Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Klamt, Johanna"'
Autor:
Cura, Francesca, Böhmer, Anne Christin, Klamt, Johanna, Schünke, Hannah, Scapoli, Luca, Martinelli, Marcella, Carinci, Francesco, Nöthen, Markus M, Knapp, Michael, Ludwig, Kerstin U, Mangold, Elisabeth
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 an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d80585327a3807da13cb6d503d18ee1d
http://hdl.handle.net/11585/541822
http://hdl.handle.net/11585/541822
Autor:
Ludwig, Kerstin U., Böhmer, Anne C., Bowes, John, Nikolić, Miloš, Ishorst, Nina, Wyatt, Niki, Hammond, Nigel L., Gölz, Lina, Thieme, Frederic, Barth, Sandra, Schuenke, Hannah, Klamt, Johanna, Spielmann, Malte, Aldhorae, Khalid, Rojas-Martinez, Augusto, Nöthen, Markus M., Rada-Iglesias, Alvaro, Dixon, Michael J., Knapp, Michael, Mangold, Elisabeth
Publikováno v:
Ludwig, K U, Böhmer, A C, Bowes, J, Nikolić, M, Ishorst, N, Wyatt, N, Hammond, N, Gölz, L, Thieme, F, Barth, S, Schuenke, H, Klamt, J, Spielmann, M, Aldhorae, K, Rojas-Martinez, A, Nöthen, M M, Rada-Iglesias, A, Dixon, M, Knapp, M & Mangold, E 2017, ' Imputation of Orofacial Clefting Data Identifies Novel Risk Loci and Sheds Light on the Genetic Background of Cleft Lip ± Cleft Palate and Cleft Palate Only. ', Human Molecular Genetics, vol. 26, no. 4, pp. 829-842 . https://doi.org/10.1093/hmg/ddx012
Human Molecular Genetics
Human Molecular Genetics
Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is among the most common human birth defects with multifactorial etiology. Here, we present results from a genome-wide imputation study of nsCL/P in which, after adding replication cohort d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ff5de9672b41eb78927d826859d5a53d
https://doi.org/10.1093/hmg/ddx012
https://doi.org/10.1093/hmg/ddx012
Autor:
Ludwig, Kerstin U., Ahmed, Syeda Tasnim, Böhmer, Anne C., Sangani, Nasim Bahram, Varghese, Sheryil, Klamt, Johanna, Schuenke, Hannah, Gültepe, Pinar, Hofmann, Andrea, Rubini, Michele, Aldhorae, Khalid Ahmed, Steegers-Theunissen, Regine P., Rojas-Martinez, Augusto, Reiter, Rudolf, Borck, Guntram, Knapp, Michael, Nakatomi, Mitsushiro, Graf, Daniel, Mangold, Elisabeth, Peters, Heiko
Publikováno v:
PLoS Genetics (online), 12(3). Public Library of Science
PLoS Genetics, Vol 12, Iss 3, p e1005914 (2016)
PLoS Genetics
PLoS Genetics, Vol 12, Iss 3, p e1005914 (2016)
PLoS Genetics
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://explore.openaire.eu/search/publication?articleId=pmid_dedup__::41e1d00668ace905bd22c3c25d4a5785
https://pure.eur.nl/en/publications/a5cad65f-9514-47ee-aa1d-7fc10d752eba
https://pure.eur.nl/en/publications/a5cad65f-9514-47ee-aa1d-7fc10d752eba
Akademický článek
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Autor:
Ludwig KU; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Ahmed ST; Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, United Kingdom., Böhmer AC; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Sangani NB; Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, United Kingdom., Varghese S; Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, United Kingdom., Klamt J; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Schuenke H; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Gültepe P; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Hofmann A; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life&Brain Center, University of Bonn, Bonn, Germany., Rubini M; Department of Biomedical and Specialty Surgical Sciences, University of Ferrara, Italy., Aldhorae KA; Orthodontic Department, College of Dentistry, Thamar University, Thamar, Yemen., Steegers-Theunissen RP; Department of Obstetrics and Gynaecology, ErasmusMC, Rotterdam, Netherlands.; Department of Epidemiology, Radboud University Medical Center, Nijmegen, Netherlands., Rojas-Martinez A; Department of Biochemistry and Molecular Medicine, School of Medicine, and Centro de Investigación y Desarrollo en Ciencias de la Salud, Universidad Autonoma de Nuevo Leon, Monterrey, Mexico., Reiter R; Department of Otolaryngology-Head and Neck Surgery, Section of Phoniatrics and Pedaudiology, University of Ulm, Ulm, Germany., Borck G; Institute of Human Genetics, University of Ulm, Ulm, Germany., Knapp M; Institute of Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn, Germany., Nakatomi M; Division of Anatomy, Kyushu Dental University, Kitakyushu, Japan., Graf D; Orofacial Development and Regeneration, Institute of Oral Biology, Center for Dental Medicine, University of Zurich, Zurich, Switzerland.; Departments of Dentistry and Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada., Mangold E; Institute of Human Genetics, University of Bonn, Bonn, Germany., Peters H; Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, United Kingdom.
Publikováno v:
PLoS genetics [PLoS Genet] 2016 Mar 11; Vol. 12 (3), pp. e1005914. Date of Electronic Publication: 2016 Mar 11 (Print Publication: 2016).
Autor:
Cura F; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy., Böhmer AC; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany., Klamt J; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany., Schünke H; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany., Scapoli L; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy., Martinelli M; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy., Carinci F; Department of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy., Nöthen MM; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany., Knapp M; Institute of Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn, Germany., Ludwig KU; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany., Mangold E; Institute of Human Genetics, University of Bonn, Bonn, Germany.
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology [Birth Defects Res A Clin Mol Teratol] 2016 Feb; Vol. 106 (2), pp. 81-7. Date of Electronic Publication: 2015 Dec 09.