Karen Snow

832 total citations
18 papers, 637 citations indexed

About

Karen Snow is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Karen Snow has authored 18 papers receiving a total of 637 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Karen Snow's work include Mitochondrial Function and Pathology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Karen Snow is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Karen Snow collaborates with scholars based in United States, India and Canada. Karen Snow's co-authors include Dusica Babovic‐Vuksanovic, Stephen N. Thibodeau, Kent E. Kruckeberg, David J. Tester, Daniel J. Schaid, Virginia V. Michels, Marc C. Patterson, Randi J. Hagerman, Claire Hull and Rong Mao and has published in prestigious journals such as Human Molecular Genetics, Clinical Chemistry and Genetics in Medicine.

In The Last Decade

Karen Snow

18 papers receiving 620 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karen Snow United States 10 398 396 230 178 53 18 637
P. Goonewardena Sweden 11 377 0.9× 491 1.2× 238 1.0× 88 0.5× 18 0.3× 23 613
Roberta Pietrobono Italy 11 515 1.3× 442 1.1× 188 0.8× 93 0.5× 17 0.3× 20 641
Stacey Beth Foti United States 4 273 0.7× 202 0.5× 77 0.3× 148 0.8× 17 0.3× 4 515
Doris Wöhrle Germany 6 425 1.1× 492 1.2× 193 0.8× 89 0.5× 17 0.3× 8 619
Terry Vrijenhoek Netherlands 8 302 0.8× 440 1.1× 104 0.5× 58 0.3× 29 0.5× 11 668
Aaron Cheung Canada 9 656 1.6× 326 0.8× 151 0.7× 95 0.5× 9 0.2× 12 777
Tetsushi Yamagata Japan 12 448 1.1× 276 0.7× 82 0.4× 221 1.2× 27 0.5× 14 736
Zhou Xp China 5 416 1.0× 306 0.8× 227 1.0× 47 0.3× 9 0.2× 8 634
A. Roche United Kingdom 9 708 1.8× 506 1.3× 216 0.9× 157 0.9× 11 0.2× 13 960
Astrid Oudakker Netherlands 14 667 1.7× 673 1.7× 177 0.8× 100 0.6× 13 0.2× 20 1.1k

Countries citing papers authored by Karen Snow

Since Specialization
Citations

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

Fields of papers citing papers by Karen Snow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Snow

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

All Works

18 of 18 papers shown
1.
Snow, Karen & Rong Mao. (2003). Extreme Expansion Detection in Spinocerebellar Ataxia Type 2 and Type 7. Neurogenetics. 217. 41–50. 2 indexed citations
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Mao, Rong, Arthur S. Aylsworth, Nicholas Potter, et al.. (2002). Childhood‐onset ataxia: Testing for large CAG‐repeats in SCA2 and SCA7. American Journal of Medical Genetics. 110(4). 338–345. 58 indexed citations
6.
Ferrance, Jerome P., Karen Snow, & James P. Landers. (2002). Evaluation of Microchip Electrophoresis as a Molecular Diagnostic Method for Duchenne Muscular Dystrophy. Clinical Chemistry. 48(2). 380–383. 14 indexed citations
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Williams, Liam, Madhuri Hegde, Richard L. M. Faull, et al.. (2000). Null Alleles at the Huntington Disease Locus: Implications for Diagnostics and CAG Repeat Instability. Genetic Testing. 4(1). 55–60. 15 indexed citations
9.
Mao, Rong, et al.. (2000). Characteristics of two cases with dup(15) (q 11.2-q 12): one of maternal and one of paternal origin. Genetics in Medicine. 2(2). 131–135. 53 indexed citations
10.
Babovic‐Vuksanovic, Dusica, Karen Snow, & Rosa Ten. (1999). Mannose-binding lectin (MBL) deficiency. Variant alleles in a Midwestern population of the United States. Annals of Allergy Asthma & Immunology. 82(2). 134–143. 42 indexed citations
11.
Babovic‐Vuksanovic, Dusica, Karen Snow, Marc C. Patterson, & Virginia V. Michels. (1998). Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. American Journal of Medical Genetics. 79(5). 383–387. 67 indexed citations
12.
Babovic‐Vuksanovic, Dusica, Karen Snow, Marc C. Patterson, & Virginia V. Michels. (1998). Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. American Journal of Medical Genetics. 79(5). 383–387. 5 indexed citations
13.
Kambouris, Marios, et al.. (1996). Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus. American Journal of Medical Genetics. 64(2). 404–407. 9 indexed citations
14.
Hagerman, Randi J., Claire Hull, Louise W. Staley, et al.. (1994). High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR‐1 mutation associated with protein expression. American Journal of Medical Genetics. 51(4). 298–308. 176 indexed citations
15.
Fisch, Gene S., David L. Nelson, Karen Snow, et al.. (1994). Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing. American Journal of Medical Genetics. 51(4). 339–345. 12 indexed citations
16.
Snow, Karen, David J. Tester, Kent E. Kruckeberg, Daniel J. Schaid, & Stephen N. Thibodeau. (1994). Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation. Human Molecular Genetics. 3(9). 1543–1551. 144 indexed citations
17.
Snow, John L., Karen Snow, & Mark R. Pittelkow. (1993). The Polymerase Chain Reaction. The Journal of Dermatologic Surgery and Oncology. 19(9). 831–845. 2 indexed citations
18.
Snow, Karen, et al.. (1992). Analysis of mutations at the fragile X locus using the DNA probe Ox1.9. American Journal of Medical Genetics. 43(1-2). 244–254. 22 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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