Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy von Marenholz, Ingo, Grosche, Sarah, Kalb, Birgit, Rüschendorf, Franz, Blümchen, Katharina, Schlags, Rupert, Harandi, Neda, Price, Mareike, Hansen, Gesine, Seidenberg, Jürgen, Röblitz, Holger, Yürek, Songül, Tschirner, Sebastian, Hong, Xiumei, Wang, Xiaobin, Homuth, Georg, Schmidt, Carsten O., Nöthen, Markus M., Hübner, Norbert, Niggemann, Bodo, Beyer, Kirsten, Lee, Young-Ae

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A functional IL-6 receptor ( IL6R ) variant is a risk factor for persistent atopic dermatitis von Esparza-Gordillo, Jorge, PhD, Schaarschmidt, Heidi, ME, Liang, Liming, PhD, Cookson, William, MD, DPhil, Bauerfeind, Anja, PhD, Lee-Kirsch, Min-Ae, MD, Nemat, Katja, MD, Henderson, John, MD, Paternoster, Lavinia, PhD, Harper, John I., MD, Mangold, Elisabeth, MD, Nothen, Markus M., MD, Rüschendorf, Franz, PhD, Kerscher, Tamara, PhD, Marenholz, Ingo, PhD, Matanovic, Anja, MSc, Lau, Susanne, MD, Keil, Thomas, MD, MSc, Bauer, Carl-Peter, MD, Kurek, Michael, MD, Ciechanowicz, Andrzej, MD, Macek, Milan, MD, DSc, Franke, Andre, PhD, Kabesch, Michael, MD, Hubner, Norbert, MD, Abecasis, Gonçalo, PhD, Weidinger, Stephan, MD, Moffatt, Miriam, DPhil, Lee, Young-Ae, MD

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Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy von Heinig, Matthias, Adriaens, Michiel E, Schafer, Sebastian, van Deutekom, Hanneke W M, Lodder, Elisabeth M, Ware, James S, Schneider, Valentin, Felkin, Leanne E, Creemers, Esther E, Meder, Benjamin, Katus, Hugo A, Rühle, Frank, Stoll, Monika, Cambien, François, Villard, Eric, Charron, Philippe, Varro, Andras, Bishopric, Nanette H, George, Jr, Alfred L, Dos Remedios, Cristobal, Moreno-Moral, Aida, Pesce, Francesco, Bauerfeind, Anja, Rüschendorf, Franz, Rintisch, Carola, Petretto, Enrico, Barton, Paul J, Cook, Stuart A, Pinto, Yigal M, Bezzina, Connie R, Hubner, Norbert

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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans von Vona, Barbara, Mazaheri, Neda, Lin, Sheng-Jia, Dunbar, Lucy A., Maroofian, Reza, Azaiez, Hela, Booth, Kevin T., Vitry, Sandrine, Rad, Aboulfazl, Rüschendorf, Franz, Varshney, Pratishtha, Fowler, Ben, Beetz, Christian, Alagramam, Kumar N., Murphy, David, Shariati, Gholamreza, Sedaghat, Alireza, Houlden, Henry, Petree, Cassidy, VijayKumar, Shruthi, Smith, Richard J. H., Haaf, Thomas, El-Amraoui, Aziz, Bowl, Michael R., Varshney, Gaurav K., Galehdari, Hamid

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PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption von Decker, Eva, Stellzig-Eisenhauer, Angelika, Fiebig, Britta S., Rau, Christiane, Kress, Wolfram, Saar, Kathrin, Rüschendorf, Franz, Hubner, Norbert, Grimm, Tiemo, Weber, Bernhard H.F.

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Eleven loci with new reproducible genetic associations with allergic disease risk von Ferreira, Manuel A.R., Vonk, Judith M., Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, Lu, Yi, Rüschendorf, Franz, Hinds, David A., Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik K.E., Jorgenson, Eric, Lee, Young-Ae, Boomsma, Dorret I., Karlsson, Robert, Almqvist, Catarina, Koppelman, Gerard H., Paternoster, Lavinia

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A systematic approach to mapping recessive disease genes in individuals from outbred populations von Hildebrandt, Friedhelm, Heeringa, Saskia F, Rüschendorf, Franz, Attanasio, Massimo, Nürnberg, Gudrun, Becker, Christian, Seelow, Dominik, Huebner, Norbert, Chernin, Gil, Vlangos, Christopher N, Zhou, Weibin, O'Toole, John F, Hoskins, Bethan E, Wolf, Matthias T F, Hinkes, Bernward G, Chaib, Hassan, Ashraf, Shazia, Schoeb, Dominik S, Ovunc, Bugsu, Allen, Susan J, Vega-Warner, Virginia, Wise, Eric, Harville, Heather M, Lyons, Robert H, Washburn, Joseph, Macdonald, James, Nürnberg, Peter, Otto, Edgar A

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ALOHOMORA: a tool for linkage analysis using 10K SNP array data von Ruschendorf, F., Nurnberg, P.

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Recessive mutations in PCBD1 cause a new type of early-onset diabetes von Simaite, Deimante, Kofent, Julia, Gong, Maolian, Rüschendorf, Franz, Jia, Shiqi, Arn, Pamela, Bentler, Kristi, Ellaway, Carolyn, Kühnen, Peter, Hoffmann, Georg F, Blau, Nenad, Spagnoli, Francesca M, Hübner, Norbert, Raile, Klemens

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A Canadian genome-wide association study and meta-analysis confirm HLA as a risk factor for peanut allergy independent of asthma von Asai, Yuka, Eslami, Aida, van Ginkel, C. Dorien, Akhabir, Loubna, Wan, Ming, Yin, David, Ellis, George, Ben-Shoshan, Moshe, Marenholz, Ingo, Martino, David, Ferreira, Manuel A., Allen, Katrina, Mazer, Bruce, de Groot, Hans, de Jong, Nicolette W., Gerth van Wijk, Roy, Dubois, Anthony E.J., Grosche, Sarah, Ashley, Sarah, Rüschendorf, Franz, Kalb, Birgit, Beyer, Kirsten, Nöthen, Markus M., Lee, Young-Ae, Chin, Rick, Cheuk, Stephen, Hoffman, Joshua, Jorgensen, Eric, Witte, John S., Melles, Ronald B., Hong, Xiumei, Wang, Xiaobin, Hui, Jennie, Musk, Arthur W. (Bill), Hunter, Michael, James, Alan L., Koppelman, Gerard H., Sandford, Andrew J., Clarke, Ann E., Daley, Denise

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Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism von Kim, Hyung-Goo, Rosenfeld, Jill A, Scott, Daryl A, Bénédicte, Gerard, Labonne, Jonathan D, Brown, Jason, McGuire, Marianne, Mahida, Sonal, Naidu, Sakkubai, Gutierrez, Jacqueline, Lesca, Gaetan, des Portes, Vincent, Bruel, Ange-Line, Sorlin, Arthur, Xia, Fan, Capri, Yline, Muller, Eric, McKnight, Dianalee, Torti, Erin, Rüschendorf, Franz, Hummel, Oliver, Islam, Zeyaul, Kolatkar, Prasanna R, Layman, Lawrence C, Ryu, Duchwan, Kong, Il-Keun, Madan-Khetarpal, Suneeta, Kim, Cheol-Hee

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Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3 von Budde, Birgit S., Mizumoto, Shuji, Kogawa, Ryo, Becker, Christian, Altmüller, Janine, Thiele, Holger, Rüschendorf, Franz, Toliat, Mohammad R., Kaleschke, Gerrit, Hämmerle, Johannes M., Höhne, Wolfgang, Sugahara, Kazuyuki, Nürnberg, Peter, Kennerknecht, Ingo

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Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy von McHenry, Christina L, Hübner, Christian A, Gal, Andreas, Thompson, Debra A, Wissinger, Bernd, Rüschendorf, Franz, Heckenlively, John, Schmid, Eduard, Utermann, Gerd, Janecke, Andreas R, Nair, Anita R, Nürnberg, Peter, Becker, Christian

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Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea von Heinz-Erian, Peter, Müller, Thomas, Krabichler, Birgit, Schranz, Melanie, Becker, Christian, Rüschendorf, Franz, Nürnberg, Peter, Rossier, Bernard, Vujic, Mihailo, Booth, Ian W., Holmberg, Christer, Wijmenga, Cisca, Grigelioniene, Giedre, Kneepkens, C. M. Frank, Rosipal, Stefan, Mistrik, Martin, Kappler, Matthias, Michaud, Laurent, Dóczy, Ludwig-Christoph, Siu, Victoria Mok, Krantz, Marie, Zoller, Heinz, Utermann, Gerd, Janecke, Andreas R.

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Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p von Lee-Kirsch, Min Ae, Gong, Maolian, Schulz, Herbert, Rüschendorf, Franz, Stein, Annette, Pfeiffer, Christiane, Ballarini, Annalisa, Gahr, Manfred, Hubner, Norbert, Linné, Maja

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Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation von Prüss, Harald, Gessner, Guido, Heinemann, Stefan H, Rüschendorf, Franz, Ruppert, Ann-Kathrin, Schulz, Herbert, Sander, Thomas, Rimpau, Wilhelm

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A major susceptibility locus for atopic dermatitis maps to chromosome 3q21 von Wahn, Ulrich, Reis, André, Wienker, Thomas, Gustafsson, Dan, Wolkertstorfer, Albert, Lee, Young-Ae, Oranje, Arnold P, Küster, Wolfgang, Kehrt, Rainer, Berg, Andrea v, Tarani, Luigi, Businco, Luisa, Rüschendorf, Franz, Hoffmann, Ute, Andersson, Florence

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar

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Childhood Hypertension in Autosomal-Dominant Hypertension With Brachydactyly von Toka, Okan, Maass, Philipp G, Aydin, Atakan, Toka, Hakan, Hübner, Norbert, Rüschendorf, Franz, Gong, Maolian, Luft, Friedrich C, Bähring, Sylvia

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Genome-wide linkage analysis of malaria infection intensity and mild disease von Timmann, Christian, Evans, Jennifer A, König, Inke R, Kleensang, André, Rüschendorf, Franz, Lenzen, Julia, Sievertsen, Jürgen, Becker, Christian, Enuameh, Yeetey, Kwakye, Kingsley Osei, Opoku, Ernest, Browne, Edmund N L, Ziegler, Andreas, Nürnberg, Peter, Horstmann, Rolf D

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