Watanabe, H;Koopmann, TT;Le Scouarnec, S;Yang, T;Ingram, CR;Schott, JJ;Demolombe, S;Probst, V;Anselme, F;Escande, D;Wiesfeld, AC;Pfeufer, A;Kääb, S;Wichmann, HE;Hasdemir, C;Aizawa, Y;Wilde, AA;Roden, DM;Bezzina, CR
Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
J Clin Invest
2008
118
6
2260-8

Gibson, J;Tapper, W;Cox, D;Zhang, W;Pfeufer, A;Gieger, C;Wichmann, HE;Kääb, S;Collins, AR;Meitinger, T;Morton, N
A multimetric approach to analysis of genome-wide association by single markers and composite likelihood.
Proc Natl Acad Sci U S A
2008
105
7
2592-7

Zirn, B;Hempel, M;Hahn, A;Neubauer, B;Wagenstaller, J;Rivera-Brugués, N;Strom, TM;Köhler, A
Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype.
Am J Med Genet A
2008
146A
22
2960-5

Gieger, C;Geistlinger, L;Altmaier, E;Hrabé de Angelis, M;Kronenberg, F;Meitinger, T;Mewes, HW;Wichmann, HE;Weinberger, KM;Adamski, J;Illig, T;Suhre, K
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.
PLoS Genet
2008
4
11
e1000282

Wermter, AK;Scherag, A;Meyre, D;Reichwald, K;Durand, E;Nguyen, TT;Koberwitz, K;Lichtner, P;Meitinger, T;Schäfer, H;Hinney, A;Froguel, P;Hebebrand, J;Brönner, G
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.
Eur J Hum Genet
2008
16
9
1126-34

Loos, RJ;Lindgren, CM;Li, S;Wheeler, E;Zhao, JH;Prokopenko, I;Inouye, M;Freathy, RM;Attwood, AP;Beckmann, JS;Berndt, SI;Jacobs, KB;Chanock, SJ;Hayes, RB;Bergmann, S;Bennett, AJ;Bingham, SA;Bochud, M;Brown, M;Cauchi, S;Connell, JM;Cooper, C;Smith, GD;Day, I;Dina, C;De, S;Dermitzakis, ET;Doney, AS;Elliott, KS;Elliott, P;Evans, DM;Sadaf Farooqi, I;Froguel, P;Ghori, J;Groves, CJ;Gwilliam, R;Hadley, D;Hall, AS;Hattersley, AT;Hebebrand, J;Heid, IM;Lamina, C;Gieger, C;Illig, T;Meitinger, T;Wichmann, HE;Herrera, B;Hinney, A;Hunt, SE;Jarvelin, MR;Johnson, T;Jolley, JD;Karpe, F;Keniry, A;Khaw, KT;Luben, RN;Mangino, M;Marchini, J;McArdle, WL;McGinnis, R;Meyre, D;Munroe, PB;Morris, AD;Ness, AR;Neville, MJ;Nica, AC;Ong, KK;O'Rahilly, S;Owen, KR;Palmer, CN;Papadakis, K;Potter, S;Pouta, A;Qi, L;Randall, JC;Rayner, NW;Ring, SM;Sandhu, MS;Scherag, A;Sims, MA;Song, K;Soranzo, N;Speliotes, EK;Syddall, HE;Teichmann, SA;Timpson, NJ;Tobias, JH;Uda, M;Vogel, CI;Wallace, C;Waterworth, DM;Weedon, MN;Willer, CJ;Wraight;Yuan, X;Zeggini, E;Hirschhorn, JN;Strachan, DP;Ouwehand, WH;Caulfield, MJ;Samani, NJ;Frayling, TM;Vollenweider, P;Waeber, G;Mooser, V;Deloukas, P;McCarthy, MI;Wareham, NJ;Barroso, I;Jacobs, KB;Chanock, SJ;Hayes, RB;Lamina, C;Gieger, C;Illig, T;Meitinger, T;Wichmann, HE;Kraft, P;Hankinson, SE;Hunter, DJ;Hu, FB;Lyon, HN;Voight, BF;Ridderstråle, M;Groop, L;Scheet, P;Sanna, S;Abecasis, GR;Albai, G;Nagaraja, R;Schlessinger, D;Jackson, AU;Tuomilehto, J;Collins, FS;Boehnke, M;Mohlke, KL
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
Nat Genet
2008
40
6
768-75

Bevan, S;Dichgans, M;Wiechmann, HE;Gschwendtner, A;Meitinger, T;Markus, HS
Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations.
Stroke
2008
39
4
1109-14

Fatar, M;Stroick, M;Steffens, M;Senn, E;Reuter, B;Bukow, S;Griebe, M;Alonso, A;Lichtner, P;Bugert, P;Meitinger, T;Wienker, TF;Hennerici, MG
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes.
Cerebrovasc Dis
2008
26
2
113-9

Gschwendtner, A;Ripke, S;Freilinger, T;Lichtner, P;Müller-Myhsok, B;Wichmann, HE;Meitinger, T;Dichgans, M
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans.
Stroke
2008
39
5
1593-6

Zimprich, F;Stogmann, E;Bonelli, S;Baumgartner, C;Mueller, JC;Meitinger, T;Zimprich, A;Strom, TM
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy.
Epilepsia
2008
49
6
1108-9