Copy number variation analysis reveals additional variants contributing to endometriosis development

Endometriosis Is Associated with Rare Copy Number Variants

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NT5E and FcGBP as key regulators of TGF-1-induced epithelial–mesenchymal transition (EMT) are associated with tumor progression and survival of patients with gallbladder cancer

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High-resolution array-comparative genomic hybridization profiling reveals 20q13.33 alterations associated with ovarian endometriosis

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The Database of Genomic Variants: a curated collection of structural variation in the human genome

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Genome-Wide Association Study Link Novel Loci to Endometriosis

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Candidate genes for schizophrenia in a mixed Brazilian population using pooled DNA

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Identification of differentially expressed genes according to chemosensitivity in advanced ovarian serous adenocarcinomas: expression of GRIA2 predicts better survival

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Genome-wide association meta-analysis identifies new endometriosis risk loci

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Brazilian urban population genetic structure reveals a high degree of admixture

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Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas

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Downregulation of IgG Fc binding protein (FcγBP) in prostate cancer

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WNT4 is required for normal ovarian follicle development and female fertility

(2010) Alexandre Boyer et al.   FASEB JOURNAL

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

(2010) Satoko Uno et al.   NATURE GENETICS

Copy Number Variation in Human Health, Disease, and Evolution

(2009) Feng Zhang et al.   Annual Review of Genomics and Human Genetics

Differentially expressed genes in eutopic and ectopic endometrium of women with endometriosis

(2009) Juliana Meola et al.   FERTILITY AND STERILITY

Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans

(2009) Yohan Bossé et al.   HUMAN GENETICS

Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome

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A genome-wide linkage and association scan reveals novel loci for autism

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Endometriosis

(2009) Serdar E. Bulun   NEW ENGLAND JOURNAL OF MEDICINE

A review of psychiatric genetics research in the Brazilian population

(2009) Quirino Cordeiro et al.   REVISTA BRASILEIRA DE PSIQUIATRIA

Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies

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Stem Cells and the Pathogenesis of Endometriosis

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A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

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Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling

(2008) Chien-hsing Lin et al.   HUMAN MUTATION

The search for genes contributing to endometriosis risk

(2008) Grant W. Montgomery et al.   HUMAN REPRODUCTION UPDATE

A HapMap harvest of insights into the genetics of common disease

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Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

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