Kate Craig

654 total citations
16 papers, 312 citations indexed

About

Kate Craig is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kate Craig has authored 16 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Kate Craig's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (5 papers) and ATP Synthase and ATPases Research (4 papers). Kate Craig is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (5 papers) and ATP Synthase and ATPases Research (4 papers). Kate Craig collaborates with scholars based in United Kingdom, United States and France. Kate Craig's co-authors include Robert W. Taylor, Patrick F. Chinnery, Sharon Keers, Emma L. Blakely, Ann Curtis, Douglass M. Turnbull, Robert McFarland, Joanna Poulton, Langping He and D. Taverner and has published in prestigious journals such as Neurology, Annals of Neurology and The Journal of Pediatrics.

In The Last Decade

Kate Craig

16 papers receiving 309 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Kate Craig United Kingdom	10	233	124	75	31	29	16	312
Silvio Ferraris Italy	12	262 1.1×	198 1.6×	34 0.5×	15 0.5×	42 1.4×	12	370
R. Mercelis Belgium	11	252 1.1×	73 0.6×	54 0.7×	19 0.6×	16 0.6×	15	301
Emma Glamuzina New Zealand	11	148 0.6×	149 1.2×	31 0.4×	31 1.0×	62 2.1×	30	323
Tim M. Strom Germany	4	173 0.7×	50 0.4×	51 0.7×	65 2.1×	76 2.6×	4	336
Colleen Muraresku United States	10	263 1.1×	175 1.4×	30 0.4×	8 0.3×	41 1.4×	19	313
India Butler South Africa	3	276 1.2×	211 1.7×	38 0.5×	19 0.6×	16 0.6×	5	320
Jose Carlo United States	6	260 1.1×	195 1.6×	23 0.3×	16 0.5×	20 0.7×	6	287
Célia Nogueira Portugal	11	249 1.1×	216 1.7×	15 0.2×	14 0.5×	27 0.9×	36	385
Magdalena Pajdowska Poland	11	316 1.4×	209 1.7×	15 0.2×	25 0.8×	76 2.6×	22	422

Countries citing papers authored by Kate Craig

Since Specialization

Citations

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

Fields of papers citing papers by Kate Craig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Craig

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

Schaefer, Andrew M., Kate Craig, Sila Hopton, et al.. (2022). Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy. BMJ Neurology Open. 4(2). e000352–e000352. 4 indexed citations

Maldergem, Lionel Van, Arnaud Besse, Emma L. Blakely, et al.. (2016). POLG2 deficiency causes adult‐onset syndromic sensory neuropathy, ataxia and parkinsonism. Annals of Clinical and Translational Neurology. 4(1). 4–14. 16 indexed citations

McKiernan, Patrick, Sarah Ball, Saikat Santra, et al.. (2016). Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure. Journal of Pediatric Gastroenterology and Nutrition. 63(6). 592–597. 34 indexed citations

Battaglia, Patrick J., Kate Craig, & Norman W. Kettner. (2015). Ultrasonography in the Assessment of Lateral Ankle Ligament Injury, Instability, and Anterior Ankle Impingement: A Diagnostic Case Report. Journal of Chiropractic Medicine. 14(4). 265–269. 8 indexed citations

Al‐Hussaini, Abdulrahman, Eissa Faqeih, Ayman W. El‐Hattab, et al.. (2013). Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure. The Journal of Pediatrics. 164(3). 553–559.e2. 36 indexed citations

Alston, Charlotte L., Andrew M. Schaefer, Nicola Solaroli, et al.. (2013). Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions. Neurology. 81(23). 2051–2053. 17 indexed citations

Blakely, Emma L., John W. Yarham, Charlotte L. Alston, et al.. (2013). Pathogenic Mitochondrial t RNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease. Human Mutation. 34(9). 1260–1268. 61 indexed citations

Wortmann, Saskia B., M. P. Champion, Lambert van den Heuvel, et al.. (2012). Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?. European Journal of Medical Genetics. 55(10). 552–556. 25 indexed citations

Craig, Kate, Matthew J. Young, Emma L. Blakely, et al.. (2011). A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunits. Mitochondrion. 12(2). 313–319. 21 indexed citations

10.

Craig, Kate, Yoshihisa Takiyama, Bing‐Wen Soong, et al.. (2008). Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?. European Journal of Human Genetics. 16(7). 841–847. 7 indexed citations

11.

Gilroy, Kathryn, Pauline Heslop, Ian G. Cowell, et al.. (2007). Differential Selection of Acridine Resistance Mutations in Human DNA Topoisomerase IIβ Is Dependent on the Acridine Structure. Molecular Pharmacology. 71(4). 1006–1014. 7 indexed citations

12.

Craig, Kate, et al.. (2005). Minimum prevalence of spinocerebellar ataxia 17 in the north east of England. Journal of the Neurological Sciences. 239(1). 105–109. 22 indexed citations

13.

Craig, Kate, et al.. (2004). Molecular epidemiology of spinocerebellar ataxia type 6. Annals of Neurology. 55(5). 752–755. 35 indexed citations

14.

Craig, Kate. (2004). London safari. 1(4). 11–11. 1 indexed citations

15.

Craig, Kate. (2004). Winter wonderland. 1(5). 52–52. 1 indexed citations

16.

Taverner, D., et al.. (1991). Effects of Exercise on Renal Function in Patients with Moderate Impairment of Renal Function Compared to Normal Men. The Nephron journals/Nephron journals. 57(3). 288–292. 17 indexed citations

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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