Petra Werner

786 total citations
27 papers, 621 citations indexed

About

Petra Werner is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Petra Werner has authored 27 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Epidemiology. Recurrent topics in Petra Werner's work include Congenital heart defects research (10 papers), Congenital Heart Disease Studies (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Petra Werner is often cited by papers focused on Congenital heart defects research (10 papers), Congenital Heart Disease Studies (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Petra Werner collaborates with scholars based in United States, Germany and Switzerland. Petra Werner's co-authors include Paula S. Henthorn, Margret L. Casal, Donald F. Patterson, M Raducha, Elaine A. Ostrander, Cathryn S. Mellersh, Susan DeRose, Elizabeth Goldmuntz, Sophie Jouquand and Christophe Hitte and has published in prestigious journals such as Journal of Thrombosis and Haemostasis, Genomics and Human Mutation.

In The Last Decade

Petra Werner

26 papers receiving 600 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Petra Werner United States 14 306 248 87 75 59 27 621
Ana Martı́nez de Aragón Spain 14 242 0.8× 125 0.5× 38 0.4× 68 0.9× 63 1.1× 54 669
Yulan Lu China 19 527 1.7× 314 1.3× 50 0.6× 80 1.1× 67 1.1× 83 1.2k
Alphonse E. Leure‐Dupree United States 18 335 1.1× 130 0.5× 65 0.7× 215 2.9× 12 0.2× 24 1.0k
Ans van der Ploeg Netherlands 13 284 0.9× 73 0.3× 149 1.7× 460 6.1× 50 0.8× 49 1.2k
Chiara Di Bella Italy 13 291 1.0× 171 0.7× 15 0.2× 60 0.8× 23 0.4× 30 668
Jessica M. Maia United States 11 524 1.7× 476 1.9× 39 0.4× 42 0.6× 7 0.1× 16 994
Mojca Stražišar Belgium 17 486 1.6× 200 0.8× 21 0.2× 25 0.3× 13 0.2× 32 863
Ľudevít Kádaši Slovakia 18 446 1.5× 155 0.6× 26 0.3× 22 0.3× 147 2.5× 56 809
Ryan Sprissler United States 8 182 0.6× 187 0.8× 108 1.2× 12 0.2× 15 0.3× 20 547
B Noël France 18 323 1.1× 466 1.9× 19 0.2× 73 1.0× 8 0.1× 63 985

Countries citing papers authored by Petra Werner

Since Specialization
Citations

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

Fields of papers citing papers by Petra Werner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petra Werner

This figure shows the co-authorship network connecting the top 25 collaborators of Petra Werner. A scholar is included among the top collaborators of Petra Werner 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 Petra Werner. Petra Werner 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.
Murgiano, Leonardo, et al.. (2024). A naturally occurring canine model of syndromic congenital microphthalmia. G3 Genes Genomes Genetics. 14(6).
2.
Xie, Hongbo, Petra Werner, Dwight Stambolian, et al.. (2017). Rare copy number variants in patients with congenital conotruncal heart defects. Birth Defects Research. 109(4). 271–295. 13 indexed citations
3.
Werner, Petra, Prasuna Paluru, Anisha M. Simpson, et al.. (2014). Mutations inNTRK3Suggest a Novel Signaling Pathway in Human Congenital Heart Disease. Human Mutation. 35(12). 1459–1468. 16 indexed citations
4.
Werner, Petra, et al.. (2011). Primary Infundibular Stenosis and Pedigree Analysis in Three Golden Retriever Littermates. Journal of the American Animal Hospital Association. 48(1). 50–53. 3 indexed citations
5.
Wang, Ping, Barbara Zangerl, Petra Werner, Elizabeth A. Mauldin, & Margret L. Casal. (2010). Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE. Immunogenetics. 63(4). 197–207. 14 indexed citations
6.
Werner, Petra, et al.. (2008). A novel locus for dilated cardiomyopathy maps to canine chromosome 8. Genomics. 91(6). 517–521. 24 indexed citations
7.
Callan, Mary Beth, Paris Margaritis, Monika E. Griot‐Wenk, et al.. (2006). A novel missense mutation responsible for factor VII deficiency in research Beagle colonies. Journal of Thrombosis and Haemostasis. 4(12). 2616–2622. 39 indexed citations
8.
Casal, Margret L., et al.. (2006). Epilepsy in Irish Wolfhounds. Journal of Veterinary Internal Medicine. 20(1). 131–131. 52 indexed citations
9.
Casal, Margret L., et al.. (2006). Epilepsy in Irish Wolfhounds. Journal of Veterinary Internal Medicine. 20(1). 131–135. 55 indexed citations
10.
Werner, Petra, M Raducha, Elaine A. Ostrander, et al.. (2005). The keeshond defect in cardiac conotruncal development is oligogenic1. Human Genetics. 116(5). 368–377. 22 indexed citations
11.
Casal, Margret L., et al.. (2005). Mutation identification in a canine model of X-linked ectodermal dysplasia. Mammalian Genome. 16(7). 524–531. 44 indexed citations
12.
Werner, Petra, M Raducha, Daesung Shin, et al.. (2004). Assignment of 10 canine genes to the canine linkage and comparative maps. Animal Genetics. 35(3). 249–251. 3 indexed citations
13.
He, Qianchuan, et al.. (2003). Canine Imerslund-Gr�sbeck syndrome maps to a region orthologous to HSA14q. Mammalian Genome. 14(11). 758–764. 25 indexed citations
14.
Mellersh, Cathryn S., Christophe Hitte, Françoise Vignaux, et al.. (2000). An integrated linkage-radiation hybrid map of the canine genome. Mammalian Genome. 11(2). 120–130. 127 indexed citations
15.
16.
17.
Werner, Petra, Cathryn S. Mellersh, M Raducha, et al.. (1999). Anchoring of canine linkage groups with chromosome-specific markers. Mammalian Genome. 10(8). 814–823. 49 indexed citations
18.
Werner, Petra, et al.. (1998). RXRA and HSPA5 map to the telomeric end of dog chromosome 9. Animal Genetics. 29(3). 220–223. 5 indexed citations
19.
Werner, Petra, et al.. (1997). Physical and Linkage Mapping of Human Chromosome 17 Loci to Dog Chromosomes 9 and 5. Genomics. 42(1). 74–82. 51 indexed citations
20.
Lyr, H. & Petra Werner. (1982). On the mechanism of action of the fungicide chloroneb. Pesticide Biochemistry and Physiology. 18(1). 69–76. 8 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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