Related references
Note: Only part of the references are listed.Estimation of Genotype Relative Risks From Pedigree Data by Retrospective Likelihoods
Daniel J. Schaid et al.
GENETIC EPIDEMIOLOGY (2010)
Software for Generating Liability Distributions for Pedigrees Conditional on Their Observed Disease States and Covariates
Desmond D. Campbell et al.
GENETIC EPIDEMIOLOGY (2010)
Exome sequencing identifies the cause of a mendelian disorder
Sarah B. Ng et al.
NATURE GENETICS (2010)
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example
Leila Mohammadi et al.
BMC CANCER (2009)
Targeted capture and massively parallel sequencing of 12 human exomes
Sarah B. Ng et al.
NATURE (2009)
Common variants at 30 loci contribute to polygenic dyslipidemia
Sekar Kathiresan et al.
NATURE GENETICS (2009)
Common disorders are quantitative traits
Robert Plomin et al.
NATURE REVIEWS GENETICS (2009)
Power of deep, all-exon resequencing for discovery of human trait genes
Gregory V. Kryukov et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
Lucia A. Hindorff et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
Sergey Nejentsev et al.
SCIENCE (2009)
A new estimate of family disease history providing improved prediction of disease risks
Rui Feng et al.
STATISTICS IN MEDICINE (2009)
A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
Bo Eskerod Madsen et al.
PLOS GENETICS (2009)
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
Bingshan Li et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Genetic similarities between latent autoimmune diabetes in adults, type 1 diabetes, and type 2 diabetes
Camilla Cervin et al.
DIABETES (2008)
Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients
E. Bakhtadze et al.
DIABETOLOGIA (2008)
Common and rare variants in multifactorial susceptibility to common diseases
Walter Bodmer et al.
NATURE GENETICS (2008)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Weizhen Ji et al.
NATURE GENETICS (2008)
Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes.
Valeriya Lyssenko et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases
Christopher G. Bell et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: A cohort allelic sums test (CAST)
Stephan Morgenthaler et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2007)
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
Stefano Romeo et al.
NATURE GENETICS (2007)
Genome-wide association studies provide new insights into type 2 diabetes aetiology
Timothy M. Frayling
NATURE REVIEWS GENETICS (2007)
Medical sequencing at the extremes of human body mass
Nadav Ahituv et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program
Jose C. Florez et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
JC Cohen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
A spectrum of PCSK9 Alleles contributes to plasma levels of low-density lipoprotein cholesterol
IK Kotowski et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Extremely discordant sib-pair study design to determine risk factors for neovascular age-related macular degeneration
MM DeAngelis et al.
ARCHIVES OF OPHTHALMOLOGY (2004)
Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onset
J Carayol et al.
GENETIC EPIDEMIOLOGY (2004)
Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
JC Cohen et al.
SCIENCE (2004)
Framingham risk score and prediction of lifetime risk for coronary heart disease
DM Lloyd-Jones et al.
AMERICAN JOURNAL OF CARDIOLOGY (2004)
Conditional likelihood inference under complex ascertainment using data augmentation
D Clayton
BIOMETRIKA (2003)
SIFT: predicting amino acid changes that affect protein function
PC Ng et al.
NUCLEIC ACIDS RESEARCH (2003)
The diabetes risk score -: A practical tool to predict type 2 diabetes risk
J Lindström et al.
DIABETES CARE (2003)
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
S Purcell et al.
BIOINFORMATICS (2003)
The role of extreme phenotype selection studies in the identification of clinically relevant genotypes in cancer research
JL Perez-Gracia et al.
CANCER (2002)
Human non-synonymous SNPs: server and survey
V Ramensky et al.
NUCLEIC ACIDS RESEARCH (2002)
Prediction of deleterious human alleles
S Sunyaev et al.
HUMAN MOLECULAR GENETICS (2001)
Extreme discordant phenotype methodology: an intuitive approach to clinical pharmacogenetics
DW Nebert
EUROPEAN JOURNAL OF PHARMACOLOGY (2000)
Power of selective genotyping in genetic association analyses of quantitative traits
S Van Gestel et al.
BEHAVIOR GENETICS (2000)
Bias and efficiency in family-based gene-characterization studies: Conditional, prospective, retrospective, and joint likelihoods
P Kraft et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)