Author

Nazanin Mirza‐Schreiber

Helmholtz MunichORCID 0000-0003-0836-8267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Assay:ChIP-seq· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Bertram Müller‐MyhsokiD· 2 shared Daniel Brandeis· 2 shared Markus Maria NötheniD· 2 shared Till F. M. AndlaueriD· 2 shared Adnan KastratiiD· 1 shared Alessandro GialluisiiD· 1 shared Ana Antic Nikolic· 1 shared Andrew P. MorrisiD· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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2 shared papersGenomics

Bertram Müller‐MyhsokORCID

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4 papers

Recent·Most cited

GenomicsProceedings of the National Academy of SciencesPeer-reviewedAug 30, 2022

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Else Eising, Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw…·Daniel Brandeis

This paper conducts genome-wide association studies on reading- and language-related skills in 34,000 people, identifying genetic variants and shared genetic factors across multiple traits.

4 citations

humanGWAS summary statistics

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GeneticsHuman Molecular GeneticsPeer-reviewedDec 7, 2021

Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation

Daniel D. Lam, Ana Antic Nikolic, Chen Zhao…·Juliane Winkelmann

The paper identifies cell type-specific epigenetic features in a conserved MEIS1 intronic region associated with insomnia and restless legs syndrome, showing their role in MEIS1 regulation.

9 citations

humanDNA methylation

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GenomicsTranslational PsychiatryPeer-reviewedFeb 11, 2019

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia.

Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber…·Gerd Schulte‐Körne

The paper conducts a GWAS to identify genetic variants associated with a cognitive predictor of dyslexia, finding significant associations with variants near MIR924HG and NKAIN3.

105 citationstop 1%

humanGWAS summary statistics

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GeneticsbioRxivPreprintJan 23, 2019

Cis-epistasis at the LPA locus and risk of coronary artery disease

Lingyao Zeng, Nazanin Mirza‐Schreiber, Claudia Lamina…·Heribert Schunkert

The paper identifies cis-epistasis at the LPA locus involving two SNPs that interact to modulate coronary artery disease risk and related traits.

1 citation

humanGWAS summary statistics

𝕏 PostBluesky