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Smith, JG;Magnani, JW;Palmer, C;Meng, YA;Soliman, EZ;Musani, SK;Kerr, KF;Schnabel, RB;Lubitz, SA;Sotoodehnia, N;Redline, S;Pfeufer, A;Muller, M;Evans, DS;Nalls, MA;Liu, Y;Newman, AB;Zonderman, AB;Evans, MK;Deo, R;Ellinor, PT;Paltoo, DN;Newton-Cheh, C;Benjamin, EJ;Mehra, R;Alonso, A;Heckbert, SR;Fox, ER
Genome-wide association studies of the PR interval in African Americans.
PLoS Genet
2011
7
2
e1001304

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Suhre, K;Shin, SY;Petersen, AK;Mohney, RP;Meredith, D;Wägele, B;Altmaier, E;Deloukas, P;Erdmann, J;Grundberg, E;Hammond, CJ;de Angelis, MH;Kastenmüller, G;Köttgen, A;Kronenberg, F;Mangino, M;Meisinger, C;Meitinger, T;Mewes, HW;Milburn, MV;Prehn, C;Raffler, J;Ried, JS;Römisch-Margl, W;Samani, NJ;Small, KS;Wichmann, HE;Zhai, G;Illig, T;Spector, TD;Adamski, J;Soranzo, N;Gieger, C
Human metabolic individuality in biomedical and pharmaceutical research.
Nature
2011
477
7362
54-60

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Schunkert, H;König, IR;Kathiresan, S;Reilly, MP;Assimes, TL;Holm, H;Preuss, M;Stewart, AF;Barbalic, M;Gieger, C;Absher, D;Aherrahrou, Z;Allayee, H;Altshuler, D;Anand, SS;Andersen, K;Anderson, JL;Ardissino, D;Ball, SG;Balmforth, AJ;Barnes, TA;Becker, DM;Becker, LC;Berger, K;Bis, JC;Boekholdt, SM;Boerwinkle, E;Braund, PS;Brown, MJ;Burnett, MS;Buysschaert, I;Carlquist, JF;Chen, L;Cichon, S;Codd, V;Davies, RW;Dedoussis, G;Dehghan, A;Demissie, S;Devaney, JM;Diemert, P;Do, R;Doering, A;Eifert, S;Mokhtari, NE;Ellis, SG;Elosua, R;Engert, JC;Epstein, SE;de Faire, U;Fischer, M;Folsom, AR;Freyer, J;Gigante, B;Girelli, D;Gretarsdottir, S;Gudnason, V;Gulcher, JR;Halperin, E;Hammond, N;Hazen, SL;Hofman, A;Horne, BD;Illig, T;Iribarren, C;Jones, GT;Jukema, JW;Kaiser, MA;Kaplan, LM;Kastelein, JJ;Khaw, KT;Knowles, JW;Kolovou, G;Kong, A;Laaksonen, R;Lambrechts, D;Leander, K;Lettre, G;Li, M;Lieb, W;Loley, C;Lotery, AJ;Mannucci, PM;Maouche, S;Martinelli, N;McKeown, PP;Meisinger, C;Meitinger, T;Melander, O;Merlini, PA;Mooser, V;Morgan, T;Mühleisen, TW;Muhlestein, JB;Münzel, T;Musunuru, K;Nahrstaedt, J;Nelson, CP;Nöthen, MM;Olivieri, O;Patel, RS;Patterson, CC;Peters, A;Peyvandi, F;Qu, L;Quyyumi, AA;Rader, DJ;Rallidis, LS;Rice, C;Rosendaal, FR;Rubin, D;Salomaa, V;Sampietro, ML;Sandhu, MS;Schadt, E;Schafer, A;Schillert, A;Schreiber, S;Schrezenmeir, J;Schwartz, SM;Siscovick, DS;Sivananthan, M;Sivapalaratnam, S;Smith, A;Smith, TB;Snoep, JD;Soranzo, N;Spertus, JA;Stark, K;Stirrups, K;Stoll, M;Tang, WH;Tennstedt, S;Thorgeirsson, G;Thorleifsson, G;Tomaszewski, M;Uitterlinden, AG;van Rij, AM;Voight, BF;Wareham, NJ;Wells, GA;Wichmann, HE;Wild, PS;Willenborg, C;Witteman, JC;Wright, BJ;Ye, S;Zeller, T;Ziegler, A;Cambien, F;Goodall, AH;Cupples, LA;Quertermous, T;März, W;Hengstenberg, C;Blankenberg, S;Ouwehand, WH;Hall, AS;Deloukas, P;Thompson, JR;Stefansson, K;Roberts, R;Thorsteinsdottir, U;O'Donnell, CJ;McPherson, R;Erdmann, J;Samani, NJ
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Nat Genet
2011
43
4
333-8

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Wain, LV;Verwoert, GC;O'Reilly, PF;Shi, G;Johnson, T;Johnson, AD;Bochud, M;Rice, KM;Henneman, P;Smith, AV;Ehret, GB;Amin, N;Larson, MG;Mooser, V;Hadley, D;Dörr, M;Bis, JC;Aspelund, T;Esko, T;Janssens, AC;Zhao, JH;Heath, S;Laan, M;Fu, J;Pistis, G;Luan, J;Arora, P;Lucas, G;Pirastu, N;Pichler, I;Jackson, AU;Webster, RJ;Zhang, F;Peden, JF;Schmidt, H;Tanaka, T;Campbell, H;Igl, W;Milaneschi, Y;Hottenga, JJ;Vitart, V;Chasman, DI;Trompet, S;Bragg-Gresham, JL;Alizadeh, BZ;Chambers, JC;Guo, X;Lehtimäki, T;Kühnel, B;Lopez, LM;Pola?ek, O;Boban, M;Nelson, CP;Morrison, AC;Pihur, V;Ganesh, SK;Hofman, A;Kundu, S;Mattace-Raso, FU;Rivadeneira, F;Sijbrands, EJ;Uitterlinden, AG;Hwang, SJ;Vasan, RS;Wang, TJ;Bergmann, S;Vollenweider, P;Waeber, G;Laitinen, J;Pouta, A;Zitting, P;McArdle, WL;Kroemer, HK;Volker, U;Völzke, H;Glazer, NL;Taylor, KD;Harris, TB;Alavere, H;Haller, T;Keis, A;Tammesoo, ML;Aulchenko, Y;Barroso, I;Khaw, KT;Galan, P;Hercberg, S;Lathrop, M;Eyheramendy, S;Org, E;Sõber, S;Lu, X;Nolte, IM;Penninx, BW;Corre, T;Masciullo, C;Sala, C;Groop, L;Voight, BF;Melander, O;O'Donnell, CJ;Salomaa, V;d'Adamo, AP;Fabretto, A;Faletra, F;Ulivi, S;Del Greco M, F;Facheris, M;Collins, FS;Bergman, RN;Beilby, JP;Hung, J;Musk, AW;Mangino, M;Shin, SY;Soranzo, N;Watkins, H;Goel, A;Hamsten, A;Gider, P;Loitfelder, M;Zeginigg, M;Hernandez, D;Najjar, SS;Navarro, P;Wild, SH;Corsi, AM;Singleton, A;de Geus, EJ;Willemsen, G;Parker, AN;Rose, LM;Buckley, B;Stott, D;Orrù, M;Uda, M;Van der Klauw, MM;Zhang, W;Li, X;Scott, J;Chen, YD;Burke, GL;Kähönen, M;Viikari, J;Döring, A;Meitinger, T;Davies, G;Starr, JM;Emilsson, V;Plump, A;Lindeman, JH;Hoen, PA;König, IR;Felix, JF;Clarke, R;Hopewell, JC;Ongen, H;Breteler, M;Debette, S;DeStefano, AL;Fornage, M;Mitchell, GF;Smith, NL;Holm, H;Stefansson, K;Thorleifsson, G;Thorsteinsdottir, U;Samani, NJ;Preuss, M;Rudan, I;Hayward, C;Deary, IJ;Wichmann, HE;Raitakari, OT;Palmas, W;Kooner, JS;Stolk, RP;Jukema, JW;Wright, AF;Boomsma, DI;Bandinelli, S;Gyllensten, UB;Wilson, JF;Ferrucci, L;Schmidt, R;Farrall, M;Spector, TD;Palmer, LJ;Tuomilehto, J;Pfeufer, A;Gasparini, P;Siscovick, D;Altshuler, D;Loos, RJ;Toniolo, D;Snieder, H;Gieger, C;Meneton, P;Wareham, NJ;Oostra, BA;Metspalu, A;Launer, L;Rettig, R;Strachan, DP;Beckmann, JS;Witteman, JC;Erdmann, J;van Dijk, KW;Boerwinkle, E;Boehnke, M;Ridker, PM;Jarvelin, MR;Chakravarti, A;Abecasis, GR;Gudnason, V;Newton-Cheh, C;Levy, D;Munroe, PB;Psaty, BM;Caulfield, MJ;Rao, DC;Tobin, MD;Elliott, P;van Duijn, CM
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Nat Genet
2011
43
10
1005-11

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Mayr, JA;Bodamer, O;Haack, TB;Zimmermann, FA;Madignier, F;Prokisch, H;Rauscher, C;Koch, J;Sperl, W
Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency.
Mol Genet Metab
2011
103
4
358-61

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Nebel, A;Kleindorp, R;Caliebe, A;Nothnagel, M;Blanche, H;Junge, O;Wittig, M;Ellinghaus, D;Flachsbart, F;Wichmann, HE;Meitinger, T;Nikolaus, S;Franke, A;Krawczak, M;Lathrop, M;Schreiber, S
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals.
Mech Ageing Dev
2011
132
6-7
324-30

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Greif, PA;Eck, SH;Konstandin, NP;Benet-Pagès, A;Ksienzyk, B;Dufour, A;Vetter, AT;Popp, HD;Lorenz-Depiereux, B;Meitinger, T;Bohlander, SK;Strom, TM
Identification of recurring tumor-specific somatic mutations in acute myeloid leukemia by transcriptome sequencing.
Leukemia
2011
25
5
821-7

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Rivera-Brugués, N;Albrecht, B;Wieczorek, D;Schmidt, H;Keller, T;Göhring, I;Ekici, AB;Tzschach, A;Garshasbi, M;Franke, K;Klopp, N;Wichmann, HE;Meitinger, T;Strom, TM;Hempel, M
Cohen syndrome diagnosis using whole genome arrays.
J Med Genet
2011
48
2
136-40

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Heeringa, SF;Chernin, G;Chaki, M;Zhou, W;Sloan, AJ;Ji, Z;Xie, LX;Salviati, L;Hurd, TW;Vega-Warner, V;Killen, PD;Raphael, Y;Ashraf, S;Ovunc, B;Schoeb, DS;McLaughlin, HM;Airik, R;Vlangos, CN;Gbadegesin, R;Hinkes, B;Saisawat, P;Trevisson, E;Doimo, M;Casarin, A;Pertegato, V;Giorgi, G;Prokisch, H;Rötig, A;Nürnberg, G;Becker, C;Wang, S;Ozaltin, F;Topaloglu, R;Bakkaloglu, A;Bakkaloglu, SA;Müller, D;Beissert, A;Mir, S;Berdeli, A;Varpizen, S;Zenker, M;Matejas, V;Santos-Ocaña, C;Navas, P;Kusakabe, T;Kispert, A;Akman, S;Soliman, NA;Krick, S;Mundel, P;Reiser, J;Nurnberg, P;Clarke, CF;Wiggins, RC;Faul, C;Hildebrandt, F
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
J Clin Invest
2011
121
5
2013-24

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Sinner, MF;Lubitz, SA;Pfeufer, A;Makino, S;Beckmann, BM;Lunetta, KL;Steinbeck, G;Perz, S;Rahman, R;Sonni, A;Greenberg, SM;Furie, KL;Wichmann, HE;Meitinger, T;Peters, A;Benjamin, EJ;Rosand, J;Ellinor, PT;Kääb, S
Lack of replication in polymorphisms reported to be associated with atrial fibrillation.
Heart Rhythm
2011
8
3
403-9