L. Pajunen

575 total citations
20 papers, 394 citations indexed

About

L. Pajunen is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, L. Pajunen has authored 20 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in L. Pajunen's work include Connective tissue disorders research (5 papers), Glycosylation and Glycoproteins Research (3 papers) and Microbial metabolism and enzyme function (2 papers). L. Pajunen is often cited by papers focused on Connective tissue disorders research (5 papers), Glycosylation and Glycoproteins Research (3 papers) and Microbial metabolism and enzyme function (2 papers). L. Pajunen collaborates with scholars based in Finland, United Kingdom and Netherlands. L. Pajunen's co-authors include Kari I. Kivirikko, Raili Myllylä, E. Solomon, Taina Pihlajaniemi, Dallas M. Swallow, Timo Hautala, Taina Turpeenniemi‐Hujanen, Jari Heikkinen, Tarja Helaakoski and T. Alwyn Jones and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical Journal and Journal of Immunological Methods.

In The Last Decade

L. Pajunen

20 papers receiving 362 citations

Peers

L. Pajunen

GENET

RHEUM

CMN

Shinu Ansari Saudi Arabia

Miia Vapola Finland

Marie-Pierre Leibovitch France

Bert Eussen Netherlands

Jill M. Shirokawa United States

Pablo Villavicencio‐Lorini Germany

Kathleen A. Soltis United States

E. Natt Germany

Erika M. Batchelder United States

K. Okui Japan

Shinu Ansari Saudi Arabia

L. Pajunen

304 ×1.1

232 ×1.7

GENET

86 ×1.2

69 ×1.3

RHEUM

15 ×0.5

CMN

Citations per year, relative to L. Pajunen L. Pajunen (= 1×) peers Shinu Ansari

Countries citing papers authored by L. Pajunen

Since Specialization

Citations

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

Fields of papers citing papers by L. Pajunen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Pajunen

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

All Works

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20 of 20 papers shown

Kaasinen, Eevi, Elisa Rahikkala, Peppi Koivunen, et al.. (2014). Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome. European Journal of Medical Genetics. 57(10). 543–551. 14 indexed citations

Ylikallio, Emil, Mridul Johari, Svetlana Konovalova, et al.. (2013). Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot–Marie–Tooth neuropathy and a mutation in HSPB1. European Journal of Human Genetics. 22(4). 522–527. 26 indexed citations

Hinttala, Reetta, Mikko Kärppä, L. Pajunen, et al.. (2010). POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype. BMC Neurology. 10(1). 29–29. 15 indexed citations

Pajunen, L., et al.. (2009). NOR activity in two families with balanced D;D translocations and numerous consecutive miscarriages. Hereditas. 92(2). 217–221. 1 indexed citations

Linna, O, Kalevi Hyrynkangas, Tuula Kaukola, & L. Pajunen. (2004). Congenital subglottic stenosis in two unrelated pairs of siblings. Acta Paediatrica. 93(4). 565–567. 4 indexed citations

Pajunen, L., Marko Suokas, Timo Hautala, et al.. (1998). A Splice-Site Mutation that Induces Exon Skipping and Reduction in Lysyl Hydroxylase mRNA Levels but Does Not Create a Nonsense Codon in Ehlers-Danlos Syndrome Type VI. DNA and Cell Biology. 17(2). 117–123. 15 indexed citations

Kauppila, Saila, Leila Risteli, Katri Vuopala, et al.. (1998). New lethal disease involving type I and III collagen defect resembling geroderma osteodysplastica, De Barsy syndrome, and Ehlers-Danlos syndrome IV.. Journal of Medical Genetics. 35(6). 513–518. 6 indexed citations

Hautala, Timo, et al.. (1994). Alu-alu recombination results in duplication of seven exons in the lysyl hydroxylase gene from a patient with the type VI variant of Ehlers-Danlos syndrome. Matrix Biology. 14(5). 399–399. 12 indexed citations

Hautala, Timo, et al.. (1994). Alu-Alu recombination results in a duplication of seven exons in the lysyl hydroxylase gene in a patient with the type VI variant of Ehlers-Danlos syndrome.. PubMed. 55(5). 899–906. 59 indexed citations

10.

Pajunen, L., T. Alwyn Jones, Audrey D. Goddard, et al.. (1991). Regional assignment of the human gene coding for a multifunctional polypeptide (P4HB) acting as the β-subunit of prolyl 4-hydroxylase and the enzyme protein disulfide isomerase to 17q25. Cytogenetic and Genome Research. 56(3-4). 165–168. 15 indexed citations

11.

Myllylä, Raili, Taina Pihlajaniemi, L. Pajunen, Taina Turpeenniemi‐Hujanen, & Kari I. Kivirikko. (1991). Molecular cloning of chick lysyl hydroxylase. Little homology in primary structure to the two types of subunit of prolyl 4-hydroxylase.. Journal of Biological Chemistry. 266(5). 2805–2810. 58 indexed citations

12.

Helaakoski, Tarja, L. Pajunen, Kari I. Kivirikko, & Taina Pihlajaniemi. (1990). Increases in mRNA concentrations of the alpha and beta subunits of prolyl 4-hydroxylase accompany increased gene expression of type IV collagen during differentiation of mouse F9 cells.. Journal of Biological Chemistry. 265(20). 11413–11416. 18 indexed citations

13.

Pajunen, L., Minna Tamminen, E. Solomon, & Taina Pihlajaniemi. (1989). Assignment of the gene coding for the α1 chain of collagen type XIII (COL13A1) to human chromosome region 10q11→qter. Cytogenetic and Genome Research. 52(3-4). 190–193. 8 indexed citations

14.

Pajunen, L., T. Alwyn Jones, Tarja Helaakoski, et al.. (1989). Assignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1.. PubMed. 45(6). 829–34. 14 indexed citations

15.

Pajunen, L., Raili Myllylä, Tarja Helaakoski, et al.. (1988). Assignment of the gene coding for both the β-subunit of prolyl 4-hydroxylase and the enzyme disulfide isomerase to human chromosome region 17p11→qter. Cytogenetic and Genome Research. 47(1-2). 37–41. 19 indexed citations

16.

Myllylä, Raili, L. Pajunen, & Kari I. Kivirikko. (1988). Polyclonal and monoclonal antibodies to human lysyl hydroxylase and studies on the molecular heterogeneity of the enzyme. Biochemical Journal. 253(2). 489–496. 26 indexed citations

17.

Pajunen, L., et al.. (1981). Radioimmunoassay for H-Y antigen. Journal of Immunological Methods. 41(3). 343–349. 6 indexed citations

18.

Chapelle, Albert de la, K. O. J. Simola, P. E. Simola, et al.. (1979). Heteromorphic X Chromosomes in 46,XX males?. Human Genetics. 52(2). 157–167. 7 indexed citations

19.

Pajunen, L., et al.. (1978). Regional mapping of chromosome 15. Cytogenetic and Genome Research. 22(1-6). 511–512. 5 indexed citations

20.

Swallow, Dallas M., E. Solomon, & L. Pajunen. (1977). Immunochemical analysis of the <i>N</i>-acetyl hexosaminidases in human-mouse hybrids made using a double selective system. Cytogenetic and Genome Research. 18(3). 136–148. 66 indexed citations

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