Reijo Norio

5.4k total citations
69 papers, 3.6k citations indexed

About

Reijo Norio is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Reijo Norio has authored 69 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 13 papers in Molecular Biology. Recurrent topics in Reijo Norio's work include Blood disorders and treatments (11 papers), Immunodeficiency and Autoimmune Disorders (10 papers) and Renal Diseases and Glomerulopathies (8 papers). Reijo Norio is often cited by papers focused on Blood disorders and treatments (11 papers), Immunodeficiency and Autoimmune Disorders (10 papers) and Renal Diseases and Glomerulopathies (8 papers). Reijo Norio collaborates with scholars based in Finland, United States and United Kingdom. Reijo Norio's co-authors include Satu Kivitie‐Kallio, Marjaleena Koskiniemi, Albert de la Chapelle, Jaakko Perheentupa, Riitta Salonen, Jinmin Miao, Anna‐Elina Lehesjoki, Juhani Rapola, N Hallman and Elena D’Amato and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Reijo Norio

69 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Reijo Norio Finland 36 1.8k 1.1k 592 447 401 69 3.6k
Ruth Gershoni‐Baruch Israel 39 1.7k 1.0× 3.1k 2.7× 409 0.7× 1.0k 2.3× 351 0.9× 145 6.1k
John R.W. Yates United Kingdom 33 1.5k 0.8× 2.2k 2.0× 194 0.3× 427 1.0× 513 1.3× 82 5.4k
Françoise Goutières France 32 579 0.3× 1.4k 1.2× 429 0.7× 563 1.3× 525 1.3× 76 3.2k
Marc De Braekeleer France 40 1.7k 0.9× 1.9k 1.6× 317 0.5× 213 0.5× 986 2.5× 235 5.6k
Luisa Bonafé Switzerland 36 1.4k 0.8× 1.8k 1.6× 502 0.8× 203 0.5× 275 0.7× 97 3.5k
Alexandre Montpetit Canada 33 897 0.5× 1.4k 1.2× 243 0.4× 621 1.4× 182 0.5× 66 3.5k
Aubrey Milunsky United States 31 1.0k 0.6× 1.6k 1.4× 537 0.9× 209 0.5× 832 2.1× 134 3.9k
Paola Grammatico Italy 34 1.9k 1.1× 1.8k 1.5× 315 0.5× 388 0.9× 348 0.9× 204 4.4k
Rong Mao United States 35 1.0k 0.6× 1.8k 1.5× 1.0k 1.7× 297 0.7× 306 0.8× 135 4.8k
Catherine Bonaïti‐Pellié France 35 2.7k 1.5× 2.1k 1.9× 210 0.4× 448 1.0× 529 1.3× 109 5.4k

Countries citing papers authored by Reijo Norio

Since Specialization
Citations

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

Fields of papers citing papers by Reijo Norio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reijo Norio

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

All Works

20 of 20 papers shown
1.
Kolehmainen, Juha, Robert N. Wilkinson, Anna-Elina Lehesjoki, et al.. (2004). Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen. The American Journal of Human Genetics. 75(1). 122–127. 69 indexed citations
2.
Kolehmainen, Juha, Graeme C. Black, Anne Saarinen, et al.. (2003). Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport. The American Journal of Human Genetics. 72(6). 1359–1369. 249 indexed citations
3.
Norio, Reijo. (2003). Finnish Disease Heritage II: population prehistory and genetic roots of Finns. Human Genetics. 112(5-6). 457–469. 89 indexed citations
4.
Norio, Reijo, et al.. (2002). The Finnish disease heritage. SHILAP Revista de lepidopterología. 7 indexed citations
5.
Kivitie‐Kallio, Satu & Reijo Norio. (2001). Cohen Syndrome: Essential features, natural history, and heterogeneity. American Journal of Medical Genetics. 102(2). 125–135. 108 indexed citations
6.
Kivitie‐Kallio, Satu, Paula Summanen, Christina Raitta, & Reijo Norio. (2000). Ophthalmologic findings in cohen syndrome. Ophthalmology. 107(9). 1737–1745. 35 indexed citations
7.
Kivitie‐Kallio, Satu, et al.. (1999). Neurological and Psychological Findings in Patients with Cohen Syndrome: A Study of 18 Patients Aged 11 Months to 57 Years. Neuropediatrics. 30(4). 181–189. 21 indexed citations
8.
Kolehmainen, Juha, Reijo Norio, Satu Kivitie‐Kallio, et al.. (1997). Refined Mapping of the Cohen Syndrome Gene by Linkage Disequilibrium. European Journal of Human Genetics. 5(4). 206–213. 28 indexed citations
9.
Höglund, Peter, P. Sistonen, Reijo Norio, et al.. (1995). Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.. PubMed. 57(1). 95–102. 51 indexed citations
10.
Tahvanainen, Esa, Reijo Norio, Susanna Ranta, et al.. (1994). Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis. Nature Genetics. 7(2). 201–204. 60 indexed citations
11.
12.
Murphy, Dennis L., Katherine B. Sims, Farouk Karoum, et al.. (1991). Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase. Journal of Neural Transmission. 83(1-2). 1–12. 25 indexed citations
13.
Salonen, Riitta, et al.. (1991). Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome). Clinical Genetics. 39(4). 287–293. 55 indexed citations
14.
Murphy, Dennis L., Katherine B. Sims, Farouk Karoum, et al.. (1990). Marked Amine and Amine Metabolite Changes in Norrie Disease Patients with an X‐Chromosomal Deletion Affecting Monoamine Oxidase. Journal of Neurochemistry. 54(1). 242–247. 44 indexed citations
15.
Kääriäinen, Helena, Soini Ryöppy, & Reijo Norio. (1989). RAPADILINO syndrome with radial and patellar aplasia/hypoplasia as main manifestations. American Journal of Medical Genetics. 33(3). 346–351. 43 indexed citations
16.
Mustajoki, Pertti, et al.. (1987). Homozygous variegate porphyria A severe skin disease of Infancy. Clinical Genetics. 32(5). 300–305. 22 indexed citations
17.
Häyry, P, Jyrki J. Reitamo, Reijo Vihko, et al.. (1982). The Desmoid Tumor. III.: A Biochemical and Genetic Analysis. American Journal of Clinical Pathology. 77(6). 681–685. 58 indexed citations
18.
Norio, Reijo. (1974). Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes.. PubMed. 10(4). 69–72. 2 indexed citations
19.
Norio, Reijo. (1970). [Mental defectiveness as a problem of practice].. PubMed. 75(11). 467–75. 1 indexed citations
20.
Norio, Reijo. (1969). The Nephrotic Syndrome and Heredity. Human Heredity. 19(2). 113–120. 21 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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