Nothnagel, Michael 1971-
Michael Nothnagel researcher
VIAF ID: 47850229 ( Personal )
Permalink: http://viaf.org/viaf/47850229
Preferred Forms
4xx's: Alternate Name Forms (4)
5xx's: Related Names (2)
Works
Title | Sources |
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Analysis of single nucleotide polymorphisms in chronic beryllium disease | |
Benchmarking of univariate pleiotropy detection methods, with an application to epilepsy phenotypes | |
definition of multilocus haplotype blocks and common diseases | |
Distinct gene-set burden patterns underlie common generalized and focal epilepsies | |
Generalized Linear Mixed Models for the interpretation of allelic drop-out observed in PCR-amplified low quality and degraded DNA samples analyzed with short tandem repeat markers in forensic genetics | |
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci | |
Statistical investigation of two current issues in genetic epidemiology | |
Statistische Aspekte genomweiter Assoziationstudien |