G Danieli

676 total citations
20 papers, 487 citations indexed

About

G Danieli is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, G Danieli has authored 20 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in G Danieli's work include Muscle Physiology and Disorders (9 papers), Genetic Neurodegenerative Diseases (4 papers) and Cardiomyopathy and Myosin Studies (3 papers). G Danieli is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Genetic Neurodegenerative Diseases (4 papers) and Cardiomyopathy and Myosin Studies (3 papers). G Danieli collaborates with scholars based in Italy, United States and Germany. G Danieli's co-authors include C. Angelini, C. Angelini, Maria Luisa Mostacciuolo, M.L. Mostacciuolo, Marta Miorin, Manuela Miorelli, C Villanova, Paola Melacini, M.P. Freda and G Fasoli and has published in prestigious journals such as The Lancet, Circulation and Genomics.

In The Last Decade

G Danieli

19 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G Danieli Italy	10	348	166	137	87	56	20	487
T. Voit Germany	13	304 0.9×	77 0.5×	109 0.8×	73 0.8×	42 0.8×	32	547
P. E. Becker Germany	11	269 0.8×	83 0.5×	117 0.9×	59 0.7×	25 0.4×	23	450
Barbara Merico Italy	5	272 0.8×	102 0.6×	87 0.6×	72 0.8×	30 0.5×	6	339
N Télerman-Toppet Belgium	13	351 1.0×	62 0.4×	137 1.0×	77 0.9×	46 0.8×	40	581
C. Sewry United Kingdom	11	382 1.1×	122 0.7×	103 0.8×	69 0.8×	52 0.9×	14	546
M. Wohlgemuth Netherlands	9	338 1.0×	103 0.6×	88 0.6×	109 1.3×	40 0.7×	9	450
J. J. Fulthorpe United Kingdom	11	285 0.8×	94 0.6×	69 0.5×	47 0.5×	46 0.8×	16	464
Satoshi Kuru Japan	12	336 1.0×	108 0.7×	90 0.7×	122 1.4×	47 0.8×	49	527
D Fontan France	14	271 0.8×	67 0.4×	149 1.1×	62 0.7×	79 1.4×	43	719
P.F. Ippel Netherlands	12	486 1.4×	121 0.7×	329 2.4×	69 0.8×	53 0.9×	25	659

Countries citing papers authored by G Danieli

Since Specialization

Citations

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

Fields of papers citing papers by G Danieli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Danieli

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

Smaniotto, Gessica, Paola Melacini, Chiara Calore, et al.. (2009). Screening of the four genes most commonly involved in hypertrophic cardiomyopathy.. 543. 1 indexed citations

Menditto, Vincenzo G., et al.. (2002). Coagulative modifications in patients with systemic sclerosis treated with iloprost or nifedipine.. PubMed. 16(3). 170–4. 7 indexed citations

Toffolatti, L., Barbara Cardazzo, Carlo Nobile, et al.. (2002). Investigating the Mechanism of Chromosomal Deletion: Characterization of 39 Deletion Breakpoints in Introns 47 and 48 of the Human Dystrophin Gene. Genomics. 80(5). 523–530. 5 indexed citations

Stephan, Douglas W., et al.. (1997). Chromosome assignment of 115 expressed sequence tags (ESTs) from human skeletal muscle. Cytogenetic and Genome Research. 76(3-4). 144–152. 5 indexed citations

Gabrielli, Armando, Paola Sambo, Silvana Savoldi, et al.. (1996). Humoral immune response and natural killer activity in patients with mixed cryoglobulinemia.. PubMed. 13 Suppl 13. S95–9. 7 indexed citations

Melacini, Paola, G Danieli, C Villanova, et al.. (1996). Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy. Circulation. 94(12). 3168–3175. 139 indexed citations

Toscano, António, Libero Vitiello, Giacomo P. Comi, et al.. (1995). Duplication of dystrophin gene and dissimilar clinical phenotype in the same family. Neuromuscular Disorders. 5(6). 475–481. 7 indexed citations

Mostacciuolo, M.L., et al.. (1995). Frequency of Duplication at 17p11.2 in Families of Northeast Italy with Charcot-Marie-Tooth Disease Type 1. Neuroepidemiology. 14(2). 49–53. 16 indexed citations

Novelli, Giuseppe, Massimo Gennarelli, E. Menegazzo, et al.. (1993). (CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients. Biochemical Medicine and Metabolic Biology. 50(1). 85–92. 47 indexed citations

10.

Mostacciuolo, Maria Luisa, Marta Miorin, Elena Pegoraro, et al.. (1993). Reappraisal of the Incidence Rate of Duchenne and Becker Muscular Dystrophies on the Basis of Molecular Diagnosis. Neuroepidemiology. 12(6). 326–330. 20 indexed citations

11.

Mostacciuolo, M.L., et al.. (1992). Epidemiology of Spinal Muscular Atrophies in a Sample of the Italian Population. Neuroepidemiology. 11(1). 34–38. 35 indexed citations

12.

Kausch, Katrin, Frank Kullmann, M.L. Mostacciuolo, et al.. (1992). Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene. Neuromuscular Disorders. 2(2). 111–115. 7 indexed citations

13.

Barbujani, Guido, et al.. (1990). Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases. Human Genetics. 84(6). 522–6. 41 indexed citations

14.

Danieli, G, et al.. (1980). Duchenne muscular dystrophy. Human Genetics. 54(1). 63–68. 13 indexed citations

15.

Danieli, G, et al.. (1977). Duchenne muscular dystrophy. Human Genetics. 35(2). 225–231. 35 indexed citations

16.

Danieli, G, et al.. (1977). Duchenne muscular dystrophy. A population study.. Human Genetics. 35(2). 225–31. 35 indexed citations

17.

Danieli, G & C. Angelini. (1976). DUCHENNE CARRIER DETECTION. The Lancet. 308(7976). 90–90. 59 indexed citations

18.

Danieli, G, C. De Vecchi, & C. Angelini. (1974). Geographic distribution of hereditary myopathies in northeast Italy. Social Biology. 21(3). 235–241. 6 indexed citations

19.

Danieli, G, et al.. (1972). Immune reactions in chronic myeloid leukaemia.. PubMed. 57(11). 697–707.

20.

Danieli, G, M Montroni, & Shirley Shizue Nagata Pignatari. (1969). [Immunoglobulins and paraproteins].. PubMed. 50(11). 1093–108. 2 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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