Dora Stauffer

4.4k total citations · 2 hit papers
15 papers, 2.2k citations indexed

About

Dora Stauffer is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Dora Stauffer has authored 15 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Dora Stauffer's work include Genomics and Rare Diseases (2 papers), Genetic factors in colorectal cancer (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Dora Stauffer is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic factors in colorectal cancer (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Dora Stauffer collaborates with scholars based in United States, Belgium and Poland. Dora Stauffer's co-authors include Vernon Anderson, Mark Leppert, R. White, Mark Leppert, Roberta Melis, Ingrid Bjerre, Gabriel M. Ronen, Robin J. Leach, Jerome V. Murphy and Andy Peiffer and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Dora Stauffer

15 papers receiving 2.2k citations

Hit Papers

A novel potassium channel gene, KCNQ2, is mutated in an i... 1987 2026 2000 2013 1998 1987 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
    1998 939 citations Nanda A. Singh, Carole Charlier et al. Nature Genetics profile →
  2. The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5
    1987 502 citations M. Leppert, Peter Scambler et al. Science profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dora Stauffer United States 12 1.2k 811 499 484 479 15 2.2k
Kazuo Washiyama Japan 23 791 0.6× 365 0.5× 137 0.3× 109 0.2× 184 0.4× 60 1.5k
Frances Elmslie United Kingdom 18 1.2k 1.0× 440 0.5× 64 0.1× 126 0.3× 566 1.2× 28 2.0k
Erik‐Jan Kamsteeg Netherlands 32 2.2k 1.8× 704 0.9× 68 0.1× 313 0.6× 470 1.0× 124 3.2k
Satoko Miyatake Japan 29 1.5k 1.2× 508 0.6× 91 0.2× 103 0.2× 766 1.6× 146 2.4k
Colleen T. Harrington United States 15 857 0.7× 401 0.5× 141 0.3× 97 0.2× 141 0.3× 20 1.5k
Albena Jordanova Belgium 32 1.9k 1.5× 1.7k 2.1× 64 0.1× 81 0.2× 479 1.0× 87 3.6k
Rossella Tupler Italy 26 1.7k 1.4× 316 0.4× 50 0.1× 284 0.6× 561 1.2× 78 2.4k
Masashi Fujitani Japan 22 931 0.8× 776 1.0× 184 0.4× 40 0.1× 126 0.3× 43 1.9k
Patrick A. Dreyfus France 26 1.1k 0.9× 359 0.4× 67 0.1× 290 0.6× 157 0.3× 49 2.0k
Jon Neumann United States 16 1.7k 1.4× 199 0.2× 50 0.1× 791 1.6× 312 0.7× 21 2.2k

Countries citing papers authored by Dora Stauffer

Since Specialization
Citations

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

Fields of papers citing papers by Dora Stauffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dora Stauffer

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

All Works

15 of 15 papers shown
1.
Flanigan, Kevin M., et al.. (2001). Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy. Neuromuscular Disorders. 11(6-7). 525–529. 87 indexed citations
2.
Charlier, Carole, Andy Peiffer, Dora Stauffer, et al.. (1999). Genes for rare idiopathic generalized epilepsies: BFNC.. PubMed. 79. 341–50. 2 indexed citations
3.
Singh, Nanda A., Carole Charlier, Dora Stauffer, et al.. (1998). A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nature Genetics. 18(1). 25–29. 939 indexed citations breakdown →
4.
Otterud, Brith, Wen‐Tsong Hsieh, María Martínez, et al.. (1995). Genetic mapping of adrenergic receptor genes in humans. Journal of Molecular Medicine. 73(6). 299–306. 22 indexed citations
5.
Melis, Roberta, Dora Stauffer, Xiao Lin Zhu, et al.. (1995). Physical and genetic localization of a Shab subfamily potassium channel (KCNB1) gene to chromosomal region 20q13.2. Genomics. 25(1). 285–287. 18 indexed citations
6.
Marshall, Hiram W., Linda Morrison, Lily Wu, et al.. (1994). Apolipoprotein polymorphisms fail to define risk of coronary artery disease. Results of a prospective, angiographically controlled study.. Circulation. 89(2). 567–577. 66 indexed citations
7.
Spirio, Lisa, Brith Otterud, Dora Stauffer, et al.. (1992). Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.. PubMed. 51(1). 92–100. 112 indexed citations
8.
Hoehe, Margret R., Rosemarie Plaetke, Brith Otterud, et al.. (1992). Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22. Human Molecular Genetics. 1(3). 175–178. 15 indexed citations
9.
Dean, Michael, Cameron Stewart, Anjanette Perry, et al.. (1991). D7S448 detects aHindIII polymorphism located in the centromere region of chromosome 7. Nucleic Acids Research. 19(1). 200–200. 2 indexed citations
10.
Lynch, Sharon, John Rose, Jack H. Petajan, et al.. (1991). Discordance of T‐cell receptor β‐chain genes in familial multiple sclerosis. Annals of Neurology. 30(3). 402–410. 48 indexed citations
11.
Lewis, Richard A., et al.. (1990). Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. Genomics. 7(2). 250–256. 90 indexed citations
12.
Leppert, Mark, Vernon Anderson, Dora Stauffer, et al.. (1989). Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature. 337(6208). 647–648. 266 indexed citations
13.
Leppert, Mark, Peter Scambler, P. O’Connell, et al.. (1987). THE GENE FOR FAMILIAL POLYPOSIS MAPS TO THE LONG ARM OF CHROMOSOME-5. UCL Discovery (University College London). 10 indexed citations
14.
Keppen, Laura Davis, Mark Leppert, Peter O'Connell, et al.. (1987). Etiological heterogeneity in X-linked spastic paraplegia.. PubMed. 41(5). 933–43. 62 indexed citations
15.
Leppert, M., Peter Scambler, P. O’Connell, et al.. (1987). The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5. Science. 238(4832). 1411–1413. 502 indexed citations breakdown →

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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