Eneli Oitmaa

591 total citations
9 papers, 477 citations indexed

About

Eneli Oitmaa is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Eneli Oitmaa has authored 9 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Sensory Systems and 3 papers in Genetics. Recurrent topics in Eneli Oitmaa's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Connexins and lens biology (3 papers) and Genetic Syndromes and Imprinting (1 paper). Eneli Oitmaa is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Connexins and lens biology (3 papers) and Genetic Syndromes and Imprinting (1 paper). Eneli Oitmaa collaborates with scholars based in Estonia, United States and Australia. Eneli Oitmaa's co-authors include Marina Pisano, Karen Brøndum‐Nielsen, M B Petersen, L. Zelante, Salvatore Melchionda, Paolo Fortina, Xavier Estivill, Paolo Gasparini, Guido Barbujani and Raquel Rabionet and has published in prestigious journals such as PEDIATRICS, European Journal of Human Genetics and Journal of Molecular Diagnostics.

In The Last Decade

Eneli Oitmaa

9 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eneli Oitmaa Estonia	6	352	293	120	103	103	9	477
Araceli Álvarez Spain	4	474 1.3×	381 1.3×	129 1.1×	122 1.2×	111 1.1×	5	559
Yin-Hung Lin Taiwan	11	292 0.8×	172 0.6×	104 0.9×	18 0.2×	115 1.1×	15	392
Marzieh Mohseni Iran	13	223 0.6×	259 0.9×	125 1.0×	53 0.5×	27 0.3×	37	470
Ana Carla Batissoco Brazil	12	246 0.7×	169 0.6×	76 0.6×	39 0.4×	66 0.6×	21	333
Kyu Yup Lee South Korea	8	270 0.8×	135 0.5×	138 1.1×	31 0.3×	95 0.9×	16	362
Suna Tokgöz-Yılmaz Türkiye	11	251 0.7×	147 0.5×	129 1.1×	16 0.2×	116 1.1×	53	361
Marta Gandía Spain	7	197 0.6×	147 0.5×	100 0.8×	33 0.3×	27 0.3×	8	277
Mark Houseman United Kingdom	7	218 0.6×	233 0.8×	69 0.6×	69 0.7×	55 0.5×	7	324
Diana L. Kolbe United States	5	325 0.9×	248 0.8×	104 0.9×	10 0.1×	86 0.8×	5	484
Kris Flothmann Belgium	8	233 0.7×	237 0.8×	90 0.8×	41 0.4×	77 0.7×	8	409

Countries citing papers authored by Eneli Oitmaa

Since Specialization

Citations

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

Fields of papers citing papers by Eneli Oitmaa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eneli Oitmaa

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

All Works

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9 of 9 papers shown

Serrano‐Fernández, Pablo, Dagmara Dymerska, Grzegorz Kurzawski, et al.. (2015). Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia. Gastroenterology Research and Practice. 2015. 1–10. 4 indexed citations

Zeitz, Christina, et al.. (2012). Arrayed Primer Extension Microarray for the Analysis of Genes Associated with Congenital Stationary Night Blindness. Methods in molecular biology. 963. 319–326. 4 indexed citations

Teek, Rita, Riina Žordania, Kairit Joost, et al.. (2010). Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia. International Journal of Pediatric Otorhinolaryngology. 74(9). 1007–1012. 15 indexed citations

Hoskins, Bethan E., Jan D. Marshall, Gayle B. Collin, et al.. (2010). Arrayed primer extension technology simplifies mutation detection in Bardet–Biedl and Alström syndrome. European Journal of Human Genetics. 19(4). 485–488. 31 indexed citations

Oitmaa, Eneli, Maire Peters, Reidar Andreson, et al.. (2010). Molecular diagnosis of Down syndrome using quantitative APEX‐2 microarrays. Prenatal Diagnosis. 30(12-13). 1170–1177. 2 indexed citations

Teek, Rita, Eneli Oitmaa, Riina Žordania, et al.. (2008). Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss. International Journal of Pediatric Otorhinolaryngology. 73(1). 103–107. 8 indexed citations

Gardner, Phyllis, Eneli Oitmaa, Anna H. Messner, et al.. (2006). Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up. PEDIATRICS. 118(3). 985–994. 63 indexed citations

Schrijver, Iris, Eneli Oitmaa, Andres Metspalu, & Phyllis Gardner. (2005). Genotyping Microarray for the Detection of More Than 200 CFTR Mutations in Ethnically Diverse Populations. Journal of Molecular Diagnostics. 7(3). 375–387. 38 indexed citations

Gasparini, Paolo, Raquel Rabionet, Guido Barbujani, et al.. (2000). High carrier frequency of the 35delG deafness mutation in European populations. European Journal of Human Genetics. 8(1). 19–23. 312 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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