المؤلفون: Redler S; Institute of Human Genetics, University of Bonn, Sigmund-Freud-Street 25, D-53127, Bonn, Germany., Birch P, Drichel D, Hofmann P, Dobson K, Böhmer AC, Becker J, Giehl KA, Tazi-Ahnini R, Kruse R, Wolff H, Miesel A, Fischer T, Böhm M, Nuwayhid R, Garcia Bartels N, Lutz G, Becker T, Blume-Peytavi U, Nöthen MM, Messenger AG, Betz RC

المصدر: The British journal of dermatology [Br J Dermatol] 2014 Apr; Vol. 170 (4), pp. 982-5.

نوع المنشور: Letter; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0004041 Publication Model: Print Cited Medium: Internet ISSN: 1365-2133 (Electronic) Linking ISSN: 00070963 NLM ISO Abbreviation: Br J Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Alopecia/*genetics , Estrogen Receptor beta/*genetics , Polymorphism, Single Nucleotide/*genetics, Adult ; Aged ; Case-Control Studies ; Female ; Genetic Predisposition to Disease/genetics ; Germany ; Humans ; Middle Aged ; United Kingdom

المؤلفون: 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

المصدر: 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

مصطلحات موضوعية: Cleft Palate, Male, Mice, Genetic Loci, Cleft Lip, Association Studies Articles, Databases, Genetic, Animals, Chromosomes, Human, Humans, Female, Polymorphism, Single Nucleotide, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ff5de9672b41eb78927d826859d5a53d
https://doi.org/10.1093/hmg/ddx012

المؤلفون: Gharahkhani, Puya, Fitzgerald, Rebecca C, Vaughan, Thomas L, Palles, Claire, Gockel, Ines, Tomlinson, Ian, Buas, Matthew F, May, Andrea, Gerges, Christian, Anders, Mario, Becker, Jessica, Kreuser, Nicole, Noder, Tania, Venerito, Marino, Veits, Lothar, Schmidt, Thomas, Manner, Hendrik, Schmidt, Claudia, Hess, Timo, Böhmer, Anne C, Izbicki, Jakob R, Hölscher, Arnulf H, Lang, Hauke, Lorenz, Dietmar, Schumacher, Brigitte, Hackelsberger, Andreas, Mayershofer, Rupert, Pech, Oliver, Vashist, Yogesh, Ott, Katja, Vieth, Michael, Weismüller, Josef, Nöthen, Markus M, Barrett's And Esophageal Adenocarcinoma Consortium (BEACON), Esophageal Adenocarcinoma GenEtics Consortium (EAGLE), Wellcome Trust Case Control Consortium 2 (WTCCC2), Attwood, Stephen, Barr, Hugh, Chegwidden, Laura, De Caestecker, John, Harrison, Rebecca, Love, Sharon B, MacDonald, David, Moayyedi, Paul, Prenen, Hans, Watson, RG Peter, Iyer, Prasad G, Anderson, Lesley A, Bernstein, Leslie, Chow, Wong-Ho, Hardie, Laura J, Lagergren, Jesper, Liu, Geoffrey, Risch, Harvey A, Wu, Anna H, Ye, Weimin, Bird, Nigel C, Shaheen, Nicholas J, Gammon, Marilie D, Corley, Douglas A, Caldas, Carlos, Moebus, Susanne, Knapp, Michael, Peters, Wilbert HM, Neuhaus, Horst, Rösch, Thomas, Ell, Christian, MacGregor, Stuart, Pharoah, Paul, Whiteman, David C, Jankowski, Janusz, Schumacher, Johannes

المساهمون: Fitzgerald, Rebecca [0000-0002-3434-3568], Caldas, Carlos [0000-0003-3547-1489], Pharoah, Paul [0000-0001-8494-732X], Apollo - University of Cambridge Repository

مصطلحات موضوعية: Risk, Barrett Esophagus, Esophageal Neoplasms, Humans, Adenocarcinoma, Polymorphism, Single Nucleotide, digestive system diseases, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::146dbf27e7906d5bcc22404627973c4a
https://www.repository.cam.ac.uk/handle/1810/282955

المؤلفون: An, Jiyuan, Gharahkhani, Puya, Law, Matthew H, Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M, Neale, Rachel E, Lai, John, Vaughan, Tom L, Gockel, Ines, Thieme, René, Böhmer, Anne C, Jankowski, Janusz, Fitzgerald, Rebecca C, Schumacher, Johannes, Palles, Claire, BEACON, 23andMe Research Team, Whiteman, David C, MacGregor, Stuart

مصطلحات موضوعية: Male, Genetic Loci, Gastroesophageal Reflux, Humans, Female, Genetic Predisposition to Disease, Esophageal Diseases, Polymorphism, Single Nucleotide, humanities, digestive system diseases, 3. Good health, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f0ece5aab5b29001b0e4b3de1b3678f1

المؤلفون: Jue-Sheng Ong, René Thieme, Janusz Jankowski, Jiyuan An, Anne C. Böhmer, Stuart MacGregor, David C. Whiteman, Johannes Schumacher, Claire Palles, Rachel E. Neale, Matthew Law, Puya Gharahkhani, Ines Gockel, John Lai, Catherine M. Olsen, Xikun Han, Beacon, Rebecca C. Fitzgerald, Tom L. Vaughan

المساهمون: Gharahkhani, Puya [0000-0002-4203-5952], Law, Matthew H [0000-0002-4303-8821], Ong, Jue-Sheng [0000-0002-6062-710X], Han, Xikun [0000-0002-3823-7308], Olsen, Catherine M [0000-0003-4483-1888], Böhmer, Anne C [0000-0002-5716-786X], Fitzgerald, Rebecca C [0000-0002-3434-3568], MacGregor, Stuart [0000-0001-6731-8142], Apollo - University of Cambridge Repository

المصدر: Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Nature Communications

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Science, General Physics and Astronomy, Genome-wide association study, Disease, Esophageal Diseases, Genome-wide association studies, Polymorphism, Single Nucleotide, Gastroenterology, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Gastro-oesophageal reflux disease, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Allele, Esophagus, Risk factor, lcsh:Science, Cancer genetics, Multidisciplinary, business.industry, Esophageal disease, Oesophageal cancer, General Chemistry, medicine.disease, humanities, digestive system diseases, 3. Good health, 030104 developmental biology, medicine.anatomical_structure, Genetic Loci, 030220 oncology & carcinogenesis, Gastroesophageal Reflux, GERD, Adenocarcinoma, lcsh:Q, Female, business, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a530542f0d7f586e929d882bc728eb4d
https://doaj.org/article/69989b38dc994e248ea97c1493de2f41

المؤلفون: 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

المساهمون: Cura, Francesca, Böhmer, Anne C., Klamt, Johanna, Schünke, Hannah, Scapoli, Luca, Martinelli, Marcella, Carinci, Francesco, Nöthen, Markus M., Knapp, Michael, Ludwig, Kerstin U., Mangold, Elisabeth

مصطلحات موضوعية: Embryology, Cleft Lip, Genetic loci, association study, genetic loci, nonsyndromic cleft lip with or without cleft palate, polymorphism, replication study, Polymorphism, Single Nucleotide, Linkage Disequilibrium, NO, Cleft Palate, Association study, Gene Frequency, Italy, Pediatrics, Perinatology and Child Health, Replication study, Humans, Genetic Predisposition to Disease, Nonsyndromic cleft lip with or without cleft palate, Polymorphism, Genome-Wide Association Study, Developmental Biology

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d80585327a3807da13cb6d503d18ee1d
http://hdl.handle.net/11585/541822