Almuth Caliebe

5.0k total citations
66 papers, 1.4k citations indexed

About

Almuth Caliebe is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Almuth Caliebe has authored 66 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 31 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Almuth Caliebe's work include Prenatal Screening and Diagnostics (19 papers), Epigenetics and DNA Methylation (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Almuth Caliebe is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Epigenetics and DNA Methylation (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Almuth Caliebe collaborates with scholars based in Germany, United Kingdom and United States. Almuth Caliebe's co-authors include Reiner Siebert, Dagmar Wieczorek, Gabriele Gillessen‐Kaesbach, Karin Buiting, J. Jenderny, Susanne Bens, Bernhard Horsthemke, Ole Ammerpohl, Ron Hochstenbach and U. Gembruch and has published in prestigious journals such as Nature, Blood and The Journal of Immunology.

In The Last Decade

Almuth Caliebe

61 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Almuth Caliebe Germany 23 678 655 324 113 97 66 1.4k
Vimla S. Aggarwal United States 17 361 0.5× 523 0.8× 238 0.7× 76 0.7× 114 1.2× 34 1.0k
Salim Aftimos New Zealand 19 690 1.0× 812 1.2× 119 0.4× 39 0.3× 253 2.6× 72 1.5k
Sibel Kantarci United States 15 1.0k 1.5× 821 1.3× 385 1.2× 50 0.4× 248 2.6× 23 1.8k
Teresa Mattina Italy 18 839 1.2× 764 1.2× 181 0.6× 60 0.5× 101 1.0× 59 1.4k
Erawati V. Bawle United States 17 442 0.7× 562 0.9× 229 0.7× 75 0.7× 91 0.9× 38 1.1k
Beate Albrecht Germany 23 1.0k 1.5× 862 1.3× 264 0.8× 52 0.5× 214 2.2× 45 1.7k
Ashwin Dalal India 20 543 0.8× 651 1.0× 202 0.6× 104 0.9× 132 1.4× 151 1.4k
Frans A. Hol Netherlands 21 407 0.6× 1.0k 1.5× 216 0.7× 68 0.6× 221 2.3× 41 1.6k
Evica Rajcan‐Separovic Canada 24 770 1.1× 775 1.2× 386 1.2× 111 1.0× 66 0.7× 58 1.6k
Alma Kuechler Germany 19 722 1.1× 649 1.0× 238 0.7× 60 0.5× 61 0.6× 46 1.2k

Countries citing papers authored by Almuth Caliebe

Since Specialization
Citations

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

Fields of papers citing papers by Almuth Caliebe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Almuth Caliebe

This figure shows the co-authorship network connecting the top 25 collaborators of Almuth Caliebe. A scholar is included among the top collaborators of Almuth Caliebe 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 Almuth Caliebe. Almuth Caliebe 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.
Händler, Kristian, et al.. (2025). Comprehensive androgen-dependent transcriptome analysis in human genital tissue. BMC Genomics. 26(1). 1047–1047.
2.
3.
Knerr, Julian, Ralf Werner, Carsten Schwan, et al.. (2023). Formin-mediated nuclear actin at androgen receptors promotes transcription. Nature. 617(7961). 616–622. 28 indexed citations
4.
Kloth, Katja, et al.. (2020). Mucopolysaccharidosis type I due to maternal uniparental disomy of chromosome 4 with partial isodisomy of 4p16.3p15.2. Molecular Genetics and Metabolism Reports. 25. 100660–100660. 2 indexed citations
5.
Hornig, Nadine, Eva Maria Murga Penas, Almuth Caliebe, et al.. (2019). Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism. The Journal of Clinical Endocrinology & Metabolism. 104(10). 4630–4638. 4 indexed citations
6.
Hoff, Kirstin, Marta Lemme, Anne‐Karin Kahlert, et al.. (2019). DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs. Clinical Epigenetics. 11(1). 89–89. 12 indexed citations
7.
Nagel, Inga, Marius Bartels, Johannes Duell, et al.. (2017). Hematopoietic stem cell involvement in BCR-ABL1–positive ALL as a potential mechanism of resistance to blinatumomab therapy. Blood. 130(18). 2027–2031. 63 indexed citations
8.
Heidemann, Simone, et al.. (2017). CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohort. Archives of Gynecology and Obstetrics. 297(1). 147–152. 6 indexed citations
9.
Kolarova, Julia, Ole Ammerpohl, Jana Gutwein, et al.. (2015). In vivo Investigations of the Effect of Short- and Long-Term Recombinant Growth Hormone Treatment on DNA-Methylation in Humans. PLoS ONE. 10(3). e0120463–e0120463. 7 indexed citations
10.
Ammerpohl, Ole, Jana Gutwein, Andreas Schmutzler, et al.. (2014). Array-based DNA methylation profiling in male infertility reveals allele-specific DNA methylation in PIWIL1 and PIWIL2. Fertility and Sterility. 101(4). 1097–1103.e1. 32 indexed citations
11.
Hotz, Alrun, Yorck Hellenbroich, Jürgen Sperner, et al.. (2013). Microdeletion 5q14.3 and anomalies of brain development. American Journal of Medical Genetics Part A. 161(9). 2124–2133. 25 indexed citations
12.
Beygo, Jasmin, Ole Ammerpohl, Julia Richter, et al.. (2013). Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient with Multiple Methylation Defects. PLoS ONE. 8(10). e76953–e76953. 25 indexed citations
13.
Eckmann-Scholz, Christel, Susanne Bens, Julia Kolarova, et al.. (2012). DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples. PLoS ONE. 7(6). e39014–e39014. 24 indexed citations
14.
Naik, Swati, N. Simon Thomas, Justin H. Davies, et al.. (2011). Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain. Molecular Syndromology. 2(2). 76–80. 4 indexed citations
15.
Helbig, Ingo, Jochen Brasch, Ingrid Haußer, et al.. (2009). Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system—a novel entity?. European Journal of Pediatrics. 169(4). 495–500. 3 indexed citations
16.
Weimer, Jörg, Almuth Caliebe, Katrin Õunap, et al.. (2006). Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay*. American Journal of Medical Genetics Part A. 140A(5). 488–495. 8 indexed citations
17.
Chavarría‐Soley, Gabriela, et al.. (2006). Novel CYP1B1 and Known PAX6 Mutations in Anterior Segment Dysgenesis (ASD). Journal of Glaucoma. 15(6). 499–504. 38 indexed citations
18.
Morava, Éva, et al.. (2002). Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics. 161(11). 619–622. 23 indexed citations
19.
Gembruch, U., Ahmet Baschat, Almuth Caliebe, & Ludwig Gortner. (1998). Prenatal diagnosis of ductus venosus agenesis: a report of two cases and review of the literature. Ultrasound in Obstetrics and Gynecology. 11(3). 185–189. 40 indexed citations
20.
Caliebe, Almuth, Stephan Waltz, & J. Jenderny. (1997). Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient. Clinical Genetics. 52(2). 116–119. 27 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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