Katrin Õunap

9.8k total citations
106 papers, 1.8k citations indexed

About

Katrin Õunap is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Katrin Õunap has authored 106 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 57 papers in Genetics and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Katrin Õunap's work include Genomic variations and chromosomal abnormalities (25 papers), Metabolism and Genetic Disorders (20 papers) and Genomics and Rare Diseases (15 papers). Katrin Õunap is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Metabolism and Genetic Disorders (20 papers) and Genomics and Rare Diseases (15 papers). Katrin Õunap collaborates with scholars based in Estonia, United States and Germany. Katrin Õunap's co-authors include Tiia Reimand, Sander Pajusalu, Riina Žordania, Oliver Bartsch, Eve Õiglane‐Shlik, Inga Talvik, Olga Žilina, Tiina Kahre, Karit Reinson and Kairit Joost and has published in prestigious journals such as Nature, Nature Communications and FEBS Letters.

In The Last Decade

Katrin Õunap

101 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrin Õunap Estonia 25 1.0k 857 264 249 191 106 1.8k
F. Lucy Raymond United Kingdom 25 1.0k 1.0× 727 0.8× 142 0.5× 183 0.7× 105 0.5× 51 1.8k
David Mowat Australia 27 1.3k 1.2× 644 0.8× 300 1.1× 91 0.4× 264 1.4× 69 2.4k
Maha S. Zaki Egypt 27 1.2k 1.2× 679 0.8× 388 1.5× 81 0.3× 118 0.6× 147 2.4k
Wafaa Eyaid Saudi Arabia 25 1.5k 1.5× 889 1.0× 255 1.0× 288 1.2× 223 1.2× 55 2.4k
Arjan P.M. de Brouwer Netherlands 30 1.6k 1.6× 923 1.1× 130 0.5× 107 0.4× 66 0.3× 77 2.4k
Renaud Touraine France 25 1.1k 1.1× 633 0.7× 120 0.5× 74 0.3× 101 0.5× 93 2.0k
David A. Koolen Netherlands 22 1.6k 1.6× 2.2k 2.6× 330 1.3× 194 0.8× 100 0.5× 53 3.1k
Stavit A. Shalev Israel 29 1.8k 1.8× 709 0.8× 126 0.5× 287 1.2× 175 0.9× 88 2.6k
Seema R. Lalani United States 30 1.5k 1.5× 1.6k 1.9× 481 1.8× 122 0.5× 61 0.3× 98 2.9k
Ziva Ben‐Neriah Israel 20 774 0.8× 404 0.5× 195 0.7× 152 0.6× 90 0.5× 40 1.4k

Countries citing papers authored by Katrin Õunap

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Õunap

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Õunap

This figure shows the co-authorship network connecting the top 25 collaborators of Katrin Õunap. A scholar is included among the top collaborators of Katrin Õunap 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 Katrin Õunap. Katrin Õunap 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.
Reinson, Karit, Kai Muru, Tiia Reimand, et al.. (2025). Exploratory analysis of epilepsy biomarkers using untargeted metabolomics across multiple cohorts. Frontiers in Neurology. 16. 1684456–1684456.
2.
Gómez‐Andrés, David, Jordi Díaz‐Manera, Katrin Õunap, et al.. (2025). Different Lower Limb Muscle MRI Patterns in Autosomal Dominant Titinopathies. European Journal of Neurology. 32(10). e70348–e70348.
3.
Tõnisson, Neeme, Margit Nõukas, Sander Pajusalu, et al.. (2023). The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General Population. Cancers. 15(14). 3663–3663. 3 indexed citations
4.
Stormorken, Astrid, Hilde Nordgarden, Rolf H. Sijmons, et al.. (2023). AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature. Molecular Genetics & Genomic Medicine. 11(6). e2157–e2157. 1 indexed citations
5.
Deans, Zandra C., Joo Wook Ahn, Isabel M. Carreira, et al.. (2022). Recommendations for reporting results of diagnostic genomic testing. European Journal of Human Genetics. 30(9). 1011–1016. 29 indexed citations
6.
Pajusalu, Sander, Monica H. Wojcik, Julia K. Goodrich, et al.. (2020). Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency. Molecular Genetics & Genomic Medicine. 8(4). e1154–e1154. 5 indexed citations
7.
Witters, Peter, Rita Barone, Katrin Õunap, et al.. (2020). Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG. Genetics in Medicine. 22(6). 1102–1107. 56 indexed citations
8.
Esch, Hilde Van, Rita Colnaghi, Kathleen Freson, et al.. (2019). Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism. The American Journal of Human Genetics. 104(5). 957–967. 26 indexed citations
9.
Kahre, Tiina, Riina Žordania, Karit Reinson, et al.. (2019). A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016. European Journal of Human Genetics. 27(11). 1649–1658. 17 indexed citations
10.
Kahre, Tiina, Sander Pajusalu, Olga Žilina, et al.. (2018). A New Case of a Rare Combination of Temple Syndrome and Mosaic Trisomy 14 and a Literature Review. Molecular Syndromology. 9(4). 182–189. 12 indexed citations
11.
Vals, Mari‐Anne, Tiina Kahre, Kai Muru, et al.. (2015). The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome. Genetic Testing and Molecular Biomarkers. 19(12). 684–691. 7 indexed citations
12.
Õiglane‐Shlik, Eve, Sanna Puusepp, Inga Talvik, et al.. (2014). Monosomy 1p36 – A multifaceted and still enigmatic syndrome: Four clinically diverse cases with shared white matter abnormalities. European Journal of Paediatric Neurology. 18(3). 338–346. 18 indexed citations
13.
Õiglane‐Shlik, Eve, et al.. (2013). A patient with the classic features of Phelan‐McDermid syndrome and a high immunoglobulin E level caused by a cryptic interstitial 0.72‐Mb deletion in the 22q13.2 region. American Journal of Medical Genetics Part A. 164(3). 806–809. 22 indexed citations
14.
Joost, Kairit, Riina Žordania, Inga Talvik, et al.. (2012). The Live-Birth Prevalence of Mucopolysaccharidoses in Estonia. Genetic Testing and Molecular Biomarkers. 16(8). 846–849. 19 indexed citations
15.
Joost, Kairit, Katrin Õunap, Riina Žordania, et al.. (2011). Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia. JIMD Reports. 2. 79–85. 14 indexed citations
16.
Jurecka, Agnieszka, Ewa Piotrowska, Loreta Cimbalistienė, et al.. (2011). Molecular analysis of mucopolysaccharidosis type VI in Poland, Belarus, Lithuania and Estonia. Molecular Genetics and Metabolism. 105(2). 237–243. 29 indexed citations
17.
Muru, Kai, et al.. (2010). A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the <i>TBX5 </i>Gene. Molecular Syndromology. 1(6). 307–310. 3 indexed citations
18.
Käll, Kerstin, Gajja S. Salomons, Inga Talvik, et al.. (2009). The screening of SLC6A8 deficiency among Estonian families with X‐linked mental retardation. Journal of Inherited Metabolic Disease. 33(S3). 5–11. 39 indexed citations
19.
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
20.
Žordania, Riina, et al.. (2008). Girl With Partial Turner Syndrome and Absence Epilepsy. Pediatric Neurology. 38(4). 289–292. 10 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

Breakdown of academic impact, for papers by F. Lucy Raymond Breakdown of academic impact, for papers by David Mowat Breakdown of academic impact, for papers by Maha S. Zaki Breakdown of academic impact, for papers by Wafaa Eyaid Breakdown of academic impact, for papers by Arjan P.M. de Brouwer Breakdown of academic impact, for papers by Renaud Touraine Breakdown of academic impact, for papers by David A. Koolen Breakdown of academic impact, for papers by Stavit A. Shalev Breakdown of academic impact, for papers by Seema R. Lalani Breakdown of academic impact, for papers by Ziva Ben‐Neriah
Rankless by CCL
2026