Multiple loci influencing hippocampal degeneration identified by genome scan
Melville, Scott A., Buros, Jacqueline, Parrado, Antonio R., Vardarajan, Badri, Logue, Mark W., Shen, Li, Risacher, Shannon L., Kim, Sungeun, Jun, Gyungah, DeCarli, Charles, Lunetta, Kathryn L., Baldwin, Clinton T., Saykin, Andrew J., Farrer, Lindsay A.
Published in Annals of neurology (01.07.2012)
Published in Annals of neurology (01.07.2012)
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A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level
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Published in BMC medical genetics (11.03.2010)
Published in BMC medical genetics (11.03.2010)
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Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels
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Published in Human molecular genetics (15.03.2011)
Published in Human molecular genetics (15.03.2011)
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Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster
DEL GRECO M, Fabiola, PATTARO, Cristian, WICHMANN, H. Erich, SCHREIBER, Stefan, HEID, Iris M, KRAWCZAK, Michael, MINELLI, Cosetta, WIEDERMANN, Christian J, PRAMSTALLER, Peter P, LUCHNER, Andreas, PICHLER, Irene, WINKLER, Thomas, HICKS, Andrew A, FUCHSBERGER, Christian, FRANKE, Andre, MELVILLE, Scott A, PETERS, Annette
Published in Human molecular genetics (15.04.2011)
Published in Human molecular genetics (15.04.2011)
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A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level
Pattaro, Cristian, De Grandi, Alessandro, Vitart, Veronique, Hayward, Caroline, Franke, Andre, Aulchenko, Yurii S, Johansson, Asa, Wild, Sarah H, Melville, Scott A, Isaacs, Aaron, Polasek, Ozren, Ellinghaus, David, Kolcic, Ivana, Nöthlings, Ute, Zgaga, Lina, Zemunik, Tatijana, Gnewuch, Carsten, Schreiber, Stefan, Campbell, Susan, Hastie, Nick, Boban, Mladen, Meitinger, Thomas, Oostra, Ben A, Riegler, Peter, Minelli, Cosetta, Wright, Alan F, Campbell, Harry, van Duijn, Cornelia M, Gyllensten, Ulf, Wilson, James F, Krawczak, Michael, Rudan, Igor, Pramstaller, Peter P
Published in BMC medical genetics (11.03.2010)
Published in BMC medical genetics (11.03.2010)
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Genetic variants in RBFOX3 are associated with sleep latency
Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G, Mbarek, Hamdi, Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-Hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger Ww, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam Cgn, Cummings, Steven R, Aulchenko, Yurii S, Gehrman, Philip R, Uitterlinden, André G, Wichmann, Heinz-Erich, Müller-Nurasyid, Martina, Fehrmann, Rudolf Sn, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred Fj, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till, van Duijn, Cornelia M
Published in European journal of human genetics : EJHG (01.10.2016)
Published in European journal of human genetics : EJHG (01.10.2016)
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