Emanuele Bellacchio

5.2k total citations
109 papers, 3.3k citations indexed

About

Emanuele Bellacchio is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Emanuele Bellacchio has authored 109 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 17 papers in Genetics and 16 papers in Cell Biology. Recurrent topics in Emanuele Bellacchio's work include Mitochondrial Function and Pathology (11 papers), Porphyrin and Phthalocyanine Chemistry (9 papers) and Molecular Sensors and Ion Detection (8 papers). Emanuele Bellacchio is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Porphyrin and Phthalocyanine Chemistry (9 papers) and Molecular Sensors and Ion Detection (8 papers). Emanuele Bellacchio collaborates with scholars based in Italy, United States and United Kingdom. Emanuele Bellacchio's co-authors include Bruno Dallapiccola, Roberto Purrello, Enza Maria Valente, Luigi Monsù Scolaro, Sergio Gurrieri, Rosaria Lauceri, Andrea Romeo, Giorgio Casari, Laura Silvestri and Viviana Caputo and has published in prestigious journals such as Journal of the American Chemical Society, Nature Genetics and PLoS ONE.

In The Last Decade

Emanuele Bellacchio

106 papers receiving 3.3k citations

Peers

Countries citing papers authored by Emanuele Bellacchio

Since Specialization

Citations

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

Fields of papers citing papers by Emanuele Bellacchio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuele Bellacchio

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuele Bellacchio. A scholar is included among the top collaborators of Emanuele Bellacchio 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 Emanuele Bellacchio. Emanuele Bellacchio 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	De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting 2024 ·International Journal of Molecular Sciences ·Beatrice Berti, Daniela Verrigni, Alessia Nasca, Michela Di Nottia, Daniela Leone, Alessandra Torraco, Teresa Rizza, Emanuele Bellacchio, (unknown), Concetta Palermo, Silvia Marchet, Costanza Lamperti, Antonio Novelli, Eugenio Mercuri, Enrico Bertini, Marika Pane, Daniele Ghezzi, Rosalba Carrozzo	2
2	Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Hypomorphic variants and two distinct disease entities 2023 ·Molecular Genetics and Metabolism ·Parith Wongkittichote, (unknown), (unknown), (unknown), (unknown), Daniel R. Carvalho, (unknown), (unknown), Claudio M. de Gusmão, Tomi L. Toler, Emanuele Bellacchio, Cristina Dallabona, Marwan Shinawi	5
3	Cerebellar Agenesis and Bilateral Polimicrogyria Associated with Rare Variants of CUB and Sushi Multiple Domains 1 Gene (CSMD1): A Longitudinal Neuropsychological and Neuroradiological Case Study 2022 ·International Journal of Environmental Research and Public Health ·Floriana Costanzo, Ginevra Zanni, Elisa Fucà, Margherita Di Paola, Sabina Barresi, Lorena Travaglini, Giovanna Stefania Colafati, Antonio Gambardella, Emanuele Bellacchio, Enrico Bertini, Deny Menghini, Stefano Vicari	1
4	Pathomorphogenesis of Glycogen-Ground Glass Hepatocytic Inclusions (Polyglucosan Bodies) in Children after Liver Transplantation 2022 ·International Journal of Molecular Sciences ·Francesco Callea, Paola Francalanci, Chiara Grimaldi, Francesca Diomedi‐Camassei, Rita De Vito, Fabio Facchetti, Rita Alaggio, Emanuele Bellacchio	2
5	Postnatal microcephaly and retinal involvement expand the phenotype of RPL10‐related disorder 2022 ·American Journal of Medical Genetics Part A ·Gerarda Cappuccio, (unknown), (unknown), (unknown), Iris Scala, Michele Pinelli, Emanuele Bellacchio, (unknown), Adriano Magli, (unknown), Mercedes Serrano, (unknown), Jaume Català, (unknown), Annalaura Torella, Vincenzo Nigro, Ginevra Zanni, Nicola Brunetti‐Pierri	3
6	Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene 2021 ·Clinical Genetics ·Emanuele Agolini, Elena Botta, (unknown), M. Cristina Digilio, Martina Rinelli, Emanuele Bellacchio, Viola Alesi, Tiziana Nardò, Giovanna Zambruno, Donata Orioli, (unknown), Luigi Boccuto, Sabrina Rossi, Andrea Carai, Giovanna Stefania Colafati, Antonella Cacchione, Bruno Dallapiccola, Antonio Novelli, Angela Mastronuzzi	5
7	Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review 2021 ·Genes ·Roberta Rotunno, Andrea Diociaiuti, Maria Lisa Dentici, Martina Rinelli, Michele Callea, (unknown), Giovanna Zambruno, Emanuele Bellacchio, May El Hachem	4
8	A Novel Splicing Variant of COL2A1 in a Fetus with Achondrogenesis Type II: Interpretation of Pathogenicity of In-Frame Deletions 2021 ·Genes ·(unknown), (unknown), (unknown), Vincenzo Dattilo, (unknown), Carmela Votino, Emanuele Bellacchio, Nicola Perrotti, Sabrina Giglio, Rodolfo Iuliano	6
9	Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis 2021 ·International Journal of Molecular Sciences ·Viola Alesi, Maria Lisa Dentici, Silvia Genovese, Sara Loddo, Emanuele Bellacchio, (unknown), Silvia Di Tommaso, (unknown), (unknown), (unknown), (unknown), Graziamaria Ubertini, Bruno Dallapiccola, Rossella Capolino, Antonio Novelli	1
10	Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease 2021 ·Human Molecular Genetics ·(unknown), (unknown), Kyle Thompson, Emanuele Bellacchio, Courtney E. French, (unknown), Toni S. Pearson, Julie Vogt, Daria Diodato, (unknown), Anja Ernst, Rita Horváth, Manali Chitre, Jakob Ek, Flemming Wibrand, Dorothy K. Grange, Lucy Raymond, Xiao-Long Zhou, Robert W. Taylor, Elsebet Østergaard	13
11	Structural Characteristics in the γ Chain Variants Associated with Fibrinogen Storage Disease Suggest the Underlying Pathogenic Mechanism 2020 ·International Journal of Molecular Sciences ·(unknown), Emanuele Bellacchio, (unknown), Alper Han Çebi, (unknown), (unknown), Güldal Yılmaz, (unknown), Murat Çakır, Francesco Callea	13
12	TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics 2020 ·International Journal of Molecular Sciences ·Antonella Sferra, Stefania Petrini, Emanuele Bellacchio, Francesco Nicita, (unknown), Maria Lisa Dentici, Paolo Alfieri, Gianluca Cestra, Enrico Bertini, Ginevra Zanni	26
13	Expanding the clinical and molecular spectrum of lethal congenital contracture syndrome 8 associated with biallelic variants of ADCY6 2019 ·Clinical Genetics ·Emanuele Agolini, Claudio Cherchi, Emanuele Bellacchio, Diego Martinelli, Dario Cocciadiferro, Renato Cutrera, Maria Beatrice Chiarini Testa, Chiara Barone, Sebastiano Bianca, Antonio Novelli	4
14	Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia 2019 ·Clinical Genetics ·Francesco Nicita, (unknown), Emanuele Bellacchio, Paolo Alfieri, Gaetano Terrone, Giorgia Piccini, Federica Graziola, Claudio Pignata, Alessandro Capuano, Enrico Bertini, Ginevra Zanni	20
15	Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation 2019 ·Clinical Genetics ·Fabrizia Stregapede, Lorena Travaglini, Adriana Rebelo, (unknown), Emanuele Bellacchio, (unknown), Paolo Alfieri, S. Pro, Stephan Züchner, Enrico Bertini, Francesco Nicita	11
16	Estudio clínico y molecular en una familia con displasia cleidocraneal 2017 ·Archivos Argentinos de Pediatria ·Michele Callea, Fabiana Fattori, Enrico Bertini, İzzet Yavuz, Emanuele Bellacchio, (unknown), (unknown), (unknown), (unknown), Francisco Cammarata‐Scalisi	3
17	Estudio clínico y molecular en una familia con displasia ectodérmica hipohidrótica autosómica dominante 2017 ·Archivos Argentinos de Pediatria ·Michele Callea, Francisco Cammarata‐Scalisi, Colin E. Willoughby, Sabrina Giglio, Ilaria Sani, Sara Bargiacchi, Giovanna Traficante, Emanuele Bellacchio, Gianluca Tadini, İzzet Yavuz, Angela Galeotti, (unknown)	0
18	A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. 2017 ·PubMed ·Michele Callea, Colin E. Willoughby, (unknown), Isabella Giovannoni, (unknown), İzzet Yavuz, Mariateresa Di Stazio, Enzo Di Iorio, (unknown), A. Benettoni, Angela Galeotti, Emanuele Bellacchio	1
19	Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage 2017 ·International Journal of Molecular Sciences ·Francesco Callea, Isabella Giovannoni, Sinan Sarı, (unknown), Buket Dalgıç, Gülen Akyol, Tsuyoshi Sogo, Abdulrahman Al‐Hussaini, Giuseppe Maggiore, Andrea Bartuli, Renata Boldrini, Paola Francalanci, Emanuele Bellacchio	18
20	ATM gene alterations in chronic lymphocytic leukemia patients induce a distinct gene expression profile and predict disease progression 2011 ·Haematologica ·Anna Guarini, M Marinelli, Simona Tavolaro, Emanuele Bellacchio, (unknown), Sabina Chiaretti, M. S. De Propris, Nadia Peragine, Simona Santangelo, Francesca Paoloni, M. Nanni, Ilaria Del Giudice, Francesca Romana Mauro, Isabella Torrente, R. Foà	70

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