Reet Rein

837 total citations
17 papers, 636 citations indexed

About

Reet Rein is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Reet Rein has authored 17 papers receiving a total of 636 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Immunology. Recurrent topics in Reet Rein's work include Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Epigenetics and DNA Methylation (2 papers). Reet Rein is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Epigenetics and DNA Methylation (2 papers). Reet Rein collaborates with scholars based in Estonia, Netherlands and United States. Reet Rein's co-authors include Hidde L. Ploegh, G. Seemann, Detlef Güssow, Ieke B. Ginjaar, Frans Hochstenbach, Katrin Õunap, C.S. Brown, Inga Talvik, Jacques Neefjes and Nico J. Stam and has published in prestigious journals such as The EMBO Journal, The Journal of Immunology and Journal of Bacteriology.

In The Last Decade

Reet Rein

17 papers receiving 600 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Reet Rein Estonia	11	280	191	127	70	51	17	636
Gumersindo Fontán Spain	14	350 1.3×	385 2.0×	168 1.3×	51 0.7×	19 0.4×	29	858
Dhirendra N. Misra United States	17	395 1.4×	280 1.5×	80 0.6×	46 0.7×	88 1.7×	38	899
Mina Nakama Japan	11	558 2.0×	126 0.7×	141 1.1×	101 1.4×	62 1.2×	27	848
Nancy Henderson United Kingdom	11	541 1.9×	97 0.5×	251 2.0×	59 0.8×	28 0.5×	14	825
Rama Gangula United States	14	651 2.3×	151 0.8×	124 1.0×	166 2.4×	84 1.6×	27	995
Katherine L. Harper United Kingdom	16	418 1.5×	384 2.0×	301 2.4×	158 2.3×	18 0.4×	23	1.0k
Masashi Yukawa Japan	16	743 2.7×	182 1.0×	141 1.1×	148 2.1×	21 0.4×	20	1.1k
Niema Ibrahim Saudi Arabia	17	411 1.5×	97 0.5×	257 2.0×	75 1.1×	37 0.7×	22	767
Jeanine Kleeman United States	10	467 1.7×	137 0.7×	181 1.4×	193 2.8×	132 2.6×	20	806
Geoffrey M. Habermacher United States	11	486 1.7×	98 0.5×	171 1.3×	44 0.6×	24 0.5×	12	870

Countries citing papers authored by Reet Rein

Since Specialization

Citations

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

Fields of papers citing papers by Reet Rein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reet Rein

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

All Works

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17 of 17 papers shown

Puusepp, Sanna, Karit Reinson, Sander Pajusalu, et al.. (2018). Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia. Molecular Genetics and Metabolism Reports. 15. 80–89. 30 indexed citations

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

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

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

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

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

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

Tomberg, Tiiu, et al.. (2008). Magnetic Resonance Imaging in Children With Bilateral Spastic Forms of Cerebral Palsy. Pediatric Neurology. 38(5). 321–328. 8 indexed citations

Õiglane‐Shlik, Eve, Reet Rein, Vallo Tillmann, Tiina Talvik, & Katrin Õunap. (2005). A Female With Angelman Syndrome and Unusual Limb Deformities. Pediatric Neurology. 33(1). 66–69. 7 indexed citations

10.

Õunap, Katrin, et al.. (2002). Sudden death of a girl with Prader-Willi syndrome.. PubMed. 13(4). 459–64. 12 indexed citations

11.

Bartsch, Oliver, et al.. (1998). Familial Williams-Beuren syndrome. American Journal of Medical Genetics. 80(5). 491–493. 25 indexed citations

12.

Raghunathan, G., Thomas Kieber‐Emmons, Reet Rein, & J. L. Alderfer. (1990). Conformational Features of DNA Containing aCis-SynPhotodimer. Journal of Biomolecular Structure and Dynamics. 7(4). 899–913. 21 indexed citations

13.

Shibata, Masayuki & Reet Rein. (1989). A computer modeling study of acetylcholine receptor-ligand interactions.. PubMed. 289. 39–54. 1 indexed citations

14.

Rein, Reet, et al.. (1987). Association with beta 2-microglobulin controls the expression of transfected human class I genes.. The Journal of Immunology. 138(4). 1178–1183. 51 indexed citations

15.

Güssow, Detlef, Reet Rein, Ieke B. Ginjaar, et al.. (1987). The human beta 2-microglobulin gene. Primary structure and definition of the transcriptional unit.. The Journal of Immunology. 139(9). 3132–3138. 281 indexed citations

16.

Seemann, G., Reet Rein, C.S. Brown, & Hidde L. Ploegh. (1986). Gene conversion-like mechanisms may generate polymorphism in human class I genes.. The EMBO Journal. 5(3). 547–552. 78 indexed citations

17.

Niedenhof, Ingrid, et al.. (1982). dnaC-dependent reconstitution of replication forks in Escherichia coli lysates. Journal of Bacteriology. 150(1). 286–292. 2 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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