Karen Rooke

5.1k total citations
7 papers, 317 citations indexed

About

Karen Rooke is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Karen Rooke has authored 7 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Physiology. Recurrent topics in Karen Rooke's work include Alzheimer's disease research and treatments (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Heat shock proteins research (2 papers). Karen Rooke is often cited by papers focused on Alzheimer's disease research and treatments (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Heat shock proteins research (2 papers). Karen Rooke collaborates with scholars based in United States, United Kingdom and Canada. Karen Rooke's co-authors include Denise A. Figlewicz, Jean‐Pierre Julien, Arthur W. Clark, Aldis Krizus, Guy A. Rouleau, Albéna Pramatarova, Oksana Suchowersky, Fei‐Yu Han, Guy A. Rouleau and John Hardy and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Karen Rooke

6 papers receiving 311 citations

Peers

Karen Rooke

NEURO

GENET

MB

PHYSI

NEURO

Lisa Taylor‐Reinwald United States

Linda Rousseau United States

Joshua D. Kidd United States

Laëtitia Miguel France

Katherine D. LaClair United States

Tsz Hang Wong Netherlands

Kanchana K. Gamage United States

Sonja Zilow Germany

Lilja Jansson Finland

Dena Hernandez United States

Lisa Taylor‐Reinwald United States

Karen Rooke

294 ×1.5

NEURO

72 ×0.6

GENET

93 ×0.9

MB

218 ×2.5

PHYSI

101 ×1.2

NEURO

Citations per year, relative to Karen Rooke Karen Rooke (= 1×) peers Lisa Taylor‐Reinwald

Countries citing papers authored by Karen Rooke

Since Specialization

Citations

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

Fields of papers citing papers by Karen Rooke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Rooke

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

All Works

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7 of 7 papers shown

1.

Xia, Yu-Rong, et al.. (1998). Mapping of three members of the mouse protein disulfide isomerase family. Mammalian Genome. 9(2). 176–177. 4 indexed citations

2.

Rooke, Karen, et al.. (1997). Mapping of the gene for calreticulin (Calr) to mouse Chromosome 8. Mammalian Genome. 8(11). 870–871. 4 indexed citations

3.

Rouleau, Guy A., Arthur W. Clark, Karen Rooke, et al.. (1996). SOD1 mutation is assosiated with accumulation of neurofilaments in amyotrophic lateral scelaries. Annals of Neurology. 39(1). 128–131. 189 indexed citations

4.

Rooke, Karen, Denise A. Figlewicz, Fei‐Yu Han, & Guy A. Rouleau. (1996). Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis. Neurology. 46(3). 789–790. 55 indexed citations

5.

Rooke, Karen, Chris J. Talbot, Louise James, et al.. (1993). A physical map of the human APP gene in YACs. Mammalian Genome. 4(11). 662–669. 3 indexed citations

6.

Fidani, Liana, Karen Rooke, Marie‐Christine Chartier‐Harlin, et al.. (1992). Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle. Human Molecular Genetics. 1(3). 165–168. 62 indexed citations

7.

Goate, Alison, Marie‐Christine Chartier‐Harlin, Michael Mullan, et al.. (1991). SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE. UCL Discovery (University College London).

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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