Winterer, G;Mittelstrass, K;Giegling, I;Lamina, C;Fehr, C;Brenner, H;Breitling, LP;Nitz, B;Raum, E;Muller, H;Gallinat, J;Gal, A;Heim, K;Prokisch, H;Meitinger, T;Hartmann, AM;Möller, HJ;Gieger, C;Wichmann, HE;Illig, T;Dahmen, N;Rujescu, D
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance.
Am J Med Genet B Neuropsychiatr Genet
2010
153B
8
1448-58

Ahting, U;Freisinger, P;Prokisch, H;Gempel, K;Hofmann, W;Rolinski, B
BIOCHEMICAL AND GENETIC ANALYSIS ON A LARGE COHORT OF PATIENTS WITH SUSPECTED MITOCHONDRIOPATHY
J Inherit Metab Dis
2010
33
S92-S92

Hemminki, K;Muller-Myhsok, B;Lichtner, P;Engel, C;Chen, BW;Burwinkel, B;Forsti, A;Sutter, C;Wappenschmidt, B;Hellebrand, H;Illig, T;Arnold, N;Niederacher, D;Dworniczak, B;Deissler, H;Kast, K;Gadzicki, D;Meitinger, T;Wichmann, HE;Kiechle, M;Bartram, CR;Schmutzler, RK;Meindl, A
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
Int J Canc Prev
2010
126
12
2858-2862

O'Toole, JF;Liu, YJ;Davis, EE;Westlake, CJ;Attanasio, M;Otto, EA;Seelow, D;Nürnberg, G;Becker, C;Nuutinen, M;Kärppä, M;Ignatius, J;Uusimaa, J;Pakanen, S;Jaakkola, E;van den Heuvel, LP;Fehrenbach, H;Wiggins, R;Goyal, M;Zhou, WB;Wolf, MTF;Wise, E;Helou, J;Allen, SJ;Murga-Zamalloa, CA;Ashraf, S;Chaki, M;Heeringa, S;Chernin, G;Hoskins, BE;Chaib, H;Gleeson, J;Kusakabe, T;Suzuki, T;Isaac, RE;Quarmby, LM;Tennant, B;Fujioka, H;Tuominen, H;Hassinen, I;Lohi, H;van Houten, JL;Rötig, A;Sayer, JA;Rolinski, B;Freisinger, P;Madhavan, SM;Herzer, M;Madignier, F;Prokisch, H;Nurnberg, P;Jackson, PK;Khanna, H;Katsanis, N;Hildebrandt, F
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (vol 120, pg 791, 2010)
Eur J Clin Invest
2010
120
4
1362-1362

Klopstock, T;Meitinger, T;Obermaier-Kusser, B
mitoNET - German network for mitochondrial disorders
Neuromuscul Disord
2010
20
9-10
671-671

Kestenbaum, B;Glazer, NL;Köttgen, A;Felix, JF;Hwang, SJ;Liu, YM;Lohman, K;Kritchevsky, SB;Hausman, DB;Petersen, AK;Gieger, C;Ried, JS;Meitinger, T;Strom, TM;Wichmann, HE;Campbell, H;Hayward, C;Rudan, I;de Boer, IH;Psaty, BM;Rice, KM;Chen, YDI;Li, M;Arking, DE;Boerwinkle, E;Coresh, J;Yang, QO;Levy, D;van Rooij, FJA;Dehghan, A;Rivadeneira, F;Uitterlinden, AG;Hofman, A;van Duijn, CM;Shlipak, MG;Kao, WHL;Witteman, JCM;Siscovick, DS;Fox, CS
Common Genetic Variants Associate with Serum Phosphorus Concentration
Clin J Am Soc Nephrol
2010
21
7
1223-1232

Winterer, G;Mittelstrass, K;Giegling, I;Lamina, C;Fehr, C;Brenner, H;Breitling, LP;Nitz, B;Raum, E;Muller, H;Gallinat, J;Gal, A;Heim, K;Prokisch, H;Meitinger, T;Hartmann, AM;Möller, HJ;Gieger, C;Wichmann, HE;Illig, T;Dahmen, N;Rujescu, D
Risk Gene Variants for Nicotine Dependence in the CHRNA5-CHRNA3-CHRNB4 Cluster Are Associated With Cognitive Performance
Am J Med Genet
2010
158B
8
1448-1458

Ellinor, PT;Lunetta, KL;Glazer, NL;Pfeufer, A;Alonso, A;Chung, MK;Sinner, MF;de Bakker, PI;Mueller, M;Lubitz, SA;Fox, E;Darbar, D;Smith, NL;Smith, JD;Schnabel, RB;Soliman, EZ;Rice, KM;Van Wagoner, DR;Beckmann, BM;van Noord, C;Wang, K;Ehret, GB;Rotter, JI;Hazen, SL;Steinbeck, G;Smith, AV;Launer, LJ;Harris, TB;Makino, S;Nelis, M;Milan, DJ;Perz, S;Esko, T;Köttgen, A;Moebus, S;Newton-Cheh, C;Li, M;Möhlenkamp, S;Wang, TJ;Kao, WH;Vasan, RS;Nöthen, MM;MacRae, CA;Stricker, BH;Hofman, A;Uitterlinden, AG;Levy, D;Boerwinkle, E;Metspalu, A;Topol, EJ;Chakravarti, A;Gudnason, V;Psaty, BM;Roden, DM;Meitinger, T;Wichmann, HE;Witteman, JC;Barnard, J;Arking, DE;Benjamin, EJ;Heckbert, SR;Kääb, S
Common variants in KCNN3 are associated with lone atrial fibrillation.
Nat Genet
2010
42
3
240-4

Pattaro, C;De Grandi, A;Vitart, V;Hayward, C;Franke, A;Aulchenko, YS;Johansson, Å;Wild, SH;Melville, SA;Isaacs, A;Polasek, O;Ellinghaus, D;Kolcic, I;Nöthlings, U;Zgaga, L;Zemunik, T;Gnewuch, C;Schreiber, S;Campbell, S;Hastie, N;Boban, M;Meitinger, T;Oostra, BA;Riegler, P;Minelli, C;Wright, AF;Campbell, H;van Duijn, CM;Gyllensten, U;Wilson, JF;Krawczak, M;Rudan, I;Pramstaller, PP
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.
BMC Med Genet
2010
11
41

Tischfield, MA;Baris, HN;Wu, C;Rudolph, G;Van Maldergem, L;He, W;Chan, WM;Andrews, C;Demer, JL;Robertson, RL;Mackey, DA;Ruddle, JB;Bird, TD;Gottlob, I;Pieh, C;Traboulsi, EI;Pomeroy, SL;Hunter, DG;Soul, JS;Newlin, A;Sabol, LJ;Doherty, EJ;de Uzcátegui, CE;de Uzcátegui, N;Collins, ML;Sener, EC;Wabbels, B;Hellebrand, H;Meitinger, T;de Berardinis, T;Magli, A;Schiavi, C;Pastore-Trossello, M;Koc, F;Wong, AM;Levin, AV;Geraghty, MT;Descartes, M;Flaherty, M;Jamieson, RV;Møller, HU;Meuthen, I;Callen, DF;Kerwin, J;Lindsay, S;Meindl, A;Gupta, ML;Pellman, D;Engle, EC
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
Cell
2010
140
1
74-87