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Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma
50 auth.
J. Wiggs,
B. Yaspan,
M. Hauser,
J. Kang,
R. Allingham,
L. Olson,
W. Abdrabou,
B. Fan,
Dan-yi Wang,
W. Brodeur,
D. Budenz,
J. Caprioli,
A. Crenshaw,
K. Crooks,
E. Delbono,
...
K. Doheny,
D. Friedman,
D. Gaasterland,
T. Gaasterland,
C. Laurie,
Richard K. Lee,
P. Lichter,
S. Loomis,
Yutao Liu,
F. Medeiros,
C. Mccarty,
D. Mirel,
S. Moroi,
D. Musch,
A. Realini,
F. Rozsa,
J. Schuman,
Kathleen M. Scott,
Kuldev Singh,
J. Stein,
E. Trager,
P. Vanveldhuisen,
D. Vollrath,
G. Wollstein,
Sachiko Yoneyama,
Kang Zhang,
R. Weinreb,
J. Ernst,
Manolis Kellis,
T. Masuda,
D. Zack,
J. Richards,
M. Pericak-Vance,
L. Pasquale,
J. Haines
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8 |
2012 |
8
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The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.
64 auth.
Soumitra S. Ghosh,
R. Watanabe,
T. Valle,
Elizabeth R. Hauser,
V. Magnuson,
C. Langefeld,
D. Ally,
K. Mohlke,
K. Silander,
K. Kohtamäki,
P. Chines,
J. Balow,
G. Birznieks,
Jennie Chang,
W. Eldridge,
...
M. Erdos,
Z. Karanjawala,
Julie I. Knapp,
Kristina Kudelko,
Colin Martin,
Anabelle Morales-Mena,
A. Musick,
Tiffany S. Musick,
C. Pfahl,
Rachel Porter,
Joseph B. Rayman,
D. Rha,
L. Segal,
Shane A. Shapiro,
Ravi Sharaf,
B. Shurtleff,
A. So,
J. Tannenbaum,
C. Te,
Jason Tovar,
A. Unni,
Christian Welch,
R. Whiten,
A. Witt,
J. Blaschak-Harvan,
J. Douglas,
W. Duren,
M. Epstein,
T. Fingerlin,
H. Kaleta,
E. Lange,
Chun Xing Li,
R. McEachin,
H. Stringham,
E. Trager,
P. P. White,
J. Eriksson,
L. Toivanen,
G. Vidgrén,
S. Nylund,
E. Tuomilehto-Wolf,
E. H. Ross,
Elza Demirchyan,
W. Hagopian,
T. Buchanan,
J. Tuomilehto,
R. Bergman,
F. Collins,
M. Boehnke
|
7 |
2000 |
7
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Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
21 auth.
Charles M. Krafchak,
H. Pawar,
S. Moroi,
A. Sugar,
P. Lichter,
D. Mackey,
S. Mian,
Theresa M. Nairus,
V. Elner,
M. Schteingart,
...
C. Downs,
T. Kijek,
Jenae M. Johnson,
E. Trager,
F. Rozsa,
M. A. Mandal,
M. Epstein,
D. Vollrath,
R. Ayyagari,
M. Boehnke,
J. Richards
|
7 |
2005 |
7
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The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
26 auth.
R. Watanabe,
S. Ghosh,
C. Langefeld,
T. Valle,
E. Hauser,
V. Magnuson,
K. Mohlke,
K. Silander,
D. Ally,
P. Chines,
J. Blaschak-Harvan,
J. Douglas,
W. Duren,
M. Epstein,
T. Fingerlin,
...
H. Kaleta,
E. Lange,
Chun Xing Li,
R. McEachin,
H. Stringham,
E. Trager,
P. P. White,
J. Balow,
G. Birznieks,
J. Chang,
W. Eldridge
|
7 |
2000 |
7
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Age-Related Macular Degeneration: A High-Resolution Genome Scan for Susceptibility Loci in a Population Enriched for Late-Stage Disease
18 auth.
G. Abecasis,
B. Yashar,
Yu Zhao,
N. Ghiasvand,
S. Zareparsi,
K. Branham,
Adam C. Reddick,
E. Trager,
Shigeo Yoshida,
John Bahling,
...
E. Filippova,
S. Elner,
Mark W. Johnson,
A. K. Vine,
P. Sieving,
S. Jacobson,
J. Richards,
A. Swaroop
|
6 |
2004 |
6
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Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
31 auth.
J. Friedman,
Joseph W. Ray,
N. Waseem,
Kory R. Johnson,
M. Brooks,
T. Hugosson,
D. Breuer,
K. Branham,
D. S. Krauth,
S. J. Bowne,
L. Sullivan,
V. Ponjavic,
Lotta Gränse,
Ritu Khanna,
E. Trager,
...
L. Gieser,
D. Hughbanks-Wheaton,
R. Cojocaru,
N. Ghiasvand,
C. Chakarova,
M. Abrahamson,
H. Göring,
A. Webster,
D. Birch,
G. Abecasis,
Y. Fann,
S. Bhattacharya,
S. Daiger,
J. Heckenlively,
S. Andreasson,
A. Swaroop
|
6 |
2009 |
6
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Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
18 auth.
G. Abecasis,
B. Yashar,
Yu Zhao,
N. Ghiasvand,
S. Zareparsi,
K. Branham,
Adam C. Reddick,
E. Trager,
S. Yoshida,
John Bahling,
...
E. Filippova,
S. Elner,
Mark W. Johnson,
A. K. Vine,
P. Sieving,
S. Jacobson,
J. Richards,
A. Swaroop
|
6 |
2004 |
6
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Evaluation of an Algorithm for Identifying Ocular Conditions in Electronic Health Record Data
12 auth.
J. Stein,
Moshiur Rahman,
Chris A. Andrews,
Joshua R. Ehrlich,
Shivani S. Kamat,
Manjool M. Shah,
...
Erin A. Boese,
Maria A. Woodward,
Jeff Cowall,
E. Trager,
Prabha Narayanaswamy,
D. Hanauer
|
5 |
2019 |
5
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A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10
14 auth.
Satoko Shimizu,
Charles M. Krafchak,
N. Fuse,
M. Epstein,
M. Schteingart,
A. Sugar,
M. Eibschitz-Tsimhoni,
C. Downs,
F. Rozsa,
E. Trager,
...
David M Reed,
M. Boehnke,
S. Moroi,
J. Richards
|
5 |
2004 |
5
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🦁
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Madeline 2.0 PDE: a new program for local and web-based pedigree drawing
7 auth.
E. Trager,
Ritu Khanna,
Adrian Marrs,
Lawrence Siden,
Kari E. H. Branham,
Anand Swaroop,
...
Julia E. Richards
|
3 |
2007 |
3
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