Corinna Friedrich

1.8k total citations
25 papers, 768 citations indexed

About

Corinna Friedrich is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Corinna Friedrich has authored 25 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 8 papers in Genetics. Recurrent topics in Corinna Friedrich's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sperm and Testicular Function (7 papers) and Sexual Differentiation and Disorders (6 papers). Corinna Friedrich is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sperm and Testicular Function (7 papers) and Sexual Differentiation and Disorders (6 papers). Corinna Friedrich collaborates with scholars based in Germany, United States and Netherlands. Corinna Friedrich's co-authors include Frank Tüttelmann, Birgit Stallmeyer, Eric Schulze‐Bahr, Sven Zumhagen, Sabine Kliesch, Margot J. Wyrwoll, Niels Decher, Susanne Rinné, Manon S. Oud and Horst Schroten and has published in prestigious journals such as Circulation Research, Endocrinology and European Heart Journal.

In The Last Decade

Corinna Friedrich

21 papers receiving 765 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinna Friedrich Germany 15 459 244 236 198 158 25 768
Akiko Takizawa Japan 13 437 1.0× 315 1.3× 188 0.8× 24 0.1× 235 1.5× 33 804
Karin Bundschu Germany 11 445 1.0× 79 0.3× 110 0.5× 42 0.2× 82 0.5× 19 613
Lyndsey Craven United Kingdom 13 784 1.7× 103 0.4× 42 0.2× 57 0.3× 125 0.8× 17 957
Hiroshi Imahie Japan 7 394 0.9× 72 0.3× 55 0.2× 98 0.5× 74 0.5× 16 513
André Stutz Switzerland 6 646 1.4× 136 0.6× 52 0.2× 34 0.2× 171 1.1× 7 886
Tania Sorg France 15 306 0.7× 120 0.5× 63 0.3× 38 0.2× 35 0.2× 27 571
Ketty Bacallao Chile 14 155 0.3× 92 0.4× 324 1.4× 14 0.1× 132 0.8× 18 579
Michela Ripolone Italy 13 349 0.8× 63 0.3× 47 0.2× 34 0.2× 33 0.2× 40 526
Maria Lucia Scaldaferri Italy 10 298 0.6× 90 0.4× 143 0.6× 6 0.0× 174 1.1× 12 545
Nathan Airhart United States 10 251 0.5× 151 0.6× 19 0.1× 185 0.9× 12 0.1× 15 589

Countries citing papers authored by Corinna Friedrich

Since Specialization
Citations

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

Fields of papers citing papers by Corinna Friedrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinna Friedrich

This figure shows the co-authorship network connecting the top 25 collaborators of Corinna Friedrich. A scholar is included among the top collaborators of Corinna Friedrich 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 Corinna Friedrich. Corinna Friedrich 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.
Gaikwad, Avinash, Margot J. Wyrwoll, Claudia Krallmann, et al.. (2025). Functional and clinical insights into nuclear receptor variants for advancing precision diagnostics in male infertility. EBioMedicine. 119. 105899–105899.
2.
Dunleavy, Jessica E. M., Daniela Fietz, Adrian Pilatz, et al.. (2025). Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes. EMBO Molecular Medicine. 17(6). 1417–1451.
3.
Friedrich, Corinna & Frank Tüttelmann. (2024). Genetics of female and male infertility. Medizinische Genetik. 36(3). 161–170.
4.
Houston, Brendan J., D. Jo Merriner, Anne E. O’Connor, et al.. (2024). AXDND1 is required to balance spermatogonial commitment and for sperm tail formation in mice and humans. Cell Death and Disease. 15(7). 499–499. 5 indexed citations
5.
Friedrich, Corinna, Eric Bareke, Frank Tüttelmann, et al.. (2024). A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertility. Journal of Assisted Reproduction and Genetics. 41(3). 751–756.
6.
Houston, Brendan J., Anne E. O’Connor, Degang Wang, et al.. (2022). Human INHBB Gene Variant (c.1079T>C:p.Met360Thr) Alters Testis Germ Cell Content, but Does Not Impact Fertility in Mice. Endocrinology. 163(3). 5 indexed citations
7.
Gaikwad, Avinash, Birgit Stallmeyer, Daniela Fietz, et al.. (2022). Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility. Fertility and Sterility. 119(2). 219–228. 7 indexed citations
8.
Wyrwoll, Margot J., Albrecht Röpke, Marius Wöste, et al.. (2022). Analysis of copy number variation in men with non‐obstructive azoospermia. Andrology. 10(8). 1593–1604. 9 indexed citations
9.
Houston, Brendan J., Antoni Riera‐Escamilla, Margot J. Wyrwoll, et al.. (2021). A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships. Human Reproduction Update. 28(1). 15–29. 140 indexed citations
10.
Fernández, Lucia Torres, Sibylle Mitschka, Marius Wöste, et al.. (2021). TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility. Frontiers in Cell and Developmental Biology. 9. 658966–658966. 18 indexed citations
11.
Rinné, Susanne, Birgit Stallmeyer, Aytuğ K. Kiper, et al.. (2020). POPDC2 a novel susceptibility gene for conduction disorders. Journal of Molecular and Cellular Cardiology. 145. 74–83. 17 indexed citations
12.
Schilit, Samantha L.P., Corinna Friedrich, Tammy Kammin, et al.. (2019). SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility. The American Journal of Human Genetics. 106(1). 41–57. 66 indexed citations
13.
Röpke, Albrecht, Marius Wöste, Rolf Jessberger, et al.. (2019). Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest. Human Reproduction. 34(11). 2112–2119. 58 indexed citations
14.
Decher, Niels, Corinna Friedrich, Marcus Schewe, et al.. (2017). Sodium permeable and “hypersensitive” TREK ‐1 channels cause ventricular tachycardia. EMBO Molecular Medicine. 9(4). 403–414. 54 indexed citations
15.
Stallmeyer, Birgit, S. Kotthoff, Sven Zumhagen, et al.. (2017). A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction. Circulation Research. 120(10). e33–e44. 32 indexed citations
16.
Wemhöner, Konstantin, Corinna Friedrich, Birgit Stallmeyer, et al.. (2015). Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. Journal of Molecular and Cellular Cardiology. 80. 186–195. 71 indexed citations
17.
Anneken, Lars, Stefan Baumann, Péter Biliczki, et al.. (2015). Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking. European Heart Journal. 37(7). 640–650. 35 indexed citations
18.
Friedrich, Corinna, Susanne Rinné, Sven Zumhagen, et al.. (2014). Gain‐of‐function mutation in TASK ‐4 channels and severe cardiac conduction disorder. EMBO Molecular Medicine. 6(7). 937–951. 50 indexed citations
19.
Tenenbaum, Tobias, Ulrike Steinmann, Corinna Friedrich, et al.. (2013). Culture models to study leukocyte trafficking across the choroid plexus. Fluids and Barriers of the CNS. 10(1). 1–1. 69 indexed citations
20.
Zumhagen, Sven, Birgit Stallmeyer, Corinna Friedrich, et al.. (2012). Inherited long QT syndrome. Herzschrittmachertherapie + Elektrophysiologie. 23(3). 211–219. 10 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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