Rita Teek

420 total citations
14 papers, 221 citations indexed

About

Rita Teek is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Rita Teek has authored 14 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Sensory Systems. Recurrent topics in Rita Teek's work include Genomic variations and chromosomal abnormalities (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Genetic Syndromes and Imprinting (2 papers). Rita Teek is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Genetic Syndromes and Imprinting (2 papers). Rita Teek collaborates with scholars based in Estonia, United States and Switzerland. Rita Teek's co-authors include Katrin Õunap, Tiia Reimand, Eve Õiglane‐Shlik, Karit Reinson, Sanna Puusepp, Tiiu Tomberg, Inga Talvik, Sander Pajusalu, Ulvi Vaher and Riina Žordania and has published in prestigious journals such as European Journal of Human Genetics, European Journal of Pediatrics and International Journal of Pediatric Otorhinolaryngology.

In The Last Decade

Rita Teek

14 papers receiving 208 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rita Teek Estonia	9	126	124	36	34	27	14	221
Leanne Moynihan United Kingdom	7	111 0.9×	71 0.6×	21 0.6×	20 0.6×	34 1.3×	7	226
Dean Phelan Australia	11	188 1.5×	180 1.5×	19 0.5×	13 0.4×	51 1.9×	15	398
Alexander Paciorkowski United States	6	109 0.9×	89 0.7×	36 1.0×	42 1.2×	4 0.1×	6	255
Anna Mikhailov Canada	7	102 0.8×	104 0.8×	14 0.4×	24 0.7×	4 0.1×	16	194
Jana Neupauerová Czechia	10	78 0.6×	68 0.5×	13 0.4×	83 2.4×	31 1.1×	14	203
Jolanda Gyftodimou Greece	10	125 1.0×	136 1.1×	56 1.6×	30 0.9×	54 2.0×	13	270
Alisha Wilkens United States	13	239 1.9×	255 2.1×	104 2.9×	13 0.4×	61 2.3×	20	438
Jennifer McCallum United States	5	280 2.2×	112 0.9×	23 0.6×	23 0.7×	41 1.5×	5	355
Jin Szatkiewicz United States	11	125 1.0×	220 1.8×	22 0.6×	16 0.5×	5 0.2×	30	321
Noriko Sangu Japan	9	101 0.8×	115 0.9×	23 0.6×	20 0.6×	3 0.1×	17	191

Countries citing papers authored by Rita Teek

Since Specialization

Citations

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

Fields of papers citing papers by Rita Teek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Teek

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

All Works

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14 of 14 papers shown

Puusepp, Sanna, et al.. (2023). Autosomal recessive Leber's hereditary optic neuropathy caused by a homozygous variant in DNAJC30 gene. European Journal of Medical Genetics. 66(9). 104821–104821. 1 indexed citations

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

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

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

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

Žilina, Olga, et al.. (2014). Chromosomal microarray analysis as a first‐tier clinical diagnostic test: Estonian experience. Molecular Genetics & Genomic Medicine. 2(2). 166–175. 21 indexed citations

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

Teek, Rita, Riina Žordania, Kairit Joost, et al.. (2013). Hearing impairment in Estonia: An algorithm to investigate genetic causes in pediatric patients. Advances in Medical Sciences. 58(2). 419–428. 11 indexed citations

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

10.

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

11.

Joost, Kairit, Rita Teek, Maire Peters, et al.. (2010). Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency. Molecular Syndromology. 1(6). 311–315. 2 indexed citations

12.

Krjutškov, Kaarel, Priit Palta, Ene Metspalu, et al.. (2009). Evaluation of the 124-plex SNP typing microarray for forensic testing. Forensic Science International Genetics. 4(1). 43–48. 22 indexed citations

13.

Muru, Kai, et al.. (2009). LEOPARD syndrome with recurrent PTPN11 mutation Y279C and different cutaneous manifestations: two case reports and a review of the literature. European Journal of Pediatrics. 169(4). 469–473. 12 indexed citations

14.

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

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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