Barbara Truitt

3.6k total citations
15 papers, 530 citations indexed

About

Barbara Truitt is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Barbara Truitt has authored 15 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Ophthalmology and 4 papers in Genetics. Recurrent topics in Barbara Truitt's work include Retinal Diseases and Treatments (3 papers), Language Development and Disorders (3 papers) and Corneal surgery and disorders (3 papers). Barbara Truitt is often cited by papers focused on Retinal Diseases and Treatments (3 papers), Language Development and Disorders (3 papers) and Corneal surgery and disorders (3 papers). Barbara Truitt collaborates with scholars based in United States, Uganda and Mexico. Barbara Truitt's co-authors include Sudha K. Iyengar, Robert P. Igo, Kristin J. Meyers, Robert B. Wallace, Zhe Liu, Chitra Karki, Julie A. Mares, Corinne D. Engelman, Gloria E. Sarto and Erin S. LeBlanc and has published in prestigious journals such as PLoS ONE, Journal of Nutrition and Antimicrobial Agents and Chemotherapy.

In The Last Decade

Barbara Truitt

15 papers receiving 524 citations

Peers

Barbara Truitt

BIOCH

OPHTH

RNMI

Chantal Martin France

Kulbhushan Sharma India

Beata Orzechowska Poland

Aikun Wang Canada

K Shimada Japan

Andrew Leber United States

Xiujuan Chen China

Thomas W. M. Crozier United Kingdom

Lixia Sun China

A. Acquafredda Italy

Chantal Martin France

Barbara Truitt

174 ×0.8

7 ×0.1

BIOCH

106 ×0.9

OPHTH

215 ×1.8

111 ×1.6

RNMI

Citations per year, relative to Barbara Truitt Barbara Truitt (= 1×) peers Chantal Martin

Countries citing papers authored by Barbara Truitt

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Truitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Truitt

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

All Works

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15 of 15 papers shown

Chan, E. Ricky, Penelope Benchek, Kim Brustoski, et al.. (2024). Importance of copy number variants in childhood apraxia of speech and other speech sound disorders. Communications Biology. 7(1). 1273–1273. 2 indexed citations

Benchek, Penelope, Robert P. Igo, Yvonne Wren, et al.. (2021). Association between genes regulating neural pathways for quantitative traits of speech and language disorders. npj Genomic Medicine. 6(1). 64–64. 9 indexed citations

Igo, Robert P., Noémi B. Hall, Jacob B. Hall, et al.. (2018). Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants. Genes and Immunity. 20(6). 473–483. 13 indexed citations

Loomis, Stephanie, Alison P. Klein, Kristine E. Lee, et al.. (2017). Exome Array Analysis of Nuclear Lens Opacity. Ophthalmic Epidemiology. 25(3). 215–219. 2 indexed citations

Chen, Fei, Priya Duggal, Barbara E.K. Klein, et al.. (2016). Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.. PubMed. 22. 783–96. 7 indexed citations

Shah, Anuja, Cynthia C. Nast, Mark D. Adams, et al.. (2014). Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing. eScholarship (California Digital Library). 1 indexed citations

Hall, Noémi B., Robert P. Igo, Barbara Truitt, et al.. (2014). Polymorphisms in TICAM2 and IL1B are associated with TB. Genes and Immunity. 16(2). 127–133. 43 indexed citations

Shah, Anuja, Cynthia C. Nast, Mark D. Adams, et al.. (2014). Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing. Nephrology Dialysis Transplantation. 29(12). 2235–2243. 22 indexed citations

Stein, Catherine M., Barbara Truitt, Allison Avrich Ciesla, et al.. (2014). Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatric Genetics. 24(5). 191–200. 8 indexed citations

10.

Chen, Fei, Alison P. Klein, Barbara E.K. Klein, et al.. (2014). Exome Array Analysis Identifies CAV1/CAV2 as a Susceptibility Locus for Intraocular Pressure. Investigative Ophthalmology & Visual Science. 56(1). 544–551. 37 indexed citations

11.

Meyers, Kristin J., Elizabeth J. Johnson, Paul S. Bernstein, et al.. (2013). Genetic Determinants of Macular Pigments in Women of the Carotenoids in Age-Related Eye Disease Study. Investigative Ophthalmology & Visual Science. 54(3). 2333–2333. 75 indexed citations

12.

Khodaverdian, Varandt Y., Barbara Truitt, Stanley Nithianantham, et al.. (2013). Discovery of Antivirulence Agents against Methicillin-Resistant Staphylococcus aureus. Antimicrobial Agents and Chemotherapy. 57(8). 3645–3652. 114 indexed citations

13.

Meyers, Kristin J., Julie A. Mares, Robert P. Igo, et al.. (2013). Genetic Evidence for Role of Carotenoids in Age-Related Macular Degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS). Investigative Ophthalmology & Visual Science. 55(1). 587–587. 102 indexed citations

14.

Engelman, Corinne D., Kristin J. Meyers, Sudha K. Iyengar, et al.. (2012). Vitamin D Intake and Season Modify the Effects of the GC and CYP2R1 Genes on 25-Hydroxyvitamin D Concentrations. Journal of Nutrition. 143(1). 17–26. 59 indexed citations

15.

Igo, Robert P., Laura J. Kopplin, Peronne Joseph, et al.. (2012). Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy. PLoS ONE. 7(10). e46742–e46742. 36 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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