Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
20485516
TITLE
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
ABSTRACT
DATE PUBLISHED
2010 May
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2010/01/25
accepted 2010/04/12
epublish 2010/05/13
entrez 2010/05/21 06:00
pubmed 2010/05/21 06:00
medline 2010/09/14 06:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Lu Y Lu Yi Y Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia.
Dimasi DP Dimasi David P DP
Hysi PG Hysi Pirro G PG
Hewitt AW Hewitt Alex W AW
Burdon KP Burdon Kathryn P KP
Toh T Toh Tze'Yo T
Ruddle JB Ruddle Jonathan B JB
Li YJ Li Yi Ju YJ
Mitchell P Mitchell Paul P
Healey PR Healey Paul R PR
Montgomery GW Montgomery Grant W GW
Hansell N Hansell Narelle N
Spector TD Spector Timothy D TD
Martin NG Martin Nicholas G NG
Young TL Young Terri L TL
Hammond CJ Hammond Christopher J CJ
Macgregor S Macgregor Stuart S
Craig JE Craig Jamie E JE
Mackey DA Mackey David A DA
INVESTIGATORS
JOURNAL
MEDLINE JOURNAL
MEDLINETA: PLoS Genet
COUNTRY: United States
ISSNLINKING: 1553-7390
NLMUNIQUEID: 101239074
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Twin Study
COMMENTS AND CORRECTIONS
REFTYPE REFSOURCE REFPMID NOTE
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GRANTS
GRANTID AGENCY COUNTRY
1R01EY018246 NEI NIH HHS United States
G20234 Biotechnology and Biological Sciences Research Council United Kingdom
Wellcome Trust United Kingdom
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Blindness genetics
Chromosomes, Human, Pair 13 genetics
Cohort Studies genetics
Corneal Diseases pathology
Epithelium, Corneal pathology
Humans pathology
Polymorphism, Single Nucleotide pathology
Quantitative Trait Loci pathology
Risk Factors pathology
Syndrome pathology
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
OTHER ID's
OTHERID SOURCE
PMC2869325 NLM