Alexander P. Drew

861 citations

15 papers · 303 indexed · h-index 10

Molecular Biology
Cellular and Molecular Neuroscience top 10%
Neurology top 10%
Cell Biology
Cardiology and Cardiovascular Medicine

Co-authors: Garth A. Nicholson Marina Kennerson Stephan Züchner Monique M. Ryan Azlina Ahmad‐Annuar Danqing Zhu Ian P. Blair David Chuang
Topics: Hereditary Neurological Disorders (9 papers)Neurological diseases and metabolism (7 papers)Cellular transport and secretion (3 papers)
Cited by: Neurology Cellular and Molecular Neuroscience Cell Biology
Journals: Annals of Neurology Journal of Cell Science Human Molecular Genetics
Partner nations: Australia United States Malaysia

In The Last Decade

Alexander P. Drew

15 papers receiving 294 citations

Peers

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

#	Work	Indexed citations
1	A laboratory framework for ongoing optimization of amplification-based genomic surveillance programs 2023 ·Microbiology Spectrum ·Connie Lam,(unknown),Kerri Basile,(unknown),C. J. E. Suster,Mailie Gall,(unknown),Shona Chandra,Jenny Draper,Elena Martínez,Alexander P. Drew,Qinning Wang,Sharon Chen,Jen Kok,Dominic E. Dwyer,Vitali Sintchenko,Rebecca J. Rockett	2
2	Guiding the design of SARS-CoV-2 genomic surveillance by estimating the resolution of outbreak detection 2022 ·Frontiers in Public Health ·C. J. E. Suster,Alicia Arnott,Grace A. Blackwell,Mailie Gall,Jenny Draper,Elena Martínez,Alexander P. Drew,Rebecca J. Rockett,Sharon C.-A. Chen,Jen Kok,Dominic E. Dwyer,Vitali Sintchenko	5
3	Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings 2021 ·Neuromuscular Disorders ·Fangzhi Jia,Alexander P. Drew,Garth A. Nicholson,Alastair Corbett,Kishore R. Kumar	13
4	The Lifeact-EGFP mouse is a translationally controlled fluorescent reporter of T cell activation 2020 ·Journal of Cell Science ·Jorge Luis Galeano Niño,Szun S. Tay,(unknown),Jianling Xie,Matt Govendir,Daryan Kempe,(unknown),Alexander P. Drew,(unknown),Sarah Kummerfeld,Christopher G. Proud,Maté Biro	7
5	Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family 2019 ·Neurogenetics ·(unknown),Nortina Shahrizaila,Alexander P. Drew,(unknown),Khean Jin Goh,Esra Battaloğlu,Derek Atkinson,Yeşim Parman,Albena Jordanova,Ki Wha Chung,Byung‐Ok Choi,(unknown),Michaela Auer‐Grumbach,Garth A. Nicholson,Marina Kennerson,Azlina Ahmad‐Annuar	13
6	Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy 2018 ·Genetics in Medicine ·André E. Minoche,(unknown),Renée Johnson,Velimir Gayevskiy,Sarah U. Morton,Alexander P. Drew,(unknown),Aaron L. Statham,Ben Lundie,Richard D. Bagnall,Jodie Ingles,Christopher Semsarian,Jonathan G. Seidman,Christine E. Seidman,Marcel E. Dinger,Mark J. Cowley,Diane Fatkin	43
7	A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34–q36.2 2016 ·Human Genetics ·Alexander P. Drew,(unknown),(unknown),Garth A. Nicholson,Marina Kennerson	9
8	Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3 2016 ·PLoS Genetics ·(unknown),(unknown),(unknown),(unknown),Alexander P. Drew,Manoj P. Menezes,Monique M. Ryan,Michelle A. Farrar,David Mowat,Gopinath M. Subramanian,Helen Young,Stephan Züchner,Stephen Reddel,Garth A. Nicholson,Marina Kennerson	27
9	Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation 2016 ·Neurobiology of Disease ·(unknown),(unknown),Adrienne Grant,Alexander P. Drew,Eppie M. Yiu,Monique M. Ryan,David Chuang,Shih-Chia Tso,Garth A. Nicholson,Marina Kennerson	14
10	Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing 2015 ·Molecular Genetics & Genomic Medicine ·Alexander P. Drew,Danqing Zhu,(unknown),(unknown),(unknown),(unknown),Azlina Ahmad‐Annuar,Garth A. Nicholson,Marina Kennerson	52
11	MORC2 mutations cause axonal Charcot–Marie–Tooth disease with pyramidal signs 2015 ·Annals of Neurology ·(unknown),Marina Kennerson,Matthew B. Harms,Alexander P. Drew,(unknown),Michaela Auer‐Grumbach,Alan Pestronk,Anne M. Connolly,Robert H. Baloh,Stephan Züchner,Stephen Reddel,Garth A. Nicholson	33
12	Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies 2015 ·Clinical Genetics ·Siok‐Keen Tey,Azlina Ahmad‐Annuar,Alexander P. Drew,Nortina Shahrizaila,Garth A. Nicholson,Marina Kennerson	7
13	Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies 2014 ·Neurogenetics ·(unknown),Azlina Ahmad‐Annuar,Alexander P. Drew,Nortina Shahrizaila,Garth A. Nicholson,Marina Kennerson	3
14	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 2013 ·Human Molecular Genetics ·Marina Kennerson,Eppie M. Yiu,David Chuang,(unknown),Shih-Chia Tso,(unknown),Rama Chaudhry,Alexander P. Drew,Gary Rance,Martin B. Delatycki,Stephan Züchner,Monique M. Ryan,Garth A. Nicholson	56
15	Molecular Genetics and Mechanisms of Disease in Distal Hereditary Motor Neuropathies: Insights Directing Future Genetic Studies 2011 ·Current Molecular Medicine ·Alexander P. Drew,Ian P. Blair,Garth A. Nicholson	19

About Alexander P. Drew

Alexander P. Drew is a scholar working on Neurology, Cellular and Molecular Neuroscience and Cell Biology, having authored 15 papers that have together received 303 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (7 papers) and Cellular transport and secretion (3 papers). The work is most often cited by research in Neurology (84 citations), Cellular and Molecular Neuroscience (148 citations) and Cell Biology (45 citations). Alexander P. Drew has collaborated with scholars based in Australia, United States and Malaysia. Frequent 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. Their work appears in journals such as Annals of Neurology, Journal of Cell Science and Human Molecular Genetics.

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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