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Author Details
Full Name
Martina M??ller-Nurasyid
Affiliation
Institute for Medical Information Processing
ORCID
Career Start Year
2003
Papers
187
H Index
72
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36701413
Proteomics biomarker discovery for individualized prevention of familial pancreatic cancer using statistical learning.
PLoS One
2023
37794016
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.
Nat Commun
2023
36701413
Proteomics biomarker discovery for individualized prevention of familial pancreatic cancer using statistical learning.
PLoS One
2023
37794016
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.
Nat Commun
2023
34142125
Chronically elevated branched chain amino acid levels are pro-arrhythmic.
Cardiovasc Res
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
36344995
Network reconstruction for trans acting genetic loci using multi-omics data and prior information.
Genome Med
2022
35489115
ExomeChip-based rare variant association study in restless legs syndrome.
Sleep Med
2022
35787517
Common electrocardiogram measures are not associated with telomere length.
Aging (Albany NY)
2022
33878186
Cis-epistasis at the LPA locus and risk of cardiovascular diseases.
Cardiovasc Res
2022
34142125
Chronically elevated branched chain amino acid levels are pro-arrhythmic.
Cardiovasc Res
2022
35217655
Author Correction: Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nat Commun
2022
35013273
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nat Commun
2022
34886679
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.
Circ Res
2022
35787517
Common electrocardiogram measures are not associated with telomere length.
Aging (Albany NY)
2022
35489115
ExomeChip-based rare variant association study in restless legs syndrome.
Sleep Med
2022
36344995
Network reconstruction for trans acting genetic loci using multi-omics data and prior information.
Genome Med
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
33878186
Cis-epistasis at the LPA locus and risk of cardiovascular diseases.
Cardiovasc Res
2022
35013273
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nat Commun
2022
35217655
Author Correction: Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nat Commun
2022
34886679
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.
Circ Res
2022
33413638
DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures.
Clin Epigenetics
2021
33491046
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.
J Gerontol A Biol Sci Med Sci
2021
34230475
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33677556
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Eur Heart J
2021
33891165
Deoxyribonuclease 1 Q222R single nucleotide polymorphism and long-term mortality after acute myocardial infarction.
Basic Res Cardiol
2021
33517400
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
Hum Mol Genet
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
34201265
Genetic Variation and Cardiovascular Risk Factors: A Cohort Study on Migrants from the Former Soviet Union and a Native German Population.
Int J Environ Res Public Health
2021
33558525
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34183656
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
34082474
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study.
Genet Epidemiol
2021
33107653
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease.
Mov Disord
2021
33413638
DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures.
Clin Epigenetics
2021
33402679
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34785669
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nat Commun
2021
34475573
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.
Nat Genet
2021
33517400
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
Hum Mol Genet
2021
33491046
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.
J Gerontol A Biol Sci Med Sci
2021
33677556
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Eur Heart J
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
33558525
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
33891165
Deoxyribonuclease 1 Q222R single nucleotide polymorphism and long-term mortality after acute myocardial infarction.
Basic Res Cardiol
2021
34785669
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nat Commun
2021
34475573
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.
Nat Genet
2021
34183656
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
34201265
Genetic Variation and Cardiovascular Risk Factors: A Cohort Study on Migrants from the Former Soviet Union and a Native German Population.
Int J Environ Res Public Health
2021
34230475
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
34082474
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study.
Genet Epidemiol
2021
1 - 50 of 374
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