John B. Vincent

3.5k total citations
19 papers, 1.1k citations indexed

About

John B. Vincent is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, John B. Vincent has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Cognitive Neuroscience. Recurrent topics in John B. Vincent's work include Genetics and Neurodevelopmental Disorders (14 papers), Autism Spectrum Disorder Research (7 papers) and RNA modifications and cancer (4 papers). John B. Vincent is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Autism Spectrum Disorder Research (7 papers) and RNA modifications and cancer (4 papers). John B. Vincent collaborates with scholars based in Canada, United States and Austria. John B. Vincent's co-authors include Stephen W. Scherer, Wendy Roberts, Péter Szatmári, James S. Sutcliffe, Jennifer Skaug, Dalila Pinto, Rainald Moessner, Lonnie Zwaigenbaum, Christian R. Marshall and Bridget A. Fernandez and has published in prestigious journals such as Nature Genetics, PLoS ONE and Scientific Reports.

In The Last Decade

John B. Vincent

19 papers receiving 1.1k citations

Peers

John B. Vincent
Matthew J. Lyst United Kingdom
James Eberwine United States
Yong-hui Jiang United States
Gregory J. Pelka Australia
Nathaniel R. Kastan United States
Frank J. Probst United States
Jean-Pierre Hardelin France
Carolyn Schanen United States
Renate K. Hukema Netherlands
Ka Ying Sharon Hung United States
Matthew J. Lyst United Kingdom
John B. Vincent
Citations per year, relative to John B. Vincent John B. Vincent (= 1×) peers Matthew J. Lyst

Countries citing papers authored by John B. Vincent

Since Specialization
Citations

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

Fields of papers citing papers by John B. Vincent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John B. Vincent. 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 John B. Vincent. The network helps show where John B. Vincent may publish in the future.

Co-authorship network of co-authors of John B. Vincent

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

All Works

19 of 19 papers shown
1.
Kim, Bo‐Hyun, et al.. (2023). MeCP2 ubiquitination and sumoylation, in search of a function. Human Molecular Genetics. 33(1). 1–11. 7 indexed citations
2.
Vincent, John B., et al.. (2021). MeCP2: The Genetic Driver of Rett Syndrome Epigenetics. Frontiers in Genetics. 12. 620859–620859. 78 indexed citations
3.
Vincent, John B. & Juan Ausió. (2021). MeCP2: latest insights fundamentally change our understanding of its interactions with chromatin and its functional attributes. BioEssays. 43(3). e2000281–e2000281. 4 indexed citations
4.
Sheikh, Taimoor I., Juan Ausió, Josh Silver, et al.. (2016). From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2. Scientific Reports. 6(1). 38590–38590. 19 indexed citations
5.
Vincent, John B.. (2016). Unstable repeat expansion in major psychiatric disorders. Psychiatric Genetics. 26(4). 156–165. 5 indexed citations
6.
Orlic-Milacic, M, Anna Mikhailov, Aaron Cheung, et al.. (2014). Over-Expression of Either MECP2_e1 or MECP2_e2 in Neuronally Differentiated Cells Results in Different Patterns of Gene Expression. PLoS ONE. 9(4). e91742–e91742. 16 indexed citations
7.
Yasui, Dag H., et al.. (2014). Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome. Human Molecular Genetics. 23(24). 6695–6695. 7 indexed citations
8.
Gianakopoulos, Peter J., Yuzhi Zhang, Nela Pencea, et al.. (2011). Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(2). 210–216. 21 indexed citations
9.
Moessner, Rainald, Christian R. Marshall, James S. Sutcliffe, et al.. (2007). Contribution of SHANK3 Mutations to Autism Spectrum Disorder. The American Journal of Human Genetics. 81(6). 1289–1297. 494 indexed citations
10.
Schwarzbraun, Thomas, Christian Windpassinger, John B. Vincent, et al.. (2005). Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS). European Journal of Medical Genetics. 49(4). 338–345. 10 indexed citations
11.
Mnatzakanian, Gevork N., Hannes Lohi, Iulia Munteanu, et al.. (2004). A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. Nature Genetics. 36(4). 339–341. 251 indexed citations
12.
Koning, Dirk‐Jan de, Chris Haley, Dawn Windsor, et al.. (2004). Segregation of QTL for production traits in commercial meat-type chickens. Genetics Research. 83(3). 211–220. 52 indexed citations
13.
14.
Vincent, John B., et al.. (2003). Association and transmission analysis of the FMR1 IVS10 + 14C‐T variant in autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 54–56. 10 indexed citations
15.
Haddad, Riad, John B. Vincent, Robert Gryfe, et al.. (2003). Chromosome 7q31 allelic imbalance and somatic mutations of RAY1/ST7 gene in colorectal cancer. Cancer Letters. 203(1). 87–90. 2 indexed citations
16.
Vincent, John B., Erwin Petek, Sandy Thevarkunnel, et al.. (2002). The RAY1/ST7 Tumor-Suppressor Locus on Chromosome 7q31 Represents a Complex Multi-transcript System. Genomics. 80(3). 283–294. 39 indexed citations
17.
Cheung, Joseph, Erwin Petek, Kazuhiko Nakabayashi, et al.. (2001). Identification of the Human Cortactin-Binding Protein-2 Gene from the Autism Candidate Region at 7q31. Genomics. 78(1-2). 7–11. 46 indexed citations
18.
19.
Parikh, Sagar V., John B. Vincent, & Kristen M. Kennedy. (1999). Clinical characteristics of bipolar disorder subjects with large CAG/CTG repeat DNA. Journal of Affective Disorders. 55(2-3). 221–224. 3 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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