Giangiorgio Crisponi

837 total citations
20 papers, 190 citations indexed

About

Giangiorgio Crisponi is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Giangiorgio Crisponi has authored 20 papers receiving a total of 190 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Oncology. Recurrent topics in Giangiorgio Crisponi's work include Cytokine Signaling Pathways and Interactions (5 papers), Hereditary Neurological Disorders (4 papers) and RNA Research and Splicing (4 papers). Giangiorgio Crisponi is often cited by papers focused on Cytokine Signaling Pathways and Interactions (5 papers), Hereditary Neurological Disorders (4 papers) and RNA Research and Splicing (4 papers). Giangiorgio Crisponi collaborates with scholars based in Italy, Germany and United Kingdom. Giangiorgio Crisponi's co-authors include A Corrias, Laura Crisponi, Rosa Maria Ibba, Giovanni Monni, Alessandra Meloni, Vassilios Fanos, Giuseppe Zampino, Loredana Boccone, Niranjan Thomas and Mara Marongiu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinica Chimica Acta and Journal of Medical Genetics.

In The Last Decade

Giangiorgio Crisponi

18 papers receiving 186 citations

Peers

Countries citing papers authored by Giangiorgio Crisponi

Since Specialization

Citations

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

Fields of papers citing papers by Giangiorgio Crisponi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giangiorgio Crisponi

This figure shows the co-authorship network connecting the top 25 collaborators of Giangiorgio Crisponi. A scholar is included among the top collaborators of Giangiorgio Crisponi 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 Giangiorgio Crisponi. Giangiorgio Crisponi 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

#	Title	Journal	Authors	Indexed citations
1	Do Rare Genetic Conditions Exhibit a Specific Phonotype? A Comprehensive Description of the Vocal Traits Associated with Crisponi/Cold-Induced Sweating Syndrome Type 1	Genes	Lucia D’Alatri, Claudia Manfredi et al.	1
2	Feeding and Nutritional Key Features of Crisponi/Cold-Induced Sweating Syndrome	Genes	Roberta Onesimo, Valentina Giorgio et al.	2
3	3MC syndrome: molecular findings in previously reported and milder patients expand the natural history and phenotypic spectrum	Clinical Dysmorphology	Rahat Perveen, Glenda M. Beaman et al.	0
4	Dental management in a patient with Crisponi/cold-induced sweating syndrome type 1: a case report	Clinical Dysmorphology	Giangiorgio Crisponi et al.	1
5	Genital anomalies in newborns	Journal of Perinatology	Vassilios Fanos, Giangiorgio Crisponi et al.	1
6	Congenital ocular anomalies in newborns: a practical atlas	SHILAP Revista de lepidopterología	Vassilios Fanos, Giangiorgio Crisponi et al.	1
7	Anomalies of the oral cavity in newborns	Journal of Perinatology	Vassilios Fanos, Giangiorgio Crisponi et al.	4
8	Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses	Clinical Genetics	Andrea Angius, Paolo Uva et al.	9
9	Crisponi/cold‐induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts	Clinical Genetics	Insa Buers, Ivana Persico et al.	11
10	New mutations in DYNC2H1 and WDR60 genes revealed by whole-exome sequencing in two unrelated Sardinian families with Jeune asphyxiating thoracic dystrophy	Clinica Chimica Acta	Carla Cossu, Alessandra Coiana et al.	13
11	Isolated ‘sign of the horns’: A simple, pathognomonic, prenatal sonographic marker of Crisponi syndrome	Journal of obstetrics and gynaecology research	Angelica Dessì, Vassilios Fanos et al.	8
12	Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders	European Journal of Human Genetics	Alessandra Meloni, Mara Marongiu et al.	32
13	Crisponi syndrome in an Indian patient: A rare differential diagnosis for neonatal tetanus	American Journal of Medical Genetics Part A	Niranjan Thomas, Sumita Danda et al.	12
14	A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosis.	PubMed	Giangiorgio Crisponi, Rossano Rossino et al.	0
15	Prenatal sonographic diagnosis of Klippel‐Trénaunay‐Weber syndrome with cardiac failure	Journal of Clinical Ultrasound	Maria Angelica Zoppi, Rosa Maria Ibba et al.	13
16	Two patients with varying combinations of sternal cleft, haemangiomas, midline abdominal raphe, coarctation of the aorta with a right aortic arch	Clinical Dysmorphology	Giangiorgio Crisponi, A Corrias et al.	8
17	Two sibs with Malpuech syndrome	American Journal of Medical Genetics	Giangiorgio Crisponi, A Corrias et al.	14
18	Autosomal recessive disorder with muscle contractions resembling neonatal tetanus, characteristic face, camptodactyly, hyperthermia, and sudden death: A new syndrome?	American Journal of Medical Genetics	Giangiorgio Crisponi	42
19	Color Doppler ultrasound and prenatal diagnosis of cleft palate	Journal of Clinical Ultrasound	Giovanni Monni, Rosa Maria Ibba et al.	9
20	X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.	Journal of Medical Genetics	G Filippi, A Rinaldi et al.	9

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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