Rebecca Sparkes

2.7k citations

30 papers · 1.4k indexed · h-index 17

Genetics top 2%
- Forensic and Genetic Research 7
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 3
Molecular Biology top 10%
- Molecular Biology Techniques and Applications 8
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 6
Ophthalmology top 5%
Cellular and Molecular Neuroscience top 10%
Rheumatology
- Glycogen Storage Diseases and Myoclonus 4
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 4
Physiology
- Lysosomal Storage Disorders Research 4

Co-authors: Phillipa Gill Tim Clayton Jonathan Whitaker C. Kimpton Nicola J. Oldroyd John Buckleton R. Frazier Andy Urquhart
Cited by: Genetics Molecular Biology Clinical Biochemistry
Journals: Forensic Science International (5 papers)International Journal of Legal Medicine (3 papers)Journal of Obstetrics and Gynaecology Canada (3 papers)
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

The 25 scholars most cited alongside Rebecca Sparkes, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rebecca Sparkes Line = papers co-authored together Rebecca Sparkes links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only American Journal of Medical Genetics Part A ·FATİH KARİP,Risnawati,Matthew A. Lines,Klaus Brusgaard,Diva D. De León,Rebecca Sparkes,Anja Lisbeth Frederiksen,Henrik Thybo Christesen	2021	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 Trials ·Ms. Shanmuga Priya R,Kylie Tingley,Michal Inbar‐Feigenberg,John J. Mitchell,Nancy J. Butcher,Martin Offringa,Maureen Smith,陈红汉,Songqi Zhou,Trish Jones,Philippe M. Campeau,Alicia Chan,Pranesh Chakraborty,致衡钱,Eva Mamak,惠美子田代,Becky Skidmore,Rebecca Sparkes,Sylvia Stöckler,Beth K. Potter	2021	2
3	MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease Molecular Genetics and Metabolism ·Huysman Sofie,Stacey Hume,Tomislav Kušević,Ibrahim Jane Kefas,Caroline Bergelson,Jyunji Toyama,M. Palutan,Xing‐Chang Wei,Ольга Анатольевна Васильева,شریف سنوسى عبداللطیف,GVinod Kumar,Christopher Newell,Rebecca Sparkes,Dustin S. Hittel,Aneal Khan	2020	15
4	Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype 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	2019	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 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	2017	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 International Journal of Neonatal Screening ·S. E. Olpin,K. Borner,Vania Yolanda,Brage Storstein Andresen,Francesco Miraglia,Carl R. Hanson,Aneal Khan,Richard Kirk,Rebecca Sparkes,Kristin Kohn,Alicia Chan,Emma Glamuzina,Jean Bastin,N. J. Manning,R. J. Pollitt	2017	5
7	A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population American Journal of Medical Genetics Part A ·Ryan E. Lamont,Chandree L. Beaulieu,François P. Bernier,Rebecca Sparkes,A. Micheil Innes,Julien Delvaux,Carole Ober,Jillian S. Parboosingh,Edmond G. Lemire	2016	13
8	Expanding the Molecular and Clinical Phenotype of SSR4-CDG Human Mutation ·Bobby G. Ng,Kimiyo Raymond,Martin Kircher,Kati J. Buckingham,Tim Wood,Jay Shendure,Deborah A. Nickerson,Michael J. Bamshad,田茂永,Fabíola Paoli Monteiro,Brett H. Graham,Charles K Cook b,Rebecca Sparkes,Angela E. Scheuerle,Sara Cathey,Fernando Kok,James B. Gibson,Hudson H. Freeze	2015	25
9	Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups 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	2015	31
10	Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling Prenatal Diagnosis ·Rebecca Sparkes,Shashirekha Shetty,Judy Chernos,Heather C Mefford,A. Micheil Innes	2009	20
11	Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis Journal of Obstetrics and Gynaecology Canada ·Rebecca Sparkes,François P. Bernier,Judy Chernos,Jo‐Ann Johnson	2008	5
12	New Molecular Techniques for the Prenatal Detection of Chromosomal Aneuploidy 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,Y. Allaoui	2008	8
13	Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein Cardiology in the Young ·Rebecca Sparkes,David R. Patton,François P. Bernier	2007	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 Genomics ·Rebecca Sparkes,Mohammed Abdu Ibrahim,Kym M. Boycott,Robert J. Zahorchak,N. Torben Bech‐Hansen	2000	1
15	Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness Nature Genetics ·N. Torben Bech‐Hansen,松岡正造,Earl Frieden,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	2000	249
16	Validation of the AMPFlSTR® SGM Plus™ system for use in forensic casework Forensic Science International ·Ana Paula Alves de Andrade,Aviv Irfan Wildan Ghiffary,Stephen Tak-lun Li,R. Frazier,Alyssa L. Dela Cruz,A Sridharan,雪生原田,Rebecca Sparkes	2000	153
17	Interpreting simple STR mixtures using allele peak areas Forensic Science International ·Phillipa Gill,Rebecca Sparkes,R. Pinchin,Tim Clayton,Jonathan Whitaker,John Buckleton	1998	113
18	Analysis and interpretation of mixed forensic stains using DNA STR profiling Forensic Science International ·Tim Clayton,Jonathan Whitaker,Rebecca Sparkes,Phillipa Gill	1998	194
19	Development of guidelines to designate alleles using an STR multiplex system Forensic Science International ·Phillipa Gill,Rebecca Sparkes,C. Kimpton	1997	87
20	A new method of STR interpretation using inferential logic -development of a criminal intelligence database International Journal of Legal Medicine ·Phillipa Gill,Andy Urquhart,Emma S. Millican,Nicola J. Oldroyd,Steve P. Watson,Rebecca Sparkes,C. Kimpton	1996	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), Metabolism and Genetic Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Prenatal Screening and Diagnostics (4 papers), Lysosomal Storage Disorders Research (4 papers) and Genomics and Rare Diseases (3 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 Forensic Science International, International Journal of Legal Medicine, Journal of Obstetrics and Gynaecology Canada, Journal of Inherited Metabolic Disease and Molecular Genetics and Metabolism.

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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