Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Margrieta A. Alblas"'
Autor:
Nina Ishorst, Holger Thiele, Lina Gölz, Michael J. Dixon, Margrieta A. Alblas, Michael Knapp, I. Graf, E. Mangold, Markus M. Nöthen, Alexander Hemprich, Khalid Aldhorae, Jill Dixon, Teresa Kruse, Johanna Klamt, Christian Gilissen, Kathleen Keppler, Anne C. Böhmer, Heiko Reutter, Nikolaos Daratsianos, Sugirthan Sivalingam, Dmitriy Drichel, Alexander Hoischen, Gül Schmidt, Anna Maaser, Ann-Kathrin Hoebel, M van de Vorst, Alexander M. Zink, Anton Dunsche, Kerstin U. Ludwig, Stefanie Nowak
Publikováno v:
Journal of dental research 96(11), 1314-1321 (2017). doi:10.1177/0022034517722761
Journal of Dental Research, 96, 11, pp. 1314-1321
Journal of Dental Research, 96, 1314-1321
Journal of Dental Research, 96, 11, pp. 1314-1321
Journal of Dental Research, 96, 1314-1321
Contains fulltext : 177554.pdf (Publisher’s version ) (Closed access) Nonsyndromic cleft palate only (nsCPO) is a facial malformation that has a livebirth prevalence of 1 in 2,500. Research suggests that the etiology of nsCPO is multifactorial, wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fba2c947aafa0cbdd67065cbfb1b9e0
Autor:
Anne C. Böhmer, Gül Schmidt, Elisabeth Mangold, Hannah Schuencke, Nadine Fricker, Bert Braumann, Kerstin U. Ludwig, Bernd Pötzsch, Margrieta A. Alblas, Michael Knapp, Markus M. Nöthen, Nikolaos Daratsianos, Taofik Al Chawa, Per Hoffmann, Rudolf H. Reich, Heide Fier, Christoph Lange
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 100:493-498
Background The genes Gremlin-1 (GREM1) and Noggin (NOG) are components of the bone morphogenetic protein 4 pathway, which has been implicated in craniofacial development. Both genes map to recently identified susceptibility loci (chromosomal region 1
Autor:
Lutz Priebe, Margrieta A. Alblas, Rami Abou Jamra, Nadine Kluck, Sibylle Eigelshoven, Susanne Moebus, Felix F. Brockschmidt, Stefanie Heilmann, Raimund Erbel, Tim Becker, Christine Herold, Holger Fröhlich, Stephen B. Harrap, Axel M. Hillmer, Christian Meesters, Karl-Heinz Jöckel, Rudolf Kruse, B. Lippke, Justine A. Ellis, Franziska Degenhardt, Sandra Hanneken, Markus M. Nöthen, Johannes Schumacher
Publikováno v:
British Journal of Dermatology. 165:1293-1302
Summary Background Male-pattern baldness (androgenetic alopecia, AGA) is the most common form of hair loss among humans. Research has shown that it is caused by genetic factors. Numerous studies have unequivocally identified two major genetic risk lo
Autor:
Sibylle Eigelshoven, A. Jung, Bettina Blaumeiser, Markus Böhm, Margrieta A. Alblas, Christian Meesters, Natalie Garcia Bartels, Matthias Goebeler, Lina M Forstbauer, Wiebke K. Peitsch, Felix F. Brockschmidt, Stefanie Heilmann, Ingrid Moll, Kathrin A. Giehl, Alexandra Herzog, Regina C. Betz, Silke Redler, George Kirov, Valentina Moskvina, Hans Christian Hennies, Ulrike Blume-Peytavi, Jennifer Kuhn, Florian Albert, Axel M. Hillmer, Gerhard Lutz, Roland Kruse, Anne-Katrin Kortüm, Hans Wolff, Dagny Jagielska, Christine Herold, Sandra Hanneken, Tim Becker, Markus M. Nöthen
Publikováno v:
European journal of human genetics
European journal of human genetics 20(3), 326-332 (2011). doi:10.1038/ejhg.2011.185
European journal of human genetics 20(3), 326-332 (2011). doi:10.1038/ejhg.2011.185
Alopecia areata (AA) is a common hair loss disorder, which is thought to be a tissue-specific autoimmune disease. Previous research has identified a few AA susceptibility genes, most of which are implicated in autoimmunity. To identify new genetic va
Autor:
Margrieta A. Alblas, Sandra Barth, Thomas Kreusch, Régine P.M. Steegers-Theunissen, Markus Martini, Bert Braumann, Anne M. Molloy, Stefanie Nowak, Borut Peterlin, B. Lippke, Peter A. Mossey, Andreas Jäger, Markus M. Nöthen, Peter Hoffmann, E. Mangold, Heiko Reutter, Mario Paredes-Zenteno, Alexander Hemprich, Kerstin U. Ludwig, Bernd Pötzsch, Anne C. Böhmer, Stefan Herms, Sergio G. Munoz-Jimenez, Augusto Rojas-Martinez, Rocio Ortiz-Lopez, Michele Rubini, Michael Knapp
Publikováno v:
Journal of Dental Research, 93, 376-81
Journal of Dental Research, 93(4), 376-381. SAGE Publishing
Journal of Dental Research, 93, 4, pp. 376-81
Journal of Dental Research, 93(4), 376-381. SAGE Publishing
Journal of Dental Research, 93, 4, pp. 376-81
Nonsyndromic orofacial clefting (nsOFC) is a common, complex congenital disorder. The most frequent forms are nonsyndromic cleft lip with or without cleft palate (nsCL/P) and nonsyndromic cleft palate only (nsCPO). Although they are generally conside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081ca6f0e99436fb2839fdea14ac39b9
http://hdl.handle.net/11392/2301818
http://hdl.handle.net/11392/2301818
Autor:
Tim Becker, Sandra Hanneken, Axel M. Hillmer, Max P. Baur, Markus M. Nöthen, Peter Propping, Anne-Katrin Kortüm, Regina C. Betz, Margrieta A. Alblas, Nicholas G. Martin, Zhen Zhen Zhao, Stefan Herms, Martina Bröcker-Preuss, Felix F. Brockschmidt, Karl-Heinz Jöckel, Susanne Moebus, Raimund Erbel, Sven Cichon, Thomas F. Wienker, Thomas W. Mühleisen, Dale R. Nyholt, Antonia Flaquer, Michael Steffens, Roland Kruse, Roman Reinartz, Sibylle Eigelshoven, Grant W. Montgomery
Publikováno v:
Nature Genetics. 40:1279-1281
We carried out a genome-wide association study in 296 individuals with male-pattern baldness (androgenetic alopecia) and 347 controls. We then investigated the 30 best SNPs in an independent replication sample and found highly significant association
Autor:
Sven Cichon, Nadine Kluck, Manuel Mattheisen, Thomas F. Wienker, Sandra Barth, Elisabeth Mangold, Nikolaos Daratsianos, Anna Paul, Jessica Becker, Taofik AlChawa, Simone Pötzsch, Peter A. Mossey, Mary L. Marazita, Margrieta A. Alblas, Terri H. Beaty, Markus M. Nöthen, Rudolf H. Reich, Stefanie Nowak, Entessar Nasser, Bert Braumann, Bettina Blaumeiser, Franz Josef Kramer, Alan F. Scott, Ingo Ruczinski, Kerstin U. Ludwig, Thomas Kreusch, Christoph Lange, Carola Lauster, Jeffrey C. Murray, Per Hoffmann, Ruth Herberz, Régine P.M. Steegers-Theunissen, Alexander Hemprich, Heiko Reutter, Peter Propping, Michael Knapp, Michele Rubini, Stefan Herms, Anne C. Böhmer
Publikováno v:
Nature Genetics, 44(9), 968-971. Nature Publishing Group
Nature genetics
Nature genetics
We have conducted the first meta-analyses for nonsyndromic cleft lip with or without cleft palate (NSCL/P) using data from the two largest genome-wide association studies published to date. We confirmed associations with all previously identified loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c31f71db52b1405af89571b0d690d69
http://hdl.handle.net/11392/1708102
http://hdl.handle.net/11392/1708102
Autor:
Heinrich Sauer, Franziska Degenhardt, Stephanie H. Witt, Ina Giegling, Manuel Mattheisen, Thomas W. Mühleisen, Jens Treutlein, Sandra Meier, Sven Cichon, Stefan Herms, Jana Strohmaier, Marcella Rietschel, Markus M. Nöthen, Per Hoffmann, Dan Rujescu, Thomas G. Schulze, Margrieta A. Alblas, Igor Nenadic
Publikováno v:
Schizophrenia research 141(2-3), 262-265 (2012). doi:10.1016/j.schres.2012.08.027
Convergent evidence from pharmacological and animal studies suggests a possible role for the synaptic vesicle glycoprotein 2A gene (SV2A) in schizophrenia susceptibility. To test systematically all common variants in the SV2A gene region for an assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59e6354170e47ce053e7a4e070e365f2
https://pub.dzne.de/record/141673
https://pub.dzne.de/record/141673
Autor:
Susanne Moebus, Torsten Paul, Sven Cichon, René Breuer, Nieratschker, Lutz Priebe, M. Rietschel, Britta Haenisch, Franziska Degenhardt, Thomas W. Mühleisen, Stefan Schreiber, Stephanie H. Witt, Wolfgang Maier, Markus M. Nöthen, Margrieta A. Alblas, Peter Propping, Manuel Mattheisen, Stefan Herms, Weingarten M, Marion Leboyer, Mark Lathrop, Maria Grigoroiu-Serbanescu
Publikováno v:
Molecular psychiatry. 17(4)
We used genome-wide single nucleotide polymorphism (SNP) data to search for the presence of copy number variants (CNVs) in 882 patients with bipolar disorder (BD) and 872 population-based controls. A total of 291 (33%) patients had an early age-at-on
Autor:
Felix F. Brockschmidt, Marcella Rietschel, Tim Becker, Elaine K. Green, Markus M. Nöthen, Rami Abou Jamra, Alexander Georgi, Mazda Adli, Johannes Schumacher, Nicholas John Craddock, Jana Strohmeier, Thomas G. Schulze, Margrieta A. Alblas, Peter Propping, Jens R. Wendland, Sven Cichon, Detelina Grozeva
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (4)
Strong evidence of linkage between chromosomal region 6q16-q22 and bipolar affective disorder (BPAD) has previously been reported. We conducted a systematic association mapping of the 6q-linkage interval using 617 SNP markers in a BPAD case–control