Reiner Schulz

3.1k total citations · 1 hit paper
41 papers, 2.0k citations indexed

About

Reiner Schulz is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Reiner Schulz has authored 41 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 22 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Reiner Schulz's work include Epigenetics and DNA Methylation (18 papers), Genetic Syndromes and Imprinting (17 papers) and Prenatal Screening and Diagnostics (9 papers). Reiner Schulz is often cited by papers focused on Epigenetics and DNA Methylation (18 papers), Genetic Syndromes and Imprinting (17 papers) and Prenatal Screening and Diagnostics (9 papers). Reiner Schulz collaborates with scholars based in United Kingdom, United States and France. Reiner Schulz's co-authors include Rebecca J. Oakey, Michael H. Malim, Kathryn Woodfine, Torsten Schaller, Andrew J. Wood, Christopher Ward, Hélène Bauby, Caroline Goujon, Olivier Moncorgé and Stéphane Hué and has published in prestigious journals such as Nature, Nucleic Acids Research and Genes & Development.

In The Last Decade

Reiner Schulz

41 papers receiving 1.9k citations

Hit Papers

Human MX2 is an interferon-induced post-entry inhibitor o... 2013 2026 2017 2021 2013 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Human MX2 is an interferon-induced post-entry inhibitor of HIV-1 infection
    2013 443 citations Torsten Schaller, Reiner Schulz et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Reiner Schulz United Kingdom 22 1.2k 740 388 380 339 41 2.0k
Valérie Cheynet France 16 1.0k 0.8× 327 0.4× 272 0.7× 119 0.3× 276 0.8× 34 1.7k
Michaël Imbeault Switzerland 22 1.8k 1.4× 412 0.6× 281 0.7× 259 0.7× 86 0.3× 23 2.4k
Cécile Esnault France 16 2.1k 1.7× 421 0.6× 316 0.8× 390 1.0× 106 0.3× 20 2.8k
Ying Lian China 25 2.1k 1.7× 489 0.7× 522 1.3× 477 1.3× 696 2.1× 70 3.4k
Guy Oriol France 16 875 0.7× 290 0.4× 213 0.5× 68 0.2× 210 0.6× 38 1.4k
Edward J. Hollox United Kingdom 28 1.2k 1.0× 1.4k 1.9× 787 2.0× 65 0.2× 144 0.4× 72 3.1k
Lorraine M. Albritton United States 25 983 0.8× 726 1.0× 782 2.0× 625 1.6× 37 0.1× 44 2.6k
Marc Friedli Switzerland 14 1.2k 1.0× 260 0.4× 419 1.1× 879 2.3× 31 0.1× 15 2.1k
Ann A. Kiessling United States 25 1.0k 0.8× 482 0.7× 144 0.4× 201 0.5× 205 0.6× 85 2.0k
Donna L. Mallery United Kingdom 24 1.4k 1.1× 402 0.5× 833 2.1× 396 1.0× 25 0.1× 29 2.9k

Countries citing papers authored by Reiner Schulz

Since Specialization
Citations

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

Fields of papers citing papers by Reiner Schulz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reiner Schulz

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

All Works

20 of 20 papers shown
1.
Rocha, Azucena, Ferdinand von Meyenn, Donal P. McLornan, et al.. (2021). Hydroxycarbamide effects on DNA methylation and gene expression in myeloproliferative neoplasms. Genome Research. 31(8). 1381–1394. 4 indexed citations
2.
Comitani, Federico, Rodrigo P. Feliciano, Leonie Johanna Jahn, et al.. (2021). Extraction and high-throughput sequencing of oak heartwood DNA: Assessing the feasibility of genome-wide DNA methylation profiling. PLoS ONE. 16(11). e0254971–e0254971. 2 indexed citations
3.
Barkas, Nikolaos, Maurício Machaim Franco, Michael Cowley, et al.. (2021). Imprinted Gene Expression and Function of the Dopa Decarboxylase Gene in the Developing Heart. Frontiers in Cell and Developmental Biology. 9. 676543–676543. 10 indexed citations
4.
Cowley, Michael, et al.. (2020). Transcription of intragenic CpG islands influences spatiotemporal host gene pre-mRNA processing. Nucleic Acids Research. 48(15). 8349–8359. 10 indexed citations
5.
Ficarelli, Mattia, Rupert Hugh-White, Andrew E. Firth, et al.. (2019). CpG Dinucleotides Inhibit HIV-1 Replication through Zinc Finger Antiviral Protein (ZAP)-Dependent and -Independent Mechanisms. Journal of Virology. 94(6). 54 indexed citations
6.
Čvoro, Aleksandra, Antonio Galleu, Carl Hobbs, et al.. (2017). Effects of maternal obesity on Wharton’s Jelly mesenchymal stromal cells. Scientific Reports. 7(1). 17595–17595. 11 indexed citations
7.
Apolonia, Luis, Reiner Schulz, Tomaž Curk, et al.. (2015). Promiscuous RNA Binding Ensures Effective Encapsidation of APOBEC3 Proteins by HIV-1. PLoS Pathogens. 11(1). e1004609–e1004609. 75 indexed citations
8.
Ishida, Miho, Stefanie Böhm, Jennifer M. Frost, et al.. (2015). Genome-wide methylation analysis in Silver–Russell syndrome patients. Human Genetics. 134(3). 317–332. 17 indexed citations
9.
Saadeh, Heba & Reiner Schulz. (2014). Protection of CpG islands against de novo DNA methylation during oogenesis is associated with the recognition site of E2f1 and E2f2. Epigenetics & Chromatin. 7(1). 26–26. 17 indexed citations
10.
11.
Cowley, Michael, et al.. (2012). Epigenetic control of alternative mRNA processing at the imprinted Herc3/Nap1l5 locus. Nucleic Acids Research. 40(18). 8917–8926. 40 indexed citations
12.
13.
Meaburn, Emma L. & Reiner Schulz. (2011). Next generation sequencing in epigenetics: Insights and challenges. Seminars in Cell and Developmental Biology. 23(2). 192–199. 63 indexed citations
14.
Hernández, Mónica, Reiner Schulz, Tracy Chaplin, et al.. (2010). The diagnosis of inherited metabolic diseases by microarray gene expression profiling. Orphanet Journal of Rare Diseases. 5(1). 34–34. 3 indexed citations
15.
Schulz, Reiner, Charlotte Proudhon, Timothy H. Bestor, et al.. (2010). The Parental Non-Equivalence of Imprinting Control Regions during Mammalian Development and Evolution. PLoS Genetics. 6(11). e1001214–e1001214. 50 indexed citations
16.
Irving, Melita, Karin Buiting, Deniz Kanber, et al.. (2010). Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14. American Journal of Medical Genetics Part A. 152A(8). 1942–1950. 27 indexed citations
17.
Schulz, Reiner, Yoko Ikeda, Melissa Spielman, et al.. (2008). MATERNALLY EXPRESSED PAB C-TERMINAL , a Novel Imprinted Gene in Arabidopsis , Encodes the Conserved C-Terminal Domain of Polyadenylate Binding Proteins. The Plant Cell. 20(9). 2387–2398. 90 indexed citations
18.
Wood, Andrew J., Roland G. Roberts, David Monk, et al.. (2007). A Screen for Retrotransposed Imprinted Genes Reveals an Association between X Chromosome Homology and Maternal Germ-Line Methylation. PLoS Genetics. 3(2). e20–e20. 102 indexed citations
19.
Schulz, Reiner. (2006). Chromosome-wide identification of novel imprinted genes using microarrays and uniparental disomies. Nucleic Acids Research. 34(12). e88–e88. 57 indexed citations
20.
Schulz, Reiner, et al.. (2006). Nondisjunction and transmission ratio distortion ofChromosome 2 in a (2.8) Robertsonian translocation mouse strain. Mammalian Genome. 17(3). 239–247. 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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