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Martina Müller-Nurasyid

Wissenschaftliche Mitarbeiterin

Name	Martina Müller-Nurasyid
Time	2024- (Wirkungsdaten)
Place	Deutschland
Gender	weiblich
Academic degree	Dr. rer. biol.hum.
Profession	Wissenschaftliche Mitarbeiterin (characteristic profession)
Variant	M. Müller-Nurasyid Martina Müller- Nurasyid
Related	Universitätsmedizin Mainz Genetik (Thema) Bioinformatik (Thema)
Record type	Person
GND-Identifier	1361140437
Record ID	1361140437
Involved in show all Genomic and phenotypic stability of fusion-driven pediatric sarcoma cell lines Bi-Gaussian analysis reveals distinct education-related alterations in spherical equivalent and axial length—results from the Gutenberg Health Study Implications of the Codominance Model for Hardy-Weinberg Testing in Genetic Association Studies Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification Proteomics biomarker discovery for individualized prevention of familial pancreatic cancer using statistical learning Network reconstruction for trans acting genetic loci using multi-omics data and prior information Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways Author Correction: Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis Common electrocardiogram measures are not associated with telomere length Deoxyribonuclease 1 Q222R single nucleotide polymorphism and long-term mortality after acute myocardial infarction DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability Cis-epistasis at the LPA locus and risk of cardiovascular diseases Genetic variation and cardiovascular risk factors: a cohort study on migrants from the former Soviet Union and a native German population Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio: a pooled analysis of 458 population-based studies in Asian and Western countries Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 Multi-ethnic genome-wide association study for atrial fibrillation Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis Sequence data and association statistics from 12,940 type 2 diabetes cases and controls Gene-gene Interaction Analyses for Atrial Fibrillation No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.

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Martina Müller-Nurasyid

Genomic and phenotypic stability of fusion-driven pediatric sarcoma cell lines

Bi-Gaussian analysis reveals distinct education-related alterations in spherical equivalent and axial length—results from the Gutenberg Health Study

Implications of the Codominance Model for Hardy-Weinberg Testing in Genetic Association Studies

Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer

Genome‐Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants

European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

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

Proteomics biomarker discovery for individualized prevention of familial pancreatic cancer using statistical learning

Network reconstruction for trans acting genetic loci using multi-omics data and prior information

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Author Correction: Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis

Common electrocardiogram measures are not associated with telomere length

Deoxyribonuclease 1 Q222R single nucleotide polymorphism and long-term mortality after acute myocardial infarction

DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures

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

Cis-epistasis at the LPA locus and risk of cardiovascular diseases

Genetic variation and cardiovascular risk factors: a cohort study on migrants from the former Soviet Union and a native German population

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

Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease

National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio: a pooled analysis of 458 population-based studies in Asian and Western countries

Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

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

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Multi-ethnic genome-wide association study for atrial fibrillation

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

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

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

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

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

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Gene-gene Interaction Analyses for Atrial Fibrillation

No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients

RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies

RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.