Arran McBride

455 total citations
6 papers, 180 citations indexed

About

Arran McBride is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Arran McBride has authored 6 papers receiving a total of 180 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Rheumatology. Recurrent topics in Arran McBride's work include RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and RNA Research and Splicing (2 papers). Arran McBride is often cited by papers focused on RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and RNA Research and Splicing (2 papers). Arran McBride collaborates with scholars based in Canada, United States and Australia. Arran McBride's co-authors include Skye McBride, Jian Gao, Zhi Yuan Wang, Kym M. Boycott, Kristin D. Kernohan, Taila Hartley, David A. Dyment, Amanda Hodge, Guillaume Paré and Peter Ainsworth and has published in prestigious journals such as Journal of Materials Chemistry, Human Molecular Genetics and Human Mutation.

In The Last Decade

Arran McBride

6 papers receiving 180 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arran McBride Canada	5	79	70	53	51	47	6	180
Martijn Kranendijk Netherlands	5	170 2.2×	20 0.3×	66 1.2×	9 0.2×	18 0.4×	5	256
Chia‐Heng Hsiung United States	8	201 2.5×	75 1.1×	27 0.5×	8 0.2×	91 1.9×	14	345
Hongliang Wang China	10	223 2.8×	52 0.7×	54 1.0×	14 0.3×	34 0.7×	24	374
Sarah Hostachy Germany	11	117 1.5×	13 0.2×	8 0.2×	11 0.2×	53 1.1×	18	283
Sebastian Richers Germany	6	329 4.2×	28 0.4×	17 0.3×	23 0.5×	20 0.4×	6	361
Liangliang Li China	12	192 2.4×	53 0.8×	8 0.2×	20 0.4×	27 0.6×	18	304
Rashmi Adhikari United States	8	172 2.2×	137 2.0×	29 0.5×	12 0.2×	108 2.3×	9	337
Denisa Hathazi United Kingdom	11	169 2.1×	39 0.6×	6 0.1×	10 0.2×	29 0.6×	22	310
Thomas C. Schwarz Austria	11	254 3.2×	72 1.0×	11 0.2×	15 0.3×	95 2.0×	14	348
Daniel Scott United Kingdom	10	218 2.8×	44 0.6×	6 0.1×	12 0.2×	14 0.3×	15	364

Countries citing papers authored by Arran McBride

Since Specialization

Citations

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

Fields of papers citing papers by Arran McBride

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arran McBride

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

All Works

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6 of 6 papers shown

1.

Warman‐Chardon, Jodi, Taila Hartley, Aren E. Marshall, et al.. (2023). Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction. Neurology Genetics. 9(5). e200088–e200088. 2 indexed citations

2.

Marshall, Aren E., Xiaomin Dong, Aziz Mhanni, et al.. (2021). Compound heterozygous variants in SHQ1 are associated with a spectrum of neurological features, including early-onset dystonia. Human Molecular Genetics. 31(4). 614–624. 10 indexed citations

3.

Kernohan, Kristin D., Arran McBride, Taila Hartley, et al.. (2019). p21 protein‐activated kinase 1 is associated with severe regressive autism, and epilepsy. Clinical Genetics. 96(5). 449–455. 15 indexed citations

4.

Schenkel, Laila C., Kristin D. Kernohan, Arran McBride, et al.. (2017). Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome. Epigenetics & Chromatin. 10(1). 10–10. 42 indexed citations

5.

Kernohan, Kristin D., Laure Frésard, Zachary Zappala, et al.. (2017). Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsy. Human Mutation. 38(6). 611–614. 20 indexed citations

6.

McBride, Arran, et al.. (2010). Colorimetric and near-infrared fluorescence turn-on molecular probe for direct and highly selective detection ofcysteine in human plasma. Journal of Materials Chemistry. 21(4). 1040–1048. 91 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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