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Rethinking genetic strategies to study complex diseases
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
review article
1 reference
stated in
Europe PubMed Central
title
Rethinking genetic strategies to study complex diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
main subject
data sharing
0 references
author name string
Brookes AJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
publication date
1 November 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
published in
Trends in Molecular Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
volume
7
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
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22 June 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
page(s)
512-516
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Europe PubMed Central
PubMed ID
11689337
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22 June 2017
cites work
In search of human variation.
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Crossref
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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902163-3
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Positional cloning: let's not call it reverse anymore
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DNA variation and the future of human genetics
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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA
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Fragile X genotype characterized by an unstable region of DNA.
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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
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Co-chairman's remarks: reverse genetics: directed modification of DNA for functional analysis
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HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome
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Initial sequencing and analysis of the human genome
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7 January 2021
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The essence of SNPs
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HGBASE: a database of SNPs and other variations in and around human genes
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dbSNP: a database of single nucleotide polymorphisms
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7 January 2021
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Linkage disequilibrium and the search for complex disease genes
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Searching for genetic determinants in the new millennium
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7 January 2021
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A full genome scan for late onset Alzheimer's disease.
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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
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Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
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From complex traits to complex alleles
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7 January 2021
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How many diseases does it take to map a gene with SNPs?
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SNP association studies in Alzheimer's disease highlight problems for complex disease analysis.
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Population choice in mapping genes for complex diseases
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7 January 2021
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Demographic history and linkage disequilibrium in human populations
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Guilt by association
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The effect of genetic variation in chemokines and their receptors on HIV transmission and progression to AIDS.
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Genomics and human disease--variations on variation
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Sequence interpretation. Functional annotation of mouse genome sequences
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The FlyBase database of the Drosophila Genome Projects and community literature
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Genome-wide RNAi
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Functional genomics: the worm scores a knockout
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Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis
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Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays
1 reference
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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902163-3
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Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease
1 reference
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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902163-3
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In silico mapping of complex disease-related traits in mice.
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Canine genetics comes of age.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902163-3
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7 January 2021
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Identifiers
DOI
10.1016/S1471-4914(01)02163-3
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
PubMed ID
11689337
1 reference
stated in
Europe PubMed Central
PubMed ID
11689337
retrieved
22 June 2017
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