Gregor Schlüter

1.3k total citations
25 papers, 486 citations indexed

About

Gregor Schlüter is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Gregor Schlüter has authored 25 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Surgery. Recurrent topics in Gregor Schlüter's work include Animal Genetics and Reproduction (5 papers), RNA and protein synthesis mechanisms (5 papers) and RNA modifications and cancer (4 papers). Gregor Schlüter is often cited by papers focused on Animal Genetics and Reproduction (5 papers), RNA and protein synthesis mechanisms (5 papers) and RNA modifications and cancer (4 papers). Gregor Schlüter collaborates with scholars based in Germany, Poland and Norway. Gregor Schlüter's co-authors include Wolfgang Engel, Hannelore Kremling, Ibrahim M. Adham, Karim Nayernia, Kerstin Reim, Andreas Meinhardt, Stephan Wolf, H. Hameister, Özlem Topaloglu and Günter Emons and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

Gregor Schlüter

25 papers receiving 469 citations

Peers

Gregor Schlüter

GENET

PHEOH

IMMUN

J. Suzanne Lindsey United States

Tiangang Zhuang United States

Trent R. Clarke United States

Miki Yoshino Japan

Yitzhak Reizel Israel

Jane M. vanWert United States

Junji Tsuchida Japan

Kuniko Nakajima Japan

Sika Ristevski Australia

Jorge Merlet France

J. Suzanne Lindsey United States

Gregor Schlüter

358 ×1.5

241 ×1.3

GENET

184 ×1.2

129 ×1.6

PHEOH

37 ×0.6

IMMUN

Citations per year, relative to Gregor Schlüter Gregor Schlüter (= 1×) peers J. Suzanne Lindsey

Countries citing papers authored by Gregor Schlüter

Since Specialization

Citations

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

Fields of papers citing papers by Gregor Schlüter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gregor Schlüter

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

All Works

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20 of 20 papers shown

Himmelreich, Nastassja, Matthias Zielonka, Georg F. Hoffmann, et al.. (2022). Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature. Molecular Genetics and Metabolism. 136(4). 274–281. 6 indexed citations

Heinrich, T., Indrajit Nanda, Karen Ernestus, et al.. (2015). Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling. Cytogenetic and Genome Research. 145(1). 25–28. 2 indexed citations

Dreha‐Kulaczewski, Steffi, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2013). A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous Females. JIMD Reports. 13. 91–99. 10 indexed citations

Gutensohn, K., et al.. (2010). Diagnostic accuracy of noninvasive polymerase chain reaction testing for the determination of fetal rhesus C, c and E status in early pregnancy. BJOG An International Journal of Obstetrics & Gynaecology. 117(6). 722–729. 26 indexed citations

Strecker, Thomas, I. Zimmermann, Gregor Schlüter, & Richard Feyrer. (2009). Antikoagulation in der Schwangerschaft nach künstlichem Herzklappenersatz. DMW - Deutsche Medizinische Wochenschrift. 134(42). 2116–2119. 1 indexed citations

Grzmil, Paweł, Kenneth C. Kleene, Ibrahim M. Adham, et al.. (2008). Prm3, the Fourth Gene in the Mouse Protamine Gene Cluster, Encodes a Conserved Acidic Protein That Affects Sperm Motility1. Biology of Reproduction. 78(6). 958–967. 40 indexed citations

Deng, Shiwei, Bettina Kulle, Gregor Schlüter, et al.. (2007). Dystrophin-Deficiency Increases the Susceptibility to Doxorubicin-Induced Cardiotoxicity. European Journal of Heart Failure. 9(10). 986–994. 19 indexed citations

Topaloglu, Özlem, Andreas Meinhardt, Arvind Dev, et al.. (2006). Premature translation of transition protein 2 mRNA causes sperm abnormalities and male infertility. Molecular Reproduction and Development. 74(3). 273–279. 47 indexed citations

Schlüter, Gregor, Holger Schiffmann, Karsten Harms, et al.. (2005). Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites. Prenatal Diagnosis. 25(7). 574–576. 36 indexed citations

10.

Topaloglu, Özlem, Gregor Schlüter, Karim Nayernia, & Wolfgang Engel. (2001). A 74-bp Promoter of the Tnp2 Gene Confers Testis- and Spermatid-Specific Expression in Transgenic Mice. Biochemical and Biophysical Research Communications. 289(2). 597–601. 5 indexed citations

11.

Schlüter, Gregor, et al.. (2000). Evidence for Translational Repression of the SOCS-1 Major Open Reading Frame by an Upstream Open Reading Frame. Biochemical and Biophysical Research Communications. 268(2). 255–261. 39 indexed citations

12.

Reim, Kerstin, et al.. (1997). Specific Binding of a 47-Kilodalton Protein to the 3' Untranslated Region of Rat Transition Protein 2 Messenger Ribonucleic Acid1. Biology of Reproduction. 56(3). 697–706. 10 indexed citations

13.

Nayernia, Karim, et al.. (1996). Stage and developmental specific gene expression during mammalian spermatogenesis. The International Journal of Developmental Biology. 40(1). 379–383. 44 indexed citations

14.

Schlüter, Gregor, et al.. (1996). Sequence analysis of the conserved protamine gene cluster shows that it contains a fourth expressed gene. Molecular Reproduction and Development. 43(1). 1–6. 42 indexed citations

15.

Schlüter, Gregor & Wolfgang Engel. (1995). The rat <i>Prm3</i> gene is an intronless member of the protamine gene cluster and is expressed in haploid male germ cells. Cytogenetic and Genome Research. 71(4). 352–355. 23 indexed citations

16.

Schlüter, Gregor & Ursula Wick. (1994). An 87 bp deletion in exon 5 of the LDL receptor gene in a mother and her son with familial hypercholesterolemia. Clinical Genetics. 45(2). 84–87. 7 indexed citations

17.

Schlüter, Gregor, et al.. (1993). A Conserved 8-Bp Motif (GCYATACAY) in the 3′UTR of Transition Protein 2 as a Putative Target for a Transcript Stabilizing Protein Factor. Biochemical and Biophysical Research Communications. 197(1). 110–115. 13 indexed citations

18.

Schlüter, Gregor, Hannelore Kremling, & Wolfgang Engel. (1992). The gene for human transition protein 2: Nucleotide sequence, assignment to the protamine gene cluster, and evidence for its low expression. Genomics. 14(2). 377–383. 34 indexed citations

19.

Engel, Wolfgang, et al.. (1992). The genes for protamine 1 and 2 (PRM1 and PRM2) and transition protein 2 (TNP2) are closely linked in the mammalian genome. Cytogenetic and Genome Research. 61(2). 158–159. 35 indexed citations

20.

Laas, J., et al.. (1987). Acute type-A dissection of the aorta: which diagnostic modes remain for surgical indication?. European Journal of Cardio-Thoracic Surgery. 1(3). 169–172. 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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