Sandro Rossetti

8.4k citations
78 papers · 5.7k · 1 hit paper · h-index 40

Impact in

  • Genetics top 0.1%
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
  • Nephrology top 1%
    • Renal Diseases and Glomerulopathies

Papers in

    • Genetic and Kidney Cyst Diseases 57
    • Genetic Syndromes and Imprinting 18
    • Renal and related cancers 38
    • Hedgehog Signaling Pathway Studies 5

Sandro Rossetti

77 papers receiving 5.5k citations

Sandro Rossetti's Hit Papers

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein 2002 · 526 citations
5260+8+16Years since publication100200300400500

Peers

Sandro Rossetti
Comparison fields: 5 of 121
  • Genetics 4.2k
  • Nephrology 417
  • Pathology and Forensic Medicine 858
  • Molecular Biology 3.0k
  • Pediatrics, Perinatology and Child Health 602
Replace Yukihiro Hasegawa with:
Yukihiro Hasegawa Japan
Sami A. Sanjad Lebanon
Luca Rampoldi Italy
Dong‐Kyu Jin South Korea
Marie‐Christine de Vernejoul France
Kathryn M. Thrailkill United States
Toshihiro Utsugi Japan
Akihiro Yasoda Japan
Shigeaki Muto Japan
Cyrille B. Confavreux France
Sandro Rossetti relative to Yukihiro Hasegawa Japan Yukihiro Hasegawa's profile →
Citations per field
00.5×3.7×
Yukihiro Hasegawa · 1×
Citations per year

Countries citing papers authored by Sandro Rossetti

Since Specialization
Citations

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

Fields of papers citing papers by Sandro Rossetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 78 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
Hit paper breakdown →
2002526
2 2007317
3 2012299
4 2010238
5 2009231
6 2006195
7 2001165
8 2017160
9 2006153
10 2006150
11 2002139
12 2003135
13 2012135
14 2005134
15 2007126
16 2017124
17 2002123
18 2014119
19 2004115
20 2006114

About Sandro Rossetti

Sandro Rossetti is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health, having authored 78 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (57 papers), Renal and related cancers (38 papers), Genetic Syndromes and Imprinting (18 papers), Biomedical Research and Pathophysiology (9 papers), Cell Adhesion Molecules Research (6 papers), Hedgehog Signaling Pathway Studies (5 papers), Kidney Stones and Urolithiasis Treatments (4 papers) and Renal Diseases and Glomerulopathies (4 papers). The work is most often cited by research in Genetics (4.2k citations), Nephrology (417 citations), Pathology and Forensic Medicine (858 citations), Molecular Biology (3.0k citations) and Pediatrics, Perinatology and Child Health (602 citations). Sandro Rossetti has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include Peter C. Harris, Vicente E. Torres, Christopher J. Ward, Mark Consugar, Vickie Kubly, Dawn S. Milliner, Denise L. Walker, Marie C. Hogan, Christopher G. Winearls and Katharina Hopp. Their work appears in journals such as Journal of the American Society of Nephrology, Kidney International, Human Mutation, American Journal of Kidney Diseases and Human Molecular 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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