Marina Murdolo

1.4k total citations
20 papers, 663 citations indexed

About

Marina Murdolo is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Marina Murdolo has authored 20 papers receiving a total of 663 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Plant Science. Recurrent topics in Marina Murdolo's work include Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (9 papers) and Prenatal Screening and Diagnostics (5 papers). Marina Murdolo is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (9 papers) and Prenatal Screening and Diagnostics (5 papers). Marina Murdolo collaborates with scholars based in Italy, United States and Spain. Marina Murdolo's co-authors include Marcella Zollino, Giovanni Neri, Giuseppe Marangi, Francesca Faravelli, Rosetta Lecce, Angelo Selicorni, Laura Mazzanti, Giuseppe Capovilla, Vanna Pecile and Luigi Memo and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and The American Journal of Human Genetics.

In The Last Decade

Marina Murdolo

20 papers receiving 638 citations

Peers

Countries citing papers authored by Marina Murdolo

Since Specialization

Citations

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

Fields of papers citing papers by Marina Murdolo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Murdolo

This figure shows the co-authorship network connecting the top 25 collaborators of Marina Murdolo. A scholar is included among the top collaborators of Marina Murdolo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marina Murdolo. Marina Murdolo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4 2017 ·European Journal of Medical Genetics ·Maria Francesca Bedeschi, Giuseppe Marangi, Mariarosaria Calvello, (unknown), (unknown), Marco Baccarin, Silvana Guerneri, Daniela Orteschi, Marina Murdolo, Serena Lattante, (unknown), Beth Keena, Margaret Harr, Elaine H. Zackai, Marcella Zollino	19
2	Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome 2016 ·European Journal of Medical Genetics ·(unknown), Randi J. Hagerman, (unknown), Marcella Zollino, Marina Murdolo, Flora Tassone	8
3	Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 2015 ·European Journal of Human Genetics ·Concetta Cafiero, Giuseppe Marangi, Daniela Orteschi, (unknown), (unknown), Emanuela Ponzi, Alice Moncada, (unknown), Marina Murdolo, (unknown), Ilaria Contaldo, Vincenzo Leuzzi, Domenica Battaglia, Eugenio Mercuri, Anne Slavotinek, Marcella Zollino	30
4	Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1 2015 ·Journal of Assisted Reproduction and Genetics ·Alina T. Midro, Marcella Zollino, Ewa Wiland, Barbara Panasiuk, Piotr Iwanowski, Marina Murdolo, Robert Śmigiel, Maria Sąsiadek, Jacek Pilch, Maciej Kurpisz	2
5	Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf‐Hirschhorn syndrome–associated seizures disorder 2014 ·Epilepsia ·Marcella Zollino, Daniela Orteschi, (unknown), Rolph Pfundt, Katharina Steindl, Concetta Cafiero, (unknown), Ilaria Contaldo, Daniela Chieffo, (unknown), (unknown), Marina Murdolo, Giuseppe Marangi, (unknown), Domenica Battaglia	23
6	Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 2012 ·Nature Genetics ·Marcella Zollino, Daniela Orteschi, Marina Murdolo, Serena Lattante, Domenica Battaglia, (unknown), Eugenio Mercuri, Pietro Chiurazzi, Giovanni Neri, Giuseppe Marangi	107
7	von Hippel-Lindau Disease and Erythrocytosis 2012 ·Journal of Clinical Oncology ·Sara Capodimonti, Luciana Teofili, Maurizio Martini, Tonia Cenci, Maria Grazia Iachininoto, Eugenia Rosa Nuzzolo, Maria Bianchi, Marina Murdolo, Giuseppe Leone, Luigi Maria Larocca	16
8	Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter 2011 ·American Journal of Medical Genetics Part A ·Piotr Iwanowski, Barbara Panasiuk, Griet Van Buggenhout, Marina Murdolo, M. Myśliwiec, Nicole Maas, Serena Lattante, L Korniszewski, Renata Posmyk, Jacek Pilch, Stanisław Zajączek, Jean‐Pierre Fryns, Marcella Zollino, Alina T. Midro	4
9	Trisomy 12p and Monosomy 4p: Phenotype–Genotype Correlation 2009 ·Genetic Testing and Molecular Biomarkers ·(unknown), Paola Costa, Marcella Zollino, Marina Murdolo, (unknown), Marco Carrozzi, Vanna Pecile	3
10	On the nosology and pathogenesis of Wolf–Hirschhorn syndrome: Genotype–phenotype correlation analysis of 80 patients and literature review 2008 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marcella Zollino, Marina Murdolo, Giuseppe Marangi, Vanna Pecile, Cinzia Galasso, Laura Mazzanti, Giovanni Neri	112
11	The first 4p euchromatic variant in a healthy carrier having an unusual reproductive history 2007 ·American Journal of Medical Genetics Part A ·Laura Rodríguez, Marcella Zollino, Elena Mansilla, M.L. Martínez‐Fernández, (unknown), Marina Murdolo, M. L. Martínez‐Frías	7
12	Mother to son amplification of a small subtelomeric deletion: A new mechanism of familial recurrence in microdeletion syndromes 2007 ·American Journal of Medical Genetics Part A ·Francesca Faravelli, Marina Murdolo, Giuseppe Marangi, F. Dagna Bricarelli, Maja Di Rocco, Marcella Zollino	42
13	The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12 2005 ·Human Genetics ·Rosetta Lecce, Marina Murdolo, (unknown), Katharina Steindl, (unknown), (unknown), Elisa Cupelli, Giovanni Neri, Marcella Zollino	12
14	The new Wolf–Hirschhorn syndrome critical region (WHSCR‐2): A description of a second case 2005 ·American Journal of Medical Genetics Part A ·Laura Rodríguez, Marcella Zollino, (unknown), Elena Mansilla, (unknown), M.L. Martínez‐Fernández, Marina Murdolo, María Luisa Martínez‐Frías	34
15	A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf–Hirschhorn syndrome 2004 ·European Journal of Human Genetics ·Marcella Zollino, Rosetta Lecce, Angelo Selicorni, Marina Murdolo, (unknown), Giuseppe Marangi, Giuseppe Zampino, Livia Garavelli, Alessandra Ferrarini, Mariano Rocchi, John M. Opitz, Giovanni Neri	25
16	Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2 2003 ·The American Journal of Human Genetics ·Marcella Zollino, Rosetta Lecce, Rita Fischetto, Marina Murdolo, Francesca Faravelli, Angelo Selicorni, (unknown), Luigi Memo, Giuseppe Capovilla, Giovanni Neri	156
17	PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome 2003 ·European Journal of Human Genetics ·Maria Inês Kavamura, Maria Grazia Pomponi, Marcella Zollino, Rosetta Lecce, Marina Murdolo, Décio Brunoni, (unknown), John M. Opitz, Giovanni Neri	22
18	Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patients 2003 ·American Journal of Medical Genetics Part A ·Maria Inês Kavamura, Marcella Zollino, Rosetta Lecce, Marina Murdolo, Décio Brunoni, (unknown), John M. Opitz, Giovanni Neri	6
19	Induction of FAS ligand expression in a human hepatoblastoma cell line by HCV core protein 2003 ·Virus Research ·Anna Ruggieri, Marina Murdolo, M. Rapicetta	17
20	Cell cycle perturbation in a human hepatoblastoma cell line constitutively expressing Hepatitis C virus core protein 2003 ·Archives of Virology ·Anna Ruggieri, Marina Murdolo, Takashi Harada, Tatsuo Miyamura, M. Rapicetta	18

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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