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	61	Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2012
	62	Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2012
	63	Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterization Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2012
	64	Tumor necrosis factor polymorphisms in psoriatic arthritis : association with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele Reich, Kristian. - Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2007
	65	Mutation in the Scyl1 gene encoding amino‐terminal kinase‐like protein causes a recessive form of spinocerebellar neurodegeneration Enthalten in European Molecular Biology Organization: EMBO reports Bd. 8, 2007, Nr. 7: 691-697. 7 S.
	66	Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates Enthalten in Human genetics Bd. 112, Nr. 1, date:1.2003: 50-56
	67	Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity Enthalten in Human genetics Bd. 111, Nr. 4-5, date:10.2002: 323-330
	68	Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosis Enthalten in Human genetics Bd. 102, Nr. 3, date:3.1998: 314-318
	69	Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14–q21 by homozygosity mapping Enthalten in Human genetics Bd. 101, Nr. 3, date:12.1997: 376-382
	70	Possible association of the allele status of the CS.7/HhaI polymorphism 5′ of the CFTR gene with postnatal female survival Enthalten in Human genetics Bd. 99, Nr. 5, date:4.1997: 565-572

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