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

par Sipos, Botond, Massingham, Tim, Stütz, Adrian M., Goldman, Nick
Publié 2012

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

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

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

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

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

par Segura-Wang, Maia, Onishi-Seebacher, Megumi, Stütz, Adrian M., Mardin, Balca R., Korbel, Jan O.
Publié dans G3 (Bethesda) (2017)

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

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

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

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

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

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

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

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

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

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

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

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

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

par 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.
Publié 2009

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

par 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.
Publié dans BMC Genomics (2016)

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

par 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.
Publié dans Cell Rep (2020)

Case-Control Association Study of TGOLN2 in Attempted Suicide

par 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.
Publié 2010

The Genomic and Transcriptomic Landscape of a HeLa Cell Line

par 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.
Publié 2013

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

par 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.
Publié dans Nat Commun (2015)

Primate genome architecture influences structural variation mechanisms and functional consequences

par 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.
Publié 2013

A cell-based model system links chromothripsis with hyperploidy

par 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
Publié dans Mol Syst Biol (2015)

Immortalization capacity of HPV types is inversely related to chromosomal instability

par 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.
Publié dans Oncotarget (2016)

A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans

par 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.
Publié 2011