Jarmo Körkkö

4.1k total citations · 1 hit paper
27 papers, 1.8k citations indexed

About

Jarmo Körkkö is a scholar working on Molecular Biology, Genetics and Immunology and Allergy. According to data from OpenAlex, Jarmo Körkkö has authored 27 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Genetics and 9 papers in Immunology and Allergy. Recurrent topics in Jarmo Körkkö's work include Connective tissue disorders research (12 papers), Cell Adhesion Molecules Research (9 papers) and Bone Metabolism and Diseases (4 papers). Jarmo Körkkö is often cited by papers focused on Connective tissue disorders research (12 papers), Cell Adhesion Molecules Research (9 papers) and Bone Metabolism and Diseases (4 papers). Jarmo Körkkö collaborates with scholars based in United States, Finland and Canada. Jarmo Körkkö's co-authors include Leena Ala‐Kokko, Shawn M. Sweeney, James D. San Antonio, Gloria A. Di Lullo, Darwin J. Prockop, Tero Pihlajamaa, Gene Kopen, David Ibberson, Donald G. Phinney and Carla M. DiGirolamo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Jarmo Körkkö

27 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen

2002 676 citations Gloria A. Di Lullo, Shawn M. Sweeney et al. Journal of Biological Chemistry profile →

Peers

Countries citing papers authored by Jarmo Körkkö

Since Specialization

Citations

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

Fields of papers citing papers by Jarmo Körkkö

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jarmo Körkkö

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability 2024 ·European Journal of Human Genetics ·(unknown), Mitja Kurki, Elisa Rahikkala, Eija Hämäläinen, Veikko Salomaa, Jaana Suvisaari, Riikka Keski‐Filppula, (unknown), (unknown), (unknown), Heli Helander, Päivi Vieira, Johanna Uusimaa, Jukka S. Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J. Daly	1
2	Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease 2023 ·Frontiers in Neuroscience ·(unknown), Leo Kager, Gina O’Grady, Hannu Tuominen, Jarmo Körkkö, Outi Kuismin, Martha Feucht, Callum Wilson, (unknown), Eleina England, Mitja Kurki, Aarno Palotie, Mikko Hallman, Riitta Kaarteenaho, Franco Laccone, Kaan Boztuǧ, Reetta Hinttala, Johanna Uusimaa	1
3	Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population 2019 ·European Journal of Human Genetics ·D.L. Polla, Elisa Rahikkala, Michaela K. Bode, Tuomo Määttä, Teppo Varilo, (unknown), (unknown), Mitja Kurki, Aarno Palotie, Jarmo Körkkö, Päivi Vieira, Kristiina Avela, (unknown), Isabelle Pirson, Marc Abramowicz, Arjan P.M. de Brouwer, Outi Kuismin, Hans van Bokhoven, Irma Järvelä	7
4	Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density 2005 ·European Journal of Human Genetics ·Marcella Devoto, Loretta D. Spotila, Deborah L. Stabley, (unknown), Halfdan Rydbeck, Jarmo Körkkö, (unknown), Darwin J. Prockop, Alan Tenenhouse, Katia Sol‐Church	41
5	Childhood‐onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg⁷⁵‐Cys mutation in procollagen type II gene (COL2A1) 2004 ·Arthritis Care & Research ·Tuija Löppönen, Jarmo Körkkö, Tuija Lundán, Ulpu Seppänen, Jaakko Ignatius, Helena Kääriäinen	32
6	Lack of correlation between the type ofCOL1A1orCOL1A2mutation and hearing loss in osteogenesis imperfecta patients 2004 ·Human Mutation ·(unknown), Kaija Kuurila, Jarmo Körkkö, Ilkka Kaitila, Reidar Grénman, Seppo Pynnönen, James Hyland, Leena Ala‐Kokko	65
7	Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS 2003 ·Journal of Clinical Investigation ·Murat Bastepe, Leopold F. Fröhlich, Geoffrey N. Hendy, Ólafur S. Indridason, Robert G. Josse, Hiroyuki Koshiyama, Jarmo Körkkö, Jon M. Nakamoto, Arlan L. Rosenbloom, Arnold H. Slyper, Toshitsugu Sugimoto, Agathocles Tsatsoulis, John D. Crawford, Harald Jüppner	186
8	Radial perivascular retinal degeneration: a key to the clinical diagnosis of an ocular variant of Stickler syndrome with minimal or no systemic manifestations 2002 ·American Journal of Ophthalmology ·(unknown), Jarmo Körkkö, William S. Hagler, Leena Ala‐Kokko	66
9	Procollagen with Skipping of α1(I) Exon 41 Has Lower Binding Affinity for α1(I) C-telopeptide, Impaired in Vitro Fibrillogenesis, and Altered Fibril Morphology 2002 ·Journal of Biological Chemistry ·Wayne A. Cabral, Andrzej Fertala, Laura K. Green, Jarmo Körkkö, Antonella Forlino, Joan C. Marini	14
10	Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions 2002 ·Journal of Medical Genetics ·Jarmo Körkkö, (unknown), (unknown), (unknown), (unknown)	50
11	Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen breakdown → 2002 ·Journal of Biological Chemistry ·Gloria A. Di Lullo, Shawn M. Sweeney, Jarmo Körkkö, Leena Ala‐Kokko, James D. San Antonio	676
12	Sequence Analysis of COL1A1 and COL1A2 Genes in Clinical Otosclerosis: No Evidence for Mutations in the Coding Regions of the Genes 2001 ·Oto-Rhino-Laryngologia Nova ·Michael J. McKenna, Arthur G. Kristiansen, Jarmo Körkkö	2
13	Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta 2001 ·Archives of Oral Biology ·Débora Pallos, Patricia Hart, José Roberto Cortelli, (unknown), Jeffrey T. Wright, Jarmo Körkkö, Décio Brunoni, Thomas C. Hart	39
14	Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita 2001 ·American Journal of Medical Genetics ·Sheila Unger, Jarmo Körkkö, Deborah Krakow, Ralph S. Lachman, David L. Rimoin, Daniel H. Cohn	25
15	Use of conformation sensitive gel electrophoresis to detect single-base changes in the gene for COL10A1 1998 ·Human Mutation ·Jarmo Körkkö, (unknown), Darwin J. Prockop, Leena Ala‐Kokko	6
16	Two new recurrent nucleotide mutations in theCOL1A1 gene in four patients with osteogenesis imperfecta: About one-fifth are recurrent 1997 ·Human Mutation ·Jarmo Körkkö, Helena Kuivaniemi, Petteri Paassilta, (unknown), Gerard Tromp, (unknown), Darwin J. Prockop, Leena Ala‐Kokko	20
17	Complete Structure of the Human COL11A2 Gene: The Exon Sizes and other Features Indicate the Gene Has Not Evolved with Genes for Other Fibriller Collagens 1996 ·Annals of the New York Academy of Sciences ·(unknown), Tero Pihlajamaa, Philipp Vandenberg, Jarmo Körkkö, Darwin J. Prockop, Leena Ala‐Kokko	4
18	Phenotypic expressions of a Gly154Arg mutation in type II collagen in two unrelated patients with spondyloepimetaphyseal dysplasia (SEMD) 1996 ·American Journal of Medical Genetics ·Ilkka Kaitila, Jarmo Körkkö, Eino Marttinen, Leena Ala‐Kokko	8
19	Identification of col2a1 gene mutations in patients with chondrodysplasias and familial osteoarthritis 1995 ·Arthritis & Rheumatism ·Pertti Ritvaniemi, Jarmo Körkkö, Jacky Bonaventure, Miikka Vikkula, James Hyland, Petteri Paassilta, Ilkka Kaitila, Helena Kääriäinen, Boris P. Sokolov, Markku Hakala, (unknown), (unknown), Tero Klemola, Charlene J. Williams, Leena Peltonen, Kari I. Kivirikko, Darwin J. Prockop, Leena Ala‐Kokko	50
20	Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy) 1993 ·PubMed ·Jarmo Körkkö, Pertti Ritvaniemi, Leena Haataja, H Kääriäinen, Kari I. Kivirikko, Darwin J. Prockop, Leena Ala‐Kokko	56

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.

Explore authors with similar magnitude of impact