G. Bartalini

676 total citations
16 papers, 332 citations indexed

About

G. Bartalini is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, G. Bartalini has authored 16 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in G. Bartalini's work include Genetics and Neurodevelopmental Disorders (5 papers), Neurofibromatosis and Schwannoma Cases (4 papers) and Tuberous Sclerosis Complex Research (3 papers). G. Bartalini is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Neurofibromatosis and Schwannoma Cases (4 papers) and Tuberous Sclerosis Complex Research (3 papers). G. Bartalini collaborates with scholars based in Italy, Belgium and Netherlands. G. Bartalini's co-authors include Paolo Balestri, A. Fois, Salvatore Grosso, Sergiusz Jóźwiak, G Morgese, Bernard A. Zonnenberg, Ans M.W. van den Ouweland, D. J. J. Halley, Dick Lindhout and Anthonie J. van Essen and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Human Genetics and Epilepsy Research.

In The Last Decade

G. Bartalini

15 papers receiving 324 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Bartalini Italy	12	129	111	106	49	43	16	332
Alina Kurolap Israel	12	118 0.9×	150 1.4×	89 0.8×	52 1.1×	24 0.6×	42	399
Krzysztof Sadowski Poland	11	52 0.4×	106 1.0×	191 1.8×	34 0.7×	72 1.7×	17	330
Moran Gal Israel	7	251 1.9×	188 1.7×	35 0.3×	21 0.4×	61 1.4×	9	439
Weiyue Gu China	11	101 0.8×	139 1.3×	47 0.4×	21 0.4×	32 0.7×	50	317
Karin Weiss Israel	13	190 1.5×	188 1.7×	86 0.8×	17 0.3×	14 0.3×	36	433
Christina Rudduck Australia	14	111 0.9×	233 2.1×	23 0.2×	43 0.9×	96 2.2×	26	442
Dariusz Kuczyński Poland	6	93 0.7×	100 0.9×	286 2.7×	22 0.4×	109 2.5×	12	399
Shobha Varma United States	7	64 0.5×	61 0.5×	30 0.3×	15 0.3×	65 1.5×	8	345
Maya Chopra United States	11	174 1.3×	151 1.4×	110 1.0×	7 0.1×	57 1.3×	25	406
Arum Oh South Korea	7	91 0.7×	109 1.0×	38 0.4×	46 0.9×	11 0.3×	18	247

Countries citing papers authored by G. Bartalini

Since Specialization

Citations

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

Fields of papers citing papers by G. Bartalini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Bartalini

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

All Works

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16 of 16 papers shown

Fogarasi, András, Liesbeth De Waele, G. Bartalini, et al.. (2016). EFFECTS: an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex. BMC Neurology. 16(1). 126–126. 15 indexed citations

Artini, Paolo Giovanni, Francesca Papini, María Ruggiero, et al.. (2011). Genetic screening in Italian infertile couples undergoing intrauterine insemination andin vitrofertilization techniques: a multicentric study. Gynecological Endocrinology. 27(7). 453–457. 5 indexed citations

Galluzzi, Paolo, Michele Sacchini, G. Bartalini, et al.. (2011). LBSL (leukoencephalopathy with brain stem and spinal cord involvement and high lactate) without sparing of the u-fibers and globi pallidi: A case report. European Journal of Radiology Extra. 79(2). e73–e76. 5 indexed citations

Nellist, Mark, Diana van den Heuvel, Miriam Goedbloed, et al.. (2008). Missense mutations to the TSC1 gene cause tuberous sclerosis complex. European Journal of Human Genetics. 17(3). 319–328. 21 indexed citations

Grosso, Salvatore, Lucia Pucci, Paolo Curatolo, et al.. (2008). Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. Epilepsy Research. 79(1). 63–70. 12 indexed citations

Grosso, Salvatore, Lucia Pucci, G. Bartalini, et al.. (2006). Photoparoxysmal responses in children with chromosomal aberrations. Epilepsy Research. 72(2-3). 164–170. 5 indexed citations

Grosso, Salvatore, Lucia Pucci, Rosanna Maria Di Bartolo, et al.. (2005). Chromosome 18 aberrations and epilepsy: A review. American Journal of Medical Genetics Part A. 134A(1). 88–94. 20 indexed citations

Grosso, Salvatore, Rosanna Maria Di Bartolo, Rosario Berardi, et al.. (2004). Electroencephalographic and Epileptic Patterns in X Chromosome Anomalies. Journal of Clinical Neurophysiology. 21(4). 249–253. 28 indexed citations

Grosso, Salvatore, M. A. Farnetani, Rosario Berardi, et al.. (2002). Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasia. American Journal of Medical Genetics Part A. 120A(1). 88–91. 34 indexed citations

10.

Grosso, Salvatore, Paolo Balestri, Cecilia Anichini, et al.. (2001). Pubertal disorders in inv dup(15) syndrome. Gynecological Endocrinology. 15(3). 165–169. 11 indexed citations

11.

Verhoef, Senno, Tadeusz Mazurczak, Sergiusz Jóźwiak, et al.. (1999). High Rate of Mosaicism in Tuberous Sclerosis Complex. The American Journal of Human Genetics. 64(6). 1632–1637. 121 indexed citations

12.

Balestri, Paolo, et al.. (1993). Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1. Child s Nervous System. 9(8). 448–451. 14 indexed citations

13.

Fois, A., Paolo Balestri, G. Bartalini, et al.. (1993). Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): A follow-up study. European Journal of Pediatrics. 152(6). 500–504. 16 indexed citations

14.

Bartalini, G., Maria Margollicci, Paolo Balestri, et al.. (1992). Biochemical diagnosis of Canavan disease. Child s Nervous System. 8(8). 468–470. 11 indexed citations

15.

Bartalini, G., Paolo Balestri, A Figus, et al.. (1991). Molecular study in von Recklinghausen neurofibromatosis (NF1). Child s Nervous System. 7(2). 98–9.

16.

Fois, A., M. Cioni, Paolo Balestri, et al.. (1986). Biotinidase deficiency: metabolites in CSF. Journal of Inherited Metabolic Disease. 9(3). 284–285. 14 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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