W. Schempp

6.3k total citations · 1 hit paper
125 papers, 4.5k citations indexed

About

W. Schempp is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, W. Schempp has authored 125 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Genetics, 70 papers in Molecular Biology and 68 papers in Plant Science. Recurrent topics in W. Schempp's work include Chromosomal and Genetic Variations (65 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (62 papers) and Genomic variations and chromosomal abnormalities (26 papers). W. Schempp is often cited by papers focused on Chromosomal and Genetic Variations (65 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (62 papers) and Genomic variations and chromosomal abnormalities (26 papers). W. Schempp collaborates with scholars based in Germany, United States and United Kingdom. W. Schempp's co-authors include Gerd Scherer, U. Wolf, Jutta Wirth, Jobst Meyer, Juan J. Pasantes, Thomas Wagner, Niels Tommerup, Michael Schmid, F. Dagna Bricarelli and Elisabeth Hustert and has published in prestigious journals such as Cell, Nature Genetics and PLoS ONE.

In The Last Decade

W. Schempp

122 papers receiving 4.3k citations

Hit Papers

Autosomal sex reversal and campomelic dysplasia are cause... 1994 2026 2004 2015 1994 400 800 1.2k
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. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
    1994 1.2k citations Thomas Wagner, Jutta Wirth et al. Cell profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
W. Schempp Germany 33 3.1k 2.8k 1.4k 627 330 125 4.5k
Toshiaki Noce Japan 29 2.0k 0.6× 3.7k 1.3× 783 0.6× 903 1.4× 218 0.7× 60 4.9k
Jamie W. Foster United Kingdom 12 3.9k 1.3× 3.1k 1.1× 571 0.4× 1.1k 1.7× 265 0.8× 12 4.6k
Stephen T. Reeders United States 37 2.9k 0.9× 2.9k 1.0× 849 0.6× 185 0.3× 263 0.8× 83 5.7k
Nigel Vivian United Kingdom 9 3.8k 1.2× 4.3k 1.5× 365 0.3× 1.3k 2.0× 314 1.0× 11 5.8k
David Zarkower United States 46 5.2k 1.7× 3.8k 1.4× 716 0.5× 1.8k 2.8× 252 0.8× 81 7.6k
Indrajit Nanda Germany 33 2.4k 0.8× 1.4k 0.5× 961 0.7× 324 0.5× 160 0.5× 75 3.6k
Silvana Guioli Italy 24 3.9k 1.3× 3.5k 1.2× 346 0.2× 1.5k 2.3× 273 0.8× 34 5.2k
H. Hameister Germany 47 2.6k 0.9× 4.3k 1.5× 1.3k 0.9× 232 0.4× 505 1.5× 193 6.7k
F.F.B. Elder United States 31 2.2k 0.7× 2.1k 0.8× 667 0.5× 175 0.3× 158 0.5× 76 3.9k
Shogo Matoba Japan 32 2.0k 0.7× 5.5k 1.9× 394 0.3× 710 1.1× 191 0.6× 76 6.4k

Countries citing papers authored by W. Schempp

Since Specialization
Citations

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

Fields of papers citing papers by W. Schempp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W. Schempp

This figure shows the co-authorship network connecting the top 25 collaborators of W. Schempp. A scholar is included among the top collaborators of W. Schempp 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 W. Schempp. W. Schempp 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.
Radner, Franz P.W., Slaheddine Marrakchi, Gwang-Jin Kim, et al.. (2013). Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans. PLoS Genetics. 9(6). 37 indexed citations
2.
Pasantes, Juan J., et al.. (2011). Heterogeneity of Pericentric Inversions of the Human Y Chromosome. Cytogenetic and Genome Research. 132(4). 219–226. 23 indexed citations
3.
Dai, Fangping, Florian Leese, W. Schempp, et al.. (2011). Diversification and Molecular Evolution of ATOH8, a Gene Encoding a bHLH Transcription Factor. PLoS ONE. 6(8). e23005–e23005. 22 indexed citations
4.
Kirsch, Stefan, Juan J. Pasantes, Nadja Bogdanova, et al.. (2009). Correction: Chromosomal evolution of the PKD1 gene family in primates (vol 8, pg 263, 2008). BMC Evolutionary Biology. 2 indexed citations
5.
Lin, Yi, et al.. (2008). Evolution of the DAZ gene and the AZFc region on primate Y chromosomes. BMC Evolutionary Biology. 8(1). 96–96. 22 indexed citations
6.
Kirsch, Stefan, Juan J. Pasantes, Andreas Wolf, et al.. (2008). Chromosomal evolution of the PKD1 gene family in primates. BMC Evolutionary Biology. 8(1). 263–263. 9 indexed citations
7.
Kirsch, Stefan, Claudia Münch, Zhaoshi Jiang, et al.. (2008). Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions. Genome Research. 18(7). 1030–1042. 26 indexed citations
8.
Kuo, Pao‐Lin, Chao‐Chin Hsu, P. H. Vogt, et al.. (2005). Polymorphisms associated with the DAZ genes on the human Y chromosome. Genomics. 86(4). 431–438. 34 indexed citations
9.
Kirsch, Stefan, Birgit Weiß, Tracie L. Miner, et al.. (2005). Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome. Genome Research. 15(2). 195–204. 28 indexed citations
10.
Tsui, Shanli, et al.. (2000). Identification of Two Novel Proteins That Interact with Germ-Cell-Specific RNA-Binding Proteins DAZ and DAZL1. Genomics. 65(3). 266–273. 114 indexed citations
11.
Schempp, W., et al.. (1997). Mapping chromosomal homology between humans and the black-handed spider monkey by fluorescence in situ hybridization. Chromosome Research. 5(8). 527–536. 54 indexed citations
12.
Toder, Roland, Birgitta Gläser, K. Schiebel, et al.. (1997). Genes Located In and Near the Human Pseudoautosomal Region are Located in the X-Y Pairing Region in Dog and Sheep. Chromosome Research. 5(5). 301–306. 35 indexed citations
13.
Arnold, Norbert, et al.. (1996). Overrepresentation of 3q and 8q material and loss of 18q material are recurrent findings in advanced human ovarian cancer. Genes Chromosomes and Cancer. 16(1). 46–54. 111 indexed citations
14.
Schempp, W., et al.. (1995). The immunoglobulin κ locus of primates. Genomics. 25(3). 623–629. 23 indexed citations
15.
Wagner, Thomas, Jutta Wirth, Jobst Meyer, et al.. (1994). Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell. 79(6). 1111–1120. 1236 indexed citations breakdown →
16.
Thompson, John R., Klaus Wagner, Sabine Barnert, et al.. (1990). The human pregnancy-specific glycoprotein genes are tightly linked on the long arm of chromosome 19 and are coordinately expressed. Biochemical and Biophysical Research Communications. 167(2). 848–859. 52 indexed citations
17.
Kiechle‐Schwarz, M., et al.. (1989). Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome. Human Genetics. 82(2). 127–130. 17 indexed citations
18.
Neumann, Hartmut P.H., Otto Müller, Bruce A.J. Ponder, et al.. (1989). Early diagnosis of multiple endocrine neoplasia type IIa. Journal of Molecular Medicine. 67(18). 951–956. 2 indexed citations
19.
Weber, Bernhard H. F., W. Schempp, & Hartmut Wiesner. (1986). An evolutionarily conserved early replicating segment on the sex chromosomes of man and the great apes. Cytogenetic and Genome Research. 43(1-2). 72–78. 24 indexed citations
20.
Schmid, Michael, W. Schempp, & J. Olert. (1982). Comparative analysis of karyotypes in European shrew species. Cytogenetic and Genome Research. 34(1-2). 124–135. 9 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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