Prof. Dr. Peter Nürnberg
Affiliation:
Director, Cologne Center for Genomics
Faculty of Mathematics and Natural Sciences, University of Cologne
Weyertal 115 b, 50931 Cologne
Phone: 0221-478-96801, Fax: 0221-478-96866
Honors & Awards (Selection)
1979-81 Goethe scholarship of the Humboldt University
1985 Humboldt Award
2004-09 Coordinator of the national genotyping platform of the NGFN
2004-present President of the"Arbeitsgemeinschaft für Gendiagnostik e.V." (AGD)
Selected Publications
- Siddiqui RA, Sauermann U, Altmüller J, Fritzer E, Nothnagel M, Dalibor N, Fellay J, Kaup FJ, Stahl-Hennig C, Nürnberg P, Krawczak M, Platzer M. (2009) X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected women. Am J Hum Genet85, 228-239.
- Henneke M, Diekmann S, Ohlenbusch A, Kaiser J, Engelbrecht V, Kohlschütter A, Krätzner R, Madruga-Garrido M, Mayer M, Opitz L, Rodriguez D, Rüschendorf F, Schumacher J, Thiele H, Thoms S, Steinfeld R, Nürnberg P, Gärtner J. (2009) RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection. Nat Genet41, 773-775.
- Rutsch F, Gailus S, Miousse IR, Suormala T, Sagné C, Toliat MR, Nürnberg G, Wittkampf T, Buers I, Sharifi A, Stucki M, Becker C, Baumgartner M, Robenek H, Marquardt T, Höhne W, Gasnier B, Rosenblatt DS, Fowler B, Nürnberg P.(2009). Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B(12) metabolism. Nat Genet41, 234-239.
- Buch S, Schafmayer C, Volzke H, Becker C, Franke A, von Eller-Eberstein H, Kluck C, Fölsch UR, Krawczak M, Schreiber S, Nürnberg P, Tepel J, and Hampe J. (2007). A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Nat Genet39, 995-999.
- Timmann C, Evans JA, König IR, Kleensang A, Rüschendorf F, Lenzen J, Sievertsen J, Becker C, Enuameh Y, Kwakye KO, Opoku E, Browne EN, Ziegler A, Nürnberg P, Horstmann RD. (2007) Genome-wide linkage analysis of malaria infection intensity and mild disease.PLoS Genet3, e48.