Paolo Fortina

Thomas Jefferson University
United States

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 Citations Publications World Ranking National Ranking

Genetics D-index 62 Citations 14,512 251 World Ranking 2164 National Ranking 976

Overview

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

As part of his studies on Genetics, Paolo Fortina often connects relevant areas like Hereditary hemochromatosis. His Hereditary hemochromatosis study frequently links to adjacent areas such as Hemochromatosis. Hemochromatosis is closely attributed to Genetics in his study. Genetic linkage and Chromosome are two areas of study in which Paolo Fortina engages in interdisciplinary work. Paolo Fortina integrates several fields in his works, including Chromosome and Haplotype. He undertakes multidisciplinary studies into Haplotype and Linkage disequilibrium in his work. Paolo Fortina conducts interdisciplinary study in the fields of Linkage disequilibrium and Gene through his research. Paolo Fortina integrates Gene with Genotype in his research. He merges many fields, such as Genotype and Mutation, in his writings.

Paolo Fortina most often published in these fields:

Genetics (100.00%)
Genetic linkage (100.00%)
Haplotype (100.00%)

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)

1233 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)

852 Citations

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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

843 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)

555 Citations

The complex transcriptional landscape of the anucleate human platelet

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

503 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)

463 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)

415 Citations

Seventy-five genetic loci influencing the human red blood cell

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

355 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)

321 Citations

Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy

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

290 Citations

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Frequent Co-Authors

External Links

Personal Website for Paolo Fortina