Christine Herold

Ludwig Erhard Allee 2
Bonn, NW 53175, Germany

Last Updated: 09/26/2026

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Found 16 publications

Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti.

Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti.

Journal: Human genomics

Published: April 13, 2017

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.

Journal: Nature communications

Published: October 27, 2016

TREM2 rare variant p.R47H is not associated with Parkinson's disease.

TREM2 rare variant p.R47H is not associated with Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: September 07, 2015

Prediction of male-pattern baldness from genotypes.

Prediction of male-pattern baldness from genotypes.

Journal: European journal of human genetics : EJHG

Published: April 17, 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

Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families.

Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families.

Journal: BMC medical genetics

Published: December 06, 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

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

A one-degree-of-freedom test for supra-multiplicativity of SNP effects.

A one-degree-of-freedom test for supra-multiplicativity of SNP effects.

Journal: PloS one

Published: May 23, 2013

Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.

Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.

Journal: The Journal of investigative dermatology

Published: January 30, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026