David Fredman

3.1k total citations
29 papers, 1.5k citations indexed

About

David Fredman is a scholar working on Molecular Biology, Genetics and Paleontology. According to data from OpenAlex, David Fredman has authored 29 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Paleontology. Recurrent topics in David Fredman's work include Genomics and Chromatin Dynamics (9 papers), Marine Invertebrate Physiology and Ecology (8 papers) and Chromosomal and Genetic Variations (8 papers). David Fredman is often cited by papers focused on Genomics and Chromatin Dynamics (9 papers), Marine Invertebrate Physiology and Ecology (8 papers) and Chromosomal and Genetic Variations (8 papers). David Fredman collaborates with scholars based in Norway, Austria and United States. David Fredman's co-authors include Boris Lenhard, Ulrich Technau, Thomas Becker, Yehu Moran, Pavla Navrátilová, Anthony J. Brookes, Pär G. Engström, Johan T. den Dunnen, Stefan J. White and Evan E. Eichler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

David Fredman

29 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Fredman Norway 21 1.0k 461 252 209 142 29 1.5k
John Reece-Hoyes United States 32 2.8k 2.6× 475 1.0× 375 1.5× 138 0.7× 128 0.9× 57 3.4k
Celina E. Juliano United States 22 1.4k 1.4× 258 0.6× 379 1.5× 357 1.7× 439 3.1× 38 2.0k
Bryony Fahey Australia 10 657 0.6× 96 0.2× 224 0.9× 256 1.2× 249 1.8× 10 1.1k
Martin Pippel Germany 14 699 0.7× 238 0.5× 195 0.8× 58 0.3× 157 1.1× 28 1.1k
Jung Shan Hwang Malaysia 16 523 0.5× 139 0.3× 144 0.6× 359 1.7× 212 1.5× 35 939
Isabelle S. Peter United States 18 1.2k 1.2× 530 1.1× 90 0.4× 52 0.2× 145 1.0× 29 1.6k
Carine Barreau France 12 1.1k 1.1× 136 0.3× 63 0.3× 130 0.6× 94 0.7× 14 1.4k
Toby Hunt United Kingdom 15 619 0.6× 501 1.1× 184 0.7× 425 2.0× 43 0.3× 21 1.9k
Mark W. Walberg United States 8 1.9k 1.8× 484 1.0× 80 0.3× 109 0.5× 54 0.4× 8 2.3k
Marie‐Luise Dirksen United States 15 1.4k 1.3× 324 0.7× 90 0.4× 110 0.5× 56 0.4× 17 1.5k

Countries citing papers authored by David Fredman

Since Specialization
Citations

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

Fields of papers citing papers by David Fredman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Fredman

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

All Works

20 of 20 papers shown
1.
Rønneseth, Anita, David Fredman, Kjell Petersen, et al.. (2018). Transcriptome-wide mapping of signaling pathways and early immune responses in lumpfish leukocytes upon in vitro bacterial exposure. Scientific Reports. 8(1). 5261–5261. 19 indexed citations
2.
Stokowy, Tomasz, Bartosz Wojtaś, Barbara Jarząb, et al.. (2016). Two-miRNA classifiers differentiate mutation-negative follicular thyroid carcinomas and follicular thyroid adenomas in fine needle aspirations with high specificity. Endocrine. 54(2). 440–447. 26 indexed citations
3.
Kraus, Johanna E. M., David Fredman, Wei Wang, Konstantin Khalturin, & Ulrich Technau. (2015). Adoption of conserved developmental genes in development and origin of the medusa body plan. EvoDevo. 6(1). 23–23. 33 indexed citations
4.
Schwaiger, Michaela, Anna Schönauer, André F. Rendeiro, et al.. (2014). Evolutionary conservation of the eumetazoan gene regulatory landscape. Genome Research. 24(4). 639–650. 116 indexed citations
5.
Fischer, Antje, et al.. (2013). Employing BAC-reporter constructs in the sea anemone Nematostella vectensis. Integrative and Comparative Biology. 53(5). 832–846. 2 indexed citations
6.
Moran, Yehu, Daniela Praher, David Fredman, & Ulrich Technau. (2013). The Evolution of MicroRNA Pathway Protein Components in Cnidaria. Molecular Biology and Evolution. 30(12). 2541–2552. 52 indexed citations
7.
Eriksson, Bo, David Fredman, G. Steïner, & Axel Schmid. (2013). Characterisation and localisation of the opsin protein repertoire in the brain and retinas of a spider and an onychophoran. BMC Evolutionary Biology. 13(1). 186–186. 45 indexed citations
8.
Moran, Yehu, David Fredman, Paweł Szczęsny, Marcin Grynberg, & Ulrich Technau. (2012). Recurrent Horizontal Transfer of Bacterial Toxin Genes to Eukaryotes. Molecular Biology and Evolution. 29(9). 2223–2230. 87 indexed citations
9.
Fredman, David, Xianjun Dong, & Boris Lenhard. (2011). Making enhancers from spare parts of the genome. Genome Biology. 12(12). 138–138. 1 indexed citations
10.
Akalin, Altuna, David Fredman, Erik Arner, et al.. (2009). Transcriptional features of genomic regulatory blocks. Genome biology. 10(4). R38–R38. 75 indexed citations
11.
Dong, Xianjun, David Fredman, & Boris Lenhard. (2009). Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes. Genome biology. 10(8). R86–R86. 20 indexed citations
12.
Navrátilová, Pavla, David Fredman, Boris Lenhard, & Thomas Becker. (2009). Regulatory divergence of the duplicated chromosomal loci sox11a/b by subpartitioning and sequence evolution of enhancers in zebrafish. Molecular Genetics and Genomics. 283(2). 171–184. 23 indexed citations
13.
Dong, Xianjun, Pavla Navrátilová, David Fredman, et al.. (2009). Exonic remnants of whole-genome duplication reveal cis-regulatory function of coding exons. Nucleic Acids Research. 38(4). 1071–1085. 43 indexed citations
14.
Luo, Minjie, Xiangfeng Cui, David Fredman, et al.. (2009). Genetic Structures of Copy Number Variants Revealed by Genotyping Single Sperm. PLoS ONE. 4(4). e5236–e5236. 2 indexed citations
15.
Navrátilová, Pavla, David Fredman, Thomas Hawkins, et al.. (2008). Systematic human/zebrafish comparative identification of cis-regulatory activity around vertebrate developmental transcription factor genes. Developmental Biology. 327(2). 526–540. 88 indexed citations
16.
Frith, Martin C., Jasmina Ponjavic, David Fredman, et al.. (2006). Evolutionary turnover of mammalian transcription start sites. Genome Research. 16(6). 713–722. 64 indexed citations
17.
Fredman, David, Sarah L. Sawyer, Salim Mottagui‐Tabar, et al.. (2006). Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection. Human Mutation. 27(2). 173–186. 8 indexed citations
18.
Fredman, David, et al.. (2004). DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applications. Human Mutation. 24(1). 1–8. 18 indexed citations
19.
Fredman, David. (2003). HGVbase: a curated resource describing human DNA variation and phenotype relationships. Nucleic Acids Research. 32(90001). 516D–519. 51 indexed citations
20.
Fredman, David. (2002). HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources. Nucleic Acids Research. 30(1). 387–391. 109 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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