
Publikationen von Nazanin Mirza-Schreiber
Alle Typen
Zeitschriftenartikel (20)
1.
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118 (4), S. 1088 - 1102 (2022)
Cis-epistasis at the LPA locus and risk of cardiovascular diseases. CARDIOVASCULAR RESEARCH 2.
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Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY (2020)
3.
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367 (6484), S. 1340 - + (2020)
The genetic architecture of the human cerebral cortex. SI 4.
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9, 77 (2019)
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY 5.
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51 (11), S. 1624 - 1636 (2019)
Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS 6.
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8, 13624 (2017)
Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS 7.
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8, 1511 (2017)
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS 8.
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19 (12), S. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE 9.
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21 (2), S. 189 - 197 (2016)
GWAS for executive function and processing speed suggests involvement of the CADM2 gene. MOLECULAR PSYCHIATRY 10.
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19 (12), S. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE 11.
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10 (8), e0135807 (2015)
Solid Organ Transplantation in Patients with Inflammatory Bowel Diseases (IBD): Analysis of Transplantation Outcome and IBD Activity in a Large Single Center Cohort. PLOS ONE 12.
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86 (5), S. 1189 - 1202 (2015)
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. NEURON 13.
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77 (8), S. 749 - 763 (2015)
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. BIOLOGICAL PSYCHIATRY 14.
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9 (10), e109290 (2014)
The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels. PLOS ONE 15.
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24 (4), S. 592 - 603 (2014)
Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon. GENOME RESEARCH 16.
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8 (6), e64872 (2013)
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLOS ONE 17.
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52 (1), S. 91 - 95 (2013)
Cost-effective GPU-Grid for Genome-wide Epistasis Calculations. METHODS OF INFORMATION IN MEDICINE 18.
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7 (3), e33682 (2012)
PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background. PLoS ONE 19.
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73 (4), S. 220 - 236 (2012)
GLIDE: GPU-Based Linear Regression for Detection of Epistasis. Human Heredity 20.
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27 (13), S. I214 - I221 (2011)
Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs. Bioinformatics