Lori S. Sullivan

4.8k total citations
80 papers, 3.2k citations indexed

About

Lori S. Sullivan is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Lori S. Sullivan has authored 80 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 39 papers in Ophthalmology and 12 papers in Genetics. Recurrent topics in Lori S. Sullivan's work include Retinal Development and Disorders (61 papers), Retinal Diseases and Treatments (37 papers) and Advanced biosensing and bioanalysis techniques (14 papers). Lori S. Sullivan is often cited by papers focused on Retinal Development and Disorders (61 papers), Retinal Diseases and Treatments (37 papers) and Advanced biosensing and bioanalysis techniques (14 papers). Lori S. Sullivan collaborates with scholars based in United States, Sweden and United Kingdom. Lori S. Sullivan's co-authors include Stephen P. Daiger, Sara J. Bowne, David G. Birch, John R. Heckenlively, Melanie M. Sohocki, Susan H. Blanton, Helen A. Mintz-Hittner, Dianna K. Hughbanks-Wheaton, Richard A. Lewis and Anisa Gire and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Lori S. Sullivan

78 papers receiving 3.1k citations

Peers

Lori S. Sullivan

OPHTH

GENET

CMN

Sara J. Bowne United States

Enrico Maria Surace Italy

Gustavo D. Aguirre United States

Rob W.J. Collin Netherlands

Elizabeth A. M. Windsor United States

Alison J. Hardcastle United Kingdom

Jijing Pang United States

Małgorzata Świder United States

Rajendra Kumar‐Singh United States

Isabelle Perrault France

Sara J. Bowne United States

Lori S. Sullivan

2.4k ×0.8

1.0k ×0.8

OPHTH

487 ×0.8

GENET

430 ×0.7

CMN

338 ×0.7

Citations per year, relative to Lori S. Sullivan Lori S. Sullivan (= 1×) peers Sara J. Bowne

Countries citing papers authored by Lori S. Sullivan

Since Specialization

Citations

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

Fields of papers citing papers by Lori S. Sullivan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lori S. Sullivan. 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 Lori S. Sullivan. The network helps show where Lori S. Sullivan may publish in the future.

Co-authorship network of co-authors of Lori S. Sullivan

This figure shows the co-authorship network connecting the top 25 collaborators of Lori S. Sullivan. A scholar is included among the top collaborators of Lori S. Sullivan 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 Lori S. Sullivan. Lori S. Sullivan 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

Birch, David G., Janet K. Cheetham, Stephen P. Daiger, et al.. (2023). Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel. Translational Vision Science & Technology. 12(6). 5–5. 9 indexed citations

Daiger, Stephen P., et al.. (2023). History of Finding Genes and Mutations Causing Inherited Retinal Diseases. Cold Spring Harbor Perspectives in Medicine. 14(9). a041287–a041287. 5 indexed citations

Fahim, Abigail T., Lori S. Sullivan, Sara J. Bowne, et al.. (2019). X-Chromosome Inactivation is a Biomarker of Clinical Severity in Female Carriers of X-linked Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 60(9). 2961–2961. 1 indexed citations

Webb-Jones, Kaylie, et al.. (2018). Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa. American Journal of Ophthalmology. 200. 76–84. 29 indexed citations

Sullivan, Lori S., Sara J. Bowne, Daniel C. Koboldt, et al.. (2017). A Novel Dominant Mutation in SAG , the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States. Investigative Ophthalmology & Visual Science. 58(5). 2774–2774. 26 indexed citations

Wheaton, Dianna K., Kaylie Webb-Jones, Sara J. Bowne, et al.. (2016). Complex Multi-Allelic Inherited Retinal Dystrophy: Multiple Genes Contributing Independently and Concurrently in Extended Families. Investigative Ophthalmology & Visual Science. 57(12). 3135–3135. 2 indexed citations

Wheaton, Dianna K., Mingchu Xu, David G. Birch, et al.. (2016). Diagnosis of a mild peroxisomal phenotype with next-generation sequencing. Molecular Genetics and Metabolism Reports. 9. 75–78. 27 indexed citations

Strom, Samuel P., Michael J. Clark, Sarah Garcia, et al.. (2016). De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa. PLoS ONE. 11(3). e0150944–e0150944. 31 indexed citations

Bowne, Sara J., Lori S. Sullivan, Dianna K. Wheaton, et al.. (2015). Retinal Targeted-Capture Next Generation Sequencing and CLIA Confirmation in a Representative Range of Patients with Inherited Retinal Degeneration. Investigative Ophthalmology & Visual Science. 56(7). 1241–1241. 1 indexed citations

10.

Daiger, Stephen P., Lori S. Sullivan, Sara J. Bowne, et al.. (2015). Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP). Advances in experimental medicine and biology. 854. 193–200. 7 indexed citations

11.

Daiger, Stephen P., Jennifer D. Churchill, Sara J. Bowne, et al.. (2014). A novel locus for autosomal dominant retinitis pigmentosa (adRP) on chromosome 19q13. Investigative Ophthalmology & Visual Science. 55(13). 3267–3267.

12.

Koboldt, Daniel C., David E. Larson, Lori S. Sullivan, et al.. (2014). Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders. The American Journal of Human Genetics. 94(3). 373–384. 30 indexed citations

13.

Koboldt, Daniel C., David E. Larson, Lori S. Sullivan, et al.. (2013). Variant prioritization and linkage mapping using whole-exome sequencing data for families with autosomal dominant retinitis pigmentosa (adRP). Investigative Ophthalmology & Visual Science. 54(15). 3357–3357. 1 indexed citations

14.

Bowne, Sara J., Lori S. Sullivan, Jennifer D. Churchill, et al.. (2012). Genome-Wide Linkage Analysis For Gene Discovery In Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 53(14). 4528–4528. 1 indexed citations

15.

Levison, Ashleigh L., Kavitha Ratnam, Austin Roorda, et al.. (2012). High Resolution Retinal Images in a Family with Autosomal Dominant Retinitis Pigmentosa Caused By a Mutation in NR2E3. Investigative Ophthalmology & Visual Science. 53(14). 4587–4587. 1 indexed citations

16.

Zhao, Chen, Deepti L. Bellur, Shasha Lu, et al.. (2009). Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs. The American Journal of Human Genetics. 85(5). 617–627. 115 indexed citations

17.

Kozma, Petra, David G. Birch, Dianna K. Hughbanks-Wheaton, et al.. (2004). Analysis of protein haplotypes in trans as factors modifying phenotypic variation of retinal dystrophies caused by a splice site mutation in the peripherin/RDS gene. Investigative Ophthalmology & Visual Science. 45(13). 3719–3719. 1 indexed citations

18.

Bowne, Sara J., Anisa Gire, Lori S. Sullivan, et al.. (2003). Frequency and Spectrum of IMPDH1 Mutations Associated with Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 44(13). 2307–2307. 1 indexed citations

19.

Sullivan, Lori S., John R. Heckenlively, Sara J. Bowne, et al.. (1999). Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa. Nature Genetics. 22(3). 255–259. 139 indexed citations

20.

Sohocki, Melanie M., Lori S. Sullivan, Helen A. Mintz-Hittner, et al.. (1998). A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene. The American Journal of Human Genetics. 63(5). 1307–1315. 220 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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