Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anna B. Stittrich"'
Autor:
Sophie Steiner, Sonya C. Becker, Jelka Hartwig, Franziska Sotzny, Sebastian Lorenz, Sandra Bauer, Madlen Löbel, Anna B. Stittrich, Patricia Grabowski, Carmen Scheibenbogen
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Single nucleotide polymorphisms (SNP) in various genes have been described to be associated with susceptibility to autoimmune disease. In this study, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) patients and controls were genotyped for
Externí odkaz:
https://doaj.org/article/efa33206a56547d091215c49a0060075
Autor:
Gustavo eGlusman, Alissa eSeverson, Varsha eDhankani, Max eRobinson, Terry eFarrah, Denise E. Mauldin, Anna B. Stittrich, Seth A. Ament, Jared C. Roach, Mary E. Brunkow, Dale L. Bodian, Joseph G. Vockley, Ilya eShmulevich, John E. Niederhuber, Leroy eHood
Publikováno v:
Frontiers in Genetics, Vol 6 (2015)
The identification of DNA copy numbers from short-read sequencing data remains a challenge for both technical and algorithmic reasons. The raw data for these analyses are measured in tens to hundreds of gigabytes per genome; transmitting, storing and
Externí odkaz:
https://doaj.org/article/ee5ba32d4beb4615b54ca8b9ce4005a6
Autor:
Joris A. Veltman, Anna B Stittrich, Michele Pinelli, Jared C. Roach, Wendy S.W. Wong, Alexander Hoischen, John E. Niederhuber, Christian Gilissen, Lisenka E.L.M. Vissers, Jakob M. Goldmann, Dale L. Bodian, Terry Farrah, Benjamin D. Solomon, Joseph G. Vockley, Gustavo Glusman
Publikováno v:
Nature Genetics. 50:1615-1615
In the version of this article published, the P values for the enrichment of single mutation categories were inadvertently not corrected for multiple testing. After multiple-testing correction, only two of the six mutation categories mentioned are st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ac860d131095265f6ac51d11d599533
https://doi.org/10.1038/s41588-018-0226-5
https://doi.org/10.1038/s41588-018-0226-5
Autor:
Gustavo Glusman, Jared C. Roach, Christian Gilissen, Wendy S.W. Wong, Anna B Stittrich, Terry Farrah, Joris A. Veltman, Michele Pinelli, Joseph G. Vockley, Lisenka E.L.M. Vissers, Alexander Hoischen, Benjamin D. Solomon, Jakob M. Goldmann, Dale L. Bodian, John E. Niederhuber
Publikováno v:
Nature Genetics, 48, 935-9
Nature Genetics, 48, 8, pp. 935-9
Nature Genetics, 48(8). Nature Publishing Group
Nature Genetics, 48, 8, pp. 935-9
Nature Genetics, 48(8). Nature Publishing Group
Item does not contain fulltext De novo mutations (DNMs) originating in gametogenesis are an important source of genetic variation. We use a data set of 7,216 autosomal DNMs with resolved parent of origin from whole-genome sequencing of 816 parent-off
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7863a2e4bd96892801841b3e351b33e8
http://hdl.handle.net/2066/168019
http://hdl.handle.net/2066/168019
Autor:
Jared C. Roach, Mary E. Brunkow, Denise E. Mauldin, Varsha Dhankani, Gustavo Glusman, Joseph G. Vockley, Terry Farrah, Alissa Severson, Seth A. Ament, John Niederhuber, Max Robinson, Ilya Shmulevich, Dale L. Bodian, Anna B Stittrich, Leroy Hood
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 6 (2015)
Frontiers in Genetics, Vol 6 (2015)
The identification of DNA copy numbers from short-read sequencing data remains a challenge for both technical and algorithmic reasons. The raw data for these analyses are measured in tens to hundreds of gigabytes per genome; transmitting, storing, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fc823a6189382a6d4e9f401541ea22
Autor:
Mude Shi, Jared C. Roach, Gustavo Glusman, David J. Galas, Shameek Biswas, Max Robinson, Justin Ashworth, Stephen L. Guthery, Richard H. Duerr, Kyle Serikawa, Jin Man Kim, Ki-Sun Kwon, Mary E. Brunkow, Jacques Peschon, Leroy Hood, Anna B Stittrich, Denise E. Mauldin, Jae U. Jung
Publikováno v:
Human Genome Variation
Currently, the best clinical predictor for inflammatory bowel disease (IBD) is family history. Over 163 sequence variants have been associated with IBD in genome-wide association studies, but they have weak effects and explain only a fraction of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed3217887ab972e4af7f618cdd120d58
http://europepmc.org/articles/PMC4785573
http://europepmc.org/articles/PMC4785573