(Q28307763)

7 January 2021

Genomic rearrangements and sporadic disease

1 reference

7 January 2021

Lamin B1 duplications cause autosomal dominant leukodystrophy

1 reference

7 January 2021

Hereditary pancreatitis caused by triplication of the trypsinogen locus

1 reference

7 January 2021

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

1 reference

7 January 2021

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

7 January 2021

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

7 January 2021

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

1 reference

7 January 2021

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

1 reference

7 January 2021

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

7 January 2021

Efficiency and power in genetic association studies

1 reference

7 January 2021

Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

7 January 2021

An SNP map of the human genome generated by reduced representation shotgun sequencing

1 reference

7 January 2021

Quality and completeness of SNP databases

1 reference

7 January 2021

Whole-genome patterns of common DNA variation in three human populations

1 reference

7 January 2021

A haplotype map of the human genome

1 reference

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

7 January 2021

Detection of large-scale variation in the human genome

1 reference

7 January 2021

Segmental duplications and copy-number variation in the human genome

1 reference

7 January 2021

Fine-scale structural variation of the human genome

1 reference

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

1 reference

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

7 January 2021

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

7 January 2021

Genome assembly comparison identifies structural variants in the human genome.

1 reference

7 January 2021

Global variation in copy number in the human genome

1 reference

7 January 2021

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

1 reference

7 January 2021

Chemical characterization of element 112

1 reference

7 January 2021

Accurate and reliable high-throughput detection of copy number variation in the human genome

1 reference

7 January 2021

The fine-scale structure of recombination rate variation in the human genome

1 reference

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

7 January 2021

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

1 reference

7 January 2021

Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma

1 reference

7 January 2021

Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysis

1 reference

7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

7 January 2021

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

7 January 2021

Demonstrating stratification in a European American population

1 reference

7 January 2021

Association mapping in structured populations

1 reference

7 January 2021

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

7 January 2021

Population structure, differential bias and genomic control in a large-scale, case-control association study

1 reference

7 January 2021

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

7 January 2021