Roslyn Simms

1.1k citations
25 papers · 550 indexed · h-index 16

Impact in

  • Genetics top 5%
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
  • Nephrology top 10%
    • Renal Diseases and Glomerulopathies

Papers in

    • Genetic and Kidney Cyst Diseases 21
    • Genetic Syndromes and Imprinting 3
    • Renal and related cancers 10
    • Hedgehog Signaling Pathway Studies 3
    • Protist diversity and phylogeny 2

Roslyn Simms

25 papers receiving 543 citations

Peers

Roslyn Simms
Comparison fields: 5 of 66
  • Genetics 355
  • Nephrology 75
  • Pediatrics, Perinatology and Child Health 125
  • Molecular Biology 328
  • Pathology and Forensic Medicine 56
Replace Diana M. Iglesias with:
Diana M. Iglesias Canada
Naoya Morisada Japan
Jolanta E. Pitera United Kingdom
Susan M. Kiefer United States
Shirlee Shril United States
Mariana F.A. Funari Brazil
Jitka Štekrová Czechia
Eiichi Kinoshita Japan
Lisa Williams‐Simons United States
Mónica Furlano Spain
Roslyn Simms relative to Diana M. Iglesias Canada Diana M. Iglesias's profile →
Citations per field
00.5×3.5×
Diana M. Iglesias · 1×
Citations per year

Countries citing papers authored by Roslyn Simms

Since Specialization
Citations

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

Fields of papers citing papers by Roslyn Simms

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201185
2 202048
3 200841
4 201137
5 201536
6 201434
7 200831
8 201629
9 201427
10 201725
11 200323
12 201122
13 201918
14 201416
15 201215
16 201415
17 200810
18 20229
19 20237
20 20226

About Roslyn Simms

Roslyn Simms is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Nephrology and Pulmonary and Respiratory Medicine, having authored 25 papers that have together received 550 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (21 papers), Renal and related cancers (10 papers), Pediatric Urology and Nephrology Studies (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic Syndromes and Imprinting (3 papers), Renal Diseases and Glomerulopathies (2 papers) and Protist diversity and phylogeny (2 papers). The work is most often cited by research in Genetics (355 citations), Nephrology (75 citations), Pediatrics, Perinatology and Child Health (125 citations), Molecular Biology (328 citations) and Pathology and Forensic Medicine (56 citations). Roslyn Simms has collaborated with scholars based in United Kingdom, Netherlands and Belgium. Frequent co-authors include Albert Ong, John A. Sayer, Lorraine Eley, Ann Marie Hynes, Helen R. Dawe, Gabriel C. Dworschak, Kah Mean Thong, Catriona Shaw, David Pitcher and Richard Sandford. Their work appears in journals such as Nephrology Dialysis Transplantation, Clinical Kidney Journal, BMJ Open, Human Molecular Genetics 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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