Lista de obras - Michael Steffens - Dominio Público Uruguay

Adverse Drug Reactions in the Emergency Department: Is There a Role for Pharmacogenomic Profiles at Risk?-Results from the ADRED Study

scientific article published on 09 June 2020

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

artículo científico publicado en 2011

CHL1, ITGB3 and SLC6A4 gene expression and antidepressant drug response: results from the Munich Antidepressant Response Signature (MARS) study

artículo científico

Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis

scientific journal article

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

artículo científico publicado en 2007

Cytokine regulation by epidermal growth factor receptor inhibitors and epidermal growth factor receptor inhibitor associated skin toxicity in cancer patients

article

Dosing to rash?--The role of erlotinib metabolic ratio from patient serum in the search of predictive biomarkers for EGFR inhibitor-mediated skin rash

artículo científico publicado en 2016

Evaluation of potential power gain with imputed genotypes in genome-wide association studies

artículo científico publicado en 2009

Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

artículo científico publicado en 2005

Evidence of palladium-defect pairing in intrinsic germanium

scholarly article by H. Timmers et al published April 2010 in Hyperfine Interactions

Familial aggregation of pure tone hearing thresholds in an aging European population

artículo científico publicado en 2013

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

article

Genetic Diversity in German and European Populations: Looking for Substructures and Genetic Patterns

article

Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study

artículo científico publicado en 2015

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

artículo científico publicado en 2011

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

artículo científico publicado en 2012

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

artículo científico publicado en 2012

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Genome-wide association study of alcohol dependence

scientific journal article

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

artículo científico publicado en 2014

Genome-wide association study reveals genetic risk underlying Parkinson's disease

artículo científico publicado en 2009

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

artículo científico publicado en 2010

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

artículo científico publicado en 2011

Genotyping NAT2 with only two SNPs (rs1041983 and rs1801280) outperforms the tagging SNP rs1495741 and is equivalent to the conventional 7-SNP NAT2 genotype

INTERSNP: genome-wide interaction analysis guided by a priori information

article

Impact of Zika Virus Infection on Human Neural Stem Cell MicroRNA Signatures

artículo científico publicado en 2020

Investigation into mechanisms mediating the inhibitory effect of 1,4-benzodiazepines on mast cells by gene expression profiling.

artículo científico publicado en 2013

Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation

artículo científico publicado en 2008

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

artículo científico publicado en 2009

Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis

artículo científico publicado en 2006

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

artículo científico publicado en 2008

Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 epression in monocyte-derived dendritic cells

Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation

artículo científico publicado en 2006

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

artículo científico publicado en 2009

Role of glycogen synthase kinase 3 (GSK-3) in innate immune response of human immature dendritic cells to Aspergillus fumigatus

artículo científico publicado en 2010

SNP-based analysis of genetic substructure in the German population.

artículo científico publicado en 2006

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

artículo científico publicado en 2008

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

Temperature dependence of the hyperfine fields of 111In in sapphire (Al2O3) single crystals

The German multi-centre study on smoking-related behavior-description of a population-based case-control study

artículo científico publicado en 2011

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss

artículo científico publicado en 2007

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

artículo científico publicado en 2007

The val158met polymorphism of human catechol-O-methyltransferase (COMT) affects anterior cingulate cortex activation in response to painful laser stimulation

artículo científico publicado en 2010

VKORCI haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation

article by Christof Geisen et al published 9 September 2005 in Thrombosis and Haemostasis

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

artículo científico publicado en 2014

Lista de obras de Michael Steffens

Adverse Drug Reactions in the Emergency Department: Is There a Role for Pharmacogenomic Profiles at Risk?-Results from the ADRED Study

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

CHL1, ITGB3 and SLC6A4 gene expression and antidepressant drug response: results from the Munich Antidepressant Response Signature (MARS) study

Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

Cytokine regulation by epidermal growth factor receptor inhibitors and epidermal growth factor receptor inhibitor associated skin toxicity in cancer patients

Dosing to rash?--The role of erlotinib metabolic ratio from patient serum in the search of predictive biomarkers for EGFR inhibitor-mediated skin rash

Evaluation of potential power gain with imputed genotypes in genome-wide association studies

Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

Evidence of palladium-defect pairing in intrinsic germanium

Familial aggregation of pure tone hearing thresholds in an aging European population

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

Genetic Diversity in German and European Populations: Looking for Substructures and Genetic Patterns

Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Genome-wide association study of alcohol dependence

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

Genotyping NAT2 with only two SNPs (rs1041983 and rs1801280) outperforms the tagging SNP rs1495741 and is equivalent to the conventional 7-SNP NAT2 genotype

INTERSNP: genome-wide interaction analysis guided by a priori information

Impact of Zika Virus Infection on Human Neural Stem Cell MicroRNA Signatures

Investigation into mechanisms mediating the inhibitory effect of 1,4-benzodiazepines on mast cells by gene expression profiling.

Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 epression in monocyte-derived dendritic cells

Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

Role of glycogen synthase kinase 3 (GSK-3) in innate immune response of human immature dendritic cells to Aspergillus fumigatus

SNP-based analysis of genetic substructure in the German population.

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Temperature dependence of the hyperfine fields of 111In in sapphire (Al2O3) single crystals

The German multi-centre study on smoking-related behavior-description of a population-based case-control study

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

The val158met polymorphism of human catechol-O-methyltransferase (COMT) affects anterior cingulate cortex activation in response to painful laser stimulation

VKORCI haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans