P Maraschio

3.3k citations

73 papers · 1.7k indexed · h-index 25

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 10%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms

Papers in

Genetics 50
- Genomic variations and chromosomal abnormalities 33
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 15
- Genetics and Neurodevelopmental Disorders 8
Developmental Biology 3

Co-authors: L. Tiepolo Orsetta Zuffardi M. Fraccaro Rossella Tupler Susi Scappaticci Giovanni Lanzi Francesco Pasquali Cristina Cuoco
Journals: Human Genetics (23 papers)Journal of Medical Genetics (10 papers)European Journal of Pediatrics (5 papers)Clinical Genetics (3 papers)Annals of Human Genetics (2 papers)
Partner nations: Italy Germany United Kingdom

In The Last Decade

P Maraschio

72 papers receiving 1.6k citations

Peers

Countries citing papers authored by P Maraschio

Since Specialization

Citations

This map shows the geographic impact of P Maraschio'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 P Maraschio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Maraschio more than expected).

Fields of papers citing papers by P Maraschio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P Maraschio. 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 P Maraschio. The network helps show where P Maraschio may publish in the future.

Co-authors

The 25 scholars most cited alongside P Maraschio, 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 P Maraschio Line = papers co-authored together P Maraschio links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Familial occurrence of Turner syndrome: casual event or increased risk? Journal of Pediatric Endocrinology and Metabolism ·Daniela Larizza, Cesare Danesino, P Maraschio, Andrea Carpentieri, Catherine Klersy, Valeria Calcaterra	2011	2
2	A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea European Journal of Medical Genetics ·Elena Rossi, Anna Verri, Maria Grazia Patricelli, Naoki Kiyama, Ivana Ricca, Annalisa Vetro, Roberto Ciccone, Roberto Giorda, Daniela Toniolo, P Maraschio, Orsetta Zuffardi	2008	59
3	Screening of Nijmegen Breakage Syndrome 1 Mutations in Four Unrelated Families by Polymerase Chain Reaction Using Sequence-Specific Primers Genetic Testing ·Alessandra di Masi, Antonio Antoccia, علیرضا خاوندی, Raymonda Varon-Mateeva, P Maraschio, C. Tanzarella	2006	1
4	XX sex reversal, palmoplantar keratoderma, and predisposition to squamous cell carcinoma: Genetic analysis in one family American Journal of Medical Genetics Part A ·Orietta Radi, P. Parma, Sandrine Imbeaud, Maria Rita Nasca, FJM Huikeshoven, P Maraschio, L. Tiepolo, Giuseppe Micali, Giovanna Camerino	2005	22
5	Smith-Magenis syndrome and growth hormone deficiency European Journal of Pediatrics ·علیرضا خاوندی, Patrizia Colapietro, Mauro Bozzola, Gian Luigi Marseglia, ŞEMSETTİN YILDIRIM, Cesare Danesino, Lidia Larizza, P Maraschio	2004	6
6	Growth hormone deficiency, anorectal agenesis, and brachycamptodactyly: A phenotype overlapping Stratton–Parker syndrome American Journal of Medical Genetics Part A ·علیرضا خاوندی, Peng Yuan, P Maraschio, K Sargsyan, Giampiero Beluffi, Wu Jie, Cesare Danesino	2004	1
7	Late diagnosis in severe and mild intellectual disability in adulthood Journal of Intellectual Disability Research ·Anna Verri, P Maraschio, C. Uggetti, Eugenio Pucci, G. Ronchi, Luca Nespoli, Naoki Kiyama, Antonio Ramponi, Antonio Federico	2004	6
8	Abnormal methylation does not prevent X inactivation in ICF patients Cytogenetic and Genome Research ·Déborah Bourc’his, Pierre Miniou, Marc Jeanpierre, D. Molina Gomes, Jean‐Michel Dupont, Geneviève de Saint Basile, P Maraschio, L. Tiepolo, E. Viégas-Pèquignot	1999	32
9	A novel mechanism for the origin of supernumerary marker chromosomes Human Genetics ·P Maraschio, Rossella Tupler, Elena Rossi, J. M. Valdez Mendia, FJM Huikeshoven, Mariano Rocchi, Orsetta Zuffardi, Pasi Vikberg	1996	1
10	Molecular analysis of a human Y;1 translocation in an azoospermic male Cytogenetic and Genome Research ·P Maraschio, Rossella Tupler, Permyakova Natalya Vyacheslavovna, 直矢橘, L. Tiepolo	1994	24
11	D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p) Human Genetics ·Antonella Minelli, Giovanna Floridia, Elena Rossi, Maurizio Clementi, Romano Tenconi, Lamberto Camurri, Franca Bernardi, 洪治平, Joachim Hüttmann, P Maraschio, Stephen Wood, Orsetta Zuffardi, Cesare Danesino	1993	25
12	Cytogenetics of multiple endocrine neoplasia syndromes. III Cancer Genetics and Cytogenetics ·P Maraschio, Annalisa Pezzolo, Ilkab Jeong, 直矢橘, Permyakova Natalya Vyacheslavovna, Susi Scappaticci, M. Fraccaro	1993	3
13	Cytogenetics of multiple endocrine neoplasia syndrome Cancer Genetics and Cytogenetics ·Susi Scappaticci, Dockery, Matovic Zoran, 直矢橘, P Maraschio, M. Fraccaro	1992	21
14	Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth. PubMed ·M Nowak, Martin C. Wapenaar, G J van Ommen, P Maraschio, Giovanna Camerino, Gudrun Rappold	1991	25
15	Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23 Human Genetics ·Kiki Adams, Silvia K. Nicolis, Paola Bianchi, Orsetta Zuffardi, Barbara Bardoni, P Maraschio, Sergio Ottolenghi, Giovanna Camerino, Barbára Giglioni	1991	8
16	Regional assignment of the loci for adenylate kinase to 9q32 and for ?1-acid glycoprotein to 9q31-q32 Human Genetics ·Orsetta Zuffardi, Kiki Adams, P Maraschio, Rossella Tupler, Elena Bianchi, Hideki Yokomizo, Giampiero Beluffi, Remigio Moratti, Gianfranco Liguri	1989	19
17	Evidence for a human mitotic mutant with pleiotropic effect Annals of Human Genetics ·Laura Papi, E Montali, Gianpiero Marconi, 路应昆, กุลนรี แนวพนิช, P Maraschio, Orsetta Zuffardi	1989	17
18	A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms Human Genetics ·Barbara Bardoni, Silvana Guioli, Emanuela Maserati, P Maraschio, Giovanna Camerino	1988	3
19	A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20 Human Genetics ·Rossella Vivarelli, Orsetta Zuffardi, P Maraschio, Cecilia Anichini, Tilahun Mengesha Afrassa	1988	2
20	Detection of aneuploid cells in fibroblast cultures from the father of two trisomy 21 patients. PubMed ·Giuseppe Simoni, T. Kinone, Martina Stefanini, Lidia Larizza, P Maraschio, Fiorella Nuzzo	1976	1

About P Maraschio

P Maraschio is a scholar working on Genetics, Developmental Biology, Plant Science, Molecular Biology and Cell Biology, having authored 73 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Chromosomal and Genetic Variations (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers), DNA Repair Mechanisms (8 papers), Microtubule and mitosis dynamics (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Chromatin Dynamics (7 papers) and Sexual Differentiation and Disorders (6 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (1.0k citations), Pediatrics, Perinatology and Child Health (263 citations), Plant Science (480 citations) and Reproductive Medicine (80 citations). P Maraschio has collaborated with scholars based in Italy, Germany and United Kingdom. Frequent co-authors include L. Tiepolo, Orsetta Zuffardi, M. Fraccaro, Rossella Tupler, Susi Scappaticci, Giovanni Lanzi, Francesco Pasquali, Cristina Cuoco, Giorgio Gimelli and U. Wolf. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, European Journal of Pediatrics, Clinical Genetics and Annals of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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