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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 3
2004 1
2005 2
2006 6
2007 3
2008 4
2009 4
2010 2
2011 3
2012 6
2013 5
2014 5
2015 3
2017 3
2018 1
2024 0

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44 results

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Page 1
Familial aggregation of alopecia areata.
Blaumeiser B, van der Goot I, Fimmers R, Hanneken S, Ritzmann S, Seymons K, Betz RC, Ruzicka T, Wienker TF, De Weert J, Lambert J, Kruse R, Nöthen MM. Blaumeiser B, et al. Among authors: kruse r. J Am Acad Dermatol. 2006 Apr;54(4):627-32. doi: 10.1016/j.jaad.2005.12.007. Epub 2006 Jan 23. J Am Acad Dermatol. 2006. PMID: 16546583
On the anisotropy of skeletal muscle tissue under compression.
Böl M, Ehret AE, Leichsenring K, Weichert C, Kruse R. Böl M, et al. Among authors: kruse r. Acta Biomater. 2014 Jul;10(7):3225-34. doi: 10.1016/j.actbio.2014.03.003. Epub 2014 Mar 14. Acta Biomater. 2014. PMID: 24636829
Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study.
Redler S, Basmanav FBÜ, Blaumeiser B, Bartels NG, Lutz G, Tafazzoli A, Kruse R, Wolff H, Böhm M, Blume-Peytavi U, Becker T, Nöthen MM, Betz RC. Redler S, et al. Among authors: kruse r. Acta Derm Venereol. 2017 Jul 6;97(7):862-863. doi: 10.2340/00015555-2658. Acta Derm Venereol. 2017. PMID: 28350042 Free article. No abstract available.
Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata.
Tafazzoli A, Forstner AJ, Broadley D, Hofmann A, Redler S, Petukhova L, Giehl KA, Kruse R, Blaumeiser B, Böhm M, Bertolini M, Rossi A, Garcia Bartels N, Lutz G, Wolff H, Blume-Peytavi U, Soreq H, Christiano AM, Botchkareva NV, Nöthen MM, Betz RC. Tafazzoli A, et al. Among authors: kruse r. J Invest Dermatol. 2018 Mar;138(3):549-556. doi: 10.1016/j.jid.2017.09.046. Epub 2017 Dec 6. J Invest Dermatol. 2018. PMID: 29080678 Free article.
Genetic variants in CTLA4 are strongly associated with alopecia areata.
John KK, Brockschmidt FF, Redler S, Herold C, Hanneken S, Eigelshoven S, Giehl KA, De Weert J, Lutz G, Kruse R, Wolff H, Blaumeiser B, Böhm M, Becker T, Nöthen MM, Betz RC. John KK, et al. Among authors: kruse r. J Invest Dermatol. 2011 May;131(5):1169-72. doi: 10.1038/jid.2010.427. Epub 2011 Feb 24. J Invest Dermatol. 2011. PMID: 21346773 Free article. No abstract available.
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: kruse r. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.
Basmanav FB, Oprisoreanu AM, Pasternack SM, Thiele H, Fritz G, Wenzel J, Größer L, Wehner M, Wolf S, Fagerberg C, Bygum A, Altmüller J, Rütten A, Parmentier L, El Shabrawi-Caelen L, Hafner C, Nürnberg P, Kruse R, Schoch S, Hanneken S, Betz RC. Basmanav FB, et al. Among authors: kruse r. Am J Hum Genet. 2014 Jan 2;94(1):135-43. doi: 10.1016/j.ajhg.2013.12.003. Am J Hum Genet. 2014. PMID: 24387993 Free PMC article.
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.
Betz RC, Petukhova L, Ripke S, Huang H, Menelaou A, Redler S, Becker T, Heilmann S, Yamany T, Duvic M, Hordinsky M, Norris D, Price VH, Mackay-Wiggan J, de Jong A, DeStefano GM, Moebus S, Böhm M, Blume-Peytavi U, Wolff H, Lutz G, Kruse R, Bian L, Amos CI, Lee A, Gregersen PK, Blaumeiser B, Altshuler D, Clynes R, de Bakker PIW, Nöthen MM, Daly MJ, Christiano AM. Betz RC, et al. Among authors: kruse r. Nat Commun. 2015 Jan 22;6:5966. doi: 10.1038/ncomms6966. Nat Commun. 2015. PMID: 25608926 Free PMC article.
44 results