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2020
Boehmer, Anne C., Hecker, Julian, Schroeder, Julia, Gharahkhani, Puya 
ORCID: 0000-0002-4203-5952, May, Andrea, Gerges, Christian, Anders, Mario, Becker, Jessica, Hess, Timo, Kreuser, Nicole, Thieme, Rene, Noder, Tania, Venerito, Marino, Veits, Lothar, Schmidt, Thomas ORCID: 0000-0002-7166-3675, Fuchs, Claudia, Izbicki, Jakob R., Hoelscher, Arnulf H., Dietrich, Arne, Moulla, Yusef, Lyros, Orestis, Lang, Hauke, Lorenz, Dietmar, Schumacher, Brigitte, Mayershofer, Rupert, Vashist, Yogesh, Ott, Katja, Vieth, Michael, Meismueller, Josef, Moebus, Susanne, Knapp, Michael, Neuhaus, Horst, Roesch, Thomas, Ell, Christian, Noethen, Markus M., Whiteman, David C., Tomlinson, Ian, Jankowski, Janusz, Fitzgerald, Rebecca C., Palles, Claire, Vaughan, Thomas L., Gockel, Ines, Thrift, Aaron P., Fier, Heide and Schumacher, Johannes
(2020).
Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies.
Cancer Epidemiol. Biomarkers Prev., 29 (2).
S. 427 - 434.
PHILADELPHIA:
AMER ASSOC CANCER RESEARCH.
ISSN 1538-7755
2017
Altmueller, Janine, Haenisch, Britta, Kawalia, Amit, Menzen, Markus, Noethen, Markus M., Fier, Heide and Molderings, Gerhard J. (2017). Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing. Immunogenetics, 69 (6). S. 359 - 370. NEW YORK: SPRINGER. ISSN 1432-1211
Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Celine S., Muehleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel ORCID: 0000-0002-8442-493X, Schumacher, Johannes, Streit, Fabian ORCID: 0000-0003-1080-4339, Meier, Sandra, Herms, Stefan ORCID: 0000-0002-2786-8200, Hoffmann, Per, Lacour, Andre ORCID: 0000-0003-2692-2583, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Schenk, Lorena M., Fischer, Sascha B., Sivalingam, Sugirthan, Czerski, Piotr M., Hauser, Joanna, Lissowska, Jolanta ORCID: 0000-0003-2695-5799, Szeszenia-Dabrowska, Neonila, Brennan, Paul, McKay, James D., Wright, Adam, Mitchell, Philip B., Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Krasnov, Valery ORCID: 0000-0002-5249-3316, Chuchalin, Alexander, Babadjanova, Gulja, Pantelejeva, Galina, Abramova, Lilia I., Tiganov, Alexander S., Polonikov, Alexey ORCID: 0000-0001-6280-247X, Khusnutdinova, Elza, Alda, Martin ORCID: 0000-0001-9544-3944, Cruceanu, Cristiana, Rouleau, Guy A., Turecki, Gustavo ORCID: 0000-0003-4075-2736, Laprise, Catherine ORCID: 0000-0001-5526-9945, Rivas, Fabio, Mayoral, Fermin, Kogevinas, Manolis ORCID: 0000-0002-9605-0461, Grigoroiu-Serbanescu, Maria ORCID: 0000-0002-1304-6687, Becker, Tim, Schulze, Thomas G., Rietschel, Marcella, Cichon, Sven ORCID: 0000-0002-9475-086X, Fier, Heide and Noethen, Markus M.
(2017).
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
PLoS One, 12 (2).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203
2014
Al Chawa, Taofik, Ludwig, Kerstin U., Fier, Heide, Poetzsch, Bernd, Reich, Rudolf H., Schmidt, Guel, Braumann, Bert, Daratsianos, Nikolaos ORCID: 0000-0003-2098-0379, Boehmer, Anne C., Schuencke, Hannah, Alblas, Margrieta, Fricker, Nadine, Hoffmann, Per, Knapp, Michael, Lange, Christoph, Noethen, Markus M. and Mangold, Elisabeth
(2014).
Nonsyndromic Cleft Lip with or without Cleft Palate: Increased Burden of Rare Variants within Gremlin-1, a Component of the Bone Morphogenetic Protein 4 Pathway.
Birth Defects Res. Part A-Clin. Mol. Teratol., 100 (6).
S. 493 - 499.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 1542-0760
2012
Nasser, Entessar, Mangold, Elisabeth, Tradowsky, Daniela C., Fier, Heide, Becker, Jessica, Boehmer, Anne C., Herberz, Ruth, Fricker, Nadine, Barth, Sandra, Wahle, Philipp ORCID: 0000-0002-4728-806X, Nowak, Stefanie, Reutter, Heiko, Reich, Rudolf H., Lauster, Carola, Braumann, Bert, Kreusch, Thomas, Hemprich, Alexander, Poetzsch, Bernd, Hoffmann, Per ORCID: 0000-0002-6573-983X, Kramer, Franz-Josef, Knapp, Michael, Lange, Christoph, Noethen, Markus M. and Ludwig, Kerstin U.
(2012).
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Birth Defects Res. Part A-Clin. Mol. Teratol., 94 (11).
S. 925 - 934.
HOBOKEN:
WILEY.
ISSN 1542-0760