E. Jaakkola

574 total citations
10 papers, 311 citations indexed

About

E. Jaakkola is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, E. Jaakkola has authored 10 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in E. Jaakkola's work include Spondyloarthritis Studies and Treatments (3 papers), Dermatological and Skeletal Disorders (2 papers) and Psoriasis: Treatment and Pathogenesis (2 papers). E. Jaakkola is often cited by papers focused on Spondyloarthritis Studies and Treatments (3 papers), Dermatological and Skeletal Disorders (2 papers) and Psoriasis: Treatment and Pathogenesis (2 papers). E. Jaakkola collaborates with scholars based in Finland, United States and United Kingdom. E. Jaakkola's co-authors include Jaakko Ignatius, Sakari Knuutila, Sirpa Ala‐Mello, Jürgen Kohlhase, Detlef Böhm, Ekaterini Tsilou, Jacek Pilch, Markku Kauppi, Michaela Auer‐Grumbach and Christopher J. Lyons and has published in prestigious journals such as Neurology, Annals of the Rheumatic Diseases and British Journal of Ophthalmology.

In The Last Decade

E. Jaakkola

10 papers receiving 302 citations

Peers

Countries citing papers authored by E. Jaakkola

Since Specialization

Citations

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

Fields of papers citing papers by E. Jaakkola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Jaakkola

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Dominant GDAP1 mutations cause predominantly mild CMT phenotypes 2011 ·Neurology ·M. Zimoń, Jonathan Baets, Gian Maria Fabrizi, E. Jaakkola, Dagmara Kabzińska, Jacek Pilch, Alice B. Schindler, David R. Cornblath, Kenneth H. Fischbeck, Michaela Auer‐Grumbach, Christian Guelly, Nina Huber, Els De Vriendt, Vincent Timmerman, Ueli Suter, I Hausmanowa-Pétrusewicz, Axel Niemann, Andrzej Kochański, Peter De Jonghe, Albena Jordanova	61
2	The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease 2010 ·British Journal of Ophthalmology ·Johane M. Robitaille, (unknown), Karin Wallace, M Beis, (unknown), Jing Yang, Tom Sheidow, (unknown), Alex V. Levin, Wai‐Ching Lam, Brian W. Arthur, Christopher J. Lyons, E. Jaakkola, Ekaterini Tsilou, Cicely A. Williams, Richard G. Weaver, Carol L. Shields, D.L. Guernsey	53
3	ERCC6 founder mutation identified in Finnish patients with COFS syndrome 2010 ·Clinical Genetics ·E. Jaakkola, Aki Mustonen, Päivi Olsén, (unknown), (unknown), Anja Raams, N.G.J. Jaspers, Hong Shao, (unknown), Jaakko Ignatius	17
4	Array CGH in molecular diagnosis of mental retardation—A study of 150 Finnish patients 2010 ·American Journal of Medical Genetics Part A ·(unknown), Sirpa Ala‐Mello, E. Jaakkola, (unknown), (unknown), Jürgen Kohlhase, Detlef Böhm, Jaakko Ignatius, Sakari Knuutila	32
5	Calvarial doughnut lesions and osteoporosis: A new three‐generation family and review 2009 ·American Journal of Medical Genetics Part A ·E. Jaakkola, Christine Lainé, Mervi K Mäyränpää, Aura Falck, Jaakko Ignatius, Outi Mäkitie	9
6	Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitis 2005 ·Annals of the Rheumatic Diseases ·E. Jaakkola, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	87
7	A novel human leucocyte antigen‐DRB1 genotyping method based on multiplex primer extension reactions 2004 ·Tissue Antigens ·E. Jaakkola, (unknown), Alison M. Crane, J. J. Pointon, Kari Laiho, Markku Kauppi, K. Kaarela, B P Wordsworth, Jaakko Tuomilehto, Matthew A. Brown	6
8	TRANSFORMING GROWTH FACTOR BETA-1 GENE POLYMORPHISMS AND ANKYLOSING SPONDYLITIS 2003 ·Lara D. Veeken ·E. Jaakkola, (unknown), (unknown), L Bradbury, A Călin, Kari Laiho, (unknown), B P Wordsworth, J. Tuomilehto, Martin M. Brown	1
9	Interleukin 10 polymorphisms in ankylosing spondylitis 2003 ·Genes and Immunity ·(unknown), Alison M. Crane, E. Jaakkola, (unknown), Kari Laiho, Daniel E. Weeks, Jonathan P. Wilson, Markku Kauppi, K. Kaarela, Jaakko Tuomilehto, B. P. Wordsworth, Matthew A. Brown	24
10	The effect of transforming growth factor 1 gene polymorphisms in ankylosing spondylitis 2003 ·British journal of rheumatology ·E. Jaakkola	21

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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