Studio portrait of Carolina Bürger nee Levison.

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Portrait of Isaac Abraham Bürger and Ella Bürger nee Cahn.

Isaac Abraham Bürger, 1791-1864; Ella Bürger nee Cahn, 1793-1879; Parents of Samuel Isaac Bürger, 1818-1885

War damage; Kunstgewerbe, Berlin.

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Living room of Henrietta Gottschalk nee Rothschild; Marienstrasse, Hannover, Germany.

The family has been curious about the family tree on the wall. Family lore suggests that it was produced by French POWs during WWI

House of Henriette Gottschalk nee Rothschild; Marienstrasse, Hannover, Germany.

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Obituary of Julie Schoenbeck nee Rothschild; Cologne, Germany.

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Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia

Several lines of evidence have implicated the catechol-O-methyltransferase (COMT) gene as a candidate for schizophrenia (SZ) susceptibility, not only because it encodes a key dopamine catabolic enzyme but also because it maps to the velocardiofacial syndrome region of chromosome 22q11 which has long been associated with SZ predisposition. The interest in COMT as a candidate SZ risk factor has led to numerous case-control and family-based studies, with the majority placing emphasis on examining a functional Val/Met polymorphism within this enzyme. Unfortunately, these studies have continually produced conflicting results. To assess the genetic contribution of other COMT variants to SZ susceptibility, we investigated three single-nucleotide polymorphisms (SNPs) (rs737865, rs4633, rs165599) in addition to the Val/Met variant (rs4680) in a highly selected sample of Australian Caucasian families containing 107 patients with SZ. The Val/Met and rs4633 variants showed nominally significant associations with SZ (P<0.05), although neither of the individual SNPs remained significant after adjusting for multiple testing (most significant P=0.1174). However, haplotype analyses showed strong evidence of an association; the most significant being the three-marker haplotype rs737865-rs4680-rs165599 (global P=0.0022), which spans more than 26 kb. Importantly, conditional analyses indicated the presence of two separate and interacting effects within this haplotype, irrespective of gender. In addition, our results indicate the Val/Met polymorphism is not disease-causing and is simply in strong linkage disequilibrium with a causative effect, which interacts with another as yet unidentified variant approximately 20 kb away. These results may help explain the inconsistent results reported on the Val/Met polymorphism and have important implications for future investigations into the role of COMT in SZ susceptibility.

Portrait of artist Rafaello Busoni.

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Artist Rafaello Busoni seated and writing at a desk; Berlin.

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Studio portraits of Rahel Bürger Apfel.

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Artist Rafaello Busoni.

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Artist Rafaello Busoni with his first wife pianist Hide Kosiwamuro.

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Pianist Hide Kosiwamuro.

First wife of artist Rafaello Busoni

Artist Rafaello Busoni (l) outdoors speaking with Dr. Heinz Kallmann.

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Artist Rafaello Busoni drawing.

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