Dynamic CpG island methylation landscape in oocytes and preimplantation embryos von Kelsey, Gavin, Smallwood, Sébastien A, Tomizawa, Shin-ichi, Krueger, Felix, Ruf, Nico, Carli, Natasha, Segonds-Pichon, Anne, Sato, Shun, Hata, Kenichiro, Andrews, Simon R

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Transcription is required for establishment of germline methylation marks at imprinted genes von Chotalia, Mita, Smallwood, Sebastien A, Ruf, Nico, Dawson, Claire, Lucifero, Diana, Frontera, Marga, James, Katherine, Dean, Wendy, Kelsey, Gavin

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Analysis of human alternative first exons and copy number variation of the GJA12 gene in patients with Pelizaeus-Merzbacher-like disease von Ruf, Nico, Uhlenberg, Birgit

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Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human von Ruf, Nico, Bähring, Sylvia, Galetzka, Danuta, Pliushch, Galyna, Luft, Friedrich C., Nürnberg, Peter, Haaf, Thomas, Kelsey, Gavin, Zechner, Ulrich

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Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes von Ruf, Nico, Dünzinger, Ulrich, Brinckmann, Anja, Haaf, Thomas, Nürnberg, Peter, Zechner, Ulrich

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Generalized arterial calcification of infancy: Different clinical courses in two affected siblings von Cheng, Kun‐Shan, Chen, Ming‐Ren, Ruf, Nico, Lin, Shuan‐Pei, Rutsch, Frank

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Hypophosphatemia, Hyperphosphaturia, and Bisphosphonate Treatment Are Associated With Survival Beyond Infancy in Generalized Arterial Calcification of Infancy von Rutsch, Frank, Boyer, Petra, Nitschke, Yvonne, Ruf, Nico, Lorenz-Depierieux, Bettina, Wittkampf, Tanja, Weissen-Plenz, Gabriele, Fischer, Rudolf-Josef, Mughal, Zulf, Gregory, John W, Davies, Justin H, Loirat, Chantal, Strom, Tim M, Schnabel, Dirk, Nurnberg, Peter, Terkeltaub, Robert, GACI Study Group

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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification von Rutsch, Frank, Suk, Anita, Ferre, Merry, Höhne, Wolfgang, Knisely, Alex, Hinrichs, Bernd, Lehmann, Mandy, Epplen, Jörg T, Ruf, Nico, Vallance, Hillary, Terkeltaub, Robert, Schnabel, Dirk, Schauer, Galen, Smith, Wendy, Sinaiko, Alan R, Roscioli, Tony, Filippone, Marco, Vaingankar, Sucheta, McGill, James, Toliat, Mohammad R, Superti-Furga, Andrea, Nürnberg, Peter

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Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease von Uhlenberg, Birgit, Schuelke, Markus, Rüschendorf, Franz, Ruf, Nico, Kaindl, Angela M, Henneke, Marco, Thiele, Holger, Stoltenburg-Didinger, Gisela, Aksu, Fuat, Topaloğlu, Haluk, Nürnberg, Peter, Hübner, Christoph, Weschke, Bernhard, Gärtner, Jutta

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The mutational spectrum of ENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI) von Ruf, Nico, Uhlenberg, Birgit, Terkeltaub, Robert, Nürnberg, Peter, Rutsch, Frank

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Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease von Uhlenberg, Birgit, Schuelke, Markus, Rüschendorf, Franz, Ruf, Nico, Kaindl, Angela M., Henneke, Marco, Thiele, Holger, Stoltenburg-Didinger, Gisela, Aksu, Fuat, Topaloğlu, Haluk, Nürnberg, Peter, Hübner, Christoph, Weschke, Bernhard, Gärtner, Jutta

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Internethandel mit Lebensmitteln von Ruf, Nico

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JVL im Wandel – innovatives Format in neuer Gestalt von Ruf, Nico, Dombrowski, Saskia

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Erratum: Transcription is required for establishment of germline methylation marks at imprinted genes von Chotalia, Mita, Smallwood, Sebastien A., Ruf, Nico, Dawson, Claire, Lucifero, Diana, Frontera, Marga, James, Katherine, Dean, Wendy, Kelsey, Gavin

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Generalized arterial calcification of infancy : two siblings with prolonged survival von CIANA, Giovanni, TRAPPAN, Antonella, BEMBI, Bruno, BENETTONI, Alessandra, MASO, Giampaolo, ZENNARO, Floriana, RUF, Nico, SCHNABEL, Dirk, RUTSCH, Frank

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Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus-Merzbacher-like leukodystrophy von Ruf, Nico, Martelli, Mara, Weschke, Bernhard, Uhlenberg, Birgit

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Insights from Keystone: advances in the understanding of epigenetic regulation of the genome von Rancourt, Rebecca C, Ruf, Nico

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Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population von Suk, Eun-Kyung, Malkin, Ida, Dahm, Stefan, Kalichman, Leonid, Ruf, Nico, Kobyliansky, Eugene, Toliat, Mohammad, Rutsch, Frank, Nürnberg, Peter, Livshits, Gregory

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Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy von Tinschert, Sigrid, Ruf, Nico, Bernascone, Ilenia, Sacherer, Kai, Lamorte, Giuseppe, Neumayer, Hans-Hellmut, Nürnberg, Peter, Luft, Friedrich C., Rampoldi, Luca

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Erratum: the mutational spectrum ofENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI) von Ruf, Nico, Uhlenberg, Birgit, Terkeltaub, Robert, Nürnberg, Peter, Rutsch, Frank

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