Franco Laccone

4.8k total citations
118 papers, 2.9k citations indexed

About

Franco Laccone is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Franco Laccone has authored 118 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 51 papers in Genetics and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Franco Laccone's work include Genetics and Neurodevelopmental Disorders (25 papers), Genetic Neurodegenerative Diseases (22 papers) and Mitochondrial Function and Pathology (20 papers). Franco Laccone is often cited by papers focused on Genetics and Neurodevelopmental Disorders (25 papers), Genetic Neurodegenerative Diseases (22 papers) and Mitochondrial Function and Pathology (20 papers). Franco Laccone collaborates with scholars based in Austria, Germany and United States. Franco Laccone's co-authors include Peter Huppke, F. Hanefeld, J. Dichgans, Michael Abele, Thomas Klockgether, Katrin Bürk, Moritz Meins, Thorsten Schmidt, Olaf Rieß and Lüdger Schöls and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Franco Laccone

108 papers receiving 2.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Franco Laccone Austria 29 1.8k 1.2k 1.1k 597 533 118 2.9k
Kathie M. Bishop United States 25 2.6k 1.5× 1.1k 0.9× 648 0.6× 654 1.1× 346 0.6× 53 4.2k
Esther de Graaff Netherlands 35 2.4k 1.3× 605 0.5× 2.1k 1.9× 668 1.1× 842 1.6× 61 4.4k
Montserrat Milà Spain 34 2.2k 1.2× 511 0.4× 1.8k 1.6× 229 0.4× 934 1.8× 140 4.0k
Vinodh Narayanan United States 25 1.2k 0.7× 418 0.4× 749 0.7× 157 0.3× 398 0.7× 67 2.3k
Sakkubai Naidu United States 33 3.2k 1.8× 351 0.3× 1.0k 0.9× 221 0.4× 645 1.2× 80 4.4k
Gabrielle Rudolf France 24 698 0.4× 708 0.6× 592 0.5× 316 0.5× 394 0.7× 69 2.1k
Klaus Wagner Austria 23 1.5k 0.8× 856 0.7× 563 0.5× 601 1.0× 104 0.2× 61 2.9k
Hideki Enomoto Japan 39 2.2k 1.2× 1.6k 1.4× 710 0.6× 340 0.6× 137 0.3× 68 5.5k
Bert van der Zwaag Netherlands 23 1.2k 0.7× 372 0.3× 704 0.6× 161 0.3× 200 0.4× 44 2.2k
Pablo V. Gejman United States 28 1.5k 0.9× 507 0.4× 980 0.9× 147 0.2× 186 0.3× 58 3.4k

Countries citing papers authored by Franco Laccone

Since Specialization
Citations

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

Fields of papers citing papers by Franco Laccone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franco Laccone

This figure shows the co-authorship network connecting the top 25 collaborators of Franco Laccone. A scholar is included among the top collaborators of Franco Laccone 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 Franco Laccone. Franco Laccone is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Rehder, Helga, Christine Bärtsch, Bárbara Fritz, et al.. (2024). Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one case. Orphanet Journal of Rare Diseases. 19(1). 114–114.
3.
Vodopiutz, Julia, et al.. (2023). Leri–Weill Dyschondrosteosis Caused by a Leaky Homozygous SHOX Splice-Site Variant. Genes. 14(4). 877–877. 2 indexed citations
4.
Rehder, Helga, Susanne Gerit Kircher, Katharina Schoner, et al.. (2023). Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations. Orphanet Journal of Rare Diseases. 18(1). 57–57. 2 indexed citations
5.
Ponleitner, Markus, Manfred Hecking, Senta Graf, et al.. (2023). Phenotyping of a novel COL4A4 and novel GLA variant in a patient presenting with microhematuria and mildly impaired kidney function: a case report. Frontiers in Genetics. 14. 1211858–1211858.
6.
Pees, Christiane, Daniel Zimpfer, Sonja Radaković, et al.. (2022). Autosomal recessive cutis laxa type Ib—Successful redo aortic root and arch replacement. SHILAP Revista de lepidopterología. 10(12). e6573–e6573. 1 indexed citations
7.
Çetin, Hakan, David T. Liu, Franco Laccone, et al.. (2022). A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation. Human Genetics. 142(8). 1077–1089. 3 indexed citations
8.
Schoner, Katharina, Martina Witsch‐Baumgartner, R. Bald, et al.. (2019). Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern. Birth Defects Research. 112(2). 175–185. 14 indexed citations
9.
Raimann, Adalbert, Julian C. Lui, Paul Roschger, et al.. (2019). De novo Missense Mutation in SP7 in a Patient with Cranial Hyperostosis, Long Bone Fragility, and Increased Osteoblast Number. 92. 2 indexed citations
10.
Ilenčíková, Denisa, et al.. (2018). Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation. Pediatric Blood & Cancer. 66(4). e27589–e27589. 15 indexed citations
11.
Rehder, Helga, Franco Laccone, Susanne Gerit Kircher, et al.. (2018). Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB‐related skeletal disorders in three fetuses and a 106‐year‐old exhibit. American Journal of Medical Genetics Part A. 176(7). 1559–1568. 2 indexed citations
12.
Raimann, Adalbert, et al.. (2016). A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up. Hormone Research in Paediatrics. 87(3). 196–204. 6 indexed citations
13.
Steinkellner, Hannes, Julia Etzler, Bernhard Gmeiner, & Franco Laccone. (2015). Detection of Survival Motor Neuron Protein in Buccal Cells Through Electrochemiluminescence-Based Assay. Assay and Drug Development Technologies. 13(3). 167–173. 6 indexed citations
14.
Steinkellner, Hannes, Julia Etzler, Jürgen Neesen, et al.. (2014). Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome. European Journal of Human Genetics. 23(9). 1186–1191. 11 indexed citations
15.
Engel, Wolfgang, Franco Laccone, & U. Sancken. (2004). Das väterliche Alter aus humangenetischer Sicht. Journal für Kardiologie (Krause & Pachernegg GmbH). 1(4). 263–267. 2 indexed citations
16.
Zoll, Barbara, Katrin Lange, Peter Gabriel, et al.. (2002). Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10. Human Mutation. 21(1). 98–98. 37 indexed citations
17.
Laccone, Franco, et al.. (2000). Klinik und Genetik des Williams-Beuren-Syndroms. Klinische Pädiatrie. 212(6). 299–307.
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Laccone, Franco, Ulrike Engel, Elke Holinski‐Feder, et al.. (1999). DNA analysis of Huntington's disease: five year experience in Germany, Austria and Switzerland (1993-1997). University of Regensburg Publication Server (University of Regensburg). 1 indexed citations
20.
Schubert, Stephanie, Franco Laccone, & I. Hansmann. (1994). Towards positional cloning of the locus for benign neonatal epilepsy (EBN1) on chromosome 20. The American Journal of Human Genetics. 55. 1 indexed citations

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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