Laura Pollard

708 total citations
43 papers, 391 citations indexed

About

Laura Pollard is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Laura Pollard has authored 43 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Physiology, 20 papers in Molecular Biology and 7 papers in Organic Chemistry. Recurrent topics in Laura Pollard's work include Lysosomal Storage Disorders Research (22 papers), Mitochondrial Function and Pathology (8 papers) and Carbohydrate Chemistry and Synthesis (7 papers). Laura Pollard is often cited by papers focused on Lysosomal Storage Disorders Research (22 papers), Mitochondrial Function and Pathology (8 papers) and Carbohydrate Chemistry and Synthesis (7 papers). Laura Pollard collaborates with scholars based in United States, Canada and United Kingdom. Laura Pollard's co-authors include Tim Wood, Julie R. Jones, Sanjay I. Bidichandani, Sara Cathey, Irene De Biase, Rebecka L. Bourn, Paul M. Rindler, Rongrong Huang, John Sowell and Richard J. Schroer and has published in prestigious journals such as Nucleic Acids Research, Scientific Reports and Clinical Chemistry.

In The Last Decade

Laura Pollard

39 papers receiving 384 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Laura Pollard United States	12	240	137	93	79	74	43	391
Nanaka Ichihara Japan	10	105 0.4×	124 0.9×	39 0.4×	24 0.3×	41 0.6×	27	309
Maja Di Rocco Italy	12	212 0.9×	131 1.0×	32 0.3×	122 1.5×	43 0.6×	20	459
M. DiRocco Italy	8	353 1.5×	78 0.6×	36 0.4×	244 3.1×	31 0.4×	11	497
Galina Baydakova Russia	12	163 0.7×	259 1.9×	22 0.2×	37 0.5×	75 1.0×	46	435
Leslie Matalonga Spain	11	219 0.9×	84 0.6×	21 0.2×	49 0.6×	26 0.4×	23	334
Patricia Yuste‐Checa Spain	11	269 1.1×	112 0.8×	23 0.2×	48 0.6×	17 0.2×	15	378
Sabine Grønborg Denmark	11	207 0.9×	64 0.5×	41 0.4×	74 0.9×	16 0.2×	25	330
Ricardo Flores Pires Brazil	15	286 1.2×	338 2.5×	43 0.5×	251 3.2×	121 1.6×	36	624
María Teresa García‐Silva Spain	12	392 1.6×	83 0.6×	32 0.3×	234 3.0×	18 0.2×	24	595
M.T. García‐Silva Spain	10	378 1.6×	86 0.6×	18 0.2×	170 2.2×	20 0.3×	16	515

Countries citing papers authored by Laura Pollard

Since Specialization

Citations

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

Fields of papers citing papers by Laura Pollard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Pollard

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

Sabir, Marya S., Vukasin M. Jovanovic, Seungmi Ryu, et al.. (2025). Lysosomal free sialic acid storage disorder iPSC-derived neural cells display altered glycosphingolipid metabolism. Scientific Reports. 15(1). 29708–29708.

Sabir, Marya S., Laura Pollard, Marjan Huizing, et al.. (2025). Lack of significant ganglioside changes in Slc17a5 heterozygous mice: Relevance to FSASD and Parkinson's disease. Biochemistry and Biophysics Reports. 42. 101979–101979. 1 indexed citations

Kubaski, Francyne, et al.. (2025). Analysis of serum oligosaccharides by UPLC-MS/MS for diagnosis and treatment monitoring of patients with alpha-mannosidosis. Molecular Genetics and Metabolism. 144(3). 109042–109042. 1 indexed citations

Yu, Seok‐Ho, Francyne Kubaski, Gavin Arno, et al.. (2024). Functional assessment of IDUA variants of uncertain significance identified by newborn screening. npj Genomic Medicine. 9(1). 68–68. 1 indexed citations

Wang, Tong, et al.. (2024). Dysregulated lysosomal exocytosis drives protease-mediated cartilage pathogenesis in multiple lysosomal disorders. iScience. 27(4). 109293–109293. 3 indexed citations

Sohn, Young Bae, Raymond Wang, Jane Ashworth, et al.. (2023). Biomarkers of Glycosaminoglycans (GAG) accumulation in patients with mucopolysaccharidosis type VI—LeukoGAG, Corneal Opacification (COM) and Carotid Intima Media Thickening (CIMT). Molecular Genetics and Metabolism Reports. 38. 101041–101041. 1 indexed citations

Orchard, Paul J., Ashish O. Gupta, Julie B. Eisengart, et al.. (2022). Hematopoietic stem cell transplant for Hurler syndrome: does using bone marrow or umbilical cord blood make a difference?. Blood Advances. 6(23). 6023–6027. 3 indexed citations

Sohn, Young Bae, Curtis Rogers, Tim Wood, et al.. (2022). RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A. Molecular Genetics and Metabolism Reports. 31. 100875–100875. 1 indexed citations

Pollard, Laura, et al.. (2020). Immune Modulation for Enzyme Replacement Therapy in A Female Patient With Hunter Syndrome. Frontiers in Immunology. 11. 1000–1000. 12 indexed citations

10.

Lund, Troy C., Weston P. Miller, Julie B. Eisengart, et al.. (2019). Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood‐onset beta‐mannosidosis. Molecular Genetics & Genomic Medicine. 7(7). e00712–e00712. 5 indexed citations

11.

Zimmermann, Michael T., Patrick R. Blackburn, Eric W. Klee, et al.. (2018). Protein modeling and clinical description of a novel in‐frame GLB1 deletion causing GM1 gangliosidosis type II. Molecular Genetics & Genomic Medicine. 6(6). 1229–1235. 4 indexed citations

12.

Gallagher, Renata C., et al.. (2018). Laboratory analysis of organic acids, 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(7). 683–691. 31 indexed citations

13.

Ellsworth, Katarzyna A., Laura Pollard, Sara Cathey, & Tim Wood. (2016). Measurement of Elevated Concentrations of Urine Keratan Sulfate by UPLC-MSMS in Lysosomal Storage Disorders (LSDs): Comparison of Urine Keratan Sulfate Levels in MPS IVA Versus Other LSDs. JIMD Reports. 34. 11–18. 11 indexed citations

14.

Leroy, Jules G., Priya S. Kishnani, Jochen Decaestecker, et al.. (2016). New observation of sialuria prompts detection of liver tumor in previously reported patient. Molecular Genetics and Metabolism. 118(2). 92–99. 2 indexed citations

15.

Sowell, John, Laura Pollard, & Tim Wood. (2011). Quantification of branched‐chain amino acids in blood spots and plasma by liquid chromatography tandem mass spectrometry for the diagnosis of maple syrup urine disease. Journal of Separation Science. 34(6). 631–639. 20 indexed citations

16.

Bourn, Rebecka L., Paul M. Rindler, Laura Pollard, & Sanjay I. Bidichandani. (2008). E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA·TTC) sequence. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 661(1-2). 71–77. 5 indexed citations

17.

Pollard, Laura, Yogesh K. Chutake, Paul M. Rindler, & Sanjay I. Bidichandani. (2007). Deficiency of RecA-dependent RecFOR and RecBCD pathways causes increased instability of the (GAA{middle dot}TTC)n sequence when GAA is the lagging strand template. Nucleic Acids Research. 35(20). 6884–6894. 7 indexed citations

18.

Rindler, Paul M., et al.. (2006). Replication in mammalian cells recapitulates the locus-specific differences in somatic instability of genomic GAA triplet-repeats. Nucleic Acids Research. 34(21). 6352–6361. 24 indexed citations

19.

Pollard, Laura. (2004). Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia. Nucleic Acids Research. 32(19). 5962–5971. 49 indexed citations

20.

Søndenaa, Karl, I. Nesvik, E. Andersen, Laura Pollard, & Jon Arne Søreide. (1995). Recurrent Pilonidal Sinus: Etiology and Treatment. Digestive Surgery. 12(2). 117–120. 6 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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