Marketta Kähkönen

1.0k total citations
16 papers, 645 citations indexed

About

Marketta Kähkönen is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Marketta Kähkönen has authored 16 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Marketta Kähkönen's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and DNA Repair Mechanisms (2 papers). Marketta Kähkönen is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and DNA Repair Mechanisms (2 papers). Marketta Kähkönen collaborates with scholars based in Finland, United States and Slovakia. Marketta Kähkönen's co-authors include Ylermi Soini, Hannu Haapasalo, Sally Järvelä, Silvia Pastoreková, Seppo Parkkila, Anna‐Kaisa Parkkila, Jaromı́r Pastorek, Jeremy Schwartzentruber, Martin Kircher and David A. Dyment and has published in prestigious journals such as Journal of Investigative Dermatology, Cancer Discovery and BMC Cancer.

In The Last Decade

Marketta Kähkönen

14 papers receiving 635 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marketta Kähkönen Finland	8	407	219	125	120	44	16	645
Radek Vrtěl Czechia	13	310 0.8×	157 0.7×	52 0.4×	127 1.1×	57 1.3×	49	616
Miriam Teeuwssen Netherlands	7	396 1.0×	107 0.5×	160 1.3×	246 2.0×	50 1.1×	8	637
Anderson T. Wang United Kingdom	11	778 1.9×	101 0.5×	191 1.5×	229 1.9×	25 0.6×	16	911
Amanda K. Ashley United States	13	461 1.1×	95 0.4×	100 0.8×	218 1.8×	21 0.5×	24	688
Yang W. Zhang United States	11	981 2.4×	101 0.5×	190 1.5×	129 1.1×	60 1.4×	13	1.2k
Akiko Fujimura Japan	13	563 1.4×	65 0.3×	81 0.6×	180 1.5×	31 0.7×	40	842
Vivek Reddy Palicharla United States	9	508 1.2×	152 0.7×	89 0.7×	115 1.0×	44 1.0×	13	649
Florence Le Page France	12	955 2.3×	171 0.8×	369 3.0×	199 1.7×	68 1.5×	15	1.1k
Hannah Williams United Kingdom	14	529 1.3×	72 0.3×	77 0.6×	79 0.7×	19 0.4×	15	702
Zarir E. Karanjawala United States	14	708 1.7×	75 0.3×	222 1.8×	330 2.8×	44 1.0×	23	1.1k

Countries citing papers authored by Marketta Kähkönen

Since Specialization

Citations

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

Fields of papers citing papers by Marketta Kähkönen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marketta Kähkönen

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

All Works

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16 of 16 papers shown

Sawyer, Sarah L., Lei Tian, Marketta Kähkönen, et al.. (2014). Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype. Cancer Discovery. 5(2). 135–142. 214 indexed citations

Haapasalo, Joonas, et al.. (2014). [Diagnosis and prognosis of gliomas--current prospects of molecular diagnostics].. PubMed. 130(9). 893–901. 5 indexed citations

Lohi, Olli, Martine Vornanen, Marketta Kähkönen, et al.. (2012). Recurrent Congenital Fibrosarcoma With Heart Metastases. Journal of Pediatric Hematology/Oncology. 34(5). e202–e205. 3 indexed citations

Gripenberg, Ulla, et al.. (2009). A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti Institution, Finland. Hereditas. 92(2). 223–228. 1 indexed citations

Gripenberg, Ulla, et al.. (2009). Fanconi's anaemia; chromosome breakage in a large African family. Hereditas. 93(2). 255–260. 1 indexed citations

Kähkönen, Marketta, et al.. (2009). Notable chromosomal anomalies in a woman receiving drugs during the period of viremia after rubella vaccination. Hereditas. 84(1). 120–123.

Kähkönen, Marketta, et al.. (2009). Mutagenicity of Bacillus thuringiensis exotoxin III. Sister chromatid exchange in rats in vivo. Hereditas. 91(1). 1–3.

Pirinen, Elina, et al.. (2009). Smooth muscle tumor of the placenta - an entrapped maternal leiomyoma: a case report. Journal of Medical Case Reports. 3(1). 7302–7302. 9 indexed citations

Järvelä, Sally, Seppo Parkkila, Marketta Kähkönen, et al.. (2008). Carbonic anhydrase IX in oligodendroglial brain tumors. BMC Cancer. 8(1). 1–1. 245 indexed citations

10.

Peippo, Maarit, K. O. J. Simola, Leena Valanne, et al.. (2006). Pitt–Hopkins syndrome in two patients and further definition of the phenotype. Clinical Dysmorphology. 15(2). 47–54. 43 indexed citations

11.

Linnankivi, Tarja, Pentti J. Tienari, Mirja Somer, et al.. (2006). 18q deletions: Clinical, molecular, and brain MRI findings of 14 individuals. American Journal of Medical Genetics Part A. 140A(4). 331–339. 48 indexed citations

12.

Muche, J. Marcus, Leena Karenko, Sylke Gellrich, et al.. (2004). Cellular Coincidence of Clonal T Cell Receptor Rearrangements and Complex Clonal Chromosomal Aberrations—A Hallmark of Malignancy in Cutaneous T Cell Lymphoma. Journal of Investigative Dermatology. 122(3). 574–578. 15 indexed citations

13.

Larramendy, Marcelo L., Mervi Heiskanen, Maija Wessman, et al.. (1993). Molecular cytogenetic study of patients with Pallister-Killian syndrome. Human Genetics. 91(2). 121–127. 18 indexed citations

14.

Väisänen, Marja‐Leena, Marketta Kähkönen, & Jaakko Leisti. (1992). Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis. American Journal of Medical Genetics. 43(1-2). 307–311. 3 indexed citations

15.

Leisti, Jaakko, Pentti Jouppila, Aki Mustonen, et al.. (1990). Prenatal Diagnosis of Single Gene Disorders in Northern Finland. Annals of Medicine. 22(2). 123–129. 3 indexed citations

16.

Knuutila, Sakari, et al.. (1978). An increased frequency of chromosomal changes and SCE's in cultured blood lymphocytes of 12 subjects vaccinated against smallpox. Human Genetics. 41(1). 89–96. 37 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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