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Susceptibility variants for male-pattern baldness on chromosome 20p11.

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Susceptibility variants for male-pattern baldness on chromosome 20p11. / Hillmer, Axel M; Brockschmidt, Felix F; Hanneken, Sandra; Eigelshoven, Sibylle; Steffens, Michael; Flaquer, Antonia; Herms, Stefan; Becker, Tim; Kortüm, Anne-Katrin; Nyholt, Dale R; Zhao, Zhen Zhen; Montgomery, Grant W; Martin, Nicholas G; Mühleisen, Thomas W; Alblas, Margrieta A; Moebus, Susanne; Jöckel, Karl-Heinz; Bröcker-Preuss, Martina; Erbel, Raimund; Reinartz, Roman; Betz, Regina C; Cichon, Sven; Propping, Peter; Baur, Max P; Wienker, Thomas F; Kruse, Roland; Nöthen, Markus M.

in: NAT GENET, Jahrgang 40, Nr. 11, 11, 2008, S. 1279-1281.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Hillmer, AM, Brockschmidt, FF, Hanneken, S, Eigelshoven, S, Steffens, M, Flaquer, A, Herms, S, Becker, T, Kortüm, A-K, Nyholt, DR, Zhao, ZZ, Montgomery, GW, Martin, NG, Mühleisen, TW, Alblas, MA, Moebus, S, Jöckel, K-H, Bröcker-Preuss, M, Erbel, R, Reinartz, R, Betz, RC, Cichon, S, Propping, P, Baur, MP, Wienker, TF, Kruse, R & Nöthen, MM 2008, 'Susceptibility variants for male-pattern baldness on chromosome 20p11.', NAT GENET, Jg. 40, Nr. 11, 11, S. 1279-1281. <http://www.ncbi.nlm.nih.gov/pubmed/18849994?dopt=Citation>

APA

Hillmer, A. M., Brockschmidt, F. F., Hanneken, S., Eigelshoven, S., Steffens, M., Flaquer, A., Herms, S., Becker, T., Kortüm, A-K., Nyholt, D. R., Zhao, Z. Z., Montgomery, G. W., Martin, N. G., Mühleisen, T. W., Alblas, M. A., Moebus, S., Jöckel, K-H., Bröcker-Preuss, M., Erbel, R., ... Nöthen, M. M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. NAT GENET, 40(11), 1279-1281. [11]. http://www.ncbi.nlm.nih.gov/pubmed/18849994?dopt=Citation

Vancouver

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A et al. Susceptibility variants for male-pattern baldness on chromosome 20p11. NAT GENET. 2008;40(11):1279-1281. 11.

Bibtex

@article{fe3be317dbb042b58fe3e794d2fa38bf,
title = "Susceptibility variants for male-pattern baldness on chromosome 20p11.",
abstract = "We carried out a genome-wide association study in 296 individuals with male-pattern baldness (androgenetic alopecia) and 347 controls. We then investigated the 30 best SNPs in an independent replication sample and found highly significant association for five SNPs on chromosome 20p11 (rs2180439 combined P = 2.7 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.",
author = "Hillmer, {Axel M} and Brockschmidt, {Felix F} and Sandra Hanneken and Sibylle Eigelshoven and Michael Steffens and Antonia Flaquer and Stefan Herms and Tim Becker and Anne-Katrin Kort{\"u}m and Nyholt, {Dale R} and Zhao, {Zhen Zhen} and Montgomery, {Grant W} and Martin, {Nicholas G} and M{\"u}hleisen, {Thomas W} and Alblas, {Margrieta A} and Susanne Moebus and Karl-Heinz J{\"o}ckel and Martina Br{\"o}cker-Preuss and Raimund Erbel and Roman Reinartz and Betz, {Regina C} and Sven Cichon and Peter Propping and Baur, {Max P} and Wienker, {Thomas F} and Roland Kruse and N{\"o}then, {Markus M}",
year = "2008",
language = "Deutsch",
volume = "40",
pages = "1279--1281",
journal = "NAT GENET",
issn = "1061-4036",
publisher = "NATURE PUBLISHING GROUP",
number = "11",

}

RIS

TY - JOUR

T1 - Susceptibility variants for male-pattern baldness on chromosome 20p11.

AU - Hillmer, Axel M

AU - Brockschmidt, Felix F

AU - Hanneken, Sandra

AU - Eigelshoven, Sibylle

AU - Steffens, Michael

AU - Flaquer, Antonia

AU - Herms, Stefan

AU - Becker, Tim

AU - Kortüm, Anne-Katrin

AU - Nyholt, Dale R

AU - Zhao, Zhen Zhen

AU - Montgomery, Grant W

AU - Martin, Nicholas G

AU - Mühleisen, Thomas W

AU - Alblas, Margrieta A

AU - Moebus, Susanne

AU - Jöckel, Karl-Heinz

AU - Bröcker-Preuss, Martina

AU - Erbel, Raimund

AU - Reinartz, Roman

AU - Betz, Regina C

AU - Cichon, Sven

AU - Propping, Peter

AU - Baur, Max P

AU - Wienker, Thomas F

AU - Kruse, Roland

AU - Nöthen, Markus M

PY - 2008

Y1 - 2008

N2 - We carried out a genome-wide association study in 296 individuals with male-pattern baldness (androgenetic alopecia) and 347 controls. We then investigated the 30 best SNPs in an independent replication sample and found highly significant association for five SNPs on chromosome 20p11 (rs2180439 combined P = 2.7 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.

AB - We carried out a genome-wide association study in 296 individuals with male-pattern baldness (androgenetic alopecia) and 347 controls. We then investigated the 30 best SNPs in an independent replication sample and found highly significant association for five SNPs on chromosome 20p11 (rs2180439 combined P = 2.7 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.

M3 - SCORING: Zeitschriftenaufsatz

VL - 40

SP - 1279

EP - 1281

JO - NAT GENET

JF - NAT GENET

SN - 1061-4036

IS - 11

M1 - 11

ER -