Lance P. Doucette

471 total citations
13 papers, 283 citations indexed

About

Lance P. Doucette is a scholar working on Molecular Biology, Ophthalmology and Sensory Systems. According to data from OpenAlex, Lance P. Doucette has authored 13 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Ophthalmology and 3 papers in Sensory Systems. Recurrent topics in Lance P. Doucette's work include Retinal Diseases and Treatments (5 papers), Retinal Development and Disorders (4 papers) and Glaucoma and retinal disorders (4 papers). Lance P. Doucette is often cited by papers focused on Retinal Diseases and Treatments (5 papers), Retinal Development and Disorders (4 papers) and Glaucoma and retinal disorders (4 papers). Lance P. Doucette collaborates with scholars based in Canada, United States and United Kingdom. Lance P. Doucette's co-authors include Michael A. Walter, Morteza Seifi, Terry‐Lynn Young, Jane Green, Bridget A. Fernandez, Patrick S. Parfrey, Tim Footz, Nancy D. Merner, Jeremy Schwartzentruber and Tracy Stockley and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Lance P. Doucette

13 papers receiving 280 citations

Peers

Lance P. Doucette

OPHTH

RNMI

GENET

Karen Y. Torrejon United States

Xavier Zanlonghi France

Pinkal D. Patel United States

Ana Fakin Slovenia

Nikolaus Trautmann United States

Annick Cabot France

Marcela Mena Spain

Christopher R. Starr United States

Ping Pan United States

Sophie Devery United Kingdom

Karen Y. Torrejon United States

Lance P. Doucette

226 ×1.6

OPHTH

138 ×1.0

107 ×2.0

RNMI

43 ×1.0

8 ×0.2

GENET

Citations per year, relative to Lance P. Doucette Lance P. Doucette (= 1×) peers Karen Y. Torrejon

Countries citing papers authored by Lance P. Doucette

Since Specialization

Citations

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

Fields of papers citing papers by Lance P. Doucette

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lance P. Doucette. 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 Lance P. Doucette. The network helps show where Lance P. Doucette may publish in the future.

Co-authorship network of co-authors of Lance P. Doucette

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

All Works

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13 of 13 papers shown

Footz, Tim, Lance P. Doucette, Nicole C. L. Noel, et al.. (2023). Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma. International Journal of Molecular Sciences. 24(19). 14423–14423. 3 indexed citations

Benson, Matthew D., et al.. (2021). PEX6 Mutations in Peroxisomal Biogenesis Disorders. SHILAP Revista de lepidopterología. 1(2). 100028–100028. 3 indexed citations

Doucette, Lance P., et al.. (2021). Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation. European Journal of Human Genetics. 29(8). 1171–1185. 2 indexed citations

Doucette, Lance P., Tim Footz, & Michael A. Walter. (2018). FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost. Investigative Ophthalmology & Visual Science. 59(6). 2548–2548. 8 indexed citations

Doucette, Lance P., et al.. (2017). FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25. PLoS ONE. 12(6). e0178518–e0178518. 8 indexed citations

Doucette, Lance P. & Michael A. Walter. (2016). Prostaglandins in the eye: Function, expression, and roles in glaucoma. Ophthalmic Genetics. 38(2). 108–116. 67 indexed citations

Doucette, Lance P., et al.. (2015). The interactions of genes, age, and environment in glaucoma pathogenesis. Survey of Ophthalmology. 60(4). 310–326. 79 indexed citations

Footz, Tim, et al.. (2014). Analysis of Exocytosis Regulation by Transcription Factor FOXC1 and its Role in Axenfeld-Rieger Syndrome Pathogenesis. Investigative Ophthalmology & Visual Science. 55(13). 3802–3802. 1 indexed citations

Doucette, Lance P., et al.. (2013). Molecular Genetics of Achromatopsia in Newfoundland Reveal Genetic Heterogeneity, Founder Effects and the First Cases of Jalili Syndrome in North America. Ophthalmic Genetics. 34(3). 119–129. 18 indexed citations

10.

Doucette, Lance P., Susan Moore, Kathy Hodgkinson, et al.. (2013). Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL. European Journal of Human Genetics. 21(10). 1112–1119. 9 indexed citations

11.

Merner, Nancy D., et al.. (2012). A Novel Deletion inSMPXCauses a Rare form of X-Linked Progressive Hearing Loss in Two Families Due to a Founder Effect. Human Mutation. 34(1). 66–69. 20 indexed citations

12.

Doucette, Lance P., et al.. (2010). A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly. European Journal of Human Genetics. 19(3). 293–299. 35 indexed citations

13.

Doucette, Lance P., Nancy D. Merner, Elizabeth Ives, et al.. (2008). Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. European Journal of Human Genetics. 17(5). 554–564. 30 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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