Riitta Sallinen

483 total citations
12 papers, 212 citations indexed

About

Riitta Sallinen is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Riitta Sallinen has authored 12 papers receiving a total of 212 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Riitta Sallinen's work include Pancreatic function and diabetes (3 papers), Diabetes and associated disorders (2 papers) and Ion channel regulation and function (2 papers). Riitta Sallinen is often cited by papers focused on Pancreatic function and diabetes (3 papers), Diabetes and associated disorders (2 papers) and Ion channel regulation and function (2 papers). Riitta Sallinen collaborates with scholars based in Finland, United States and Sweden. Riitta Sallinen's co-authors include Maija Wessman, Mari Kaunisto, Per‐Henrik Groop, Kim Pettersson-Fernholm, Carol Forsblom, Johan Fagerudd, Nina Horelli‐Kuitunen, Göran Bergström, Maja Neiman and Linn Fagerberg and has published in prestigious journals such as PLoS ONE, Diabetes and Journal of Nutrition.

In The Last Decade

Riitta Sallinen

12 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Riitta Sallinen Finland	9	97	59	53	35	22	12	212
Jasmine Lew United States	4	204 2.1×	55 0.9×	26 0.5×	28 0.8×	19 0.9×	4	361
Mònica Arribas United Kingdom	10	189 1.9×	38 0.6×	44 0.8×	19 0.5×	34 1.5×	20	418
Ming Yu China	8	167 1.7×	73 1.2×	59 1.1×	14 0.4×	5 0.2×	11	370
Teodora Niculescu United States	8	142 1.5×	38 0.6×	165 3.1×	13 0.4×	22 1.0×	8	356
U Bucher Switzerland	9	100 1.0×	34 0.6×	63 1.2×	16 0.5×	18 0.8×	57	345
Reema B. Davis United States	9	223 2.3×	58 1.0×	46 0.9×	22 0.6×	28 1.3×	12	361
Emre Aldinc United States	10	161 1.7×	18 0.3×	25 0.5×	43 1.2×	53 2.4×	22	255
Madeeha H. Sheikh United Kingdom	5	171 1.8×	14 0.2×	77 1.5×	17 0.5×	23 1.0×	5	268
Zhi Fang China	14	188 1.9×	25 0.4×	61 1.2×	17 0.5×	16 0.7×	22	395

Countries citing papers authored by Riitta Sallinen

Since Specialization

Citations

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

Fields of papers citing papers by Riitta Sallinen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Riitta Sallinen

This figure shows the co-authorship network connecting the top 25 collaborators of Riitta Sallinen. A scholar is included among the top collaborators of Riitta Sallinen 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 Riitta Sallinen. Riitta Sallinen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Sallinen, Riitta, Sanni Ruotsalainen, Robert Mills, et al.. (2020). Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults. Journal of Nutrition. 151(2). 281–292. 7 indexed citations

Neiman, Maja, Cecilia Hellström, David Just, et al.. (2019). Individual and stable autoantibody repertoires in healthy individuals. Autoimmunity. 52(1). 1–11. 46 indexed citations

Wessman, Maija, Carol Forsblom, Mari Kaunisto, et al.. (2011). Novel Susceptibility Locus at 22q11 for Diabetic Nephropathy in Type 1 Diabetes. PLoS ONE. 6(9). e24053–e24053. 10 indexed citations

Sallinen, Riitta, Jenny Söderlund, Carol Forsblom, et al.. (2010). DDOST, PRKCSH and LGALS3, which encode AGE-receptors 1, 2 and 3, respectively, are not associated with diabetic nephropathy in type 1 diabetes. Diabetologia. 53(9). 1903–1907. 9 indexed citations

Sallinen, Riitta, Mari Kaunisto, Carol Forsblom, et al.. (2010). Association of theSLC22A1,SLC22A2, andSLC22A3genes encoding organic cation transporters with diabetic nephropathy and hypertension. Annals of Medicine. 42(4). 296–304. 23 indexed citations

Kaunisto, Mari, Riitta Sallinen, Kim Pettersson-Fernholm, et al.. (2009). Elevated MBL Concentrations Are Not an Indication of Association Between the MBL2 Gene and Type 1 Diabetes or Diabetic Nephropathy. Diabetes. 58(7). 1710–1714. 29 indexed citations

Sallinen, Riitta, Anna Vihola, Linda L. Bachinski, et al.. (2004). New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscular Disorders. 14(4). 274–283. 37 indexed citations

Miettinen, Päivi J., J. Vesa, Arto Orpana, et al.. (2004). Novel splice site CACNA1A mutation causing episodic ataxia type 2. Neurogenetics. 5(1). 69–73. 24 indexed citations

Sallinen, Riitta, et al.. (2001). Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K+-Cl– cotransporter (KCC2) defines a new region of conserved homology. Cytogenetic and Genome Research. 94(1-2). 67–70. 9 indexed citations

10.

Sallinen, Riitta, Ari-Pekka Kvist, Marko Rehn, et al.. (2001). Physical mapping of mouse collagen genes on Chromosome 10 by high-resolution FISH. Mammalian Genome. 12(5). 340–346. 2 indexed citations

11.

Bodnar, Jackie, Riitta Sallinen, Lawrence W. Castellani, et al.. (2001). Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL. Mammalian Genome. 12(3). 238–245. 15 indexed citations

12.

Sallinen, Riitta, Wenhuan Kuang, Eva Engvall, et al.. (1999). Assignment<footref rid="foot01">1</footref> of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4–B1 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 87(3-4). 195–196. 1 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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