Alexander P. Drew

861 total citations
15 papers, 303 citations indexed

About

Alexander P. Drew is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Alexander P. Drew has authored 15 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Neurology and 4 papers in Molecular Biology. Recurrent topics in Alexander P. Drew's work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (7 papers) and Cellular transport and secretion (3 papers). Alexander P. Drew is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (7 papers) and Cellular transport and secretion (3 papers). Alexander P. Drew collaborates with scholars based in Australia, United States and Malaysia. Alexander P. Drew's co-authors include Garth A. Nicholson, Marina Kennerson, Stephan Züchner, Monique M. Ryan, Azlina Ahmad‐Annuar, Danqing Zhu, Ian P. Blair, David Chuang, Eppie M. Yiu and Shih-Chia Tso and has published in prestigious journals such as Annals of Neurology, Journal of Cell Science and Human Molecular Genetics.

In The Last Decade

Alexander P. Drew

15 papers receiving 294 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander P. Drew Australia	10	152	148	84	45	37	15	303
Eduardo Calpena Spain	11	153 1.0×	114 0.8×	29 0.3×	39 0.9×	11 0.3×	21	272
Hannah E. Steele United Kingdom	9	180 1.2×	77 0.5×	33 0.4×	51 1.1×	14 0.4×	14	275
Kishin Koh Japan	11	136 0.9×	194 1.3×	99 1.2×	51 1.1×	8 0.2×	38	295
Simona Capponi Italy	12	211 1.4×	222 1.5×	74 0.9×	76 1.7×	11 0.3×	16	405
Esther Gill Germany	10	151 1.0×	62 0.4×	29 0.3×	23 0.5×	16 0.4×	13	224
Vincent Meyer France	5	110 0.7×	68 0.5×	27 0.3×	29 0.6×	20 0.5×	8	242
Vedrana Milić Rašić Serbia	8	151 1.0×	70 0.5×	12 0.1×	29 0.6×	19 0.5×	12	211
Danique Beijer United States	9	124 0.8×	72 0.5×	27 0.3×	31 0.7×	6 0.2×	15	231
Alessandro Geroldi Italy	13	214 1.4×	285 1.9×	94 1.1×	90 2.0×	8 0.2×	30	461
Misti C. White United States	10	265 1.7×	189 1.3×	20 0.2×	54 1.2×	10 0.3×	11	349

Countries citing papers authored by Alexander P. Drew

Since Specialization

Citations

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

Fields of papers citing papers by Alexander P. Drew

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander P. Drew. 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 Alexander P. Drew. The network helps show where Alexander P. Drew may publish in the future.

Co-authorship network of co-authors of Alexander P. Drew

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

All Works

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15 of 15 papers shown

Lam, Connie, Kerri Basile, C. J. E. Suster, et al.. (2023). A laboratory framework for ongoing optimization of amplification-based genomic surveillance programs. Microbiology Spectrum. 11(6). e0220223–e0220223. 2 indexed citations

Suster, C. J. E., Alicia Arnott, Grace A. Blackwell, et al.. (2022). Guiding the design of SARS-CoV-2 genomic surveillance by estimating the resolution of outbreak detection. Frontiers in Public Health. 10. 1004201–1004201. 5 indexed citations

Jia, Fangzhi, Alexander P. Drew, Garth A. Nicholson, Alastair Corbett, & Kishore R. Kumar. (2021). Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings. Neuromuscular Disorders. 31(11). 1101–1112. 13 indexed citations

Niño, Jorge Luis Galeano, Szun S. Tay, Jianling Xie, et al.. (2020). The Lifeact-EGFP mouse is a translationally controlled fluorescent reporter of T cell activation. Journal of Cell Science. 133(5). 7 indexed citations

Shahrizaila, Nortina, Alexander P. Drew, Khean Jin Goh, et al.. (2019). Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family. Neurogenetics. 20(3). 117–127. 13 indexed citations

Minoche, André E., Renée Johnson, Velimir Gayevskiy, et al.. (2018). Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Genetics in Medicine. 21(3). 650–662. 43 indexed citations

Drew, Alexander P., et al.. (2016). A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34–q36.2. Human Genetics. 135(11). 1269–1278. 9 indexed citations

Drew, Alexander P., Manoj P. Menezes, Monique M. Ryan, et al.. (2016). Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3. PLoS Genetics. 12(7). e1006177–e1006177. 27 indexed citations

Grant, Adrienne, Alexander P. Drew, Eppie M. Yiu, et al.. (2016). Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation. Neurobiology of Disease. 94. 237–244. 14 indexed citations

10.

Drew, Alexander P., et al.. (2015). Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing. Molecular Genetics & Genomic Medicine. 3(2). 143–154. 52 indexed citations

11.

Kennerson, Marina, Matthew B. Harms, Alexander P. Drew, et al.. (2015). MORC2 mutations cause axonal Charcot–Marie–Tooth disease with pyramidal signs. Annals of Neurology. 79(3). 419–427. 33 indexed citations

12.

Tey, Siok‐Keen, Azlina Ahmad‐Annuar, Alexander P. Drew, et al.. (2015). Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies. Clinical Genetics. 90(2). 127–133. 7 indexed citations

13.

Ahmad‐Annuar, Azlina, et al.. (2014). Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies. Neurogenetics. 15(4). 229–235. 3 indexed citations

14.

Kennerson, Marina, Eppie M. Yiu, David Chuang, et al.. (2013). A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene. Human Molecular Genetics. 22(7). 1404–1416. 56 indexed citations

15.

Drew, Alexander P., Ian P. Blair, & Garth A. Nicholson. (2011). Molecular Genetics and Mechanisms of Disease in Distal Hereditary Motor Neuropathies: Insights Directing Future Genetic Studies. Current Molecular Medicine. 11(8). 650–665. 19 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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