Jolene R. Guide

700 total citations
7 papers, 366 citations indexed

About

Jolene R. Guide is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jolene R. Guide has authored 7 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 1 paper in Neurology. Recurrent topics in Jolene R. Guide's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (5 papers) and Fungal and yeast genetics research (2 papers). Jolene R. Guide is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (5 papers) and Fungal and yeast genetics research (2 papers). Jolene R. Guide collaborates with scholars based in United States, Canada and Portugal. Jolene R. Guide's co-authors include Vanessa C. Wheeler, Tammy Gillis, Jason St. Claire, Ella Dragileva, Ricardo Mouro Pinto, Edith Lopez, Guo‐Min Li, Caixia Hou, Paula E. Cohen and Mark J. Daly and has published in prestigious journals such as PLoS ONE, Genetics and The American Journal of Human Genetics.

In The Last Decade

Jolene R. Guide

7 papers receiving 362 citations

Peers

Jolene R. Guide

MB

CMN

GENET

NEURO

CN

Zhe Long China

Alejandro Lloret United States

Claudia Cagnoli Italy

Charlotte Nguyen Canada

Emilia K. Bijlsma Netherlands

Fernando Morales Costa Rica

Olaf Rieß Germany

Tania Cruz Mariño Canada

A. K. Mosemiller United States

María Moreno‐Igoa Spain

Zhe Long China

Jolene R. Guide

189 ×0.6

MB

141 ×0.6

CMN

57 ×0.6

GENET

88 ×1.2

NEURO

44 ×1.5

CN

Citations per year, relative to Jolene R. Guide Jolene R. Guide (= 1×) peers Zhe Long

Countries citing papers authored by Jolene R. Guide

Since Specialization

Citations

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

Fields of papers citing papers by Jolene R. Guide

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jolene R. Guide. 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 Jolene R. Guide. The network helps show where Jolene R. Guide may publish in the future.

Co-authorship network of co-authors of Jolene R. Guide

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Kovalenko, Marina, Austen J. Milnerwood, Jason St. Claire, et al.. (2018). HttQ111/+ Huntington’s Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic Dysfunction. Journal of Huntington s Disease. 7(1). 17–33. 25 indexed citations

2.

Lee, Jong‐Min, Tammy Gillis, Jolene R. Guide, et al.. (2016). Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington’s Disease Knock-In Mice. Genetics. 205(2). 503–516. 20 indexed citations

3.

Carroll, Jeffrey B., Amy Deik, Elisa Fossale, et al.. (2015). HdhQ111 Mice Exhibit Tissue Specific Metabolite Profiles that Include Striatal Lipid Accumulation. PLoS ONE. 10(8). e0134465–e0134465. 16 indexed citations

4.

Ramos, Eliana Marisa, Marina Kovalenko, Jolene R. Guide, et al.. (2015). Chromosome substitution strain assessment of a Huntington’s disease modifier locus. Mammalian Genome. 26(3-4). 119–130. 3 indexed citations

5.

Blumenthal, Ian, Ashok Ragavendran, Serkan Erdin, et al.. (2014). Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families. The American Journal of Human Genetics. 94(6). 870–883. 88 indexed citations

6.

Pinto, Ricardo Mouro, Ella Dragileva, Andrew Kirby, et al.. (2013). Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches. PLoS Genetics. 9(10). e1003930–e1003930. 155 indexed citations

7.

Kovalenko, Marina, Ella Dragileva, Jason St. Claire, et al.. (2012). Msh2 Acts in Medium-Spiny Striatal Neurons as an Enhancer of CAG Instability and Mutant Huntingtin Phenotypes in Huntington’s Disease Knock-In Mice. PLoS ONE. 7(9). e44273–e44273. 59 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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