Alessandro De Luca

6.8k citations

113 papers · 2.9k indexed · h-index 31

Rheumatology top 2%
Neurology top 5%
- Neurofibromatosis and Schwannoma Cases 13
Genetics top 5%
- Genetic Syndromes and Imprinting 8
Molecular Biology top 5%
- Congenital heart defects research 15
- Protein Tyrosine Phosphatases 12
- RNA modifications and cancer 8
Reproductive Medicine top 5%
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 13
Epidemiology
- Congenital Heart Disease Studies 7
Pulmonary and Respiratory Medicine
- Sarcoma Diagnosis and Treatment 7

Co-authors: Bruno Dallapiccola Valentina Guida Bruno Marino M. Cristina Digilio Melinda A. Miller C. Blake Gilks David G. Huntsman Isabella Torrente
Cited by: Rheumatology Neurology Genetics
Journals: Proceedings of the National Academy of Sciences (1 paper)SHILAP Revista de lepidopterología (2 papers)Applied and Environmental Microbiology (1 paper)
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

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

All Works

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20 of 20 papers shown

#	Work
1	Novel ATP2A2 Gene Mutation c.118G>A Causing Keratinocyte and Cardiomyocyte Disconnection in Darier Disease Biomedicines ·Andrea Frustaci,Alessandro De Luca,Romina Verardo,Valentina Guida,Maria Alfarano,Camilla Calvieri,Luigi Sansone,Matteo Antonio Russo,Cristina Chimenti	2024	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 Journal of Personalized Medicine ·Federica Graziola,Sabrina Maffi,Melissa Grasso,Giacomo Garone,Simone Migliore,Eugenia Scaricamazza,Consuelo Ceccarelli,Melissa Casella,Ludovica Busi,Barbara D’Alessio,Alessandro De Luca,Giovanna Stefania Colafati,Umberto Sabatini,Alessandro Capuano,Ferdinando Squitieri	2022	2
3	Sliding ureteral inguinal hernia International Journal of Surgery Case Reports ·R. Isernia,Giuseppe Massimiliano De Luca,Alessandro De Luca,Lucia Franzoso,Lorenzo Ramon Navazio,Riccardo Caruso,Valentina Ferri,Benedetto Ielpo,Simone Giungato	2022	2
4	Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings Clinical Genetics ·Alessandra D’Amico,Carmen L. Rosano,Luca Pannone,Valentina Pinna,Antonia Assunto,Marialetizia Motta,Lorenzo Ugga,Paola Daniele,Roberta Mandile,Lucio Mariniello,Maria Siano,Claudia Santoro,Giulio Piluso,Simone Martinelli,Pietro Strisciuglio,Alessandro De Luca,Marco Tartaglia,Daniela Melis	2021	5
5	The Global Emergency of Novel Coronavirus (SARS-CoV-2): An Update of the Current Status and Forecasting International Journal of Environmental Research and Public Health ·Hossein Hozhabri,Francesca Piceci‐Sparascio,Hamidreza Sohrabi,Leila Mousavifar,René Roy,Daniela Scribano,Alessandro De Luca,Cecilia Ambrosi,Meysam Sarshar	2020	51
6	Azidothymidine “Clicked” into 1,2,3-Triazoles: First Report on Carbonic Anhydrase–Telomerase Dual-Hybrid Inhibitors Journal of Medicinal Chemistry ·Emanuela Berrino,Andrea Angeli,Dmitry D. Zhdanov,Anna P. Kiryukhina,Andrea Milaneschi,Alessandro De Luca,Murat Bozdağ,Simone Carradori,Silvia Selleri,Gianluca Bartolucci,Thomas S. Peat,Marta Ferraroni,Claudiu T. Supuran,Fabrizio Carta	2020	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 Stem Cell Research ·Giovannina Rotundo,Eris Bidollari,Daniela Ferrari,Iolanda Spasari,Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Simone Migliore,Ferdinando Squitieri,Angelo L. Vescovi,Jessica Rosati	2018	1
8	Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage Stem Cell Research ·Eris Bidollari,Giovannina Rotundo,Daniela Ferrari,Ornella Candido,Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Andrea Ilari,Ferdinando Squitieri,Angelo L. Vescovi,Jessica Rosati	2018	6
9	Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease Stem Cell Research ·Jessica Rosati,Eris Bidollari,Giovannina Rotundo,Daniela Ferrari,Bárbara Torres,Laura Bernardini,Federica Consoli,Alessandro De Luca,Iolanda Santimone,Giuseppe Lamorte,Ferdinando Squitieri,Angelo L. Vescovi	2018	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 Human Molecular Genetics ·José A. Caparrós‐Martín,Alessandro De Luca,François Cartault,Mona Aglan,Samia A. Temtamy,Ghada A. Otaify,Mennat Mehrez,Eulalia Valencia,Laura Vázquez,Jean-Luc Alessandri,Julián Nevado,Inmaculada Rueda‐Arenas,Karen E. Heath,M. Cristina Digilio,Bruno Dallapiccola,Judith A. Goodship,Pleasantine Mill,Pablo Lapunzina,Víctor L. Ruiz‐Pérez	2015	42
11	Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis European Journal of Medical Genetics ·Maria Cecilia D’Asdia,Isabella Torrente,Federica Consoli,Rosangela Ferese,Monia Magliozzi,Laura Bernardini,Valentina Guida,M. Cristina Digilio,Bruno Marino,Bruno Dallapiccola,Alessandro De Luca	2012	49
12	CArdiac Resynchronization In combination with BEta blocker treatment in advanced chronic Heart Failure (CARIBE-HF): the results of the CARIBE-HF study Acta cardiologica. Supplementum ·Aurelia Grosu,Michele Senni,Attilio Iacovoni,Mauro Gori,Francesco Cantù,Silvia Bisetti,Tiziana De Santo,Alessandro De Luca,Antonello Gavazzi	2011	8
13	Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion Neurogenetics ·Antonio Pizzuti,Irene Bottillo,Francesca Inzana,Valentina Lanari,Francesca Romana Buttarelli,Isabella Torrente,Anna Teresa Giallonardo,Alessandro De Luca,Bruno Dallapiccola	2011	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 Human Molecular Genetics ·Lothar Gremer,Alessandro De Luca,Torsten Merbitz-Zahradnik,Bruno Dallapiccola,Susanne Morlot,Marco Tartaglia,Kerstin Kutsche,Mohammad Reza Ahmadian,Georg Rosenberger	2009	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 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	2008	51
16	Functional analysis of splicing mutations in exon 7 of NF1gene BMC Medical Genetics ·Irene Bottillo,Alessandro De Luca,Annalisa Schirinzi,Valentina Guida,Isabella Torrente,Stefano Calvieri,Cristina Gervasini,Lidia Larizza,Antonio Pizzuti,Bruno Dallapiccola	2007	27
17	Combinatorial Sequencing-by-Hybridization: Analysis of the NF1 Gene Genetic Testing ·Annalisa Schirinzi,Snezana Drmanac,Bruno Dallapiccola,Steve Huang,Kathryn Scott,Alessandro De Luca,Donald A. Swanson,Radoje Drmanac,Saul Surrey,Paolo Fortina	2006	5
18	Validation of dHPLC for Molecular Diagnosis of β-Thalassemia in Southern Italy Genetic Testing ·Alessia Colosimo,Valentina Guida,Anna Scolari,Alessandro De Luca,Giandomenico Palka,Luciana Rigoli,Anna Meo,D. C. Salpietro,Bruno Dallapiccola	2003	8
19	A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene Journal of Human Genetics ·Massimo Mangino,Isabella Torrente,Alessandro De Luca,Otto Sánchez,Bruno Dallapiccola,Giuseppe Novelli	1999	20
20	Localization of a Gene for Familial Patella Aplasia-Hypoplasia (PTLAH) to Chromosome 17q21–22 The American Journal of Human Genetics ·Massimo Mangino,Otto Sánchez,Isabella Torrente,Alessandro De Luca,Francesca Capon,Giuseppe Novelli,Bruno Dallapiccola	1999	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), Neurofibromatosis and Schwannoma Cases (13 papers), Protein Tyrosine Phosphatases (12 papers), Genetic Syndromes and Imprinting (8 papers), RNA modifications and cancer (8 papers), Congenital Heart Disease Studies (7 papers) and Sarcoma Diagnosis and Treatment (7 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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