Ilona Visapää

755 total citations
7 papers, 510 citations indexed

About

Ilona Visapää is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Ilona Visapää has authored 7 papers receiving a total of 510 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Surgery and 3 papers in Genetics. Recurrent topics in Ilona Visapää's work include Metabolism and Genetic Disorders (2 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Ilona Visapää is often cited by papers focused on Metabolism and Genetic Disorders (2 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Ilona Visapää collaborates with scholars based in Finland, United States and Australia. Ilona Visapää's co-authors include Leena Peltonen, Marjo Kestilä, Vineta Fellman, Jouni Vesa, Christer Holmberg, Jaakko Patrakka, Juhani Rapola, Jorma Wartiovaara, Hannu Jalanko and Päivi Tissari and has published in prestigious journals such as Kidney International, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Ilona Visapää

7 papers receiving 498 citations

Peers

Ilona Visapää

MB

NEPHR

GENET

CB

PFM

Yujing Shu Japan

Rafael Muley Spain

Soledad Kleppe United States

Oraly Sanchez-Ferras Canada

Meredith P. Millis United States

Daisuke Yoshihara Japan

Isabelle Redonnet‐Vernhet France

Enrique Urdanivia United States

Shinya Ishiko Japan

Nanyawan Rungroj Thailand

Yujing Shu Japan

Ilona Visapää

161 ×0.4

MB

196 ×1.0

NEPHR

65 ×0.5

GENET

23 ×0.2

CB

29 ×0.7

PFM

Citations per year, relative to Ilona Visapää Ilona Visapää (= 1×) peers Yujing Shu

Countries citing papers authored by Ilona Visapää

Since Specialization

Citations

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

Fields of papers citing papers by Ilona Visapää

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilona Visapää

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

All Works

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7 of 7 papers shown

1.

Mee, Lisa, Outi Kopra, Jouni Vesa, et al.. (2005). Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1. Human Molecular Genetics. 14(11). 1475–1488. 50 indexed citations

2.

Visapää, Ilona, Vineta Fellman, Jouni Vesa, et al.. (2002). GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L. The American Journal of Human Genetics. 71(4). 863–876. 199 indexed citations

3.

Visapää, Ilona, et al.. (2002). ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis. American Journal of Medical Genetics. 109(3). 202–205. 5 indexed citations

4.

Fellman, Vineta, Ilona Visapää, Mihailo Vujic, Ulla‐Britt Wennerholm, & Leena Peltonen. (2002). Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant. Acta Obstetricia Et Gynecologica Scandinavica. 81(5). 398–402. 9 indexed citations

5.

Patrakka, Jaakko, Marjo Kestilä, Jorma Wartiovaara, et al.. (2000). Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients. Kidney International. 58(3). 972–980. 209 indexed citations

6.

Visapää, Ilona, Riitta Salonen, Teppo Varilo, Paulina Paavola, & Leena Peltonen. (1999). Assignment of the Locus for Hydrolethalus Syndrome to a Highly Restricted Region on 11q23-25. The American Journal of Human Genetics. 65(4). 1086–1095. 21 indexed citations

7.

Visapää, Ilona, Vineta Fellman, Teppo Varilo, et al.. (1998). Assignment of the Locus for a New Lethal Neonatal Metabolic Syndrome to 2q33-37. The American Journal of Human Genetics. 63(5). 1396–1403. 17 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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