Sandro Rossetti

8.3k total citations · 1 hit paper
79 papers, 5.6k citations indexed

About

Sandro Rossetti is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Sandro Rossetti has authored 79 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Genetics, 56 papers in Molecular Biology and 13 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Sandro Rossetti's work include Genetic and Kidney Cyst Diseases (57 papers), Renal and related cancers (47 papers) and Genetic Syndromes and Imprinting (22 papers). Sandro Rossetti is often cited by papers focused on Genetic and Kidney Cyst Diseases (57 papers), Renal and related cancers (47 papers) and Genetic Syndromes and Imprinting (22 papers). Sandro Rossetti collaborates with scholars based in United States, Italy and United Kingdom. Sandro Rossetti's 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 and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Sandro Rossetti

78 papers receiving 5.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

2002 525 citations Christopher J. Ward, Marie C. Hogan et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandro Rossetti United States	41	4.3k	3.7k	996	865	861	79	5.6k
Yoshiki Seino Japan	39	1.4k 0.3×	1.9k 0.5×	1.4k 1.5×	639 0.7×	396 0.5×	238	6.0k
Yukihiro Hasegawa Japan	31	1.5k 0.4×	2.1k 0.6×	447 0.4×	396 0.5×	638 0.7×	258	5.0k
Lars Sävendahl Sweden	40	1.7k 0.4×	1.7k 0.5×	206 0.2×	543 0.6×	199 0.2×	154	4.9k
Sami A. Sanjad Lebanon	16	704 0.2×	2.6k 0.7×	259 0.3×	239 0.3×	703 0.8×	46	3.8k
Hunter Heath United States	38	981 0.2×	1.7k 0.5×	1.1k 1.1×	136 0.2×	635 0.7×	129	5.9k
Luca Rampoldi Italy	32	595 0.1×	1.5k 0.4×	446 0.4×	628 0.7×	861 1.0×	63	4.0k
Dong‐Kyu Jin South Korea	33	1.1k 0.2×	917 0.2×	225 0.2×	219 0.3×	232 0.3×	261	3.9k
Mark B. Meyer United States	38	885 0.2×	2.2k 0.6×	2.4k 2.5×	171 0.2×	262 0.3×	82	4.9k
Toshihiro Utsugi Japan	21	1.9k 0.4×	1.2k 0.3×	404 0.4×	99 0.1×	268 0.3×	45	4.6k
John L. Fowlkes United States	38	549 0.1×	1.8k 0.5×	315 0.3×	177 0.2×	203 0.2×	89	4.1k

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-authorship network of co-authors of Sandro Rossetti

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

Rastogi, Anjay, et al.. (2020). Management of Hyperphosphatemia in End-Stage Renal Disease: A New Paradigm. Journal of Renal Nutrition. 31(1). 21–34. 46 indexed citations

Blanchette, Christopher M., et al.. (2014). Hospital-based inpatient resource utilization associated with autosomal dominant polycystic kidney disease in the US. Journal of Medical Economics. 18(4). 303–311. 11 indexed citations

Consugar, Mark, Jamie L. Sundsbak, Christina M. Heyer, et al.. (2013). Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families. Kidney International. 85(2). 383–392. 25 indexed citations

Rossetti, Sandro & Peter C. Harris. (2013). The Genetics of Vascular Complications in Autosomal Dominant Polycystic Kidney Disease (ADPKD). Current Hypertension Reviews. 9(1). 37–43. 28 indexed citations

Hopp, Katharina, Christopher J. Ward, Cynthia J. Hommerding, et al.. (2012). Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity. Journal of Clinical Investigation. 122(11). 4257–4273. 294 indexed citations

Ward, Christopher J., Yanhong Wu, Ruth Johnson, et al.. (2011). Germline PKHD1 mutations are protective against colorectal cancer. Human Genetics. 129(3). 345–349. 22 indexed citations

Pelleymounter, Linda L., Irene Moon, Julie A. Johnson, et al.. (2011). A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: Targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian population. Molecular Genetics and Metabolism. 104(4). 457–469. 16 indexed citations

Hogan, Marie C., Tatyana V. Masyuk, Vickie Kubly, et al.. (2010). Randomized Clinical Trial of Long-Acting Somatostatin for Autosomal Dominant Polycystic Kidney and Liver Disease. Journal of the American Society of Nephrology. 21(6). 1052–1061. 237 indexed citations

Harris, Peter C. & Sandro Rossetti. (2010). Molecular diagnostics for autosomal dominant polycystic kidney disease. Nature Reviews Nephrology. 6(4). 197–206. 112 indexed citations

10.

Xu, Chang, Boris E. Shmukler, Katherine K. Nishimura, et al.. (2009). Attenuated, flow-induced ATP release contributes to absence of flow-sensitive, purinergic Ca_i²⁺signaling in human ADPKD cyst epithelial cells. American Journal of Physiology-Renal Physiology. 296(6). F1464–F1476. 70 indexed citations

11.

Rossetti, Sandro, Mark Consugar, Arlene B. Chapman, et al.. (2007). Comprehensive Molecular Diagnostics in Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 18(7). 2143–2160. 311 indexed citations

12.

Parker, Ernest T., Linda J. Newby, Claire C. Sharpe, et al.. (2007). Hyperproliferation of PKD1 cystic cells is induced by insulin-like growth factor-1 activation of the Ras/Raf signalling system. Kidney International. 72(2). 157–165. 71 indexed citations

13.

Xu, Nancy, et al.. (2006). Autosomal dominant polycystic kidney disease coexisting with cystic fibrosis. Journal of Nephrology. 19(4). 529–534. 43 indexed citations

14.

Consugar, Mark, Sarah Anderson, Sandro Rossetti, et al.. (2005). Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease. American Journal of Kidney Diseases. 45(1). 77–87. 24 indexed citations

15.

Monico, Carla G., Sandro Rossetti, Julie B. Olson, & Dawn S. Milliner. (2005). Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele. Kidney International. 67(5). 1704–1709. 134 indexed citations

16.

Ward, Christopher J., Marie C. Hogan, Sandro Rossetti, et al.. (2002). The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nature Genetics. 30(3). 259–269. 525 indexed citations breakdown →

17.

Turco, Alberto, Elena Bresin, Sandro Rossetti, et al.. (1997). Molecular Genetic Investigations in Autosomal Dominant Polycystic Kidney Disease. Gene Mutation Detection, Linkage Analysis, and Preliminary ACE Gene I/D Polymorphism Association Studies: An Update. Contributions to nephrology. 122. 53–57. 3 indexed citations

18.

Turco, Alberto, Maurizio Clementi, Sandro Rossetti, Romano Tenconi, & Pier Franco Pignatti. (1996). An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene. American Journal of Kidney Diseases. 28(5). 759–761. 40 indexed citations

19.

Rossetti, Sandro, Elena Bresin, Gabriella Restagno, et al.. (1996). Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 gene. American Journal of Medical Genetics. 65(2). 155–159. 40 indexed citations

20.

Turco, Alberto, E Padovani, Bernard Peissel, et al.. (1995). Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case report. Journal of Perinatal Medicine. 23(3). 205–212. 4 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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