Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Felix F Brockschmidt"'
Autor:
Rui Li, Felix F Brockschmidt, Amy K Kiefer, Hreinn Stefansson, Dale R Nyholt, Kijoung Song, Sita H Vermeulen, Stavroula Kanoni, Daniel Glass, Sarah E Medland, Maria Dimitriou, Dawn Waterworth, Joyce Y Tung, Frank Geller, Stefanie Heilmann, Axel M Hillmer, Veronique Bataille, Sibylle Eigelshoven, Sandra Hanneken, Susanne Moebus, Christine Herold, Martin den Heijer, Grant W Montgomery, Panos Deloukas, Nicholas Eriksson, Andrew C Heath, Tim Becker, Patrick Sulem, Massimo Mangino, Peter Vollenweider, Tim D Spector, George Dedoussis, Nicholas G Martin, Lambertus A Kiemeney, Vincent Mooser, Kari Stefansson, David A Hinds, Markus M Nöthen, J Brent Richards
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002746 (2012)
Androgenetic alopecia (AGA) is a highly heritable condition and the most common form of hair loss in humans. Susceptibility loci have been described on the X chromosome and chromosome 20, but these loci explain a minority of its heritable variance. W
Externí odkaz:
https://doaj.org/article/9681c1f1d7c841d4900a974fc86ce27d
Autor:
Felix F. Brockschmidt, Kenneth Pfarr, Christine Herold, Achim Hoerauf, Linda Batsa Debrah, Tim Becker, Yusif Mubarik, Anna Albers, Holger Fröhlich, Andrea Hofmann, Alexander Yaw Debrah, Jubin Osei-Mensah
Publikováno v:
Human Genomics, Vol 11, Iss 1, Pp 1-13 (2017)
Human Genomics
Human Genomics
Background Lymphedema (LE) is a chronic clinical manifestation of filarial nematode infections characterized by lymphatic dysfunction and subsequent accumulation of protein-rich fluid in the interstitial space—lymphatic filariasis. A number of stud
Autor:
Cornelia Kraus, N. Katzorke, Trine Prescott, S. Blichfeldt, J. Rehnitz, Eva Wohlleber, Hartmut Engels, Peter H. Vogt, Felix F. Brockschmidt, Stefanie Heilmann, Heiko Reutter, O.K. Rødningen, Per Hoffmann, Jennifer A. Lee, Zeynep Tümer, Kirstine Ravn, Martina Kreiß-Nachtsheim, Alexander M. Zink
Publikováno v:
Molecular Syndromology. 5:65-75
Fragile X syndrome (FXS) is one of the most common causes of intellectual disability/developmental delay (ID/DD), especially in males. It is caused most often by CGG trinucleotide repeat expansions, and less frequently by point mutations and partial
Autor:
Joyce Y. Tung, Axel M. Hillmer, Silke Redler, Vincent Mooser, Nicholas Eriksson, Dale R. Nyholt, Christine Herold, Amy K. Kiefer, Kari Stefansson, Nicholas G. Martin, Felix F. Brockschmidt, Stefanie Heilmann, J. Brent Richards, David A. Hinds, Ari Karason, Stavroula Kanoni, Nadine Fricker, Rui Li, George Dedoussis, Tim Becker, Sita H. Vermeulen, Regina C. Betz, Dmitriy Drichel, Markus M. Nöthen, Lambertus A. Kiemeney, Kijoung Song
Publikováno v:
Journal of Investigative Dermatology, 133, 6, pp. 1489-96
The journal of investigative dermatology 133(6), 1489-1496 (2013). doi:10.1038/jid.2013.43
Journal of Investigative Dermatology, 133, 1489-96
The journal of investigative dermatology 133(6), 1489-1496 (2013). doi:10.1038/jid.2013.43
Journal of Investigative Dermatology, 133, 1489-96
Item does not contain fulltext The pathogenesis of androgenetic alopecia (AGA, male-pattern baldness) is driven by androgens, and genetic predisposition is the major prerequisite. Candidate gene and genome-wide association studies have reported that
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
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
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:
Gerhard Lutz, Roland Kruse, Kathrin A. Giehl, Hans Wolff, Sibylle Eigelshoven, Silke Redler, Regina C. Betz, Markus Böhm, Karsten K-G John, Felix F. Brockschmidt, Bettina Blaumeiser, Jozef De Weert, Markus M. Nöthen, Tim Becker, Sandra Hanneken, Christine Herold
Publikováno v:
The journal of investigative dermatology
The journal of investigative dermatology 131(5), 1169-1172 (2011). doi:10.1038/jid.2010.427
The journal of investigative dermatology 131(5), 1169-1172 (2011). doi:10.1038/jid.2010.427
Autor:
Heiko Reutter, Lutz Priebe, Friederike Baudisch, Stefan Holland-Cunz, Michael Ludwig, Stuart Hosie, Felix F. Brockschmidt, Markus M. Nöthen, Alexander M. Zink, Eberhard Schmiedeke, Per Hoffmann, Markus Draaken, Stefanie Märzheuser, Stefan Aretz, Charlotte Schramm, Hartmut Engels, Sabine Grasshoff-Derr, Thomas M. Boemers, Enrika Bartels
Publikováno v:
American Journal of Medical Genetics Part A. 155:445-449
De Novo Duplication of 18p11.21–18q12.1 in a Female With Anorectal Malformation Charlotte Schramm, Markus Draaken, Enrika Bartels, Thomas M. Boemers, Eberhard Schmiedeke, Sabine Grasshoff-Derr, Stefanie M€arzheuser, Stuart Hosie, Stefan Holland-C