Thorsten Enklaar

821 total citations
12 papers, 531 citations indexed

About

Thorsten Enklaar is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Thorsten Enklaar has authored 12 papers receiving a total of 531 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Thorsten Enklaar's work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (5 papers) and Prenatal Screening and Diagnostics (5 papers). Thorsten Enklaar is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (5 papers) and Prenatal Screening and Diagnostics (5 papers). Thorsten Enklaar collaborates with scholars based in Germany, United States and Austria. Thorsten Enklaar's co-authors include Dirk Prawitt, Bernhard Zabel, Mahealani K. Monteilh‐Zoller, Andrea Fleig, Reinhold Penner, Christian Spangenberg, Dirk Reutzel, Monika Oswald, Ekkehart Lausch and Peter Schmidtke and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer Research and Biochemical and Biophysical Research Communications.

In The Last Decade

Thorsten Enklaar

12 papers receiving 521 citations

Peers

Thorsten Enklaar

GENET

PPCH

ONCOL

Mónika Mórocz Hungary

Bernard Pellissier France

Laura L. Wootton United Kingdom

Shubana Kazi United Kingdom

Miranda Menniti Italy

Andrea Salazar-Lázaro Germany

Yongyi Zou China

D L Lips United States

Yvonne Munari‐Silem France

Ruth M. Lightfoot United States

Mónika Mórocz Hungary

Thorsten Enklaar

355 ×1.0

63 ×0.3

GENET

15 ×0.1

PPCH

19 ×0.2

98 ×1.4

ONCOL

Citations per year, relative to Thorsten Enklaar Thorsten Enklaar (= 1×) peers Mónika Mórocz

Countries citing papers authored by Thorsten Enklaar

Since Specialization

Citations

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

Fields of papers citing papers by Thorsten Enklaar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thorsten Enklaar

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

All Works

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12 of 12 papers shown

Enklaar, Thorsten, Sebastian Frees, Joachim W. Thüroff, et al.. (2018). In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself. Cell Communication and Signaling. 16(1). 35–35. 17 indexed citations

Langer, David, Ursula Martiné, Regina Cencic, et al.. (2016). Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation. Clinical Epigenetics. 8(1). 47–47. 15 indexed citations

Bachmann, Nadine, Roman Crazzolara, Dieter Kotzot, et al.. (2016). Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis. Pediatric Blood & Cancer. 64(3). 10 indexed citations

Beygo, Jasmin, Valentina Citro, Angela Sparago, et al.. (2012). The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites. Human Molecular Genetics. 22(3). 544–557. 64 indexed citations

Monteilh‐Zoller, Mahealani K., Andrea Fleig, Reinhold Penner, et al.. (2010). TRPM5 regulates glucose-stimulated insulin secretion. Pflügers Archiv - European Journal of Physiology. 460(1). 69–76. 93 indexed citations

Enklaar, Thorsten, Bernhard Zabel, & Dirk Prawitt. (2006). Beckwith–Wiedemann syndrome: multiple molecular mechanisms. Expert Reviews in Molecular Medicine. 8(17). 1–19. 64 indexed citations

Lausch, Ekkehart, Steffen Schmitt, Thorsten Enklaar, et al.. (2005). Premature Senescence Is a Primary Fail-safe Mechanism of ERBB2-Driven Tumorigenesis in Breast Carcinoma Cells. Cancer Research. 65(3). 840–849. 70 indexed citations

Prawitt, Dirk, Thorsten Enklaar, Christian Spangenberg, et al.. (2005). Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith–Wiedemann syndrome and Wilms' tumor. Proceedings of the National Academy of Sciences. 102(11). 4085–4090. 107 indexed citations

Enklaar, Thorsten, et al.. (2000). Mapping and Structure of DMXL1, a Human Homologue of the DmX Gene from Drosophila melanogaster Coding for a WD Repeat Protein. Genomics. 64(1). 97–101. 17 indexed citations

10.

Bahn, Andrew, Dirk Prawitt, Glen Reid, et al.. (2000). Genomic Structure and in Vivo Expression of the Human Organic Anion Transporter 1 (hOAT1) Gene. Biochemical and Biophysical Research Communications. 275(2). 623–630. 35 indexed citations

11.

Enklaar, Thorsten, Monika Oswald, Katja Hilbert, et al.. (2000). Mtr1, a Novel Biallelically Expressed Gene in the Center of the Mouse Distal Chromosome 7 Imprinting Cluster, is a Member of the Trp Gene Family. Genomics. 67(2). 179–187. 35 indexed citations

12.

Winterpacht, Andreas, et al.. (1996). Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2→q13.3. Cytogenetic and Genome Research. 75(2-3). 132–135. 4 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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