Irma López

5.5k total citations
34 papers, 2.0k citations indexed

About

Irma López is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Irma López has authored 34 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 13 papers in Ophthalmology and 11 papers in Genetics. Recurrent topics in Irma López's work include Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (12 papers) and Genomics and Rare Diseases (4 papers). Irma López is often cited by papers focused on Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (12 papers) and Genomics and Rare Diseases (4 papers). Irma López collaborates with scholars based in Canada, United States and Netherlands. Irma López's co-authors include Robert K. Koenekoop, Frans P.M. Cremers, Anneke I. den Hollander, L. Ingeborgh van den Born, Carel B. Hoyng, Suzanne Yzer, Klaus Rohrschneider, Marijke N. Zonneveld, Tim M. Strom and Maarten Arends and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The American Journal of Human Genetics.

In The Last Decade

Irma López

34 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irma López Canada 23 1.7k 656 655 251 225 34 2.0k
Kerstin Nagel‐Wolfrum Germany 20 1.3k 0.8× 180 0.3× 349 0.5× 257 1.0× 156 0.7× 42 1.6k
Judith Mosinger Ogilvie United States 17 818 0.5× 171 0.3× 146 0.2× 193 0.8× 318 1.4× 36 1.2k
Kazuto Kajiwara United States 12 1.3k 0.8× 339 0.5× 258 0.4× 278 1.1× 237 1.1× 18 1.6k
Visvanathan Ramamurthy United States 23 1.4k 0.9× 383 0.6× 400 0.6× 240 1.0× 400 1.8× 55 1.6k
Sheila A. Baker United States 19 1.4k 0.8× 142 0.2× 646 1.0× 443 1.8× 587 2.6× 40 1.6k
Nadine S. Dejneka United States 17 1.1k 0.7× 484 0.7× 439 0.7× 39 0.2× 332 1.5× 21 1.4k
Paulo A. Ferreira United States 24 1.4k 0.8× 207 0.3× 261 0.4× 418 1.7× 223 1.0× 45 1.6k
Jijing Pang United States 32 3.6k 2.1× 1.7k 2.5× 1.2k 1.8× 181 0.7× 978 4.3× 78 4.0k
Norman Michaud United States 25 947 0.6× 1.1k 1.7× 64 0.1× 187 0.7× 284 1.3× 47 2.2k
Anne K. Hennig United States 18 637 0.4× 115 0.2× 129 0.2× 174 0.7× 149 0.7× 27 1.0k

Countries citing papers authored by Irma López

Since Specialization
Citations

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

Fields of papers citing papers by Irma López

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irma López

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

All Works

20 of 20 papers shown
1.
Hussain, Hafiz Muhammad Jafar, Mark E. Pennesi, Paul Yang, et al.. (2024). Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases. Human Molecular Genetics. 33(11). 945–957. 5 indexed citations
2.
Wen, Shu, Meng C. Wang, Yumei Li, et al.. (2023). Systematic assessment of the contribution of structural variants to inherited retinal diseases. Human Molecular Genetics. 32(12). 2005–2015. 7 indexed citations
3.
Accogli, Andrea, Christine Saint‐Martin, Irma López, et al.. (2021). PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy. European Journal of Medical Genetics. 65(2). 104405–104405. 3 indexed citations
4.
Keser, Vafa, Ayesha Khan, Sorath Noorani Siddiqui, et al.. (2017). The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families. Investigative Ophthalmology & Visual Science. 58(2). 1028–1028. 16 indexed citations
5.
Soens, Zachry T., Yuanyuan Li, Li Zhao, et al.. (2016). Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1. Genetics in Medicine. 18(10). 1044–1051. 31 indexed citations
6.
Xu, Mingchu, Zixi Sun, Aiden Eblimit, et al.. (2016). Mutations inPOMGNT1cause non-syndromic retinitis pigmentosa. Human Molecular Genetics. 25(8). 1479–1488. 29 indexed citations
7.
Zaneveld, Jacques, Sorath Noorani Siddiqui, Huajin Li, et al.. (2014). Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype–phenotype correlations and unexpected diagnostic revisions. Genetics in Medicine. 17(4). 262–270. 41 indexed citations
8.
Asai-Coakwell, Mika, Michèle G. DuVal, Irma López, et al.. (2013). Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies. Human Molecular Genetics. 22(7). 1432–1442. 52 indexed citations
9.
Yzer, Suzanne, Anneke I. den Hollander, Irma López, et al.. (2012). Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290.. PubMed. 18. 412–25. 41 indexed citations
10.
Wang, Hui, Anneke I. den Hollander, Yalda Moayedi, et al.. (2010). Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa. The American Journal of Human Genetics. 86(2). 293–293. 4 indexed citations
11.
Chakarova, Christina, Hemant Khanna, Amna Z. Shah, et al.. (2010). TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein. Human Molecular Genetics. 20(5). 975–987. 46 indexed citations
12.
Danis‐Lozano, Rogelio, Jorge X. Velasco‐Hernández, Gilma Sánchez-Burgos, et al.. (2010). Evolution of dengue virus in Mexico is characterized by frequent lineage replacement. Archives of Virology. 155(9). 1401–1412. 45 indexed citations
13.
Ebermann, Inga, Jennifer B. Phillips, Max C. Liebau, et al.. (2010). PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome. Journal of Clinical Investigation. 120(6). 1812–1823. 181 indexed citations
14.
Wang, Hui, Anneke I. den Hollander, Yalda Moayedi, et al.. (2009). Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa. The American Journal of Human Genetics. 84(3). 380–387. 85 indexed citations
15.
Ebermann, Inga, et al.. (2008). An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians. European Journal of Human Genetics. 17(1). 80–84. 28 indexed citations
16.
Ebermann, Inga, Irma López, Maria Bitner‐Glindzicz, et al.. (2007). Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1Cgene provides the first genetic link with the Acadian population. Genome biology. 8(4). R47–R47. 36 indexed citations
17.
Koenekoop, Robert K., Irma López, Anneke I. den Hollander, Rando Allikmets, & Frans P.M. Cremers. (2007). Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions. Clinical and Experimental Ophthalmology. 35(5). 473–485. 89 indexed citations
18.
McEwen, Dyke P., Robert K. Koenekoop, Hemant Khanna, et al.. (2007). Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons. Proceedings of the National Academy of Sciences. 104(40). 15917–15922. 126 indexed citations
19.
Hollander, Anneke I. den, Robert K. Koenekoop, Suzanne Yzer, et al.. (2006). Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis. The American Journal of Human Genetics. 79(3). 556–561. 488 indexed citations
20.
Papaioannou, Myrto, Christina Chakarova, Quincy Prescott, et al.. (2005). A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p. Human Genetics. 118(3-4). 501–503. 12 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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