Research Topics
Genomes and GenesSpecies | Axel M HillmerSummaryAffiliation: University of Bonn Country: Germany Publications
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Detail Information
Publications
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26Axel M Hillmer
Department of Genomics, Life and Brain Center, University of Bonn, D 53127 Bonn, Germany
Am J Hum Genet 82:737-43. 2008..97 (empirical p value = 0.00055). This is the first step toward the identification of new susceptibility genes in AGA, a process which will provide important insights into the molecular and cellular basis of scalp hair loss...
Susceptibility variants for male-pattern baldness on chromosome 20p11Axel M Hillmer
Department of Genomics, Life and Brain Center, University of Bonn, D 53127 Bonn, Germany
Nat Genet 40:1279-81. 2008..7 x 10(-15)). No interaction was detected with the X-chromosomal androgen receptor locus, suggesting that the 20p11 locus has a role in a yet-to-be-identified androgen-independent pathway...
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldnessAxel M Hillmer
Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany
Hum Genet 126:255-64. 2009..It is therefore probable that the AGA risk haplotype rose to high frequency in combination with this EDA2R variant, possibly by hitchhiking on a positively selected 57K haplotype...
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataLina M Forstbauer
Institute of Human Genetics, University of Bonn, Bonn, Germany
Eur J Hum Genet 20:326-32. 2012..43 × 10(-4) (OR=1.24 (1.10-1.39)). This SNP maps to an intronic region of the SPATA5 (spermatogenesis-associated protein 5) gene on chromosome 4. The results therefore suggest the SPATA5 locus is a new susceptibility locus for AA...
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaAxel M Hillmer
Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany
Am J Hum Genet 77:140-8. 2005..The X-chromosomal location of AR stresses the importance of the maternal line in the inheritance of AGA...
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic diseaseRegina C Betz
Institute of Human Genetics, University of Bonn, Bonn, Germany
J Invest Dermatol 127:2539-43. 2007..003; odds ratio (OR)=5.47 (95% confidence interval (CI): 1.59-18.76)). In conclusion, our data suggest that when AA occurs in conjunction with FLG-associated atopic disorder, the clinical presentation of AA may be more severe...
The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein functionFelix F Brockschmidt
Department of Genomics, Life and Brain Center, University of Bonn, Sigmund Freud Strasse 25, 53127 Bonn, Germany
J Mol Endocrinol 39:1-8. 2007..In conclusion, our data provide evidence of functional differences between the two most common alleles of the AR GGN repeat, supporting its potential role in the development of human traits...
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexiaJohannes Schumacher
Institute of Human Genetics, University of Bonn, Bonn, Germany
Am J Hum Genet 78:52-62. 2006....
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthSandra M Pasternack
Institute of Human Genetics, University of Bonn, Bonn 53111, Germany
Nat Genet 40:329-34. 2008..This finding may provide opportunities for new therapeutic approaches to the treatment of hair loss in humans...
