Ngā hua rapu - Bettina Blaumeiser
- E whakaatu ana i te 1 - 14 hua o te 14
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1
Genetic Variants in CTLA4 Are Strongly Associated with Alopecia Areata mā Karsten K-G John, Felix F. Brockschmidt, Silke Redler, Christine Herold, S. Hanneken, Sibylle Eigelshoven, Kathrin Giehl, J. De Weert, Gerhard Lutz, Roland Kruse, Hans Wolff, Bettina Blaumeiser, Markus Böhm, Tim Becker, Markus M. Nöthen, Regina C. Betz
I whakaputaina 2011Carta -
2
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies mā Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, Jessica M.E. van den Oever, Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch
I whakaputaina 2016Artigo -
3
Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease mā Regina C. Betz, Jana Pforr, Antònia Flaquer, Silke Redler, S. Hanneken, Sibylle Eigelshoven, Anne-Katrin Kortüm, Thomas Tüting, Julien Lambert, J. De Weert, Axel M. Hillmer, Christine Schmael, Thomas F. Wienker, Roland Kruse, Gerhard Lutz, Bettina Blaumeiser, Markus M. Nöthen
I whakaputaina 2007Artigo -
4
Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance mā Dagny Jagielska, Silke Redler, Felix F. Brockschmidt, Christine Herold, Sandra M. Pasternack, Natalie Garcia Bartels, S. Hanneken, Sibylle Eigelshoven, Melanie Refke, Sandra Barth, Kathrin Giehl, Roland Kruse, Gerhard Lutz, Hans Wolff, Bettina Blaumeiser, Markus Böhm, Ulrike Blume‐Peytavi, Tim Becker, Markus M. Nöthen, Regina C. Betz
I whakaputaina 2012Revisão -
5
Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies mā Laura Southgate, Rajiv D. Machado, Katie Snape, Martin Primeau, Dimitra Dafou, Deborah Ruddy, Peter Branney, Malcolm E Fisher, Grace J. Lee, Michael A. Simpson, Yi He, Teisha Y. Bradshaw, Bettina Blaumeiser, W S Winship, William Reardon, Eamonn R. Maher, David Fitzpatrick, Wim Wuyts, Martin Zenker, Nathalie Lamarche‐Vane, Richard C. Trembath
I whakaputaina 2011Artigo -
6
Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia mā Axel M. Hillmer, S. Hanneken, Sibylle Ritzmann, Tim Becker, Jan Freudenberg, Felix F. Brockschmidt, Antònia Flaquer, Yun Freudenberg‐Hua, Rami Abou Jamra, Christine Metzen, Uwe Heyn, Nadine Schweiger, Regina C. Betz, Bettina Blaumeiser, Jochen Hampe, Stefan Schreiber, Thomas G. Schulze, Hans Christian Hennies, Johannes Schumacher, Peter Propping, Thomas Ruzicka, Sven Cichon, Thomas F. Wienker, Roland Kruse, Markus M. Nöthen
I whakaputaina 2005Artigo -
7
Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 mā Hanyin Cheng, Leah Gottlieb, Elaine Marchi, Robert Kleyner, Puja Bhardwaj, Alan F. Rope, Sarah Rosenheck, Sébastien Moutton, Christophe Philippe, Wafaa Eyaid, Fowzan S. Alkuraya, Janet Toribio, Rafael Mena, Carlos E. Prada, Holly A.F. Stessman, Raphael Bernier, Marieke Wermuth, Brice Kauffmann, Bettina Blaumeiser, R. Frank Kooy, Diana Baralle, Grazia M.S. Mancini, Simon J. Conway, Fan Xia, Chen Zhao, Linyan Meng, Ljubisa Mihajlovic, Ronen Marmorstein, Gholson J. Lyon
I whakaputaina 2019Artigo -
8
Outcome of publicly funded nationwide first-tier noninvasive prenatal screening mā Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gâtinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener, Marjan De Rademaeker, Julie Désir, Annelies Dheedene, Armelle Duquenne, Nathalie Fieremans, Annelies Fieuw, Jean‐Stéphane Gatot, Bernard Grisart, Katrien Janssens, Sandra Janssens, Damien Lederer, Axel Marichal, Björn Menten, Colombine Meunier, Léonor Palmeira, Bruno Pichon, Eva Sammels, Guillaume Smits, Yves Sznajer, Elise Vantroys, Koenraad Devriendt, Joris Vermeesch
I whakaputaina 2021Artigo -
9
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata mā Lina M Forstbauer, Felix F Brockschmidt, Valentina Moskvina, Christine Herold, Silke Redler, Alexandra Herzog, Axel M. Hillmer, Christian Meesters, Stefanie Heilmann‐Heimbach, Florian Albert, Margrieta A Alblas, S. Hanneken, Sibylle Eigelshoven, Kathrin Giehl, Dagny Jagielska, Ulrike Blume‐Peytavi, Natalie Garcia Bartels, Jennifer Kuhn, Hans Christian Hennies, Matthias Goebeler, Andreas Jung, Wiebke K. Peitsch, Anne-Katrin Kortüm, Ingrid Moll, Roland Kruse, Gerhard Lutz, Hans Wolff, Bettina Blaumeiser, Markus Böhm, George Kirov, Tim Becker, Markus M. Nöthen, Regina C Betz
I whakaputaina 2011Artigo -
10
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci mā Regina C. Betz, Lynn Petukhova, Stephan Ripke, Hailiang Huang, Androniki Menelaou, Silke Redler, Tim Becker, Stefanie Heilmann‐Heimbach, Tarek Yamany, Madeliene Duvic, Maria Hordinsky, David A. Norris, Vera H. Price, Julian Mackay‐Wiggan, Annemieke de Jong, Gina M. DeStefano, Susanne Moebus, Markus Böhm, Ulrike Blume‐Peytavi, Hans Wolff, Gerhard Lutz, Roland Kruse, Bian Li, Christopher I. Amos, Annette Lee, Peter K. Gregersen, Bettina Blaumeiser, David Altshuler, Raphael Clynes, Paul I. W. de Bakker, Markus M. Nöthen, Mark J. Daly, Angela M. Christiano
I whakaputaina 2015Revisão -
11
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate mā Elisabeth Mangold, Kerstin U. Ludwig, Stefanie Birnbaum, Carlotta Baluardo, Melissa Ferrian, Stefan Herms, Heiko Reutter, Nilma Almeida de Assis, Taofik Al Chawa, Manuel Mattheisen, Michael Steffens, Sandra Barth, Nadine Kluck, Anna Paul, Jessica Becker, Carola Lauster, Gül Schmidt, Bert Braumann, Martin Scheer, Rudolf H. Reich, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Susanne Moebus, Michael Krawczak, Stefan Schreiber, Thomas Meitinger, Hans-Erich Wichmann, Régine P.M. Steegers‐Theunissen, Franz-Josef Kramer, Sven Cichon, Peter Propping, Thomas F. Wienker, Michael Knapp, Michele Rubini, Peter Mossey, Per Hoffmann, Markus M. Nöthen
I whakaputaina 2009Artigo -
12
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci mā Kerstin U. Ludwig, Elisabeth Mangold, Stefan Herms, Stefanie Nowak, Heiko Reutter, Anna Paul, Jessica Becker, Ruth Herberz, Taofik AlChawa, Entessar Nasser, Anne C. Böhmer, Manuel Mattheisen, Margrieta A Alblas, Sandra Barth, Nadine Kluck, Carola Lauster, Bert Braumann, Rudolf H. Reich, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Nikolaos Daratsianos, Thomas Kreusch, Jeffrey C. Murray, Mary L. Marazita, Ingo Ruczinski, Alan F. Scott, Terri H. Beaty, Franz-Josef Kramer, Thomas F. Wienker, Régine P.M. Steegers‐Theunissen, Michele Rubini, Peter Mossey, Per Hoffmann, Christoph Lange, Sven Cichon, Peter Propping, Michael Knapp, Markus M. Nöthen
I whakaputaina 2012Revisão -
13
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 mā Robin Walters, Sébastien Jacquemont, Armand Valsesia, Adam J. de Smith, Danielle Martinet, Johanna C. Andersson‐Assarsson, Mario Falchi, Fei Chen, Joris Andrieux, Stéphane Lobbens, B Delobel, Fanny Stutzmann, Julia S. El-Sayed Moustafa, Jean-Claude Chèvre, Cécile Lecœur, Vincent Vatin, Sonia Bouquillon, Jessica L. Buxton, Odile Boute, Muriel Holder‐Espinasse, Jean‐Marie Cuisset, M. Lemaître, Anne‐Emmanuelle Ambresin, Andrea Brioschi, Muriel Gaillard, Vittorio Giusti, Florence Fellmann, Alessandra Ferrarini, Nouchine Hadjikhani, Dominique Campion, Audrey Guilmatre, Anna Goldenberg, Nadège Calmels, Jean‐Louis Mandel, Cédric Le Caignec, A. David, Bertrand Isidor, Marie‐Pierre Cordier, Sophie Dupuis‐Girod, Audrey Labalme, Damien Sanlaville, Mylène Béri‐Dexheimer, Philippe Jonveaux, Bruno Leheup, Katrin Õunap, Elena G. Bochukova, Elana Henning, Julia M. Keogh, Richard J. Ellis, K D MacDermot, Mieke M. van Haelst, C. Vincent‐Delorme, Ghislaine Plessis, Renaud Touraine, Anne Philippe, Valérie Malan, M. Mathieu‐Dramard, Jean Chiésa, Bettina Blaumeiser, R. Frank Kooy, Robert Caïazzo, Marie Pigeyre, Beverley Balkau, Robert Sladek, Sven Bergmann, Vincent Mooser, Dawn Waterworth, Alexandre Reymond, Péter Vollenweider, Gérard Waeber, Ants Kurg, Priit Palta, Tõnu Esko, Andres Metspalu, Mari Nelis, Paul Elliott, Anna‐Liisa Hartikainen, Mark I. McCarthy, L. Peltonen, Lena Carlsson, Peter Jacobson, Lars Sjöström, Ni Huang, Matthew E. Hurles, Stephen O’Rahilly, I. Sadaf Farooqi, Katrin Männik, Marjo‐Riitta Järvelin, François Pattou, Stephen Eyre, Andrew J. Walley, Lachlan Coin, Alexandra I. F. Blakemore, Philippe Froguel, J. Beckmann
I whakaputaina 2010Artigo -
14
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus mā Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D. Beckmann, Guðmar Þorleifsson, Marco Belfiore, Sonia Bouquillon, Dominique Campion, Nicole de Leeuw, Bert B.A. de Vries, Tõnu Esko, Bridget A. Fernandez, Fernando Fernández‐Aranda, José Manuel Fernández‐Real, Mónica Gratacòs, Audrey Guilmatre, Juliane Hoyer, Marjo‐Riitta Järvelin, R. Frank Kooy, Ants Kurg, Cédric Le Caignec, Katrin Männik, Orah S. Platt, Damien Sanlaville, Mieke M. van Haelst, Sergi Villatoro, Faida Walha, Bai-Lin Wu, Yongguo Yu, Azzedine Aboura, Marie‐Claude Addor, Yves Alembik, Stylianos E. Antonarakis, Benoı̂t Arveiler, Magalie Barth, Nathalie Bednarek, Frédérique Béna, Sven Bergmann, Mylène Béri, Laura Bernardini, Bettina Blaumeiser, Dominique Bonneau, Armand Bottani, Odile Boute, Han G. Brunner, Dorothée Cailley, Patrick Callier, Jean Chiésa, Jacqueline Chrast, Lachlan Coin, Charles Coutton, Jean‐Marie Cuisset, J. Cuvellier, Albert David, Bénédicte de Fréminville, Bruno Delobel, Marie‐Ange Delrue, Bénédicte Demeer, Dominique Descamps, Gérard Didelot, Klaus Dieterich, Vittoria Disciglio, Martine Doco‐Fenzy, Séverine Drunat, Bénédicte Duban‐Bedu, Christèle Dubourg, Julia S. El-Sayed Moustafa, Paul Elliott, Brigitte H. W. Faas, Laurence Faivre, Anne Faudet, Florence Fellmann, Alessandra Ferrarini, Richard Fisher, Elisabeth Flori, Lukas Forer, Dominique Gaillard, Marion Gérard, Christian Gieger, Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin, Anna‐Liisa Hartikainen, Delphine Héron, Loyse Hippolyte, Muriel Holder, Georg Homuth, Bertrand Isidor, Sylvie Jaillard, Zdenek Jaros, Susana Jiménez‐Múrcia, Géraldine Joly Helas
I whakaputaina 2011Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Medicine
Gene
Genome-wide association study
Genotype
Internal medicine
Single-nucleotide polymorphism
Alopecia areata
Environmental health
Genetic association
Population
Phenotype
Copy-number variation
Dermatology
Disease
Endocrinology
Exome sequencing
Fetus
Genetic heterogeneity
Genome
Immunology
Locus (genetics)
Obesity
Odds ratio
Pregnancy
Prenatal diagnosis
Risk factor
Actin cytoskeleton
Allele