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Entries: 1-8  
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Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon.
Authors: Spieler, Derek; Kaffe, Maria; Knauf, Franziska; Bessa, José; Tena, Juan J; Giesert, Florian; Schormair, Barbara; Tilch, Erik; Lee, Hyun-Ok Kate; Horsch, Marion; Czamara, Darina; Karbalai, Nazanin; Toerne, Christine von; Waldenberger, Melanie; Gieger, Christian; Lichtner, Peter; Claussnitzer, Melina; Naumann, Ronald; Müller-Myhsok, Bertram; Torres, Miguel; Garrett, Lillian; Rozman, Jan; Klingenspor, Martin; Gailus-Durner, Valérie; Fuchs, Helmut; Angelis, Martin Hrabe de; Beckers, Johannes; Hölter, Sabine M; Meitinger, Thomas; Hauck, Stefanie M; Laumen, Helmut; Wurst, Wolfgang; Casares, Fernando; Gómez-Skarmeta, Jose Luis; Winkelmann, Juliane
Date of Publication (YYYY-MM-DD): 2014
Title of Journal: Genome Research
Volume: 24
Issue / Number: 4
Start Page: 592
End Page: 603
Document Type: Article
ID: 705777.0
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy
Authors: Sibbing, Dirk; Pfeufer, Arne; Perisic, Tamara; Mannes, Alexander M.; Fritz−Wolf, Karin; Unwin, Sarah; Sinner, Moritz F.; Gieger, Christian; Gloeckner, Christian J.; Wichmann, Heinz−Erich; Kremmer, Elisabeth; Schäfer, Zasie; Walch, Axel; Hinterseer, Martin; Näbauer, Michael; Kääb, Stefan; Kastrati, Adnan; Schömig, Albert; Meitinger, Thomas; Bornkamm, Georg W.; Conrad, Marcus; von Beckerath, Nicolas
Date of Publication (YYYY-MM-DD): 2011-05-01
Title of Journal: European Heart Journal
Volume: 32
Issue / Number: 9
Start Page: 1121
End Page: 1133
Document Type: Article
ID: 597809.0
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy
Authors: Sibbing, Dirk; Pfeufer, Arne; Perisic, Tamara; Mannes, Alexander M.; Fritz−Wolf, Karin; Unwin, Sarah; Sinner, Moritz F.; Gieger, Christian; Gloeckner, Christian J.; Wichmann, Heinz−Erich; Kremmer, Elisabeth; Schäfer, Zasie; Walch, Axel; Hinterseer, Martin; Näbauer, Michael; Kääb, Stefan; Kastrati, Adnan; Schömig, Albert; Meitinger, Thomas; Bornkamm, Georg W.; Conrad, Marcus; von Beckerath, Nicolas
Date of Publication (YYYY-MM-DD): 2011-01-18
Title of Journal: European Heart Journal
Volume: 32
Start Page: 1
End Page: 13
Document Type: Article
ID: 565629.0
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy
Authors: Sibbing, Dirk; Pfeufer, Arne; Perisic, Tamara; Mannes, Alexander M.; Fritz−Wolf, Karin; Unwin, Sarah; Sinner, Moritz F.; Gieger, Christian; Gloeckner, Christian J.; Wichmann, Heinz−Erich; Kremmer, Elisabeth; Schäfer, Zasie; Walch, Axel; Hinterseer, Martin; Näbauer, Michael; Kääb, Stefan; Kastrati, Adnan; Schömig, Albert; Meitinger, Thomas; Bornkamm, Georg W.; Conrad, Marcus; von Beckerath, Nicolas
Date of Publication (YYYY-MM-DD): 2011-01-18
Title of Journal: European Heart Journal
Volume: 32
Start Page: 1
End Page: 13
Document Type: Article
ID: 567897.0
Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia
Authors: Stöber, Gerald; Kohlmann, Bernd; Siekiera, Markus; Rubie, Claudia; Gawlik, Micha; Möller-Ehrlich, Kerstin; Meitinger, Thomas; Bettecken, Thomas
Date of Publication (YYYY-MM-DD): 2005-10-14
Title of Journal: BMC Psychiatry
Volume: 5
Sequence Number of Article: doi:10.1186/1471-244X-5-36
Document Type: Article
ID: 246519.0
 
Full text / Content available
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
Authors: Binder, Elisabeth B.; Salyakina, Daria; Lichtner, Peter; Wochnik, Gabriele M.; Ising, Marcus; Pütz, Benno; Papiol, Sergi; Seaman, Shaun; Lucae, Susanne; Kohli, Martin; Nickel, Thomas; Künzel, Heike; Fuchs, Brigitte; Majer, Matthias; Pfennig, Andrea; Kern, Nikola; Brunner, Jürgen; Modell, Sieglinde; Baghai, Thomas; Deiml, Tobias; Zill, Peter; Bondy, Brigitte; Rupprecht, Rainer; Messer, Thomas; Köhnlein, Oliver; Dabitz, Heike; Brückl, Tanja; Müller, Nina; Pfister, Hildegard; Lieb, Roselind; Mueller, Jacob C.; Löhmussaar, Elin; Strom, Tim M.; Bettecken, Thomas; Meitinger, Thomas; Uhr, Manfred; Rein, Theo; Holsboer, Florian; Müller-Myhsok, Bertram
Date of Publication (YYYY-MM-DD): 2004
Title of Journal: Nature Genetics
Volume: 36
Start Page: 1319
End Page: 1325
Document Type: Article
ID: 210643.0
The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted
Authors: Grabowski, Monika; Zimprich, Alexander; Lorenz-Depiereux, Bettina; Kalscheuer, Vera; Asmus, Friedrich; Gasser, Thomas; Meitinger, Thomas; Strom, Tim M.
Date of Publication (YYYY-MM-DD): 2003-02
Title of Journal: European Journal of Human Genetics
Volume: 11
Issue / Number: 2
Start Page: 138
End Page: 144
Document Type: Article
ID: 194847.0
Epsilon-sarcoglycan (SGCE), the gene mutated in myoclonus-dystonia syndrome, is imprinted.
Authors: Grabowski, Monika; Zimprich, Alexander; Lorenz-Depiereux, Bettina; Kalscheuer, Vera; Asmus, Friedrich; Gasser, Thomas; Meitinger, Thomas; Strom, Tim M.
Date of Publication (YYYY-MM-DD): 2002-05
Title of Journal: European Journal of Human Genetics
Volume: 10
Issue / Number: Suppl. Suppl. 1
Start Page: 233
End Page: 234
Document Type: Article
ID: 127600.0
Entries: 1-8  
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