Tiina Kahre

647 total citations
30 papers, 328 citations indexed

About

Tiina Kahre is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tiina Kahre has authored 30 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tiina Kahre's work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (6 papers). Tiina Kahre is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (6 papers). Tiina Kahre collaborates with scholars based in Estonia, United States and United Kingdom. Tiina Kahre's co-authors include Katrin Õunap, Tiina Talvik, Sander Pajusalu, Riina Žordania, Vallo Tillmann, Tiia Reimand, Mari‐Anne Vals, Anneli Kolk, Kai Muru and Inga Talvik and has published in prestigious journals such as British Journal of Clinical Pharmacology, Cancers and Acta Paediatrica.

In The Last Decade

Tiina Kahre

30 papers receiving 313 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tiina Kahre Estonia 13 146 133 75 43 28 30 328
Sevcan Tuğ Bozdoğan Türkiye 10 86 0.6× 77 0.6× 33 0.4× 49 1.1× 40 1.4× 35 296
Muhammad Talal Alrifai Saudi Arabia 12 157 1.1× 82 0.6× 53 0.7× 45 1.0× 16 0.6× 28 444
C. M. Hall United Kingdom 12 177 1.2× 121 0.9× 59 0.8× 12 0.3× 71 2.5× 14 490
Gianluca Casara Italy 11 98 0.7× 57 0.4× 103 1.4× 18 0.4× 23 0.8× 20 296
Paola Nicolaides United Kingdom 11 188 1.3× 63 0.5× 130 1.7× 42 1.0× 48 1.7× 19 507
Artemis Doulgeraki Greece 12 145 1.0× 89 0.7× 27 0.4× 16 0.4× 37 1.3× 33 358
Jessica Connor United States 9 80 0.5× 59 0.4× 25 0.3× 26 0.6× 34 1.2× 13 293
Marie McDonald United States 8 308 2.1× 207 1.6× 53 0.7× 52 1.2× 42 1.5× 13 505
Mona Seibt Palmér Sweden 12 119 0.8× 48 0.4× 60 0.8× 86 2.0× 43 1.5× 17 472
Satoko Nakahara Japan 10 102 0.7× 79 0.6× 32 0.4× 22 0.5× 17 0.6× 12 391

Countries citing papers authored by Tiina Kahre

Since Specialization
Citations

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

Fields of papers citing papers by Tiina Kahre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tiina Kahre

This figure shows the co-authorship network connecting the top 25 collaborators of Tiina Kahre. A scholar is included among the top collaborators of Tiina Kahre 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 Tiina Kahre. Tiina Kahre 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.
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
2.
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
3.
Pajusalu, Sander, et al.. (2023). High Prevalence of Collagenopathies in Preterm- and Term-Born Children With Periventricular Venous Hemorrhagic Infarction. Journal of Child Neurology. 38(6-7). 373–388. 3 indexed citations
4.
Õunap, Katrin, et al.. (2022). The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016–2021. Frontiers in Genetics. 13. 1020543–1020543. 2 indexed citations
5.
Muru, Kai, et al.. (2021). A two‐year prospective study assessing the performance of fetal chromosomal microarray analysis and next‐generation sequencing in high‐risk pregnancies. Molecular Genetics & Genomic Medicine. 9(10). e1787–e1787. 3 indexed citations
6.
Kahre, Tiina, Sander Pajusalu, Kai Muru, et al.. (2021). The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia. Frontiers in Genetics. 12. 796862–796862. 6 indexed citations
7.
8.
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
9.
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
10.
Grigorova, Marina, Margus Punab, Tiina Kahre, et al.. (2017). The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young men. Andrology. 5(3). 495–504. 25 indexed citations
11.
Pajusalu, Sander, et al.. (2017). Large gene panel sequencing in clinical diagnostics—results from 501 consecutive cases. Clinical Genetics. 93(1). 78–83. 23 indexed citations
12.
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
13.
Vals, Mari‐Anne, Tiina Kahre, Kai Muru, et al.. (2015). Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes. Molecular Syndromology. 6(3). 147–151. 24 indexed citations
14.
Kahre, Tiina, et al.. (2014). Are Methylenetetrahydrofolate Reductase (<i>MTHFR</i>) Gene Polymorphisms C677T and A1298C Associated with Higher Risk of Pediatric Migraine in Boys and Girls?. Journal of Biomedical Science and Engineering. 7(8). 464–472. 7 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.
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
17.
Talvik, Inga, Andres Kulla, Tiina Kahre, et al.. (2006). Descriptive Epidemiology of Spinal Muscular Atrophy Type I in Estonia. Neuroepidemiology. 27(3). 164–168. 10 indexed citations
18.
Õiglane‐Shlik, Eve, Tiina Talvik, Riina Žordania, et al.. (2006). Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented. American Journal of Medical Genetics Part A. 140A(18). 1936–1943. 25 indexed citations
19.
Kahre, Tiina, et al.. (2004). Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient. Journal of Cystic Fibrosis. 3(1). 58–60. 6 indexed citations
20.
Kahre, Tiina, et al.. (2003). A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia. European Journal of Paediatric Neurology. 7(5). 221–226. 13 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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