Kruse R - Search Results

1

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.

Hillmer AM, Kruse R, Macciardi F, Heyn U, Betz RC, Ruzicka T, Propping P, Nöthen MM, Cichon S. Hillmer AM, et al. Among authors: kruse r. Br J Dermatol. 2002 Apr;146(4):601-8. doi: 10.1046/j.1365-2133.2002.04766.x. Br J Dermatol. 2002. PMID: 11966690

2

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM. Hillmer AM, et al. Among authors: kruse r. Am J Hum Genet. 2005 Jul;77(1):140-8. doi: 10.1086/431425. Epub 2005 May 18. Am J Hum Genet. 2005. PMID: 15902657 Free PMC article.

3

Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.

Redler S, Kruse R, Eigelshoven S, Hanneken S, Refke M, Wen Y, Zhang X, Cichon S, Betz RC, Nöthen MM. Redler S, et al. Among authors: kruse r. J Am Acad Dermatol. 2011 Apr;64(4):e45-50. doi: 10.1016/j.jaad.2010.06.013. Epub 2010 Jul 24. J Am Acad Dermatol. 2011. PMID: 20659777

4

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Cichon S, Anker M, Vogt IR, Rohleder H, Pützstück M, Hillmer A, Farooq SA, Al-Dhafri KS, Ahmad M, Haque S, Rietschel M, Propping P, Kruse R, Nöthen MM. Cichon S, et al. Among authors: kruse r. Hum Mol Genet. 1998 Oct;7(11):1671-9. doi: 10.1093/hmg/7.11.1671. Hum Mol Genet. 1998. PMID: 9736769

5

Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.

Kruse R, Cichon S, Anker M, Hillmer AM, Barros-Núñez P, Cantú JM, Leal E, Weinlich G, Schmuth M, Fritsch P, Ruzicka T, Propping P, Nöthen MM. Kruse R, et al. J Invest Dermatol. 1999 Dec;113(6):954-9. doi: 10.1046/j.1523-1747.1999.00790.x. J Invest Dermatol. 1999. PMID: 10594736 Free article.

6

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.

Cichon S, Kruse R, Hillmer AM, Kukuk G, Anker M, Altland K, Knapp M, Propping P, Nöthen MM. Cichon S, et al. Among authors: kruse r. Br J Dermatol. 2000 Oct;143(4):811-4. doi: 10.1046/j.1365-2133.2000.03781.x. Br J Dermatol. 2000. PMID: 11069461

7

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.

Betz RC, König K, Flaquer A, Redler S, Eigelshoven S, Kortüm AK, Hanneken S, Hillmer A, Tüting T, Lambert J, De Weert J, Kruse R, Lutz G, Blaumeiser B, Nöthen MM. Betz RC, et al. Among authors: kruse r. Br J Dermatol. 2008 Feb;158(2):389-91. doi: 10.1111/j.1365-2133.2007.08312.x. Epub 2007 Nov 19. Br J Dermatol. 2008. PMID: 18028494

8

The TRAF1/C5 locus confers risk for familial and severe alopecia areata.

Redler S, Brockschmidt FF, Forstbauer L, Giehl KA, Herold C, Eigelshoven S, Hanneken S, De Weert J, Lutz G, Wolff H, Kruse R, Blaumeiser B, Böhm M, Becker T, Nöthen MM, Betz RC. Redler S, et al. Among authors: kruse r. Br J Dermatol. 2010 Apr;162(4):866-9. doi: 10.1111/j.1365-2133.2009.09598.x. Epub 2009 Dec 17. Br J Dermatol. 2010. PMID: 20030635

9

Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.

Brockschmidt FF, Heilmann S, Ellis JA, Eigelshoven S, Hanneken S, Herold C, Moebus S, Alblas MA, Lippke B, Kluck N, Priebe L, Degenhardt FA, Jamra RA, Meesters C, Jöckel KH, Erbel R, Harrap S, Schumacher J, Fröhlich H, Kruse R, Hillmer AM, Becker T, Nöthen MM. Brockschmidt FF, et al. Among authors: kruse r. Br J Dermatol. 2011 Dec;165(6):1293-302. doi: 10.1111/j.1365-2133.2011.10708.x. Br J Dermatol. 2011. PMID: 22032556

10

Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss.

Redler S, Brockschmidt FF, Tazi-Ahnini R, Drichel D, Birch MP, Dobson K, Giehl KA, Herms S, Refke M, Kluck N, Kruse R, Lutz G, Wolff H, Böhm M, Becker T, Nöthen MM, Messenger AG, Betz RC. Redler S, et al. Among authors: kruse r. Br J Dermatol. 2012 Jun;166(6):1314-8. doi: 10.1111/j.1365-2133.2012.10877.x. Br J Dermatol. 2012. PMID: 22309448

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