Mathew Nightingale

1.4k total citations
14 papers, 625 citations indexed

About

Mathew Nightingale is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Mathew Nightingale has authored 14 papers receiving a total of 625 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Genetics. Recurrent topics in Mathew Nightingale's work include Multiple Myeloma Research and Treatments (2 papers), Metabolism and Genetic Disorders (2 papers) and Hereditary Neurological Disorders (2 papers). Mathew Nightingale is often cited by papers focused on Multiple Myeloma Research and Treatments (2 papers), Metabolism and Genetic Disorders (2 papers) and Hereditary Neurological Disorders (2 papers). Mathew Nightingale collaborates with scholars based in Canada, United Kingdom and United States. Mathew Nightingale's co-authors include Haiyan Jiang, Andrew Orr, Mark D. Ludman, Makoto Matsuoka, Duane L. Guernsey, Susan C. Evans, Meghan Ferguson, Andrea L. Rideout, Karen Bedard and Mark Samuels and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Mathew Nightingale

13 papers receiving 613 citations

Peers

Mathew Nightingale

HEMAT

GENET

ONCOL

GENET

Frédéric Esnard France

Andrea Šoltýsová Slovakia

Stefan Lang Sweden

M.C. Sparkes United States

Chun Cao Switzerland

Michael W. Harr United States

Ilenia Simeoni United Kingdom

Nasim Yousaf United Kingdom

Motohiro Nishimura Japan

Edith Rian Norway

Frédéric Esnard France

Mathew Nightingale

320 ×0.8

80 ×0.4

HEMAT

50 ×0.4

GENET

62 ×0.6

ONCOL

96 ×1.0

GENET

Citations per year, relative to Mathew Nightingale Mathew Nightingale (= 1×) peers Frédéric Esnard

Countries citing papers authored by Mathew Nightingale

Since Specialization

Citations

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

Fields of papers citing papers by Mathew Nightingale

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathew Nightingale

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

All Works

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14 of 14 papers shown

Bedard, Karen, Karin Wallace, Michael P. Mackley, et al.. (2025). Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel. Investigative Ophthalmology & Visual Science. 66(2). 23–23. 2 indexed citations

Walsh, Noreen M., Daniel Gaston, Thai Yen Ly, et al.. (2022). RB1-deficient squamous cell carcinoma: the proposed source of combined Merkel cell carcinoma. Modern Pathology. 35(12). 1829–1836. 13 indexed citations

Elhaji, Youssef, et al.. (2021). Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family. SHILAP Revista de lepidopterología. 1(3). 100022–100022. 2 indexed citations

Orr, Andrew, et al.. (2021). Familial Optic Disc Pits in 2 Father-Son Pairs: Clinical Features and Genetic Analysis. Case Reports in Ophthalmology. 12(2). 603–610.

Greenshields, Anna L., et al.. (2016). Resveratrol, piperine and apigenin differ in their NADPH-oxidase inhibitory and reactive oxygen species-scavenging properties. Phytomedicine. 23(12). 1494–1503. 32 indexed citations

LeBlanc, Marissa A., Lynette S. Penney, Daniel Gaston, et al.. (2013). A novel rearrangement of occludin causes brain calcification and renal dysfunction. Human Genetics. 132(11). 1223–1234. 22 indexed citations

Orr, Andrew, Marie‐Pierre Dubé, Juan Carlos Zenteno, et al.. (2011). Mutations in a novel serine protease PRSS56 in families with nanophthalmos.. PubMed. 17. 1850–61. 43 indexed citations

Guernsey, Duane L., Haiyan Jiang, Karen Bedard, et al.. (2010). Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease. PLoS Genetics. 6(8). e1001081–e1001081. 52 indexed citations

Guernsey, Duane L., Haiyan Jiang, Susan C. Evans, et al.. (2009). Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2. The American Journal of Human Genetics. 85(1). 120–129. 61 indexed citations

10.

Guernsey, D.L., Marie‐Pierre Dubé, Haiyan Jiang, et al.. (2009). Novel mutations in the sacsin gene in ataxia patients from Maritime Canada. Journal of the Neurological Sciences. 288(1-2). 79–87. 12 indexed citations

11.

Guernsey, Duane L., Haiyan Jiang, Dean R. Campagna, et al.. (2009). Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nature Genetics. 41(6). 651–653. 181 indexed citations

12.

Jenner, Matthew, Paola Leone, Brian A. Walker, et al.. (2007). Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma. Blood. 110(9). 3291–3300. 100 indexed citations

13.

Chiecchio, Laura, R.K.M. Protheroe, Ashraf Ibrahim, et al.. (2006). Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma. Leukemia. 20(9). 1610–1617. 104 indexed citations

14.

Jenner, Matthew, Paola Leone, Brian A. Walker, et al.. (2006). Abnormalities of 16q in Multiple Myeloma Are Associated with Poor Prognosis: 500K Gene Mapping and Expression Correlations Identify Two Potential Tumor Suppressor Genes, WWOX and CYLD.. Blood. 108(11). 110–110. 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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