Lista de obras - Peter Ahnert - Dominio Público Uruguay

5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population.

artículo científico publicado en 2009

A Biomathematical Model of Pneumococcal Lung Infection and Antibiotic Treatment in Mice

artículo científico publicado en 2016

A biomathematical model of immune response and barrier function in mice with pneumococcal lung infection

artículo científico publicado en 2020

A family-based study does not support the association of a functional polymorphism in the gene for endothelial nitric oxide synthase with risk for rheumatoid arthritis

artículo científico publicado en 2009

Adverse drug reactions in elderly people : First data from the Leipzig Research Center for Civilization Diseases (LIFE)

artículo científico publicado en 2016

Association of Human Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study ⬇️

artículo científico publicado en 2019

Association of MICA with rheumatoid arthritis independent of known HLA-DRB1 risk alleles in a family-based and a case control study

artículo científico publicado en 2009

Association of proteome and metabolome signatures with severity in patients with community-acquired pneumonia

scientific article published on 30 December 2019

Association of rs2069459 in the CDK5 gene with dyslexia in a German cohort.

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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

artículo científico publicado en 2012

Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort

artículo científico publicado en 2016

Asymmetric interactions of hexameric bacteriophage T7 DNA helicase with the 5'- and 3'-tails of the forked DNA substrate.

artículo científico publicado en 1997

Attenuated PDGF signaling drives alveolar and microvascular defects in neonatal chronic lung disease.

artículo científico publicado en 2017

Body surface assessment with 3D laser-based anthropometry: reliability, validation, and improvement of empirical surface formulae.

artículo científico publicado en 2017

Bortezomib sensitizes primary human astrocytoma cells of WHO grades I to IV for tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis.

artículo científico publicado en 2007

Cell cycle, oncogenic and tumor suppressor pathways regulate numerous long and macro non-protein-coding RNAs

artículo científico publicado en 2014

Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression

artículo científico publicado en 2014

Central neurocytoma: SNP array analyses, subtel FISH, and review of the literature

scientific article published on 27 March 2019

Comparing performance of modern genotype imputation methods in different ethnicities

scientific article published on 04 October 2016

Comprehensive cytogenetic characterization of an esthesioneuroblastoma

artículo científico publicado en 2007

Comprehensive high-resolution genomic profiling and cytogenetics of human chondrocyte cultures by GTG-banding, locus-specific FISH, SKY and SNP array

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Copy number variants in lipid metabolism genes are associated with gallstones disease in men

scientific article published on 04 September 2019

Cytogenetic and molecular biological characterization of an adult medulloblastoma.

artículo científico publicado en 2007

Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array ⬇️

artículo científico publicado el 8 de mayo de 2012

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

artículo científico publicado en 2012

Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

artículo científico publicado en 2015

Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

artículo científico publicado en 2014

Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.

artículo científico publicado en 2008

HLA Class II Allele Analyses Implicate Common Genetic Components in Type 1 and Non-Insulin-Treated Type 2 Diabetes

scientific article published on 01 March 2020

High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas

artículo científico publicado en 2011

Identification of New, Functionally Relevant Mutations in the Coding Regions of the Human Fos and Jun Proto-Oncogenes in Rheumatoid Arthritis Synovial Tissue

artículo científico publicado en 2020

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2011

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2012

Impact of pre-imputation SNP-filtering on genotype imputation results.

artículo científico publicado en 2014

Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis.

artículo científico publicado en 2011

Markov State Modelling of Disease Courses and Mortality Risks of Patients with Community-Acquired Pneumonia

artículo científico publicado en 2020

Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics

artículo científico publicado en 2011

Neutralizing Complement C5a Protects Mice with Pneumococcal Pulmonary Sepsis

artículo científico publicado en 2020

No association between systemic sclerosis and C77G polymorphism in the human PTPRC (CD45) gene

artículo científico publicado en 2008

Novel Anthropometry Based on 3D-Bodyscans Applied to a Large Population Based Cohort

artículo científico publicado en 2016

PROGRESS - prospective observational study on hospitalized community acquired pneumonia

artículo científico publicado en 2016

Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays

artículo científico publicado en 2011

Relevance of the gene variant PTPN22 620W for rheumatology

artículo científico publicado en 2008

Reliability of 3D laser-based anthropometry and comparison with classical anthropometry

artículo científico publicado en 2016

Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints

artículo científico publicado en 2013

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

artículo científico publicado en 2006

Sequential organ failure assessment score is an excellent operationalization of disease severity of adult patients with hospitalized community acquired pneumonia - results from the prospective observational PROGRESS study

artículo científico publicado en 2019

The LIFE-Adult-Study: objectives and design of a population-based cohort study with 10,000 deeply phenotyped adults in Germany

artículo científico publicado en 2015

The pore size of PLGA bone implants determines the de novo formation of bone tissue in tibial head defects in rats

artículo científico publicado en 2012

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.

artículo científico publicado en 2015

The role of gene DCDC2 in German dyslexics.

artículo científico publicado en 2009

Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature.

artículo científico publicado en 2014

[Self-reported infections in the German National Cohort (GNC) in the context of the current research landscape]

artículo científico publicado en 2020

Lista de obras de Peter Ahnert

5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population.

A Biomathematical Model of Pneumococcal Lung Infection and Antibiotic Treatment in Mice

A biomathematical model of immune response and barrier function in mice with pneumococcal lung infection

A family-based study does not support the association of a functional polymorphism in the gene for endothelial nitric oxide synthase with risk for rheumatoid arthritis

Adverse drug reactions in elderly people : First data from the Leipzig Research Center for Civilization Diseases (LIFE)

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 proteome and metabolome signatures with severity in patients with community-acquired pneumonia

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.

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

Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort

Asymmetric interactions of hexameric bacteriophage T7 DNA helicase with the 5'- and 3'-tails of the forked DNA substrate.

Attenuated PDGF signaling drives alveolar and microvascular defects in neonatal chronic lung disease.

Body surface assessment with 3D laser-based anthropometry: reliability, validation, and improvement of empirical surface formulae.

Bortezomib sensitizes primary human astrocytoma cells of WHO grades I to IV for tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis.

Cell cycle, oncogenic and tumor suppressor pathways regulate numerous long and macro non-protein-coding RNAs

Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression

Central neurocytoma: SNP array analyses, subtel FISH, and review of the literature

Comparing performance of modern genotype imputation methods in different ethnicities

Comprehensive cytogenetic characterization of an esthesioneuroblastoma

Comprehensive high-resolution genomic profiling and cytogenetics of human chondrocyte cultures by GTG-banding, locus-specific FISH, SKY and SNP array

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

Copy number variants in lipid metabolism genes are associated with gallstones disease in men

Cytogenetic and molecular biological characterization of an adult medulloblastoma.

Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array ⬇️

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

Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.

HLA Class II Allele Analyses Implicate Common Genetic Components in Type 1 and Non-Insulin-Treated Type 2 Diabetes

High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas

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

Imaging genetics of FOXP2 in dyslexia

Impact of pre-imputation SNP-filtering on genotype imputation results.

Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis.

Markov State Modelling of Disease Courses and Mortality Risks of Patients with Community-Acquired Pneumonia

Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics

Neutralizing Complement C5a Protects Mice with Pneumococcal Pulmonary Sepsis

No association between systemic sclerosis and C77G polymorphism in the human PTPRC (CD45) gene

Novel Anthropometry Based on 3D-Bodyscans Applied to a Large Population Based Cohort

PROGRESS - prospective observational study on hospitalized community acquired pneumonia

Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays

Relevance of the gene variant PTPN22 620W for rheumatology

Reliability of 3D laser-based anthropometry and comparison with classical anthropometry

Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints

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

Sequential organ failure assessment score is an excellent operationalization of disease severity of adult patients with hospitalized community acquired pneumonia - results from the prospective observational PROGRESS study

The LIFE-Adult-Study: objectives and design of a population-based cohort study with 10,000 deeply phenotyped adults in Germany

The pore size of PLGA bone implants determines the de novo formation of bone tissue in tibial head defects in rats

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.

The role of gene DCDC2 in German dyslexics.

Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature.

[Self-reported infections in the German National Cohort (GNC) in the context of the current research landscape]