Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma

10.1371/journal.pgen.1002654

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Main Authors: Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L.
Other Authors: DUKE-NUS MEDICAL SCHOOL
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Published: 2019
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/161641
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spelling sg-nus-scholar.10635-1616412023-10-31T08:36:23Z Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma Wiggs J.L. Yaspan B.L. Hauser M.A. Kang J.H. Allingham R.R. Olson L.M. Abdrabou W. Fan B.J. Wang D.Y. Brodeur W. Budenz D.L. Caprioli J. Crenshaw A. Crooks K. DelBono E. Doheny K.F. Friedman D.S. Gaasterland D. Gaasterland T. Laurie C. Lee R.K. Lichter P.R. Loomis S. Liu Y. Medeiros F.A. McCarty C. Mirel D. Moroi S.E. Musch D.C. Realini A. Rozsa F.W. Schuman J.S. Scott K. Singh K. Stein J.D. Trager E.H. VanVeldhuisen P. Vollrath D. Wollstein G. Yoneyama S. Zhang K. Weinreb R.N. Ernst J. Kellis M. Masuda T. Zack D. Richards J.E. Pericak-Vance M. Pasquale L.R. Haines J.L. DUKE-NUS MEDICAL SCHOOL animal experiment animal model animal tissue article CDKN2BAS gene chromosome 14q chromosome 8q chromosome 9p controlled study disease association disease classification DNA sequence exfoliation syndrome gene gene expression profiling gene function gene location gene locus genetic association genetic identification genetic susceptibility genetic variability human intraocular pressure LRP12 gene major clinical study mouse nerve degeneration nonhuman open angle glaucoma optic nerve disease signal transduction single nucleotide polymorphism ZFPM2 gene allele chromosome 8 chromosome 9 exfoliation syndrome genetic association genetics meta analysis metabolism nerve degeneration optic nerve pathology ANRIL long non coding RNA, human ANRIL long non-coding RNA, human homeodomain protein SIX1 protein, human transforming growth factor beta untranslated RNA Alleles Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 9 Exfoliation Syndrome Genome-Wide Association Study Glaucoma, Open-Angle Homeodomain Proteins Humans Nerve Degeneration Optic Nerve Polymorphism, Single Nucleotide RNA, Untranslated Transforming Growth Factor beta 10.1371/journal.pgen.1002654 PLoS Genetics 8 4 e1002654 2019-11-06T09:29:54Z 2019-11-06T09:29:54Z 2012 Article Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L. (2012). Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genetics 8 (4) : e1002654. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1002654 15537390 https://scholarbank.nus.edu.sg/handle/10635/161641 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic animal experiment
animal model
animal tissue
article
CDKN2BAS gene
chromosome 14q
chromosome 8q
chromosome 9p
controlled study
disease association
disease classification
DNA sequence
exfoliation syndrome
gene
gene expression profiling
gene function
gene location
gene locus
genetic association
genetic identification
genetic susceptibility
genetic variability
human
intraocular pressure
LRP12 gene
major clinical study
mouse
nerve degeneration
nonhuman
open angle glaucoma
optic nerve disease
signal transduction
single nucleotide polymorphism
ZFPM2 gene
allele
chromosome 8
chromosome 9
exfoliation syndrome
genetic association
genetics
meta analysis
metabolism
nerve degeneration
optic nerve
pathology
ANRIL long non coding RNA, human
ANRIL long non-coding RNA, human
homeodomain protein
SIX1 protein, human
transforming growth factor beta
untranslated RNA
Alleles
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Exfoliation Syndrome
Genome-Wide Association Study
Glaucoma, Open-Angle
Homeodomain Proteins
Humans
Nerve Degeneration
Optic Nerve
Polymorphism, Single Nucleotide
RNA, Untranslated
Transforming Growth Factor beta
spellingShingle animal experiment
animal model
animal tissue
article
CDKN2BAS gene
chromosome 14q
chromosome 8q
chromosome 9p
controlled study
disease association
disease classification
DNA sequence
exfoliation syndrome
gene
gene expression profiling
gene function
gene location
gene locus
genetic association
genetic identification
genetic susceptibility
genetic variability
human
intraocular pressure
LRP12 gene
major clinical study
mouse
nerve degeneration
nonhuman
open angle glaucoma
optic nerve disease
signal transduction
single nucleotide polymorphism
ZFPM2 gene
allele
chromosome 8
chromosome 9
exfoliation syndrome
genetic association
genetics
meta analysis
metabolism
nerve degeneration
optic nerve
pathology
ANRIL long non coding RNA, human
ANRIL long non-coding RNA, human
homeodomain protein
SIX1 protein, human
transforming growth factor beta
untranslated RNA
Alleles
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Exfoliation Syndrome
Genome-Wide Association Study
Glaucoma, Open-Angle
Homeodomain Proteins
Humans
Nerve Degeneration
Optic Nerve
Polymorphism, Single Nucleotide
RNA, Untranslated
Transforming Growth Factor beta
Wiggs J.L.
Yaspan B.L.
Hauser M.A.
Kang J.H.
Allingham R.R.
Olson L.M.
Abdrabou W.
Fan B.J.
Wang D.Y.
Brodeur W.
Budenz D.L.
Caprioli J.
Crenshaw A.
Crooks K.
DelBono E.
Doheny K.F.
Friedman D.S.
Gaasterland D.
Gaasterland T.
Laurie C.
Lee R.K.
Lichter P.R.
Loomis S.
Liu Y.
Medeiros F.A.
McCarty C.
Mirel D.
Moroi S.E.
Musch D.C.
Realini A.
Rozsa F.W.
Schuman J.S.
Scott K.
Singh K.
Stein J.D.
Trager E.H.
VanVeldhuisen P.
Vollrath D.
Wollstein G.
Yoneyama S.
Zhang K.
Weinreb R.N.
Ernst J.
Kellis M.
Masuda T.
Zack D.
Richards J.E.
Pericak-Vance M.
Pasquale L.R.
Haines J.L.
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
description 10.1371/journal.pgen.1002654
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
Wiggs J.L.
Yaspan B.L.
Hauser M.A.
Kang J.H.
Allingham R.R.
Olson L.M.
Abdrabou W.
Fan B.J.
Wang D.Y.
Brodeur W.
Budenz D.L.
Caprioli J.
Crenshaw A.
Crooks K.
DelBono E.
Doheny K.F.
Friedman D.S.
Gaasterland D.
Gaasterland T.
Laurie C.
Lee R.K.
Lichter P.R.
Loomis S.
Liu Y.
Medeiros F.A.
McCarty C.
Mirel D.
Moroi S.E.
Musch D.C.
Realini A.
Rozsa F.W.
Schuman J.S.
Scott K.
Singh K.
Stein J.D.
Trager E.H.
VanVeldhuisen P.
Vollrath D.
Wollstein G.
Yoneyama S.
Zhang K.
Weinreb R.N.
Ernst J.
Kellis M.
Masuda T.
Zack D.
Richards J.E.
Pericak-Vance M.
Pasquale L.R.
Haines J.L.
format Article
author Wiggs J.L.
Yaspan B.L.
Hauser M.A.
Kang J.H.
Allingham R.R.
Olson L.M.
Abdrabou W.
Fan B.J.
Wang D.Y.
Brodeur W.
Budenz D.L.
Caprioli J.
Crenshaw A.
Crooks K.
DelBono E.
Doheny K.F.
Friedman D.S.
Gaasterland D.
Gaasterland T.
Laurie C.
Lee R.K.
Lichter P.R.
Loomis S.
Liu Y.
Medeiros F.A.
McCarty C.
Mirel D.
Moroi S.E.
Musch D.C.
Realini A.
Rozsa F.W.
Schuman J.S.
Scott K.
Singh K.
Stein J.D.
Trager E.H.
VanVeldhuisen P.
Vollrath D.
Wollstein G.
Yoneyama S.
Zhang K.
Weinreb R.N.
Ernst J.
Kellis M.
Masuda T.
Zack D.
Richards J.E.
Pericak-Vance M.
Pasquale L.R.
Haines J.L.
author_sort Wiggs J.L.
title Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
title_short Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
title_full Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
title_fullStr Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
title_full_unstemmed Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
title_sort common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
publishDate 2019
url https://scholarbank.nus.edu.sg/handle/10635/161641
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