Sara Mole
Impact in
- Physiology top 0.2%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
- Cell Biology top 0.2%
- Cellular transport and secretion
Papers in
- Physiology 124
- Lysosomal Storage Disorders Research 124
- Calcium signaling and nucleotide metabolism 16
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- Glycosylation and Glycoproteins Research 34
- RNA regulation and disease 10
- Co-authors
- Ruth Williams (10 shared papers)Emily Gardner (10 shared papers)Anna‐Elina Lehesjoki (6 shared papers)Susan L. Cotman (4 shared papers)Alan Tunnacliffe (4 shared papers)Lois M. Mulligan (4 shared papers)Catherine S. Healey (2 shared papers)Julia K. Moore (3 shared papers)
- Journals
- European Journal of Paediatric Neurology (14 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (12 papers)Human Mutation (8 papers)Human Molecular Genetics (7 papers)Neurology (6 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Sara Mole
161 papers receiving 7.6k citations
Sara Mole's Hit Papers
Peers
Comparison fields: 5 of 108
- Physiology 4.4k
- Physiology 741
- Cell Biology 2.4k
- Endocrinology, Diabetes and Metabolism 889
- Neurology 782
Countries citing papers authored by Sara Mole
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
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-authors
The 25 scholars most cited alongside Sara Mole, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 172 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A Hit paper breakdown → | 1993 | 1590 |
| 2 | 2012 | 380 | |
| 3 | 2011 | 272 | |
| 4 | 1999 | 268 | |
| 5 | 2015 | 244 | |
| 6 | 2005 | 238 | |
| 7 | 2012 | 213 | |
| 8 | 2011 | 212 | |
| 9 | 1997 | 172 | |
| 10 | 2012 | 172 | |
| 11 | 2002 | 164 | |
| 12 | 2006 | 154 | |
| 13 | 2018 | 128 | |
| 14 | 2016 | 110 | |
| 15 | 2009 | 110 | |
| 16 | 2013 | 100 | |
| 17 | 2004 | 95 | |
| 18 | 2004 | 86 | |
| 19 | 1993 | 84 | |
| 20 | 1993 | 80 |
About Sara Mole
Sara Mole is a scholar working on Physiology, Molecular Biology, Cell Biology, Organic Chemistry and Rheumatology, having authored 172 papers that have together received 7.9k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (124 papers), Cellular transport and secretion (45 papers), Glycosylation and Glycoproteins Research (34 papers), Carbohydrate Chemistry and Synthesis (23 papers), Glycogen Storage Diseases and Myoclonus (21 papers), Calcium signaling and nucleotide metabolism (16 papers), Trypanosoma species research and implications (12 papers) and RNA regulation and disease (10 papers). The work is most often cited by research in Physiology (4.4k citations), Physiology (741 citations), Cell Biology (2.4k citations), Endocrinology, Diabetes and Metabolism (889 citations) and Neurology (782 citations). Sara Mole has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Ruth Williams, Emily Gardner, Anna‐Elina Lehesjoki, Susan L. Cotman, Alan Tunnacliffe, Lois M. Mulligan, Catherine S. Healey, Julia K. Moore, Laura Papi and Donald R. Love. Their work appears in journals such as European Journal of Paediatric Neurology, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Human Mutation, Human Molecular Genetics and Neurology.
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.