Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Johanna Klamt"'
Autor:
Kerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, Nasim Bahram Sangani, Sheryil Varghese, Johanna Klamt, Hannah Schuenke, Pinar Gültepe, Andrea Hofmann, Michele Rubini, Khalid Ahmed Aldhorae, Regine P Steegers-Theunissen, Augusto Rojas-Martinez, Rudolf Reiter, Guntram Borck, Michael Knapp, Mitsushiro Nakatomi, Daniel Graf, Elisabeth Mangold, Heiko Peters
Publikováno v:
PLoS Genetics, Vol 12, Iss 3, p e1005914 (2016)
Nonsyndromic orofacial clefts are common birth defects with multifactorial etiology. The most common type is cleft lip, which occurs with or without cleft palate (nsCLP and nsCLO, respectively). Although genetic components play an important role in n
Externí odkaz:
https://doaj.org/article/86fcbe5b9eae4ed2819aa96fe4a4aa5d
Autor:
Jessica Becker, Kerstin U. Ludwig, Gül Schmidt, Martin Scheer, Ann-Kathrin Hoebel, Lina Gölz, Andrea Hofmann, Alexander M. Zink, Elisabeth Mangold, Anne C. Böhmer, Markus Draaken, Markus Martini, Franziska Degenhardt, Alexander Hemprich, Michael Knapp, Johanna Klamt
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 106:767-772
Background Nonsyndromic cleft with or without cleft palate (nsCL/P) is a common birth defect. Although genome-wide association studies (GWAS) have identified numerous risk variants, a considerable fraction of the genetic heritability remains unknown.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90290b2681b00ea80310ffad891f25cc
https://doi.org/10.1002/bdra.23539
https://doi.org/10.1002/bdra.23539
Autor:
Elisabeth Mangold, Johanna Klamt, Hannah Schünke, Luca Scapoli, Kerstin U. Ludwig, Francesco Carinci, Marcella Martinelli, Michael Knapp, Francesca Cura, Markus M. Nöthen, Anne C. Böhmer
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 106:81-87
BACKGROUND Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is one of the most common congenital malformations in humans. Its average global incidence is 1.7 per 1000 live births, with wide variation according to geographical location and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454991dbeb093b3949f11e3642f72f57
https://doi.org/10.1002/bdra.23454
https://doi.org/10.1002/bdra.23454
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:
Johanna, Klamt, Andrea, Hofmann, Anne C, Böhmer, Ann-Kathrin, Hoebel, Lina, Gölz, Jessica, Becker, Alexander M, Zink, Markus, Draaken, Alexander, Hemprich, Martin, Scheer, Gül, Schmidt, Markus, Martini, Michael, Knapp, Elisabeth, Mangold, Franziska, Degenhardt, Kerstin U, Ludwig
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 106(9)
Nonsyndromic cleft with or without cleft palate (nsCL/P) is a common birth defect. Although genome-wide association studies (GWAS) have identified numerous risk variants, a considerable fraction of the genetic heritability remains unknown. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9755a11ea880a3c1453754d9dfc7bd64
https://pubmed.ncbi.nlm.nih.gov/27384521
https://pubmed.ncbi.nlm.nih.gov/27384521
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