Cinzia Cameli

406 citations
14 papers · 254 · h-index 10

Impact in

    • Migraine and Headache Studies
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Autism Spectrum Disorder Research 9
    • Genomic variations and chromosomal abnormalities 6
    • Genetics and Neurodevelopmental Disorders 5

Cinzia Cameli

14 papers receiving 253 citations

Peers

Cinzia Cameli
Comparison fields: 5 of 61
  • Psychiatry and Mental health 49
  • Genetics 86
  • Cognitive Neuroscience 55
  • Cellular and Molecular Neuroscience 28
  • Endocrine and Autonomic Systems 9
Replace Delphine Bernoux with:
Delphine Bernoux France
Aneek Das Bhowmik India
Rena Vanzo United States
Amaia Muñoz‐Lopetegi Spain
Bàrbara Torrico Spain
Calwing Liao Canada
Madeleine Fannemel Norway
Alexander J. Sandweiss United States
Yoko Sugie Japan
Raúl Alelú‐Paz Spain
Cinzia Cameli relative to Delphine Bernoux France Delphine Bernoux's profile →
Citations per field
00.5×1.5×1.9×
Delphine Bernoux · 1×
Citations per year

Countries citing papers authored by Cinzia Cameli

Since Specialization
Citations

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

Fields of papers citing papers by Cinzia Cameli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Cinzia Cameli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Cinzia Cameli Line = papers co-authored together Cinzia Cameli links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 201547
2 201942
3 202038
4 201638
5 201815
6 201815
7 201912
8 201912
9 202411
10 20209
11 20229
12 20213
13 20152
14
Identification of a rare deletion encompassing ELMOD3 and CAPG in two siblings with Autism Spectrum Disorder
20151

About Cinzia Cameli

Cinzia Cameli is a scholar working on Cognitive Neuroscience, Genetics, Molecular Biology, Pharmacology and Genetics, having authored 14 papers that have together received 254 indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (2 papers), Nicotinic Acetylcholine Receptors Study (2 papers), Epigenetics and DNA Methylation (1 paper), Ion channel regulation and function (1 paper) and Cholinesterase and Neurodegenerative Diseases (1 paper). The work is most often cited by research in Psychiatry and Mental health (49 citations), Genetics (86 citations), Cognitive Neuroscience (55 citations), Cellular and Molecular Neuroscience (28 citations) and Endocrine and Autonomic Systems (9 citations). Cinzia Cameli has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Elena Bacchelli, Elena Maestrini, Agatino Battaglia, Raffaella Tancredi, Michèle Zoli, Luigi Alberto Pini, Maria Michela Cainazzo, Susanne Thomson, Silvia Lomartire and James S. Sutcliffe. Their work appears in journals such as The Journal of Headache and Pain, Journal of Cellular and Molecular Medicine, npj Genomic Medicine, Annals of Clinical and Translational Neurology and European Journal of Human Genetics.

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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