Susan A. Cook

2.3k total citations
32 papers, 1.8k citations indexed

About

Susan A. Cook is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Susan A. Cook has authored 32 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 6 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in Susan A. Cook's work include Renal and related cancers (5 papers), RNA regulation and disease (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Susan A. Cook is often cited by papers focused on Renal and related cancers (5 papers), RNA regulation and disease (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Susan A. Cook collaborates with scholars based in United States, Germany and United Kingdom. Susan A. Cook's co-authors include Muriel T. Davisson, Roderick T. Bronson, Kenneth R. Johnson, Qing Yin Zheng, Lawrence C. Erway, Chantal M. Longo-Guess, Keith R. Johnson, James F. Willott, Susan L. Ackerman and Jae-Seon Jang and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Susan A. Cook

32 papers receiving 1.8k citations

Peers

Susan A. Cook

CMN

GENET

J. Hikke van Doorninck Netherlands

Farideh Hooshmand United States

Nobuko Hagiwara United States

Jacqueline Gabrion France

Mitsuhiro Hashimoto Japan

Ji Eun Lee South Korea

Takahiro Gotow Japan

G. Giacomo Consalez Italy

Daniel Gibbs United States

Olivia Bermingham‐McDonogh United States

J. Hikke van Doorninck Netherlands

Susan A. Cook

971 ×0.8

328 ×1.0

CMN

249 ×0.8

GENET

121 ×0.6

Citations per year, relative to Susan A. Cook Susan A. Cook (= 1×) peers J. Hikke van Doorninck

Countries citing papers authored by Susan A. Cook

Since Specialization

Citations

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

Fields of papers citing papers by Susan A. Cook

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susan A. Cook. 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 Susan A. Cook. The network helps show where Susan A. Cook may publish in the future.

Co-authorship network of co-authors of Susan A. Cook

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

Jia, Yichang, et al.. (2015). Loss ofClcc1Results in ER Stress, Misfolded Protein Accumulation, and Neurodegeneration. Journal of Neuroscience. 35(7). 3001–3009. 29 indexed citations

Korstanje, Ron, Rosalinda Doty, Susan A. Cook, et al.. (2014). A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers. Kidney International. 85(6). 1461–1468. 37 indexed citations

Collin, Gayle B., Jungyeon Won, Wanda L. Hicks, et al.. (2012). Meckelin Is Necessary for Photoreceptor Intraciliary Transport and Outer Segment Morphogenesis. Investigative Ophthalmology & Visual Science. 53(2). 967–967. 28 indexed citations

Cook, Susan A., Gayle B. Collin, Roderick T. Bronson, et al.. (2009). A Mouse Model for Meckel Syndrome Type 3. Journal of the American Society of Nephrology. 20(4). 753–764. 38 indexed citations

Miki, Takafumi, Theresa A. Zwingman, Minoru Wakamori, et al.. (2008). Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies. Neuroscience. 155(1). 31–44. 40 indexed citations

Lee, Jeong-Woong, Kirk Beebe, Leslie A. Nangle, et al.. (2006). Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration. Nature. 443(7107). 50–55. 488 indexed citations

Longo-Guess, Chantal M., et al.. (2005). A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry ( hscy ) mice. Proceedings of the National Academy of Sciences. 102(22). 7894–7899. 83 indexed citations

Cook, Susan A., Ellen C. Akeson, Keith R. Johnson, et al.. (2001). Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenetic and Genome Research. 93(1-2). 77–82. 5 indexed citations

Davisson, Muriel T., Kenneth R. Johnson, Roderick T. Bronson, et al.. (2000). Grey intense: a new mouse mutation affecting pigmentation. Mammalian Genome. 11(12). 1139–1141. 1 indexed citations

10.

Johnson, Keith R., Susan A. Cook, Lawrence C. Erway, et al.. (1999). Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome. Human Molecular Genetics. 8(4). 645–653. 71 indexed citations

11.

Jager, Philip L. De, Jianping Zuo, Susan A. Cook, & Nathaniel Heintz. (1997). A new allele of the lurcher gene, lurcher. Mammalian Genome. 8(9). 647–650. 7 indexed citations

12.

Birkenmeier, E H, et al.. (1997). Identification and Genetic Mapping of a New Polycystic Kidney Disease on Mouse Chromosome 8. Genomics. 40(1). 101–107. 45 indexed citations

13.

Cook, Susan A., Keith Johnson, & Muriel T. Davisson. (1997). The mouse urate oxidase gene, Uox, maps to distal Chromosome 3. Mammalian Genome. 8(8). 623–624. 2 indexed citations

14.

Patel, Vishal, et al.. (1996). Effect of the mouse scid mutation on meiotic recombination. Mammalian Genome. 7(7). 497–500. 1 indexed citations

15.

Sweet, Hope O., Roderick T. Bronson, Keith R. Johnson, Susan A. Cook, & Muriel T. Davisson. (1996). Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration. Mammalian Genome. 7(11). 798–802. 129 indexed citations

16.

Johnson, Keith R., Susan A. Cook, & Muriel T. Davisson. (1994). Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse. Mammalian Genome. 5(11). 670–687. 26 indexed citations

17.

Davisson, Muriel T., et al.. (1994). Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects. Journal of Heredity. 85(2). 134–136. 18 indexed citations

18.

Buckwalter, Marion S., Susan A. Cook, Muriel T. Davisson, William F. White, & Sally A. Camper. (1994). A frameshift mutation in the mouse α₁ glycine receptor gene (Gira1) results in progressive neurological symptoms and juvenile death. Human Molecular Genetics. 3(11). 2025–2030. 100 indexed citations

19.

Bronson, Roderick T., et al.. (1993). Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease). Annals of Neurology. 33(4). 381–385. 129 indexed citations

20.

Johnson, Kenneth R., et al.. (1993). Genetic mapping of variable length rDNA segments to centromeric regions of mouse Chromosomes 11, 12, 15, 16, and 18. Mammalian Genome. 4(1). 49–52. 6 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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