Sarah E. Lloyd

4.0k citations

41 papers · 3.0k indexed · 2 hit papers · h-index 21

Impact in

Neurology top 2%
- Neurological diseases and metabolism
Nephrology top 2%
- Parathyroid Disorders and Treatments

Papers in

Neurology 16
- Neurological diseases and metabolism 15
- Neuroblastoma Research and Treatments 3
Nutrition and Dietetics 18
- Trace Elements in Health 16

Co-authors: John Collinge Rajesh V. Thakker Elizabeth Fisher Majid Hafezparast J. Beck Janan T. Eppig Michael F. W. Festing Simon H. S. Pearce
Journals: PLoS ONE (3 papers)Journal of Bone and Mineral Research (2 papers)The American Journal of Human Genetics (2 papers)Neurogenetics (2 papers)Mammalian Genome (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Sarah E. Lloyd

39 papers receiving 2.9k citations

Hit Papers

align trajectories log scale

Genealogies of mouse inbred strains 2000 · 645 citations

Peers

Countries citing papers authored by Sarah E. Lloyd

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Sarah E. Lloyd Line = papers co-authored together Sarah E. Lloyd links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Emotion recognition in people with Huntington's disease: A comprehensive systematic review Journal of Huntington s Disease ·Nicolò Zarotti, Zou Yunjing, Sarah E. Lloyd, Maximilian Filsinger, Helen Caswell, Sigmar de Mello, Jane Simpson	2025	0
2	A Single-Step Protein Extraction for Lung Extracellular Matrix Proteomics Enabled by the Photocleavable Surfactant Azo and timsTOF Pro Molecular & Cellular Proteomics ·Fuchs, JULIANY B. CAVALHEIRO, Zulema Sánchez Bazán, Yanlong Zhu, Fei Wang, Sarah E. Lloyd, Kuniko Kadoya, Yupeng He, Yu Tian, Ying Ge	2025	1
3	Asking questions that are “close to the bone”: integrating thematic analysis and natural language processing to explore the experiences of people with traumatic brain injuries engaging with patient-reported outcome measures Frontiers in Digital Health ·(unknown), M. Biegen, Sarah E. Lloyd, Irma Ruslina Defi, Matthew Shardlow	2024	0
4	Rare structural genetic variation in human prion diseases Neurobiology of Aging ·Ana Lukić, James Uphill, Craig Brown, John S. Beck, Mark Poulter, Tracy Campbell, Gary Adamson, Holger Hummerich, Jerome Whitfield, Claudia Ponto, Inga Zerr, Sarah E. Lloyd, John Collinge, Simon Mead	2015	6
5	Microglial Cx3cr1knockout reduces prion disease incubation time in mice BMC Neuroscience ·篠田洋子, Alwiyah Alwiyah, Sebastian Brandner, John Collinge, Sarah E. Lloyd	2014	25
6	Genetics of Prion Disease Topics in current chemistry ·Sarah E. Lloyd, Simon Mead, John Collinge	2011	85
7	The Retinoic Acid Receptor Beta (Rarb) Region of Mmu14 Is Associated with Prion Disease Incubation Time in Mouse PLoS ONE ·篠田洋子, Alwiyah Alwiyah, John Collinge, Sarah E. Lloyd	2010	11
8	Shadoo (Sprn) and prion disease incubation time in mice Mammalian Genome ·Sarah E. Lloyd, 篠田洋子, Hirva Pota, John Collinge	2009	12
9	HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q BMC Medical Genetics ·Sarah E. Lloyd, Martin N. Rossor, Nick C. Fox, Simon Mead, John Collinge	2009	13
10	A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse Neurogenetics ·Sarah E. Lloyd, Wang Xueliang, 篠田洋子, Holger Hummerich, John Collinge	2009	17
11	Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype Science ·Jonathan D. F. Wadsworth, Emmanuel A. Asante, Melanie Desbruslais, Jacqueline M. Linehan, Susan Joiner, Ian Gowland, Julie L. Welch, 輝美青木, Sarah E. Lloyd, Andrew F. Hill, Sebastian Brandner, John Collinge	2004	197
12	Identification and characterization of a novel mouse prion gene allele Mammalian Genome ·Sarah E. Lloyd, Simon R. Thompson, Jonathan Beck, Jacqueline M. Linehan, Jonathan D. F. Wadsworth, Sebastian Brandner, John Collinge, Elizabeth Fisher	2004	22
13	Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice Neurogenetics ·Sarah E. Lloyd, James Uphill, Paul V. Targonski, Elizabeth Fisher, John Collinge	2002	56
14	Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria Kidney International ·Steven J. Scheinman, Anton Sarpila, Sarah E. Lloyd, Simon H. S. Pearce, José Cretella Neto, R R Hoopes, David A. Bushinsky, Oliver Wrong, John R. Asplin, Craig B. Langman, Anthony G.W. Norden, Rajesh V. Thakker	2000	49
15	Genealogies of mouse inbred strains Nature Genetics ·J. Beck, Sarah E. Lloyd, Majid Hafezparast, Wang Chang, Janan T. Eppig, Michael F. W. Festing, Elizabeth Fisher Hit paper breakdown →	2000	645
16	Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13. Journal of Bone and Mineral Research ·Sarah E. Lloyd, Michael P. Whyte, Rajesh V. Thakker	1997	1
17	Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis. Journal of Bone and Mineral Research ·Sarah E. Lloyd, Ho-yee Leung, A D Thomson, Maria Luisa Bianchi, Ian Craig, Simon E. Fisher, Steven J. Scheinman, O M Wrong, Rajesh V. Thakker	1996	1
18	Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene Human Genetics ·J T Pang, Sarah E. Lloyd, C Wooding, Bernadette Farren, Y Legrand-Lambling, Brian Harding, S. E. A. Leigh, Mark A. Pook, Rajesh V. Thakker, Frances Benham, G. T. Gillett, R. Thomas Taggart	1996	29
19	A common molecular basis for three inherited kidney stone diseases Nature ·Sarah E. Lloyd, Simon H. S. Pearce, Simon E. Fisher, Klaus Steinmeyer, Blanche Schwappach, Steven J. Scheinman, Brian Harding, Alessandra Bolino, Marcella Devoto, Paul Goodyer, Susan P. A. Rigden, Oliver Wrong, Thomas J. Jentsch, Ian Craig, Rajesh V. Thakker Hit paper breakdown →	1996	556
20	ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA Journal of the American Society of Nephrology ·Steven J. Scheinman, Sarah E. Lloyd, Ho-yee Leung, Jack Safely, Simon E. Fisher, Ian Craig, Thomas J. Jentsch, David A. Bushinsky, Rajesh V. Thakker	1995	3

About Sarah E. Lloyd

Sarah E. Lloyd is a scholar working on Neurology, Nutrition and Dietetics, Molecular Biology, Nephrology and Cellular and Molecular Neuroscience, having authored 41 papers that have together received 3.0k indexed citations. Recurring topics across this work include Prion Diseases and Protein Misfolding (20 papers), Trace Elements in Health (16 papers), Neurological diseases and metabolism (15 papers), Ion Transport and Channel Regulation (6 papers), Kidney Stones and Urolithiasis Treatments (3 papers), Neuroblastoma Research and Treatments (3 papers), Biomedical Research and Pathophysiology (3 papers) and Nuclear Receptors and Signaling (3 papers). The work is most often cited by research in Neurology (510 citations), Nephrology (297 citations), Nutrition and Dietetics (518 citations), Molecular Biology (2.0k citations) and Neurology (239 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, Majid Hafezparast, J. Beck, Janan T. Eppig, Michael F. W. Festing, Simon H. S. Pearce, Ian Craig and Simon E. Fisher. Their work appears in journals such as PLoS ONE, Journal of Bone and Mineral Research, The American Journal of Human Genetics, Neurogenetics and Mammalian Genome.

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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