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 and Molecular Biology D-index 53 Citations 10,637 164 World Ranking 3264 National Ranking 1565

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Mutation

His primary areas of study are Genetics, Molecular biology, Cancer research, microRNA and Cancer. While working in this field, Paolo Fortina studies both Genetics and GJB6. The various areas that Paolo Fortina examines in his Molecular biology study include genomic DNA, Multiplex polymerase chain reaction, Silicon, Amplicon and Cell isolation.

Paolo Fortina combines subjects such as Metastatic tumor, Carcinogenesis, Cancer stem cell and Phosphorylation, MAPK/ERK pathway with his study of Cancer research. In his study, Transcriptome and Bioinformatics is inextricably linked to RNA, which falls within the broad field of microRNA. His work in the fields of Cancer, such as Colorectal cancer, intersects with other areas such as Thermal ablation and Guanylate cyclase 2C.

His most cited work include:

  • The reverse Warburg effect: Aerobic glycolysis in cancer associated fibroblasts and the tumor stroma (798 citations)
  • Connexin-26 mutations in sporadic and inherited sensorineural deafness (573 citations)
  • Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans (520 citations)

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

Paolo Fortina focuses on Genetics, Gene, Molecular biology, Cancer research and Internal medicine. His study involves Mutation, Single-nucleotide polymorphism, Sequence analysis, Allele and Exome sequencing, a branch of Genetics. His biological study spans a wide range of topics, including genomic DNA, Multiplex polymerase chain reaction, Polymerase chain reaction and Genotyping.

Within one scientific family, he focuses on topics pertaining to Prostate cancer under Cancer research, and may sometimes address concerns connected to Prostate. Metastatic breast cancer is closely connected to Oncology in his research, which is encompassed under the umbrella topic of Internal medicine. His Transcriptome study combines topics in areas such as RNA and Computational biology.

He most often published in these fields:

  • Genetics (46.73%)
  • Gene (23.86%)
  • Molecular biology (16.99%)

What were the highlights of his more recent work (between 2013-2021)?

  • Genetics (46.73%)
  • Cancer research (16.34%)
  • Gene (23.86%)

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

Paolo Fortina mainly focuses on Genetics, Cancer research, Gene, Bioinformatics and Transcriptome. Genetics is a component of his Ichthyosis, Consanguinity, Exome sequencing, Disease gene identification and microRNA studies. He interconnects RNA, Regulation of gene expression and Immunology in the investigation of issues within microRNA.

His work deals with themes such as Epithelial–mesenchymal transition, Circulating tumor cell, Mutation, Retinoblastoma protein and Metastatic breast cancer, which intersect with Cancer research. His Bioinformatics research includes elements of Medical laboratory, Engineering ethics, MEDLINE and Genomics. His Transcriptome research incorporates elements of DNA microarray, Transcription factor and Computational biology.

Between 2013 and 2021, his most popular works were:

  • Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- And tissue-specific microRNAs (285 citations)
  • Human platelet microRNA-mRNA networks associated with age and gender revealed by integrated plateletomics (134 citations)
  • Human platelet microRNA-mRNA networks associated with age and gender revealed by integrated plateletomics (134 citations)

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

  • Gene
  • DNA
  • Mutation

Paolo Fortina mainly investigates Cancer research, Genetics, Bioinformatics, Gene and Pathology. The concepts of his Cancer research study are interwoven with issues in Epithelial–mesenchymal transition, Retinoblastoma protein, Metastatic breast cancer, Signal transduction and Cyclin D1. His work is connected to RNA, Exome sequencing, Consanguinity, Genomics and Epidermolysis bullosa, as a part of Genetics.

His RNA research is multidisciplinary, relying on both Transcriptome, Receptor, Messenger RNA, microRNA and Genetic association. In his study, Emerging technologies and MEDLINE is strongly linked to Engineering ethics, which falls under the umbrella field of Bioinformatics. The Pathology study combines topics in areas such as In situ hybridization, Circulating tumor cell, Mutation, Fluorescence-lifetime imaging microscopy and Colorectal cancer.

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 reverse Warburg effect: Aerobic glycolysis in cancer associated fibroblasts and the tumor stroma

Stephanos Pavlides;Diana Whitaker-Menezes;Remedios Castello-Cros;Neal Flomenberg.
Cell Cycle (2009)

1070 Citations

Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

Leopoldo Zelante;Paolo Gasparini;Xavier Estivill;Salvatore Melchionda.
Human Molecular Genetics (1997)

837 Citations

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Xavier Estivill;Paolo Fortina;Saul Surrey;Raquel Rabionet.
The Lancet (1998)

827 Citations

The complex transcriptional landscape of the anucleate human platelet

Paul F. Bray;Steven E. McKenzie;Leonard C. Edelstein;Srikanth Nagalla.
BMC Genomics (2013)

570 Citations

High carrier frequency of the 35delG deafness mutation in European populations

Paolo Gasparini;Raquel Rabionet;Guido Barbujani;Salvatore Melchionda.
European Journal of Human Genetics (2000)

548 Citations

Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- And tissue-specific microRNAs

Eric Londina;Phillipe Lohera;Aristeidis G. Telonis;Kevin Quann.
Proceedings of the National Academy of Sciences of the United States of America (2015)

421 Citations

Integrated cell isolation and polymerase chain reaction analysis using silicon microfilter chambers.

Peter Wilding;Larry J. Kricka;Jing Cheng;Gia Hvichia.
Analytical Biochemistry (1998)

402 Citations

Seventy-five genetic loci influencing the human red blood cell

Pim Van Der Harst;Weihua Zhang;Irene Mateo Leach;Augusto Rendon.
Nature (2012)

332 Citations

Nanobiotechnology: the promise and reality of new approaches to molecular recognition.

Paolo Fortina;Larry J. Kricka;Saul Surrey;Piotr Grodzinski.
Trends in Biotechnology (2005)

312 Citations

Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy

Eloisa Arbustini;Marta Diegoli;Roberta Fasani;Maurizia Grasso.
American Journal of Pathology (1998)

284 Citations

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