Pia Bernardo

424 citations
32 papers · 245 · h-index 9

Impact in

  • Neurology top 10%
    • Neurofibromatosis and Schwannoma Cases
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genetics and Neurodevelopmental Disorders 9
    • Genomic variations and chromosomal abnormalities 4
    • Genomics and Rare Diseases 3
    • Congenital heart defects research 2

Pia Bernardo

30 papers receiving 243 citations

Peers

Pia Bernardo
Comparison fields: 5 of 47
  • Neurology 77
  • Genetics 75
  • Psychiatry and Mental health 30
  • Cognitive Neuroscience 32
  • Rheumatology 18
Replace Marisela Dy-Hollins with:
Marisela Dy-Hollins United States
Heejong Sung United States
Thea Giacomini Italy
Precilla D’Souza United States
Veneta Bojinova Bulgaria
Amina Gargouri Tunisia
Abeer Shehab Egypt
Alessandro F. Fois Australia
Marta Galdós Spain
Weiyi Mu United States
Pia Bernardo relative to Marisela Dy-Hollins United States Marisela Dy-Hollins's profile →
Citations per field
00.5×2.7×
Marisela Dy-Hollins · 1×
Citations per year

Countries citing papers authored by Pia Bernardo

Since Specialization
Citations

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

Fields of papers citing papers by Pia Bernardo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Pia Bernardo, 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 Pia Bernardo Line = papers co-authored together Pia Bernardo links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 202028
2 201826
3 202020
4 201715
5 201913
6 201712
7 202011
8 201910
9 20209
10 20178
11 20218
12 20198
13 20208
14 20207
15 20167
16 20196
17 20226
18 20216
19 20186
20 20225

About Pia Bernardo

Pia Bernardo is a scholar working on Genetics, Molecular Biology, Neurology, Clinical Psychology and Psychiatry and Mental health, having authored 32 papers that have together received 245 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Autism Spectrum Disorder Research (3 papers), Genomics and Rare Diseases (3 papers), Family and Disability Support Research (3 papers), Congenital heart defects research (2 papers) and Child Nutrition and Feeding Issues (2 papers). The work is most often cited by research in Neurology (77 citations), Genetics (75 citations), Psychiatry and Mental health (30 citations), Cognitive Neuroscience (32 citations) and Rheumatology (18 citations). Pia Bernardo has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Claudia Santoro, Giuseppe Cinalli, Carmela Bravaccio, Antonietta Coppola, Giulio Piluso, Salvatore Striano, Teresa Giugliano, Mario Cirillo, Silverio Perrotta and Nicola Brunetti‐Pierri. Their work appears in journals such as Clinical Neurology and Neurosurgery, International Journal of Molecular Sciences, Brain and Development, Child s Nervous System and Epileptic Disorders.

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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