Bolzer, A;Kreth, G;Solovei, I;Koehler, D;Saracoglu, K;Fauth, C;Müller, S;Eils, R;Cremer, C;Speicher, MR;Cremer, T
Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes
PLoS Biol
2005
3
5
826-842

Baumeister, FA;Auer, DP;Hortnagel, K;Freisinger, P;Meitinger, T
The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome.
Neuropediatrics
2005
36
3
221-2

Rivera, A;Fisher, SA;Fritsche, LG;Keilhauer, CN;Lichtner, P;Meitinger, T;Weber, BH
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
Hum Mol Genet
2005
14
21
3227-36

Lombardo, F;Chiurazzi, P;Hortnagel, K;Arrigo, T;Valenzise, M;Meitinger, T;Messina, MF;Salzano, G;Barberi, I;de Luca, F
Clinical picture, evolution and peculiar molecular findings in a very large pedigree with Wolfram syndrome.
J Pediatr Endocrinol Metab
2005
18
12
1391-7

Mueller, JC;Lõhmussaar, E;Magi, R;Remm, M;Bettecken, T;Lichtner, P;Biskup, S;Illig, T;Pfeufer, A;Luedemann, J;Schreiber, S;Pramstaller, P;Pichler, I;Romeo, G;Gaddi, A;Testa, A;Wichmann, HE;Metspalu, A;Meitinger, T
Linkage disequilibrium patterns and tagSNP transferability among European populations.
Am J Hum Genet
2005
76
3
387-98

Barth, AS;Merk, S;Arnoldi, E;Zwermann, L;Kloos, P;Gebauer, M;Steinmeyer, K;Bleich, M;Kääb, S;Pfeufer, A;Uberfuhr, P;Dugas, M;Steinbeck, G;Näbauer, M
Functional profiling of human atrial and ventricular gene expression.
Pflugers Arch
2005
450
4
201-8

Lõhmussaar, E;Gschwendtner, A;Mueller, JC;Org, T;Wichmann, E;Hamann, G;Meitinger, T;Dichgans, M
ALOX5AP gene and the PDE4D gene in a central European population of stroke patients.
Stroke
2005
36
4
731-6

Mueller, JC;Fuchs, J;Hofer, A;Zimprich, A;Lichtner, P;Illig, T;Berg, D;Wüllner, U;Meitinger, T;Gasser, T
Multiple regions of alpha-synuclein are associated with Parkinson's disease.
Ann Neurol
2005
57
4
535-41

Koch, W;Hoppmann, P;Michou, E;Jung, V;Pfeufer, A;Muller, J;Meitinger, T;Schömig, A;Kastrati, A
TaqMan assays for genotyping of single nucleotide polymorphisms present at a disease susceptibility locus on chromosome 6.
Clin Chem Lab Med
2005
43
2
167-72

Benet-Pagès, A;Orlik, P;Strom, TM;Lorenz-Depiereux, B
An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.
Hum Mol Genet
2005
14
3
385-90