Franz Rüschendorf

发表

ALOHOMORA: a tool for linkage analysis using 10K SNP array data

Peter J. Nürnberg, Franz Rüschendorf, F. Rüschendorf, 2005, Bioinform..

Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE

Manuel Mattheisen, Franz Rüschendorf, Konstantin Strauch, 2007, Bioinform..

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.

Peter Nürnberg, Markus Schuelke, Franz Rüschendorf, 2004, American journal of human genetics.

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation

Juliane Hoyer, Peter Nürnberg, André Reis, 2006, American journal of medical genetics. Part A.

RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection

Lennart Opitz, Peter Nürnberg, Johannes Schumacher, 2009, Nature Genetics.

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Peter Nürnberg, Dominik Seelow, Shazia Ashraf, 2009, PLoS genetics.

Erratum: Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause severe childhood-onset retinal dystrophy (Nature Genetics (2004) 36 (850-854))

Peter Nürnberg, Eduard Schmid, Franz Rüschendorf, 2004 .

Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

Christian Gieger, David Torrents, Kari Stefansson, 2018, Nature Genetics.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Andreas Busjahn, Jens Jordan, Herbert Schulz, 2015, Nature Genetics.

A Genetic Basis for Mechanosensory Traits in Humans

Jens Jordan, Jens Tank, Gary R. Lewin, 2012, PLoS biology.