Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Christine, Herold"'
Autor:
Wiesje M. van der Flier, Eckart Rüther, Henne Holstege, Johannes Kornhuber, Jens Wiltfang, Charlotte E. Teunissen, Alison Goate, Piotr Lewczuk, Carlos Cruchaga, David Ramonet, Frank Jessen, Markus M. Nöthen, Oliver Peters, Michael T. Heneka, Adam C. Naj, Markus P. Kummer, Christine Herold, Heike Kölsch, R. Heun, Wolfgang Maier, Philip Scheltens, Lutz Frölich, Amy Gerrish, Julius Popp, Vincent Chouraki, Céline Bellenguez, Alzheimer's Disease Neuroimaging Initiative, Dmitriy Drichel, Tim Becker, Lara Buscemi, André Lacour, Monique M.B. Breteler, Stefan Herms, Michael Hüll, Stefanie Heilmann, Alfredo Ramirez, Per Hoffmann, Eva Louwersheimer
Publikováno v:
Human Molecular Genetics, Vol. 23, No 24 (2014) pp. 6644-6658
Ramirez, A, van der Flier, W M, Herold, C, Ramonet, D, Heilmann, S, Lewczuk, P, Popp, J, Lacour, A, Drichel, D, Louwersheimer, E, Kummer, M P, Cruchaga, C, Hoffmann, P, Teunissen, C E, Holstege, H, Kornhuber, J, Peters, O, Naj, A C, Chouraki, V, Bellenguez, C, Gerrish, A, Heun, R, Frolich, L, Hull, M, Buscemi, L, Herms, S, Kolsch, H, Scheltens, P, Breteler, M M, Ruther, E, Wiltfang, J, Goate, A, Jessen, F, Maier, W, Heneka, M T, Becker, T & Nothen, M M 2014, ' SUCLG2 identified as both a determinator of CSF Abeta1-42 levels and an attenuator of cognitive decline in Alzheimer's disease ', Human Molecular Genetics, vol. 23, no. 24, pp. 6644-6658 . https://doi.org/10.1093/hmg/ddu372
Human molecular genetics 23(24), 6644-6658 (2014). doi:10.1093/hmg/ddu372
Human Molecular Genetics, 23(24), 6644-6658. Oxford University Press
Ramirez, A, van der Flier, W M, Herold, C, Ramonet, D, Heilmann, S, Lewczuk, P, Popp, J, Lacour, A, Drichel, D, Louwersheimer, E, Kummer, M P, Cruchaga, C, Hoffmann, P, Teunissen, C E, Holstege, H, Kornhuber, J, Peters, O, Naj, A C, Chouraki, V, Bellenguez, C, Gerrish, A, Heun, R, Frolich, L, Hull, M, Buscemi, L, Herms, S, Kolsch, H, Scheltens, P, Breteler, M M, Ruther, E, Wiltfang, J, Goate, A, Jessen, F, Maier, W, Heneka, M T, Becker, T & Nothen, M M 2014, ' SUCLG2 identified as both a determinator of CSF Abeta1-42 levels and an attenuator of cognitive decline in Alzheimer's disease ', Human Molecular Genetics, vol. 23, no. 24, pp. 6644-6658 . https://doi.org/10.1093/hmg/ddu372
Human molecular genetics 23(24), 6644-6658 (2014). doi:10.1093/hmg/ddu372
Human Molecular Genetics, 23(24), 6644-6658. Oxford University Press
Cerebrospinal fluid amyloid-beta 1-42 (Aβ1-42) and phosphorylated Tau at position 181 (pTau181) are biomarkers of Alzheimer's disease (AD). We performed an analysis and meta-analysis of genome-wide association study data on Aβ1-42 and pTau181 in AD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e0346a024e4af22aa36d41fa2a4beaf
http://doc.rero.ch/record/296237/files/ddu372.pdf
http://doc.rero.ch/record/296237/files/ddu372.pdf
Autor:
George Dedoussis, Rui Li, Elaine G.Y. Chew, George Papanikolaou, Tim D. Spector, David A. Hinds, Susanne Moebus, Asif Javed, Dale R. Nyholt, Axel M. Hillmer, Gérard Waeber, Zoltán Kutalik, Nicholas G. Martin, Michael P. Philpott, Lara M. Hochfeld, Tessel E. Galesloot, Xiu Ting Heng, Rico Rueedi, Thomas Anhalt, Markus M. Nöthen, Dmitriy Drichel, Michael Nothnagel, Stavroula Kanoni, Ralf Paus, Lambertus A. Kiemeney, Christine Herold, Stefanie Heilmann-Heimbach, J. Brent Richards, Tim Becker, Panos Deloukas, Peter Vollenweider, Julian Hecker, Sonali Pechlivanis, Ricardo C.H. del Rosario, Heide Loehlein Fier, Shyam Prabhakar
Publikováno v:
Heilmann-Heimbach, S, Herold, C, Hochfeld, L M, Hillmer, A M, Nyholt, D R, Hecker, J, Javed, A, Chew, E G Y, Pechlivanis, S, Drichel, D, Heng, X T, Del Rosario, R C H, Fier, H L, Paus, R, Rueedi, R, Galesloot, T E, Moebus, S, Anhalt, T, Prabhakar, S, Li, R, Kanoni, S, Papanikolaou, G, Kutalik, Z, Deloukas, P, Philpott, M P, Waeber, G, Spector, T D, Vollenweider, P, Kiemeney, L A L M, Dedoussis, G, Richards, J B, Nothnagel, M, Martin, N G, Becker, T, Hinds, D A & Nöthen, M M 2017, ' Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness ', Nature Communications, vol. 8, 14694 . https://doi.org/10.1038/ncomms14694
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Nature Communications 8(1), 14694 (2017). doi:10.1038/ncomms14694
Nature Communications
Nature Communications, 8, 14694
Nature Communications, 8, pp. 14694
Nature communications, vol. 8, pp. 14694
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Nature Communications 8(1), 14694 (2017). doi:10.1038/ncomms14694
Nature Communications
Nature Communications, 8, 14694
Nature Communications, 8, pp. 14694
Nature communications, vol. 8, pp. 14694
Male-pattern baldness (MPB) is a common and highly heritable trait characterized by androgen-dependent, progressive hair loss from the scalp. Here, we carry out the largest GWAS meta-analysis of MPB to date, comprising 10,846 early-onset cases and 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c457dad93623b5473179a9e54aca6e3
https://doi.org/10.1038/ncomms14694
https://doi.org/10.1038/ncomms14694
Autor:
Markus M. Nöthen, Merel A. Hamer, Christine Herold, Susanne Moebus, Fan Liu, Stefanie Heilmann, Tamar Nijsten, Albert Hofman, Cornelia M. van Duijn, Manfred Kayser, André G. Uitterlinden
Publikováno v:
European Journal of Human Genetics, 24(6), 895-902. Nature Publishing Group
European journal of human genetics 24(6), 895-902 (2015). doi:10.1038/ejhg.2015.220
European journal of human genetics 24(6), 895-902 (2015). doi:10.1038/ejhg.2015.220
The global demand for products that effectively prevent the development of male-pattern baldness (MPB) has drastically increased. However, there is currently no established genetic model for the estimation of MPB risk. We conducted a prediction analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9195ed49252b5d05d3f43dc5dbed08
https://pure.eur.nl/en/publications/17f54741-2850-4107-bb30-89839cb9600b
https://pure.eur.nl/en/publications/17f54741-2850-4107-bb30-89839cb9600b
Autor:
Martin Scherer, Richard Dodel, David Mengel, Steffi G. Riedel-Heller, Mathias Thelen, Jan-Philipp Bach, Eva Schaeffer, Tim Becker, Frank Jessen, Inga Liepelt, Christine Herold, Wolfgang Maier, J Becker, Monika Balzer-Geldsetzer, Alfredo Ramirez, Charlotte Söling
Publikováno v:
Parkinsonism & related disorders 23, 109-111 (2016). doi:10.1016/j.parkreldis.2015.11.026
Variant p.R47H of triggering receptor expressed on myeloid cells 2 (TREM2) has been associated with Parkinson's disease (PD). We screened this TREM2-variant in 821 PD patients including 261 demented PD patients (PDD) and in healthy controls (n = 919)
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:
Pauline Ho, Gerd-Marie Alenius, Steffen Uebe, Ross McManus, André Reis, Jörg Lohmann, Maria Apel, Beate Böhm, Ian N. Bruce, Heinz-Erich Wichmann, Harald Burkhardt, Emiliano Giardina, Jesús Lascorz, Thomas F. Wienker, Neil McHugh, Heiko Traupe, John Bowes, Christian Gieger, Arif B. Ekici, Kristina Juneblad, Giuseppe Novelli, Frank Behrens, Lars Klareskog, Oliver FitzGerald, Anne Barton, Michael Steffens, Anthony W. Ryan, Eleanor Korendowych, Ulrike Hüffmeier, Christine Herold
Publikováno v:
Nature genetics
Psoriatic arthritis (PsA) is an inflammatory joint disease that is distinct from other chronic arthritides and which is frequently accompanied by psoriasis vulgaris (PsV) and seronegativity for rheumatoid factor. We conducted a genome-wide associatio
Autor:
Felix F. Brockschmidt, Stefanie Heilmann, Markus M. Nöthen, Axel M. Hillmer, Christine Herold, Sibylle Eigelshoven, Tim Becker, Sandra Barth, Sandra Hanneken, Rudolf Kruse
Publikováno v:
British Journal of Dermatology. 162:899-903
Autor:
L. Forstbauer, Bettina Blaumeiser, Markus M. Nöthen, Kathrin A. Giehl, Sibylle Eigelshoven, Silke Redler, Regina C. Betz, Rudolf Kruse, Tim Becker, Helmut H. Wolff, Felix F. Brockschmidt, Markus Böhm, Sandra Hanneken, J. De Weert, Gerhard Lutz, Christine Herold
Publikováno v:
British Journal of Dermatology. 162:866-869
Summary Background Alopecia areata (AA) is a common hair loss disorder with a complex mode of inheritance. Autoimmune mechanisms are presumed to be crucial aetiologically. It is plausible that a number of autoimmune disorders may share a common genet