Domenico Coviello

8.0k citations

175 papers · 3.4k indexed · h-index 32

Genetics top 2%
- Genetic Syndromes and Imprinting 15
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 14
- BRCA gene mutations in cancer 11
- Genetics and Neurodevelopmental Disorders 11
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 12
Genetics top 5%
- Genetic Syndromes and Imprinting 15
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 14
- BRCA gene mutations in cancer 11
- Genetics and Neurodevelopmental Disorders 11
Molecular Biology top 10%
- Congenital heart defects research 16
Cardiology and Cardiovascular Medicine top 5%
Surgery
- Lipoproteins and Cardiovascular Health 9

Co-authors: Celine Lewis Heather Skirton Alastair Kent Paolo Spirito D. Degiorgio Hugh Watkins Carla Colombo L. Castagnetta
Cited by: Genetics Pediatrics, Perinatology and Child Health
Partner nations: Italy United States United Kingdom

In The Last Decade

Domenico Coviello

165 papers receiving 3.4k citations

Peers

Countries citing papers authored by Domenico Coviello

Since Specialization

Citations

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

Fields of papers citing papers by Domenico Coviello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency Giuseppina Conteduca,Chiara Baldo,Alessia Arado,Joana Soraia Martinheira Da Silva,Renata Bocciardi,Barbara Testa,Sımona Baldassari,Maria Margherita Mancardi,Federico Zara,Michela Malacarne,Domenico Coviello	2025	1
2	Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome Giulio Calcagni,Federica Ferrigno,Alessio Franceschini,Maria Lisa Dentici,Rossella Capolino,Lorenzo Sinibaldi,Chiara Minotti,Alessia Micalizzi,Viola Alesi,Antonio Novelli,Anwar Baban,Giovanni Parlapiano,Domenico Coviello,Paolo Versacci,Carolina Putotto,Marcello Chinali,Fabrizio Drago,Andrea Bartuli,Bruno Marino,M. Cristina Digilio	2024	1
3	Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts Giuseppina Conteduca,Davide Cangelosi,Chiara Baldo,Alessia Arado,Barbara Testa,Ryan T. Wagner,Keith D. Robertson,Samuel Dequiedt,Lane Fitzsimmons,Michela Malacarne,Gilberto Filaci,Domenico Coviello	2024	0
4	Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome Rute Luísa Cabrita Pinto,Silvia Viaggi,Edoardo Canale,Marina Martinez Popple,Valeria Capra,Giuseppina Conteduca,Barbara Testa,Domenico Coviello,Angela Elvira Covone	2023	1
5	Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome Barbara Testa,Giuseppina Conteduca,Marina Grasso,Maurizio Cecconi,Francesca Lantieri,Chiara Baldo,Alessia Arado,Laura Andraghetti,Michela Malacarne,Donatella Milani,Domenico Coviello,(unknown)	2023	9
6	Esophageal Cancer with Early Onset in a Patient with Cri du Chat Syndrome Cesare Danesino,Monica Gualtierotti,Matteo Origi,Angelina Cistaro,Michela Malacarne,Matteo Massidda,Katia Bencardino,Domenico Coviello,Giovanni Albani,Irene Giovanna Schiera,Alexandra Liava,Andrea Guala	2023	1
7	EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias Jesse B.G. Hayesmoore,Zahurul A. Bhuiyan,Domenico Coviello,Desirée du Sart,Matthew Edwards,Maria Iascone,Déborah Morris-Rosendahl,Katie Sheils,Marjon van Slegtenhorst,Kate Thomson	2023	11
8	Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid Margherita Vinciguerra,Filippo Leto,Filippo Cassarà,Viviana Tartaglia,Michela Malacarne,Domenico Coviello,Valentina Cigna,Emanuela Orlandi,Francesco Picciotto,Gaspare Cucinella,Emanuela Salzano,Maria Piccione,Aurelio Maggio,Antonino Giambona	2022	1
9	Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability Loredana Poeta,Michela Malacarne,Agnese Padula,Denise Drongitis,Lucia Verrillo,Maria Brigida Lioi,Andrea M. Chiariello,Simona Bianco,Mario Nicodemi,Maria Piccione,Emanuela Salzano,Domenico Coviello,Maria Giuseppina Miano	2022	3
10	The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs Elvira Sondo,Federico Cresta,Cristina Pastorino,Valeria Tomati,Valeria Capurro,Emanuela Pesce,Mariateresa Lena,Michele Iacomino,Ave Maria Baffico,Domenico Coviello,Tiziano Bandiera,Federico Zara,Luis J. V. Galietta,Renata Bocciardi,Carlo Castellani,Nicoletta Pedemonte	2022	31
11	Fluorescent In Situ Staining and Flow Cytometric Procedures as New Pre-Diagnostic Tests for Sialidosis, GM1 Gangliosidosis and Niemann–Pick Type C Claudia Capitini,Federica Feo,Anna Caciotti,Rodolfo Tonin,Matteo Lulli,Domenico Coviello,Renzo Guerrini,Martino Calamai,Amelia Morrone	2022	4
12	NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint Giuseppina Conteduca,Davide Cangelosi,Simona Coco,Michela Malacarne,Chiara Baldo,Alessia Arado,Rute Luísa Cabrita Pinto,Barbara Testa,Domenico Coviello	2022	6
13	Hemoglobin A2 and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene Noraesah Mahmud,Massimo Maffei,Massimo Mogni,Gian Luca Forni,Valeria Maria Pinto,Giuseppina Barberio,Silvana Ungari,Antonella Maffé,Cristina Curcio,Francesco Zanolli,Raffaella Paventa,Mariarosa Carta,Alberta Caleffi,Mariella Mercadanti,Sauro Maoggi,Gilles Ivaldi,Domenico Coviello	2021	0
14	High-Throughput Gene and Protein Analysis Revealed the Response of Disc Cells to Vitamin D, Depending on the VDR FokI Variants Alessandra Colombini,Paola De Luca,Davide Cangelosi,Carlotta Perucca Orfei,Enrico Ragni,Marco Viganò,Michela Malacarne,Mauro Castagnetta,Marco Brayda‐Bruno,Domenico Coviello,Laura de Girolamo	2021	6
15	Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease Khalda Amr,Hala T. El‐Bassyouni,Sawsan Abdel Hady,Mostafa I. Mostafa,Mennat Mehrez,Domenico Coviello,Ghada El‐Kamah	2021	5
16	Comprehensive Profiling of Secretome Formulations from Fetal- and Perinatal Human Amniotic Fluid Stem Cells Ambra Costa,Davide Ceresa,Antonella De Palma,Rossana Rossi,Sara Turturo,Sara Santamaria,Carolina Balbi,Federico Villa,Daniele Reverberi,Katia Cortese,Pierangela De Biasio,D. Paladini,Domenico Coviello,Silvia Ravera,Paolo Malatesta,Pierluigi Mauri,Rodolfo Quarto,Sveva Bollini	2021	16
17	Intervertebral disc and endplate cells response to IL-1β inflammatory cell priming and identification of molecular targets of tissue degeneration (unknown),Paola De Luca,Laura de Girolamo,Dimitrios Kouroupis,Mauro Castagnetta,Carlotta Perucca Orfei,Domenico Coviello,Simona Coco,Diego Correa,Marco Brayda‐Bruno,Alessandra Colombini	2020	16
18	Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma Francesca Piaggio,Veronica Tozzo,Cinzia Bernardi,Michela Croce,Roberto Puzone,Silvia Viaggi,Serena Patrone,Annalisa Barla,Domenico Coviello,Martine J. Jager,Pieter A. van der Velden,Michael Zeschnigk,Davide Cangelosi,Alessandra Eva,Ulrich Pfeffer,Adriana Amaro	2019	22
19	Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries Thomas Liehr,Isabel M. Carreira,Zsófia Balogh,Elena Domínguez‐Garrido,Irmgard Verdorfer,Domenico Coviello,Lina Florentin,Hans Scheffer,Martina Rinčić,Heather Williams	2019	9
20	Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome Giuseppe Vezzoli,Teresa Arcidiacono,Vera Paloschi,Annalisa Terranegra,R. Biasion,Giovanna Weber,Stefano Mora,Marie‐Louise Syrén,Domenico Coviello,Daniele Cusi,Giuseppe Bianchi,Laura Soldati	2006	33

About Domenico Coviello

Domenico Coviello is a scholar working on Genetics, Genetics and Molecular Biology, having authored 175 papers that have together received 3.4k indexed citations. Recurring topics across this work include Congenital heart defects research (16 papers), Genetic Syndromes and Imprinting (15 papers), Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (12 papers), BRCA gene mutations in cancer (11 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Lipoproteins and Cardiovascular Health (9 papers). The work is most often cited by research in Genetics (795 citations), Pediatrics, Perinatology and Child Health (418 citations) and Genetics (207 citations). Domenico Coviello has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Celine Lewis, Heather Skirton, Alastair Kent, Paolo Spirito, D. Degiorgio, Hugh Watkins, Carla Colombo, L. Castagnetta, Giuseppe Carruba and David A. Zanis.

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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