Alessandro De Luca

6.8k citations

113 papers · 2.9k indexed · h-index 31

Molecular Biology top 5%
Pulmonary and Respiratory Medicine top 5%
Genetics top 5%
Rheumatology top 2%
Oncology top 10%

Co-authors: Bruno Dallapiccola Valentina Guida Bruno Marino M. Cristina Digilio Melinda A. Miller C. Blake Gilks David G. Huntsman Isabella Torrente
Topics: Congenital heart defects research (15 papers)Genetic Neurodegenerative Diseases (13 papers)Neurofibromatosis and Schwannoma Cases (13 papers)
Cited by: Rheumatology Neurology Genetics
Journals: Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterologíaApplied and Environmental Microbiology
Partner nations: Italy Canada United States

In The Last Decade

Alessandro De Luca

107 papers receiving 2.9k citations

Peers

Countries citing papers authored by Alessandro De Luca

Since Specialization

Citations

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

Fields of papers citing papers by Alessandro De Luca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alessandro De Luca. 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 Alessandro De Luca. The network helps show where Alessandro De Luca may publish in the future.

Co-authorship network of co-authors of Alessandro De Luca

This figure shows the co-authorship network connecting the top 25 collaborators of Alessandro De Luca. A scholar is included among the top collaborators of Alessandro De Luca 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 Alessandro De Luca. Alessandro De Luca 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	Novel ATP2A2 Gene Mutation c.118G>A Causing Keratinocyte and Cardiomyocyte Disconnection in Darier Disease 2024 ·Biomedicines ·Andrea Frustaci,Alessandro De Luca,Romina Verardo,Valentina Guida,(unknown),Camilla Calvieri,Luigi Sansone,Matteo Antonio Russo,Cristina Chimenti	0
2	“Spazio Huntington”: Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats 2022 ·Journal of Personalized Medicine ·Federica Graziola,(unknown),(unknown),Giacomo Garone,Simone Migliore,Eugenia Scaricamazza,(unknown),(unknown),(unknown),Barbara D’Alessio,Alessandro De Luca,Giovanna Stefania Colafati,Umberto Sabatini,Alessandro Capuano,Ferdinando Squitieri	2
3	Sliding ureteral inguinal hernia 2022 ·International Journal of Surgery Case Reports ·(unknown),(unknown),Alessandro De Luca,(unknown),(unknown),Riccardo Caruso,Valentina Ferri,Benedetto Ielpo,(unknown)	2
4	Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings 2021 ·Clinical Genetics ·Alessandra D’Amico,Carmen L. Rosano,Luca Pannone,Valentina Pinna,(unknown),Marialetizia Motta,Lorenzo Ugga,Paola Daniele,(unknown),(unknown),Maria Siano,Claudia Santoro,Giulio Piluso,Simone Martinelli,Pietro Strisciuglio,Alessandro De Luca,Marco Tartaglia,Daniela Melis	5
5	The Global Emergency of Novel Coronavirus (SARS-CoV-2): An Update of the Current Status and Forecasting 2020 ·International Journal of Environmental Research and Public Health ·(unknown),Francesca Piceci‐Sparascio,(unknown),(unknown),René Roy,Daniela Scribano,Alessandro De Luca,Cecilia Ambrosi,Meysam Sarshar	51
6	Azidothymidine “Clicked” into 1,2,3-Triazoles: First Report on Carbonic Anhydrase–Telomerase Dual-Hybrid Inhibitors 2020 ·Journal of Medicinal Chemistry ·Emanuela Berrino,Andrea Angeli,Dmitry D. Zhdanov,(unknown),(unknown),Alessandro De Luca,Murat Bozdağ,Simone Carradori,Silvia Selleri,Gianluca Bartolucci,Thomas S. Peat,Marta Ferraroni,Claudiu T. Supuran,Fabrizio Carta	42
7	Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease 2018 ·Stem Cell Research ·(unknown),(unknown),Daniela Ferrari,(unknown),Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Simone Migliore,Ferdinando Squitieri,Angelo L. Vescovi,Jessica Rosati	1
8	Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage 2018 ·Stem Cell Research ·(unknown),(unknown),Daniela Ferrari,(unknown),Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Andrea Ilari,Ferdinando Squitieri,Angelo L. Vescovi,Jessica Rosati	6
9	Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease 2018 ·Stem Cell Research ·Jessica Rosati,(unknown),(unknown),Daniela Ferrari,Bárbara Torres,Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Ferdinando Squitieri,Angelo L. Vescovi	3
10	Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium 2015 ·Human Molecular Genetics ·José A. Caparrós‐Martín,Alessandro De Luca,François Cartault,Mona Aglan,Samia A. Temtamy,Ghada A. Otaify,(unknown),Eulalia Valencia,(unknown),(unknown),Julián Nevado,(unknown),Karen E. Heath,M. Cristina Digilio,Bruno Dallapiccola,Judith A. Goodship,Pleasantine Mill,Pablo Lapunzina,Víctor L. Ruiz‐Pérez	42
11	Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis 2012 ·European Journal of Medical Genetics ·(unknown),Isabella Torrente,Federica Consoli,Rosangela Ferese,(unknown),Laura Bernardini,Valentina Guida,M. Cristina Digilio,Bruno Marino,Bruno Dallapiccola,Alessandro De Luca	49
12	CArdiac Resynchronization In combination with BEta blocker treatment in advanced chronic Heart Failure (CARIBE-HF): the results of the CARIBE-HF study 2011 ·Acta cardiologica. Supplementum ·Aurelia Grosu,Michele Senni,Attilio Iacovoni,Mauro Gori,Francesco Cantù,(unknown),Tiziana De Santo,Alessandro De Luca,Antonello Gavazzi	8
13	Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion 2011 ·Neurogenetics ·Antonio Pizzuti,Irene Bottillo,Francesca Inzana,(unknown),Francesca Romana Buttarelli,Isabella Torrente,Anna Teresa Giallonardo,Alessandro De Luca,Bruno Dallapiccola	6
14	Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation 2009 ·Human Molecular Genetics ·Lothar Gremer,Alessandro De Luca,Torsten Merbitz-Zahradnik,Bruno Dallapiccola,Susanne Morlot,Marco Tartaglia,Kerstin Kutsche,Mohammad Reza Ahmadian,Georg Rosenberger	32
15	Xenografts of primary human gynecological tumors grown under the renal capsule of NOD/SCID mice show genetic stability during serial transplantation and respond to cytotoxic chemotherapy 2008 ·Gynecologic Oncology ·Joshua Z. Press,Jennifer Kenyon,Hui Xue,Melinda A. Miller,Alessandro De Luca,Dianne Miller,David G. Huntsman,C. Blake Gilks,Jessica N. McAlpine,Yuzhuo Wang	51
16	Functional analysis of splicing mutations in exon 7 of NF1gene 2007 ·BMC Medical Genetics ·Irene Bottillo,Alessandro De Luca,Annalisa Schirinzi,Valentina Guida,Isabella Torrente,Stefano Calvieri,Cristina Gervasini,Lidia Larizza,Antonio Pizzuti,Bruno Dallapiccola	27
17	Combinatorial Sequencing-by-Hybridization: Analysis of the NF1 Gene 2006 ·Genetic Testing ·Annalisa Schirinzi,Snezana Drmanac,Bruno Dallapiccola,Steve Huang,Kathryn Scott,Alessandro De Luca,Donald A. Swanson,Radoje Drmanac,Saul Surrey,Paolo Fortina	5
18	Validation of dHPLC for Molecular Diagnosis of β-Thalassemia in Southern Italy 2003 ·Genetic Testing ·Alessia Colosimo,Valentina Guida,(unknown),Alessandro De Luca,Giandomenico Palka,Luciana Rigoli,Anna Meo,(unknown),Bruno Dallapiccola	8
19	A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene 1999 ·Journal of Human Genetics ·Massimo Mangino,Isabella Torrente,Alessandro De Luca,Otto Sánchez,Bruno Dallapiccola,Giuseppe Novelli	20
20	Localization of a Gene for Familial Patella Aplasia-Hypoplasia (PTLAH) to Chromosome 17q21–22 1999 ·The American Journal of Human Genetics ·Massimo Mangino,Otto Sánchez,Isabella Torrente,Alessandro De Luca,Francesca Capon,Giuseppe Novelli,Bruno Dallapiccola	15

About Alessandro De Luca

Alessandro De Luca is a scholar working on Neurology, Genetics and Molecular Biology, having authored 113 papers that have together received 2.9k indexed citations. Recurring topics across this work include Congenital heart defects research (15 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurofibromatosis and Schwannoma Cases (13 papers). The work is most often cited by research in Rheumatology (433 citations), Neurology (378 citations) and Genetics (639 citations). Alessandro De Luca has collaborated with scholars based in Italy, Canada and United States. Frequent co-authors include Bruno Dallapiccola, Valentina Guida, Bruno Marino, M. Cristina Digilio, Melinda A. Miller, C. Blake Gilks, David G. Huntsman, Isabella Torrente, Federica Consoli and Torsten O. Nielsen. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Applied and Environmental Microbiology.

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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