C. Angelini

University of Pisa (IT)

Research Areas

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H-index

108

Publications

1827

Citations

51469

i10-index

732

Publications & Citations Over Time

Top Cited Publications

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Title	Year	Citations
Assessment of mitochondrial respiratory chain enzy...	2012	991
Dysferlin, a novel skeletal muscle gene, is mutate...	1998	916
Carnitine Deficiency of Human Skeletal Muscle with...	1973	510
MELAS: Clinical features, biochemistry, and molecu...	1992	507
MELAS mutation in mtDNA binding site for transcrip...	1992	495
β–sarcoglycan (A3b) mutations cause autosomal rece...	1995	446
Exploring the molecular basis for variability amon...	1991	401
Gene for chronic proximal spinal muscular atrophie...	1990	397
229th ENMC international workshop: Limb girdle mus...	2018	374
Nuclear envelope dystrophies show a transcriptiona...	2006	323

Publications

1.
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells
Year: 2012Citations: 991DOI: 10.1038/nprot.2012.058
2.
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Year: 1998Citations: 916DOI: 10.1038/1682
3.
Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome
Year: 1973Citations: 510DOI: 10.1126/science.179.4076.899
4.
MELAS: Clinical features, biochemistry, and molecular genetics
Year: 1992Citations: 507DOI: 10.1002/ana.410310408
5.
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.
Year: 1992Citations: 495DOI: 10.1073/pnas.89.10.4221
6.
β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
Year: 1995Citations: 446DOI: 10.1038/ng1195-266
7.
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
Year: 1991Citations: 401
8.
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q
Year: 1990Citations: 397DOI: 10.1038/344767a0
9.
229th ENMC international workshop: Limb girdle muscular dystrophies – Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017
Year: 2018Citations: 374DOI: 10.1016/j.nmd.2018.05.007
10.
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration
Year: 2006Citations: 323DOI: 10.1093/brain/awl023

About C. Angelini

C. Angelini is a researcher with 1827 publications and 51469 citations. They are affiliated with University of Pisa. Their research focuses on . With an h-index of 108, they are among the top researchers in their field.

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Distribution of citations across publications

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Impact Metrics Over Time

Citations per publication by year