Ulvi Vaher

1.3k total citations
15 papers, 303 citations indexed

About

Ulvi Vaher is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Ulvi Vaher has authored 15 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Molecular Biology and 6 papers in Psychiatry and Mental health. Recurrent topics in Ulvi Vaher's work include Neonatal and fetal brain pathology (6 papers), Epilepsy research and treatment (6 papers) and Genomics and Rare Diseases (3 papers). Ulvi Vaher is often cited by papers focused on Neonatal and fetal brain pathology (6 papers), Epilepsy research and treatment (6 papers) and Genomics and Rare Diseases (3 papers). Ulvi Vaher collaborates with scholars based in Estonia, Australia and Denmark. Ulvi Vaher's co-authors include Tiina Talvik, Pilvi Ilves, Inga Talvik, Katrin Õunap, Tiia Reimand, Mare Lintrop, Tuuli Metsvaht, Eve Õiglane‐Shlik, Andres Piirsoo and Reet Rein and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Language and Acta Paediatrica.

In The Last Decade

Ulvi Vaher

13 papers receiving 284 citations

Peers

Ulvi Vaher
In Goo Lee South Korea
Judith Weisenberg United States
Sanem Yılmaz Türkiye
Sébastien Lebon Switzerland
M A McShane United Kingdom
In Goo Lee South Korea
Ulvi Vaher
Citations per year, relative to Ulvi Vaher Ulvi Vaher (= 1×) peers In Goo Lee

Countries citing papers authored by Ulvi Vaher

Since Specialization
Citations

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

Fields of papers citing papers by Ulvi Vaher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulvi Vaher

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

All Works

15 of 15 papers shown
1.
Vaher, Ulvi, et al.. (2024). General ability and specific cognitive functions are lower in children with epilepsy after perinatal ischemic stroke. SHILAP Revista de lepidopterología. 3. 1371093–1371093.
2.
Vaher, Ulvi, et al.. (2024). Vascular syndrome predicts the development and course of epilepsy after perinatal stroke. Epileptic Disorders. 26(4). 471–483.
3.
Vaher, Ulvi, et al.. (2023). The thalamus and basal ganglia are smaller in children with epilepsy after perinatal stroke. Frontiers in Neurology. 14. 3 indexed citations
4.
Männamaa, Mairi, et al.. (2022). Language lateralization and outcome in perinatal stroke patients with different vascular types. Brain and Language. 228. 105108–105108. 8 indexed citations
5.
Laugesaar, Rael, Ulvi Vaher, Anneli Kolk, et al.. (2018). Epilepsy after perinatal stroke with different vascular subtypes. Epilepsia Open. 3(2). 193–202. 29 indexed citations
6.
Veri, Kadi, Inga Talvik, Ulvi Vaher, et al.. (2018). Incidence of Childhood Epilepsy in Estonia. Journal of Child Neurology. 33(9). 587–592. 3 indexed citations
7.
Reinson, Karit, Eve Õiglane‐Shlik, Inga Talvik, et al.. (2016). Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American Journal of Medical Genetics Part A. 170(8). 2173–2176. 62 indexed citations
8.
Talvik, Inga, Ulvi Vaher, Katrin Õunap, et al.. (2016). CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature. Neuropediatrics. 47(6). 361–367. 10 indexed citations
9.
Talvik, Inga, Rikke S. Møller, Ulvi Vaher, et al.. (2015). Clinical Phenotype of De Novo GNAO1 Mutation. SHILAP Revista de lepidopterología. 2(2). 2329048X15583717–2329048X15583717. 20 indexed citations
10.
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
11.
Veri, Kadi, Raivo Uibo, Tiina Talvik, et al.. (2013). Newly-diagnosed pediatric epilepsy is associated with elevated autoantibodies to glutamic acid decarboxylase but not cardiolipin. Epilepsy Research. 105(1-2). 86–91. 10 indexed citations
12.
Vaher, Ulvi, Margit Nõukas, Tiit Nikopensius, et al.. (2013). De NovoSCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders. Journal of Child Neurology. 29(12). NP202–NP206. 52 indexed citations
13.
Õunap, Katrin, Maire Peters, Ulvi Vaher, et al.. (2012). A novel c.2T > C mutation of the KDM5C/JARID1C gene in one large family with X-linked intellectual disability. European Journal of Medical Genetics. 55(3). 178–184. 31 indexed citations
14.
Ilves, Pilvi, Mare Lintrop, Tuuli Metsvaht, Ulvi Vaher, & Tiina Talvik. (2004). Cerebral blood‐flow velocities in predicting outcome of asphyxiated newborn infants. Acta Paediatrica. 93(4). 523–528. 50 indexed citations
15.
Vaher, Ulvi, et al.. (2001). Four siblings with Hallervorden–Spatz disease. Brain and Development. 23(4). 236–239. 7 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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