Peter N. Robinson

The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process

Sebastian Bauer, Thorsten Dickhaus, Peter M. Krawitz, 2011, Nucleic acids research.

MicroRNAs Differentially Expressed in Postnatal Aortic Development Downregulate Elastin via 3′ UTR and Coding-Sequence Binding Sites

Thomas Manke, Gao Guo, Marten Jäger, 2011, PloS one.

The molecular genetics of Marfan syndrome and related microfibrillopathies

P. Robinson, Peter N. Robinson, Maurice Godfrey, 2000, Journal of medical genetics.

PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.

Na Zhu, Peter M. Krawitz, Stefan Mundlos, 2013, American journal of human genetics.

Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome

Damian Smedley, Yves Moreau, Melissa Haendel, 2014, Science Translational Medicine.

Filtering for Compound Heterozygous Sequence Variants in Non-Consanguineous Pedigrees

Tom Kamphans, Na Zhu, Peter M. Krawitz, 2013, PloS one.

Microindel detection in short-read sequence data

Sebastian Bauer, Christian Rödelsperger, Peter M. Krawitz, 2010, Bioinform..

Computational Exome and Genome Analysis

Rosario M. Piro, Marten Jäger, P. Robinson, 2017 .