Rebecca Sparkes

2.7k citations

30 papers · 1.4k indexed · h-index 17

Molecular Biology top 10%
Genetics top 2%
Ecology top 10%
Cellular and Molecular Neuroscience top 10%
Cell Biology

Co-authors: Phillipa Gill Tim Clayton Jonathan Whitaker C. Kimpton Nicola J. Oldroyd John Buckleton R. Frazier Andy Urquhart
Topics: Molecular Biology Techniques and Applications (8 papers)Forensic and Genetic Research (7 papers)Metabolism and Genetic Disorders (6 papers)
Cited by: Genetics Molecular Biology Clinical Biochemistry
Journals: Proceedings of the National Academy of Sciences Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Canada United Kingdom United States

In The Last Decade

Rebecca Sparkes

30 papers receiving 1.3k citations

Peers

Countries citing papers authored by Rebecca Sparkes

Since Specialization

Citations

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

Fields of papers citing papers by Rebecca Sparkes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca Sparkes

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only 2021 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Matthew A. Lines,Klaus Brusgaard,Diva D. De León,Rebecca Sparkes,Anja Lisbeth Frederiksen,Henrik Thybo Christesen	5
2	Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys 2021 ·Trials ·(unknown),Kylie Tingley,Michal Inbar‐Feigenberg,John J. Mitchell,Nancy J. Butcher,Martin Offringa,Maureen Smith,(unknown),(unknown),(unknown),Philippe M. Campeau,Alicia Chan,Pranesh Chakraborty,(unknown),Eva Mamak,(unknown),Becky Skidmore,Rebecca Sparkes,Sylvia Stöckler,Beth K. Potter	2
3	MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease 2020 ·Molecular Genetics and Metabolism ·(unknown),Stacey Hume,(unknown),(unknown),(unknown),(unknown),(unknown),Xing‐Chang Wei,(unknown),(unknown),(unknown),Christopher Newell,Rebecca Sparkes,Dustin S. Hittel,Aneal Khan	15
4	Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype 2019 ·Proceedings of the National Academy of Sciences ·Eline Blommaert,Romain Péanne,Н. А. Черепанова,Daisy Rymen,Frederik Staels,Jaak Jaeken,Valérie Race,Liesbeth Keldermans,Erika Souche,Anniek Corveleyn,Rebecca Sparkes,Kaustuv Bhattacharya,Christine Devalck,Rik Schrijvers,François Foulquier,Reid Gilmore,Gert Matthijs	61
5	Cardiopulmonary Exercise Testing Reflects Improved Exercise Capacity in Response to Treatment in Morquio A Patients: Results of a 52-Week Pilot Study of Two Different Doses of Elosulfase Alfa 2017 ·JIMD Reports ·Kenneth I. Berger,Barbara K. Burton,Gregory D. Lewis,Mark A. Tarnopolsky,Paul Harmatz,John J. Mitchell,Nicole Muschol,Simon Jones,V. Reid Sutton,Gregory M. Pastores,Heather Lau,Rebecca Sparkes,Adam J. Shaywitz	4
6	Fibroblast Fatty-Acid Oxidation Flux Assays Stratify Risk in Newborns with Presumptive-Positive Results on Screening for Very-Long Chain Acyl-CoA Dehydrogenase Deficiency 2017 ·International Journal of Neonatal Screening ·S. E. Olpin,(unknown),(unknown),Brage Storstein Andresen,(unknown),(unknown),Aneal Khan,Richard Kirk,Rebecca Sparkes,(unknown),Alicia Chan,Emma Glamuzina,Jean Bastin,N. J. Manning,R. J. Pollitt	5
7	A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population 2016 ·American Journal of Medical Genetics Part A ·Ryan E. Lamont,Chandree L. Beaulieu,François P. Bernier,Rebecca Sparkes,A. Micheil Innes,(unknown),Carole Ober,Jillian S. Parboosingh,Edmond G. Lemire	13
8	Expanding the Molecular and Clinical Phenotype of SSR4-CDG 2015 ·Human Mutation ·Bobby G. Ng,Kimiyo Raymond,Martin Kircher,Kati J. Buckingham,Tim Wood,Jay Shendure,Deborah A. Nickerson,Michael J. Bamshad,(unknown),Fabíola Paoli Monteiro,Brett H. Graham,(unknown),Rebecca Sparkes,Angela E. Scheuerle,Sara Cathey,Fernando Kok,James B. Gibson,Hudson H. Freeze	25
9	Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups 2015 ·Journal of Inherited Metabolic Disease ·Sara D. Khangura,Kylie Tingley,Pranesh Chakraborty,Doug Coyle,Jonathan B. Kronick,Anne‐Marie Laberge,Julian Little,Fiona A. Miller,John J. Mitchell,Chitra Prasad,Shabnaz Siddiq,Komudi Siriwardena,Rebecca Sparkes,Kathy N. Speechley,Sylvia Stöckler,Yannis Trakadis,Brenda J. Wilson,Kumanan Wilson,Beth K. Potter	31
10	Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling 2009 ·Prenatal Diagnosis ·Rebecca Sparkes,Shashirekha Shetty,Judy Chernos,Heather C Mefford,A. Micheil Innes	20
11	Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis 2008 ·Journal of Obstetrics and Gynaecology Canada ·Rebecca Sparkes,François P. Bernier,Judy Chernos,Jo‐Ann Johnson	5
12	New Molecular Techniques for the Prenatal Detection of Chromosomal Aneuploidy 2008 ·Journal of Obstetrics and Gynaecology Canada ·Rebecca Sparkes,Jo-Ann Johnson,Sylvie Langlois,R. Douglas Wilson,Victoria M. Allen,Claire Blight,Valérie Désilets,Alain Gagnon,Anne Summers,(unknown)	8
13	Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein 2007 ·Cardiology in the Young ·Rebecca Sparkes,David R. Patton,François P. Bernier	35
14	Development of a 1.4-Mb BAC/PAC Contig and Physical Map within the Critical Region for Complete X-Linked Congenital Stationary Night Blindness in Xp11.4 2000 ·Genomics ·Rebecca Sparkes,(unknown),Kym M. Boycott,Robert J. Zahorchak,N. Torben Bech‐Hansen	1
15	Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness 2000 ·Nature Genetics ·N. Torben Bech‐Hansen,(unknown),(unknown),Rebecca Sparkes,Ben F. Koop,David G. Birch,Arthur A. Bergen,Clemens Prinsen,Robert C. Polomeno,Andreas Gal,Arlene V. Drack,Maria A. Musarella,Samuel G. Jacobson,Rockefeller S.L. Young,Richard G. Weleber	249
16	Validation of the AMPFlSTR® SGM Plus™ system for use in forensic casework 2000 ·Forensic Science International ·(unknown),(unknown),(unknown),R. Frazier,(unknown),(unknown),(unknown),Rebecca Sparkes	153
17	Interpreting simple STR mixtures using allele peak areas 1998 ·Forensic Science International ·Phillipa Gill,Rebecca Sparkes,R. Pinchin,Tim Clayton,Jonathan Whitaker,John Buckleton	113
18	Analysis and interpretation of mixed forensic stains using DNA STR profiling 1998 ·Forensic Science International ·Tim Clayton,Jonathan Whitaker,Rebecca Sparkes,Phillipa Gill	194
19	Development of guidelines to designate alleles using an STR multiplex system 1997 ·Forensic Science International ·Phillipa Gill,Rebecca Sparkes,C. Kimpton	87
20	A new method of STR interpretation using inferential logic -development of a criminal intelligence database 1996 ·International Journal of Legal Medicine ·Phillipa Gill,Andy Urquhart,Emma S. Millican,Nicola J. Oldroyd,Steve P. Watson,Rebecca Sparkes,C. Kimpton	66

About Rebecca Sparkes

Rebecca Sparkes is a scholar working on Clinical Biochemistry, Genetics and Rheumatology, having authored 30 papers that have together received 1.4k indexed citations. Recurring topics across this work include Molecular Biology Techniques and Applications (8 papers), Forensic and Genetic Research (7 papers) and Metabolism and Genetic Disorders (6 papers). The work is most often cited by research in Genetics (780 citations), Molecular Biology (914 citations) and Clinical Biochemistry (73 citations). Rebecca Sparkes has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include Phillipa Gill, Tim Clayton, Jonathan Whitaker, C. Kimpton, Nicola J. Oldroyd, John Buckleton, R. Frazier, Andy Urquhart, R. Pinchin and Steve P. Watson. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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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