Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Nadine Kluck"'
Autor:
Kathrin A. Giehl, M.P. Birch, Markus M. Nöthen, Rachid Tazi-Ahnini, Andrew G. Messenger, Regina C. Betz, Silke Redler, Dmitriy Drichel, Stefan Herms, Tim Becker, Helmut H. Wolff, Felix F. Brockschmidt, Markus Böhm, Melanie Refke, Gerhard Lutz, Rudolf Kruse, K. Dobson, Nadine Kluck
Publikováno v:
British Journal of Dermatology. 166:1314-1318
Summary Background The aetiology of female pattern hair loss (FPHL) is largely unknown. However, it is hypothesized that FPHL and male pattern baldness (AGA) share common susceptibility alleles. The two major susceptibility loci for AGA are the andro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf5eedf3a5b1b0a82c71667c4177de08
https://doi.org/10.1111/j.1365-2133.2012.10877.x
https://doi.org/10.1111/j.1365-2133.2012.10877.x
Autor:
Felix F. Brockschmidt, Rachid Tazi-Ahnini, Markus M. Nöthen, Hans Wolff, Kathrin A. Giehl, Nadine Kluck, Mary P. Birch, Silke Redler, Melanie Refke, K. Dobson, Regina C. Betz, Andrew G. Messenger, Tim Becker, Markus Böhm, Dmitriy Drichel, Roland Kruse, Gerhard Lutz
Publikováno v:
Experimental dermatology 21(5), 390-393 (2012). doi:10.1111/j.1600-0625.2012.01469.x
Female pattern hair loss (FPHL) is a common disorder with a complex mode of inheritance. Although understanding of its etiopathogenesis is incomplete, an interaction between genetic and hormonal factors is assumed to be important. The involvement of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5a70742498e086f565e0c966e6e567
https://doi.org/10.1111/j.1600-0625.2012.01469.x
https://doi.org/10.1111/j.1600-0625.2012.01469.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24c2fa5834824c125d19875eaaa1d8f2
https://doi.org/10.1111/j.1365-2133.2011.10708.x
https://doi.org/10.1111/j.1365-2133.2011.10708.x
Autor:
Andreas Ziegler, Andreas Warnke, Gerd Schulte-Körne, Myriam Peyrard-Janvid, Nadine Kluck, Heidi Anthoni, Faten Dahdouh, Malou Manthey, Helmut Remschmidt, Juha Kere, Axel M. Hillmer, Marco Zucchelli, Sven Cichon, Markus M. Nöthen, Ellen Plume, Jutta Hülsmann, Peter Propping, Cecilia M. Lindgren, Johannes Schumacher, Inke R. König
Publikováno v:
The American Journal of Human Genetics. 78(1):52-62
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the most-replicated dyslexia susceptibility region on 6p21-p22, and found association between the disease and markers within the VMP/DCDC2/KAAG1 locus. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78709fa697d83633e3fa642a3d4b4eeb
Autor:
Nadine Kluck, J Winantea, Peter Propping, Markus M. Nöthen, Jan Freudenberg, Sven Cichon, Yun Freudenberg-Hua, Michael Brüss
Publikováno v:
The Pharmacogenomics Journal. 5:183-192
In order to identify single-nucleotide polymorphisms (SNPs) and analyze their characteristics in a set of 111 genes, we resequenced exons and flanking regions in an average of 170 chromosomes from individuals of European origin. Genetic variability w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d32a88f786f8f65e6163d21818a05ff1
https://doi.org/10.1038/sj.tpj.6500306
https://doi.org/10.1038/sj.tpj.6500306
Autor:
Rudolf Kruse, K. Dobson, Tim Becker, Markus M. Nöthen, Helmut H. Wolff, Gerhard Lutz, Nadine Kluck, Dmitriy Drichel, Felix F. Brockschmidt, Kathrin A. Giehl, Rachid Tazi-Ahnini, Regina C. Betz, Andrew G. Messenger, Silke Redler, M.P. Birch
Publikováno v:
British Journal of Dermatology. 165:703-705
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2d3223b1e31af1167d514f93b39bf5d
https://doi.org/10.1111/j.1365-2133.2011.10456.x
https://doi.org/10.1111/j.1365-2133.2011.10456.x
Autor:
Peter Propping, Martin Scheer, Michael Knapp, Stefan Herms, Carlotta Baluardo, Sandra Barth, Thomas Meitinger, Bettina Blaumeiser, Simone Pötzsch, Markus M. Nöthen, Jessica Becker, Bert Braumann, Per Hoffmann, Thomas F. Wienker, Sven Cichon, Melissa Ferrian, Peter A. Mossey, Stefan Schreiber, Michele Rubini, Nadine Kluck, Michael Steffens, Régine P.M. Steegers-Theunissen, Michael Krawczak, Nilma Almeida de Assis, Anna Paul, Stefanie Birnbaum, Heiko Reutter, Gül Schmidt, Manuel Mattheisen, Kerstin U. Ludwig, Rudolf H. Reich, Carola Lauster, Hans Erich Wichmann, Taofik Al Chawa, Elisabeth Mangold, Susanne Moebus, Franz Josef Kramer, Alexander Hemprich
Publikováno v:
Nature Genetics, 42(1), 24-26. Nature Publishing Group
Nature genetics
Nature genetics
We conducted a genome-wide association study for nonsyndromic cleft lip with or without cleft palate (NSCL/P) in 401 affected individuals and 1,323 controls, with replication in an independent sample of 793 NSCL/P triads. We report two new loci assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3659d9b2d52ba43732da75f8902086
https://doi.org/10.1038/ng.506
https://doi.org/10.1038/ng.506
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:
Heiko Reutter, Stefanie Nowak, Elisabeth Mangold, Markus M. Nöthen, Bert Braumann, Kerstin U. Ludwig, Nadine Kluck, Carola Lauster, Nilma Almeida de Assis, Per Hoffmann, Thomas F. Wienker, Rudolf H. Reich, Alexander Hemprich, Jennifer Vollmer, Michael Knapp, Franz-Josef Kramer, Stefanie Heilmann
Publikováno v:
International journal of pediatric otorhinolaryngology. 75(1)
Objective Studies in mice and humans have suggested that SUMO1, which codes for the small ubiquitin-related modifier 1 (SUMO1), is a promising candidate gene for non-syndromic cleft lip with or without cleft palate (NSCL/P). To investigate the possib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9dc024d7a8ceebecf1bb19e85b27f1a
https://pubmed.ncbi.nlm.nih.gov/21044801
https://pubmed.ncbi.nlm.nih.gov/21044801
Autor:
Markus M. Nöthen, Peter Propping, Nadine Kluck, Jan Freudenberg, Yun Freudenberg-Hua, Sven Cichon
Publikováno v:
Genome research
The detailed investigation of variation in functionally important regions of the human genome is expected to promote understanding of genetically complex diseases. We resequenced 65 candidate genes for CNS disorders in an average of 85 European indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2902598542ce291855392550e56e7ca
https://hdl.handle.net/10067/428980151162165141
https://hdl.handle.net/10067/428980151162165141