Paula J. Waters

3.2k total citations
75 papers, 2.0k citations indexed

About

Paula J. Waters is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Paula J. Waters has authored 75 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Clinical Biochemistry, 46 papers in Molecular Biology and 23 papers in Rheumatology. Recurrent topics in Paula J. Waters's work include Metabolism and Genetic Disorders (47 papers), Folate and B Vitamins Research (17 papers) and Mitochondrial Function and Pathology (16 papers). Paula J. Waters is often cited by papers focused on Metabolism and Genetic Disorders (47 papers), Folate and B Vitamins Research (17 papers) and Mitochondrial Function and Pathology (16 papers). Paula J. Waters collaborates with scholars based in Canada, United States and United Kingdom. Paula J. Waters's co-authors include Charles R. Scriver, Piotr Nowacki, Michael A. Parniak, Eileen P. Treacy, Susan Byck, C. A. Pennock, Emre Kayaalp, Hilary Vallance, Eduard A. Struys and Sylvia Stöckler‐Ipsiroglu and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and Biochemical Journal.

In The Last Decade

Paula J. Waters

72 papers receiving 2.0k citations

Peers

Paula J. Waters

PHYSI

RHEUM

GENET

José E. Abdenur United States

Celia Pérez‐Cerdá Spain

Chris Mühlhausen Germany

Silvia Tortorelli United States

Annette Feigenbaum Canada

Belén Pérez Spain

Ewa Pronicka Poland

Birgit Assmann Germany

Mikio Iijima Japan

Kuniaki Narisawa Japan

José E. Abdenur United States

Paula J. Waters

978 ×0.8

818 ×0.7

446 ×1.0

PHYSI

454 ×1.1

RHEUM

325 ×1.0

GENET

Citations per year, relative to Paula J. Waters Paula J. Waters (= 1×) peers José E. Abdenur

Countries citing papers authored by Paula J. Waters

Since Specialization

Citations

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

Fields of papers citing papers by Paula J. Waters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paula J. Waters. 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 Paula J. Waters. The network helps show where Paula J. Waters may publish in the future.

Co-authorship network of co-authors of Paula J. Waters

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

All Works

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20 of 20 papers shown

Waters, Paula J., et al.. (2025). Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trial. Journal of Neurology. 272(4). 307–307.

Boutin, Michel, Bruno Maranda, & Paula J. Waters. (2024). Analysis of Globotriaosylceramide (Gb₃) in Liquid Urine: A Straightforward Assay Using Tandem Mass Spectrometry. Current Protocols. 4(6). e1087–e1087.

Bouva, Marelle J., Monique G. de Sain-van der Velden, Klaas Koop, et al.. (2023). Maleic acid is a biomarker for maleylacetoacetate isomerase deficiency; implications for newborn screening of tyrosinemia type 1. Journal of Inherited Metabolic Disease. 46(6). 1104–1113. 7 indexed citations

Yang, Hao, Youlin Wang, Paula J. Waters, et al.. (2022). Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers. Molecular Genetics and Metabolism. 137(3). 257–264. 3 indexed citations

Agudelo, Daniel, Sophie Carter, Sébastien Levesque, et al.. (2020). Versatile and robust genome editing with Streptococcus thermophilus CRISPR1-Cas9. Genome Research. 30(1). 107–117. 54 indexed citations

Chénier, Sébastien, Valérie Désilets, Bruno Maranda, et al.. (2018). Clinical validity of phenotype-driven analysis software PhenoVar as a diagnostic aid for clinical geneticists in the interpretation of whole-exome sequencing data. Genetics in Medicine. 20(9). 942–949. 9 indexed citations

Yang, Hao, Francis Rossignol, Denis Cyr, et al.. (2017). Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles. Molecular Genetics and Metabolism Reports. 14. 55–58. 7 indexed citations

Waters, Paula J., Thomas M. Kitzler, Annette Feigenbaum, et al.. (2017). Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment. JIMD Reports. 39. 89–96. 12 indexed citations

Lévesque, Sébastien, Christiane Auray‐Blais, Michel Boutin, et al.. (2016). Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing. Orphanet Journal of Rare Diseases. 11(1). 8–8. 43 indexed citations

10.

Wang, Jing, Ariel Brautbar, Fangyuan Li, et al.. (2008). Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family. Molecular Genetics and Metabolism. 96(2). 59–65. 18 indexed citations

11.

Waters, Paula J., et al.. (2007). Isolated Sulfite Oxidase Deficiency in the Newborn: Lactic Acidaemia and Leukoencephalopathy. Neuropediatrics. 38(1). 38–41. 18 indexed citations

12.

Andrade, Jason G., et al.. (2007). Screening for Fabry Disease in Patients with Chronic Kidney Disease. Clinical Journal of the American Society of Nephrology. 3(1). 139–145. 48 indexed citations

13.

Hueber, Pierre‐Alain, Paula J. Waters, Philip A. Clarke, Michael R. Eccles, & Paul Goodyer. (2006). PAX2 inactivation enhances cisplatin-induced apoptosis in renal carcinoma cells. Kidney International. 69(7). 1139–1145. 41 indexed citations

14.

Waters, Paula J., Minesh Khashu, Yolanda Lillquist, et al.. (2005). Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?. Molecular Genetics and Metabolism. 86. 148–152. 4 indexed citations

15.

Waters, Paula J.. (2001). Degradation of Mutant Proteins, Underlying "Loss of Function" Phenotypes, Plays a Major Role in Genetic Disease. Current Issues in Molecular Biology. 3(3). 57–65. 41 indexed citations

16.

Waters, Paula J., Michael A. Parniak, Beverly R. Akerman, & Charles R. Scriver. (2000). Characterization of Phenylketonuria Missense Substitutions, Distant from the Phenylalanine Hydroxylase Active Site, Illustrates a Paradigm for Mechanism and Potential Modulation of Phenotype. Molecular Genetics and Metabolism. 69(2). 101–110. 44 indexed citations

17.

Scriver, Charles R. & Paula J. Waters. (1999). Monogenic traits are not simple: lessons from phenylketonuria. Trends in Genetics. 15(7). 267–272. 304 indexed citations

18.

Kayaalp, Emre, Eileen P. Treacy, Paula J. Waters, et al.. (1997). Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations. The American Journal of Human Genetics. 61(6). 1309–1317. 154 indexed citations

19.

Waters, Paula J., M. D. Flynn, & C. A. Pennock. (1994). Association between Serum Cholesterol and Leucocyte Lysosomal Function. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 31(1). 91–93. 2 indexed citations

20.

Waters, Paula J., M. D. Flynn, R. J. M. Corrall, & C. A. Pennock. (1992). Increases in plasma lysosomal enzymes in Type 1 (insulin-dependent) diabetes mellitus: relationship to diabetic complications and glycaemic control. Diabetologia. 35(10). 991–995. 19 indexed citations

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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