Müller, TD;Reichwald, K;Wermter, AK;Brönner, G;Nguyen, TT;Friedel, S;Koberwitz, K;Engeli, S;Lichtner, P;Meitinger, T;Schäfer, H;Hebebrand, J;Hinney, A
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.
Mol Genet Metab
2007
90
4
429-34

Haubenberger, D;Bonelli, S;Hotzy, C;Leitner, P;Lichtner, P;Samal, D;Katzenschlager, R;Djamshidian, A;Brücke, T;Steffelbauer, M;Bancher, C;Grossmann, J;Ransmayr, G;Strom, TM;Meitinger, T;Gasser, T;Auff, E;Zimprich, A
A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.
Mov Disord
2007
22
11
1640-3

Kemlink, D;Polo, O;Montagna, P;Provini, F;Stiasny-Kolster, K;Oertel, W;de Weerd, A;Nevsimalova, S;Sonka, K;Högl, B;Frauscher, B;Poewe, W;Trenkwalder, C;Pramstaller, PP;Ferini-Strambi, L;Zucconi, M;Konofal, E;Arnulf, I;Hadjigeorgiou, GM;Happe, S;Klein, C;Hiller, A;Lichtner, P;Meitinger, T;Müller-Myshok, B;Winkelmann, J
Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.
Mov Disord
2007
22
2
207-12

Samani, NJ;Erdmann, J;Hall, AS;Hengstenberg, C;Mangino, M;Mayer, B;Dixon, RJ;Meitinger, T;Braund, P;Wichmann, HE;Barrett, JH;König, IR;Stevens, SE;Szymczak, S;Trégouët, DA;Iles, MM;Pahlke, F;Pollard, H;Lieb, W;Cambien, F;Fischer, M;Ouwehand, W;Blankenberg, S;Balmforth, AJ;Baessler, A;Ball, SG;Strom, TM;Braenne, I;Gieger, C;Deloukas, P;Tobin, MD;Ziegler, A;Thompson, JR;Schunkert, H
Genomewide association analysis of coronary artery disease.
N Engl J Med
2007
357
5
443-53

den Hollander, AI;Lopez, I;Yzer, S;Zonneveld, MN;Janssen, IM;Strom, TM;Hehir-Kwa, JY;Veltman, JA;Arends, ML;Meitinger, T;Musarella, MA;van den Born, LI;Fishman, GA;Maumenee, IH;Rohrschneider, K;Cremers, FP;Koenekoop, RK
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.
Invest Ophthalmol Vis Sci
2007
48
12
5690-8

Prokisch, H;Hartig, M;Hellinger, R;Meitinger, T;Rosenberg, T
A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.
Invest Ophthalmol Vis Sci
2007
48
9
4012-8

Panza, E;Gimelli, G;Passalacqua, M;Cohen, A;Gimelli, S;Giglio, S;Ghezzi, C;Sparatore, B;Heye, B;Zuffardi, O;Rugarli, E;Meitinger, T;Romeo, G;Ravazzolo, R;Seri, M
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies.
Int J Mol Med
2007
19
3
429-35

Lyon, HN;Emilsson, V;Hinney, A;Heid, IM;Lasky-Su, J;Zhu, X;Thorleifsson, G;Gunnarsdottir, S;Walters, GB;Thorsteinsdottir, U;Kong, A;Gulcher, J;Nguyen, TT;Scherag, A;Pfeufer, A;Meitinger, T;Brönner, G;Rief, W;Soto-Quirós, ME;Avila, L;Klanderman, B;Raby, BA;Silverman, EK;Weiss, ST;Laird, N;Ding, X;Groop, L;Tuomi, T;Isomaa, B;Bengtsson, K;Butler, JL;Cooper, RS;Fox, CS;O'Donnell, CJ;Vollmert, C;Celedón, JC;Wichmann, HE;Hebebrand, J;Stefansson, K;Lange, C;Hirschhorn, JN
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts.
PLoS Genet
2007
3
4
e61

Fisher, SA;Rivera, A;Fritsche, LG;Keilhauer, CN;Lichtner, P;Meitinger, T;Rudolph, G;Weber, BH
Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).
Hum Mutat
2007
28
4
406-13

Winkelmann, J;Schormair, B;Lichtner, P;Ripke, S;Xiong, L;Jalilzadeh, S;Fulda, S;Pütz, B;Eckstein, G;Hauk, S;Trenkwalder, C;Zimprich, A;Stiasny-Kolster, K;Oertel, W;Bachmann, CG;Paulus, W;Peglau, I;Eisensehr, I;Montplaisir, J;Turecki, G;Rouleau, G;Gieger, C;Illig, T;Wichmann, HE;Holsboer, F;Müller-Myhsok, B;Meitinger, T
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.
Nat Genet
2007
39
8
1000-6