Pichler, I;Mueller, JC;Stefanov, SA;De Grandi, A;Volpato, CB;Pinggera, GK;Mayr, A;Ogriseg, M;Ploner, F;Meitinger, T;Pramstaller, PP
Genetic Structure in Contemporary South Tyrolean Isolated Populations Revealed by Analysis of Y-Chromosome, mtDNA, and Alu Polymorphisms
Am J Hum Biol
2009
81
5-6
875-898

Newton-Cheh, C;Johnson, T;Gateva, V;Tobin, MD;Bochud, M;Coin, L;Najjar, SS;Zhao, JH;Heath, SC;Eyheramendy, S;Papadakis, K;Voight, BF;Scott, LJ;Zhang, F;Farrall, M;Tanaka, T;Wallace, C;Chambers, JC;Khaw, KT;Nilsson, P;van der Harst, P;Polidoro, S;Grobbee, DE;Onland-Moret, NC;Bots, ML;Wain, LV;Elliott, KS;Teumer, A;Luan, J;Lucas, G;Kuusisto, J;Burton, PR;Hadley, D;McArdle, WL;Brown, M;Dominiczak, A;Newhouse, SJ;Samani, NJ;Webster, J;Zeggini, E;Beckmann, JS;Bergmann, S;Lim, N;Song, K;Vollenweider, P;Waeber, G;Waterworth, DM;Yuan, X;Groop, L;Orho-Melander, M;Allione, A;Di Gregorio, A;Guarrera, S;Panico, S;Ricceri, F;Romanazzi, V;Sacerdote, C;Vineis, P;Barroso, I;Sandhu, MS;Luben, RN;Crawford, GJ;Jousilahti, P;Perola, M;Boehnke, M;Bonnycastle, LL;Collins, FS;Jackson, AU;Mohlke, KL;Stringham, HM;Valle, TT;Willer, CJ;Bergman, RN;Morken, MA;Döring, A;Gieger, C;Illig, T;Meitinger, T;Org, E;Pfeufer, A;Wichmann, HE;Kathiresan, S;Marrugat, J;O'Donnell, CJ;Schwartz, SM;Siscovick, DS;Subirana, I;Freimer, NB;Hartikainen, AL;McCarthy, MI;O'Reilly, PF;Peltonen, L;Pouta, A;de Jong, PE;Snieder, H;van Gilst, WH;Clarke, R;Goel, A;Hamsten, A;Peden, JF;Seedorf, U;Syvänen, AC;Tognoni, G;Lakatta, EG;Sanna, S;Scheet, P;Schlessinger, D;Scuteri, A;Dörr, M;Ernst, F;Felix, SB;Homuth, G;Lorbeer, R;Reffelmann, T;Rettig, R;Volker, U;Galan, P;Gut, IG;Hercberg, S;Lathrop, GM;Zelenika, D;Deloukas, P;Soranzo, N;Williams, FM;Zhai, G;Salomaa, V;Laakso, M;Elosua, R;Forouhi, NG;Völzke, H;Uiterwaal, CS;van der Schouw, YT;Numans, ME;Matullo, G;Navis, G;Berglund, G;Bingham, SA;Kooner, JS;Connell, JM;Bandinelli, S;Ferrucci, L;Watkins, H;Spector, TD;Tuomilehto, J;Altshuler, D;Strachan, DP;Laan, M;Meneton, P;Wareham, NJ;Uda, M;Jarvelin, MR;Mooser, V;Melander, O;Loos, RJF;Elliott, P;Abecasis, GR;Caulfield, M;Munroe, PB;Wellcome, Trust
Genome-wide association study identifies eight loci associated with blood pressure
Nat Genet
2009
41
6
666-676

Klopstock, T;Ahting, U;Floss, T;Meitinger, T;Wurst, W;Prokisch, H
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import
J Neurol
2009
256
S192-S192

Pham, TT;Giesert, F;Rothig, A;Floss, T;Kallnik, M;Weindl, K;Hölter, SM;Ahting, U;Prokisch, H;Becker, L;Klopstock, T;de Angelis, MH;Beyer, K;Gorner, K;Kahle, PJ;Weisenhorn, DMV;Wurst, W
DJ-1-deficient mice show less TH-positive neurons in the ventral tegmental area and exhibit non-motoric behavioural impairments
Genes Brain Behav
2009
9
3
305-317

Pattaro, C;Aulchenko, YS;Isaacs, A;Vitart, V;Hayward, C;Franklin, CS;Polasek, O;Kolcic, I;Biloglav, Z;Campbell, S;Hastie, N;Lauc, G;Meitinger, T;Oostra, BA;Gyllensten, U;Wilson, JF;Pichler, I;Hicks, AA;Campbell, H;Wright, AF;Rudan, I;van Duijn, CM;Riegler, P;Marroni, F;Pramstaller, PP
Genome-wide linkage analysis of serum creatinine in three isolated European populations.
Kidney Int
2009
76
3
297-306

Schlachter, K;Gruber-Sedlmayr, U;Stogmann, E;Lausecker, M;Hotzy, C;Balzar, J;Schuh, E;Baumgartner, C;Mueller, JC;Illig, T;Wichmann, HE;Lichtner, P;Meitinger, T;Strom, TM;Zimprich, A;Zimprich, F
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures.
Neurology
2009
72
11
974-8

Stogmann, E;El Tawil, S;Wagenstaller, J;Gaber, A;Edris, S;Abdelhady, A;Assem-Hilger, E;Leutmezer, F;Bonelli, S;Baumgartner, C;Zimprich, F;Strom, TM;Zimprich, A
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.
Neurogenetics
2009
10
1
73-7

Elstner, M;Andreoli, C;Klopstock, T;Meitinger, T;Prokisch, H
The mitochondrial proteome database: MitoP2.
Methods Enzymol
2009
457
3-20

Fritsche, LG;Freitag-Wolf, S;Bettecken, T;Meitinger, T;Keilhauer, CN;Krawczak, M;Weber, BH
Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene.
Hum Mutat
2009
30
7
1048-53

Johansson, Å;Marroni, F;Hayward, C;Franklin, CS;Kirichenko, AV;Jonasson, I;Hicks, AA;Vitart, V;Isaacs, A;Axenovich, T;Campbell, S;Dunlop, MG;Floyd, J;Hastie, N;Hofman, A;Knott, S;Kolcic, I;Pichler, I;Polasek, O;Rivadeneira, F;Tenesa, A;Uitterlinden, AG;Wild, SH;Zorkoltseva, IV;Meitinger, T;Wilson, JF;Rudan, I;Campbell, H;Pattaro, C;Pramstaller, P;Oostra, BA;Wright, AF;van Duijn, CM;Aulchenko, YS;Gyllensten, U
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
Hum Mol Genet
2009
18
2
373-80