Allison Matthews

621 total citations
14 papers, 254 citations indexed

About

Allison Matthews is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Allison Matthews has authored 14 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Allison Matthews's work include Genomics and Rare Diseases (4 papers), Epigenetics and DNA Methylation (3 papers) and Prenatal Screening and Diagnostics (3 papers). Allison Matthews is often cited by papers focused on Genomics and Rare Diseases (4 papers), Epigenetics and DNA Methylation (3 papers) and Prenatal Screening and Diagnostics (3 papers). Allison Matthews collaborates with scholars based in Canada, Netherlands and United Kingdom. Allison Matthews's co-authors include Wyeth W. Wasserman, Clara van Karnebeek, Maja Tarailo‐Graovac, Jing Zhu, Carolyn J. Brown, Wendy P. Robinson, Victor Yuan, Linhua Zhang, Chaini Konwar and Jessica Lee and has published in prestigious journals such as PLANT PHYSIOLOGY, Scientific Reports and Genetics in Medicine.

In The Last Decade

Allison Matthews

13 papers receiving 253 citations

Peers

Countries citing papers authored by Allison Matthews

Since Specialization

Citations

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

Fields of papers citing papers by Allison Matthews

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Allison Matthews

This figure shows the co-authorship network connecting the top 25 collaborators of Allison Matthews. A scholar is included among the top collaborators of Allison Matthews 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 Allison Matthews. Allison Matthews 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

#	Work	Indexed citations
1	Breaking rules: the complex relationship between DNA methylation and X-chromosome inactivation in the human placenta 2025 ·Biology of Sex Differences ·(unknown), Allison Matthews, Tanya N. Phung, Seema B. Plaisier, Melissa A. Wilson, Carolyn J. Brown, Wendy P. Robinson	0
2	A simple method to visualize pre-mRNA splicing with the naked eye using a genetically encoded visual splicing reporter 2024 ·PLANT PHYSIOLOGY ·Kasavajhala V. S. K. Prasad, (unknown), (unknown), Allison Matthews, (unknown), Enamul Huq, Anireddy S. N. Reddy	3
3	Who’s afraid of the X? Incorporating the X and Y chromosomes into the analysis of DNA methylation array data 2023 ·Epigenetics & Chromatin ·(unknown), (unknown), Allison Matthews, Carolyn J. Brown, Wendy P. Robinson	15
4	Is the diagnostic rate for the common subtypes of A1AT deficiency consistent across two Canadian Provinces? 2021 ·Clinical Biochemistry ·Mathew P. Estey, (unknown), Tanya N. Nelson, Michelle Parker, Terence A. Agbor, Hui-Min Yang, Rachel Jen, Vilte Barakauskas, Grace Y. Lam, Allison Matthews, André Mattman	1
5	Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effects 2021 ·Neurogenetics ·Clara D. van Karnebeek, (unknown), Allison Matthews, (unknown), (unknown), Britt I. Drögemöller, Casper Shyr, Jessica Lee, Jill Mwenifumbo, (unknown), Sylvia Stöckler, Jan M. Friedman, Anna Lehman, (unknown), Colin J.D. Ross, Wyeth W. Wasserman, Maja Tarailo‐Graovac, Gabriella Horváth	2
6	A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta 2021 ·Biology of Sex Differences ·(unknown), Victor Yuan, Chaini Konwar, Allison Matthews, Carolyn J. Brown, Wendy P. Robinson	24
7	Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review 2018 ·Journal of Inherited Metabolic Disease ·(unknown), Jessica Lee, (unknown), Maja Tarailo‐Graovac, Allison Matthews, Udo F. H. Engelke, Jeffrey Tang, Leo A. J. Kluijtmans, Ron A. Wevers, Wyeth W. Wasserman, Clara van Karnebeek, Sara Mostafavi	34
8	Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders 2017 ·Genetics in Medicine ·Maja Tarailo‐Graovac, Jing Zhu, Allison Matthews, Clara van Karnebeek, Wyeth W. Wasserman	48
9	A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder 2017 ·European Journal of Medical Genetics ·Allison Matthews, Maja Tarailo‐Graovac, E. Magda Price, (unknown), (unknown), Britt I. Drögemöller, Wendy P. Robinson, Colin J.D. Ross, Wyeth W. Wasserman, Harold Siden, Clara D. van Karnebeek	11
10	Novel homozygous PCK1 mutation causing cytosolic phosphoenolpyruvate carboxykinase deficiency presenting as childhood hypoglycemia, an abnormal pattern of urine metabolites and liver dysfunction 2017 ·Molecular Genetics and Metabolism ·Päivi Vieira, Jessie M. Cameron, Elisa Rahikkala, Riikka Keski‐Filppula, Linhua Zhang, Saikat Santra, Allison Matthews, Päivi Myllynen, Matti Nuutinen, Jukka S. Moilanen, Richard J. Rodenburg, Arndt Rolfs, Johanna Uusimaa, Clara van Karnebeek	28
11	Bone health and SATB2‐associated syndrome 2017 ·Clinical Genetics ·Yuri A. Zárate, Michelle Steinraths, Allison Matthews, Wendy E. Smith, Angela Sun, Louise C. Wilson, Caroline Brain, (unknown), Benjamin Jacobs, Jennifer L. Fish, Cynthia M. Powell, Wyeth W. Wasserman, Clara D. van Karnebeek, Emma Wakeling, (unknown)	15
12	Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutation 2016 ·Molecular Case Studies ·(unknown), Katelin N. Townsend, Casper Shyr, Allison Matthews, Scott A. Lear, (unknown), Anna Lehman, Wyeth W. Wasserman, Clara van Karnebeek, Graham Sinclair, Hilary Vallance, William T. Gibson	10
13	YY1 binding association with sex-biased transcription revealed through X-linked transcript levels and allelic binding analyses 2016 ·Scientific Reports ·Chih‐Yu Chen, Wenqiang Shi, Bradley P. Balaton, Allison Matthews, Yifeng Li, David J. Arenillas, Anthony Mathelier, Masayoshi Itoh, Hideya Kawaji, Timo Lassmann, Yoshihide Hayashizaki, Piero Carninci, Alistair R. R. Forrest, Carolyn J. Brown, Wyeth W. Wasserman	30
14	Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target? 2015 ·Molecular Genetics and Metabolism ·Gabriella Horváth, Michelle Demos, Casper Shyr, Allison Matthews, Linhua Zhang, (unknown), Sylvia Stöckler‐Ipsiroglu, Margot I. Van Allen, B. Ogan Mancarci, Lilah Toker, Paul Pavlidis, Colin J.D. Ross, Wyeth W. Wasserman, Natalie Trump, (unknown), Simon Pope, J. Helen Cross, Clara van Karnebeek	33

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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