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N. Hornig · SciRah

Researcher profile · Semantic Scholar

N. Hornig

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N. Hornig — researcher profile on SciRah

h-index: 13
Works: 35
Citations: 2,076

Most-cited papers

The regulated retrotransposon transcriptome of mammalian cells
G. Faulkner, Y. Kimura, Carsten O. Daub, Shivangi Wani +18 more
2009Nature Genetics807 citations
Semantic Scholar
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing
J. Richter, M. Schlesner, S. Hoffmann, M. Kreuz +51 more
2012Nature Genetics540 citations
Semantic Scholar
The dual mechanism of separase regulation by securin.
N. Hornig, P. P. Knowles, N. McDonald, F. Uhlmann
2002Current Biology146 citations Open access
Semantic Scholar
Preferential cleavage of chromatin‐bound cohesin after targeted phosphorylation by Polo‐like kinase
N. Hornig, F. Uhlmann
2004EMBO Journal91 citations Open access
Semantic Scholar
Enhancer of zeste homolog 2 overexpression has a role in the development of anaplastic thyroid carcinomas.
E. Borbone, G. Troncone, A. Ferraro, Zuzana Jasencakova +5 more
2011Journal of Clinical Endocrinology and Metabolism76 citations Open access
Semantic Scholar
Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity
N. Hornig, M. Ukat, H. Schweikert, O. Hiort +21 more
2016Journal of Clinical Endocrinology and Metabolism68 citations Open access
Semantic Scholar
Studies on Substrate Recognition by the Budding Yeast Separase*
M. Sullivan, N. Hornig, T. Porstmann, F. Uhlmann
2004Journal of Biological Chemistry60 citations Open access
Semantic Scholar
Formin-mediated nuclear actin at androgen receptors promotes transcription
Julian Knerr, R. Werner, Carsten Schwan, Hong Wang +7 more
2023Nature53 citations Open access
Semantic Scholar
A Recurrent Germline Mutation in the 5’UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF Translation
N. Hornig, C. D. de Beaufort, Friederike Denzer, M. Cools +10 more
2016PLoS ONE52 citations Open access
Semantic Scholar
Molecular basis of androgen insensitivity syndromes.
N. Hornig, P. Holterhus
2020Molecular and Cellular Endocrinology48 citations
Semantic Scholar
A quantitative proteomics tool to identify DNA-protein interactions in primary cells or blood.
N. Hubner, L. Nguyen, N. Hornig, H. Stunnenberg
2015Journal of Proteome Research43 citations
Semantic Scholar
Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II)
N. Hornig, P. Rodens, H. Dörr, N. Hubner +14 more
2018Journal of Clinical Endocrinology and Metabolism27 citations Open access
Semantic Scholar
Determination of 17OHPreg and DHEAS by LC-MS/MS: Impact of Age, Sex, Pubertal Stage, and BMI on the &Dgr;5 Steroid Pathway
A. Kulle, T. Reinehr, G. Šimić-Schleicher, N. Hornig +1 more
2017Journal of Clinical Endocrinology and Metabolism17 citations
Semantic Scholar
Growth, puberty and testicular function in boys born small for gestational age with a nonspecific disorder of sex development
L. Tack, S. van der Straaten, S. Riedl, A. Springer +21 more
2021Clinical Endocrinology9 citations
Semantic Scholar
Multiples of Median-Transformed, Normalized Reference Ranges of Steroid Profiling Data Independent of Age, Sex, and Units
D. Zalas, T. Reinehr, M. Niedziela, C. Borzikowsky +7 more
2018Hormone Research in Paediatrics8 citations
Semantic Scholar
Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?
H. Fabbri-Scallet, R. Werner, M. Guaragna, J. R. D. de Andrade +5 more
2022Sexual Development7 citations
Semantic Scholar
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
J. Pozojevic, Radhika Sivaprasad, J. Laß, Franziska Haarich +11 more
2024Scientific Reports6 citations Open access
Semantic Scholar
Carbon source-dependent transcriptional regulation of the QCR8 gene in Kluyveromyces lactis.
J. F. Brons, Agnieszka Dryla, Esther B. Plüger, T. M. F. Vinkenvleugel +3 more
2001Current Genetics6 citations
Semantic Scholar
The past and future of “sex genes”
C. Rehmann-Sutter, N. Hornig, Birgit Stammberger, H. Stoff
2023Medizinische Genetik5 citations Open access
Semantic Scholar
Reduced androgen receptor expression in genital skin fibroblasts from patients with 45,X/46,XY mosaicism.
N. Hornig, J. Demiri, P. Rodens, E. M. Murga Penas +9 more
2019Journal of Clinical Endocrinology and Metabolism5 citations Open access
Semantic Scholar
Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development
Hannah L Marko, N. Hornig, R. Betz, P. Holterhus +6 more
2022Human Mutation3 citations Open access
Semantic Scholar
Comprehensive androgen-dependent transcriptome analysis in human genital tissue
Radhika Sivaprasad, K. Händler, A. Caliebe, M. Spielmann +2 more
2025BMC Genomics2 citations Open access
Semantic Scholar
Hormonal Control of Fetal Sex Development
N. Hornig, A. Kulle, P. Holterhus
2019Encyclopedia of Endocrine Diseases1 citations
Semantic Scholar
Exonisation of an Alu element in the 3’-UTR contributes to SRD5A2 deficiency
R. Werner, Anna Basina, A. Künstner, S. Prakash +8 more
2026Scientific Reports0 citations Open access
Semantic Scholar
Modeling hormone-associated differences in human neurodevelopment using hiPSC-derived GnRH neurons
Alisa Weltken, P. Ramesh, L. Blobaum, B. Brandl +3 more
2026Endocrine Abstracts0 citations
Semantic Scholar
A new variant in the 3'-UTR of the SRD5A2 gene leads to highly efficient exonisation of an Alu element and contributes to 5[alpha]-steroid reductase type 2 deficiency
R. Werner, Anna Basina, A. Künstner, Chandra Prakash Sudharsan Agas +8 more
2026Endocrine Abstracts0 citations
Semantic Scholar
Robust prediction of response to growth hormone therapy by five PBMC-based transcripts
Valerie van Kekem, Irene Victoria Bermúdez-Pérez, A. Kulle, M. Welzel +5 more
2026Genes and Diseases0 citations Open access
Semantic Scholar
A Case of Gonadal Dysgenesis Due to a Novel Homozygous Mutation in NR5A2 Gene
Friederike Denzer, C. Denzer, N. Hornig, P. Holterhus +2 more
20180 citations
Semantic Scholar
A Laboratory Harmonization Strategy for Steroid Hormone Profiling by MoM-Transformed, Normalized Reference Ranges Independent of Age, Sex and Units
A. Kulle, D. Zalas, T. Reinehr, M. Niedziela +9 more
20180 citations
Semantic Scholar
The use of apolipoprotein D as a biomarker for androgen sensitivity identifies a new type of androgen insensitivity syndrome that is not associated with a mutation in the androgen receptor gene
N. Hornig, M. Ukat, H. Schweikert, O. Hiort +21 more
20160 citations
Semantic Scholar
Correlation of AR Expression and AR Transcriptional Activity in Cultured Human Genital Fibroblasts
N. Hornig, P. Rodens, M. Ukat, J. Demiri +5 more
20150 citations
Semantic Scholar
Next generation sequencing and functional characterization of the androgen receptor (AR) gene in patients with androgen insensitivity syndrome (AIS) and controls
N. Hornig, H. Schweikert, M. Ukat, A. Kulle +14 more
20150 citations
Semantic Scholar
LC-MSMS Profiling of Plasma Steroids in Different Types of Congenital Adrenal Hyperplasia
A. Kulle, T. Reinehr, H. I. Akkurt, Christian Commentz +5 more
20140 citations
Semantic Scholar
Next Generation Sequencing of the Androgen Receptor Gene in Patients With Androgen Insensitivity Syndrome and Controls
N. Hornig, H. Schweikert, M. Ukat, A. Kulle +10 more
20140 citations
Semantic Scholar
Regulation of cohesin cleavage by separase in Saccharomyces cerevisiae.
N. Hornig
20040 citations
Semantic Scholar

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O. Ammerpohl×9
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H. Schweikert — researcher profile on SciRah

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M. Ukat — researcher profile on SciRah

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