Alexandra Kulle

1.6k total citations
57 papers, 995 citations indexed

About

Alexandra Kulle is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Alexandra Kulle has authored 57 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Endocrinology, Diabetes and Metabolism, 32 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in Alexandra Kulle's work include Sexual Differentiation and Disorders (30 papers), Hormonal and reproductive studies (29 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Alexandra Kulle is often cited by papers focused on Sexual Differentiation and Disorders (30 papers), Hormonal and reproductive studies (29 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Alexandra Kulle collaborates with scholars based in Germany, Italy and Netherlands. Alexandra Kulle's co-authors include Paul‐Martin Holterhus, Felix G. Riepe, Olaf Hiort, Thomas Reinehr, Nina Lass, D. Melchior, Barbara Wolters, Stefan A. Wudy, Ralf Werner and Juliane Rothermel and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Alexandra Kulle

55 papers receiving 985 citations

Peers

Alexandra Kulle

EDM

GENET

PHEOH

Laëtitia Martinerie France

Lam P Ly Australia

Willem de Ronde Netherlands

Kerry J. McInnes United Kingdom

L.J.G. Gooren Netherlands

J. Homoki Germany

Carina Ankarberg‐Lindgren Sweden

Stefano Lello Italy

C. Wang United States

Mónica Fernández‐Cancio Spain

Laëtitia Martinerie France

Alexandra Kulle

635 ×1.2

EDM

648 ×1.2

309 ×1.3

GENET

188 ×1.0

107 ×0.9

PHEOH

Citations per year, relative to Alexandra Kulle Alexandra Kulle (= 1×) peers Laëtitia Martinerie

Countries citing papers authored by Alexandra Kulle

Since Specialization

Citations

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

Fields of papers citing papers by Alexandra Kulle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandra Kulle

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra Kulle. A scholar is included among the top collaborators of Alexandra Kulle 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 Alexandra Kulle. Alexandra Kulle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kulle, Alexandra, Paul Martin Holterhus, Manfred Fobker, et al.. (2024). The sperm-specific K+ channel Slo3 is inhibited by albumin and steroids contained in reproductive fluids. Frontiers in Cell and Developmental Biology. 12. 1275116–1275116. 1 indexed citations

Kulle, Alexandra, Amke Caliebe, Thomas Reinehr, et al.. (2024). New liquid chromatography tandem mass spectrometry reference data for estradiol show mini-puberty in both sexes and typical pre-pubertal and pubertal patterns. European Journal of Endocrinology. 190(5). 401–408. 1 indexed citations

Holterhus, Paul‐Martin, et al.. (2023). Pilot study shows suppression of mineralocorticoid precursors under high-dose glucocorticoid therapy in pediatric acute lymphoblastic leukemia. Endocrine Connections. 12(10). 2 indexed citations

Holterhus, Paul‐Martin, Alexandra Kulle, Hauke Busch, & Malte Spielmann. (2023). Classic genetic and hormonal switches during fetal sex development and beyond. Medizinische Genetik. 35(3). 163–171.

Schreiner, Felix, et al.. (2023). Salivary Diurnal Glucocorticoid Profiles in Monozygotic Twins With Intratwin Birthweight Differences. The Journal of Clinical Endocrinology & Metabolism. 109(1). e40–e50.

Wagner, Isabel Viola, Nora Klöting, Alexandra Kulle, et al.. (2021). Diabetes Type 1 Negatively Influences Leydig Cell Function in Rats, Which is Partially Reversible By Insulin Treatment. Endocrinology. 162(4). 17 indexed citations

Hirtz, Raphael, Lars Libuda, Anke Hinney, et al.. (2021). Lack of Evidence for a Relationship Between the Hypothalamus-Pituitary-Adrenal and the Hypothalamus-Pituitary-Thyroid Axis in Adolescent Depression. Frontiers in Endocrinology. 12. 662243–662243. 19 indexed citations

Aherrahrou, Rédouane, Alexandra Kulle, Natália Alenina, et al.. (2020). CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development. Scientific Reports. 10(1). 8792–8792. 24 indexed citations

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

10.

Tasić, Velibor, Adele Mitrotti, Alexandra Kulle, et al.. (2019). Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature. SHILAP Revista de lepidopterología. 22(1). 81–88. 12 indexed citations

11.

Hornig, Nadine, Helmuth G. Dörr, Nina C. Hubner, et al.. (2018). Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II). The Journal of Clinical Endocrinology & Metabolism. 103(12). 4617–4627. 22 indexed citations

12.

Reinehr, Thomas, Marek Niedziela, Christoph Borzikowsky, et al.. (2018). Multiples of Median-Transformed, Normalized Reference Ranges of Steroid Profiling Data Independent of Age, Sex, and Units. Hormone Research in Paediatrics. 89(4). 255–264. 6 indexed citations

13.

Niederberger, Uwe, et al.. (2017). Prenatal maternal distress seems to be associated with the infant’s temperament and motor development: an explorative study. Journal of Neural Transmission. 124(7). 881–890. 11 indexed citations

14.

Hornig, Nadine, Carine de Beaufort, Friederike Denzer, et al.. (2016). A Recurrent Germline Mutation in the 5’UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation. PLoS ONE. 11(4). e0154158–e0154158. 33 indexed citations

15.

Ellaithi, Mona, Ralf Werner, Felix G. Riepe, et al.. (2014). 46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 Gene. Sexual Development. 8(4). 151–155. 8 indexed citations

16.

Wudy, Stefan A., Felix G. Riepe, Paul‐Martin Holterhus, et al.. (2014). 17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene. Hormone Research in Paediatrics. 81(5). 350–355. 4 indexed citations

17.

Kulle, Alexandra, Züleyha Karaca, Ilker Akkurt, et al.. (2014). Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency. European Journal of Endocrinology. 170(5). 697–706. 19 indexed citations

18.

Yüksel, Bilgin, Alexandra Kulle, Fatih Gürbüz, et al.. (2013). The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development. Hormone Research in Paediatrics. 80(3). 163–169. 7 indexed citations

19.

Charfeddine, Ilhem Ben, Felix G. Riepe, Alexandra Kulle, et al.. (2011). Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family. General and Comparative Endocrinology. 175(3). 514–518. 15 indexed citations

20.

Riepe, Felix G., et al.. (2011). CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency. PLoS ONE. 6(9). e25492–e25492. 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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