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Recurrent PTPRB and PLCG1 mutations in angiosarcoma

Nature genetics, 2014-04, Vol.46 (4), p.376-379

2014

Volltextzugriff (PDF)

Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution

Nature genetics, 2023-12, Vol.55 (12), p.2255-2268

2023

Volltextzugriff (PDF)

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Nature genetics, 2018-04, Vol.50 (4), p.524-537

2018

Volltextzugriff (PDF)

Tissue-specific enhancer-gene maps from multimodal single-cell data identify causal disease alleles

Nature genetics, 2024-04, Vol.56 (4), p.615-626

2024

Volltextzugriff (PDF)

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Nature genetics, 2012-09, Vol.44 (9), p.991-1005

2012

Volltextzugriff (PDF)

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature genetics, 2012-06, Vol.44 (6), p.659-669

2012

Volltextzugriff (PDF)

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Nature genetics, 2012-05, Vol.44 (5), p.545-551

2012

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Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations

Nature genetics, 2012-08, Vol.44 (8), p.904-909

2012

Volltextzugriff (PDF)

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Nature genetics, 2003-05, Vol.34 (1), p.91-96

2003

Volltextzugriff (PDF)

Common variants at 12q15 and 12q24 are associated with infant head circumference

Nature genetics, 2012-05, Vol.44 (5), p.532-538

2012

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Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

Nature genetics, 2016-08, Vol.48 (8), p.867-876

2016

Volltextzugriff (PDF)

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Nature genetics, 2019-07, Vol.51 (7), p.1192-1193

2019

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Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Nature genetics, 2016-11, Vol.48 (12), p.1591-1591

2016

Volltextzugriff (PDF)

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Nature genetics, 2016-07, Vol.48 (8), p.970-970

2016

Volltextzugriff (PDF)

Genome-wide association analyses of risk tolerance and risky behaviors in over one million individuals identify hundreds of loci and shared genetic influences

Nature genetics, 2019-01, Vol.51 (2), p.245-257

2019

Volltextzugriff (PDF)

Common variants at 6q22 and 17q21 are associated with intracranial volume

Nature genetics, 2013-06, Vol.45 (6), p.713-713

2013

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Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

Nature genetics, 2012-06, Vol.44 (6), p.732-732

2012

Volltextzugriff (PDF)

Common variants at 6q22 and 17q21 are associated with intracranial volume

Nature genetics, 2012-06, Vol.44 (6), p.732

2012

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Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways

Nature genetics, 2012-01, Vol.44 (3), p.260-268

2012

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Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Tissue-specific enhancer-gene maps from multimodal single-cell data identify causal disease alleles

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Common variants at 12q15 and 12q24 are associated with infant head circumference

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Genome-wide association analyses of risk tolerance and risky behaviors in over one million individuals identify hundreds of loci and shared genetic influences

Common variants at 6q22 and 17q21 are associated with intracranial volume

Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

Common variants at 6q22 and 17q21 are associated with intracranial volume

Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways

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