Michele D’Urso

7.6k citations

100 papers · 4.2k indexed · h-index 35

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Molecular Biology top 2%
- Retinal Development and Disorders
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics

Papers in

Genetics 35
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Genetics and Neurodevelopmental Disorders 10
Clinical Biochemistry 8
- Metabolism and Genetic Disorders 8

Co-authors: Alfredo Ciccodicola Daniela Toniolo Lucio Luzzatto G. Martini David Schlessinger M. Graziella Persico G. Battistuzzi Maurizio D’Esposito
Journals: Genomics (16 papers)Proceedings of the National Academy of Sciences (9 papers)Gene (7 papers)Human Molecular Genetics (6 papers)Nucleic Acids Research (5 papers)
Partner nations: Italy United States United Kingdom

In The Last Decade

Michele D’Urso

100 papers receiving 4.1k citations

Peers

Countries citing papers authored by Michele D’Urso

Since Specialization

Citations

This map shows the geographic impact of Michele D’Urso's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michele D’Urso with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michele D’Urso more than expected).

Fields of papers citing papers by Michele D’Urso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michele D’Urso. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michele D’Urso. The network helps show where Michele D’Urso may publish in the future.

Co-authors

The 25 scholars most cited alongside Michele D’Urso, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michele D’Urso Line = papers co-authored together Michele D’Urso links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Functional Characterization of Wiskott-Aldrich Syndrome Protein and Scar Homolog (WASH), a Bi-modular Nucleation-promoting Factor Able to Interact with Biogenesis of Lysosome-related Organelle Subunit 2 (BLOS2) and γ-Tubulin Journal of Biological Chemistry ·Jlenia Monfregola, Gennaro Napolitano, Michele D’Urso, Pekka Lappalainen, Matilde Valeria Ursini	2010	37
2	Functional characterization of the TMLH gene: promoter analysis, in situ hybridization, identification and mapping of alternative splicing variants Gene ·Jlenia Monfregola, Gennaro Napolitano, Iván Conte, Armando Cevenini, José de Jesús Alderete-Gutiérrez, Michele D’Urso, Matilde Valeria Ursini	2007	4
3	Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting Journal of Cellular Physiology ·Jlenia Monfregola, Armando Cevenini, Antonio Terracciano, Naomi van Vlies, Salvatore Arbucci, Ronald J. A. Wanders, Michele D’Urso, Frédéric M. Vaz, Matilde Valeria Ursini	2005	10
4	Mapping of MRX81 in Xp11.2‐Xq12 suggests the presence of a new gene involved in nonspecific X‐linked mental retardation American Journal of Medical Genetics Part A ·Ida Annunziata, Carmela Lanzara, Iván Conte, Alberto Zullo, V. Ventruto, Maria Michela Rinaldi, Michele D’Urso, Giorgio Casari, Alfredo Ciccodicola, Maria Giuseppina Miano	2003	10
5	High‐resolution methylation analysis of the hMLH1 promoter in sporadic endometrial and colorectal carcinomas Cancer ·Maria Strazzullo, Antonio Cossu, Frank Kolpak, Maria Colombino, María Paola Satta, Francesco Tanda, Maria Luigia De Bonis, Andrea Cerase, Michele D’Urso, Mark D’Esposito, Giuseppe Palmieri	2003	28
6	New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease. PubMed ·Francesca Simonelli, Francesco Testa, Giuseppe de Crecchio, E. Rinaldi, Amy Hutchinson, Andrew Atkinson, Michael Dean, Michele D’Urso, Rando Allikmets	2000	69
7	Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 American Journal of Medical Genetics ·Swaroop Aradhya, صلاح أحمد الكبيسي, Richard A. Lewis, David L. Nelson, Teresa Esposito, Alfredo Ciccodicola, Tiziana Bardaro, Michele D’Urso, Hayley Woffendin, Susan Kenwrick, Asma Smahi, S. Heuertz, Arnold Munnich, Nina S. Heiss, Annemarie Poustka, Athar H. Chishti	2000	3
8	DNA methylation in transcriptional repression of two differentially expressed X-linked genes,GPC3andSYBL1 Proceedings of the National Academy of Sciences ·Reid Huber, R. Scott Hansen, Maria Strazzullo, Gina Pengue, Richard Mazzarella, Michele D’Urso, David Schlessinger, Giuseppe Pilia, Stanley M. Gartler, Mark D’Esposito	1999	42
9	Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21→q22 Cytogenetic and Genome Research ·Mark D’Esposito, Maria Strazzullo, A. Mlynik, C. Mirella Spalluto, Mariano Rocchi, Michele D’Urso, Alfredo Ciccodicola	1998	9
10	Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse European Journal of Human Genetics ·Bettina Lorenz, Carmela Migliaccio, Peter Lichtner, Carsten Meyer, Tim M. Strom, Michele D’Urso, Jörg D. Becker, Alfredo Ciccodicola, Thomas Meitinger	1998	14
11	Integrated YAC/STS Physical and Genetic Map of 22.5 Mb of Human Xq24–q26 at 56-kb Inter-STS Resolution Genomics ·Ramaiah Nagaraja, Sandra MacMillan, C. Hal Jones, Camila Andrea Gutiérrez Vera, Gina Pengue, Giovanni Porta, Marianna Augusta Ferrari do Outeiro Bernstein, Amelia Casamassimi, Michele D’Urso, Bernard H. Brownstein, David Schlessinger	1998	18
12	Expressed STSs and transcription of human Xq28 Gene ·Teresa Esposito, Alfredo Ciccodicola, Hu Shuixun, Maria R. Matarazzo, Carmela Migliaccio, Rosa Anna Cifarelli, Gaurav Drlami, Anderson da Silva Sampaio, Richard Mazzarella, David Schlessinger, Michele D’Urso, Maurizio D’Esposito	1997	1
13	Sequence-Based Exon Prediction around the Synaptophysin Locus Reveals a Gene-Rich Area Containing Novel Genes in Human Proximal Xp Genomics ·Simon E. Fisher, Alfredo Ciccodicola, Karo Tanaka, Anna Curci, 杨自佑, Michele D’Urso, Ian Craig	1997	31
14	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) Nature Genetics ·A Meindl, Katherine L. Dry, Karin A. Herrmann, Forbes Manson, Alfredo Ciccodicola, Yu.F. Berdnychenko, Maria Raquel Santos Carvalho, Helene Achatz, Heide Hellebrand, Alan Lennon, Carmela Migliaccio, Keith Porter, Eberhart Zrenner, Alan C. Bird, Marcelle Jay, Birgit Lorenz, B Wittwer, Michele D’Urso, Thomas Meitinger, Alan F. Wright	1996	391
15	PCR-based immortalization and screening of hierarchical pools of cDNAs Nucleic Acids Research ·Maurizio D’Esposito, Richard Mazzarella, Gina Pengue, Carol Jones, Michele D’Urso, David Schlessinger	1994	18
16	1.5-Mb YAC Contig in Xq28 Formatted with Sequence-Tagged Sites and Including a Region Unstable in the Clones Genomics ·Giuseppe Palmieri, Giovanna Romano, Amelia Casamassimi, Michele D’Urso, Randall D. Little, Fatima Abidi, David Schlessinger, Ulrike Mossbacher, Helena Malmgren, James Hardymon, Ulf Pettersson, Ulf Landegren	1993	12
17	YAC-assisted cloning of transcribed sequences from the human chromosome 3p21 region Human Molecular Genetics ·Gina Pengue, Viola Calabrò, N. S. Barsukova, Pasquale De Luca, Teresa Esposito, Patricia Taillon‐Miller, Sal LaForgia, Teresa Druck, Kay Huebner, Michele D’Urso, Luigi Lania	1993	11
18	The iduronate sulfatase gene: Isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome Genomics ·Giuseppe Palmieri, Valeria Capra, Giovanna Romano, Michele D’Urso, Sandra Johnson, David Schlessinger, C. Phillip Morris, John J. Hopwood, Paola Di Natale, Rosanna Gatti, Andrea Ballabio	1992	33
19	Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome Genomics ·Ellson Y. Chen, Andre Cheng, Angela Lee, Helen Happer, LaDeana Hillier, Philip Green, David Schlessinger, Alfredo Ciccodicola, Michele D’Urso	1991	91
20	Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome. Europe PMC (PubMed Central) ·Robert Feil, Giuseppe Palmieri, Michele D’Urso, Roland Heilig, I. Oberlé, Jean‐Louis Mandel	1990	25

About Michele D’Urso

Michele D’Urso is a scholar working on Genetics, Clinical Biochemistry, Aging, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 100 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (17 papers), Chromosomal and Genetic Variations (15 papers), Neonatal Health and Biochemistry (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), CRISPR and Genetic Engineering (10 papers), Genetics and Neurodevelopmental Disorders (10 papers), RNA Research and Splicing (10 papers) and Metabolism and Genetic Disorders (8 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (2.8k citations), Pediatrics, Perinatology and Child Health (706 citations), Cell Biology (469 citations) and Clinical Biochemistry (182 citations). Michele D’Urso has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Alfredo Ciccodicola, Daniela Toniolo, Lucio Luzzatto, G. Martini, David Schlessinger, M. Graziella Persico, David Schlessinger, G. Battistuzzi, Maurizio D’Esposito and Giuseppe Viglietto. Their work appears in journals such as Genomics, Proceedings of the National Academy of Sciences, Gene, Human Molecular Genetics and Nucleic Acids Research.

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