioinformatics.

Between 2012 and 2021, her most popular works were:

  • A high-throughput kinome screen reveals serum/glucocorticoid-regulated kinase 1 as a therapeutic target for NF2-deficient meningiomas (28 citations)
  • CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies (14 citations)
  • Survival benefit and phenotypic improvement by hamartin gene therapy in a tuberous sclerosis mouse brain model. (11 citations)

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

  • Gene
  • Mutation
  • Genetics

Her primary scientific interests are in TSC1, mTORC1, Cancer research, Kinome and TSC2. Her studies in TSC1 integrate themes in fields like Transcriptome, Ubiquitin ligase and RHEB. Her mTORC1 study contributes to a more complete understanding of Cell biology.

Her Cancer research research is multidisciplinary, relying on both mTORC2, Immediate early protein, Molecular biology, Signal transduction and Meningioma. Her research in Kinome intersects with topics in Proto-oncogene tyrosine-protein kinase Src, Receptor tyrosine kinase, Erythropoietin-producing hepatocellular receptor, Tumor suppressor gene and Tumor progression. Her study on TSC2 is covered under Genetics.

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

Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis

Dan Ehninger;Sangyeul Han;Carrie Shilyansky;Yu Zhou.
Nature Medicine (2008)

887 Citations

The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane

Athar H. Chishti;Anthony C. Kim;Shirin M. Marfatia;Mohini Lutchman.
Trends in Biochemical Sciences (1998)

646 Citations

Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.

R. Wellenreuther;J. A. Kraus;D. Lenartz;A. G. Menon.
American Journal of Pathology (1995)

336 Citations

NHE-RF, a Regulatory Cofactor for Na+-H+Exchange, Is a Common Interactor for Merlin and ERM (MERM) Proteins

Anita Murthy;Charo Gonzalez-Agosti;Etchell Cordero;Denise Pinney.
Journal of Biological Chemistry (1998)

298 Citations

NF2/Merlin Is a Novel Negative Regulator of mTOR Complex 1, and Activation of mTORC1 Is Associated with Meningioma and Schwannoma Growth

Marianne James;S Han;Carolyn Polizzano;Scott Randall Plotkin.
Molecular and Cellular Biology (2009)

290 Citations

Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.

Bianchi Ab;Hara T;Ramesh;Gao J.
Nature Genetics (1994)

289 Citations

Association of Mammalian Trp4 and Phospholipase C Isozymes with a PDZ Domain-containing Protein, NHERF

Yufang Tang;Jisen Tang;Zhangguo Chen;Claudia Trost.
Journal of Biological Chemistry (2000)

285 Citations

Exon scanning for mutation of the NF2 gene in schwannomas

Lee B. Jacoby;Mia MacCollin;David N. Louls;Trina Mohney.
Human Molecular Genetics (1994)

247 Citations

The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation.

A I McClatchey;I Saotome;V Ramesh;J F Gusella.
Genes & Development (1997)

244 Citations

Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

Jeffrey Hewett;Charo Gonzalez-Agosti;Damien Slater;Philipp Ziefer.
Human Molecular Genetics (2000)

236 Citations

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