W. Schempp

6.3k citations

125 papers · 4.5k indexed · 1 hit paper · h-index 33

Impact in

Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Animal Genetics and Reproduction
Reproductive Medicine top 1%
- Sperm and Testicular Function

Papers in ⓘ

Genetics 93
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 62
- Genomic variations and chromosomal abnormalities 26
- Animal Genetics and Reproduction 13
Plant Science 68
- Chromosomal and Genetic Variations 65

Co-authors: Gerd Scherer (10 shared papers)U. Wolf (8 shared papers)Jutta Wirth (3 shared papers)Juan J. Pasantes (12 shared papers)Jobst Meyer (3 shared papers)Thomas Wagner (2 shared papers)Niels Tommerup (2 shared papers)Michael Schmid (7 shared papers)
Journals: Human Genetics (27 papers)Cytogenetic and Genome Research (25 papers)Chromosome Research (14 papers)Chromosoma (7 papers)BMC Evolutionary Biology (4 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

W. Schempp

122 papers receiving 4.3k citations

Hit Papers

align trajectories log scale

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 1994 · 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside W. Schempp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with W. Schempp Line = papers co-authored together W. Schempp links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 125 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 Cell ·Thomas Wagner, Jutta Wirth, Jobst Meyer, Bernhard Zabel, M. Held, Jürgen Zimmer, Juan J. Pasantes, F. Dagna Bricarelli, Jürgen Keutel, Elisabeth Hustert, U. Wolf, Niels Tommerup, W. Schempp, Gerd Scherer Hit paper breakdown →	1994	1236
2	Assignment of an autosomal sex reversa– locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3–q25.1 Nature Genetics ·Niels Tommerup, W. Schempp, Peter Meinecke, S. Pedersen, Lars Bolund, C. Brandt, Carll Goodpasture, Per Guldberg, K. R. Held, H. Reinwein, Ola Didrik Saugstad, Gerd Scherer, Ola H. Skjeldal, Roland Toder, Jostein Westvik, C. B. van der Hagen, U. Wolf	1993	143
3	Centromere repositioning in mammals Heredity ·Mariano Rocchi, Nicoletta Archidiacono, W. Schempp, Oronzo Capozzi, Roscoe Stanyon	2011	137
4	Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans PLoS Genetics ·Franz P.W. Radner, Slaheddine Marrakchi, Peter Kirchmeier, Gwang-Jin Kim, Florence Ribiérre, B. Kamoun, Leïla Abid, M. Leipoldt, H. Turki, W. Schempp, Roland Heilig, Mark Lathrop, Judith Fischer	2013	115
5	Identification of Two Novel Proteins That Interact with Germ-Cell-Specific RNA-Binding Proteins DAZ and DAZL1 Genomics ·Shanli Tsui, Tiane Dai, Susanne Roettger, W. Schempp, Eduardo Salido, Pauline H. Yen	2000	114
6	Overrepresentation of 3q and 8q material and loss of 18q material are recurrent findings in advanced human ovarian cancer Genes Chromosomes and Cancer ·Norbert Arnold, Lorenz Hägele, Lioba Walz, W. Schempp, Jacobus Pfisterer, Thomas Bauknecht, Marion Kiechle	1996	111
7	Chromosome banding and DNA replication patterns in bird karyotypes Cytogenetic and Genome Research ·Michael Schmid, E. Enderle, Detlev Schindler, W. Schempp	1989	97
8	Chromosome banding in amphibia Chromosoma ·W. Schempp, Michael Schmid	1981	93
9	Cytologic evidence for three human X-chromosomal segments escaping inactivation Human Genetics ·W. Schempp, Barbara Meer	1983	89
10	Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9 Human Genetics ·Jutta Wirth, Thomas Wagner, Jobst Meyer, Rudolf A. Pfeiffer, H. U. Tietze, W. Schempp, Gerd Scherer	1996	82
11	Comparative mapping ofYRRM- andTSPY-related cosmids in man and hominoid apes Chromosome Research ·W. Schempp, Andreas Binkele, Joachim Arnemann, Birgitta Gl�ser, Kun Ma, Kay Taylor, Roland Toder, Jonathan Wolfe, S. Zeitler, Ann C. Chandley	1995	81
12	Chromosomal localization of the carcinoembryonic antigen gene family and differential expression in various tumors. PubMed ·Wolfgang Zimmermann, Bernhard H. F. Weber, B. Ortlieb, Fritz Rudert, W. Schempp, H. H. Fiebig, John E. Shively, S. von Kleist, John A. Thompson	1988	77
13	Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man Human Genetics ·Gerd Scherer, W. Schempp, C Baccichetti, Elisabetta Lenzini, FrancaDagna Bricarelli, LauraDoriaLamba Carbone, U. Wolf	1989	64
14	A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates PLoS Genetics ·Anne Averdam, Beatrix Petersen, Cornelia Rosner, Jennifer Neff, Christian Roos, Manfred Eberle, Fabienne Aujard, Claudia Münch, W. Schempp, Mary Carrington, Takashi Shiina, Hidetoshi Inoko, Florian Knaust, Penny Coggill, Harminder Sehra, Stephan Beck, Laurent Abi-Rached, Richard Reinhardt, Lutz Walter	2009	58
15	Mapping chromosomal homology between humans and the black-handed spider monkey by fluorescence in situ hybridization Chromosome Research ·M. A. Morescalchi, W. Schempp, Stefania Consigliere, F. Bigoni, Johannes Wienberg, Roscoe Stanyon	1997	54
16	Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome Human Genetics ·Violaine Goidts, D.N. Cooper, Lluı́s Armengol, W. Schempp, Jeffrey M. Conroy, Xavier Estivill, Norma J. Nowak, H. Hameister, Hildegard Kehrer‐Sawatzki	2006	54
17	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 ·John R. Thompson, Rosa Koumari, Klaus Wagner, Sabine Barnert, Cathrin Schleussner, Heinrich Schrewe, Wolfgang Zimmermann, Gaby Müller, W. Schempp, Daniela Zaninetta, Domenico Ammaturo, Norman Hardman	1990	52
18	Simian Y Chromosomes: species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY Mammalian Genome ·Birgitta Gläser, Frank Grützner, Ulrike Willmann, Roscoe Stanyon, Norbert Arnold, Kay Taylor, W. Rietschel, S. Zeitler, Roland Toder, W. Schempp	1998	50
19	Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs) Chromosome Research ·Hjalmar S. Kühl, Susanne Röttger, H. Heilbronner, H. Enders, W. Schempp	2001	44
20	Human Endogenous Retrovirus Family HERV-K(HML-5): Status, Evolution, and Reconstruction of an Ancient Betaretrovirus in the Human Genome Journal of Virology ·Laurence Lavie, Patrik Medstrand, W. Schempp, Eckart Meese, Jens Mayer	2004	43

About W. Schempp

W. Schempp is a scholar working on Genetics, Plant Science, Reproductive Medicine, Molecular Biology and Cancer Research, having authored 125 papers that have together received 4.5k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (65 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (62 papers), Genomic variations and chromosomal abnormalities (26 papers), Genomics and Chromatin Dynamics (23 papers), Sexual Differentiation and Disorders (17 papers), Sperm and Testicular Function (14 papers), Animal Genetics and Reproduction (13 papers) and Genomics and Phylogenetic Studies (6 papers). The work is most often cited by research in Genetics (3.1k citations), Reproductive Medicine (627 citations), Molecular Biology (2.8k citations), Plant Science (1.4k citations) and Developmental Biology (61 citations). W. Schempp has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Gerd Scherer, U. Wolf, Jutta Wirth, Juan J. Pasantes, Jobst Meyer, Thomas Wagner, Niels Tommerup, Michael Schmid, Bernhard Zabel and Elisabeth Hustert. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Chromosome Research, Chromosoma and BMC Evolutionary Biology.

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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