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Bruno Dallapiccola

ResearcherPublications, citations & collaboration network

Bruno Dallapiccola is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Bruno Dallapiccola have?

ScholarIQindexed works

Bruno Dallapiccola has 1,758 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Bruno Dallapiccola have?

ScholarIQcitation count

Bruno Dallapiccola has 53,495 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Bruno Dallapiccola?

ScholarIQh-index

Bruno Dallapiccola has an h-index of 106 in OpenAlex.

What is the i10-index of Bruno Dallapiccola?

ScholarIQi10-index

Bruno Dallapiccola has an i10-index of 681 in OpenAlex.

What is the ORCID of Bruno Dallapiccola?

ScholarIQorcid

The ORCID for Bruno Dallapiccola is on the source record.

What is the OpenAlex record for Bruno Dallapiccola?

ScholarIQopenalex

The OpenAlex for Bruno Dallapiccola is on the source record.

What are the most-cited papers on Bruno Dallapiccola?

ScholarIQmost cited works
Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C
Giuseppe Novelli, Antoine Muchir, Federica Sangiuolo, A. Leclerc, Maria Rosaria D’Apice, Catherine Massart, Francesca Capon, Paolo Sbraccia, Massimo Federici, Renato Lauro, Cosimo Tudisco, R Pallotta, Gioacchino Scarano, Bruno Dallapiccola, Luciano Merlini, Gisèle Bonne
The American Journal of Human Genetics. 2002535 CitationsOPEN ACCESS
Common variants at five new loci associated with early-onset inflammatory bowel disease
Marcin Imieliński, Robert N. Baldassano, Anne M. Griffiths, Richard K. Russell, Vito Annese, Marla Dubinsky, Subra Kugathasan, Jonathan P. Bradfield, Thomas D. Walters, Patrick Sleiman, Cecilia E Kim, Aleixo M. Muise, Kai Wang, Joseph Glessner, Shehzad A. Saeed, Haitao Zhang, Edward C. Frackelton, Cuiping Hou, James H. Flory, George Otieno, Rosetta Chiavacci, Robert W. Grundmeier, Massimo Castro, Anna Latiano, Bruno Dallapiccola, Joanne M. Stempak, Debra Abrams, Kent D. Taylor, Dermot McGovern, Melvin B. Heyman, George D. Ferry, Barbara S. Kirschner, Jessica Lee, Jonah Essers, Richard J. Grand, Michael C. Stephens, Arie Levine, David A. Piccoli, Johan Van Limbergen, Salvatore Cucchiara, Dimitri Monos, Stephen L. Guthery, Lee A. Denson, David C. Wilson, Struan F.A. Grant, Mark J. Daly, Mark S. Silverberg, Jack Satsangi, Håkon Håkonarson
Nature Genetics. 2009488 CitationsOPEN ACCESS
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
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
The American Journal of Human Genetics. 2017462 CitationsOPEN ACCESS
The origin of the major cystic fibrosis mutation (ΔF508) in European populations
Núria Morral, Jaume Bertranpetit, Xavier Estivill, Virginia Nunes, Teresa Casals, Juliette Gimenez, André Reis, Raymonda Varon-Mateeva, Milan Maçek, Luba Kalaydjieva, Dora Angelicheva, R. Dancheva, G. Romeo, Maria Pia Russo, S. Garnerone, Gabriella Restagno, Maurizio Ferrari, Carmelina Magnani, Mireille Claustres, Marie Desgeorges, M. Schwartz, Martin Schwarz, Bruno Dallapiccola, Giuseppe Novelli, Claude Férec, M. De Arce, M Németi, Juha Kere, Maria Anvret, Niklas Dahl, L Kádasi
Nature Genetics. 1994349 Citations
Genetic Susceptibility to Nonsteroidal Anti-Inflammatory Drug–Related Gastroduodenal Bleeding: Role of Cytochrome P450 2C9 Polymorphisms
Alberto Pilotto, Davide Seripa, Marilisa Franceschi, Carlo Scarcelli, Donatella Colaizzo, Elvira Grandone, Valeria Niro, Angelo Andriulli, Gioacchino Leandro, Francesco Di Mario, Bruno Dallapiccola
Gastroenterology. 2007174 CitationsOPEN ACCESS

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