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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Nature genetics, 2010-07, Vol.42 (7), p.579-589

2010

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Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Nature genetics, 2009-01, Vol.41 (1), p.25-34

2009

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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

Nature genetics, 2008-05, Vol.40 (5), p.638-645

2008

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Variants in MTNR1B influence fasting glucose levels

Nature genetics, 2009-01, Vol.41 (1), p.77-81

2009

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Nature genetics, 2008-02, Vol.40 (2), p.161-169

2008

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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.(Correction notice)

Nature genetics, 2010-05, Vol.42 (5), p.464

2010

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Variants in the melatonin receptor 1B gene (MTNR1B) influence fasting glucose levels

Nature genetics, 2008-12, Vol.41 (1), p.77-81

2008

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-09, Vol.45 (9), p.1044-1049

2013

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Large-scale association analyses identify host factors influencing human gut microbiome composition

Nature genetics, 2021-02, Vol.53 (2), p.156-5

2021

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-11, Vol.45 (11), p.1409-1409

2013

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Corrigendum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-11, Vol.45 (11), p.1409

2013

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Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-10, Vol.45 (11), p.1409-1409

2013

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Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Common variants in the GDF5-UQCC region are associated with variation in human height

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

Variants in MTNR1B influence fasting glucose levels

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Exome array analysis identifies novel loci and low-frequency variants for insulin processing and secretion

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.(Correction notice)

Common variant in MTNRIB associated with increased risk of type 2 diabetes and impaired early insulin secretion

A common variant in the melatonin receptor gene (MTNR1B) is associated with increased risk of future type 2 diabetes and impaired early insulin secretion

Variants in the melatonin receptor 1B gene (MTNR1B) influence fasting glucose levels

Common variants in the GDF5-BFZB region are associated with variation in human height

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Large-scale association analyses identify host factors influencing human gut microbiome composition

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Corrigendum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

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