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List of works by Holger Kirsten

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The role of HPV RNA transcription, immune response-related gene expression and disruptive TP53 mutations in diagnostic and prognostic profiling of head and neck cancer.

scientific article published on 20 June 2015
The role of gene DCDC2 in German dyslexics.

scientific article published on 24 February 2009
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

scientific article published on 27 May 2015
A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019
Association of MICA with rheumatoid arthritis independent of known HLA-DRB1 risk alleles in a family-based and a case control study

scientific article published on May 2009
Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study

scientific article
Association of the X-chromosomal genes TIMP1 and IL9R with rheumatoid arthritis.

scientific article published in September 2009
Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

scholarly article published 19 October 2018
Impact of pre-imputation SNP-filtering on genotype imputation results.

scientific article
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

scientific article published on 02 October 2019
A stereotaxic, population-averaged T1w ovine brain atlas including cerebral morphology and tissue volumes

scientific article published on 4 June 2015
Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood

scientific article
Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis

scientific article
Comparing performance of modern genotype imputation methods in different ethnicities

scientific article published on 04 October 2016
Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives

scientific article
Robustness of single-base extension against mismatches at the site of primer attachment in a clinical assay.

scientific article
Association study of a functional genetic variant in KIAA0319 in German dyslexics

scientific article published on 01 August 2012
Comprehensive cytogenetic characterization of an esthesioneuroblastoma

scientific article published on 01 March 2007
NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school.

scientific article published on 24 June 2016
Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics

scientific article published on 01 January 2011
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin

scientific article
Dyslexia risk gene relates to representation of sound in the auditory brainstem.

scientific article
Complexin2 modulates working memory-related neural activity in patients with schizophrenia.

scientific article
Differential allelic expression of IL13 and CSF2 genes associated with asthma.

scientific article published on July 2012
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

scientific article published on 11 September 2019
Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.

scientific article published in July 2008
Comparison of scoring methods for the detection of causal genes with or without rare variants

scientific article published on November 29, 2011
Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis.

scientific article published on 9 February 2011
Human brain arousal in the resting state: a genome-wide association study

scientific article published on 27 April 2018
Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

scientific article published on 3 February 2014
Association of Human Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study

scientific article published on 19 March 2019
No association between systemic sclerosis and C77G polymorphism in the human PTPRC (CD45) gene

scientific article published in September 2008
Measurement of Cerebral Biomarkers Proving Traumatic Brain Injuries in Post-Mortem Body Fluids

scientific article published on 06 July 2018
Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array

scientific article published on May 8, 2012
5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population.

scientific article published on 26 March 2009
Intra-individual alterations of serum markers routinely used in forensic pathology depending on increasing post-mortem interval

scientific article published in Scientific Reports
Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature.

scientific article
Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes

scientific article published on 01 May 2018
Effectiveness of different central venous catheter fixation suture techniques: An in vitro crossover study

scientific article published on 12 September 2019
Biomechanical properties of polymer-infiltrated ceramic crowns on one-piece zirconia implants after long-term chewing simulation

scientific article
Comprehensive high-resolution genomic profiling and cytogenetics of two pediatric and one adult medulloblastoma.

scientific article published on 4 July 2013
High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas

scientific article published on 01 October 2011
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

scientific article published on 12 October 2020
Genome-wide association study data reveal genetic susceptibility to chronic inflammatory intestinal diseases and pancreatic ductal adenocarcinoma risk

scientific article published on 08 July 2020
Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2

scientific article published on 01 March 2022
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

scientific article published on 14 October 2020
Prognostic Factors for Iatrogenic Tracheal Rupture: A Single-Center Retrospective Cohort Study

scientific article published on 01 February 2020
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis

scientific article published on 10 January 2022
Reply to Loughlin et al.

scientific article published in February 2007
Transcriptome Analyses of Adipose Tissue Samples Identify EGFL6 as a Candidate Gene Involved in Obesity-Related Adipose Tissue Dysfunction in Children

scientific article published on 14 April 2022

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