Andre Lacour

Ludwig Erhard Allee 2
Bonn, NW 53175, Germany

Last Updated: 09/26/2026

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Found 16 publications

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.

Journal: Journal of affective disorders

Published: July 20, 2017

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.

Journal: PloS one

Published: October 10, 2016

Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci.

Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci.

Journal: Bioinformatics (Oxford, England)

Published: October 02, 2015

Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment.

Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: September 16, 2015

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.

Journal: Translational psychiatry

Published: August 20, 2015

Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment.

Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment.

Journal: Molecular psychiatry

Published: June 30, 2015

Analysis of the progression of systolic blood pressure using imputation of missing phenotype values.

Analysis of the progression of systolic blood pressure using imputation of missing phenotype values.

Journal: BMC proceedings

Published: December 19, 2014

METAINTER: meta-analysis of multiple regression models in genome-wide association studies.

METAINTER: meta-analysis of multiple regression models in genome-wide association studies.

Journal: Bioinformatics (Oxford, England)

Published: September 26, 2014

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.

Journal: Human molecular genetics

Published: July 17, 2014

PLD3 in non-familial Alzheimer's disease.

PLD3 in non-familial Alzheimer's disease.

Journal: Nature

Published: July 15, 2014

Novel genetic matching methods for handling population stratification in genome-wide association studies.

Novel genetic matching methods for handling population stratification in genome-wide association studies.

Journal: BMC bioinformatics

Published: July 11, 2014

Rare variant testing of imputed data: an analysis pipeline typified.

Rare variant testing of imputed data: an analysis pipeline typified.

Journal: Human heredity

Published: June 10, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026