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S. Sabrautzki · SciRah

Researcher profile · Semantic Scholar

S. Sabrautzki

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S. Sabrautzki — researcher profile on SciRah

h-index: 13
Works: 36
Citations: 443

Most-cited papers

Peroxidasin is essential for eye development in the mouse
Xiaohe Yan, S. Sabrautzki, M. Horsch, H. Fuchs +4 more
2014Human Molecular Genetics68 citations Open access
Semantic Scholar
The elevation of circulating fibroblast growth factor 23 without kidney disease does not increase cardiovascular disease risk.
E. Pastor-Arroyo, N. Gehring, C. Krudewig, S. Costantino +11 more
2018Kidney International61 citations Open access
Semantic Scholar
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia
S. Diener, S. Bayer, S. Sabrautzki, T. Wieland +14 more
2016Mammalian Genome32 citations
Semantic Scholar
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
S. Sabrautzki, I. Rubio-Aliaga, W. Hans, H. Fuchs +13 more
2012Mammalian Genome28 citations Open access
Semantic Scholar
New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts
S. Kunze, C. Dalke, H. Fuchs, M. Klaften +8 more
2015PLoS ONE26 citations Open access
Semantic Scholar
An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.
S. Sabrautzki, E. Janas, B. Lorenz-Depiereux, J. Calzada-Wack +15 more
2013American Journal of Pathology24 citations Open access
Semantic Scholar
Cytoplasmic Mislocalization of POU3F4 Due to Novel Mutations Leads to Deafness in Humans and Mice
T. Parzefall, Shaked Shivatzki, Danielle R. Lenz, B. Rathkolb +11 more
2013Human Mutation22 citations Open access
Semantic Scholar
Point mutation of Ffar1 abrogates fatty acid-dependent insulin secretion, but protects against HFD-induced glucose intolerance
S. Sabrautzki, G. Kaiser, Gerhard K. H. Przemeck, F. Gerst +8 more
2017Molecular Metabolism20 citations Open access
Semantic Scholar
Combining fish and environmental PCR for diagnostics of diseased laboratory zebrafish in recirculating systems
Manuel Miller, S. Sabrautzki, Andreas Beyerlein, M. Brielmeier
2019PLoS ONE19 citations Open access
Semantic Scholar
A point mutation in the Pdia6 gene results in loss of pancreatic β-cell identity causing overt diabetes
N. Chhabra, Anna-Lena Amend, Aimée Bastidas-Ponce, S. Sabrautzki +9 more
2021Molecular Metabolism18 citations Open access
Semantic Scholar
Systemic Jak1 activation provokes hepatic inflammation and imbalanced FGF23 production and cleavage
Arezoo Daryadel, P. Ruiz, N. Gehring, D. Stojanović +11 more
2021The FASEB Journal17 citations Open access
Semantic Scholar
Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice
Sudhir Kumar, B. Rathkolb, E. Kemter, S. Sabrautzki +21 more
2016PLoS ONE15 citations Open access
Semantic Scholar
Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice
Xiaohe Yan, J. Atorf, D. Ramos, F. Thiele +14 more
2020Investigative Ophthalmology and Visual Science13 citations Open access
Semantic Scholar
Gender-, strain-, and inheritance-dependent variation in aldosterone secretion in mice.
A. Spyroglou, S. Sabrautzki, B. Rathkolb, T. Bozoglu +4 more
2012Journal of Endocrinology12 citations Open access
Semantic Scholar
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1I27N mutant mice
Sudhir Kumar, B. Rathkolb, S. Sabrautzki, S. Krebs +19 more
2017Journal of Biomedical Sciences10 citations Open access
Semantic Scholar
Enhanced oxidative stress and endocrine pancreas alterations are linked to a novel glucokinase missense mutation in ENU-derived Munich Gck(D217V) mutants.
L. van Buerck, M. Schuster, B. Rathkolb, S. Sabrautzki +5 more
2012Molecular and Cellular Endocrinology8 citations
Semantic Scholar
Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon
O. Puk, Xiaohe Yan, S. Sabrautzki, H. Fuchs +3 more
2013Molecular Vision7 citations
Semantic Scholar
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
H. Fuchs, S. Sabrautzki, H. Seedorf, B. Rathkolb +14 more
2012European Journal of Oral Sciences7 citations Open access
Semantic Scholar
Welfare Assessment of Adult Laboratory Zebrafish: A Practical Guide
S. Sabrautzki, Manuel Miller, E. Kague, M. Brielmeier
2021Zebrafish6 citations
Semantic Scholar
Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia
S. Vetrivel, N. Tiso, Andrea Kügler, M. Irmler +9 more
2019Experimental Eye Research6 citations Open access
Semantic Scholar
Viable EdnraY129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation
S. Sabrautzki, Michael Sandholzer, B. Lorenz-Depiereux, R. Brommage +24 more
2016Mammalian Genome5 citations Open access
Semantic Scholar
The Calcium-sensing receptor (CaSR) has only a PTH-dependent role in the acute response of renal phosphatetransporters to phosphate intake.
Arezoo Daryadel, Catharina Küng, Betul Haykir, S. Sabrautzki +4 more
2024AJP - Renal Physiology4 citations
Semantic Scholar
New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance
Tanja Klein-Rodewald, Kateryna Micklich, A. Sanz-Moreno, Monica Tost +28 more
2022bioRxiv3 citations Open access
Semantic Scholar
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels
B. Rathkolb, M. Klempt, S. Sabrautzki, Dian Michel +12 more
2015Biometals3 citations
Semantic Scholar
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia
S. Diener, S. Bayer, S. Sabrautzki, T. Wieland +14 more
2016Mammalian Genome2 citations
Semantic Scholar
Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
S. Sabrautzki, I. Rubio-Aliaga, W. Hans, H. Fuchs +13 more
2014Mammalian Genome2 citations Open access
Semantic Scholar
In Vitro Characterization Of TNSALP Mutations From Two Novel Mouse Models For Hypophosphatasia
B. Mentrup, S. Sabrautzki, C. Hofmann, M. D. de Angelis +1 more
20122 citations
Semantic Scholar
Role of free fatty acid signaling in islet function
E. Lorza-Gil, G. Przemeck, ER Ulven, S. Sabrautzki +6 more
2018Diabetologie und Stoffwechsel0 citations
Semantic Scholar
Mutation in the Crybb1 gene encoding beta-B1-crystallin leads to recessive cataracts in the mouse
J. Graw, O. Amarie, D. Kumar, Angelika Scheideler +3 more
20170 citations
Semantic Scholar
Splice‐site mutation in the Bmpr1b gene of the mouse causes optic nerve head dysgenesis and retinal gliosis
J. Graw, Xiaohe Yan, O. Amarie, O. Puk +5 more
20160 citations
Semantic Scholar
Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over
S. Derdak, S. Sabrautzki, M. D. de Angelis, M. Gut +2 more
2015BMC Genomics0 citations Open access
Semantic Scholar
Mutation in the Ercc2 gene of the mouse causes cataracts
J. Graw, S. Kunze, C. Dalke, H. Fuchs +3 more
20150 citations
Semantic Scholar
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels
B. Rathkolb, M. Klempt, S. Sabrautzki, Dian Michel +12 more
2015Biometals0 citations
Semantic Scholar
Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
S. Sabrautzki, I. Rubio-Aliaga, W. Hans, H. Fuchs +13 more
2014Mammalian Genome0 citations Open access
Semantic Scholar
Mice with point mutations in Ffar1 display impaired glucose tolerance
G. Kaiser, F. Gerst, S. Ullrich, H. Häring +3 more
20140 citations
Semantic Scholar
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
S. Sabrautzki, I. Rubio-Aliaga, W. Hans, H. Fuchs +13 more
2012Mammalian Genome0 citations Open access
Semantic Scholar

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