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Lista de obras de Augustine Kong

A common variant associated with prostate cancer in European and African populations

artículo científico publicado en 2006

A common variant at 8q24.21 is associated with renal cell cancer.

artículo científico publicado en 2013

A direct characterization of human mutation based on microsatellites

artículo científico publicado en 2012

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

artículo científico publicado en 2016

A genetic risk factor for periodic limb movements in sleep

artículo científico publicado en 2007

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

artículo científico publicado en 2011

A major susceptibility gene for asthma maps to chromosome 14q24

artículo científico publicado en 2002

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

artículo científico publicado en 2012

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)

artículo científico publicado en 2004

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

article by Hannes Helgason et al published 15 September 2013 in Nature Genetics

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

artículo científico publicado en 2011

A sequence variant associating with educational attainment also affects childhood cognition

artículo científico publicado en 2016

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2010

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

artículo científico publicado en 2009

A sequence variant on 17q21 is associated with age at onset and severity of asthma

artículo científico publicado en 2010

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

artículo científico publicado en 2012

A theory of statistical models for Monte Carlo integration

article

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

artículo científico publicado en 2008

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

artículo científico publicado en 2008

Allegro version 2

Allegro, a new computer program for multipoint linkage analysis

artículo científico publicado en 2000

Allele-sharing models: LOD scores and accurate linkage tests

artículo científico publicado en 1997

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

artículo científico publicado en 2017

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

artículo científico publicado en 2003

Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases

scientific journal article

Asymptotic theory for gene mapping

artículo científico publicado en 1994

Blocking Gibbs sampling for linkage analysis in large pedigrees with many loops.

artículo científico publicado en 1999

CDKN2A mutations and melanoma risk in the Icelandic population

artículo científico publicado en 2008

CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD

artículo científico publicado en 2006

Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family

artículo científico publicado en 2004

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

artículo científico publicado en 2017

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

artículo científico publicado en 2009

Common and low-frequency variants associated with genome-wide recombination rate

artículo científico publicado en 2013

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

artículo científico publicado en 2007

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

artículo científico publicado en 2010

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

artículo científico publicado en 2008

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

artículo científico publicado en 2009

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

artículo científico publicado en 2007

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

artículo científico publicado en 2009

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

artículo científico publicado en 2017

Covariance Structure and Convergence Rate of the Gibbs Sampler with Various Scans

Deconstructing the sources of genotype-phenotype associations in humans

scientific article published on 01 September 2019

Detection of sharing by descent, long-range phasing and haplotype imputation

artículo científico publicado en 2008

Diabetes, dependence, asymptotics, selection and significance

artículo científico publicado en 1997

Discovery of common variants associated with low TSH levels and thyroid cancer risk

scientific journal article

Epigenetic and genetic components of height regulation

artículo científico publicado en 2016

Erratum: Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor

article

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

European bone mineral density loci are also associated with BMD in East-Asian populations

artículo científico publicado en 2010

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene

artículo científico publicado en 2011

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

Familial Aggregation of Parkinson's Disease in Iceland

scholarly article by Sigurlaug Sveinbjörnsdóttir et al published 14 December 2000 in The New England Journal of Medicine

Finding the missing heritability of complex diseases

artículo científico publicado en 2009

Fine-scale recombination rate differences between sexes, populations and individuals

artículo científico publicado en 2010

Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets

artículo científico publicado en 2013

Genetic correction of PSA values using sequence variants associated with PSA levels

artículo científico publicado en 2010

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

Genetics of gene expression and its effect on disease

artículo científico publicado en 2008

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

artículo científico publicado en 2009

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

artículo científico publicado en 2009

Genome-wide association study identifies 74 loci associated with educational attainment

artículo científico publicado en 2016

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

artículo científico publicado en 2007

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

artículo científico publicado en 2009

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

artículo científico publicado en 2014

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

artículo científico publicado en 2009

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk

artículo científico publicado en 2011

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3 ⬇️

artículo científico publicado el 7 de mayo de 2003

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

scientific journal article

Graphical templates for model registration

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

artículo científico publicado en 2016

How medical professionals evaluate expressions of probability.

artículo científico

Identification of a large set of rare complete human knockouts

artículo científico publicado en 2015

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

artículo científico publicado en 2011

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

artículo científico publicado en 2014

Identification of low-frequency variants associated with gout and serum uric acid levels

artículo científico publicado en 2011

Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer

artículo científico publicado en 2016

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Large-scale whole-genome sequencing of the Icelandic population

artículo científico publicado en 2015

Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling.

artículo científico publicado en 1992

Linkage of osteoporosis to chromosome 20p12 and association to BMP2

artículo científico publicado en 2003

Localization of a susceptibility gene for common forms of stroke to 5q12

artículo científico publicado en 2002

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

artículo científico publicado en 2014

Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

artículo científico publicado en 2015

Male-pattern baldness susceptibility locus at 20p11.

artículo científico publicado en 2008

Many sequence variants affecting diversity of adult human height

artículo científico publicado en 2008

Measuring the relative information in allele-sharing linkage studies

artículo científico publicado en 2004

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

artículo científico publicado en 2008

Multi-nucleotide de novo Mutations in Humans

artículo científico publicado en 2016

Multiple genetic loci for bone mineral density and fractures

artículo científico publicado en 2008

Multiple transmissions of de novo mutations in families

article

Mutations in BRIP1 confer high risk of ovarian cancer

artículo científico publicado en 2011

Neuregulin 1 and susceptibility to schizophrenia

artículo científico publicado en 2002

New basal cell carcinoma susceptibility loci

artículo científico publicado en 2015

New common variants affecting susceptibility to basal cell carcinoma

artículo científico publicado en 2009

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

New sequence variants associated with bone mineral density

artículo científico publicado en 2009

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

artículo científico publicado en 2013

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

On a randomization procedure.

artículo científico publicado en 2000

Parental influence on human germline de novo mutations in 1,548 trios from Iceland

artículo científico publicado en 2017

Parental origin of sequence variants associated with complex diseases

scientific article published on December 2009

Physical and neurobehavioral determinants of reproductive onset and success

artículo científico publicado en 2016

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

artículo científico publicado en 2015

Rate of de novo mutations and the importance of father's age to disease risk

artículo científico publicado en 2012

Recombination rate and reproductive success in humans

artículo científico publicado en 2004

Reconstructing an African haploid genome from the 18th century.

artículo científico publicado en 2018

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

article

Relatedness disequilibrium regression estimates heritability without environmental bias

article

Reproductive fitness and genetic risk of psychiatric disorders in the general population

artículo científico publicado en 2017

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

artículo científico publicado en 2008

Selection against variants in the genome associated with educational attainment

scientific article published on 17 January 2017

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

artículo científico publicado en 2017

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2008

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

artículo científico publicado en 2009

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

artículo científico publicado en 2011

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

artículo científico publicado en 2009

Sequence variants from whole genome sequencing a large group of Icelanders

artículo científico publicado en 2015

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

scientific journal article

Sequence variants in the RNF212 gene associate with genome-wide recombination rate

artículo científico publicado en 2008

Sequential Imputations and Bayesian Missing Data Problems

article by Augustine Kong et al published March 1994 in Journal of the American Statistical Association

Sequential imputation for multilocus linkage analysis

artículo científico publicado en 1994

Several common variants modulate heart rate, PR interval and QRS duration

article by Hilma Holm et al published 10 January 2010 in Nature Genetics

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.

artículo científico publicado en 2014

Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals

artículo científico publicado en 2011

Support for involvement of the AHI1 locus in schizophrenia

The BARD1 Cys557Ser variant and breast cancer risk in Iceland

artículo científico publicado en 2006

The Y-chromosome point mutation rate in humans.

artículo científico publicado en 2015

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

artículo científico publicado en 2007

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

artículo científico publicado en 2014

The impact of divergence time on the nature of population structure: an example from Iceland

artículo científico publicado en 2009

The nature of nurture: Effects of parental genotypes

artículo científico publicado en 2018

The properties of the cross-match estimate and split sampling

article

The rate of meiotic gene conversion varies by sex and age.

artículo científico publicado en 2016

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

article

Truncating mutations in RBM12 are associated with psychosis

artículo científico publicado en 2017

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

artículo científico publicado en 2010

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

artículo científico publicado en 2009

Two newly identified genetic determinants of pigmentation in Europeans

artículo científico publicado en 2008

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

scientific journal article

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

artículo científico publicado en 2013

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

artículo científico publicado en 2006

Variants conferring risk of atrial fibrillation on chromosome 4q25.

artículo científico publicado en 2007

Variants in MTNR1B influence fasting glucose levels

artículo científico publicado en 2008

Weighting sequence variants based on their annotation increases power of whole-genome association studies

artículo científico publicado en 2016

Whole genome characterization of sequence diversity of 15,220 Icelanders

artículo científico publicado en 2017

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

artículo científico publicado en 2017

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