(Q22337234)

7 February 2023

2

Celeste L. Pearce

Celeste L.

Pearce

1 reference

7 February 2023

5

Joel N. Hirschhorn

Joel N.

Hirschhorn

1 reference

7 February 2023

1

Kirk E. Lohmueller

Kirk E.

Lohmueller

1 reference

7 February 2023

Malcolm Pike

3

Malcolm

Pike

1 reference

1047659846

Genetic dissection of complex traits

7 February 2023

language of work or name

English

0 references

publication date

13 January 2003

0 references

published in

Nature Genetics

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volume

33

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issue

2

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page(s)

177-182

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cites work

1 reference

7 January 2021

The future of genetic studies of complex human diseases

1 reference

7 January 2021

Variations on a theme: cataloging human DNA sequence variation

1 reference

7 January 2021

Searching for genetic determinants in the new millennium

1 reference

7 January 2021

Association study designs for complex diseases

1 reference

7 January 2021

Genetic Polymorphisms and Disease

1 reference

7 January 2021

Candidate-gene approaches for studying complex genetic traits: practical considerations

1 reference

7 January 2021

A comprehensive review of genetic association studies

1 reference

7 January 2021

Bias in meta-analysis detected by a simple, graphical test

1 reference

7 January 2021

Replication validity of genetic association studies

1 reference

7 January 2021

Large upward bias in estimation of locus-specific effects from genomewide scans

1 reference

7 January 2021

Once and Again—Issues Surrounding Replication in Genetic Association Studies

1 reference

7 January 2021

Exact and asymptotic tests for homogeneity in several 2 x 2 tables

1 reference

7 January 2021

Estimators of the Mantel-Haenszel variance consistent in both sparse data and large-strata limiting models

1 reference

7 January 2021

Meta-analysis of published data using a linear mixed-effects model

1 reference

7 January 2021

Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians

1 reference

7 January 2021

Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension

1 reference

7 January 2021

Apolipoprotein E type ϵ4 allele frequency is increased in patients with schizophrenia

1 reference

7 January 2021

Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease

1 reference

7 January 2021

Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene

1 reference

7 January 2021

Catechol-O-methyltransferase Vall58Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder

1 reference

7 January 2021

Preferential transmission of the high activity allele of COMT in schizophrenia

1 reference

7 January 2021

The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

1 reference

7 January 2021

A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia

1 reference

7 January 2021

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene

1 reference

7 January 2021

Association between glutathione S-transferase M1, P1, and T1 genetic polymorphisms and development of breast cancer

1 reference

7 January 2021

Glutathione s-transferase genotypes as risk factors for head and neck cancer

1 reference

7 January 2021

Association between polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus.

1 reference

7 January 2021

Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia

1 reference

7 January 2021

Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians

1 reference

7 January 2021

Neurotrophin-3 gene polymorphism associated with schizophrenia

1 reference

7 January 2021

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease

1 reference

7 January 2021

A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity

1 reference

7 January 2021

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

1 reference

7 January 2021

Association of genetic variant of the glucose transporter with non-insulin-dependent diabetes mellitus

1 reference

7 January 2021

Association between a restriction fragment length polymorphism at the liver/islet cell (GluT 2) glucose transporter and familial Type 2 (non-insulin-dependent) diabetes mellitus

1 reference

7 January 2021

Association Between the Tryptophan Hydroxylase Gene and Manic-depressive Illness

1 reference

7 January 2021