Patricia Hall

1.6k total citations
57 papers, 926 citations indexed

About

Patricia Hall is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Patricia Hall has authored 57 papers receiving a total of 926 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 19 papers in Physiology and 17 papers in Molecular Biology. Recurrent topics in Patricia Hall's work include Metabolism and Genetic Disorders (20 papers), Lysosomal Storage Disorders Research (11 papers) and Neonatal Health and Biochemistry (8 papers). Patricia Hall is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Lysosomal Storage Disorders Research (11 papers) and Neonatal Health and Biochemistry (8 papers). Patricia Hall collaborates with scholars based in United States, Canada and Netherlands. Patricia Hall's co-authors include James H. Gilchrist, David B. Collum, Piero Rinaldo, Aidan T. Harrison, Renata Raina, David J. Fuller, Arthur F. Hagar, Denis C. Lehotay, Robert J. Currier and Robert S. Bandurski and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Environmental Science & Technology.

In The Last Decade

Patricia Hall

48 papers receiving 889 citations

Peers

Patricia Hall

PHYSI

GENET

Wilfred L.F. Armarego Australia

Christian Bauch Switzerland

Takahiro Hatanaka United States

Katrina Peariso United States

Anand Balakrishnan United States

H. Olin Spivey United States

Bolesław T. Karwowski Poland

Zhong‐Xian Huang China

Charles A. Lewis United States

Leonard F. Blackwell New Zealand

Wilfred L.F. Armarego Australia

Patricia Hall

570 ×1.9

167 ×0.6

476 ×1.8

86 ×0.5

PHYSI

42 ×0.3

GENET

Citations per year, relative to Patricia Hall Patricia Hall (= 1×) peers Wilfred L.F. Armarego

Countries citing papers authored by Patricia Hall

Since Specialization

Citations

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

Fields of papers citing papers by Patricia Hall

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Hall

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Hall. A scholar is included among the top collaborators of Patricia Hall 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 Patricia Hall. Patricia Hall 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

Hall, Patricia, Christina Lam, Lynne A. Wolfe, & Andrew C. Edmondson. (2025). Biochemical testing for congenital disorders of glycosylation: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(4). 101328–101328. 1 indexed citations

Hall, Patricia, Wouter F. Visser, Klaas Koop, et al.. (2025). Reducing False Positives in Newborn Screening: The Role of Perinatal Factors in the Dutch NBS Program. Metabolites. 15(9). 634–634.

Turgeon, Coleman, Kari Casas, Ryan Flanagan, et al.. (2024). Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase. Molecular Genetics and Metabolism Reports. 40. 101110–101110. 1 indexed citations

Sterner, Rosalie M., Patricia Hall, Dietrich Matern, John L. Black, & Ann M. Moyer. (2024). Genotype and Phenotype Correlation of the TPMT∗8 Allele in Thiopurine Metabolism. Journal of Molecular Diagnostics. 26(11). 988–994.

White, Amy, Tiffany Grider, Josef Alawneh, et al.. (2024). P004: Urine polyols for diagnosis of sorbitol dehydrogenase (SORD) deficiency-related peripheral neuropathy*. SHILAP Revista de lepidopterología. 2. 100881–100881.

Matern, Dietrich, et al.. (2024). Newborn Screening for Krabbe Disease: Status Quo and Recommendations for Improvements. International Journal of Neonatal Screening. 10(1). 10–10. 3 indexed citations

Stiles, Ashlee R., Taraka Donti, Patricia Hall, & William R. Wilcox. (2024). Biomarker testing for lysosomal diseases: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(1). 101242–101242. 1 indexed citations

Schultz, Matthew, et al.. (2023). Incorrect laboratory test selection is common in the evaluation of alpha-gal syndrome and Fabry disease. The Journal of Allergy and Clinical Immunology In Practice. 11(10). 3263–3264. 3 indexed citations

Li, Hong, Heather M. Byers, Miriam B. Vos, et al.. (2018). Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Molecular Genetics and Metabolism. 123(4). 428–432. 29 indexed citations

10.

Hall, Patricia, Christina Lam, John Alexander, et al.. (2018). Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency. Molecular Genetics and Metabolism. 124(1). 82–86. 28 indexed citations

11.

Tortorelli, Silvia, Joseph J. Orsini, Colleen F. Stevens, et al.. (2017). Moonlighting newborn screening markers: the incidental discovery of a second-tier test for Pompe disease. Genetics in Medicine. 20(8). 840–846. 44 indexed citations

12.

Garber, Kathryn B., et al.. (2016). Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing. Genetics in Medicine. 19(1). 77–82. 28 indexed citations

13.

Hall, Patricia, et al.. (2014). Newborn screening for medium chain acyl-CoA dehydrogenase deficiency: Performance improvement by monitoring a new ratio. Molecular Genetics and Metabolism. 113(4). 274–277. 16 indexed citations

14.

Hall, Patricia, Virginia V. Michels, Dimitar Gavrilov, et al.. (2013). Aripiprazole and trazodone cause elevations of 7-dehydrocholesterol in the absence of Smith–Lemli–Opitz Syndrome. Molecular Genetics and Metabolism. 110(1-2). 176–178. 34 indexed citations

15.

Eichhorst, J., Michele L. Etter, Patricia Hall, & Denis C. Lehotay. (2012). LC-MS/MS Techniques for High-Volume Screening of Drugs of Abuse and Target Drug Quantitation in Urine/Blood Matrices. Methods in molecular biology. 902. 29–41. 7 indexed citations

16.

Eichhorst, J., Michele L. Etter, Patricia Hall, & Denis C. Lehotay. (2012). Opiate Screening and Quantitation in Urine/Blood Matrices Using LC-MS/MS Techniques. Methods in molecular biology. 902. 53–64. 3 indexed citations

17.

Hall, Patricia. (2011). Moral Decision-making By Wives Of Patients With Life Threatening Cardiovascular Disease. Journal of Family Nursing. 14. 1 indexed citations

18.

Antonishyn, Nick A., et al.. (2011). A Polymerase Chain Reaction–Based Genotyping Assay for Detecting a Novel Sandhoff Disease–Causing Mutation. Genetic Testing and Molecular Biomarkers. 16(5). 401–405. 5 indexed citations

19.

Aimone, Lisa D., et al.. (1992). Synthesis and substance P receptor binding activity of androstano[3,2-b]pyrimido[1,2-a]benzimidazoles. Journal of Medicinal Chemistry. 35(2). 374–378. 47 indexed citations

20.

Hall, Patricia & Robert S. Bandurski. (1978). Movement of Indole-3-acetic Acid and Tryptophan-derived Indole-3-acetic Acid from the Endosperm to the Shoot of Zea mays L.. PLANT PHYSIOLOGY. 61(3). 425–429. 27 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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