Juha Kolehmainen

1.2k total citations
12 papers, 893 citations indexed

About

Juha Kolehmainen is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, Juha Kolehmainen has authored 12 papers receiving a total of 893 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Immunology and 3 papers in Molecular Biology. Recurrent topics in Juha Kolehmainen's work include Immunodeficiency and Autoimmune Disorders (5 papers), Blood disorders and treatments (5 papers) and Retinal Development and Disorders (2 papers). Juha Kolehmainen is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (5 papers), Blood disorders and treatments (5 papers) and Retinal Development and Disorders (2 papers). Juha Kolehmainen collaborates with scholars based in Finland, Hungary and Denmark. Juha Kolehmainen's co-authors include Ville Sallinen, Pertti Panula, Albert de la Chapelle, Satu Kivitie‐Kallio, Piotr Podlasz, Maxim Moshnyakov, Maria Sundvik, Reijo Norio, Anna‐Elina Lehesjoki and Kate Chandler and has published in prestigious journals such as The American Journal of Human Genetics, Neurobiology of Disease and Genomics.

In The Last Decade

Juha Kolehmainen

12 papers receiving 858 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juha Kolehmainen Finland 12 311 298 247 190 98 12 893
Jeannette Nardelli France 18 124 0.4× 184 0.6× 931 3.8× 110 0.6× 179 1.8× 31 1.4k
Hyong Kyu Kim South Korea 21 135 0.4× 107 0.4× 606 2.5× 131 0.7× 347 3.5× 48 1.2k
Abdul Karim Sesay United Kingdom 20 101 0.3× 447 1.5× 949 3.8× 106 0.6× 138 1.4× 45 1.9k
Maryam Faiz Bangladesh 23 87 0.3× 198 0.7× 474 1.9× 133 0.7× 281 2.9× 45 1.4k
Margarita Díaz‐Guerra Spain 21 160 0.5× 289 1.0× 638 2.6× 249 1.3× 430 4.4× 40 1.5k
Marie Schaeffer France 18 49 0.2× 185 0.6× 472 1.9× 457 2.4× 115 1.2× 33 1.8k
Néstor Guerrero Chile 17 85 0.3× 157 0.5× 554 2.2× 100 0.5× 67 0.7× 22 1.0k
Scott J. Nowak United States 13 242 0.8× 162 0.5× 1.3k 5.1× 108 0.6× 119 1.2× 19 1.5k
Sophie Chauvet France 14 236 0.8× 96 0.3× 543 2.2× 73 0.4× 561 5.7× 28 1.1k
Mark Barnett United Kingdom 20 120 0.4× 433 1.5× 986 4.0× 118 0.6× 164 1.7× 32 1.5k

Countries citing papers authored by Juha Kolehmainen

Since Specialization
Citations

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

Fields of papers citing papers by Juha Kolehmainen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juha Kolehmainen

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

All Works

12 of 12 papers shown
1.
Sallinen, Ville, et al.. (2010). Dopaminergic cell damage and vulnerability to MPTP in Pink1 knockdown zebrafish. Neurobiology of Disease. 40(1). 93–101. 63 indexed citations
2.
Korpelainen, Helena, Irène Bisang, Lars Hedenäs, & Juha Kolehmainen. (2008). The First Sex-Specific Molecular Marker Discovered in the Moss Pseudocalliergon trifarium. Journal of Heredity. 99(6). 581–587. 55 indexed citations
3.
Rimhanen‐Finne, Ruska, et al.. (2007). Evaluation of immunofluorescence microscopy and enzyme-linked immunosorbent assay in detection of Cryptosporidium and Giardia infections in asymptomatic dogs. Veterinary Parasitology. 145(3-4). 345–348. 65 indexed citations
4.
Panula, Pertti, Ville Sallinen, Maria Sundvik, et al.. (2006). Modulatory Neurotransmitter Systems and Behavior: Towards Zebrafish Models of Neurodegenerative Diseases. Zebrafish. 3(2). 235–247. 237 indexed citations
5.
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
6.
Falk, Marni J., Heidi S. Feiler, Derek Neilson, et al.. (2004). Cohen syndrome in the Ohio Amish. American Journal of Medical Genetics Part A. 128A(1). 23–28. 31 indexed citations
7.
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
8.
Kolehmainen, Juha, et al.. (1998). Refined mapping of the Cohen syndrome gene by linkage disequilibrium.. PubMed. 5(4). 206–13. 30 indexed citations
9.
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
10.
Tahvanainen, Esa, et al.. (1996). The genetics of cornea plana congenita.. Journal of Medical Genetics. 33(2). 116–119. 14 indexed citations
11.
Tahvanainen, Esa, Henrik Forsius, Juha Kolehmainen, et al.. (1995). Linkage Disequilibrium Mapping of the Cornea Plana Congenita Gene CNA2. Genomics. 30(3). 409–414. 14 indexed citations
12.
Wallgren‐Pettersson, Carina, Kristiina Avela, Stéphanie Marchand, et al.. (1995). A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis. Neuromuscular Disorders. 5(6). 441–443. 38 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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