|
🐜
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Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis
30 auth.
U. Hüffmeier,
S. Uebe,
A. Ekici,
J. Bowes,
E. Giardina,
E. Korendowych,
K. Juneblad,
Maria Apel,
R. McManus,
P. Ho,
I. Bruce,
A. Ryan,
F. Behrens,
J. Lascorz,
B. Böhm,
...
H. Traupe,
J. Lohmann,
C. Gieger,
H. Wichmann,
C. Herold,
M. Steffens,
L. Klareskog,
T. Wienker,
O. FitzGerald,
G. Alenius,
N. McHugh,
G. Novelli,
H. Burkhardt,
A. Barton,
A. Reis
|
8 |
2010 |
8
🐜
|
|
🐜
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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
158 auth.
A. Pardiñas,
P. Holmans,
A. Pocklington,
V. Escott-Price,
S. Ripke,
N. Carrera,
S. Legge,
Sophie Bishop,
Darren Cameron,
M. Hamshere,
Jun Han,
L. Hubbard,
A. Lynham,
K. Mantripragada,
E. Rees,
...
J. MacCabe,
S. Mccarroll,
B. Baune,
Gerome Breen,
Enda M. Byrne,
U. Dannlowski,
T. Eley,
C. Hayward,
N. G. Martin,
A. McIntosh,
R. Plomin,
D. Porteous,
N. Wray,
A. Caballero,
D. Geschwind,
Laura M. Huckins,
D. Ruderfer,
Enrique Santiago,
P. Sklar,
E. Stahl,
H. Won,
E. Agerbo,
T. Als,
O. Andreassen,
Marie Bækvad-Hansen,
P. Mortensen,
C. B. Pedersen,
A. Børglum,
J. Bybjerg-Grauholm,
S. Djurovic,
N. Durmishi,
M. Pedersen,
V. Golimbet,
J. Grove,
D. Hougaard,
M. Mattheisen,
E. Molden,
O. Mors,
M. Nordentoft,
M. Pejović-Milovančević,
E. Sigurdsson,
T. Silagadze,
C. Hansen,
K. Stefánsson,
H. Stefánsson,
S. Steinberg,
S. Tosato,
T. Werge,
D. Harold,
R. Sims,
A. Gerrish,
J. Chapman,
R. Abraham,
P. Hollingworth,
J. Pahwa,
N. Denning,
C. Thomas,
Sarah Taylor,
J. Powell,
P. Proitsi,
Michelle K. Lupton,
S. Lovestone,
P. Passmore,
D. Craig,
B. McGuinness,
J. Johnston,
S. Todd,
Wolfgang Maier,
F. Jessen,
R. Heun,
Britta Schurmann,
A. Ramírez,
T. Becker,
C. Herold,
A. Lacour,
D. Drichel,
M. Nothen,
A. Goate,
C. Cruchaga,
P. Nowotny,
John X. Morris,
K. Mayo,
Michael C. O’Donovan,
Michael J. Owen,
Julie Williams,
E. Achilla,
E. Agerbo,
C. Barr,
Theresa Wimberly Böttger,
Gerome Breen,
D. Cohen,
D. Collier,
S. Curran,
E. Dempster,
D. Dima,
R. Sabés-Figuera,
R. Flanagan,
S. Frangou,
J. Frank,
C. Gasse,
F. Gaughran,
I. Giegling,
J. Grove,
E. Hannon,
A. Hartmann,
B. Heisserer,
M. Helthuis,
H. T. Horsdal,
O. Ingimarsson,
Karel Jollie,
J. Kennedy,
O. Köhler,
B. Konte,
M. Lang,
S. Legge,
C. Lewis,
J. MacCabe,
A. Malhotra,
Paul McCrone,
S. Meier,
J. Mill,
M. Nöthen,
Michael C. O’Donovan,
Michael J. Owen,
A. Pardiñas,
C. B. Pedersen,
M. Rietschel,
D. Rujescu,
A. Schwalber,
E. Sigurdsson,
H. Sørensen,
Benjamin W. Spencer,
H. Støvring,
J. Strohmaier,
P. Sullivan,
E. Vassos,
M. Verbelen,
James T. R. Walters,
D. Collier,
G. Kirov,
Michael J. Owen,
Michael C. O’Donovan,
James T. R. Walters
|
7 |
2018 |
7
🐜
|
|
🦁
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INTERSNP: genome-wide interaction analysis guided by a priori information
C. Herold,
M. Steffens,
F. F. Brockschmidt,
M. Baur,
T. Becker
|
7 |
2009 |
7
🦁
|
|
🐬
|
Reviewing the relevance of dioxin and PCB sources for food from animal origin and the need for their inventory, control and management
R. Weber,
C. Herold,
H. Hollert,
J. Kamphues,
Markus Blepp,
K. Ballschmiter
|
7 |
2018 |
7
🐬
|
|
🐜
|
Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.
20 auth.
Dagny Jagielska,
S. Redler,
F. F. Brockschmidt,
C. Herold,
S. M. Pasternack,
N. Garcia Bartels,
S. Hanneken,
S. Eigelshoven,
M. Refke,
S. Barth,
...
K. Giehl,
R. Kruse,
G. Lutz,
H. Wolff,
B. Blaumeiser,
M. Böhm,
U. Blume-Peytavi,
T. Becker,
M. Nöthen,
R. Betz
|
6 |
2012 |
6
🐜
|
|
🐜
|
Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
39 auth.
Rui Li,
F. F. Brockschmidt,
A. Kiefer,
H. Stefánsson,
D. Nyholt,
Kijoung Song,
S. Vermeulen,
S. Kanoni,
D. Glass,
S. Medland,
M. Dimitriou,
D. Waterworth,
J. Tung,
F. Geller,
S. Heilmann,
...
A. Hillmer,
V. Bataille,
S. Eigelshoven,
S. Hanneken,
S. Moebus,
C. Herold,
M. den Heijer,
G. Montgomery,
P. Deloukas,
N. Eriksson,
Andrew C. Heath,
T. Becker,
P. Sulem,
M. Mangino,
P. Vollenweider,
T. Spector,
G. Dedoussis,
N. G. Martin,
L. Kiemeney,
V. Mooser,
K. Stefánsson,
D. Hinds,
M. Nöthen,
J. Richards
|
6 |
2012 |
6
🐜
|
|
🐜
|
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.
26 auth.
S. Heilmann,
A. Kiefer,
Nadine Fricker,
D. Drichel,
A. Hillmer,
C. Herold,
J. Tung,
N. Eriksson,
S. Redler,
R. Betz,
Rui Li,
Ari Kárason,
D. Nyholt,
Kijoung Song,
S. Vermeulen,
...
S. Kanoni,
G. Dedoussis,
N. Martin,
L. Kiemeney,
V. Mooser,
K. Stefánsson,
J. B. Richards,
T. Becker,
F. F. Brockschmidt,
D. Hinds,
M. Nöthen
|
6 |
2013 |
6
🐜
|
|
🐜
|
CFH, C3 and ARMS2 Are Significant Risk Loci for Susceptibility but Not for Disease Progression of Geographic Atrophy Due to AMD
16 auth.
H. Scholl,
M. Fleckenstein,
L. Fritsche,
S. Schmitz-Valckenberg,
A. Göbel,
C. Adrion,
C. Herold,
C. Keilhauer,
F. Mackensen,
A. Mößner,
...
D. Pauleikhoff,
A. Weinberger,
U. Mansmann,
F. Holz,
T. Becker,
B. Weber
|
6 |
2009 |
6
🐜
|
|
🦁
|
Family-based Association Analyses of Imputed Genotypes Reveal Genome-Wide Significant Association of Alzheimer’s disease with OSBPL6, PTPRG and PDCL3
10 auth.
C. Herold,
B. Hooli,
K. Mullin,
Tian Liu,
J. T. Roehr,
M. Mattheisen,
...
A. Parrado,
L. Bertram,
C. Lange,
R. Tanzi
|
6 |
2015 |
6
🦁
|
|
🐜
|
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
18 auth.
J. Schumacher,
G. Laje,
R. Abou Jamra,
T. Becker,
Thomas W. Mühleisen,
Catalina Vasilescu,
M. Mattheisen,
S. Herms,
P. Hoffmann,
A. Hillmer,
...
A. Georgi,
C. Herold,
T. Schulze,
P. Propping,
M. Rietschel,
F. McMahon,
M. Nöthen,
S. Cichon
|
6 |
2009 |
6
🐜
|
