Sarah E. Lloyd
Impact in
- Neurology top 1%
- Neurological diseases and metabolism
- Nephrology top 2%
- Parathyroid Disorders and Treatments
Papers in
-
- Prion Diseases and Protein Misfolding 20
- Ion Transport and Channel Regulation 6
-
- Trace Elements in Health 15
- Co-authors
- John Collinge (21 shared papers)Rajesh V. Thakker (14 shared papers)Elizabeth Fisher (5 shared papers)J. Beck (1 shared paper)Michael F. W. Festing (1 shared paper)Janan T. Eppig (1 shared paper)Majid Hafezparast (1 shared paper)Simon H. S. Pearce (5 shared papers)
- Journals
- PLoS ONE (3 papers)Human Genetics (2 papers)Journal of Bone and Mineral Research (2 papers)Mammalian Genome (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Sarah E. Lloyd
40 papers receiving 3.4k citations
Sarah E. Lloyd's Hit Papers
Peers
Comparison fields: 5 of 113
- Neurology 647
- Nephrology 339
- Nutrition and Dietetics 579
- Molecular Biology 2.3k
- Genetics 468
Countries citing papers authored by Sarah E. Lloyd
This map shows the geographic impact of Sarah E. Lloyd'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 Sarah E. Lloyd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah E. Lloyd more than expected).
Fields of papers citing papers by Sarah E. Lloyd
This network shows the impact of papers produced by Sarah E. Lloyd. 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 Sarah E. Lloyd. The network helps show where Sarah E. Lloyd may publish in the future.
Co-authors
The 25 scholars most cited alongside Sarah E. Lloyd, 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 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genealogies of mouse inbred strains Hit paper breakdown → | 2000 | 679 |
| 2 | A common molecular basis for three inherited kidney stone diseases Hit paper breakdown → | 1996 | 614 |
| 3 | 1998 | 344 | |
| 4 | 2002 | 287 | |
| 5 | 2004 | 209 | |
| 6 | 2001 | 154 | |
| 7 | Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). | 1994 | 139 |
| 8 | 1997 | 133 | |
| 9 | 1995 | 121 | |
| 10 | 1999 | 116 | |
| 11 | 2011 | 95 | |
| 12 | 1997 | 69 | |
| 13 | 2009 | 63 | |
| 14 | 2000 | 61 | |
| 15 | 2019 | 60 | |
| 16 | 2002 | 56 | |
| 17 | 2013 | 50 | |
| 18 | 2004 | 41 | |
| 19 | 1996 | 30 | |
| 20 | 2014 | 25 |
About Sarah E. Lloyd
Sarah E. Lloyd is a scholar working on Molecular Biology, Nutrition and Dietetics, Neurology, Pulmonary and Respiratory Medicine and Oncology, having authored 42 papers that have together received 3.6k indexed citations. Recurring topics across this work include Prion Diseases and Protein Misfolding (20 papers), Trace Elements in Health (15 papers), Neurological diseases and metabolism (15 papers), Ion Transport and Channel Regulation (6 papers), Neuroblastoma Research and Treatments (3 papers), Kidney Stones and Urolithiasis Treatments (3 papers), Advanced Proteomics Techniques and Applications (2 papers) and Biomedical Research and Pathophysiology (2 papers). The work is most often cited by research in Neurology (647 citations), Nephrology (339 citations), Nutrition and Dietetics (579 citations), Molecular Biology (2.3k citations) and Genetics (468 citations). Sarah E. Lloyd has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include John Collinge, Rajesh V. Thakker, Elizabeth Fisher, J. Beck, Michael F. W. Festing, Janan T. Eppig, Majid Hafezparast, Simon H. S. Pearce, Ian Craig and Simon E. Fisher. Their work appears in journals such as PLoS ONE, Human Genetics, Journal of Bone and Mineral Research, Mammalian Genome and The American Journal of Human Genetics.
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.