Sara Mole

10.8k total citations · 1 hit paper
147 papers, 7.2k citations indexed

About

Sara Mole is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Sara Mole has authored 147 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Physiology, 77 papers in Molecular Biology and 52 papers in Cell Biology. Recurrent topics in Sara Mole's work include Lysosomal Storage Disorders Research (109 papers), Cellular transport and secretion (46 papers) and Glycosylation and Glycoproteins Research (29 papers). Sara Mole is often cited by papers focused on Lysosomal Storage Disorders Research (109 papers), Cellular transport and secretion (46 papers) and Glycosylation and Glycoproteins Research (29 papers). Sara Mole collaborates with scholars based in United Kingdom, United States and Germany. Sara Mole's co-authors include Ruth Williams, Anna‐Elina Lehesjoki, Emily Gardner, Susan L. Cotman, Alan Tunnacliffe, Lois M. Mulligan, Catherine S. Healey, Laura Papi, Bruce A.J. Ponder and Håkan Telenius and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Sara Mole

142 papers receiving 7.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

1993 1.4k citations Emily Gardner, Sara Mole et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sara Mole United Kingdom	41	4.1k	3.0k	2.5k	1.1k	877	147	7.2k
Anna‐Elina Lehesjoki Finland	39	1.4k 0.3×	2.1k 0.7×	943 0.4×	286 0.3×	1.6k 1.8×	126	4.9k
Mirella Filocamo Italy	34	2.5k 0.6×	1.9k 0.6×	1.1k 0.4×	903 0.8×	431 0.5×	158	4.3k
Vijaya Ramesh United States	48	1.0k 0.3×	2.7k 0.9×	1.2k 0.5×	1.2k 1.1×	716 0.8×	113	6.6k
G I Bell United States	31	696 0.2×	4.0k 1.3×	335 0.1×	1.2k 1.1×	1.1k 1.2×	55	6.4k
William F. Simonds United States	45	409 0.1×	4.0k 1.3×	675 0.3×	1.0k 0.9×	782 0.9×	138	6.5k
Paola Bruni Italy	41	886 0.2×	3.6k 1.2×	978 0.4×	418 0.4×	322 0.4×	168	5.1k
Patrick Aubourg France	44	1.7k 0.4×	4.7k 1.6×	227 0.1×	254 0.2×	481 0.5×	96	5.8k
Uwe Kornak Germany	36	579 0.1×	3.3k 1.1×	700 0.3×	261 0.2×	1.2k 1.3×	136	5.1k
Lawrence A. Quilliam United States	46	989 0.2×	5.3k 1.8×	2.2k 0.9×	227 0.2×	388 0.4×	91	7.5k
Alastair D. Reith United Kingdom	35	832 0.2×	4.6k 1.5×	1.2k 0.5×	357 0.3×	555 0.6×	52	7.1k

Countries citing papers authored by Sara Mole

Since Specialization

Citations

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

Fields of papers citing papers by Sara Mole

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Mole

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Hermey, Guido, Sara Mole, Tatyana A. Shelkovnikova, et al.. (2023). The Batten disease protein CLN3 is important for stress granules dynamics and translational activity. Journal of Biological Chemistry. 299(5). 104649–104649. 4 indexed citations

Little, Daniel, et al.. (2023). Characterization of two human induced pluripotent stem cell lines derived from Batten disease patient fibroblasts harbouring CLN5 mutations. Stem Cell Research. 74. 103291–103291. 2 indexed citations

Townsend, StJohn, Julia Petschnigg, Elisa Tinelli, et al.. (2021). Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease. Scientific Reports. 11(1). 6332–6332. 9 indexed citations

Holthaus, Sophia-Martha kleine, Saúl Herranz-Martín, Giulia Massaro, et al.. (2019). Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease. Human Molecular Genetics. 28(23). 3867–3879. 23 indexed citations

Nita, Dragos A., Sara Mole, & Berge A. Minassian. (2016). Neuronal ceroid lipofuscinoses. Epileptic Disorders. 18(s2). 73–88. 106 indexed citations

Mole, Sara & Susan L. Cotman. (2015). Genetics of the neuronal ceroid lipofuscinoses (Batten disease). Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(10). 2237–2241. 228 indexed citations

Nosková, Lenka, Viktor Stránecký, Hana Hartmannová, et al.. (2011). Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis. The American Journal of Human Genetics. 89(4). 589–589. 10 indexed citations

Codlin, Sandra, Rebecca L. Haines, Ian J. White, et al.. (2010). Deletion of btn 1, an orthologue of CLN 3, increases glycolysis and perturbs amino acidmetabolism in the fission yeast model of Batten disease. Molecular BioSystems. 6(6). 1093–1102. 17 indexed citations

Åberg, L., et al.. (2009). A 30-year Follow-Up of a Neuronal Ceroid Lipofuscinosis Patient With Mutations in CLN3 and Protracted Disease Course. Pediatric Neurology. 40(2). 134–137. 11 indexed citations

10.

Al-Din, A. S. Najim, et al.. (2007). Adult neuronal ceroid lipofuscinosis caused by deficiency in palmitoyl protein thioesterase 1. Neurology. 68(5). 387–388. 38 indexed citations

11.

Sharp, Julie D., Ruth B. Wheeler, Keith A. Parker, et al.. (2003). Spectrum ofCLN6mutations in variant late infantile neuronal ceroid lipofuscinosis. Human Mutation. 22(1). 35–42. 60 indexed citations

12.

Mole, Sara, Nanbert Zhong, W. P. D. Logan, et al.. (2001). New mutations in the neuronal ceroid lipofuscinosisgenes. European Journal of Paediatric Neurology. 5. 7–10. 26 indexed citations

13.

Mole, Sara & Mark Gardiner. (1999). Molecular Genetics of the Neuronal Ceroid Lipofuscinoses. Epilepsia. 40(s3). 29–32. 19 indexed citations

14.

Vos, Nathalie De, et al.. (1999). A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999). UCL Discovery (University College London).

15.

Munroe, Patricia B., Yanick J. Crow, Robert W. Williams, et al.. (1998). Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits (vol 7, pg 291, 1998). UCL Discovery (University College London). 1 indexed citations

16.

Mitchison, Hannah M., Angela O'Rawe, Terry J. Lerner, et al.. (1995). Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288‐D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits. American Journal of Medical Genetics. 57(2). 312–315. 14 indexed citations

17.

Gardner, Emily, et al.. (1991). EXTENDING THE GENETIC-MAP OF THE PERICENTROMERIC REGION OF CHROMOSOME-10. UCL Discovery (University College London). 1 indexed citations

18.

Gardner, Emily, et al.. (1991). IS THE RET PROTOONCOGENE A CANDIDATE FOR THE MEN2 GENE. UCL Discovery (University College London). 6 indexed citations

19.

Mole, Sara, Julian Gannon, M J Ford, & David P. Lane. (1987). Structure and function of SV40 large-T antigen. Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 317(1187). 455–469. 56 indexed citations

20.

Lane, David P., et al.. (1985). Cellular targets for SV40 Large T-antigen. Proceedings of the Royal Society of London. Series B, Biological sciences. 226(1242). 25–42. 24 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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