Rapid evolution of RNA editing sites in a small non-essential plastid gene

per Fiebig, Andreas, Stegemann, Sandra, Bock, Ralph
Publicat 2004

Heritability of chronic venous disease

per Fiebig, Andreas, Krusche, Petra, Wolf, Andreas, Krawczak, Michael, Timm, Birgitt, Nikolaus, Susanna, Frings, Norbert, Schreiber, Stefan
Publicat 2010

TFG, a target of chromosome translocations in lymphoma and soft tissue tumors, fuses to GPR128 in healthy individuals

per Chase, Andrew, Ernst, Thomas, Fiebig, Andreas, Collins, Andrew, Grand, Francis, Erben, Philipp, Reiter, Andreas, Schreiber, Stefan, Cross, Nicholas C.P.
Publicat 2010

Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe

per Salmela, Elina, Lappalainen, Tuuli, Fransson, Ingegerd, Andersen, Peter M., Dahlman-Wright, Karin, Fiebig, Andreas, Sistonen, Pertti, Savontaus, Marja-Liisa, Schreiber, Stefan, Kere, Juha, Lahermo, Päivi
Publicat 2008

Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci

per Ellinghaus, Eva, Ellinghaus, David, Krusche, Petra, Greiner, Aljoscha, Schreiber, Claudia, Nikolaus, Susanna, Gieger, Christian, Strauch, Konstantin, Lieb, Wolfgang, Rosenstiel, Philip, Frings, Norbert, Fiebig, Andreas, Schreiber, Stefan, Franke, Andre
Publicat a Sci Rep (2017)

Structural Variation of Chromosomes in Autism Spectrum Disorder

per Marshall, Christian R., Noor, Abdul, Vincent, John B., Lionel, Anath C., Feuk, Lars, Skaug, Jennifer, Shago, Mary, Moessner, Rainald, Pinto, Dalila, Ren, Yan, Thiruvahindrapduram, Bhooma, Fiebig, Andreas, Schreiber, Stefan, Friedman, Jan, Ketelaars, Cees E.J., Vos, Yvonne J., Ficicioglu, Can, Kirkpatrick, Susan, Nicolson, Rob, Sloman, Leon, Summers, Anne, Gibbons, Clare A., Teebi, Ahmad, Chitayat, David, Weksberg, Rosanna, Thompson, Ann, Vardy, Cathy, Crosbie, Vicki, Luscombe, Sandra, Baatjes, Rebecca, Zwaigenbaum, Lonnie, Roberts, Wendy, Fernandez, Bridget, Szatmari, Peter, Scherer, Stephen W.
Publicat 2008

Disruption at the PTCHD1 locus on Xp22.11 in autism spectrum disorder and intellectual disability

per Noor, Abdul, Whibley, Annabel, Marshall, Christian R., Gianakopoulos, Peter J., Piton, Amelie, Carson, Andrew R., Orlic-Milacic, Marija, Lionel, Anath, Sato, Daisuke, Pinto, Dalila, Drmic, Irene, Noakes, Carolyn, Senman, Lili, Zhang, Xiaoyun, Mo, Rong, Gauthier, Julie, Crosbie, Jennifer, Pagnamenta, Alistair T., Munson, Jeffrey, Estes, Annette M., Fiebig, Andreas, Franke, Andre, Schreiber, Stefan, Stewart, Alexandre F.R., Roberts, Robert, McPherson, Ruth, Guter, Stephen J., Cook, Edwin H., Dawson, Geraldine, Schellenberg, Gerard D., Battaglia, Agatino, Maestrini, Elena, Jeng, Linda, Hutchison, Terry, Rajcan-Separovic, Evica, Chudley, Albert E., Lewis, Suzanne M.E., Liu, Xudong, Holden, Jeanette, Fernandez, Bridget, Zwaigenbaum, Lonnie, Bryson, Susan E., Roberts, Wendy, Szatmari, Peter, Gallagher, Louise, Stratton, Michael R., Gecz, Jozef, Brady, Angela F., Schwartz, Charles E., Schachar, Russell J., Monaco, Anthony P., Rouleau, Guy A., Hui, Chi-chung, Raymond, F. Lucy, Scherer, Stephen W., Vincent, John B.
Publicat 2010