Catherine A. Brownstein

5.0k total citations · 1 hit paper
57 papers, 1.6k citations indexed

About

Catherine A. Brownstein is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Catherine A. Brownstein has authored 57 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 20 papers in Molecular Biology and 5 papers in Nephrology. Recurrent topics in Catherine A. Brownstein's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Catherine A. Brownstein is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Catherine A. Brownstein collaborates with scholars based in United States, Hong Kong and Germany. Catherine A. Brownstein's co-authors include Paul Wicks, Michael P. Massagli, James Heywood, Timothy E. Vaughan, Jeana Frost, Sally Okun, Richard N Bradley, Pankaj B. Agrawal, Alan H. Beggs and Meghan C. Towne and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Catherine A. Brownstein

52 papers receiving 1.5k 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.

Sharing Health Data for Better Outcomes on PatientsLikeMe

2010 436 citations Paul Wicks, Michael P. Massagli et al. Journal of Medical Internet Research profile →

Peers

Catherine A. Brownstein

GENET

GHP

NEPHR

HEALT

Sharon L. R. Kardia United States

Robert P. Finger Germany

Haifeng Hou China

Chen‐Tian Shen China

Arjun K. Manrai United States

Amy C. Sturm United States

Yvonne Bombard Canada

Maria Hägglund Sweden

Robert Logan United States

John A. Robertson United States

Sharon L. R. Kardia United States

Catherine A. Brownstein

903 ×2.0

729 ×1.8

GENET

68 ×0.2

GHP

162 ×0.9

NEPHR

41 ×0.2

HEALT

Citations per year, relative to Catherine A. Brownstein Catherine A. Brownstein (= 1×) peers Sharon L. R. Kardia

Countries citing papers authored by Catherine A. Brownstein

Since Specialization

Citations

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

Fields of papers citing papers by Catherine A. Brownstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine A. Brownstein. 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 Catherine A. Brownstein. The network helps show where Catherine A. Brownstein may publish in the future.

Co-authorship network of co-authors of Catherine A. Brownstein

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Brownstein, Catherine A., Jacqui Clinch, Dawn Marie R. Davis, et al.. (2025). Pediatric erythromelalgia from multidisciplinary perspectives: a scoping review. Pediatric Research. 98(3). 786–799.

Garrett, Amanda L., Stuart B. Bauer, Rosalyn M. Adam, et al.. (2025). Variability in the Diagnosis and Treatment of Interstitial Cystitis/Bladder Pain Syndrome: Internet Survey. JMIR Formative Research. 9. e70813–e70813.

Fitzpatrick, Sarah E., Erika L. Nurmi, Thomas Fernandez, et al.. (2024). Review: Child Psychiatry in the Era of Genomics: The Promise of Translational Genetics Research for the Clinic. PubMed. 3(2). 157–170. 2 indexed citations

Dias, Caroline, Alisa Mo, Chunhui Cai, et al.. (2024). Cell-type-specific effects of autism-associated 15q duplication syndrome in the human brain. The American Journal of Human Genetics. 111(8). 1544–1558. 6 indexed citations

Beggs, Alan H., et al.. (2023). X-linked hypophosphatemia in 4 generations due to an exon 13–15 duplication in PHEX, in the absence of the c.*231A>G variant. Bone. 172. 116763–116763. 2 indexed citations

Garrett, Amanda L., et al.. (2023). Using social media listening to understand barriers to genomic medicine for those living with Ehlers–Danlos syndromes and hypermobility spectrum disorders. Health Expectations. 26(4). 1524–1535. 7 indexed citations

Hojlo, Margaret A., Casie A. Genetti, Richard S. Smith, et al.. (2023). Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes. 14(4). 779–779. 5 indexed citations

Li, Qifei, Klaus Schmitz‐Abe, Casie A. Genetti, et al.. (2023). Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders. European Journal of Human Genetics. 31(6). 712–715. 4 indexed citations

Sahajpal, Nikhil, Alex Hastie, Maximilian Schieck, et al.. (2023). Genetic Predisposition to Neurological Complications in Patients with COVID-19. Biomolecules. 13(1). 133–133.

10.

Smith, Richard S., Marta Florio, Shyam K. Akula, et al.. (2021). Early role for a Na ⁺ ,K ⁺ -ATPase ( ATP1A3 ) in brain development. Proceedings of the National Academy of Sciences. 118(25). 28 indexed citations

11.

Li, Jianqiao, Margaret A. Hojlo, Kent Shefchek, et al.. (2021). Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study. Journal of Medical Internet Research. 23(3). e21023–e21023. 3 indexed citations

12.

Wojcik, Monica H., Klaas J. Wierenga, Lance H. Rodan, et al.. (2017). Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals. JIMD Reports. 39. 45–54. 7 indexed citations

13.

Lo, Mindy S., Meghan C. Towne, Grace E. VanNoy, et al.. (2017). Monogenic Hashimoto thyroiditis associated with a variant in the thyroglobulin (TG) gene. Journal of Autoimmunity. 86. 116–119. 14 indexed citations

14.

Morton, Sarah U., Sanjay P. Prabhu, Hart G.W. Lidov, et al.. (2017). AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant. Molecular Case Studies. 3(2). a001560–a001560. 39 indexed citations

15.

Towne, Meghan C., Phillip L. Pearl, Casie A. Genetti, et al.. (2016). SLC6A1 Mutation and Ketogenic Diet in Epilepsy With Myoclonic-Atonic Seizures. Pediatric Neurology. 64. 77–79. 33 indexed citations

16.

Brownstein, Catherine A., David Margulies, & Shannon Manzi. (2014). Misinterpretation of TPMT by a DTC Genetic Testing Company. Clinical Pharmacology & Therapeutics. 95(6). 598–600. 5 indexed citations

17.

Wicks, Paul, Dorothy L. Keininger, Michael P. Massagli, et al.. (2011). Perceived benefits of sharing health data between people with epilepsy on an online platform. Epilepsy & Behavior. 23(1). 16–23. 84 indexed citations

18.

Wicks, Paul, Michael P. Massagli, Jeana Frost, et al.. (2010). Sharing Health Data for Better Outcomes on PatientsLikeMe. Journal of Medical Internet Research. 12(2). e19–e19. 436 indexed citations breakdown →

19.

Brownstein, Catherine A. & Paul Wicks. (2010). The Potential Research Impact of Patient Reported Outcomes on Osteogenesis Imperfecta. Clinical Orthopaedics and Related Research. 468(10). 2581–2585. 7 indexed citations

20.

Brownstein, Catherine A., F.T. Adler, Carol Nelson‐Williams, et al.. (2008). A translocation causing increased α-Klotho level results in hypophosphatemic rickets and hyperparathyroidism. Proceedings of the National Academy of Sciences. 105(9). 3455–3460. 165 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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