Ruth E. Williams

3.3k citations

63 papers · 2.5k · h-index 25

Impact in

Physiology top 2%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Cell Biology top 2%
- Cellular transport and secretion

Papers in

Physiology 32
- Lysosomal Storage Disorders Research 26
- Diet and metabolism studies 6
Cell Biology 12
- Cellular transport and secretion 10

Co-authors: Sara Mole (11 shared papers)Hans Hilmar Goebel (3 shared papers)Alessandro Simonati (4 shared papers)Alfried Kohlschütter (2 shared papers)Ruth B. Wheeler (9 shared papers)Julie D. Sharp (8 shared papers)Angela Schulz (3 shared papers)Jonathan W. Mink (2 shared papers)
Journals: Molecular Genetics and Metabolism (4 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (3 papers)The Lancet Neurology (2 papers)Epilepsia (2 papers)Seizure (2 papers)
Partner nations: United Kingdom Australia United States

In The Last Decade

Ruth E. Williams

63 papers receiving 2.5k citations

Peers

Countries citing papers authored by Ruth E. Williams

Since Specialization

Citations

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

Fields of papers citing papers by Ruth E. Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruth E. Williams. 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 Ruth E. Williams. The network helps show where Ruth E. Williams may publish in the future.

Co-authors

The 25 scholars most cited alongside Ruth E. Williams, 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 Ruth E. Williams Line = papers co-authored together Ruth E. Williams links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses Neurogenetics ·Sara Mole, Ruth E. Williams, Hans Hilmar Goebel	2005	241
2	Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens Journal of Neurology Neurosurgery & Psychiatry ·Yael Hacohen, Sukhvir K. Wright, Patrick Joseph Waters, Shakti Agrawal, Lucinda Carr, Judith Helen Cross, Carlos de Sousa, Catherine J DeVile	2012	211
3	NCL diseases — clinical perspectives Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Angela Schulz, Alfried Kohlschütter, Jonathan W. Mink, Alessandro Simonati, Ruth E. Williams	2013	200
4	New nomenclature and classification scheme for the neuronal ceroid lipofuscinoses Neurology ·Ruth E. Williams, Sara Mole	2012	183
5	The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein The American Journal of Human Genetics ·Ruth B. Wheeler, Julie D. Sharp, Roger Alan Schultz, John M. Joslin, Ruth E. Williams, Sara Mole	2002	159
6	Repairing a critical-sized bone defect with highly porous modified and unmodified baghdadite scaffolds Acta Biomaterialia ·Seyed‐Iman Roohani‐Esfahani, Colin Robert Dunstan, B. Davies, S. G. PEARCE, Ruth E. Williams, Hala Zreiqat	2012	111
7	Diagnosis of the neuronal ceroid lipofuscinoses: An update Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Ruth E. Williams, Laura E Åberg, Taina H Autti, Hans Hilmar Goebel, Alfried Kohlschütter, Tuula R I Lönnqvist	2006	92
8	Management Strategies for CLN2 Disease Pediatric Neurology ·Ruth E. Williams, Heather Adams, Martin E. G. Blohm, Jessica L. Cohen-Pfeffer, Emily de los Reyes, Jonas Denecke, Kristen Drago, Charlie Fairhurst	2017	91
9	Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic marker Clinical Chemistry ·Peter J. Meikle, Doug A. Brooks, Elaine M. Ravenscroft, Miao Yan, Ruth E. Williams, Alvis Jaunzems, Tim Chataway, Litsa Karageorgos	1997	90
10	Spectrum ofCLN6mutations in variant late infantile neuronal ceroid lipofuscinosis Human Mutation ·Julie D. Sharp, Ruth B. Wheeler, Keith A. Parker, R. Mark Gardiner, Ruth E. Williams, Sara Mole	2003	65
11	The clinical utility of an SCN1A genetic diagnosis in infantile‐onset epilepsy Developmental Medicine & Child Neurology ·Andreas Brunklaus, Liam Dorris, Rachael Ellis, Eleanor Reavey, Elizabeth Lee, GORDON FORBES, Richard E Appleton, Judith Helen Cross	2012	61
12	Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis Human Mutation ·Chiara Aiello, Alessandro Simonati, Giancarlo Discepoli, Natalia Cannelli, Dianela Claps, Yanick Joseph Crow, Marzia Bianchi, Claudia Kitzmüller	2009	61
13	Unique microstructural design of ceramic scaffolds for bone regeneration under load Acta Biomaterialia ·Seyed‐Iman Roohani‐Esfahani, Colin Robert Dunstan, Jiao Jiao Li, Zufu Lu, B. Davies, S. G. PEARCE, John K. Field, Ruth E. Williams	2013	56
14	Bone marrow lesions detected by specific combination of MRI sequences are associated with severity of osteochondral degeneration Arthritis Research & Therapy ·Dzenita Muratovic, Flavia Cicuttini, Anita E. Wluka, David M. Findlay, Yuanyuan Wang, Sophia Otto, DAVID J. TAYLOR, Julia M. Humphries	2016	54
15	Incorporating epilepsy genetics into clinical practice: a 360°evaluation npj Genomic Medicine ·Stephanie Oates, Shan S. Tang, Richard Ewald Rosch, Rosalie Lear, Elaine Hughes, Ruth E. Williams, Line H.G. Larsen, Qin Hao	2018	53
16	Pharmacokinetics, Safety, and 48-Week Efficacy of Oral Raltegravir in HIV-1-Infected Children Aged 2 Through 18 Years Clinical Infectious Diseases ·Sharon Nachman, Naiyu Zheng, Edward P. Acosta, Hedy Teppler, Brenda Homony, Bobbie Graham, T. R. Fenton, Xin Xu	2013	51
17	Neuronal Ceroid Lipofuscinosis: The Multifaceted Approach to the Clinical Issues, an Overview Frontiers in Neurology ·Alessandro Simonati, Ruth E. Williams	2022	50
18	A New Locus for Variant Late Infantile Neuronal Ceroid Lipofuscinosis—CLN7 Molecular Genetics and Metabolism ·Ruth B. Wheeler, Julie D. Sharp, Wayne A. Mitchell, S. Louise Bate, Ruth E. Williams, Brian D. Lake, R M Gardiner	1999	45
19	Frequency of pancreatitis in fulminant hepatic failure using isoenzyme markers. Gut ·Roland J. Ede, Kevin P. Moore, William Marshall, Ruth E. Williams	1988	45
20	Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8 European Journal of Paediatric Neurology ·Wayne A. Mitchell, Ruth B. Wheeler, Julie D. Sharp, S. Louise Bate, R. Mark Gardiner, U. Susanna Ranta, Liina Lonka, Ruth E. Williams	2001	43

About Ruth E. Williams

Ruth E. Williams is a scholar working on Physiology, Cell Biology, Rheumatology, Psychiatry and Mental health and Molecular Biology, having authored 63 papers that have together received 2.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (26 papers), Cellular transport and secretion (10 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Glycosylation and Glycoproteins Research (8 papers), Epilepsy research and treatment (6 papers), Diet and metabolism studies (6 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Trypanosoma species research and implications (4 papers). The work is most often cited by research in Physiology (1.4k citations), Physiology (179 citations), Cell Biology (584 citations), Rheumatology (307 citations) and Neurology (277 citations). Ruth E. Williams has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Sara Mole, Hans Hilmar Goebel, Alessandro Simonati, Alfried Kohlschütter, Ruth B. Wheeler, Julie D. Sharp, Angela Schulz, Jonathan W. Mink, Roger Alan Schultz and John M. Joslin. Their work appears in journals such as Molecular Genetics and Metabolism, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, The Lancet Neurology, Epilepsia and Seizure.

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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