Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Peter Tessmann"'
Autor:
Elisabeth Mangold, Peter Tessmann, Rocio Ortiz-Lopez, Heiko Reutter, Markus M. Nöthen, Anne C. Böhmer, Stefanie Nowak, Philipp Wahle, Kerstin U. Ludwig, Augusto Rojas-Martinez, Mario Paredes-Zenteno, Sergio G. Munoz-Jimenez, Michael Knapp
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 100:43-47
Background: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is among the most frequently occurring congenital malformations worldwide. The number of genetic loci identified as being involved in NSCL/P etiology was recently increased by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5588fb41733986bdd2c473229a4679
https://doi.org/10.1002/bdra.23209
https://doi.org/10.1002/bdra.23209
Autor:
Khalid Aldhorae, Franz-Josef Kramer, Hannah Schuenke, Gül Schmidt, Elisabeth Mangold, Johanna Klamt, Janis Stavusis, Heiko Reutter, Rudolf Reiter, Pinar Gültepe, Guntram Borck, Markus M. Nöthen, Andrea Hofmann, Miho Ishida, Bert Braumann, Ruth Raff, Philip Stanier, Nina Ishorst, Baiba Lace, Anne C. Böhmer, Michael Knapp, Alexander Hemprich, Sibylle Brosch, Lina Gölz, Gudrun E. Moore, Ann-Kathrin Hoebel, Peter Tessmann, Rimante Seselgyte, Stefanie Nowak, Kerstin U. Ludwig, Andreas Jäger, Rudolf H. Reich, Thomas Kreusch
Publikováno v:
American journal of human genetics. 98(4)
Nonsyndromic cleft lip with/without cleft palate (nsCL/P) and nonsyndromic cleft palate only (nsCPO) are the most frequent subphenotypes of orofacial clefts. A common syndromic form of orofacial clefting is Van der Woude syndrome (VWS) where individu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93973bc5ede729d0f80a6972287667e
https://pubmed.ncbi.nlm.nih.gov/27018475
https://pubmed.ncbi.nlm.nih.gov/27018475
Autor:
K. Dobson, Silke Redler, Pattie Birch, Kathrin A. Giehl, Hans Wolff, Peter Teßmann, Dmitriy Drichel, Markus M. Nöthen, Regina C. Betz, Rachid Tazi-Ahnini, Sandra Hanneken, Andrew G. Messenger, Ulrike Blume-Peytavi, Markus Böhm, Hassnaa Mahmoudi, Tim Becker, Gerhard Lutz, Roland Kruse
Publikováno v:
Archives of dermatological research 305(3), 249-253 (2012). doi:10.1007/s00403-012-1296-3
Female pattern hair loss (FPHL) is a common hair loss disorder in women with a complex mode of inheritance. Its etiopathogenesis is poorly understood. Widespread assumptions of overlapping susceptibility variants between FPHL and male pattern baldnes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e0299d7eec0b1fa4e907557f97db48
https://pub.dzne.de/record/136859
https://pub.dzne.de/record/136859
Autor:
Paola Franceschelli, Marieke Bouwman-Both, Peter A. Mossey, Régine P.M. Steegers-Theunissen, Kerstin U. Ludwig, Markus M. Nöthen, Peter Tessmann, Jan Lindemans, Anne C. Böhmer, Anne M. Molloy, Elisabeth Mangold, Borut Peterlin, V. Aiello, Michael Knapp, Michele Rubini
Publikováno v:
American Journal of Medical Genetics. Part A, 161, 2545-2549
American Journal of Medical Genetics. Part A, 161, 10, pp. 2545-2549
American Journal of Medical Genetics Part A, 161(10), 2545-2549. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 161, 10, pp. 2545-2549
American Journal of Medical Genetics Part A, 161(10), 2545-2549. Wiley-Liss Inc.
Contains fulltext : 126522.pdf (Publisher’s version ) (Closed access) Nonsyndromic cleft lip with or without cleft palate (NSCL/P), the most common type of orofacial clefting, is one of the most frequent congenital defects. Based on epidemiological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::906d3792c095f56d71e63e323b04b937
https://doi.org/10.1002/ajmg.a.36141
https://doi.org/10.1002/ajmg.a.36141
Autor:
Silke Redler, Felix F. Brockschmidt, Stefanie Heilmann, Hans Wolff, Markus M. Nöthen, Gerhard Lutz, Kathrin A. Giehl, Roland Kruse, Sabrina Wolf, Ulrike Blume-Peytavi, Natalie Garcia Bartels, K. Dobson, Peter Teßmann, Pattie Birch, Dmitriy Drichel, Markus Böhm, Andrew G. Messenger, Regina C. Betz, Rachid Tazi-Ahnini, Sandra Hanneken, Tim Becker
Publikováno v:
Journal of dermatological science 72(2), 186-188 (2013). doi:10.1016/j.jdermsci.2013.06.012
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b99b4048c31cc905163f1bc1212c073
https://pubmed.ncbi.nlm.nih.gov/23928227
https://pubmed.ncbi.nlm.nih.gov/23928227
Autor:
Martin Hautzinger, Manuel Mattheisen, Srdjan Djurovic, Jennifer Vollmer, Marian L. Hamshere, Michael Alexander, Alexander S. Tiganov, Maria Grigoroiu-Serbanescu, Johanna Sasse, Markus J. Schwarz, Scott D. Gordon, Michael Bauer, Lilia I. Abramova, René Breuer, H.-Erich Wichmann, Susanne Lucae, Susanne Moebus, Britta Haenisch, Carmen C. Diaconu, Grant W. Montgomery, Johannes Schumacher, Kari Stefansson, Jean-Pierre Kahn, Nicholas G. Martin, Wolfgang Maier, Piotr M. Czerski, Michael Steffens, Frank Bellivier, Ole A. Andreassen, Mark Lathrop, Joanna Hauser, Bertram Müller-Myhsok, Stéphane Jamain, Thomas F. Wienker, Omar Gustafsson, Hreinn Stefansson, Nicholas John Craddock, Lejla Kapur-Pojskić, Peter Tessmann, Chantal Henry, Fermín Mayoral, Michael Conlon O'Donovan, Jutta Kammerer-Ciernioch, Fabio Rivas, Liliana Oruc, Markus M. Nöthen, Alexander Chuchalin, Andreas Zimmer, Moritz Weingarten, Stefan Schreiber, Engilbert Sigurdsson, Sven Cichon, Adam Wright, Bruno Etain, Marcella Rietschel, Peter Propping, Franziska Degenhardt, Simon Heath, Thomas G. Schulze, Christine Schmäl, Galina Pantelejeva, Michael John Owen, Helmut Vedder, Christian Meesters, Andreas Reif, Gulja Babadjanova, Philip B. Mitchell, Jana Strohmaier, Thomas W. Mühleisen, Peter R. Schofield, Stefan Herms, Marion Leboyer, Stacy Steinberg, Sarah E. Medland, Lutz Priebe, Xavier Miró
Publikováno v:
The American Journal of Human Genetics. (3):372-381
We conducted a genome-wide association study (GWAS) and a follow-up study of bipolar disorder (BD), a common neuropsychiatric disorder. In the GWAS, we investigated 499,494 autosomal and 12,484 X-chromosomal SNPs in 682 patients with BD and in 1300 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8372750100a2d11d32ccfa1515e67abf
Autor:
von Lowtzow, Catharina1, Hofmann, Andrea1,2, Rong Zhang1,2, Marsch, Florian1, Ebert, Anne-Karoline3, Rösch, Wolfgang4, Stein, Raimund5, Boemers, Thomas M.6, Hirsch, Karin7, Marcelis, Carlo8, Feitz, Wouter F. J.9, Brusco, Alfredo10, Migone, Nicola10, Di Grazia, Massimo11, Moebus, Susanne12, Nöthen, Markus M.1,2, Reutter, Heiko1,13, Ludwig, Michael14 mludwig@uni-bonn.de, Draaken, Markus1,2
Publikováno v:
BMC Medical Genetics. 4/30/2016, Vol. 17, p1-9. 9p.
Autor:
Basmanav, F. Buket, Forstner, Andreas J., Fier, Heide, Herms, Stefan, Meier, Sandra, Degenhardt, Franziska, Hoffmann, Per, Barth, Sandra, Fricker, Nadine, Strohmaier, Jana, Witt, Stephanie H., Ludwig, Michael, Schmael, Christine, Moebus, Susanne, Maier, Wolfgang, Mössner, Rainald, Rujescu, Dan, Rietschel, Marcella, Lange, Christoph, Nöthen, Markus M.
Publikováno v:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics; Jul2015, Vol. 168B Issue 5, p354-362, 9p
Autor:
Horpaopan, Sukanya, Spier, Isabel, Zink, Alexander M., Altmüller, Janine, Holzapfel, Stefanie, Laner, Andreas, Vogt, Stefanie, Uhlhaas, Siegfried, Heilmann, Stefanie, Stienen, Dietlinde, Pasternack, Sandra M., Keppler, Kathleen, Adam, Ronja, Kayser, Katrin, Moebus, Susanne, Draaken, Markus, Degenhardt, Franziska, Engels, Hartmut, Hofmann, Andrea, Nöthen, Markus M.
Publikováno v:
International Journal of Cancer; Mar2015, Vol. 136 Issue 6, pE578-E589, 12p
Autor:
Forstner, Andreas J., Basmanav, F. Buket, Mattheisen, Manuel, Böhmer, Anne C., Hollegaard, Mads V., Janson, Esther, Strengman, Eric, Priebe, Lutz, Degenhardt, Franziska, Hoffmann, Per, Herms, Stefan, Maier, Wolfgang, Mössner, Rainald, Rujescu, Dan, Ophoff, Roel A., Moebus, Susanne, Mortensen, Preben B., Børglum, Anders D., Hougaard, David M., Frank, Josef
Publikováno v:
Journal of Psychiatry & Neuroscience; Nov2014, Vol. 39 Issue 6, p386-396, 11p, 3 Color Photographs, 3 Charts