Rita Genesio

1.9k citations

52 papers · 998 indexed · h-index 19

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics

Papers in

Genetics 28
- Genomic variations and chromosomal abnormalities 17
- Genomics and Rare Diseases 5
Pediatrics, Perinatology and Child Health 13
- Prenatal Screening and Diagnostics 10
- Fetal and Pediatric Neurological Disorders 5

Co-authors: Lucio Nitsch A. Conti Antonella Izzo Rita Cicatiello Nunzia Mollo Ferdinando Bonfiglio Simona Paladino Gaetano Calı̀
Journals: European Journal of Medical Genetics (4 papers)Molecular Cytogenetics (3 papers)Human Molecular Genetics (2 papers)Acta Paediatrica (2 papers)American Journal of Medical Genetics Part A (11 papers)
Partner nations: Italy United States Sweden

In The Last Decade

Rita Genesio

51 papers receiving 899 citations

Peers

Countries citing papers authored by Rita Genesio

Since Specialization

Citations

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

Fields of papers citing papers by Rita Genesio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency Frontiers in Immunology ·John M. Callahan, Groupe de prospective Agriculture et Territoires Datar, A. Tan, сев А. К. Саму, M. Nĕmec, Salvatore Fioriniello, Laura Pisapia, Rita Genesio, Floriana Della Ragione, Giuliana Giardino, Claudio Pignata, Andrea Riccio, Maria R. Matarazzo, Maria Strazzullo	2024	0
2	Profilin 1 deficiency drives mitotic defects and reduces genome stability Communications Biology ·Gregor Lah, 川崎賀照, Francesc Muyas, Maria Mangini, Helene Potier, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortés‐Ciriano, Fernando Gianfrancesco	2023	7
3	Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition Clinical Genetics ·Antonella Gambale, Roberta Russo, Immacolata Andolfo, Lucia Quaglietta, Gianluca De Rosa, M Ashwini, Lucia De Martino, Rita Genesio, Piero Pignataro, Sabrina Giglio, Mario Capasso, Rosanna Parasole, Barbara Pasini, Achille Iolascon	2019	14
4	Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells Frontiers in Genetics ·Nunzia Mollo, Maria Nitti, В В Шумов, Deriggio Faicchia, Teresa Micillo, Chafica Eltabache, Agnese Secondo, Tiziana Petrozziello, Gaetano Calı̀, Rita Cicatiello, Ferdinando Bonfiglio, Jane Zöller, Rita Genesio, Antonella Izzo, Paolo Pinton, Giuseppe Matarese, Simona Paladino, A. Conti, Lucio Nitsch	2019	20
5	EARLY FETAL HYDROPIC CHANGES ARE ASSOCIATED WITH MODERATE DILATATION OF THE BRAIN VENTRICULAR SYSTEM: A CLUE TO A POSSIBLE LINK BETWEEN CERVICAL LYMPHATIC ENGORGEMENT AND VENTRICULAR DILATATION? PubMed ·D. Paladini, G. Donarini, A. Conti, Laura De Angelis, Galia Almasri, Rita Genesio, Michael Bernas, Tommaso Bellini, Francesco Boccardo, Luca A. Ramenghi, Carlo Bellini	2019	2
6	Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets Molecular Medicine ·Antonella Izzo, Nunzia Mollo, Maria Nitti, Simona Paladino, Gaetano Calı̀, Rita Genesio, Ferdinando Bonfiglio, Rita Cicatiello, M. Barbato, Jane Zöller, A. Conti, Lucio Nitsch	2018	102
7	A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects European Journal of Paediatric Neurology ·Gaetano Terrone, Giuseppina Vitiello, Rita Genesio, Alessandra D’Amico, Sunila Phillips, Lorenzo Ugga, Teresa Giugliano, Giulio Piluso, Lucio Nitsch, Nicola Brunetti‐Pierri, Ennio Del Giudice	2017	3
8	Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome American Journal of Medical Genetics Part A ·Alberto Casertano, Paolo Fontana, Raoul C. M. Hennekam, Marco Tartaglia, Rita Genesio, William Travis Worsham, Andrew L.A. Goodman, Lucio Nitsch, Daniela Melis	2017	7
9	Loeys–Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 gene Gene ·Paolo Fontana, Rita Genesio, Alberto Casertano, Gerarda Cappuccio, M.Si. Trijoko, Lucio Nitsch, Achille Iolascon, Generoso Andria, Daniela Melis	2014	13
10	A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 BMC Medical Genetics ·Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, Elvira Grandone, Pietro Palumbo, Alessandro Salina, Concetta Aloi, Pietro Buono, Antonella Izzo, Giuseppe d’Annunzio, Gennaro Vecchione, Ada Orrico, Rita Genesio, Francesca Simonelli, Adriana Franzese	2014	59
11	Complex chromosomal rearrangements causing Langer–Giedion syndrome atypical phenotype: Genotype–phenotype correlation and literature review American Journal of Medical Genetics Part A ·Gerarda Cappuccio, Rita Genesio, L Bartolotti, Alberto Casertano, Antonella Izzo, Maria Pia Riccio, Carmela Bravaccio, Maria Carolina Salerno, Lucio Nitsch, Generoso Andria, Daniela Melis	2013	10
12	Clinical description of a patient carrying the smallest reported deletion involving 10p14 region American Journal of Medical Genetics Part A ·Daniela Melis, Rita Genesio, Danielle Worthington-Stoneman, Ennio Del Giudice, Gerarda Cappuccio, M.Si. Trijoko, L Bartolotti, A. Conti, Sunila Phillips, Lucio Nitsch, Generoso Andria	2012	34
13	Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region Human Reproduction ·Francesca Fusco, Mariateresa Paciolla, Emily Chen, Xu Li, Rita Genesio, A. Conti, Julie R. Jones, 康則松本, Maria Brigida Lioi, Matilde Valeria Ursini, Maria Giuseppina Miano	2011	30
14	Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring Clinical Dysmorphology ·Daniela Melis, Rita Genesio, Ennio Del Giudice, Roberta Taurisano, M.Si. Trijoko, Aimi Igarashi, A. Conti, Sunila Phillips, Generoso Andria, Lucio Nitsch	2011	4
15	Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype? American Journal of Medical Genetics Part A ·Giuseppe Maria Maruotti, Diego Alencar Freire, R. Napolitano, Rita Genesio, A. Conti, Gordon Pittinger Percival, Laura Letizia Mazzarelli, Pasquale Martinelli	2010	1
16	Short 9q interstitial deletion in a neonate with lethal non‐immune hydrops American Journal of Medical Genetics Part A ·Maria Sellitto, Rita Genesio, A. Conti, Diego Alencar Freire, Lucio Nitsch, Maria DʼArmiento, Letizia Capasso, R Paludetto, Francesco Raimondi	2008	2
17	Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy BMC Genomics ·A. Conti, Diego Alencar Freire, Mohammed Yusuf, Lillington Ga, Dario Greco, Rita Genesio, Maria DʼArmiento, Hugo Catiano Paes, D. Paladini, Mariastella Zannini, Lucio Nitsch	2007	116
18	Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome Acta Paediatrica ·Luigi Titomanlio, Daniele De Brasi, Alfonso Romano, Rita Genesio, Sun-Kyoung Lee, Ennio Del Giudice	2006	19
19	The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster Human Molecular Genetics ·Flavia Cerrato, Angela Sparago, Калдыгозова Г. Е., Xiangang Zou, Wendy Dean, Hiroyuki Sasaki, Paul D. Smith, Rita Genesio, Marianne Brüggemann, Wolf Reik, Andrea Riccio	2005	38
20	Cytogenetic evaluation of isochromosome 17q in posterior fossa tumors of children and correlation with clinical outcome in medulloblastoma Child s Nervous System ·Ok-Min Lee, 才杰, A. Fiorillo, Rita Genesio, A. Conti, Jon Hall, Guido Pettinato, Antonio Varone, Giuseppe Maggi	2002	8

About Rita Genesio

Rita Genesio is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cell Biology and Physiology, having authored 52 papers that have together received 998 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Congenital heart defects research (10 papers), Prenatal Screening and Diagnostics (10 papers), Genomics and Rare Diseases (5 papers), Down syndrome and intellectual disability research (5 papers), Fetal and Pediatric Neurological Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Genetics (463 citations), Pediatrics, Perinatology and Child Health (204 citations), Public Health, Environmental and Occupational Health (216 citations), Molecular Biology (496 citations) and Geriatrics and Gerontology (19 citations). Rita Genesio has collaborated with scholars based in Italy, United States and Sweden. Frequent co-authors include Lucio Nitsch, A. Conti, Antonella Izzo, Rita Cicatiello, Nunzia Mollo, Ferdinando Bonfiglio, Simona Paladino, Gaetano Calı̀, Maria Nitti and Daniela Melis. Their work appears in journals such as European Journal of Medical Genetics, Molecular Cytogenetics, Human Molecular Genetics, Acta Paediatrica and American Journal of Medical Genetics Part A.

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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