Publications by Altmüller, Janine

Sauvigny, Thomas, Alawi, Malik, Krause, Linda , Renner, Sina, Spohn, Michael, Busch, Alice, Kolbe, Verena, Altmüller, Janine, Löscher, Britt-Sabina, Franke, Andre, Brockmann, Christian, Lieb, Wolfgang, Westphal, Manfred, Schmidt, Nils Ole , Regelsberger, Jan and Rosenberger, Georg (2020) Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage. Journal of Neurology 267 (9), pp. 2533-2545. Fulltext not available.

Lindner, Angie, Marbach, Felix, Tschernitz, Sebastian, Ortner, Christine, Berneburg, Mark, Felthaus, Oliver, Prantl, Lukas, Kye, Min Jeong , Rappl, Gunter, Altmüller, Janine, Thiele, Holger, Schreml, Stephan and Schreml, Julia (2019) Calcyphosine-like (CAPSL) is regulated in Multiple Symmetric Lipomatosis and is involved in Adipogenesis. Scientific Reports 9 (1). Fulltext not available.

Hauke, Jan, Horvath, Judit, Groß, Eva, Gehrig, Andrea, Honisch, Ellen, Hackmann, Karl, Schmidt, Gunnar, Arnold, Norbert , Faust, Ulrike, Sutter, Christian, Hentschel, Julia, Wang-Gohrke, Shan, Smogavec, Mateja, Weber, Bernhard H. F., Weber-Lassalle, Nana, Weber-Lassalle, Konstantin, Borde, Julika, Ernst, Corinna, Altmüller, Janine, Volk, Alexander E., Thiele, Holger, Hübbel, Verena, Nürnberg, Peter, Keupp, Katharina, Versmold, Beatrix, Pohl, Esther, Kubisch, Christian , Grill, Sabine, Paul, Victoria, Herold, Natalie, Lichey, Nadine, Rhiem, Kerstin, Ditsch, Nina, Ruckert, Christian , Wappenschmidt, Barbara, Auber, Bernd, Rump, Andreas, Niederacher, Dieter, Haaf, Thomas, Ramser, Juliane, Dworniczak, Bernd, Engel, Christoph , Meindl, Alfons, Schmutzler, Rita K. and Hahnen, Eric (2018) Gene panel testing of 5589 BRCA1/2 -negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer. Cancer Medicine 7 (4), pp. 1349-1358. Fulltext not available.

Schlingmann, Karl P., Bandulik, Sascha, Mammen, Cherry, Tarailo-Graovac, Maja , Holm, Rikke, Baumann, Matthias, König, Jens, Lee, Jessica J. Y., Drögemöller, Britt , Imminger, Katrin, Beck, Bodo B., Altmüller, Janine, Thiele, Holger, Waldegger, Siegfried, van’t Hoff, William, Kleta, Robert, Warth, Richard , van Karnebeek, Clara D. M., Vilsen, Bente , Bockenhauer, Detlef and Konrad, Martin (2018) Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability. The American Journal of Human Genetics 103 (5), pp. 808-816. Fulltext not available.

Demenais, Florence , Margaritte-Jeannin, Patricia, Barnes, Kathleen C., Cookson, William O. C. , Altmüller, Janine, Ang, Wei, Barr, R. Graham, Beaty, Terri H., Becker, Allan B., Beilby, John, Bisgaard, Hans , Bjornsdottir, Unnur Steina, Bleecker, Eugene, Bønnelykke, Klaus , Boomsma, Dorret I., Bouzigon, Emmanuelle, Brightling, Christopher E., Brossard, Myriam, Brusselle, Guy G., Burchard, Esteban, Burkart, Kristin M., Bush, Andrew, Chan-Yeung, Moira, Chung, Kian Fan, Couto Alves, Alexessander, Curtin, John A., Custovic, Adnan , Daley, Denise, de Jongste, Johan C., Del-Rio-Navarro, Blanca E., Donohue, Kathleen M., Duijts, Liesbeth, Eng, Celeste, Eriksson, Johan G., Farrall, Martin, Fedorova, Yuliya, Feenstra, Bjarke, Ferreira, Manuel A., Freidin, Maxim B. , Gajdos, Zofia, Gauderman, Jim, Gehring, Ulrike, Geller, Frank , Genuneit, Jon , Gharib, Sina A., Gilliland, Frank, Granell, Raquel, Graves, Penelope E., Gudbjartsson, Daniel F., Haahtela, Tari, Heckbert, Susan R., Heederik, Dick, Heinrich, Joachim , Heliövaara, Markku, Henderson, John, Himes, Blanca E., Hirose, Hiroshi, Hirschhorn, Joel N., Hofman, Albert, Holt, Patrick , Hottenga, Jouke, Hudson, Thomas J., Hui, Jennie , Imboden, Medea, Ivanov, Vladimir, Jaddoe, Vincent W. V., James, Alan, Janson, Christer, Jarvelin, Marjo-Riitta, Jarvis, Deborah, Jones, Graham, Jonsdottir, Ingileif, Jousilahti, Pekka, Kabesch, Michael, Kähönen, Mika , Kantor, David B., Karunas, Alexandra S. , Khusnutdinova, Elza, Koppelman, Gerard H., Kozyrskyj, Anita L., Kreiner, Eskil, Kubo, Michiaki, Kumar, Rajesh, Kumar, Ashish, Kuokkanen, Mikko, Lahousse, Lies , Laitinen, Tarja, Laprise, Catherine , Lathrop, Mark, Lau, Susanne, Lee, Young-Ae, Lehtimäki, Terho, Letort, Sébastien, Levin, Albert M., Li, Guo, Liang, Liming, Loehr, Laura R., London, Stephanie J. , Loth, Daan W., Manichaikul, Ani, Marenholz, Ingo, Martinez, Fernando J., Matheson, Melanie C., Mathias, Rasika A., Matsumoto, Kenji, Mbarek, Hamdi , McArdle, Wendy L., Melbye, Mads, Melén, Erik, Meyers, Deborah, Michel, Sven, Mohamdi, Hamida, Musk, Arthur W., Myers, Rachel A., Nieuwenhuis, Maartje A. E., Noguchi, Emiko, O’Connor, George T., Ogorodova, Ludmila M., Palmer, Cameron D., Palotie, Aarno, Park, Julie E., Pennell, Craig E. , Pershagen, Göran, Polonikov, Alexey , Postma, Dirkje S., Probst-Hensch, Nicole, Puzyrev, Valery P. , Raby, Benjamin A., Raitakari, Olli T., Ramasamy, Adaikalavan , Rich, Stephen S., Robertson, Colin F., Romieu, Isabelle, Salam, Muhammad T., Salomaa, Veikko, Schlünssen, Vivi , Scott, Robert, Selivanova, Polina A., Sigsgaard, Torben, Simpson, Angela, Siroux, Valérie, Smith, Lewis J., Solodilova, Maria, Standl, Marie, Stefansson, Kari, Strachan, David P., Stricker, Bruno H., Takahashi, Atsushi, Thompson, Philip J., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tiesler, Carla M. T., Torgerson, Dara G., Tsunoda, Tatsuhiko , Uitterlinden, André G., van der Valk, Ralf J. P., Vaysse, Amaury , Vedantam, Sailaja, von Berg, Andrea, von Mutius, Erika, Vonk, Judith M. , Waage, Johannes, Wareham, Nick J., Weiss, Scott T., White, Wendy B., Wickman, Magnus, Widén, Elisabeth, Willemsen, Gonneke, Williams, L. Keoki, Wouters, Inge M. , Yang, James J., Zhao, Jing Hua, Moffatt, Miriam F., Ober, Carole and Nicolae, Dan L. (2018) Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nature Genetics 50 (1), pp. 42-53. Fulltext not available.