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Claudia Langenberg (1972-)

Name	Claudia Langenberg
Zeit	1972- (Lebensdaten)
Ort	München (Geburtsort) Deutschland
Weitere Angaben	Diss. Fachbereich Medizin
Quelle	AM Metadaten
Datensatztyp	Person
GND-Nummer	129408182
Datensatz-ID	129408182
Beteiligt an alle anzeigen Obesity due to MC4R deficiency is associated with reduced cholesterol, triglycerides and cardiovascular disease risk Machine learning-guided deconvolution of plasma protein levels A genetic map of human metabolism across the allele frequency spectrum Sex differences in the genetic regulation of the human plasma proteome Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes Author Correction: Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats Large-scale multi-omics identifies drug targets for heart failure with reduced and preserved ejection fraction Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery disease Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats Genetic basis of early onset and progression of type 2 diabetes in South Asians Genetic architecture of routinely acquired blood tests in a British South Asian cohort Disease coverage of human genome-wide association studies and pharmaceutical research and development Mapping biological influences on the human plasma proteome beyond the genome Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health The genetic landscape of neuro-related proteins in human plasma Proteomic signatures improve risk prediction for common and rare diseases Reporting guidelines for precision medicine research of clinical relevance: the BePRECISE checklist Complex patterns of multimorbidity associated with severe COVID-19 and long COVID Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications Plasma Metabolites Related to the Consumption of Different Types of Dairy Products and Their Association with New‐Onset Type 2 Diabetes: Analyses in the Fenland and EPIC‐Norfolk Studies, United Kingdom Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism Identification of circulating proteins associated with general cognitive function among middle-aged and older adults Multi-omic prediction of incident type 2 diabetes ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenon Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases Circulating metabolites modulated by diet are associated with depression Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism Circulating proteins to predict COVID-19 severity Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals Metabolomic profiles predict individual multidisease outcomes Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ELF5 is a potential respiratory epithelial cell-specific risk gene for severe COVID-19 Author Correction: Metabolomic profiling reveals extensive adrenal suppression due to inhaled corticosteroid therapy in asthma Metabolomic profiling reveals extensive adrenal suppression due to inhaled corticosteroid therapy in asthma Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes Rare and common genetic determinants of metabolic individuality and their effects on human health Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19 Genetic disruption of serine biosynthesis is a key driver of macular telangiectasia type 2 aetiology and progression A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women A cross-platform approach identifies genetic regulators of human metabolism and health Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease A Mendelian Randomization Study Genetic architecture of host proteins involved in SARS-CoV-2 infection Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study Integrating Genetics and the Plasma Proteome to Predict the Risk of Type 2 Diabetes rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis Autoimmunity plays a role in the onset of diabetes after 40 years of age Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 Interleukin-18 as a drug repositioning opportunity for inflammatory bowel disease: A Mendelian randomization study Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

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Katalog der Deutschen Nationalbibliothek

Claudia Langenberg (1972-)

Obesity due to MC4R deficiency is associated with reduced cholesterol, triglycerides and cardiovascular disease risk

Machine learning-guided deconvolution of plasma protein levels

A genetic map of human metabolism across the allele frequency spectrum

Sex differences in the genetic regulation of the human plasma proteome

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

Author Correction: Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats

Large-scale multi-omics identifies drug targets for heart failure with reduced and preserved ejection fraction

Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery disease

Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats

Genetic basis of early onset and progression of type 2 diabetes in South Asians

Genetic architecture of routinely acquired blood tests in a British South Asian cohort

Disease coverage of human genome-wide association studies and pharmaceutical research and development

Mapping biological influences on the human plasma proteome beyond the genome

Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health

The genetic landscape of neuro-related proteins in human plasma

Proteomic signatures improve risk prediction for common and rare diseases

Reporting guidelines for precision medicine research of clinical relevance: the BePRECISE checklist

Complex patterns of multimorbidity associated with severe COVID-19 and long COVID

Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers

Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Plasma Metabolites Related to the Consumption of Different Types of Dairy Products and Their Association with New‐Onset Type 2 Diabetes: Analyses in the Fenland and EPIC‐Norfolk Studies, United Kingdom

Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

Multi-omic prediction of incident type 2 diabetes

ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenon

Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases

Circulating metabolites modulated by diet are associated with depression

Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

Circulating proteins to predict COVID-19 severity

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals

The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals

Metabolomic profiles predict individual multidisease outcomes

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

ELF5 is a potential respiratory epithelial cell-specific risk gene for severe COVID-19

Author Correction: Metabolomic profiling reveals extensive adrenal suppression due to inhaled corticosteroid therapy in asthma

Metabolomic profiling reveals extensive adrenal suppression due to inhaled corticosteroid therapy in asthma

Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes

Rare and common genetic determinants of metabolic individuality and their effects on human health

Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19

Genetic disruption of serine biosynthesis is a key driver of macular telangiectasia type 2 aetiology and progression

A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity

Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women

A cross-platform approach identifies genetic regulators of human metabolism and health

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease A Mendelian Randomization Study

Genetic architecture of host proteins involved in SARS-CoV-2 infection

Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study

Integrating Genetics and the Plasma Proteome to Predict the Risk of Type 2 Diabetes

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis

Autoimmunity plays a role in the onset of diabetes after 40 years of age

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

Interleukin-18 as a drug repositioning opportunity for inflammatory bowel disease: A Mendelian randomization study

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity