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Bruno Dallapiccola

Active 1976–2025

206
Papers
37,165
Citations
105
h-index
204
i10-index

Citations

Citations per year for Bruno Dallapiccola1955: 5 citations1969: 1 citations1979: 2 citations1982: 4 citations1983: 1 citations1984: 3 citations1985: 5 citations1986: 5 citations1987: 4 citations1988: 1 citations1989: 1 citations1991: 6 citations1992: 11 citations1993: 7 citations1994: 16 citations1995: 18 citations1996: 23 citations1997: 31 citations1998: 43 citations1999: 53 citations2000: 68 citations2001: 87 citations2002: 101 citations2003: 144 citations2004: 204 citations2005: 269 citations2006: 308 citations2007: 334 citations2008: 382 citations2009: 369 citations2010: 502 citations2011: 530 citations2012: 456 citations2013: 442 citations2014: 364 citations2015: 399 citations2016: 375 citations2017: 344 citations2018: 375 citations2019: 991 citations2020: 1,110 citations2021: 1,073 citations2022: 785 citations2023: 471 citations2024: 743 citations2025: 313 citations2026: 8 citations1956–1968: no citations, so these years are not shown1970–1978: no citations, so these years are not shown1980–1981: no citations, so these years are not shown1990: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,232 citing papers, 24.4% of this breakdownUnited Kingdom: 1,478 citing papers, 8.5% of this breakdownItaly: 1,332 citing papers, 7.7% of this breakdownChina: 1,103 citing papers, 6.4% of this breakdownGermany: 1,021 citing papers, 5.9% of this breakdownCanada: 714 citing papers, 4.1% of this breakdownFrance: 709 citing papers, 4.1% of this breakdownNetherlands: 586 citing papers, 3.4% of this breakdownSpain: 489 citing papers, 2.8% of this breakdownAustralia: 488 citing papers, 2.8% of this breakdownJapan: 483 citing papers, 2.8% of this breakdownSwitzerland: 294 citing papers, 1.7% of this breakdown
0%24.4%Other 25.4%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology50%
  • Medicine40.1%
  • Neuroscience4.6%
  • Immunology and Microbiology2.2%
  • Agricultural and Biological Sciences0.6%
  • Psychology0.4%
  • Other2.1%

Topics

  • Parkinson's Disease Mechanisms and Treatments3.9%
  • Autophagy in Disease and Therapy2.7%
  • Gut microbiota and health2.6%
  • Mitochondrial Function and Pathology2.2%
  • Liver Disease Diagnosis and Treatment2.1%
  • Congenital heart defects research1.9%
  • Other84.6%

Coauthors

All papers

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  1. Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

    Authors: Enza Maria Valente, Patrick M. Abou‐Sleiman, Viviana Caputo, Miratul M. K. Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G. Healy, Alberto Albanese, Robert Nussbaum, Rafael González-Maldonado, Thomas Deller, Sergio Salvi, Pietro Cortelli, William P. Gilks, David S. Latchman, Robert J. Harvey, Bruno Dallapiccola, Georg Auburger, Nicholas Wood - Science 2004 cited by 3,491

  2. Gut microbiota profiling of pediatric nonalcoholic fatty liver disease and obese patients unveiled by an integrated meta‐omics‐based approach

    Authors: Federica Del Chierico, Valério Nobili, Pamela Vernocchi, Alessandra Russo, Cristiano De Stefanis, Daniela Gnani, Cesare Furlanello, Alessandro Zandonà, Paola Paci, Giorgio Capuani, Bruno Dallapiccola, Alfredo Miccheli, Anna Alisi, Lorenza Putignani - Hepatology 2016 cited by 711

  3. Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease

    Authors: Paola Dongiovanni, Salvatore Petta, Cristina Maglio, Anna Ludovica Fracanzani, Rosaria Maria Pipitone, Enrico Mozzi, Benedetta Maria Motta, Dorota Kamińska, Raffaela Rametta, Stefania Grimaudo, Serena Pelusi, Tiziana Montalcini, Anna Alisi, Marco Maggioni, Vesa Kärjä, Jan Borén, Pirjo Käkelä, V. Di Marco, Chao Xing, Valério Nobili, Bruno Dallapiccola, Antonio Craxı̀, Jussi Pihlajamäki, Silvia Fargion, Lars Sjöström, Lena Carlsson, Stefano Romeo, Luca Valenti - Hepatology 2014 cited by 529

  4. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

    Authors: Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, Philippe Lemay, Dan Spiegelman, Alexandre D. Laporte, Christina Nassif, Ousmane Diallo, Jean Monlong, Maxime Cadieux‐Dion, Sylvia Dobrzeniecka, Caroline Meloche, Kyle Retterer, Megan T. Cho, Jill A. Rosenfeld, Weimin Bi, Christine Massicotte, Marguerite Miguet, Ledia Brunga, Brigid M. Regan, Kelly Mo, Cory Tam, Amy Schneider, Georgie Hollingsworth, David Fitzpatrick, Alan Donaldson, Natalie Canham, Edward Blair, Bronwyn Kerr, Andrew E. Fry, Rhys H. Thomas, Joss Shelagh, Jane A. Hurst, Helen Brittain, Moira Blyth, Robert Roger Lebel, Erica H. Gerkes, Laura Davis‐Keppen, Quinn Stein, Wendy K. Chung, Sara J. Dorison, Paul J. Benke, Emily Fassi, Nicole Corsten‐Janssen, Erik‐Jan Kamsteeg, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Alain Verloès, Katrin Õunap, Monica H. Wojcik, Dara V.F. Albert, Sunita Venkateswaran, Tyson L. Ware, Dean Jones, Yu‐Chi Liu, Shekeeb S. Mohammad, Peyman Bizargity, Carlos A. Bacino, Vincenzo Leuzzi, Simone Martinelli, Bruno Dallapiccola, Marco Tartaglia, Lubov Blumkin, Klaas J. Wierenga, Gabriela Purcarin, James J. O’Byrne, Sylvia Stöckler, Anna Lehman, Boris Keren, Marie‐Christine Nouguès, Cyril Mignot, Stéphane Auvin, Caroline Nava, Susan M. Hiatt, Martina Bebin, Yunru Shao, Fernando Scaglia, Seema R. Lalani, Richard E. Frye, Imad T. Jarjour, Stéphanie Jacques, Renee-Myriam Boucher, Émilie Riou, Myriam Srour, Lionel Carmant, Anne Lortie, Philippe Major, Paola Diadori, François Dubeau, Guy D’Anjou, Guillaume Bourque, Samuel F. Berkovic, Lynette G. Sadleir, Philippe M. Campeau, Zoha Kibar, Ronald G. Lafrenière, Simon Girard, Saadet Mercimek‐Mahmutoglu, Cyrus Boelman, Guy A. Rouleau and 6 more - The American Journal of Human Genetics 2017 cited by 456

  5. LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

    Authors: Yaoqin Gong, Roger B. Slee, Naomi Fukai, Georges Rawadi, Sergio Roman‐Roman, Anthony M. Reginato, Hongwei Wang, Tim Cundy, F. H. Glorieux, Dorit Lev, Margaret Zacharin, Konrad Oexle, J. R. Marcelino, W. Suwairi, Shauna Heeger, G. Sabatakos, Suneel Apte, William N. Adkins, Jeremy Allgrove, Mine Arslan‐Kirchner, Jennifer Batch, Peter Beighton, Graeme C. Black, Richard G. Boles, Laurence M. Boon, C Borrone, HG Brunner, Georges F. Carle, Bruno Dallapiccola, Anne De Paepe, B. Floege, M. L. Halfhide, Bryan Hall, Raoul C. M. Hennekam, Tatsuo Hirose, Anneke Jans, Harald Jüppner, Chong Ae Kim, Kim M. Keppler‐Noreuil, A. Kohlschuetter, Didier Lacombe, Marie Lambert, Emmanuelle Lemyre, Tom G.W. Letteboer, Leena Peltonen, Raj Ramesar, Marta Romanengo, Hannu Somer, Elisabeth Steichen‐Gersdorf, B Steinmann, Beth Sullivan, Andrea Superti‐Furga, Walter Swoboda, M. J. van den Boogaard, Wim Van Hul, Miikka Vikkula, Marcela Votruba, Bernhard Zabel, Teresa García, Roland Baron, Bjørn R. Olsen, Matthew L. Warman - Cell 2001 cited by 2,248

  6. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

    Authors: Víctor Faùndes, William G. Newman, Laura Bernardini, Natalie Canham, Jill Clayton‐Smith, Bruno Dallapiccola, Sally Davies, Michelle Demos, Amy Goldman, Harinder Gill, Rachel Horton, Bronwyn Kerr, Dhavendra Kumar, Anna Lehman, Shane McKee, Jenny Morton, Michael Parker, Julia Rankin, Lisa Robertson, I. Karen Temple, Shelin Adam, Christèle du Souich, Alison M. Elliott, Anna Lehman, Jill Mwenifumbo, Tanya N. Nelson, Clara van Karnebeek, Jan M. Friedman, Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Munaza Ahmed, Uruj Anjum, Hayley Archer, Ruth Armstrong, Jana Awada, Meena Balasubramanian, Siddharth Banka, Diana Baralle, Angela Barnicoat, Paul Batstone, David Baty, Chris Bennett, Jonathan Berg, Birgitta Bernhard, A. Paul Bevan, Maria Bitner‐Glindzicz, Edward Blair, Moira Blyth, David Bohanna, Louise Bourdon, David Bourn, Lisa Bradley, Angela F. Brady, Simon Brent, Carole Brewer, Kate Brunstrom, David J. Bunyan, John Burn, Natalie Canham, Bruce Castle, Kate Chandler, Elena Chatzimichali, Deirdre Cilliers, Angus Clarke, Susan Clasper, Jill Clayton‐Smith, Virginia Clowes, Andrea Coates, Trevor Cole, Irina Colgiu, Amanda Collins, Morag N. Collinson, Fiona Connell, Nicola Cooper, Helen Cox, Lara Cresswell, Gareth Cross, Yanick J. Crow, Mariella D’Alessandro, Tabib Dabir, Rosemarie Davidson, Sally Davies and 231 more - The American Journal of Human Genetics 2017 cited by 278

  7. Development and Validation of a Multidimensional Prognostic Index for One-Year Mortality from Comprehensive Geriatric Assessment in Hospitalized Older Patients

    Authors: Alberto Pilotto, Luigi Ferrucci, Marilisa Franceschi, Luigi D’Ambrosio, Carlo Scarcelli, Leandro Cascavilla, Francesco Paris, Giuliana Placentino, Davide Seripa, Bruno Dallapiccola, Gioacchino Leandro - Rejuvenation Research 2008 cited by 502

  8. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

    Authors: Bhaswati Pandit, Anna Sárközy, L Pennacchio, Claudio Carta, Kimihiko Oishi, Simone Martinelli, Edgar A. Pogna, Wendy Schackwitz, Anna Ustaszewska, Andrew P. Landstrom, J. Martijn Bos, Steve R. Ommen, Giorgia Esposito, Francesca Romana Lepri, Christian Faul, Peter Mündel, Juan Pedro López Siguero, Romano Tenconi, Angelo Selicorni, Cesare Rossi, Laura Mazzanti, Isabella Torrente, Bruno Marino, M. Cristina Digilio, Giuseppe Zampino, Michael J. Ackerman, Bruno Dallapiccola, Marco Tartaglia, Bruce D. Gelb - Nature Genetics 2007 cited by 702

  9. The human gut microbiota: a dynamic interplay with the host from birth to senescence settled during childhood

    Authors: Lorenza Putignani, Federica Del Chierico, Andrea Petrucca, Pamela Vernocchi, Bruno Dallapiccola - Pediatric Research 2014 cited by 246

  10. SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

    Authors: Marialetizia Motta, Giulia Fasano, Sina Gredy, Julia Brinkmann, Adeline Bonnard, Pelin Özlem Şimşek‐Kiper, Elif Yılmaz Güleç, L. Essaddam, Gülen Eda Ütine, Ingrid G. Prandi, Martina Venditti, Francesca Pantaleoni, Francesca Clementina Radio, Andrea Ciolfi, Stefania Petrini, Federica Consoli, Cédric Vignal, Denis Hepbasli, Melanie Ullrich, Elke de Boer, Lisenka E.L.M. Vissers, Sami Gritli, Cesare Rossi, Alessandro De Luca, S. Ben Bêcher, Bruce D. Gelb, Bruno Dallapiccola, Antonella Lauri, Giovanni Chillemi, Kai Schuh, Hélène Cavé, Martin Zenker, Marco Tartaglia - The American Journal of Human Genetics 2021 cited by 80

  11. PINK1 mutations are associated with sporadic early‐onset parkinsonism

    Authors: Enza Maria Valente, Sergio Salvi, Tàmara Ialongo, Roberta Marongiu, Antonio Emanuele Elia, Viviana Caputo, Luigi Romito, Alberto Albanese, Bruno Dallapiccola, Anna Rita Bentivoglio - Annals of Neurology 2004 cited by 498

  12. Mediterranean Diet and Health: Food Effects on Gut Microbiota and Disease Control

    Authors: Federica Del Chierico, Pamela Vernocchi, Bruno Dallapiccola, Lorenza Putignani - International Journal of Molecular Sciences 2014 cited by 204

  13. Joubert Syndrome and related disorders

    Authors: Francesco Brancati, Bruno Dallapiccola, Enza Maria Valente - Orphanet Journal of Rare Diseases 2010 cited by 468

  14. Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype

    Authors: Pamela Vernocchi, Federica Del Chierico, Alessandra Russo, Fabio Majo, Martina Rossitto, Mariacristina Valerio, Luca Casadei, Antonietta La Storia, Francesca De Filippis, Cristiano Rizzo, Cesare Manetti, Paola Paci, Danilo Ercolini, Federico Marini, Ersilia Fiscarelli, Bruno Dallapiccola, V. Lucidi, Alfredo Miccheli, Lorenza Putignani - PLoS ONE 2018 cited by 123

  15. GermlineBRAFmutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: Molecular diversity and associated phenotypic spectrum

    Authors: Anna Sárközy, Claudio Carta, Sonia Moretti, Giuseppe Zampino, M. Cristina Digilio, Francesca Pantaleoni, Anna Paola Scioletti, Giorgia Esposito, Viviana Cordeddu, Francesca Romana Lepri, Valentina Petrangeli, Maria Lisa Dentici, Grazia M.S. Mancini, Angelo Selicorni, Cesare Rossi, Laura Mazzanti, Bruno Marino, Giovanni Battista Ferrero, Margherita Silengo, Luigi Memo, Franco Stanzial, Francesca Faravelli, Liborio Stuppia, Efisio Puxeddu, Bruce D. Gelb, Bruno Dallapiccola, Marco Tartaglia - Human Mutation 2009 cited by 305

  16. Whole genome sequencing diagnostic yield for paediatric patients with suspected genetic disorders: systematic review, meta-analysis, and GRADE assessment

    Authors: Mario Cesare Nurchis, Gerardo Altamura, Maria Teresa Riccardi, Francesca Clementina Radio, Giovanni Chillemi, Enrico Bertini, Jacopo Garlasco, Marco Tartaglia, Bruno Dallapiccola, Gianfranco Damiani - Archives of Public Health 2023 cited by 63

  17. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused byRASA1 mutations

    Authors: Nicole Revençu, Laurence M. Boon, John B. Mulliken, O Enjolras, Maria Cordisco, Patricia E. Burrows, Philippe Clapuyt, Frank Hammer, Josée Dubois, Eulàlia Baselga, Francesco Brancati, Robin Carder, José Miguel Ceballos Quintal, Bruno Dallapiccola, Gayle Fischer, Ilona J. Frieden, Maria C. Garzón, John Harper, Jennifer Johnson-Patel, Christine Labrèze, Loreto Martorell, Harriet J. Paltiel, Annette Pohl, Julie Prendiville, I. Quéré, Dawn H. Siegel, Enza Maria Valente, Annet van Hagen, Liselot van Hest, Keith K. Vaux, Asunción Vicente, Lisa Weibel, David Chitayat, Miikka Vikkula - Human Mutation 2008 cited by 430

  18. Gut Microbiota Dysbiosis as Risk and Premorbid Factors of IBD and IBS Along the Childhood–Adulthood Transition

    Authors: Lorenza Putignani, Federica Del Chierico, Pamela Vernocchi, Michele Cicala, Salvatore Cucchiara, Bruno Dallapiccola - Inflammatory Bowel Diseases 2015 cited by 154

  19. Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum

    Authors: Marialetizia Motta, Luca Pannone, Francesca Pantaleoni, Gianfranco Bocchinfuso, Francesca Clementina Radio, Serena Cecchetti, Andrea Ciolfi, Martina Di Rocco, Mariet W. Elting, Eva H. Brilstra, Stefania Boni, Laura Mazzanti, Federica Tamburrino, Larry Walsh, Katelyn Payne, Alberto Fernández‐Jaén, Mythily Ganapathi, Wendy K. Chung, Dorothy K. Grange, Ashita Dave‐Wala, Shalini C. Reshmi, Dennis W. Bartholomew, Danielle Mouhlas, Giovanna Carpentieri, Alessandro Bruselles, Simone Pizzi, Emanuele Bellacchio, Francesca Piceci‐Sparascio, Christina Lißewski, Julia Brinkmann, Ronald R. Waclaw, Quinten Waisfisz, Koen L.I. van Gassen, Ingrid M. Wentzensen, Michelle M. Morrow, Sara Álvarez, Mónica Mártinez‐García, Alessandro De Luca, Luigi Memo, Giuseppe Zampino, Cesare Rossi, Marco Seri, Bruce D. Gelb, Martin Zenker, Bruno Dallapiccola, Lorenzo Stella, Carlos E. Prada, Simone Martinelli, Elisabetta Flex, Marco Tartaglia - The American Journal of Human Genetics 2020 cited by 95

  20. Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene

    Authors: M. Cristina Digilio, Emanuela Conti, Anna Sárközy, Rita Mingarelli, Tania Dottorini, Bruno Marino, Antonio Pizzuti, Bruno Dallapiccola - The American Journal of Human Genetics 2002 cited by 422

  21. Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

    Authors: Stephanie Bielas, Jennifer L. Silhavy, Francesco Brancati, Marina V. Kisseleva, Lihadh Al‐Gazali, László Sztriha, Riad Bayoumi, Maha S. Zaki, Alice Abdel Aleem, Rasim Özgür Rosti, Hülya Kayserili, Dominika Swistun, Lesley C. Scott, Enrico Bertini, Eugen Boltshauser, Elisa Fazzi, Lorena Travaglini, Seth J. Field, Stéphanie Gayral, Monique Jacoby, Stéphane Schurmans, Bruno Dallapiccola, Philip W. Majerus, Enza Maria Valente, Joseph G. Gleeson - Nature Genetics 2009 cited by 412

  22. Gut Microbiota Markers in Obese Adolescent and Adult Patients: Age-Dependent Differential Patterns

    Authors: Federica Del Chierico, Francesca Abbatini, Alessandra Russo, Andrea Quagliariello, Sofia Reddel, Danila Capoccia, Romina Caccamo, Stefano Ginanni Corradini, Valério Nobili, Francesco De Peppo, Bruno Dallapiccola, Frida Leonetti, Gianfranço Silecchia, Lorenza Putignani - Frontiers in Microbiology 2018 cited by 181

  23. Gut Microbiota Profiling and Gut–Brain Crosstalk in Children Affected by Pediatric Acute-Onset Neuropsychiatric Syndrome and Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections

    Authors: Andrea Quagliariello, Federica Del Chierico, Alessandra Russo, Sofia Reddel, Giulia Conte, Loris Riccardo Lopetuso, Gianluca Ianiro, Bruno Dallapiccola, Francesco Cardona, Antonio Gasbarrini, Lorenza Putignani - Frontiers in Microbiology 2018 cited by 119

  24. Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome

    Authors: Christiane K. Bauer, Paolo Calligari, Francesca Clementina Radio, Viviana Caputo, Maria Lisa Dentici, N Falah, Frances A. High, Francesca Pantaleoni, Sabina Barresi, Andrea Ciolfi, Simone Pizzi, Alessandro Bruselles, Richard Person, Sarah Richards, Megan T. Cho, Daniela Judith Claps Sepulveda, S. Pro, Roberta Battini, Giuseppe Zampino, M. Cristina Digilio, Gianfranco Bocchinfuso, Bruno Dallapiccola, Lorenzo Stella, Marco Tartaglia - The American Journal of Human Genetics 2018 cited by 94