List of works - Andreas Ziegler

No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma

article

Interrelationship and familiality of dyslexia related quantitative measures

scientific article published on 13 October 2006

Association of single nucleotide polymorphisms in the genes ATM, GSTP1, SOD2, TGFB1, XPD and XRCC1 with risk of severe erythema after breast conserving radiotherapy

scientific article

What Do We Mean by ‘Replication’ and ‘Validation’ in Genome-Wide Association Studies?

scientific article published on 17 October 2008

Ankylosing spondylitis: a beta2m-deposition disease?

scientific article

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design

scientific article published on 2 May 2005

BiomarCaRE: rationale and design of the European BiomarCaRE project including 300,000 participants from 13 European countries

scientific article

Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents

scientific article

Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data

scientific article

Association tests for X-chromosomal markers--a comparison of different test statistics

scientific article

Analysis of the base excision repair genes MTH1, OGG1 and MUTYH in patients with squamous oral carcinomas

article

HLA-B27 heavy chains distinguished by a micropolymorphism exhibit differential flexibility

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

article

Picking single-nucleotide polymorphisms in forests

scientific article

Data mining, neural nets, trees--problems 2 and 3 of Genetic Analysis Workshop 15.

scientific article

Novel intronic polymorphisms in theRET proto-oncogene and their association with Hirschsprung disease

Hypofractionation with simultaneous integrated boost for early breast cancer

scientific article published on 16 April 2014

Complex transcription and splicing of odorant receptor genes

scientific article

No evidence for an involvement of alleles of polymorphisms in the serotonin1Dβ and 7 receptor genes in obesity, underweight or anorexia nervosa

article

Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome

scientific article published on 01 October 1996

Treatment with an Anti-CD44v10-Specific Antibody Inhibits the Onset of Alopecia Areata in C3H/HeJ Mice

article

NMR spectroscopy reveals unexpected structural variation at the protein-protein interface in MHC class I molecules

scientific article published on 5 September 2013

Update of Familial Pancreatic Cancer in Germany

article

Variations of the melanocortin-1 receptor and the glutathione-S transferase T1 and M1 genes in cutaneous malignant melanoma

scientific article published on 28 October 2006

Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability

article

Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.

scientific article published in August 2000

Observation and execution of upper-limb movements as a tool for rehabilitation of motor deficits in paretic stroke patients: protocol of a randomized clinical trial

scientific article

HLA class I-associated diseases with a suspected autoimmune etiology: HLA-B27 subtypes as a model system

scientific article published on 12 June 2011

Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults

scientific article published in January 1997

Ras-associated small GTPase 33A, a novel T cell factor, is down-regulated in patients with tuberculosis

scientific article

Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus

scientific article published on 4 May 2015

Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population

scientific article published in November 2008

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

scientific article published on 03 August 2005

Reduced body fat in long-term followed-up female patients with anorexia nervosa

scientific article published on 01 January 2000

The choice of the filtering method in microarrays affects the inference regarding dosage compensation of the active X-chromosome

scientific article

Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis

scientific article published on January 2011

Association of polymorphisms in the human surfactant protein-D (SFTPD) gene and postnatal pulmonary adaptation in the preterm infant

article

Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences

scientific article

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

scientific article published on 26 December 2013

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome

scientific article published in July 1997

TLR4andIL-18gene variants in aggressive periodontitis

article

Sample size calculations for controlled clinical trials using generalized estimating equations (GEE).

scientific article published in January 2004

Secular trends in body mass index measurements in preschool children from the City of Aachen, Germany

scientific article published on 9 January 2003

Serum leptin levels, body fat deposition, and weight in females with anorexia or bulimia nervosa

scientific article published in April 1999

Citrullination-dependent differential presentation of a self-peptide by HLA-B27 subtypes

scientific article

Influence of sex and genetic variability on expression of X-linked genes in human monocytes.

scientific article

Influence of inflammation-related changes on conformational characteristics of HLA-B27 subtypes as detected by IR spectroscopy

scientific article published on 4 April 2011

Significant weight gains in a clinical sample of obese children and adolescents between 1985 and 1995

scientific article published on 01 February 1997

Probability estimation with machine learning methods for dichotomous and multicategory outcome: applications.

scientific article published on 12 February 2014

Detection rates for genotyping errors in SNPs using the trio design

scientific article published in January 2002

List of works by Andreas Ziegler

No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma

Interrelationship and familiality of dyslexia related quantitative measures

Association of single nucleotide polymorphisms in the genes ATM, GSTP1, SOD2, TGFB1, XPD and XRCC1 with risk of severe erythema after breast conserving radiotherapy

What Do We Mean by ‘Replication’ and ‘Validation’ in Genome-Wide Association Studies?

Ankylosing spondylitis: a beta2m-deposition disease?

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design

BiomarCaRE: rationale and design of the European BiomarCaRE project including 300,000 participants from 13 European countries

Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents

Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data

Association tests for X-chromosomal markers--a comparison of different test statistics

Analysis of the base excision repair genes MTH1, OGG1 and MUTYH in patients with squamous oral carcinomas

HLA-B27 heavy chains distinguished by a micropolymorphism exhibit differential flexibility

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

Picking single-nucleotide polymorphisms in forests

Data mining, neural nets, trees--problems 2 and 3 of Genetic Analysis Workshop 15.

Novel intronic polymorphisms in theRET proto-oncogene and their association with Hirschsprung disease

Hypofractionation with simultaneous integrated boost for early breast cancer

Complex transcription and splicing of odorant receptor genes

No evidence for an involvement of alleles of polymorphisms in the serotonin1Dβ and 7 receptor genes in obesity, underweight or anorexia nervosa

Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome

Treatment with an Anti-CD44v10-Specific Antibody Inhibits the Onset of Alopecia Areata in C3H/HeJ Mice

NMR spectroscopy reveals unexpected structural variation at the protein-protein interface in MHC class I molecules

Update of Familial Pancreatic Cancer in Germany

Variations of the melanocortin-1 receptor and the glutathione-S transferase T1 and M1 genes in cutaneous malignant melanoma

Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability

Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.

Observation and execution of upper-limb movements as a tool for rehabilitation of motor deficits in paretic stroke patients: protocol of a randomized clinical trial

HLA class I-associated diseases with a suspected autoimmune etiology: HLA-B27 subtypes as a model system

Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults

Ras-associated small GTPase 33A, a novel T cell factor, is down-regulated in patients with tuberculosis

Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus

Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

Reduced body fat in long-term followed-up female patients with anorexia nervosa

The choice of the filtering method in microarrays affects the inference regarding dosage compensation of the active X-chromosome

Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis

Association of polymorphisms in the human surfactant protein-D (SFTPD) gene and postnatal pulmonary adaptation in the preterm infant

Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome

TLR4andIL-18gene variants in aggressive periodontitis

Sample size calculations for controlled clinical trials using generalized estimating equations (GEE).

Secular trends in body mass index measurements in preschool children from the City of Aachen, Germany

Serum leptin levels, body fat deposition, and weight in females with anorexia or bulimia nervosa

Citrullination-dependent differential presentation of a self-peptide by HLA-B27 subtypes

Influence of sex and genetic variability on expression of X-linked genes in human monocytes.

Influence of inflammation-related changes on conformational characteristics of HLA-B27 subtypes as detected by IR spectroscopy

Significant weight gains in a clinical sample of obese children and adolescents between 1985 and 1995

Probability estimation with machine learning methods for dichotomous and multicategory outcome: applications.

Detection rates for genotyping errors in SNPs using the trio design