Darek Kedra

2.9k total citations
28 papers, 1.0k citations indexed

About

Darek Kedra is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Darek Kedra has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Darek Kedra's work include RNA modifications and cancer (5 papers), Congenital heart defects research (3 papers) and Chromatin Remodeling and Cancer (3 papers). Darek Kedra is often cited by papers focused on RNA modifications and cancer (5 papers), Congenital heart defects research (3 papers) and Chromatin Remodeling and Cancer (3 papers). Darek Kedra collaborates with scholars based in Sweden, United States and Poland. Darek Kedra's co-authors include Jan P. Dumanski, Ingegerd Fransson, Eyal Seroussi, Bruce A. Roe, Nikolaus Blin, Josiane Grosgeorge, Nicolas Sirvent, Nils Mandahl, Gabriella Sozzi and Claude Turc‐Carel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Bioinformatics.

In The Last Decade

Darek Kedra

28 papers receiving 1.0k citations

Peers

Darek Kedra

PRM

ONCOL

GENET

RHEUM

Wei-Wu He United States

L. Michael Glode United States

J. Christopher Grimaldi United States

Yves Courty France

Andy Blanchard United Kingdom

Astrid Weins United States

Warren Kaplan Australia

René Hubert United States

Ute Raffetseder Germany

Wei-Wu He United States

Darek Kedra

1.0k ×2.1

204 ×0.7

PRM

198 ×1.0

ONCOL

194 ×1.2

GENET

51 ×0.4

RHEUM

Citations per year, relative to Darek Kedra Darek Kedra (= 1×) peers Wei-Wu He

Countries citing papers authored by Darek Kedra

Since Specialization

Citations

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

Fields of papers citing papers by Darek Kedra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Darek Kedra

This figure shows the co-authorship network connecting the top 25 collaborators of Darek Kedra. A scholar is included among the top collaborators of Darek Kedra 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 Darek Kedra. Darek Kedra 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

Rydzanicz, Małgorzata, Paweł Olszewski, Darek Kedra, et al.. (2020). Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications. Molecular Genetics & Genomic Medicine. 9(1). e1526–e1526. 5 indexed citations

Prieto, Pablo, Pascale Pescher, Giovanni Bussotti, et al.. (2017). Haplotype selection as an adaptive mechanism in the protozoan pathogen Leishmania donovani. Nature Ecology & Evolution. 1(12). 1961–1969. 75 indexed citations

Seroussi, Eyal, Micha Ron, & Darek Kedra. (2002). ShiftDetector: detection of shift mutations. Bioinformatics. 18(8). 1137–1138. 16 indexed citations

Kiss, Hajnalka, Darek Kedra, Csaba Kiss, et al.. (2001). The LZTFL1 Gene Is a Part of a Transcriptional Map Covering 250 kb within the Common Eliminated Region 1 (C3CER1) in 3p21.3. Genomics. 73(1). 10–19. 32 indexed citations

Grigelioniené, Giedré, O. Eklöf, Sten A. Ivarsson, et al.. (2000). Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia. Human Genetics. 107(2). 145–149. 30 indexed citations

Tapia‐Páez, Isabel, Kevin P. O'Brien, Maria Kost‐Alimova, et al.. (2000). Fine mapping of the constitutional translocation t(11;22)(q23;q11). Human Genetics. 106(5). 506–516. 18 indexed citations

Kiss, Hajnalka, Darek Kedra, Ying Yang, et al.. (1999). A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3. Human Genetics. 105(6). 552–559. 58 indexed citations

Seroussi, Eyal, Darek Kedra, Huaqin Pan, et al.. (1999). Duplications on Human Chromosome 22 Reveal a Novel Ret Finger Protein-Like Gene Family with Sense and Endogenous Antisense Transcripts. Genome Research. 9(9). 803–814. 23 indexed citations

Yang, Ying, Hajnalka Kiss, Maria Kost‐Alimova, et al.. (1999). A 1-Mb PAC Contig Spanning the Common Eliminated Region 1 (CER1) in Microcell Hybrid-Derived SCID Tumors. Genomics. 62(2). 147–155. 25 indexed citations

10.

Betz, Regina C., Jacob Lagercrantz, Darek Kedra, Jan P. Dumanski, & Agneta Nordenskjöld. (1999). Genomic Structure, 5′ Flanking Sequences, and Precise Localization in 1P31.1 of the Human Prostaglandin F Receptor Gene. Biochemical and Biophysical Research Communications. 254(2). 413–416. 16 indexed citations

11.

Bruder, Carl E.G., Jan P. Dumanski, & Darek Kedra. (1999). The Mouse Ortholog of the HumanSMARCB1Gene Encodes Two Splice Forms. Biochemical and Biophysical Research Communications. 257(3). 886–890. 26 indexed citations

12.

Seroussi, Eyal, Darek Kedra, Maria Kost‐Alimova, et al.. (1999). TOM1Genes Map to Human Chromosome 22q13.1 and Mouse Chromosome 8C1 and Encode Proteins Similar to the Endosomal Proteins HGS and STAM. Genomics. 57(3). 380–388. 17 indexed citations

13.

Seroussi, Eyal, Huaqin Pan, Darek Kedra, Bruce A. Roe, & Jan P. Dumanski. (1998). Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family. Gene. 212(1). 13–20. 44 indexed citations

14.

Kedra, Darek, Huaqin Pan, Eyal Seroussi, et al.. (1998). Characterization of the human synaptogyrin gene family. Human Genetics. 103(2). 131–141. 52 indexed citations

15.

Kedra, Darek, Eyal Seroussi, Ingegerd Fransson, et al.. (1997). The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13. Human Genetics. 100(5-6). 611–619. 26 indexed citations

16.

Konturek, Stanisław J., et al.. (1997). Role ofl-arginine, a substrate for nitric oxide-synthase, in gastroprotection and ulcer healing. Journal of Gastroenterology. 32(4). 442–452. 50 indexed citations

17.

Pédeutour, Florence, Nicolas Sirvent, Josiane Grosgeorge, et al.. (1997). Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma. Nature Genetics. 15(1). 95–98. 364 indexed citations

18.

Lagercrantz, Jacob, Darek Kedra, Emma Carson, et al.. (1996). Sequence and Expression of the Mouse Homologue to Human Phospholipase C β3 Neighboring Gene. Biochemical and Biophysical Research Communications. 223(2). 335–340. 6 indexed citations

19.

Peyrard, Myriam, Huaqin Pan, Darek Kedra, et al.. (1996). Structure of the Promoter and Genomic Organization of the Human β′-Adaptin Gene (BAM22) from Chromosome 22q12. Genomics. 36(1). 112–117. 19 indexed citations

20.

Kedra, Darek. (1996). Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11. Human Molecular Genetics. 5(5). 625–631. 51 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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