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Michele D'Urso

Michele D'Urso

D-Index & Metrics

Genetics

D-Index
50
Citations
10418
World Ranking
3920
National Ranking
1691

Overview

Michele D'Urso is affiliated with United Way in the United States and has contributed to research primarily in the field of Medicine. Their work focuses on Surgery as a subfield, with particular attention to Diverticular Disease and its complications.

The scientist's research includes the study titled "General practitioners' management of symptomatic uncomplicated diverticular disease of the colon by using rifaximin, a non-adsorbable antibiotic," published in 2021 in PubMed.

  • General practitioners' management of symptomatic uncomplicated diverticular disease of the colon by using rifaximin, a non-adsorbable antibiotic. (2021, PubMed)

Michele D'Urso has collaborated with several co-authors over the course of their research activities. Frequent co-authors include:

  • Rudi De Bastiani
  • G. Sanna
  • L. Bertolusso
  • Gianni Casella
  • M. De Polo

Their publication record is concentrated in venues such as:

  • PubMed

The main scientific topics addressed by Michele D'Urso center on Diverticular Disease and Complications, reflecting a specialized engagement with this area as reflected in multiple publications.

Best Publications

  • The DNA sequence of the human X chromosome

    Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer

  • Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

    Asmae Smahi;G. Courtois;P. Vabres;S. Yamaoka

  • A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3).

    A. Meindl;K. Dry;K. Herrmann;F. Manson

  • Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia

    Diego Ingrosso;Amelia Cimmino;Alessandra F Perna;Lucia Masella

  • Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region.

    M G Persico;G Viglietto;G Martini;D Toniolo

  • Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia

    T J Vulliamy;M D'Urso;G Battistuzzi;M Estrada

  • Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.

    G. Martini;D. Toniolo;T. Vulliamy;L. Luzzatto

  • A recurrent deletion in the ubiquitously expressed NEMO (IKK-γ) gene accounts for the vast majority of incontinentia pigmenti mutations

    Swaroop Aradhya;Hayley Woffendin;Tracy Jakins;Tiziana Bardaro

  • Transcriptome analysis of mouse stem cells and early embryos.

    Alexei A Sharov;Yulan Piao;Ryo Matoba;Dawood B Dudekula

  • Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-κB activation

    Francesca Fusco;Tiziana Bardaro;Giorgia Fimiani;Vincenzo Mercadante

  • Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome.

    S. Kenwrick;H. Woffendin;T. Jakins;S. Garry Shuttleworth

  • Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

    M. D’Esposito;N. A. Quaderi;A. Ciccodicola;P. Bruni

  • Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome.

    Ellson Y. Chen;Andre Cheng;Angela Lee;Wun Jing Kuang

  • Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations.

    Francesca Fusco;Alessandra Pescatore;Elodie Bal;Aida Ghoul

  • Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain

    Francesco Filippini;Valeria Rossi;Thierry Galli;Alberta Budillon

  • Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.

    Alfredo Ciccodicola;Maurizio D’Esposito;Teresa Esposito;Fernando Gianfrancesco

  • Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer

    Minna Nyström-Lahti;Claudia Perrera;Markus Räschle;Elena Panyushkina-Seiler

  • X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content.

    R Nagaraja;S MacMillan;J Kere;C Jones

  • Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts.

    Juha Kere;Ramaiah Nagaraja;Steven Mumm;Alfredo Ciccodicola

  • Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes

    Christoph Lengauer;Michael R. Speicher;Susanne Popp;Anna Jauch

Frequent Co-Authors

Alfredo Ciccodicola
Alfredo Ciccodicola National Research Council (CNR)
Maurizio D'Esposito
Maurizio D'Esposito National Research Council (CNR)
Giuseppe Palmieri
Giuseppe Palmieri National Academies of Sciences, Engineering, and Medicine
David L. Nelson
David L. Nelson Baylor College of Medicine
David Schlessinger
David Schlessinger National Institutes of Health
Annemarie Poustka
Annemarie Poustka German Cancer Research Center
Mariano Rocchi
Mariano Rocchi University of Bari Aldo Moro
Richard A. Lewis
Richard A. Lewis Baylor College of Medicine
Ellson Y. Chen
Ellson Y. Chen Applied Biosystems
Daniela Toniolo
Daniela Toniolo Vita-Salute San Raffaele University

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