Sarah J. Beecroft

924 total citations
16 papers, 270 citations indexed

About

Sarah J. Beecroft is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sarah J. Beecroft has authored 16 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Genetics. Recurrent topics in Sarah J. Beecroft's work include Neurogenetic and Muscular Disorders Research (7 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (5 papers). Sarah J. Beecroft is often cited by papers focused on Neurogenetic and Muscular Disorders Research (7 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (5 papers). Sarah J. Beecroft collaborates with scholars based in Australia, United States and United Kingdom. Sarah J. Beecroft's co-authors include Nigel G. Laing, Gianina Ravenscroft, Mark R. Davis, Phillipa J. Lamont, Catriona McLean, Miriam Rodrigues, Richard Roxburgh, Teddy Y. Wu, Andrea Cortese and Mary M. Reilly and has published in prestigious journals such as Brain, Genome biology and Journal of Medical Genetics.

In The Last Decade

Sarah J. Beecroft

16 papers receiving 270 citations

Peers

Countries citing papers authored by Sarah J. Beecroft

Since Specialization

Citations

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

Fields of papers citing papers by Sarah J. Beecroft

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah J. Beecroft. 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 Sarah J. Beecroft. The network helps show where Sarah J. Beecroft may publish in the future.

Co-authorship network of co-authors of Sarah J. Beecroft

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Hecatomb: an integrated software platform for viral metagenomics 2024 ·GigaScience ·Michael J. Roach, Sarah J. Beecroft, Kathie A. Mihindukulasuriya, Leran Wang, (unknown), (unknown), (unknown), Laís Farias Oliveira Lima, Elizabeth A. Dinsdale, Robert A. Edwards, Scott A. Handley	7
2	Koverage: Read-coverage analysis for massive(meta)genomics datasets 2024 ·The Journal of Open Source Software ·Michael J. Roach, (unknown), Sarah J. Beecroft, Bhavya Papudeshi, (unknown), (unknown), Vijini Mallawaarachchi, George Bouras, Robert A. Edwards	2
3	Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications 2023 ·Genome biology ·(unknown), Velimir Gayevskiy, Ryan L. Davis, Marie Wong, Chelsea Mayoh, Amali Mallawaarachchi, Yvonne Hort, Mark J. McCabe, Sarah J. Beecroft, Matilda R. Jackson, Peer Arts, Andrew Dubowsky, Nigel G. Laing, Marcel E. Dinger, Hamish S. Scott, Emily C. Oates, Mark Pinese, Mark J. Cowley	10
4	STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci 2022 ·Genome biology ·Harriet Dashnow, Brent S. Pedersen, (unknown), Joe Brown, Sarah J. Beecroft, Gianina Ravenscroft, Amy Lacroix, Phillipa J. Lamont, Richard Roxburgh, Miriam Rodrigues, Mark R. Davis, Heather C. Mefford, Nigel G. Laing, Aaron R. Quinlan	24
5	Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects 2021 ·Human Mutation ·Sarah J. Beecroft, (unknown), George McGillivray, Vikas Nanda, Emanuele Agolini, Antonio Novelli, M. Cristina Digilio, Andrea Dotta, Rosalba Carrozzo, Joshua S. Clayton, (unknown), Catriona McLean, Jessica M.Y. Ng, Nigel G. Laing, Paul G. Matteson, James H. Millonig, Gianina Ravenscroft	12
6	The Impact of Next-Generation Sequencing on the Diagnosis, Treatment, and Prevention of Hereditary Neuromuscular Disorders 2020 ·Molecular Diagnosis & Therapy ·Sarah J. Beecroft, Phillipa J. Lamont, Samantha Edwards, Hayley Goullée, Mark R. Davis, Nigel G. Laing, Gianina Ravenscroft	7
7	A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele 2020 ·Brain ·Sarah J. Beecroft, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Zoe Dyer, Teddy Y. Wu, Eoin Mulroy, Luciana Pelosi, Miriam Rodrigues, Rachael L. Taylor, Stuart Mossman, (unknown), James Cleland, Tim Anderson, Gianina Ravenscroft, Nigel G. Laing, Henry Houlden, Mary M. Reilly, Richard Roxburgh	45
8	A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families 2020 ·Brain ·Carolin K. Scriba, Sarah J. Beecroft, Joshua S. Clayton, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Natalia Dominik, Miriam Rodrigues, Elizabeth Walker, Zoe Dyer, Teddy Y. Wu, Mark R. Davis, David Chandler, Ben Weisburd, Henry Houlden, Mary M. Reilly, Nigel G. Laing, Phillipa J. Lamont, Richard Roxburgh, Gianina Ravenscroft	53
9	Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience 2020 ·Annals of Clinical and Translational Neurology ·Sarah J. Beecroft, Kyle S. Yau, Richard J. N. Allcock, Kym Mina, Rebecca Gooding, Fathimath Faiz, (unknown), C. Wise, Padma Sivadorai, (unknown), Nina Kresoje, Royston Ong, Rachael M. Duff, Macarena Cabrera‐Serrano, Kristen L. Nowak, Nicholas Pachter, Gianina Ravenscroft, Phillipa J. Lamont, Mark R. Davis, Nigel G. Laing	24
10	NEW GENES AND DISEASES / NGS & RELATED TECHNIQUES 2020 ·Neuromuscular Disorders ·Patricia A. Sullivan, Chelsea Mayoh, Marie Wong, Velimir Gayevskiy, Sarah J. Beecroft, Mark Pinese, Emily C. Oates, Mark J. Cowley	1
11	Cylindrical spirals in two families: Clinical and genetic investigations 2019 ·Neuromuscular Disorders ·Sarah J. Beecroft, Montse Olivé, Lidia González‐Quereda, P. Gallano, Isabel Ojanguren, Catriona McLean, Pamela McCombe, Nigel G. Laing, Gianina Ravenscroft	7
12	Recessive MYH7-related myopathy in two families 2019 ·Neuromuscular Disorders ·Sarah J. Beecroft, (unknown), Josine M. de Winter, Coen A. C. Ottenheijm, Caroline A. Sewry, Shehla Mohammed, Monique M. Ryan, Ian Woodcock, Lauren Sanders, Rebecca Gooding, Mark R. Davis, Emily C. Oates, Nigel G. Laing, Gianina Ravenscroft, Catriona McLean, Heinz Jungbluth	8
13	Genetics of neuromuscular fetal akinesia in the genomics era 2018 ·Journal of Medical Genetics ·Sarah J. Beecroft, (unknown), David Mowat, Catriona McLean, Anita Cairns, Mark R. Davis, Nigel G. Laing, Gianina Ravenscroft	26
14	Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin gene 2017 ·Neuromuscular Disorders ·Ebtesam Abdalla, Gianina Ravenscroft, (unknown), Sarah J. Beecroft, Nigel G. Laing	17
15	Expanding the phenotypic spectrum associated with mutations of DYNC1H1 2017 ·Neuromuscular Disorders ·Sarah J. Beecroft, Catriona McLean, Martin B. Delatycki, (unknown), Eppie M. Yiu, Göknur Haliloğlu, Dıclehan Orhan, Phillipa J. Lamont, Mark R. Davis, Nigel G. Laing, Gianina Ravenscroft	26
16	Autosomal dominant lower limb restricted congenital myopathy 2016 ·Neuromuscular Disorders ·Martin B. Delatycki, Andrew Churchyard, Eppie M. Yiu, Mark R. Davis, Sarah J. Beecroft, Gianina Ravenscroft, Catriona McLean, Nigel G. Laing	1

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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