2009
Seifert W, Beninde J, Hoffmann K, Lindner TH, Bassir C, Aksu F, Hübner C, Verbeek NE, Mundlos S, Horn D.
HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing. Eur J Hum Genet 17: 1570-1576, 2009 [PDF ]
Hoffmann K, Planitz C, Rüschendorf F, Müller-Myhsok B, Stassen HH, Lucke B, Mattheisen M, Stumvoll M, Bochmann R, Zschornack M, Wienker TF, Nürnberg P, Reis A, Luft FC, Lindner TH.
A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. J Hypertens 27: 983-990, 2009 [Abstract ]
Seelow D, Göhler H, Hoffmann K.
FragIdent - Automatic identification and characterisation of cDNA-fragments. BMC Genomics 10: 95, 2009 [PDF ]
Stassen HH, Hoffmann K, Scharfetter C.
The difficulties of reproducing conventionally derived results through 500k-chip technology. BMC Genetics Suppl. 7: S66, 2009 [PDF ]
Türkmen S, Guo G, Garshasbi M, Hoffmann K, Alshalah AJ, Mischung C, Kuss A, Humphrey N, Mundlos S, Robinson PN.
CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait. PLoS Genet 5: e1000487, 2009 [PDF ]
Tönjes A, Zeggini E, Kovacs P, Böttcher Y, Schleinitz D, Dietrich K, Morris AP, Enigk B, Rayner NW, Koriath M, Eszlinger M, Kemppinen A, Prokopenko I, Hoffmann K, Teupser D, Thiery J, Krohn K, McCarthy MI, Stumvoll M.
Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany. Eur J Hum Genet 18: 104-110, 2009 [PDF ]
Tönjes A, Koriath M, Schleinitz D, Dietrich K, Böttcher Y, Rayner NW, Almgren P, Enigk B, Richter O, Rohm S, Fischer-Rosinsky A, Pfeiffer A, Hoffmann K, Krohn K, Aust G, Spranger J, Groop L, Blüher M, Kovacs P, Stumvoll M.
Genetic variation in GPR133 is associated with height - Genome wide association study in the self-contained population of Sorbs. Hum Mol Genet 18: 4662-4668, 2009 [PDF ]
Pegoraro G, Kubben N, Wickert U, Göhler H, Hoffmann K, Misteli T.
Ageing-related chromatin defects through loss of the NURD complex. Nat Cell Biol 11: 1261-1267, 2009 [PDF ]