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Genome-wide association studies of the PR interval in African Americans.
PLoS Genet
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Human metabolic individuality in biomedical and pharmaceutical research.
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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Nat Genet
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Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Nat Genet
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43
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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
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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
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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
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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
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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
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121
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2013-24

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