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Experimental Dermatology|April 19, 2012
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identifiedSilke Redler, Rachid Tazi-Ahnini, Dmitriy Drichel, et al.
Archives of Dermatological Research|November 6, 2012
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair lossHassnaa Mahmoudi, Silke Redler, Pattie Birch, et al.
Familial Cancer|January 19, 2016
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposisIsabel Spier, Martin Kerick, Dmitriy Drichel, et al.
Journal of Medical Genetics|November 29, 2015
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis casesIsabel Spier, Dmitriy Drichel, Martin Kerick, et al.
Plos One|July 23, 2013
High-throughput miRNA and mRNA sequencing of paired colorectal normal, tumor and metastasis tissues and bioinformatic modeling of miRNA-1 therapeutic applicationsChristina Röhr, Martin Kerick, Axel Fischer, et al.
Archives of Dermatological Research|December 20, 2013
Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair lossRima Nuwaihyd, Silke Redler, Stefanie Heilmann, et al.
Nature Communications|May 3, 2018
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval EuropeansBen Krause-Kyora, Marcel Nutsua, Lisa Boehme, et al.
European Journal of Human Genetics : EJHG|December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish modelsNina Ishorst, Selina Hölzel, Carola Greve, et al.
The Journal of Investigative Dermatology|January 30, 2013
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiologyStefanie Heilmann, Amy K Kiefer, Nadine Fricker, et al.
Nature Communications|December 14, 2017
Identification and characterization of two functional variants in the human longevity gene FOXO3Friederike Flachsbart, Janina Dose, Liljana Gentschew, et al.
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