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

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

#	Work	Indexed citations
1	The sperm-specific K+ channel Slo3 is inhibited by albumin and steroids contained in reproductive fluids 2024 ·Frontiers in Cell and Developmental Biology ·(unknown), (unknown), (unknown), Alexandra Kulle, Paul Martin Holterhus, Manfred Fobker, (unknown), Verena Nordhoff, Hermann M. Behre, Timo Strünker, Christoph Brenker	1
2	New liquid chromatography tandem mass spectrometry reference data for estradiol show mini-puberty in both sexes and typical pre-pubertal and pubertal patterns 2024 ·European Journal of Endocrinology ·Alexandra Kulle, Amke Caliebe, (unknown), Thomas Reinehr, (unknown), Esther Schulz, Michaela Kleber, Juliane Rothermel, Sabine Heger, Olaf Hiort, Paul‐Martin Holterhus	1
3	Pilot study shows suppression of mineralocorticoid precursors under high-dose glucocorticoid therapy in pediatric acute lymphoblastic leukemia 2023 ·Endocrine Connections ·Paul‐Martin Holterhus, Alexandra Kulle, (unknown), (unknown), (unknown), Simon Vieth, Melchior Lauten	2
4	Classic genetic and hormonal switches during fetal sex development and beyond 2023 ·Medizinische Genetik ·Paul‐Martin Holterhus, Alexandra Kulle, Hauke Busch, Malte Spielmann	0
5	Salivary Diurnal Glucocorticoid Profiles in Monozygotic Twins With Intratwin Birthweight Differences 2023 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), (unknown), Felix Schreiner, (unknown), Peter Bartmann, Paul‐Martin Holterhus, Alexandra Kulle, Bettina Gohlke	0
6	Diabetes Type 1 Negatively Influences Leydig Cell Function in Rats, Which is Partially Reversible By Insulin Treatment 2021 ·Endocrinology ·Isabel Viola Wagner, Nora Klöting, (unknown), (unknown), Alexandra Kulle, (unknown), Jörg Dötsch, Olaf Hiort, Konstantin Svechnikov, Olle Söder	17
7	Lack of Evidence for a Relationship Between the Hypothalamus-Pituitary-Adrenal and the Hypothalamus-Pituitary-Thyroid Axis in Adolescent Depression 2021 ·Frontiers in Endocrinology ·Raphael Hirtz, Lars Libuda, Anke Hinney, Manuel Föcker, Judith Bühlmeier, Jochen Antel, Paul‐Martin Holterhus, Alexandra Kulle, (unknown), Johannes Hebebrand, Corinna Grasemann	19
8	CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development 2020 ·Scientific Reports ·Rédouane Aherrahrou, Alexandra Kulle, Natália Alenina, Ralf Werner, (unknown), Michael Bäder, Heribert Schunkert, Jeanette Erdmann, Zouhair Aherrahrou	24
9	Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY Mosaicism 2019 ·The Journal of Clinical Endocrinology & Metabolism ·Nadine Hornig, (unknown), (unknown), Eva Maria Murga Penas, Almuth Caliebe, (unknown), Hans‐Udo Schweikert, Laura Audí, Olaf Hiort, Ralf Werner, Alexandra Kulle, Ole Ammerpohl, Paul‐Martin Holterhus	4
10	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 2019 ·SHILAP Revista de lepidopterología ·Velibor Tasić, Adele Mitrotti, (unknown), Alexandra Kulle, Nidal Abu Laban, Momir Polenaković, (unknown), Simone Sanna‐Cherchi, (unknown), Zoran Gucev	12
11	Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II) 2018 ·The Journal of Clinical Endocrinology & Metabolism ·Nadine Hornig, (unknown), Helmuth G. Dörr, Nina C. Hubner, Alexandra Kulle, (unknown), (unknown), Susanne Bens, Olaf Hiort, Ralf Werner, (unknown), (unknown), Martine Cools, (unknown), Hendrik G. Stunnenberg, Reiner Siebert, Ole Ammerpohl, Paul-Martin Holterhus	22
12	Multiples of Median-Transformed, Normalized Reference Ranges of Steroid Profiling Data Independent of Age, Sex, and Units 2018 ·Hormone Research in Paediatrics ·(unknown), Thomas Reinehr, Marek Niedziela, Christoph Borzikowsky, (unknown), (unknown), (unknown), Sabine Heger, Nadine Hornig, Paul‐Martin Holterhus, Alexandra Kulle	6
13	Prenatal maternal distress seems to be associated with the infant’s temperament and motor development: an explorative study 2017 ·Journal of Neural Transmission ·(unknown), Uwe Niederberger, Alexandra Kulle, (unknown), (unknown), (unknown), Paul‐Martin Holterhus, Wolf‐Dieter Gerber, Michael Siniatchkin	11
14	A Recurrent Germline Mutation in the 5’UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation 2016 ·PLoS ONE ·Nadine Hornig, Carine de Beaufort, Friederike Denzer, Martine Cools, Martin Wabitsch, (unknown), Alexandra Kulle, Hans‐Udo Schweikert, Ralf Werner, Olaf Hiort, Laura Audí, Reiner Siebert, Ole Ammerpohl, Paul‐Martin Holterhus	33
15	46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the <b><i>HSD17B3</i></b> Gene 2014 ·Sexual Development ·Mona Ellaithi, Ralf Werner, Felix G. Riepe, Nils Krone, Alexandra Kulle, (unknown), Alaa K. Kamel, Wiebke Arlt, Paul‐Martin Holterhus, (unknown), Olaf Hiort	8
16	17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the <b><i>CYP17A1</i></b> Gene 2014 ·Hormone Research in Paediatrics ·(unknown), Stefan A. Wudy, Felix G. Riepe, Paul‐Martin Holterhus, (unknown), Michaela F. Hartmann, Alexandra Kulle, (unknown), Joachim Grötzinger, Ralf L. Schild, Sabine Heger	4
17	Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency 2014 ·European Journal of Endocrinology ·(unknown), Alexandra Kulle, Züleyha Karaca, Ilker Akkurt, (unknown), Fahrettin Keleştimur, Joachim Grötzinger, Paul‐Martin Holterhus, Felix G. Riepe	19
18	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 2013 ·Hormone Research in Paediatrics ·Bilgin Yüksel, Alexandra Kulle, Fatih Gürbüz, (unknown), Leman Damla Kotan, Eda Mengen, Paul‐Martin Holterhus, A. Kemal Topaloğlu, Joachim Grötzinger, Felix G. Riepe	7
19	Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family 2011 ·General and Comparative Endocrinology ·Ilhem Ben Charfeddine, Felix G. Riepe, (unknown), Alexandra Kulle, (unknown), Ons Mamaï, (unknown), A. Mili, (unknown), Saad Hasan Mohammed Ali, Paul‐Martin Holterhus, Moez Gribaa	15
20	CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency 2011 ·PLoS ONE ·(unknown), (unknown), Felix G. Riepe, Richard J. Auchus, Alexandra Kulle, Paul Martin Holterhus, (unknown), (unknown), (unknown), Hung Chun Chen	18

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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