Maigi Külm

432 total citations
7 papers, 349 citations indexed

About

Maigi Külm is a scholar working on Molecular Biology, Ophthalmology and Plant Science. According to data from OpenAlex, Maigi Külm has authored 7 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Ophthalmology and 3 papers in Plant Science. Recurrent topics in Maigi Külm's work include Retinal Development and Disorders (3 papers), Retinal Diseases and Treatments (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Maigi Külm is often cited by papers focused on Retinal Development and Disorders (3 papers), Retinal Diseases and Treatments (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Maigi Külm collaborates with scholars based in United States, Norway and Hungary. Maigi Külm's co-authors include Francesca Simonelli, Francesco Testa, Rando Allikmets, James R. Lupski, Carel B. Hoyng, Meira R. Meltzer, Peter Gouras, Neeme Tõnisson, Marko Hawlina and F.P.M. Cremers and has published in prestigious journals such as PLoS ONE, Investigative Ophthalmology & Visual Science and Human Mutation.

In The Last Decade

Maigi Külm

7 papers receiving 342 citations

Peers

Maigi Külm

MB

OPHTH

SS

CMN

RNMI

María Isabel López-Molina Spain

Jean-Louis Dufier France

T. P. Dryja United States

Sophie Devery United Kingdom

N S Davis Israel

F.P.M. Cremers Netherlands

Xavier Zanlonghi France

Annick Cabot France

Lance P. Doucette Canada

T.J.R. van de Pol Netherlands

María Isabel López-Molina Spain

Maigi Külm

287 ×1.0

MB

130 ×0.7

OPHTH

45 ×0.8

SS

45 ×1.0

CMN

21 ×0.5

RNMI

Citations per year, relative to Maigi Külm Maigi Külm (= 1×) peers María Isabel López-Molina

Countries citing papers authored by Maigi Külm

Since Specialization

Citations

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

Fields of papers citing papers by Maigi Külm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maigi Külm

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

All Works

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7 of 7 papers shown

1.

Vámos, Rita, Maigi Külm, Miklós Schneider, et al.. (2015). Leber Congenital Amaurosis: First Genotyped Hungarian Patients and Report of 2 Novel Mutations in the CRB1 and CEP290 Genes. European Journal of Ophthalmology. 26(1). 78–84. 5 indexed citations

2.

Vijayalakshmi, P, et al.. (2013). Mutational Screening of LCA Genes Emphasizing RPE65 in South Indian Cohort of Patients. PLoS ONE. 8(9). e73172–e73172. 33 indexed citations

3.

Vozzi, Diego, Anu Aaspõllu, Emmanouil Athanasakis, et al.. (2011). Molecular epidemiology of Usher syndrome in Italy.. PubMed. 17. 1662–8. 28 indexed citations

4.

Jaijo, Teresa, Elena Aller, Gema García‐García, et al.. (2010). Microarray-Based Mutation Analysis of 183 Spanish Families with Usher Syndrome. Investigative Ophthalmology & Visual Science. 51(3). 1311–1311. 51 indexed citations

5.

Külm, Maigi, et al.. (2008). Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease. Clinical Genetics. 73(5). 441–452. 16 indexed citations

6.

Schrijver, Iris, Maigi Külm, Phyllis Gardner, Eugene Pergament, & Morris Fiddler. (2007). Comprehensive Arrayed Primer Extension Array for the Detection of 59 Sequence Variants in 15 Conditions Prevalent Among the (Ashkenazi) Jewish Population. Journal of Molecular Diagnostics. 9(2). 228–236. 14 indexed citations

7.

Zernant, Jana, Maigi Külm, Amy Hutchinson, et al.. (2003). Genotyping microarray (gene chip) for theABCR(ABCA4) gene. Human Mutation. 22(5). 395–403. 202 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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