Jennifer Duff

1.8k total citations
30 papers, 728 citations indexed

About

Jennifer Duff is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Jennifer Duff has authored 30 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 8 papers in Clinical Biochemistry. Recurrent topics in Jennifer Duff's work include Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (8 papers) and Genetic Neurodegenerative Diseases (7 papers). Jennifer Duff is often cited by papers focused on Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (8 papers) and Genetic Neurodegenerative Diseases (7 papers). Jennifer Duff collaborates with scholars based in United Kingdom, Germany and Spain. Jennifer Duff's co-authors include Rita Horváth, Patrick F. Chinnery, Angela Pyle, Helen Griffin, Venkateswaran Ramesh, Patrick Yu‐Wai‐Man, Robert W. Taylor, Mauro Santibanez‐Koref, David Lewis‐Smith and Konstantinos Douroudis and has published in prestigious journals such as Brain, Neurology and Scientific Reports.

In The Last Decade

Jennifer Duff

29 papers receiving 704 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jennifer Duff United Kingdom 15 447 198 141 124 101 30 728
Joanna Kosińska Poland 19 544 1.2× 74 0.4× 117 0.8× 188 1.5× 39 0.4× 54 891
Laia Pedrola Spain 14 416 0.9× 477 2.4× 56 0.4× 57 0.5× 213 2.1× 31 1.0k
Ľudevít Kádaši Slovakia 18 446 1.0× 99 0.5× 147 1.0× 155 1.3× 39 0.4× 56 809
Bart Kanon Netherlands 12 748 1.7× 146 0.7× 42 0.3× 40 0.3× 82 0.8× 13 879
Nay-Wei Soong United States 9 694 1.6× 84 0.4× 204 1.4× 224 1.8× 15 0.1× 10 927
Debra A. Tokarz United States 13 240 0.5× 154 0.8× 16 0.1× 91 0.7× 124 1.2× 36 741
Margaret A. Johnson United Kingdom 11 728 1.6× 103 0.5× 197 1.4× 131 1.1× 12 0.1× 17 873
Tadashi Mabuchi Japan 16 452 1.0× 37 0.2× 28 0.2× 65 0.5× 84 0.8× 34 905
RD Jolly New Zealand 16 264 0.6× 64 0.3× 61 0.4× 101 0.8× 135 1.3× 49 754
Henry Hoff United States 12 540 1.2× 61 0.3× 27 0.2× 72 0.6× 20 0.2× 18 897

Countries citing papers authored by Jennifer Duff

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Duff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Duff

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

All Works

20 of 20 papers shown
1.
Johari, Mridul, Ana Töpf, Jennifer Duff, et al.. (2024). Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement. Journal of Medical Genetics. 61(10). 992–998.
2.
Kadhim, Hazim, et al.. (2023). A pathogenic CTBP1 variant featuring HADDTS with dystrophic myopathology. Neuromuscular Disorders. 33(5). 410–416. 2 indexed citations
3.
Mroczek, Magdalena, Cheryl Longman, Maria Elena Farrugia, et al.. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of Medical Genetics. 59(11). 1069–1074. 3 indexed citations
4.
Specht, Sabine, Jennifer Duff, Richard Charlton, et al.. (2021). A cryptic intronic LAMA2 insertion in a boy with mild congenital muscular dystrophy type 1A. Neuromuscular Disorders. 31(7). 660–665. 1 indexed citations
5.
Alonso‐Pérez, Jorge, Jennifer Duff, Ricard Rojas‐García, et al.. (2021). Late onset Sandhoff disease presenting with lower motor neuron disease and stuttering. Neuromuscular Disorders. 31(8). 769–772. 4 indexed citations
6.
Pyle, Angela, Maria Suo‐Palosaari, Jennifer Duff, et al.. (2020). Homozygous TAF1C variants are associated with a novel childhood‐onset neurological phenotype. Clinical Genetics. 98(5). 493–498. 3 indexed citations
7.
Mroczek, Magdalena, Hacer Durmuş, Sunita Bijarnia‐Mahay, et al.. (2020). Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patients. Neuromuscular Disorders. 30(4). 310–314. 16 indexed citations
8.
Nilipour, Yalda, Farzad Fatehi, Jennifer Duff, et al.. (2020). Multiple acyl-coenzyme A dehydrogenase deficiency shows a possible founder effect and is the most frequent cause of lipid storage myopathy in Iran. Journal of the Neurological Sciences. 411. 116707–116707. 15 indexed citations
9.
Mroczek, Magdalena, Dimitrios Zafeiriou, Andreas Roos, et al.. (2020). Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular Disease. Neuropediatrics. 52(5). 390–393. 8 indexed citations
10.
Bánsági, Boglárka, Mark R. Baker, Julia O’Sullivan, et al.. (2018). Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation. Neurology. 90(21). e1842–e1848. 5 indexed citations
11.
Pyle, Angela, Maria Lucia Valentino, Rocco Liguori, et al.. (2018). Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. Scientific Reports. 8(1). 11682–11682. 17 indexed citations
12.
Connor, Thomas M., Simon Hoer, Andrew J. Mallett, et al.. (2017). Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. PLoS Genetics. 13(3). e1006620–e1006620. 40 indexed citations
13.
Duff, Jennifer, et al.. (2015). Variation in complement protein C1q is not a major contributor to cognitive impairment in Parkinson’s disease. Neuroscience Letters. 594. 66–69. 10 indexed citations
14.
Keogh, Michael J., Hannah E. Steele, Konstantinos Douroudis, et al.. (2015). Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia. Journal of Neurology. 262(8). 1822–1827. 11 indexed citations
15.
Pyle, Angela, Venkateswaran Ramesh, Marina Bartsakoulia, et al.. (2014). Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene. Journal of Neuromuscular Diseases. 1(1). 55–63. 14 indexed citations
16.
Griffin, Helen, Angela Pyle, Emma L. Blakely, et al.. (2014). Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations. Genetics in Medicine. 16(12). 962–971. 48 indexed citations
17.
Pyle, Angela, Helen Griffin, Jennifer Duff, et al.. (2013). Late-Onset Sacsinopathy Diagnosed by Exome Sequencing and Comparative Genomic Hybridization. Journal of Neurogenetics. 27(4). 176–182. 6 indexed citations
18.
Pyle, Angela, Helen Griffin, Patrick Yu‐Wai‐Man, et al.. (2012). Prominent Sensorimotor Neuropathy Due to SACS Mutations Revealed by Whole-Exome Sequencing. Archives of Neurology. 69(10). 1351–4. 19 indexed citations
19.
Duff, Jennifer, et al.. (1995). Courtship and mortality in foxes (Vulpes vulpes). Veterinary Record. 136(14). 367–367. 6 indexed citations
20.
Kirkwood, James, Andrew A. Cunningham, S. K. Macgregor, Simon N. Thornton, & Jennifer Duff. (1994). Salmonella enteritidis excretion by carnivorous animals fed on day-old chicks. Veterinary Record. 134(26). 683–683. 6 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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