Laura Watts

428 total citations
14 papers, 234 citations indexed

About

Laura Watts is a scholar working on Rheumatology, Genetics and Genetics. According to data from OpenAlex, Laura Watts has authored 14 papers receiving a total of 234 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Rheumatology, 5 papers in Genetics and 3 papers in Genetics. Recurrent topics in Laura Watts's work include Neurogenetic and Muscular Disorders Research (3 papers), Health Systems, Economic Evaluations, Quality of Life (3 papers) and Spondyloarthritis Studies and Treatments (2 papers). Laura Watts is often cited by papers focused on Neurogenetic and Muscular Disorders Research (3 papers), Health Systems, Economic Evaluations, Quality of Life (3 papers) and Spondyloarthritis Studies and Treatments (2 papers). Laura Watts collaborates with scholars based in United Kingdom, United States and Australia. Laura Watts's co-authors include M K Javaid, Harriet Teare, B P Wordsworth, Alison Turner, Rafael Pinedo‐Villanueva, Jane Kaye, Cyrus Cooper, P Wordsworth, Richard Eastell and Raashid Luqmani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Osteoporosis International.

In The Last Decade

Laura Watts

13 papers receiving 228 citations

Peers

Countries citing papers authored by Laura Watts

Since Specialization

Citations

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

Fields of papers citing papers by Laura Watts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Watts

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6 2024 ·Brain Communications ·Laura Watts, David J. Bunyan, Edoardo Giacopuzzi, Susan Walker, (unknown), N. Simon Thomas, Volker Straub, (unknown), (unknown), Julie Vogt, Shagufta Khan, Tracey Willis, Jenny C. Taylor, Alistair T. Pagnamenta	0
2	Neuropathic-like Pain in Fibrous Dysplasia/McCune-Albright Syndrome 2022 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Laura Watts, Anushka Soni, Rafael Pinedo‐Villanueva, Anne‐Marie Heegaard, Alison M. Boyce, M K Javaid	16
3	Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance 2020 ·Orphanet Journal of Rare Diseases ·(unknown), Kristina Staley, (unknown), (unknown), Amy Hunter, Richard Keen, (unknown), (unknown), (unknown), Stuart H. Ralston, Elaine Rush, Sheela Upadhyaya, Sandra Regan, Laura Watts, Jennifer Walsh, P. Bruce White, Roger M. Francis, M K Javaid	9
4	The severity of ankylosing spondylitis and responses to anti-tumour necrosis factor biologics are not influenced by the tumour necrosis factor receptor polymorphism incriminated in multiple sclerosis 2018 ·Genes and Immunity ·Laura Watts, Tugce Karaderi, (unknown), Louise Appleton, (unknown), C. Cohen, B P Wordsworth, Matteo Vecellio	6
5	ERAP1 association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations 2017 ·Proceedings of the National Academy of Sciences ·(unknown), Louise Appleton, Adrián Cortés, Matteo Vecellio, Jonathan C. Lau, Laura Watts, Matthew A. Brown, B P Wordsworth	23
6	The RUDY study: using digital technologies to enable a research partnership 2017 ·European Journal of Human Genetics ·Harriet Teare, Joanna Hogg, Jane Kaye, Raashid Luqmani, Elaine Rush, Alison Turner, Laura Watts, Melanie Williams, M K Javaid	28
7	Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnership 2017 ·Archives of Osteoporosis ·Alison M. Boyce, Alison Turner, Laura Watts, (unknown), (unknown), Rafael Pinedo‐Villanueva, Fergal Monsell, Daniele Tessaris, Christine Burren, Laura Masi, N.A.T. Hamdy, Maria Luisa Brandi, Roland Chapurlat, Michael T. Collins, M K Javaid	12
8	Using the RUDY study platform to capture quality of life of adults with rare diseases of the bone 2016 ·Osteoporosis International ·(unknown), Laura Watts, Amy S. Turner, Harriet Teare, Jennifer H. Barrett, B P Wordsworth, Jeffrey Kaye, M K Javaid, (unknown)	1
9	The RUDY study platform – a novel approach to patient driven research in rare musculoskeletal diseases 2016 ·Orphanet Journal of Rare Diseases ·M K Javaid, (unknown), Laura Watts, Alison Turner, Cristina Ponte, Harriet Teare, Debra Gray, Nathanael S. Gray, Rick Popert, James Hogg, (unknown), Rafael Pinedo‐Villanueva, Cyrus Cooper, Richard Eastell, Nick Bishop, Raashid Luqmani, B P Wordsworth, Jane Kaye	49
10	Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia 2016 ·Orphanet Journal of Rare Diseases ·(unknown), Laura Watts, Alison Turner, Harriet Teare, Jane Kaye, (unknown), Cyrus Cooper, Richard Eastell, B P Wordsworth, M K Javaid, Rafael Pinedo‐Villanueva	51
11	Chiari malformation, syringomyelia and bulbar palsy in X linked hypophosphataemia 2015 ·BMJ Case Reports ·Laura Watts, P Wordsworth	14
12	Patient experiences of participation in a medical student teaching workshop 2014 ·Medical Teacher ·Laura Watts, Tess McPherson, Joanna Robson, (unknown), Susan Burge	10
13	Now I know what I don’t know: how to reform the foundation years to fit 21st-century medicine 2013 ·Clinical Medicine ·Laura Watts	6
14	Serial Alu sequence transposition interrupting a human B creatine kinase pseudogene 1991 ·Genomics ·S. Tony, (unknown), Laura Watts, Michael J. Siciliano, Robert Roberts, M. Benjamin Perryman	9

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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