Kirsten, Holger 1976-
Holger Kirsten researcher
VIAF ID: 172683073 (Personal)
Permalink: http://viaf.org/viaf/172683073
Preferred Forms
- 100 0 _ ‡a Holger Kirsten ‡c researcher
- 100 1 _ ‡a Kirsten, Holger ‡d 1976-
- 100 1 _ ‡a Kirsten, Holger ‡d 1976-
4xx's: Alternate Name Forms (1)
5xx's: Related Names (1)
Works
Title | Sources |
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5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population. | |
Association of Human Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study | |
Association of MICA with rheumatoid arthritis independent of known HLA-DRB1 risk alleles in a family-based and a case control study | |
Association of rs2069459 in the CDK5 gene with dyslexia in a German cohort. | |
Association of the X-chromosomal genes TIMP1 and IL9R with rheumatoid arthritis. | |
Biomechanical properties of polymer-infiltrated ceramic crowns on one-piece zirconia implants after long-term chewing simulation. | |
A catalog of genetic loci associated with kidney function from analyses of a million individuals | |
Common variants in glyoxalase I do not increase chronic pancreatitis risk | |
Comparing performance of modern genotype imputation methods in different ethnicities | |
Complexin2 modulates working memory-related neural activity in patients with schizophrenia. | |
Cytogenetic and molecular biological characterization of an adult medulloblastoma. | |
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†. | |
Dyslexia risk gene relates to representation of sound in the auditory brainstem. | |
Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1. | |
Effectiveness of different central venous catheter fixation suture techniques: An in vitro crossover study | |
Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes | |
Genetic risk variants for dyslexia on chromosome 18 in a German cohort. | |
Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study | |
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | |
Genome-wide association study data reveal genetic susceptibility to chronic inflammatory intestinal diseases and pancreatic ductal adenocarcinoma risk | |
Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis | |
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia | |
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin | |
Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery | |
High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas | |
Human brain arousal in the resting state: a genome-wide association study | |
Identification of New, Functionally Relevant Mutations in the Coding Regions of the Human Fos and Jun Proto-Oncogenes in Rheumatoid Arthritis Synovial Tissue | |
Imaging genetics of FOXP2 in dyslexia | |
Impact of medication on blood transcriptome reveals off-target regulations of beta-blockers | |
Impact of pre-imputation SNP-filtering on genotype imputation results. | |
Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives | |
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 | |
Intra-individual alterations of serum markers routinely used in forensic pathology depending on increasing post-mortem interval | |
Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis. | |
MALDI-TOF basierte Genotypisierung Charakterisierung und Optimierung der Methode sowie Anwendung in genetischen Studien zur Rheumatoiden Arthritis | |
Measurement of Cerebral Biomarkers Proving Traumatic Brain Injuries in Post-Mortem Body Fluids | |
Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2 | |
Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics | |
National and subnational short-term forecasting of COVID-19 in Germany and Poland during early 2021 | |
Neurobiological origins of individual differences in mathematical ability | |
No association between systemic sclerosis and C77G polymorphism in the human PTPRC (CD45) gene | |
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits | |
NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school. | |
On the Parametrization of Epidemiologic Models—Lessons from Modelling COVID-19 Epidemic | |
Post-mortem in situ stability of serum markers of cerebral damage and acute phase response | |
Prognostic Factors for Iatrogenic Tracheal Rupture: A Single-Center Retrospective Cohort Study | |
Reply to Loughlin et al. | |
Robustness of single-base extension against mismatches at the site of primer attachment in a clinical assay. | |
The role of gene DCDC2 in German dyslexics. | |
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. | |
A stereotaxic, population-averaged T1w ovine brain atlas including cerebral morphology and tissue volumes | |
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | |
Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature. | |
Transcriptome Analyses of Adipose Tissue Samples Identify <i>EGFL6</i> as a Candidate Gene Involved in Obesity-Related Adipose Tissue Dysfunction in Children | |
Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis |