K. Schmitt

Somatic mutations and promotor methylation of the ryanodine receptor 2 is a common event in the pathogenesis of head and neck cancer

R. Eils, C. Plass, W. Weichert, 2019, International journal of cancer.

Genome-wide search for schizophrenia susceptibility loci: the NIMH Genetics Initiative and Millennium Consortium.

T. Matise, S. Faraone, M. Tsuang, 1998, American journal of medical genetics.

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees.

T. Matise, S. Faraone, Joanne M. Meyer, 1998, American journal of medical genetics.

Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium.

T. Matise, S. Faraone, M. Tsuang, 1998, American journal of medical genetics.

RMRP gene sequence analysis confirms a cartilage‐hair hypoplasia variant with only skeletal manifestations and reveals a high density of single‐nucleotide polymorphisms

A. Superti-Furga, L. Bonafė, A. Giedion, 2002, Clinical genetics.