Laura Bryant

497 total citations
7 papers, 184 citations indexed

About

Laura Bryant is a scholar working on Molecular Biology, Genetics and Biomedical Engineering. According to data from OpenAlex, Laura Bryant has authored 7 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Biomedical Engineering. Recurrent topics in Laura Bryant's work include Retinal Development and Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Laura Bryant is often cited by papers focused on Retinal Development and Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Laura Bryant collaborates with scholars based in United States and France. Laura Bryant's co-authors include Jesse L. Rodriguez, Josh Tycko, James M. Wilson, Christian Hinderer, Jenessa B. Smith, Elizabeth A. Traxler, April R. Giles, Olga Lozynska, Albert M. Maguire and Tomás S. Alemán and has published in prestigious journals such as British Journal of Ophthalmology, Human Genetics and Microscopy Research and Technique.

In The Last Decade

Laura Bryant

7 papers receiving 179 citations

Peers

Laura Bryant

MB

GENET

ONCOL

PHYSI

CCM

Adrian Westhaus Australia

Rwik Sen United States

Cecilia Rosales United Kingdom

Samuel Koller Switzerland

Julie Berthy United States

Jonas Weinmann Germany

Dexuan Cui Hong Kong

David Cano-Rodríguez Netherlands

Caiyong Yin China

Syed Anees India

Adrian Westhaus Australia

Laura Bryant

190 ×1.3

MB

178 ×1.8

GENET

20 ×0.5

ONCOL

20 ×1.1

PHYSI

30 ×1.7

CCM

Citations per year, relative to Laura Bryant Laura Bryant (= 1×) peers Adrian Westhaus

Countries citing papers authored by Laura Bryant

Since Specialization

Citations

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

Fields of papers citing papers by Laura Bryant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Bryant

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

All Works

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7 of 7 papers shown

1.

Bryant, Laura, Annabel K. Sangree, Kelly James Clark, & Elizabeth Bhoj. (2023). Histone 3.3-related chromatinopathy: missense variants throughout H3-3A and H3-3B cause a range of functional consequences across species. Human Genetics. 143(4). 497–510. 3 indexed citations

2.

Bryant, Laura, et al.. (2022). Analysis of histone variant constraint and tissue expression suggests five potential novel human disease genes: H2AFY2, H2AFZ, H2AFY, H2AFV, H1F0. Human Genetics. 141(8). 1409–1421. 3 indexed citations

3.

Bryant, Laura, Olga Lozynska, Tyler E. Papp, et al.. (2018). Identification of a novel pathogenic missense mutation inPRPF31using whole exome sequencing: a case report. British Journal of Ophthalmology. 103(6). 761–767. 7 indexed citations

4.

Bryant, Laura, Olga Lozynska, Albert M. Maguire, Tomás S. Alemán, & Jean Bennett. (2017). Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration. Clinical ophthalmology. Volume 12. 49–63. 15 indexed citations

5.

Bryant, Laura, Olga Lozynska, Grace Han, et al.. (2017). On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness. Ophthalmic Genetics. 39(1). 144–146. 3 indexed citations

6.

Bryant, Laura, April R. Giles, Christian Hinderer, et al.. (2013). Lessons Learned from the Clinical Development and Market Authorization of Glybera. PubMed. 24(2). 55–64. 145 indexed citations

7.

Ziady, Assem, et al.. (2010). Bioluminescent imaging of reporter gene expression in the lungs of wildtype and model mice following the administration of PEG‐stabilized DNA nanoparticles. Microscopy Research and Technique. 73(9). 918–928. 8 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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