An Improved Protocol for Sequencing of Repetitive Genomic Regions and Structural Variations Using Mutagenesis and Next Generation Sequencing

od Sipos, Botond, Massingham, Tim, Stütz, Adrian M., Goldman, Nick
Wydane 2012

DELLY: structural variant discovery by integrated paired-end and split-read analysis

od Rausch, Tobias, Zichner, Thomas, Schlattl, Andreas, Stütz, Adrian M., Benes, Vladimir, Korbel, Jan O.
Wydane 2012

Functional identification of the promoter of SLC4A5, a gene associated with cardiovascular and metabolic phenotypes in the HERITAGE Family Study

od Stütz, Adrian M, Teran-Garcia, Margarita, Rao, D C, Rice, Treva, Bouchard, Claude, Rankinen, Tuomo
Wydane 2009

Systematic Identification of Determinants for Single-Strand Annealing-Mediated Deletion Formation in Saccharomyces cerevisiae

od Segura-Wang, Maia, Onishi-Seebacher, Megumi, Stütz, Adrian M., Mardin, Balca R., Korbel, Jan O.
Wydane w G3 (Bethesda) (2017)

KIF5B gene sequence variation and response of cardiac stroke volume to regular exercise

od Argyropoulos, George, Stütz, Adrian M., Ilnytska, Olha, Rice, Treva, Teran-Garcia, Margarita, Rao, D. C., Bouchard, Claude, Rankinen, Tuomo
Wydane 2009

Molecular Mechanisms for Activation of the Agouti-Related Protein and Stimulation of Appetite

od Ilnytska, Olha, Stütz, Adrian M., Park-York, MieJung, York, David A., Ribnicky, David M., Zuberi, Aamir, Cefalu, William T., Argyropoulos, George
Wydane 2011

Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing

od Zichner, Thomas, Garfield, David A., Rausch, Tobias, Stütz, Adrian M., Cannavó, Enrico, Braun, Martina, Furlong, Eileen E.M., Korbel, Jan O.
Wydane 2013

Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity

od Waszak, Sebastian M., Hasin, Yehudit, Zichner, Thomas, Olender, Tsviya, Keydar, Ifat, Khen, Miriam, Stütz, Adrian M., Schlattl, Andreas, Lancet, Doron, Korbel, Jan O.
Wydane 2010

A scalable CRISPR/Cas9-based fluorescent reporter assay to study DNA double-strand break repair choice

od Roidos, Paris, Sungalee, Stephanie, Benfatto, Salvatore, Serçin, Özdemirhan, Stütz, Adrian M., Abdollahi, Amir, Mauer, Jan, Zenke, Frank T., Korbel, Jan O., Mardin, Balca R.
Wydane w Nat Commun (2020)

Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study

od Rice, Treva K., Sarzynski, Mark A., Sung, Yun Ju, Argyropoulos, George, Stütz, Adrian M., Teran-Garcia, Margarita, Rao, D. C., Bouchard, Claude, Rankinen, Tuomo
Wydane 2011

Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library

od Lam, Hugo Y. K., Mu, Xinmeng Jasmine, Stütz, Adrian M., Tanzer, Andrea, Cayting, Philip D., Snyder, Michael, Kim, Philip M., Korbel, Jan O., Gerstein, Mark B.
Wydane 2009

Next-generation sequencing-based detection of germline L1-mediated transductions

od Tica, Jelena, Lee, Eunjung, Untergasser, Andreas, Meiers, Sascha, Garfield, David A., Gokcumen, Omer, Furlong, Eileen E.M., Park, Peter J., Stütz, Adrian M., Korbel, Jan O.
Wydane w BMC Genomics (2016)

Genome-wide Screens Implicate Loss of Cullin Ring Ligase 3 in Persistent Proliferation and Genome Instability in TP53-Deficient Cells

od Drainas, Alexandros P., Lambuta, Ruxandra A., Ivanova, Irina, Serçin, Özdemirhan, Sarropoulos, Ioannis, Smith, Mike L., Efthymiopoulos, Theocharis, Raeder, Benjamin, Stütz, Adrian M., Waszak, Sebastian M., Mardin, Balca R., Korbel, Jan O.
Wydane w Cell Rep (2020)

Case-Control Association Study of TGOLN2 in Attempted Suicide

od Mahon, Pamela B., Stütz, Adrian M., Seifuddin, Fayaz, Huo, Yuqing, Goes, Fernando S., Jancic, Dubravka, Judy, Jennifer T., DePaulo, J. Raymond, Gershon, Elliot S., McMahon, Francis J., Zandi, Peter P., Potash, James B., Willour, Virginia L.
Wydane 2010

The Genomic and Transcriptomic Landscape of a HeLa Cell Line

od Landry, Jonathan J. M., Pyl, Paul Theodor, Rausch, Tobias, Zichner, Thomas, Tekkedil, Manu M., Stütz, Adrian M., Jauch, Anna, Aiyar, Raeka S., Pau, Gregoire, Delhomme, Nicolas, Gagneur, Julien, Korbel, Jan O., Huber, Wolfgang, Steinmetz, Lars M.
Wydane 2013

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms

od Abyzov, Alexej, Li, Shantao, Kim, Daniel Rhee, Mohiyuddin, Marghoob, Stütz, Adrian M., Parrish, Nicholas F., Mu, Xinmeng Jasmine, Clark, Wyatt, Chen, Ken, Hurles, Matthew, Korbel, Jan O., Lam, Hugo Y. K., Lee, Charles, Gerstein, Mark B.
Wydane w Nat Commun (2015)

Primate genome architecture influences structural variation mechanisms and functional consequences

od Gokcumen, Omer, Tischler, Verena, Tica, Jelena, Zhu, Qihui, Iskow, Rebecca C., Lee, Eunjung, Fritz, Markus Hsi-Yang, Langdon, Amy, Stütz, Adrian M., Pavlidis, Pavlos, Benes, Vladimir, Mills, Ryan E., Park, Peter J., Lee, Charles, Korbel, Jan O.
Wydane 2013

A cell-based model system links chromothripsis with hyperploidy

od Mardin, Balca R, Drainas, Alexandros P, Waszak, Sebastian M, Weischenfeldt, Joachim, Isokane, Mayumi, Stütz, Adrian M, Raeder, Benjamin, Efthymiopoulos, Theocharis, Buccitelli, Christopher, Segura-Wang, Maia, Northcott, Paul, Pfister, Stefan M, Lichter, Peter, Ellenberg, Jan, Korbel, Jan O
Wydane w Mol Syst Biol (2015)

Immortalization capacity of HPV types is inversely related to chromosomal instability

od Schütze, Denise M., Krijgsman, Oscar, Snijders, Peter J.F., Ylstra, Bauke, Weischenfeldt, Joachim, Mardin, Balca R., Stütz, Adrian M., Korbel, Jan O., de Winter, Johan P., Meijer, Chris J.L.M., Quint, Wim G.V., Bosch, Leontien, Wilting, Saskia M., Steenbergen, Renske D.M.
Wydane w Oncotarget (2016)

A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans

od Stewart, Chip, Kural, Deniz, Strömberg, Michael P., Walker, Jerilyn A., Konkel, Miriam K., Stütz, Adrian M., Urban, Alexander E., Grubert, Fabian, Lam, Hugo Y. K., Lee, Wan-Ping, Busby, Michele, Indap, Amit R., Garrison, Erik, Huff, Chad, Xing, Jinchuan, Snyder, Michael P., Jorde, Lynn B., Batzer, Mark A., Korbel, Jan O., Marth, Gabor T.
Wydane 2011