Joanne Sutherland

2.0k total citations
16 papers, 874 citations indexed

About

Joanne Sutherland is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Joanne Sutherland has authored 16 papers receiving a total of 874 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Ophthalmology and 6 papers in Genetics. Recurrent topics in Joanne Sutherland's work include Retinal Development and Disorders (6 papers), Ocular Disorders and Treatments (4 papers) and Ophthalmology and Visual Impairment Studies (4 papers). Joanne Sutherland is often cited by papers focused on Retinal Development and Disorders (6 papers), Ocular Disorders and Treatments (4 papers) and Ophthalmology and Visual Impairment Studies (4 papers). Joanne Sutherland collaborates with scholars based in Canada, United States and United Kingdom. Joanne Sutherland's co-authors include Huntington F. Willard, Kirby D. Smith, Brenda L. Gallie, Patrícia Branco, Katherine Zhang, Ning Chen, Julie Anderson, Suzanne Richter, Liping Han and Thaddeus P. Dryja and has published in prestigious journals such as Science, Nucleic Acids Research and The American Journal of Human Genetics.

In The Last Decade

Joanne Sutherland

16 papers receiving 841 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joanne Sutherland Canada	11	492	315	264	231	160	16	874
Robert W. Rapkins Australia	13	395 0.8×	107 0.3×	212 0.8×	118 0.5×	45 0.3×	18	727
Carmen Ramos Spain	15	450 0.9×	125 0.4×	268 1.0×	39 0.2×	67 0.4×	32	720
H. Allen Gardner Canada	14	456 0.9×	65 0.2×	193 0.7×	129 0.6×	32 0.2×	32	745
Geoffrey J. Maher United Kingdom	14	801 1.6×	111 0.4×	326 1.2×	43 0.2×	39 0.2×	26	1.2k
Alexander N. Yatsenko United States	18	787 1.6×	197 0.6×	527 2.0×	35 0.2×	51 0.3×	35	1.4k
Kusum P. Lele United States	10	201 0.4×	86 0.3×	175 0.7×	84 0.4×	37 0.2×	19	449
Greg B. Peters Australia	14	382 0.8×	27 0.1×	385 1.5×	262 1.1×	44 0.3×	22	785
Atsuko Fujimoto United States	19	310 0.6×	50 0.2×	489 1.9×	42 0.2×	153 1.0×	45	868
Leslie Boghosian-Sell United States	9	320 0.7×	40 0.1×	124 0.5×	105 0.5×	23 0.1×	10	536
Diane Beysen Belgium	12	397 0.8×	53 0.2×	357 1.4×	20 0.1×	79 0.5×	20	951

Countries citing papers authored by Joanne Sutherland

Since Specialization

Citations

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

Fields of papers citing papers by Joanne Sutherland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanne Sutherland

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

16 of 16 papers shown

Hayeems, Robin Z., et al.. (2021). Gene therapy: perspectives from young adults with Leber’s congenital amaurosis. Eye. 36(11). 2088–2093. 4 indexed citations

Vincent, Ajoy, Nicole Forster, Jason T. Maynes, et al.. (2014). OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium. Journal of Medical Genetics. 51(12). 797–805. 31 indexed citations

Sutherland, Joanne, et al.. (2011). Advantages and disadvantages of molecular testing in ophthalmology. Expert Review of Ophthalmology. 6(2). 221–245. 4 indexed citations

Mallipatna, Ashwin, Joanne Sutherland, Brenda L. Gallie, Helen S. L. Chan, & Élise Héon. (2009). Management and outcome of unilateral retinoblastoma. Journal of American Association for Pediatric Ophthalmology and Strabismus. 13(6). 546–550. 41 indexed citations

Sutherland, Joanne, et al.. (2009). Genetic counseling and genetic testing in ophthalmology. Current Opinion in Ophthalmology. 20(5). 343–350. 16 indexed citations

Morad, Yair, et al.. (2007). The Ocular Genetics Program: multidisciplinary care of patients with ocular genetic eye disease. Canadian Journal of Ophthalmology. 42(5). 734–738. 19 indexed citations

Ganesh, Anuradha, et al.. (2007). Psychosocial Adjustment to Visual Loss in Patients with Retinitis Pigmentosa. Ophthalmic Genetics. 28(1). 25–30. 30 indexed citations

Roche, Olivier, Carolina O. Jaliffa, Dominique Marchant, et al.. (2006). Eight previously unidentified mutations found in the OA1ocular albinism gene. BMC Medical Genetics. 7(1). 41–41. 13 indexed citations

Mezer, Eedy, Joanne Sutherland, Stephanie Goei, Elise Héon, & Alex V. Levin. (2006). Utility of molecular testing for related retinal dystrophies. Canadian Journal of Ophthalmology. 41(2). 190–196. 4 indexed citations

10.

Punnett, Angela, Ikuko Teshima, Élise Héon, et al.. (2003). Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma. American Journal of Medical Genetics Part A. 120A(1). 105–109. 16 indexed citations

11.

Richter, Suzanne, Ning Chen, Katherine Zhang, et al.. (2003). Sensitive and Efficient Detection of RB1 Gene Mutations Enhances Care for Families with Retinoblastoma. The American Journal of Human Genetics. 72(2). 253–269. 222 indexed citations

12.

Allingham‐Hawkins, Diane, et al.. (1998). Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry. American Journal of Medical Genetics. 75(2). 171–175. 6 indexed citations

13.

Sippel, Kimberly C., et al.. (1998). Frequency of Somatic and Germ-Line Mosaicism in Retinoblastoma: Implications for Genetic Counseling. The American Journal of Human Genetics. 62(3). 610–619. 120 indexed citations

14.

Fitzpatrick, Jennifer, et al.. (1996). Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions. Journal of Genetic Counseling. 5(1). 1–15. 1 indexed citations

15.

Worton, Ronald G., Joanne Sutherland, James E. Sylvester, et al.. (1988). Human Ribosomal RNA Genes: Orientation of the Tandem Array and Conservation of the 5′ End. Science. 239(4835). 64–68. 110 indexed citations

16.

Willard, Huntington F., Kirby D. Smith, & Joanne Sutherland. (1983). Isolation and characterization of a major tandem repeat family from the human X chromosome. Nucleic Acids Research. 11(7). 2017–2034. 237 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