Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Kazimierz O Wrzeszczynski"'
Autor:
Kazimierz O Wrzeszczynski, Vinay Varadan, James Byrnes, Elena Lum, Sitharthan Kamalakaran, Douglas A Levine, Nevenka Dimitrova, Michael Q Zhang, Robert Lucito
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28503 (2011)
The identification of genetic and epigenetic alterations from primary tumor cells has become a common method to identify genes critical to the development and progression of cancer. We seek to identify those genetic and epigenetic aberrations that ha
Externí odkaz:
https://doaj.org/article/d8119b5d5ba64a6e9bd932ccfaf8886c
Autor:
Daniel A. Rodriguez, Jessica Yang, Michael A. Durante, Alexander N. Shoushtari, Stergios J. Moschos, Kazimierz O. Wrzeszczynski, J. William Harbour, Richard D. Carvajal
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-6 (2021)
Abstract Uveal melanoma (UM) is the most common primary intraocular malignancy in adults and leads to deadly metastases for which there is no approved treatment. Genetic events driving early tumor development are well-described, but those occurring l
Externí odkaz:
https://doaj.org/article/a14dce398f0e41c38acdb3290d8128a5
Autor:
Mayu O. Frank, Takahiko Koyama, Kahn Rhrissorrakrai, Nicolas Robine, Filippo Utro, Anne-Katrin Emde, Bo-Juen Chen, Kanika Arora, Minita Shah, Heather Geiger, Vanessa Felice, Esra Dikoglu, Sadia Rahman, Alice Fang, Vladimir Vacic, Ewa A. Bergmann, Julia L. Moore Vogel, Catherine Reeves, Depinder Khaira, Anthony Calabro, Duyang Kim, Michelle F. Lamendola-Essel, Cecilia Esteves, Phaedra Agius, Christian Stolte, John Boockvar, Alexis Demopoulos, Dimitris G. Placantonakis, John G. Golfinos, Cameron Brennan, Jeffrey Bruce, Andrew B. Lassman, Peter Canoll, Christian Grommes, Mariza Daras, Eli Diamond, Antonio Omuro, Elena Pentsova, Dana E. Orange, Stephen J. Harvey, Jerome B. Posner, Vanessa V. Michelini, Vaidehi Jobanputra, Michael C. Zody, John Kelly, Laxmi Parida, Kazimierz O. Wrzeszczynski, Ajay K. Royyuru, Robert B. Darnell
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-16 (2019)
Abstract Background Prompted by the revolution in high-throughput sequencing and its potential impact for treating cancer patients, we initiated a clinical research study to compare the ability of different sequencing assays and analysis methods to a
Externí odkaz:
https://doaj.org/article/11a5273709844f08a3cc53b25ce39717
Autor:
Mayu O. Frank, Takahiko Koyama, Kahn Rhrissorrakrai, Nicolas Robine, Filippo Utro, Anne-Katrin Emde, Bo-Juen Chen, Kanika Arora, Minita Shah, Heather Geiger, Vanessa Felice, Esra Dikoglu, Sadia Rahman, Xiaolan Fang, Vladimir Vacic, Ewa A. Bergmann, Julia L. Moore Vogel, Catherine Reeves, Depinder Khaira, Anthony Calabro, Duyang Kim, Michelle F. Lamendola-Essel, Cecilia Esteves, Phaedra Agius, Christian Stolte, John Boockvar, Alexis Demopoulos, Dimitris G. Placantonakis, John G. Golfinos, Cameron Brennan, Jeffrey Bruce, Andrew B. Lassman, Peter Canoll, Christian Grommes, Mariza Daras, Eli Diamond, Antonio Omuro, Elena Pentsova, Dana E. Orange, Stephen J. Harvey, Jerome B. Posner, Vanessa V. Michelini, Vaidehi Jobanputra, Michael C. Zody, John Kelly, Laxmi Parida, Kazimierz O. Wrzeszczynski, Ajay K. Royyuru, Robert B. Darnell
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-1 (2019)
Following publication of the original article [1], it was reported that the given name of the fourteenth author was incorrectly published. The incorrect and the correct names are given below.
Externí odkaz:
https://doaj.org/article/1d97177535aa4c4aae7304b51c8609fd
Autor:
Ferrah London, Inessa Hakker, Peter Andrews, Vaidehi Jobanputra, Michael Ronemus, Kazimierz O. Wrzeszczynski, Lukasz Kozon, Avinash Abhyankar, Vanessa Felice, Dino Robinson
Publikováno v:
J Mol Diagn
Chromosomal microarray testing is indicated for patients with diagnoses including unexplained developmental delay or intellectual disability, autism spectrum disorders, and multiple congenital anomalies. The short multiply aggregated sequence homolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee2308a089c2f07f80ba193c36d4f58
https://doi.org/10.1016/j.jmoldx.2020.09.009
https://doi.org/10.1016/j.jmoldx.2020.09.009
Autor:
Marilena Melas, Heather Geiger, Sowmya T. Srinivasa, Saurav Guha, Vanessa Felice, Lena Fielding, Amanda Thomas-Wilson, Ashley Wilson, Theresa MacDonald, Ryan Smith, Jyothi Manohar, Michelle Primiano, Olivier Elemento, Ravi Sharaf, Kazimierz O. Wrzeszczynski, Vaidehi Jobanputra
Publikováno v:
Cancer Genetics. :32-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1a893cbc09bd812c09e64c1054f6417
https://doi.org/10.1016/j.cancergen.2022.10.105
https://doi.org/10.1016/j.cancergen.2022.10.105
Autor:
Arianna Di Napoli, Davide Vacca, Giorgio Bertolazzi, Gianluca Lopez, Maria Piane, Aldo Germani, Evelina Rogges, Giuseppina Pepe, Fabio Santanelli Di Pompeo, Marzia Salgarello, Vaidehi Jobanputra, Susan Hsiao, Kazimierz O. Wrzeszczynski, Emilio Berti, Govind Bhagat
Publikováno v:
Cancers; Volume 13; Issue 24; Pages: 6174
Cancers
Cancers, Vol 13, Iss 6174, p 6174 (2021)
Cancers
Cancers, Vol 13, Iss 6174, p 6174 (2021)
Simple Summary Cutaneous and breast implant-associated anaplastic large-cell lymphomas are usually localized neoplasms with an indolent clinical course compared to systemic ALCL. However comparative analyses of the molecular features of these two ent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cd66e5a883ce0329e85c5d1e18abf0f
Autor:
Jessica Yang, J. William Harbour, Daniel A. Rodriguez, Richard D. Carvajal, Stergios J. Moschos, Alexander N. Shoushtari, Kazimierz O. Wrzeszczynski, Michael A. Durante
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-6 (2021)
NPJ Genomic Medicine
NPJ Genomic Medicine
Uveal melanoma (UM) is the most common primary intraocular malignancy in adults and leads to deadly metastases for which there is no approved treatment. Genetic events driving early tumor development are well-described, but those occurring later duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d42d5a5445788d625ff9e7d8089145a
https://doi.org/10.1038/s41525-021-00233-5
https://doi.org/10.1038/s41525-021-00233-5
Autor:
Kazimierz O. Wrzeszczynski, Heather Geiger, Sowmya T. Srinivasa, Marilena Melas, Valisha Shah, Vanessa Felice, Luisa Suarez, Endre Hegedus, Shruti Phadke, Saurav Guha, Dina Manaa, Dino Robinson, Lena Fielding, Vaidehi Jobanputra
Publikováno v:
Cancer Research. 82:757-757
The New York Genome Center CLIA laboratory has been providing New York State approved molecular diagnostic whole genome and whole transcriptome sequencing (WGTS) since October 2018. Indications for testing are cancers (solid tumors or hematological m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe30acb3993e8706019f8664c2b4431d
https://doi.org/10.1158/1538-7445.am2022-757
https://doi.org/10.1158/1538-7445.am2022-757
Autor:
Torsten Haferlach, Reinhard Büttner, Sean M. Grimmond, Kazimierz O. Wrzeszczynski, Charles G. Mullighan, Anna Schuh, Carlos Caldas, Vaidehi Jobanputra, Olivier Elemento, Edwin Cuppen
Publikováno v:
Seminars in cancer biology. 84
Whole-genome sequencing either alone or in combination with whole-transcriptome sequencing has started to be used to analyze clinical tumor samples to improve diagnosis, provide risk stratification, and select patient-specific therapies. Compared wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::903bbb3bf6119d5d78a39d15e136d3ca
https://pubmed.ncbi.nlm.nih.gov/34256129
https://pubmed.ncbi.nlm.nih.gov/34256129