Simon Zwolinski

1.5k total citations
5 papers, 91 citations indexed

About

Simon Zwolinski is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Simon Zwolinski has authored 5 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Simon Zwolinski's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital heart defects research (2 papers). Simon Zwolinski is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital heart defects research (2 papers). Simon Zwolinski collaborates with scholars based in United Kingdom, Italy and United States. Simon Zwolinski's co-authors include Sally Ann Lynch, John Burn, Ingrid Simonic, Sarju Mehta, Mark S. Bateman, John Barber, Lionel Willatt, Kristin M. Abbott, Domenico Coviello and Francesca Faravelli and has published in prestigious journals such as Journal of Medical Genetics, American Journal of Medical Genetics Part A and Journal of Neurogenetics.

In The Last Decade

Simon Zwolinski

5 papers receiving 68 citations

Peers

Simon Zwolinski

GENET

MB

PS

PPCH

PHARM

Leigh Anne Flore United States

Sinitdhorn Rujirabanjerd Thailand

Chieko Chijiwa Canada

A.L. Mosca France

Alessandra Ferrarini Switzerland

Ko‐ichiro Yoshiura Japan

Lina Ramos Portugal

Nobuhiko Okamoto Japan

C Schluth France

Jin Fang Chai China

Leigh Anne Flore United States

Simon Zwolinski

84 ×1.2

GENET

35 ×1.3

MB

16 ×1.1

PS

27 ×2.3

PPCH

0 ×0.0

PHARM

Citations per year, relative to Simon Zwolinski Simon Zwolinski (= 1×) peers Leigh Anne Flore

Countries citing papers authored by Simon Zwolinski

Since Specialization

Citations

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

Fields of papers citing papers by Simon Zwolinski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Zwolinski

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

All Works

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5 of 5 papers shown

1.

Pyle, Angela, Helen Griffin, Jennifer Duff, et al.. (2013). Late-Onset Sacsinopathy Diagnosed by Exome Sequencing and Comparative Genomic Hybridization. Journal of Neurogenetics. 27(4). 176–182. 6 indexed citations

2.

Mandrile, Giorgia, Anna Dubois, Jodi D. Hoffman, et al.. (2013). 3q26.33–3q27.2 microdeletion: A new microdeletion syndrome?. European Journal of Medical Genetics. 56(4). 216–221. 26 indexed citations

3.

Bateman, Mark S., Sarju Mehta, Lionel Willatt, et al.. (2010). A de novo 4q34 interstitial deletion of at least 9.3 Mb with no discernible phenotypic effect. American Journal of Medical Genetics Part A. 152A(7). 1764–1769. 25 indexed citations

4.

Lynch, Sally Ann, et al.. (1995). Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13.. Journal of Medical Genetics. 32(3). 227–230. 33 indexed citations

5.

Mutton, David, Eva Alberman, Martin Bobrow, et al.. (1992). Abstracts of the annual scientific meeting of the Association of Clinical Cytogeneticists held on 3 to 5 July 1991 at Earnshaw Hall, Sheffield. Journal of Medical Genetics. 29(3). 203–213. 1 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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