Ronnie Wright

1.2k total citations
8 papers, 81 citations indexed

About

Ronnie Wright is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Ronnie Wright has authored 8 papers receiving a total of 81 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Ronnie Wright's work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Glycosylation and Glycoproteins Research (1 paper). Ronnie Wright is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Glycosylation and Glycoproteins Research (1 paper). Ronnie Wright collaborates with scholars based in United Kingdom, Belgium and Netherlands. Ronnie Wright's co-authors include Julija Pavaine, Alexander Broomfield, Helen Prunty, Simon Jones, Pauline Hensman, Marcus Lowe, Nicola Bates, Philip A. Lewis, Lisa Grady and Alan Kerby and has published in prestigious journals such as Journal of Medical Genetics, Theriogenology and Stem Cell Research & Therapy.

In The Last Decade

Ronnie Wright

7 papers receiving 80 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ronnie Wright United Kingdom	5	37	27	18	11	8	8	81
Ksenija Gorni Italy	5	99 2.7×	37 1.4×	10 0.6×	8 0.7×	20 2.5×	10	129
Sara Nagy Switzerland	6	59 1.6×	19 0.7×	5 0.3×	5 0.5×	13 1.6×	12	97
Ludo van der Pol Netherlands	6	89 2.4×	27 1.0×	9 0.5×	12 1.1×	29 3.6×	8	144
Lucia Laugwitz Germany	7	47 1.3×	26 1.0×	6 0.3×	12 1.1×	7 0.9×	15	97
Laura Lorioli Italy	6	68 1.8×	87 3.2×	8 0.4×	16 1.5×	9 1.1×	10	151
Elena Alonso Spain	4	40 1.1×	24 0.9×	14 0.8×	26 2.4×	3 0.4×	10	89
Willem De Ridder Belgium	6	32 0.9×	8 0.3×	10 0.6×	7 0.6×	5 0.6×	16	68
Maria Asif Germany	7	67 1.8×	26 1.0×	7 0.4×	27 2.5×	5 0.6×	13	147
Girolamo Alfieri Italy	8	29 0.8×	8 0.3×	16 0.9×	7 0.6×	6 0.8×	11	82
Keryn G. Woodman United States	5	95 2.6×	25 0.9×	3 0.2×	18 1.6×	15 1.9×	9	108

Countries citing papers authored by Ronnie Wright

Since Specialization

Citations

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

Fields of papers citing papers by Ronnie Wright

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ronnie Wright

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

All Works

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8 of 8 papers shown

1.

Burghel, George J., Jamie M. Ellingford, Ronnie Wright, et al.. (2024). Systematic reanalysis of copy number losses of uncertain clinical significance. Journal of Medical Genetics. 61(7). 621–625.

2.

Vassallo, Grace, Julija Pavaine, Ronnie Wright, et al.. (2022). Anticipatory banking of samples enables diagnosis of adenylosuccinase deficiency following molecular autopsy in an infant with vacuolating leukoencephalopathy. American Journal of Medical Genetics Part A. 191(1). 234–237. 5 indexed citations

3.

Paesschen, Wim Van, Ataf Sabir, Francis H. Sansbury, et al.. (2021). ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy. European Journal of Human Genetics. 29(9). 1377–1383. 6 indexed citations

4.

Cruz, Pedro M. Rodríguez, Imelda Hughes, Adnan Manzur, et al.. (2020). Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter. Neuromuscular Disorders. 31(1). 21–28. 14 indexed citations

5.

Wright, Ronnie, et al.. (2019). A maternally inherited frameshift CDKL5 variant in a male with global developmental delay and late‐onset generalized epilepsy. American Journal of Medical Genetics Part A. 179(3). 507–511. 1 indexed citations

6.

Broomfield, Alexander, Pauline Hensman, Ronnie Wright, et al.. (2017). Rapidly Progressive White Matter Involvement in Early Childhood: The Expanding Phenotype of Infantile Onset Pompe?. JIMD Reports. 39. 55–62. 23 indexed citations

7.

Bates, Nicola, Despina Soteriou, Lisa Grady, et al.. (2017). High quality clinical grade human embryonic stem cell lines derived from fresh discarded embryos. Stem Cell Research & Therapy. 8(1). 128–128. 29 indexed citations

8.

Crenshaw, Carlyle, et al.. (2000). The use of buck and ram extenders and two packaging systems to cryopreserve aoudad (Ammotragus lervia) spermatozoa. Theriogenology. 54(1). 69–74. 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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