Items where Division is "Medicine > Lehrstuhl für Humangenetik" and Year is 2011

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Bernstein, Jonathan A. and Bernstein, Daniel and Hehr, Ute and Hudgins, Louanne (2011) Familial Cardiac Valvulopathy Due to Filamin A Mutation. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 155A (9). pp. 2236-2241. ISSN 1552-4825

Bygum, Anette and Fagerberg, Christina R. and Clemmensen, Ole J. and Fiebig, Britta and Hafner, Christian (2011) Systemic epidermal nevus with involvement of the oral mucosa due to FGFR3 mutation. BMC MEDICAL GENETICS, 12: 79. ISSN 1471-2350

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Cox, David G. and Simard, Jacques and Sinnett, Daniel and Hamdi, Yosr and Soucy, Penny and Ouimet, Manon and Barjhoux, Laure and Verny-Pierre, Carole and McGuffog, Lesley and Healey, Sue and Szabo, Csilla and Greene, Mark H. and Mai, Phuong L. and Andrulis, Irene L. and Thomassen, Mads and Gerdes, Anne-Marie and Caligo, Maria A. and Friedman, Eitan and Laitman, Yael and Kaufman, Bella and Paluch, Shani S. and Borg, Ake and Karlsson, Per and Askmalm, Marie Stenmark and Bustinza, Gisela Barbany and Nathanson, Katherine L. and Domchek, Susan M. and Rebbeck, Timothy R. and Benitez, Javier and Hamann, Ute and Rookus, Matti A. and van den Ouweland, Ans M. W. and Ausems, Margreet G. E. M. and Aalfs, Cora M. and van Asperen, Christi J. and Devilee, Peter and Gille, Hans J. J. P. and Peock, Susan and Frost, Debra and Evans, D. Gareth and Eeles, Ros and Izatt, Louise and Adlard, Julian and Paterson, Joan and Eason, Jacqueline and Godwin, Andrew K. and Remon, Marie-Alice and Moncoutier, Virginie and Gauthier-Villars, Marion and Lasset, Christine and Giraud, Sophie and Hardouin, Agnes and Berthet, Pascaline and Sobol, Hagay and Eisinger, Francois and de Paillerets, Brigitte Bressac and Caron, Olivier and Delnatte, Capucine and Goldgar, David and Miron, Alex and Ozcelik, Hilmi and Buys, Saundra and Southey, Melissa C. and Terry, Mary Beth and Singer, Christian F. and Dressler, Anne-Catharina and Tea, Muy-Kheng and Hansen, Thomas V. O. and Johannsson, Oskar and Piedmonte, Marion and Rodriguez, Gustavo C. and Basil, Jack B. and Blank, Stephanie and Toland, Amanda E. and Montagna, Marco and Isaacs, Claudine and Blanco, Ignacio and Gayther, Simon A. and Moysich, Kirsten B. and Schmutzler, Rita K. and Wappenschmidt, Barbara and Engel, Christoph and Meindl, Alfons and Ditsch, Nina and Arnold, Norbert and Niederacher, Dieter and Sutter, Christian and Gadzicki, Dorothea and Fiebig, Britta and Caldes, Trinidad and Laframboise, Rachel and Nevanlinna, Heli and Chen, Xiaoqing and Beesley, Jonathan and Spurdle, Amanda B. and Neuhausen, Susan L. and Ding, Yuan C. and Couch, Fergus J. and Wang, Xianshu and Peterlongo, Paolo and Manoukian, Siranoush and Bernard, Loris and Radice, Paolo and Easton, Douglas F. and Chenevix-Trench, Georgia and Antoniou, Antonis C. and Stoppa-Lyonnet, Dominique and Mazoyer, Sylvie and Sinilnikova, Olga M. (2011) Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. HUMAN MOLECULAR GENETICS, 20 (23). pp. 4732-4747. ISSN 0964-6906

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Dauwerse, Johannes G. and Dixon, Jill and Seland, Saskia and Ruivenkamp, Claudia A. L. and van Haeringen, Arie and Hoefsloot, Lies H. and Peters, Dorien J. M. and Boers, Agnes Clement-de and Daumer-Haas, Cornelia and Maiwald, Robert and Zweier, Christiane and Kerr, Bronwyn and Cobo, Ana M. and Toral, Joaquin F. and Hoogeboom, A. Jeannette M. and Lohmann, Dietmar R. and Hehr, Ute and Dixon, Michael J. and Breuning, Martijn H. and Wieczorek, Dagmar (2011) Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. NATURE GENETICS, 43 (1). pp. 20-22. ISSN 1061-4036

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Fernandez-Martinez, Lorena and Letteboer, Stef and Mardin, Christian Y. and Weisschuh, Nicole and Gramer, Eugen and Weber, Bernhard H. F. and Rautenstrauss, Bernd and Ferreira, Paulo A. and Kruse, Friedrich E. and Reis, Andre and Roepman, Ronald and Pasutto, Francesca (2011) Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma. EUROPEAN JOURNAL OF HUMAN GENETICS, 19 (4). pp. 445-451. ISSN 1018-4813, 1476-5438

Friedrich, Ulrike and Myers, Connie A. and Fritsche, Lars G. and Milenkovich, Andrea and Wolf, Armin and Corbo, Joseph C. and Weber, Bernhard H. F. (2011) Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency. HUMAN MOLECULAR GENETICS, 20 (7). pp. 1387-1399. ISSN 0964-6906, 1460-2083

Friedrich, Ulrike and Stoehr, Heidi and Hilfinger, Daniela and Loenhardt, Thomas and Schachner, Melitta and Langmann, Thomas and Weber, Bernhard H. F. (2011) The Na/K-ATPase is obligatory for membrane anchorage of retinoschisin, the protein involved in the pathogenesis of X-linked juvenile retinoschisis. HUMAN MOLECULAR GENETICS, 20 (6). pp. 1132-1142. ISSN 0964-6906, 1460-2083

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Grunewald, Thomas G. P. and Herbst, Saskia M. and Heinze, Juergen and Burdach, Stefan (2011) Understanding tumor heterogeneity as functional compartments - superorganisms revisited. JOURNAL OF TRANSLATIONAL MEDICINE, 9: 79. ISSN 1479-5876

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Hehr, A. and Paulmann, B. and Seifert, B. and Hehr, U. (2011) Preimplantation genetic diagnosis for monogenic inherited disorders. MEDIZINISCHE GENETIK, 23 (4). pp. 469-478. ISSN 1863-5490

Hehr, U. and Schuierer, G. (2011) Genetic Assessment of Cortical Malformations. NEUROPEDIATRICS, 42 (2). pp. 43-50. ISSN 0174-304X

Heid, I. M. and Winkler, T. W. and Grassmann, F. and Weber, B. H. F. (2011) How big are the small genetic risks? MEDIZINISCHE GENETIK, 23 (3). pp. 377-384. ISSN 1863-5490

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Karlstetter, M. and Walczak, Y. and Ebert, S. and Weigelt, K. and Van den Brulle, J. and Schwer, H. (2011) THE NOVEL ACTIVATED MICROGLIA/MACROPHAGE WAP DOMAIN PROTEIN, AMWAP, IS INDUCED DURING MICROGLIAL ACTIVATION AND ACTS AS A NEGATIVE REGULATOR OF THE PRO-INFLAMMATORY RESPONSE. GLIA, 59 (s1). S124. ISSN 0894-1491

Karlstetter, Marcus and Lippe, Elena and Walczak, Yana and Moehle, Christoph and Aslanidis, Alexander and Mirza, Myriam and Langmann, Thomas (2011) Curcumin is a potent modulator of microglial gene expression and migration. JOURNAL OF NEUROINFLAMMATION, 8: 125. ISSN 1742-2094

Keilhauer, Claudia N. and Fritsche, Lars G. and Weber, Bernhard H. F. (2011) Age-related macular degeneration with discordant late stage phenotypes in monozygotic twins. OPHTHALMIC GENETICS, 32 (4). pp. 237-244. ISSN 1381-6810

Kraus, Dominik and Karlstetter, Marcus and Walczak, Yana and Hilfinger, Daniela and Langmann, Thomas and Weber, Bernhard H. F. (2011) Retinal expression of the X-linked juvenile retinoschisis (RS1) gene is controlled by an upstream CpG island and two opposing CRX-bound regions. BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 1809 (4-6). pp. 245-254. ISSN 1874-9399

Krumbiegel, Mandy and Pasutto, Francesca and Schloetzer-Schrehardt, Ursula and Uebe, Steffen and Zenkel, Matthias and Mardin, Christian Y. and Weisschuh, Nicole and Paoli, Daniela and Gramer, Eugen and Becker, Christian and Ekici, Arif B. and Weber, Bernhard H. F. and Nuernberg, Peter and Kruse, Friedrich E. and Reis, Andre (2011) Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS, 19 (2). pp. 186-193. ISSN 1018-4813

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Langmann, T. (2011) MICROGLIA IN RETINAL DEGENERATION: PU.1 AND EGR1 CONTROL POLARIZED TRANSCRIPTIONAL PHENOTYPES. GLIA, 59 (s1). S25. ISSN 0894-1491

Lauer, Nadine and Mihlan, Michael and Hartmann, Andrea and Schloetzer-Schrehardt, Ursula and Keilhauer, Claudia and Scholl, Hendrik P. N. and Issa, Peter Charbel and Holz, Frank and Weber, Bernhard H. F. and Skerka, Christine and Zipfel, Peter F. (2011) Complement Regulation at Necrotic Cell Lesions Is Impaired by the Age-Related Macular Degeneration-Associated Factor-H His(402) Risk Variant. JOURNAL OF IMMUNOLOGY, 187 (8). pp. 4374-4383. ISSN 0022-1767

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McKay, Gareth J. and Patterson, Chris C. and Chakravarthy, Usha and Dasari, Shilpa and Klaver, Caroline C. and Vingerling, Johannes R. and Ho, Lintje and de Jong, Paulus T. V. M. and Fletcher, Astrid E. and Young, Ian S. and Seland, Johan H. and Rahu, Mati and Soubrane, Gisele and Tomazzoli, Laura and Topouzis, Fotis and Vioque, Jesus and Hingorani, Aroon D. and Sofat, Reecha and Dean, Michael and Sawitzke, Julie and Seddon, Johanna M. and Peter, Inga and Webster, Andrew R. and Moore, Anthony T. and Yates, John R. W. and Cipriani, Valentina and Fritsche, Lars G. and Weber, Bernhard H. F. and Keilhauer, Claudia N. and Lotery, Andrew J. and Ennis, Sarah and Klein, Michael L. and Francis, Peter J. and Stambolian, Dwight and Orlin, Anton and Gorin, Michael B. and Weeks, Daniel E. and Kuo, Chia-Ling and Swaroop, Anand and Othman, Mohammad and Kanda, Atsuhiro and Chen, Wei and Abecasis, Goncalo R. and Wright, Alan F. and Hayward, Caroline and Baird, Paul N. and Guymer, Robyn H. and Attia, John and Thakkinstian, Ammarin and Silvestri, Giuliana (2011) Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies. HUMAN MUTATION, 32 (12). pp. 1407-1416. ISSN 1059-7794

McKay, Gareth J. and Silvestri, Giuliana and Chakravarthy, Usha and Dasari, Shilpa and Fritsche, Lars G. and Weber, Bernhard H. and Keilhauer, Claudia N. and Klein, Michael L. and Francis, Peter J. and Klaver, Caroline C. and Vingerling, Johannes R. and Ho, Lintje and De Jong, Paulus T. D. V. and Dean, Michael and Sawitzke, Julie and Baird, Paul N. and Guymer, Robyn H. and Stambolian, Dwight and Orlin, Anton and Seddon, Johanna M. and Peter, Inga and Wright, Alan F. and Hayward, Caroline and Lotery, Andrew J. and Ennis, Sarah and Gorin, Michael B. and Weeks, Daniel E. and Kuo, Chia-Ling and Hingorani, Aroon D. and Sofat, Reecha and Cipriani, Valentina and Swaroop, Anand and Othman, Mohammad and Kanda, Atsuhiro and Chen, Wei and Abecasis, Goncalo R. and Yates, John R. and Webster, Andrew R. and Moore, Anthony T. and Seland, Johan H. and Rahu, Mati and Soubrane, Gisele and Tomazzoli, Laura and Topouzis, Fotis and Vioque, Jesus and Young, Ian S. and Fletcher, Astrid E. and Patterson, Chris C. (2011) Variations in Apolipoprotein E Frequency With Age in a Pooled Analysis of a Large Group of Older People. AMERICAN JOURNAL OF EPIDEMIOLOGY, 173 (12). pp. 1357-1364. ISSN 0002-9262

Milenkovic, Vladimir M. and Roehrl, Elena and Weber, Bernhard H. F. and Strauss, Olaf (2011) Disease-associated missense mutations in bestrophin-1 affect cellular trafficking and anion conductance. JOURNAL OF CELL SCIENCE, 124 (17). pp. 2988-2996. ISSN 0021-9533

Mirza, M. and Jaegle, H. and Langmann, T. (2011) RETINAL DEGENERATION AND MICROGLIAL ACTIVATION IN MOUSE MODELS OF NEURONAL CEROID LIPOFUSCINOSES. GLIA, 59 (s1). S125. ISSN 0894-1491

Mulligan, Anna Marie and Couch, Fergus J. and Barrowdale, Daniel and Domchek, Susan M. and Eccles, Diana and Nevanlinna, Heli and Ramus, Susan J. and Robson, Mark and Sherman, Mark and Spurdle, Amanda B. and Wappenschmidt, Barbara and Lee, Andrew and McGuffog, Lesley and Healey, Sue and Sinilnikova, Olga M. and Janavicius, Ramunas and Hansen, Thomas V. O. and Nielsen, Finn C. and Ejlertsen, Bent and Osorio, Ana and Munoz-Repeto, Ivan and Duran, Mercedes and Godino, Javier and Pertesi, Maroulio and Benitez, Javier and Peterlongo, Paolo and Manoukian, Siranoush and Peissel, Bernard and Zaffaroni, Daniela and Cattaneo, Elisa and Bonanni, Bernardo and Viel, Alessandra and Pasini, Barbara and Papi, Laura and Ottini, Laura and Savarese, Antonella and Bernard, Loris and Radice, Paolo and Hamann, Ute and Verheus, Martijn and Meijers-Heijboer, Hanne E. J. and Wijnen, Juul and Garcia, Encarna B. Gomez and Nelen, Marcel R. and Kets, C. Marleen and Seynaeve, Caroline and Tilanus-Linthorst, Madeleine M. A. and van der Luijt, Rob B. and van Os, Theo and Rookus, Matti and Frost, Debra and Jones, J. Louise and Evans, D. Gareth and Lalloo, Fiona and Eeles, Ros and Izatt, Louise and Adlard, Julian and Davidson, Rosemarie and Cook, Jackie and Donaldson, Alan and Dorkins, Huw and Gregory, Helen and Eason, Jacqueline and Houghton, Catherine and Barwell, Julian and Side, Lucy E. and McCann, Emma and Murray, Alex and Peock, Susan and Godwin, Andrew K. and Schmutzler, Rita K. and Rhiem, Kerstin and Engel, Christoph and Meindl, Alfons and Ruehl, Ina and Arnold, Norbert and Niederacher, Dieter and Sutter, Christian and Deissler, Helmut and Gadzicki, Dorothea and Kast, Karin and Preisler-Adams, Sabine and Varon-Mateeva, Raymonda and Schoenbuchner, Ines and Fiebig, Britta and Heinritz, Wolfram and Schaefer, Dieter and Gevensleben, Heidrun and Caux-Moncoutier, Virginie and Fassy-Colcombet, Marion and Cornelis, Francois and Mazoyer, Sylvie and Leone, Melanie and Boutry-Kryza, Nadia and Hardouin, Agnes and Berthet, Pascaline and Muller, Daniele and Fricker, Jean-Pierre and Mortemousque, Isabelle and Pujol, Pascal and Coupier, Isabelle and Lebrun, Marine and Kientz, Caroline and Longy, Michel and Sevenet, Nicolas and Stoppa-Lyonnet, Dominique and Isaacs, Claudine and Caldes, Trinidad and de la Hoya, Miguel and Heikkinen, Tuomas and Aittomaki, Kristiina and Blanco, Ignacio and Lazaro, Conxi and Barkardottir, Rosa B. and Soucy, Penny and Dumont, Martine and Simard, Jacques and Montagna, Marco and Tognazzo, Silvia and D'Andrea, Emma and Fox, Stephen and Yan, Max and Rebbeck, Tim and Olopade, Olufunmilayo I. and Weitzel, Jeffrey N. and Lynch, Henry T. and Ganz, Patricia A. and Tomlinson, Gail E. and Wang, Xianshu and Fredericksen, Zachary and Pankratz, Vernon S. and Lindor, Noralane M. and Szabo, Csilla and Offit, Kenneth and Sakr, Rita and Gaudet, Mia and Bhatia, Jasmine and Kauff, Noah and Singer, Christian F. and Tea, Muy-Kheng and Gschwantler-Kaulich, Daphne and Fink-Retter, Anneliese and Mai, Phuong L. and Greene, Mark H. and Imyanitov, Evgeny and O'Malley, Frances P. and Ozcelik, Hilmi and Glendon, Gordon and Toland, Amanda E. and Gerdes, Anne-Marie and Thomassen, Mads and Kruse, Torben A. and Jensen, Uffe Birk and Skytte, Anne-Bine and Caligo, Maria A. and Soller, Maria and Henriksson, Karin and Wachenfeldt, von Anna and Arver, Brita and Stenmark-Askmalm, Marie and Karlsson, Per and Ding, Yuan Chun and Neuhausen, Susan L. and Beattie, Mary and Pharoah, Paul D. P. and Moysich, Kirsten B. and Nathanson, Katherine L. and Karlan, Beth Y. and Gross, Jenny and John, Esther M. and Daly, Mary B. and Buys, Saundra M. and Southey, Melissa C. and Hopper, John L. and Terry, Mary Beth and Chung, Wendy and Miron, Alexander F. and Goldgar, David and Chenevix-Trench, Georgia and Easton, Douglas F. and Andrulis, Irene L. and Antoniou, Antonis C. (2011) Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. BREAST CANCER RESEARCH, 13 (6): R110. ISSN 1465-542X, 1465-5411

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Ramus, Susan J. and Kartsonaki, Christiana and Gayther, Simon A. and Pharoah, Paul D. P. and Sinilnikova, Olga M. and Beesley, Jonathan and Chen, Xiaoqing and McGuffog, Lesley and Healey, Sue and Couch, Fergus J. and Wang, Xianshu and Fredericksen, Zachary and Peterlongo, Paolo and Manoukian, Siranoush and Peissel, Bernard and Zaffaroni, Daniela and Roversi, Gaia and Barile, Monica and Viel, Alessandra and Allavena, Anna and Ottini, Laura and Papi, Laura and Gismondi, Viviana and Capra, Fabio and Radice, Paolo and Greene, Mark H. and Mai, Phuong L. and Andrulis, Irene L. and Glendon, Gord and Ozcelik, Hilmi and Thomassen, Mads and Gerdes, Anne-Marie and Kruse, Torben A. and Cruger, Dorthe and Jensen, Uffe Birk and Caligo, Maria Adelaide and Olsson, Hakan and Kristoffersson, Ulf and Lindblom, Annika and Arver, Brita and Karlsson, Per and Askmalm, Marie Stenmark and Borg, Ake and Neuhausen, Susan L. and Ding, Yuan Chun and Nathanson, Katherine L. and Domchek, Susan M. and Jakubowska, Anna and Lubinski, Jan and Huzarski, Tomasz and Byrski, Tomasz and Gronwald, Jacek and Gorski, Bohdan and Cybulski, Cezary and Debniak, Tadeusz and Osorio, Ana and Duran, Mercedes and Tejada, Maria-Isabel and Benitez, Javier and Hamann, Ute and Rookus, Matti A. and Verhoef, Senno and Tilanus-Linthorst, Madeleine A. and Vreeswijk, Maaike P. and Bodmer, Danielle and Ausems, Margreet G. E. M. and van Os, Theo A. and Asperen, Christi J. and Blok, Marinus J. and Meijers-Heijboer, Hanne E. J. and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Dunning, Alison M. and Evans, D. Gareth and Eeles, Ros and Pichert, Gabriella and Cole, Trevor and Hodgson, Shirley and Brewer, Carole and Morrison, Patrick J. and Porteous, Mary and Kennedy, M. John and Rogers, Mark T. and Side, Lucy E. and Donaldson, Alan and Gregory, Helen and Godwin, Andrew and Stoppa-Lyonnet, Dominique and Moncoutier, Virginie and Castera, Laurent and Mazoyer, Sylvie and Barjhoux, Laure and Bonadona, Valerie and Leroux, Dominique and Faivre, Laurence and Lidereau, Rosette and Nogues, Catherine and Bignon, Yves-Jean and Prieur, Fabienne and Collonge-Rame, Marie-Agnes and Venat-Bouvet, Laurence and Fert-Ferrer, Sandra and Miron, Alex and Buys, Saundra S. and Hopper, John L. and Daly, Mary B. and John, Esther M. and Terry, Mary Beth and Goldgar, David and Hansen, Thomas V. O. and Jonson, Lars and Ejlertsen, Bent and Agnarsson, Bjarni A. and Offit, Kenneth and Kirchhoff, Tomas and Vijai, Joseph and Dutra-Clarke, Ana V. C. and Przybylo, Jennifer A. and Montagna, Marco and Casella, Cinzia and Imyanitov, Evgeny N. and Janavicius, Ramunas and Blanco, Ignacio and Lazaro, Conxi and Moysich, Kirsten B. and Karlan, Beth Y. and Gross, Jenny and Beattie, Mary S. and Schmutzler, Rita and Wappenschmidt, Barbara and Meindl, Alfons and Ruehl, Ina and Fiebig, Britta and Sutter, Christian and Arnold, Norbert and Deissler, Helmut and Varon-Mateeva, Raymonda and Kast, Karin and Niederacher, Dieter and Gadzicki, Dorothea and Caldes, Trinidad and de la Hoya, Miguel and Nevanlinna, Heli and Aittomaeki, Kristiina and Simard, Jacques and Soucy, Penny and Spurdle, Amanda B. and Holland, Helene and Chenevix-Trench, Georgia and Easton, Douglas F. and Antoniou, Antonis C. (2011) Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 103 (2). ISSN 0027-8874, 1460-2105

Refke, M. and Pasternack, S. M. and Fiebig, B. and Wenzel, S. and Ishorst, N. and Ludwig, M. and Noethen, M. M. and Seyger, M. M. and Hamel, B. C. and Betz, Regina C. (2011) Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay. BRITISH JOURNAL OF DERMATOLOGY, 165 (5). pp. 1127-1132. ISSN 0007-0963

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Shamsara, Jamal and Behravan, Javad and Falsoleiman, Homa and Mohammadpour, Amir Hooshang and Rendeirs, Joerg and Ramezani, Mohammad (2011) Pentoxifylline administration changes protein expression profile of coronary artery disease patients. GENE, 487 (1). pp. 107-111. ISSN 0378-1119, 1879-0038

Smailhodzic, Dzenita and Fleckenstein, Monika and Theelen, Thomas and Boon, Camiel J. F. and van Huet, Ramon A. C. and de Ven, Johannes P. H. van and Den Hollander, Anneke I. and Schmitz-Valckenberg, Steffen and Hoyng, Carel B. and Weber, Bernhard H. F. and Holz, Frank G. and Klevering, B. Jeroen (2011) Central Areolar Choroidal Dystrophy (CACD) and Age-Related Macular Degeneration (AMD): Differentiating Characteristics in Multimodal Imaging. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 52 (12). pp. 8908-8918. ISSN 0146-0404, 1552-5783

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Yang, Rongxi and Dick, Michelle and Marme, Frederik and Schneeweiss, Andreas and Langheinz, Anne and Hemminki, Kari and Sutter, Christian and Bugert, Peter and Wappenschmidt, Barbara and Varon, Raymonda and Schott, Sarah and Weber, Bernhard H. F. and Niederacher, Dieter and Arnold, Norbert and Meindl, Alfons and Bartram, Claus R. and Schmutzler, Rita K. and Mueller, Heiko and Arndt, Volker and Brenner, Hermann and Sohn, Christof and Burwinkel, Barbara (2011) Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk. BREAST CANCER RESEARCH AND TREATMENT, 127 (2). pp. 549-554. ISSN 0167-6806

Yis, Uluc and Uyanik, Goekhan and Heck, Pinar Bambul and Smitka, Martin and Nobel, Hannes and Ebinger, Friedrich and Dirik, Eray and Feng, Lucy and Kurul, Semra H. and Brocke, Katja and Unalp, Aycan and Oezer, Erdener and Cakmakci, Handan and Sewry, Caroline and Cirak, Sebahattin and Muntoni, Francesco and Hehr, Ute and Morris-Rosendahl, Deborah J. (2011) Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: Less severe mutations predominate in patients with a non-Walker-Warburg phenotype. NEUROMUSCULAR DISORDERS, 21 (1). pp. 20-30. ISSN 0960-8966, 1873-2364