Lorenzo Sinibaldi

2.5k total citations
46 papers, 1.5k citations indexed

About

Lorenzo Sinibaldi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lorenzo Sinibaldi has authored 46 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lorenzo Sinibaldi's work include Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Functional Brain Connectivity Studies (6 papers). Lorenzo Sinibaldi is often cited by papers focused on Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Functional Brain Connectivity Studies (6 papers). Lorenzo Sinibaldi collaborates with scholars based in Italy, United States and Lebanon. Lorenzo Sinibaldi's co-authors include Bruno Dallapiccola, Marco Castori, Gianluca Ursini, Giuseppe Blasi, Alessandro Bertolino, Grazia Caforio, Paolo Taurisano, Teresa Popolizio, Annabella Di Giorgio and Leonardo Fazio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Lorenzo Sinibaldi

44 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lorenzo Sinibaldi Italy	20	509	447	414	290	284	46	1.5k
Janine A. Lamb United Kingdom	25	937 1.8×	928 2.1×	673 1.6×	124 0.4×	187 0.7×	56	2.6k
Giovanni Lanzi Italy	28	248 0.5×	554 1.2×	374 0.9×	549 1.9×	239 0.8×	62	2.0k
Kiran K. Mantripragada United Kingdom	22	853 1.7×	773 1.7×	274 0.7×	241 0.8×	87 0.3×	41	1.8k
Maria T. Acosta United States	20	253 0.5×	386 0.9×	333 0.8×	273 0.9×	163 0.6×	63	1.3k
Pablo V. Gejman United States	28	980 1.9×	1.5k 3.4×	186 0.4×	288 1.0×	507 1.8×	58	3.4k
Carlo Cianchetti Italy	26	250 0.5×	764 1.7×	315 0.8×	698 2.4×	466 1.6×	103	2.4k
Ryoichi Sakuta Japan	22	408 0.8×	841 1.9×	256 0.6×	359 1.2×	194 0.7×	59	1.7k
Domenica Battaglia Italy	27	702 1.4×	563 1.3×	288 0.7×	1.2k 4.3×	414 1.5×	115	2.3k
Helen Petropoulos United States	22	169 0.3×	556 1.2×	525 1.3×	249 0.9×	163 0.6×	35	1.7k
Gabrielle Rudolf France	24	592 1.2×	698 1.6×	394 1.0×	658 2.3×	708 2.5×	69	2.1k

Countries citing papers authored by Lorenzo Sinibaldi

Since Specialization

Citations

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

Fields of papers citing papers by Lorenzo Sinibaldi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorenzo Sinibaldi

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Travaglini, Lorena, Marina Macchiaiolo, Giacomo Garone, et al.. (2024). Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes. 15(4). 508–508.

Calcagni, Giulio, Federica Ferrigno, Maria Lisa Dentici, et al.. (2024). Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome. Diagnostics. 14(6). 594–594. 1 indexed citations

Garone, Giacomo, Alessandro Capuano, Flaminia Frascarelli, et al.. (2024). Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology. Parkinsonism & Related Disorders. 126. 107057–107057. 4 indexed citations

Onesimo, Roberta, Valentina Trevisan, Chiara Leoni, et al.. (2023). From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome. Genes. 14(10). 1843–1843. 6 indexed citations

Trivisano, Marina, Fabrizia Stregapede, Alessia Micalizzi, et al.. (2023). Refining of the electroclinical phenotype in familial and sporadic cases of CSNK2B-related Neurodevelopmental Syndrome. Epilepsy & Behavior. 147. 109436–109436. 1 indexed citations

Iarossi, Giancarlo, Lorenzo Sinibaldi, Chiara Passarelli, et al.. (2022). A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients. Diagnostics. 12(9). 2183–2183. 2 indexed citations

Squeo, Gabriella Maria, Tommaso Mazza, Stefano Castellana, et al.. (2022). Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed case. Journal of Human Genetics. 67(9). 547–551. 5 indexed citations

Alfieri, Paolo, Lorenzo Sinibaldi, Giovanni Valeri, et al.. (2020). Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases. Genes Brain & Behavior. 19(7). e12687–e12687. 5 indexed citations

Cocciadiferro, Dario, Emanuele Agolini, M. Cristina Digilio, et al.. (2020). The splice c.1815G>A variant in KIAA0586 results in a phenotype bridging short-rib-polydactyly and oral-facial-digital syndrome. Medicine. 99(8). e19169–e19169. 6 indexed citations

10.

Dentici, Maria Lisa, Paola De Rose, Viola Alesi, et al.. (2020). 7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling. Brain Sciences. 10(11). 839–839. 5 indexed citations

11.

Baeza‐Velasco, Carolina, Lorenzo Sinibaldi, & Marco Castori. (2018). Attention-deficit/hyperactivity disorder, joint hypermobility-related disorders and pain: expanding body-mind connections to the developmental age. ADHD Attention Deficit and Hyperactivity Disorders. 10(3). 163–175. 28 indexed citations

12.

Sinibaldi, Lorenzo, Gianluca Ursini, & Marco Castori. (2015). Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers–Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revised. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 97–106. 55 indexed citations

13.

Pasini, Augusto, Lorenzo Sinibaldi, Claudio Paloscia, et al.. (2013). Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: A longitudinal open label trial. European Journal of Paediatric Neurology. 17(4). 407–414. 26 indexed citations

14.

Ursini, Gianluca, Valentina Bollati, Leonardo Fazio, et al.. (2011). Stress-Related Methylation of the Catechol- O -Methyltransferase Val ¹⁵⁸ Allele Predicts Human Prefrontal Cognition and Activity. Journal of Neuroscience. 31(18). 6692–6698. 143 indexed citations

15.

Sinibaldi, Lorenzo, Ghita Harifi, Irene Bottillo, et al.. (2010). A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathy.. PubMed. 28(2). 153–7. 29 indexed citations

16.

Bertolino, Alessandro, Paolo Taurisano, Giuseppe Blasi, et al.. (2010). Genetically Determined Measures of Striatal D2 Signaling Predict Prefrontal Activity during Working Memory Performance. PLoS ONE. 5(2). e9348–e9348. 73 indexed citations

17.

Bertolino, Alessandro, Leonardo Fazio, Annabella Di Giorgio, et al.. (2009). Genetically Determined Interaction between the Dopamine Transporter and the D₂Receptor on Prefronto-Striatal Activity and Volume in Humans. Journal of Neuroscience. 29(4). 1224–1234. 86 indexed citations

18.

Sinibaldi, Lorenzo, Laura Bernardini, Roberto De Simone, et al.. (2007). Duplication 18q21.31‐q22.2. American Journal of Medical Genetics Part A. 143A(4). 343–348. 23 indexed citations

19.

Bertolino, Alessandro, Giuseppe Blasi, Valeria Latorre, et al.. (2006). Additive Effects of Genetic Variation in Dopamine Regulating Genes on Working Memory Cortical Activity in Human Brain. Journal of Neuroscience. 26(15). 3918–3922. 172 indexed citations

20.

Novelli, Antonio, Enza Maria Valente, Laura Bernardini, et al.. (2004). Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian family. European Journal of Human Genetics. 12(7). 579–583. 10 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.

Explore authors with similar magnitude of impact