Andrew Orr

1.8k total citations
17 papers, 735 citations indexed

About

Andrew Orr is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Andrew Orr has authored 17 papers receiving a total of 735 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Ophthalmology. Recurrent topics in Andrew Orr's work include Genomics and Rare Diseases (4 papers), Glaucoma and retinal disorders (3 papers) and BRCA gene mutations in cancer (2 papers). Andrew Orr is often cited by papers focused on Genomics and Rare Diseases (4 papers), Glaucoma and retinal disorders (3 papers) and BRCA gene mutations in cancer (2 papers). Andrew Orr collaborates with scholars based in Canada, United States and Australia. Andrew Orr's co-authors include Duane L. Guernsey, Haiyan Jiang, Marie‐Pierre Dubé, Meghan Ferguson, Mark Samuels, Mathew Nightingale, Mark D. Ludman, Makoto Matsuoka, Susan C. Evans and Mark E. Samuels and has published in prestigious journals such as Nature Genetics, PLoS ONE and Nature Reviews Genetics.

In The Last Decade

Andrew Orr

15 papers receiving 701 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Andrew Orr Canada	12	348	226	95	79	76	17	735
Gabriella Esposito Italy	19	650 1.9×	137 0.6×	74 0.8×	20 0.3×	24 0.3×	56	923
Vedam L. Ramprasad India	18	534 1.5×	207 0.9×	382 4.0×	277 3.5×	27 0.4×	61	1.1k
Oscar Suzuki United States	15	539 1.5×	109 0.5×	72 0.8×	61 0.8×	53 0.7×	25	817
M.C. Sparkes United States	16	379 1.1×	295 1.3×	41 0.4×	26 0.3×	30 0.4×	29	724
JT den Dunnen Netherlands	3	402 1.2×	244 1.1×	15 0.2×	8 0.1×	44 0.6×	6	825
Hisham Alkuraya Saudi Arabia	12	313 0.9×	147 0.7×	267 2.8×	155 2.0×	15 0.2×	17	653
Elżbieta Ciara Poland	17	647 1.9×	278 1.2×	16 0.2×	12 0.2×	40 0.5×	88	1.1k
Andrea Šoltýsová Slovakia	14	354 1.0×	56 0.2×	12 0.1×	22 0.3×	35 0.5×	37	624
Alison J. Coffey United Kingdom	17	699 2.0×	242 1.1×	28 0.3×	9 0.1×	79 1.0×	27	1.0k
Yuan-Yuan Ho Hong Kong	12	325 0.9×	275 1.2×	14 0.1×	6 0.1×	32 0.4×	18	785

Countries citing papers authored by Andrew Orr

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Orr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Orr

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Orr. A scholar is included among the top collaborators of Andrew Orr 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 Andrew Orr. Andrew Orr 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:

17 of 17 papers shown

Vu, T. Robert, et al.. (2024). Internal Medicine Acting Internship Trends in Rotation Structure and Student Responsibilities: Results from a 2023 National Survey. Journal of General Internal Medicine. 40(1). 287–293.

Orr, Andrew, et al.. (2021). Familial Optic Disc Pits in 2 Father-Son Pairs: Clinical Features and Genetic Analysis. Case Reports in Ophthalmology. 12(2). 603–610.

Labelle‐Dumais, Cassandre, Nicholas Tolman, Andrew Orr, et al.. (2018). Müller glia-derived PRSS56 is required to sustain ocular axial growth and prevent refractive error. PLoS Genetics. 14(3). e1007244–e1007244. 32 indexed citations

Fernandez, Conrad V., Colleen O’Connell, Meghan Ferguson, et al.. (2015). Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study. Public Health Genomics. 18(5). 299–308. 9 indexed citations

Fernandez, Conrad V., Éric Bouffet, David Malkin, et al.. (2014). Attitudes of parents toward the return of targeted and incidental genomic research findings in children. Genetics in Medicine. 16(8). 633–640. 79 indexed citations

LeBlanc, Marissa A., Lynette S. Penney, Daniel Gaston, et al.. (2013). A novel rearrangement of occludin causes brain calcification and renal dysfunction. Human Genetics. 132(11). 1223–1234. 22 indexed citations

Orr, Andrew, Marie‐Pierre Dubé, Juan Carlos Zenteno, et al.. (2011). Mutations in a novel serine protease PRSS56 in families with nanophthalmos.. PubMed. 17. 1850–61. 43 indexed citations

Guernsey, Duane L., Haiyan Jiang, Karen Bedard, et al.. (2010). Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease. PLoS Genetics. 6(8). e1001081–e1001081. 52 indexed citations

Guernsey, Duane L., Haiyan Jiang, Susan C. Evans, et al.. (2009). Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2. The American Journal of Human Genetics. 85(1). 120–129. 61 indexed citations

10.

Guernsey, D.L., Marie‐Pierre Dubé, Haiyan Jiang, et al.. (2009). Novel mutations in the sacsin gene in ataxia patients from Maritime Canada. Journal of the Neurological Sciences. 288(1-2). 79–87. 12 indexed citations

11.

Jiang, Haiyan, Andrew Orr, Duane L. Guernsey, et al.. (2009). Application of Homozygosity Haplotype Analysis to Genetic Mapping with High-Density SNP Genotype Data. PLoS ONE. 4(4). e5280–e5280. 20 indexed citations

12.

Guernsey, Duane L., Haiyan Jiang, Dean R. Campagna, et al.. (2009). Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nature Genetics. 41(6). 651–653. 181 indexed citations

13.

Samuels, Mark E., Andrew Orr, Duane L. Guernsey, et al.. (2008). Is gene discovery research or diagnosis?. Genetics in Medicine. 10(6). 385–390. 6 indexed citations

14.

Orr, Andrew, Marie‐Pierre Dubé, Julien Marcadier, et al.. (2007). Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy. PLoS ONE. 2(8). e685–e685. 110 indexed citations

15.

Brinkman, Ryan R., Marie‐Pierre Dubé, Guy A. Rouleau, Andrew Orr, & Mark Samuels. (2006). Human monogenic disorders — a source of novel drug targets. Nature Reviews Genetics. 7(4). 249–260. 68 indexed citations

16.

Orr, Andrew, Johane M. Robitaille, Paul A. Price, et al.. (2001). Exfoliation syndrome: Clinical and genetic features. Ophthalmic Genetics. 22(3). 171–185. 38 indexed citations

17.

Orr, Andrew. (1993). Anterior chamber reaction after mitomycin and 5-fluorouracil trabeculectomy: A comparative study. Survey of Ophthalmology. 38(3). 316–317. 2 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.

Explore authors with similar magnitude of impact