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Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Nature genetics, 2009-06, Vol.41 (6), p.718-723

2009

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Nature genetics, 2012-01, Vol.44 (1), p.78-84

2012

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X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Nature genetics, 2008-06, Vol.40 (6), p.776-781

2008

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Genome-wide association study identifies three loci associated with melanoma risk

Nature genetics, 2009-08, Vol.41 (8), p.920-925

2009

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Genome-wide association study identifies a common variant associated with risk of endometrial cancer

Nature genetics, 2011-05, Vol.43 (5), p.451-454

2011

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Nature genetics, 2013-03, Vol.45 (3), p.314-318

2013

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Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior

Nature Genetics, 2010-05, Vol.42 (5), p.448-453

2010

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Susceptibility variants for male-pattern baldness on chromosome 20p11

Nature genetics, 2008-11, Vol.40 (11), p.1279-1281

2008

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OPCML at 11q25 is epigenetically inactivated and has tumor-suppressor function in epithelial ovarian cancer

Nature genetics, 2003-07, Vol.34 (3), p.337-343

2003

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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Nature genetics, 2009-01, Vol.41 (1), p.47-55

2009

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Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Nature genetics, 2013-02, Vol.45 (2), p.155-163

2013

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Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures

Nature genetics, 2001-05, Vol.28 (1), p.49-52

2001

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Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Genome-wide association study identifies three loci associated with melanoma risk

Genome-wide association study identifies a common variant associated with risk of endometrial cancer

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior

Susceptibility variants for male-pattern baldness on chromosome 20p11

OPCML at 11q25 is epigenetically inactivated and has tumor-suppressor function in epithelial ovarian cancer

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures

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