Peter Wieacker

7.8k total citations
141 papers, 3.8k citations indexed

About

Peter Wieacker is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Peter Wieacker has authored 141 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Molecular Biology, 72 papers in Genetics and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Peter Wieacker's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (48 papers), Sexual Differentiation and Disorders (39 papers) and Prenatal Screening and Diagnostics (17 papers). Peter Wieacker is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (48 papers), Sexual Differentiation and Disorders (39 papers) and Prenatal Screening and Diagnostics (17 papers). Peter Wieacker collaborates with scholars based in Germany, United States and Poland. Peter Wieacker's co-authors include Susanne Ledig, Hans‐Hilger Ropers, Sibylle Jakubiczka, Ilse Wieland, Albrecht Röpke, Thomas F. Wienker, Markus Stümm, Petra Muschke, Sabine Kliesch and Kay E. Davies and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Cancer Research.

In The Last Decade

Peter Wieacker

134 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Wieacker Germany 35 2.4k 1.6k 397 393 392 141 3.8k
Marc Jeanpierre France 37 3.8k 1.6× 1.3k 0.8× 515 1.3× 209 0.5× 181 0.5× 120 4.7k
Hong Lei United States 21 5.0k 2.1× 1.8k 1.1× 584 1.5× 198 0.5× 268 0.7× 27 5.7k
Veronica J. Roberts United States 29 2.0k 0.8× 502 0.3× 124 0.3× 890 2.3× 884 2.3× 41 3.3k
Laurence Legeai‐Mallet France 36 2.7k 1.1× 2.5k 1.5× 199 0.5× 394 1.0× 364 0.9× 87 4.7k
Svetlana A. Yatsenko United States 26 1.5k 0.6× 1.8k 1.1× 628 1.6× 523 1.3× 519 1.3× 110 3.0k
Giandomenico Palka Italy 31 1.5k 0.6× 1.5k 0.9× 515 1.3× 648 1.6× 330 0.8× 145 3.3k
Maki Fukami Japan 35 3.7k 1.5× 3.6k 2.2× 881 2.2× 787 2.0× 398 1.0× 307 5.9k
Hoon‐Ki Sung Canada 26 3.4k 1.4× 555 0.3× 128 0.3× 172 0.4× 303 0.8× 63 5.2k
Michael B. Petersen Greece 34 1.7k 0.7× 1.9k 1.1× 1.1k 2.8× 87 0.2× 412 1.1× 172 4.1k
Marika Charalambous United Kingdom 22 1.7k 0.7× 1.0k 0.6× 792 2.0× 48 0.1× 124 0.3× 39 3.0k

Countries citing papers authored by Peter Wieacker

Since Specialization
Citations

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

Fields of papers citing papers by Peter Wieacker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Wieacker

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Wieacker. A scholar is included among the top collaborators of Peter Wieacker 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 Peter Wieacker. Peter Wieacker 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.
Römer, Thomas, Karina Kapczuk, Cordula Schippert, et al.. (2019). Sequence Variants in <b><i>TBX6</i></b> Are Associated with Disorders of the Müllerian Ducts: An Update. Sexual Development. 13(1). 35–40. 8 indexed citations
2.
Röpke, Albrecht, et al.. (2013). Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report. Journal of Assisted Reproduction and Genetics. 30(12). 1553–1558. 6 indexed citations
3.
Psathaki, Olympia E., Karin Hübner, Davood Sabour, et al.. (2011). Ultrastructural Characterization of Mouse Embryonic Stem Cell-Derived Oocytes and Granulosa Cells. Stem Cells and Development. 20(12). 2205–2215. 16 indexed citations
4.
Tüttelmann, Frank, Manuela Simoni, Sabine Kliesch, et al.. (2011). Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome. PLoS ONE. 6(4). e19426–e19426. 105 indexed citations
5.
Pennekamp, Petra, et al.. (2009). 11-P013 Gene expression in WT and Pkd2 mutant mouse embryos. Mechanisms of Development. 126. S187–S188. 1 indexed citations
6.
Wieacker, Peter, I. Knoke, & Sibylle Jakubiczka. (2009). Clinical and molecular aspects of androgen receptor defects. Experimental and Clinical Endocrinology & Diabetes. 106(6). 446–452. 3 indexed citations
7.
Skalej, Martin, et al.. (2007). Novel chromosomal aberrations in a recurrent malignant meningioma. Cancer Genetics and Cytogenetics. 174(1). 48–53. 7 indexed citations
8.
Köhler, Birgit, Lin Lin, Bruno Ferraz‐de‐Souza, et al.. (2007). Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency. Human Mutation. 29(1). 59–64. 106 indexed citations
9.
Wieacker, Peter, et al.. (2005). Empfehlungen zur genetischen Diagnostik bei Aborten. Journal für Kardiologie (Krause & Pachernegg GmbH). 2(3). 148–150. 1 indexed citations
10.
Röpke, Albrecht, Peter Buhtz, Malte Böhm, et al.. (2005). Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer. Oncogene. 24(44). 6667–6675. 27 indexed citations
11.
Ludwig, Michael, Jörg Gromoll, Ute Hehr, & Peter Wieacker. (2004). Stellungnahme der Arbeitsgemeinschaft Reproduktionsgenetik der Deutschen Gesellschaft für Reproduktionsmedizin: Empfehlung zur genetischen Diagnostik bei Kinderwunschpaaren. Journal für Kardiologie (Krause & Pachernegg GmbH). 1(3). 190–193. 3 indexed citations
12.
Röpke, Albrecht, et al.. (2004). Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes. American Journal of Obstetrics and Gynecology. 190(4). 1059–1062. 18 indexed citations
13.
Röpke, Albrecht, E. P. Allhoff, & Peter Wieacker. (2004). Mutationen des Androgenrezeptor-Gens als mögliche Ursache der Antiandrogenresistenz beim Prostatakarzinom. 1(3). 194–201. 1 indexed citations
14.
Jentsch‐Ullrich, Kathleen, Holger Braun, Michael Koenigsmann, et al.. (2004). Complete molecular remission in a patient with Philadelphia-chromosome positive acute myeloid leukemia after conventional therapy and imatinib.. PubMed. 89(5). ECR15–ECR15. 31 indexed citations
15.
Winter, Carsten, Susanne tom Dieck, Tobias M. Boeckers, et al.. (1999). The Presynaptic Cytomatrix Protein Bassoon: Sequence and Chromosomal Localization of the HumanBSNGene. Genomics. 57(3). 389–397. 22 indexed citations
16.
Knoke, I., et al.. (1997). A(870)E mutation of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and sertoli cell tumor. Cancer Genetics and Cytogenetics. 98(2). 139–141. 10 indexed citations
17.
Wieacker, Peter, et al.. (1990). Prognose von Drillingsschwangerschaften. Geburtshilfe und Frauenheilkunde. 50(9). 701–709. 1 indexed citations
18.
Wieacker, Peter, G. Wolff, Thomas F. Wienker, et al.. (1985). A new X‐linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia. American Journal of Medical Genetics. 20(4). 597–606. 39 indexed citations
19.
Wieacker, Peter, Kay E. Davies, Howard J. Cooke, et al.. (1984). Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.. PubMed. 36(2). 265–76. 137 indexed citations
20.
Wieacker, Peter, Nina Horn, P. Pearson, et al.. (1983). Menkes kinky hair disease: A search for closely linked restriction fragment length polymorphism. Human Genetics. 64(2). 139–142. 18 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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