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🐜
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A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration
19 auth.
Zhenglin Yang,
N. Camp,
Hui Sun,
Z. Tong,
D. Gibbs,
D. J. Cameron,
H. Chen,
Yu Zhao,
E. Pearson,
Xi Li,
...
J. Chien,
A. Dewan,
J. Harmon,
P. Bernstein,
V. Shridhar,
N. Zabriskie,
J. Hoh,
K. Howes,
Kang Zhang
|
9 |
2006 |
9
🐜
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🦁
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HTRA1 promoter polymorphism in wet age-related macular degeneration.
13 auth.
A. Dewan,
Mugen Liu,
S. Hartman,
S. S. Zhang,
D. T. Liu,
Connie Zhao,
P. Tam,
W. Chan,
D. Lam,
Michael Snyder,
...
C. Barnstable,
C. Pang,
J. Hoh
|
8 |
2007 |
8
🦁
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|
🦁
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HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration
13 auth.
A. Dewan,
Mugen Liu,
S. Hartman,
S. S. Zhang,
D. T. Liu,
Connie Zhao,
P. Tam,
W. Chan,
D. Lam,
Michael Snyder,
...
C. Barnstable,
C. Pang,
J. Hoh
|
8 |
2006 |
8
🦁
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|
🐜
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Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
47 auth.
G. Thorleifsson,
G. Walters,
A. Hewitt,
G. Másson,
Agnar Helgason,
A. Dewan,
A. Sigurdsson,
Adalbjorg Jonasdottir,
S. A. Gudjonsson,
K. Magnússon,
H. Stefánsson,
D. S. Lam,
P. Tam,
Gudrun J Gudmundsdottir,
L. Southgate,
...
K. Burdon,
M. Gottfredsdóttir,
M. Aldred,
P. Mitchell,
D. S. Clair,
D. Collier,
Nelson L. S. Tang,
Orn Sveinsson,
S. Macgregor,
Nicholas G. Martin,
A. Cree,
J. Gibson,
A. Macleod,
Aby Jacob,
S. Ennis,
Terri L. Young,
J. C. Chan,
Wojciech S S Karwatowski,
Christopher J. Hammond,
K. Thordarson,
Mingzhi Zhang,
C. Wadelius,
Andrew J. Lotery,
R. Trembath,
C. Pang,
J. Hoh,
Jamie E. Craig,
A. Kong,
David A. Mackey,
F. Jónasson,
U. Thorsteinsdóttir,
K. Stefansson
|
8 |
2010 |
8
🐜
|
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🐜
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Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
16 auth.
I. Bespalova,
I. Bespalova,
G. Camp,
S. Bom,
David J. Brown,
K. Cryns,
A. Dewan,
A. E. Erson,
K. Flothmann,
H. Kunst,
...
Purnima Kurnool,
T. Sivakumaran,
C. Cremers,
S. Leal,
M. Burmeister,
M. Lesperance
|
7 |
2001 |
7
🐜
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|
🐜
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Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
10 auth.
Mei Zhu,
Tao Yang,
Sainan Wei,
A. Dewan,
R. Morell,
J. Elfenbein,
...
R. Fisher,
S. Leal,
Richard J. H. Smith,
K. Friderici
|
7 |
2003 |
7
🐜
|
|
🐜
|
Evidence for a putative bipolar disorder locus on 2p13–16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21–24, 13q32, 14q21 and 17q11–12
16 auth.
Jianjun Liu,
S. Juo,
A. Dewan,
A. Grunn,
Xiaomei Tong,
M. Brito,
N. Park,
J. E. Loth,
K. Kanyas,
B. Lerer,
...
J. Endicott,
G. Penchaszadeh,
J. Knowles,
J. Ott,
T. Gilliam,
M. Baron
|
7 |
2003 |
7
🐜
|
|
🐜
|
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
10 auth.
M. Zhu,
T. Yang,
S. Wei,
A. Dewan,
R. Morell,
J. Elfenbein,
...
R. Fisher,
S. Leal,
R. L. Smith,
K. Friderici
|
6 |
2003 |
6
🐜
|
|
🐜
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HTRA1 promoter polymorphism predisposes Japanese to age-related macular degeneration
13 auth.
Tsunehiko Yoshida,
A. Dewan,
Hong Zhang,
Ryosuke Sakamoto,
H. Okamoto,
M. Minami,
M. Obazawa,
A. Mizota,
Minoru Tanaka,
Yoshihiro Saito,
...
Ikue Takagi,
J. Hoh,
T. Iwata
|
6 |
2007 |
6
🐜
|
|
🐜
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Mitochondrial DNA Variants of Respiratory Complex I that Uniquely Characterize Haplogroup T2 Are Associated with Increased Risk of Age-Related Macular Degeneration
20 auth.
J. Sangiovanni,
D. Arking,
S. Iyengar,
M. Elashoff,
T. Clemons,
G. Reed,
A. Henning,
T. Sivakumaran,
Xuming Xu,
A. Dewan,
...
E. Agrón,
E. Rochtchina,
C. Sue,
Jie-Jin Wang,
P. Mitchell,
J. Hoh,
P. Francis,
M. Klein,
E. Chew,
A. Chakravarti
|
6 |
2009 |
6
🐜
|
|
🐬
|
A Comparison of Association Methods Correcting for Population Stratification in Case–Control Studies
Chengqing Wu,
A. Dewan,
J. Hoh,
Zuoheng Wang
|
6 |
2011 |
6
🐬
|
