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Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
25 auth.
A. Hillmer,
S. Hanneken,
S. Ritzmann,
T. Becker,
J. Freudenberg,
F. F. Brockschmidt,
A. Flaquer,
Y. Freudenberg-Hua,
R. Jamra,
C. Metzen,
Uwe Heyn,
N. Schweiger,
R. Betz,
B. Blaumeiser,
J. Hampe,
...
S. Schreiber,
T. Schulze,
H. Hennies,
J. Schumacher,
P. Propping,
T. Ruzicka,
S. Cichon,
T. Wienker,
R. Kruse,
M. Nothen
|
7 |
2005 |
7
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|
|
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Susceptibility variants for male-pattern baldness on chromosome 20p11
27 auth.
A. Hillmer,
F. F. Brockschmidt,
S. Hanneken,
S. Eigelshoven,
M. Steffens,
A. Flaquer,
S. Herms,
T. Becker,
Anne-Katrin Kortüm,
D. Nyholt,
Z. Zhao,
G. Montgomery,
N. Martin,
Thomas W. Mühleisen,
M. Alblas,
...
S. Moebus,
K. Jöckel,
M. Bröcker-Preuss,
R. Erbel,
R. Reinartz,
R. Betz,
S. Cichon,
P. Propping,
M. Baur,
T. Wienker,
R. Kruse,
M. Nöthen
|
7 |
2008 |
7
🐜
|
|
🐜
|
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 disease.
17 auth.
R. Betz,
J. Pforr,
A. Flaquer,
S. Redler,
S. Hanneken,
S. Eigelshoven,
Anne-Katrin Kortüm,
T. Tüting,
J. Lambert,
J. De Weert,
...
A. Hillmer,
C. Schmael,
T. Wienker,
R. Kruse,
G. Lutz,
B. Blaumeiser,
M. Nöthen
|
6 |
2007 |
6
🐜
|
|
🦁
|
The human pseudoautosomal regions: a review for genetic epidemiologists
A. Flaquer,
G. Rappold,
T. Wienker,
C. Fischer
|
6 |
2008 |
6
🦁
|
|
🐜
|
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
16 auth.
A. Hillmer,
A. Flaquer,
S. Hanneken,
S. Eigelshoven,
Anne-Katrin Kortüm,
F. F. Brockschmidt,
A. Golla,
C. Metzen,
H. Thiele,
S. Kolberg,
...
R. Reinartz,
R. Betz,
T. Ruzicka,
H. Hennies,
R. Kruse,
M. Nöthen
|
6 |
2008 |
6
🐜
|
|
🐜
|
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.
31 auth.
J. Huyghe,
L. Van Laer,
J. Hendrickx,
E. Fransen,
K. Demeester,
V. Topsakal,
S. Kunst,
M. Manninen,
M. Jensen,
A. Bonaconsa,
M. Mazzoli,
M. Baur,
S. Hannula,
E. Mäki-Torkko,
A. Espeso,
...
E. Van Eyken,
A. Flaquer,
C. Becker,
D. Stephens,
M. Sorri,
E. Orzan,
M. Bille,
A. Parving,
I. Pyykkö,
C. Cremers,
H. Kremer,
P. H. Van de Heyning,
T. Wienker,
P. Nürnberg,
M. Pfister,
G. Van Camp
|
5 |
2008 |
5
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|
|
🐜
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Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.
39 auth.
J. Schumacher,
R. Kaneva,
R. Jamra,
G. O. Diaz,
S. Ohlraun,
V. Milanova,
Young-Ae Lee,
F. Rivas,
F. Mayoral,
R. Fuerst,
A. Flaquer,
C. Windemuth,
E. Gay,
S. Sanz,
Maria José González,
...
Susana Gil,
F. Cabaleiro,
F. del Rio,
F. Perez,
Jesus Haro,
Chris Kostov,
Vesselin M. Chorbov,
Amelia Nikolova-Hill,
V. Stoyanova,
G. Onchev,
I. Kremensky,
K. Strauch,
T. Schulze,
P. Nürnberg,
W. Gaebel,
A. Klimke,
G. Auburger,
T. Wienker,
L. Kalaydjieva,
P. Propping,
S. Cichon,
A. Jablensky,
M. Rietschel,
M. Nöthen
|
5 |
2005 |
5
🐜
|
|
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The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata
15 auth.
S. Eigelshoven,
K. König,
A. Flaquer,
S. Redler,
S. Hanneken,
Anne-Katrin Kortüm,
A. Hillmer,
T. Tüting,
J. Lambert,
J. D. Weert,
...
Rudolf Kruse,
G. Lutz,
B. Blaumeiser,
Mm Nothen,
R. Betz
|
5 |
2007 |
5
🐜
|
|
🦁
|
Mitochondrial Genetic Variants Identified to Be Associated with BMI in Adults
8 auth.
A. Flaquer,
C. Baumbach,
J. Kriebel,
T. Meitinger,
A. Peters,
M. Waldenberger,
...
H. Grallert,
K. Strauch
|
5 |
2014 |
5
🦁
|
