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The impact of divergence time on the nature of population structure: an example from IcelandGenome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionCancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear familyThe association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsFinding the missing heritability of complex diseasesVariant of TREM2 Associated with the Risk of Alzheimer's DiseaseA mutation in APP protects against Alzheimer’s disease and age-related cognitive declineTwenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studiesGenomewide scan for hand osteoarthritis: a novel mutation in matrilin-3.Association of neuregulin 1 with schizophrenia confirmed in a Scottish populationTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisA major susceptibility gene for asthma maps to chromosome 14q24Common variants conferring risk of schizophreniaNew common variants affecting susceptibility to basal cell carcinomaRate of de novo mutations and the importance of father's age to disease riskLocalization of a susceptibility gene for common forms of stroke to 5q12Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypesVariants in MTNR1B influence fasting glucose levels.Large recurrent microdeletions associated with schizophreniaLinkage of osteoporosis to chromosome 20p12 and association to BMP2CFH Y402H confers similar risk of soft drusen and both forms of advanced AMDMutations in BRIP1 confer high risk of ovarian cancerA novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesMany sequence variants affecting diversity of adult human heightGenome-wide association yields new sequence variants at seven loci that associate with measures of obesityNew sequence variants associated with bone mineral densityA rare variant in MYH6 is associated with high risk of sick sinus syndromeSequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionA direct characterization of human mutation based on microsatellitesA genome-wide association search for type 2 diabetes genes in African AmericansEuropean bone mineral density loci are also associated with BMD in East-Asian populationsGermline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinomaAssociation of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesDiscovery of common variants associated with low TSH levels and thyroid cancer riskSequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityCommon sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancerVariant in the sequence of the LINGO1 gene confers risk of essential tremorGenome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
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P50
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Augustine Kong
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P108
P106
P21
P31
P496
0000-0001-8193-5438