Marco Fichera

10.0k citations

87 papers · 1.8k indexed · h-index 21

Genetics top 2%
- Genetics and Neurodevelopmental Disorders 30
- Genomic variations and chromosomal abnormalities 28
- Genomics and Rare Diseases 9
Molecular Biology top 10%
- Congenital heart defects research 8
Genetics top 10%
- Genetics and Neurodevelopmental Disorders 30
- Genomic variations and chromosomal abnormalities 28
- Genomics and Rare Diseases 9
Cell Biology top 10%
Bioengineering top 10%
- Analytical Chemistry and Sensors 6
Electrical and Electronic Engineering
- Electrochemical sensors and biosensors 8
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 7
Cognitive Neuroscience
- Autism Spectrum Disorder Research 6

Co-authors: Corrado Romano Mariangela Lo Giudice Sebania Libertino Daniela Benedetto Venera Aiello S Musumeci Fulvia Sinatra Antonino Scandurra
Cited by: Genetics Molecular Biology
Journals: Nature Genetics (1 paper)Neurology (2 papers)Nature Methods (1 paper)
Partner nations: Italy United States United Kingdom

In The Last Decade

Marco Fichera

81 papers receiving 1.8k citations

Peers

Countries citing papers authored by Marco Fichera

Since Specialization

Citations

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

Fields of papers citing papers by Marco Fichera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis International Journal of Molecular Sciences ·Pinella Failla,Lucia Saccuzzo,Ornella Galesi,Donatella Greco,Vincenza Barresi,Silvestra Amata,Corrado Romano,Marco Fichera	2024	0
2	Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes Genes & Genomics ·Martina Miceli,Pinella Failla,Lucia Saccuzzo,Ornella Galesi,Silvestra Amata,Corrado Romano,María Clara Bonaglia,Marco Fichera	2023	4
3	Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion European Journal of Medical Genetics ·María Clara Bonaglia,Marco Fichera,Susan Marelli,Romina Romaniello,Orsetta Zuffardi	2022	0
4	Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity European Journal of Human Genetics ·Elena Cellini,Annalisa Vetro,Valerio Conti,Carla Marini,Viola Doccini,Claudia Clementella,Elena Parrini,Sabrina Giglio,Matteo Della Monica,Marco Fichera,S Musumeci,Renzo Guerrini	2019	21
5	Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorder European Journal of Human Genetics ·Carmela Scuderi,Lucia Saccuzzo,Mirella Vinci,Lucia Castiglia,Ornella Galesi,Michele Salemi,Teresa Mattina,Eugenia Borgione,Santina Città,Corrado Romano,Marco Fichera	2019	19
6	Familial 18q12.2 deletion supports the role of RNA‐binding protein CELF4 in autism spectrum disorders American Journal of Medical Genetics Part A ·Rita Barone,Marco Fichera,Mariaclara De Grandi,Marta Battaglia,Valeria Lo Faro,Teresa Mattina,Renata Rizzo	2017	27
7	Antitumoural activity of a cytotoxic peptide of Lactobacillus casei peptidoglycan and its interaction with mitochondrial-bound hexokinase Anti-Cancer Drugs ·Giuseppe A. Fichera,Marco Fichera,Giuseppe Milone	2016	20
8	Definition of minimal duplicated region encompassing the XIAP and STAG2 genes in the Xq25 microduplication syndrome American Journal of Medical Genetics Part A ·Daniela Benedetto,S Musumeci,Emanuela Avola,A Alberti,Serafino Buono,Carmela Scuderi,Lucia Grillo,Ornella Galesi,Angela Spalletta,Mariangela Lo Giudice,D Luciano,Mirella Vinci,Sebastiano Bianca,Corrado Romano,Marco Fichera	2014	9
9	Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response Molecular Cytogenetics ·Marco Fichera,Rita Barone,Lucia Grillo,Mariaclara De Grandi,Valerio Fiore,Morana Ignazio,Tiziana Maniscalchi,Mirella Vinci,Silvestra Amata,Angela Spalletta,Giovanni Sorge,Salvatore Santo Signorelli	2014	3
10	Apneic crises: A clue for MECP2 testing in severe neonatal hypotonia-respiratory failure European Journal of Paediatric Neurology ·Raffaele Falsaperla,Piero Pavone,Marco Fichera,Pasquale Striano	2012	9
11	Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders Journal of Genetics ·Maria Piccione,Cinzia Sanfilippo,Simona Cavani,PATRIZIA SALATIELLO,Michela Malacarne,Mauro Pierluigi,Marco Fichera,D Luciano,Giovanni Corsello	2011	4
12	Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex Mitochondrion ·Carmela Scuderi,Eugenia Borgione,F Castelló,Mariangela Lo Giudice,Marco Fichera,Maurizio Elia,Carmelo Amato,Maria Savio,Francesco Domenico Di Blasi,Girolamo Aurelio Vitello,Salvatore Romano,Salvatore DiMauro,S Musumeci	2010	2
13	A Syndrome with Coarse Face, Mental Retardation and Unusual Stereotyped Movements Neuropediatrics ·Piero Pavone,R. R. Trifiletti,Enrico Parano,Marco Fichera,Martino Ruggieri	2009	1
14	A novel L1CAM mutation in a fetus detected by prenatal diagnosis European Journal of Pediatrics ·Maria Piccione,Federico Matina,Marco Fichera,Mariangela Lo Giudice,Gianfranca Damiani,Maria Cristina Jakil,Giovanni Corsello	2009	6
15	12q12 deletion: A new patient contributing to genotype–phenotype correlation American Journal of Medical Genetics Part A ·Pinella Failla,Corrado Romano,S Reitano,Daniela Benedetto,Lucia Grillo,Marco Fichera,Lucia Castiglia	2008	10
16	The molecular landscape of ASPM mutations in primary microcephaly Journal of Medical Genetics ·Adeline K. Nicholas,Eric A. Swanson,James J. Cox,Gulshan Karbani,Sabreena Malik,Kelly Springell,Daniel J. Hampshire,M Ahmed,Jacquelyn Bond,Daniela Benedetto,Marco Fichera,Corrado Romano,William B. Dobyns,C. Geoffrey Woods	2008	68
17	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism Nature Genetics ·David A. Koolen,Lisenka E.L.M. Vissers,Rolph Pfundt,Nicole de Leeuw,Samantha J.L. Knight,Regina Regan,R. Frank Kooy,Edwin Reyniers,Corrado Romano,Marco Fichera,Albert Schinzel,Alessandra Baumer,Britt-Marie Anderlid,Jacqueline Schoumans,Nine V.A.M. Knoers,Ad Geurts van Kessel,Erik A. Sistermans,Joris A. Veltman,Han G. Brunner,Bert B.A. de Vries	2006	305
18	Nail aplasia, microcephaly, severe mental retardation and MRI abnormalities: report of two unrelated cases Neurological Sciences ·S Musumeci,Maurizio Elia,Marco Fichera,Carmelo Amato,Raffaele Ferri,Corrado Romano,Antonio Federico	2006	2
19	Mutational analysis of the ATRX gene by DGGE: A powerful diagnostic approach for the ATRX syndrome Human Mutation ·Eugenia Borgione,Maurizio Sturnio,Angela Spalletta,Mariangela Lo Giudice,Lucia Castiglia,Ornella Galesi,Angela Ragusa,Marco Fichera	2003	7
20	Spontaneous transmission from a father to his son of a Y chromosome microdeletion involving the deleted in azoospermia (DAZ) gene Journal of Endocrinological Investigation ·Aldo E. Calogero,Maria Garofalo,Nunziata Barone,G. Longo,Adele De Palma,Marco Fichera,Giancarlo Rappazzo,Roberta D’Agata,Enzo Vicari	2002	35

About Marco Fichera

Marco Fichera is a scholar working on Genetics, Bioengineering and Molecular Biology, having authored 87 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (30 papers), Genomic variations and chromosomal abnormalities (28 papers), Genomics and Rare Diseases (9 papers), Congenital heart defects research (8 papers), Electrochemical sensors and biosensors (8 papers), Prenatal Screening and Diagnostics (7 papers), Analytical Chemistry and Sensors (6 papers) and Autism Spectrum Disorder Research (6 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (890 citations) and Genetics (131 citations). Marco Fichera has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Corrado Romano, Mariangela Lo Giudice, Sebania Libertino, Daniela Benedetto, Venera Aiello, S Musumeci, Fulvia Sinatra, Antonino Scandurra, Marcella Neri and Marcella Renis. Their work appears in journals such as Nature Genetics, Neurology and Nature Methods.

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