Katherine B. Sims

12.2k total citations · 1 hit paper
117 papers, 6.9k citations indexed

About

Katherine B. Sims is a scholar working on Physiology, Molecular Biology and Neurology. According to data from OpenAlex, Katherine B. Sims has authored 117 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Physiology, 43 papers in Molecular Biology and 28 papers in Neurology. Recurrent topics in Katherine B. Sims's work include Lysosomal Storage Disorders Research (38 papers), Glycogen Storage Diseases and Myoclonus (16 papers) and Cellular transport and secretion (12 papers). Katherine B. Sims is often cited by papers focused on Lysosomal Storage Disorders Research (38 papers), Glycogen Storage Diseases and Myoclonus (16 papers) and Cellular transport and secretion (12 papers). Katherine B. Sims collaborates with scholars based in United States, United Kingdom and Germany. Katherine B. Sims's co-authors include Maryam Banikazemi, Philip Lee, Sami I. Said, Juan Politei, Earl A. Zimmerman, Donald L. Hoffman, Winnie Xin, Ian Craig, Robert J. Hopkin and John F. Staropoli and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Katherine B. Sims

115 papers receiving 6.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

2014 372 citations Sumit Parikh, Amy Goldstein et al. Genetics in Medicine profile →

Peers

Katherine B. Sims

PHYSI

NEURO

EPIDE

Lamya S. Shihabuddin United States

Raphael Schiffmann United States

Matthias Vorgerd Germany

S. Pablo Sardi United States

E. Schwinger Germany

Berge A. Minassian Canada

Ellen Sidransky United States

Krystyna E. Wisniewski United States

Raji P. Grewal United States

Carlo Minetti Italy

Lamya S. Shihabuddin United States

Katherine B. Sims

1.9k ×0.6

PHYSI

3.1k ×1.1

1.8k ×1.3

NEURO

1.0k ×0.9

473 ×0.4

EPIDE

Citations per year, relative to Katherine B. Sims Katherine B. Sims (= 1×) peers Lamya S. Shihabuddin

Countries citing papers authored by Katherine B. Sims

Since Specialization

Citations

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

Fields of papers citing papers by Katherine B. Sims

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katherine B. Sims. 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 Katherine B. Sims. The network helps show where Katherine B. Sims may publish in the future.

Co-authorship network of co-authors of Katherine B. Sims

This figure shows the co-authorship network connecting the top 25 collaborators of Katherine B. Sims. A scholar is included among the top collaborators of Katherine B. Sims 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 Katherine B. Sims. Katherine B. Sims 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

Guelbert, Norberto, et al.. (2015). The neuronal ceroid lipofuscinoses program: A translational research experience in Argentina. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(10). 2301–2311. 18 indexed citations

Walker, Melissa, Stefano Volpi, Katherine B. Sims, Jolán E. Walter, & Elisabetta Traggiai. (2014). Powering the Immune System: Mitochondria in Immune Function and Deficiency. Journal of Immunology Research. 2014. 1–8. 60 indexed citations

Parikh, Sumit, Amy Goldstein, Mary Kay Koenig, et al.. (2014). Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genetics in Medicine. 17(9). 689–701. 372 indexed citations breakdown →

Lieber, Daniel S., Steven G. Hershman, Nancy G. Slate, et al.. (2014). Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency. BMC Medical Genetics. 15(1). 30–30. 35 indexed citations

Wadley, Virginia G., Leslie A. McClure, David G. Warnock, et al.. (2014). Cognitive Function in Adults Aging with Fabry Disease: A Case–Control Feasibility Study Using Telephone-Based Assessments. JIMD Reports. 18. 41–50. 8 indexed citations

Velinov, Milen, Natalia Dolzhanskaya, Michael Gonzalez, et al.. (2012). Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families. PLoS ONE. 7(9). 7 indexed citations

Xin, Winnie, Katherine B. Sims, Norberto Guelbert, et al.. (2012). Neuronal ceroid lipofuscinosis type CLN2: A new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America. Gene. 516(1). 114–121. 34 indexed citations

Ploeg, Ans T. van der, Richard J. Barohn, Lisa Carlson, et al.. (2012). Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa. Molecular Genetics and Metabolism. 107(3). 456–461. 85 indexed citations

Smith, Katherine R., John A. Damiano, Silvana Franceschetti, et al.. (2012). Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage. The American Journal of Human Genetics. 90(6). 1102–1107. 356 indexed citations

10.

Brown, Jeffrey A., John F. Staropoli, Xin Feng, et al.. (2012). SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: A United States clinical testing lab experience. Amyotrophic Lateral Sclerosis. 13(2). 217–222. 45 indexed citations

11.

Nosková, Lenka, Viktor Stránecký, Hana Hartmannová, et al.. (2011). Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis. The American Journal of Human Genetics. 89(4). 589–589. 10 indexed citations

12.

Sims, Katherine B., Juan Politei, Gary J. Bennett, et al.. (2011). Early diagnosis of peripheral nervous system involvement in Fabry disease and treatment of neuropathic pain: the report of an expert panel. BMC Neurology. 11(1). 61–61. 93 indexed citations

13.

Jansen, Anna, Őzgür Sancak, Daniela D’Agostino, et al.. (2005). Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations. Epilepsia. 46. 52–52. 2 indexed citations

14.

Sims, Katherine B., et al.. (2005). Risperidone-Induced Psychosis and Depression in a Child with a Mitochondrial Disorder. Journal of Child and Adolescent Psychopharmacology. 15(3). 520–525. 8 indexed citations

15.

Niida, Yo, Anat Stemmer‐Rachamimov, Marian L. Logrip, et al.. (2001). Survey of Somatic Mutations in Tuberous Sclerosis Complex (TSC) Hamartomas Suggests Different Genetic Mechanisms for Pathogenesis of TSC Lesions. The American Journal of Human Genetics. 69(3). 493–503. 148 indexed citations

16.

Klein, Christine, Jennifer Friedman, S. B. Bressman, et al.. (1999). Genetic Testing for Early-Onset Torsion Dystonia ( DYT1 ): Introduction of a Simple Screening Method, Experiences from Testing of a Large Patient Cohort, and Ethical Aspects. Genetic Testing. 3(4). 323–328. 48 indexed citations

17.

Beauchamp, Roberta L., Patrick McNamara, Hope Northrup, et al.. (1998). Exon scanning of the entireTSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis. Human Mutation. 12(6). 408–416. 46 indexed citations

18.

Murphy, Dennis L., Katherine B. Sims, Farouk Karoum, et al.. (1991). Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase. Journal of Neural Transmission. 83(1-2). 1–12. 25 indexed citations

19.

Diergaarde, P.J., Bé Wieringa, E. M. Bleeker‐Wagemakers, et al.. (1989). Physical fine-mapping of a deletion spanning the Norrie gene. Human Genetics. 84(1). 22–26. 13 indexed citations

20.

Barks, John, Faye S. Silverstein, Katherine B. Sims, J. Timothy Greenamyre, & Michael V. Johnston. (1988). Glutamate recognition sites in human fetal brain. Neuroscience Letters. 84(2). 131–136. 55 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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