Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Helio A. Costa"'
Autor:
Christine G. Preston, Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L. Goldstein, Xi Luo, Hannah Wand, Bryan Wulf, Gloria Cheung, Mark E. Mandell, Howard Tong, Shaung Cheng, Michael A. Iacocca, Arturo Lopez Pineda, Alice B. Popejoy, Karen Dalton, Jimmy Zhen, Selina S. Dwight, Lawrence Babb, Marina DiStefano, Julianne M. O’Daniel, Kristy Lee, Erin R. Riggs, Diane B. Zastrow, Jessica L. Mester, Deborah I. Ritter, Ronak Y. Patel, Sai Lakshmi Subramanian, Aleksander Milosavljevic, Jonathan S. Berg, Heidi L. Rehm, Sharon E. Plon, J. Michael Cherry, Carlos D. Bustamante, Helio A. Costa, on behalf of the Clinical Genome Resource (ClinGen)
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-12 (2022)
Abstract Background Identification of clinically significant genetic alterations involved in human disease has been dramatically accelerated by developments in next-generation sequencing technologies. However, the infrastructure and accessible compre
Externí odkaz:
https://doaj.org/article/c5ae77d69fae41bca5be493d02302150
Autor:
Eliah G. Overbey, Amanda M. Saravia-Butler, Zhe Zhang, Komal S. Rathi, Homer Fogle, Willian A. da Silveira, Richard J. Barker, Joseph J. Bass, Afshin Beheshti, Daniel C. Berrios, Elizabeth A. Blaber, Egle Cekanaviciute, Helio A. Costa, Laurence B. Davin, Kathleen M. Fisch, Samrawit G. Gebre, Matthew Geniza, Rachel Gilbert, Simon Gilroy, Gary Hardiman, Raúl Herranz, Yared H. Kidane, Colin P.S. Kruse, Michael D. Lee, Ted Liefeld, Norman G. Lewis, J. Tyson McDonald, Robert Meller, Tejaswini Mishra, Imara Y. Perera, Shayoni Ray, Sigrid S. Reinsch, Sara Brin Rosenthal, Michael Strong, Nathaniel J. Szewczyk, Candice G.T. Tahimic, Deanne M. Taylor, Joshua P. Vandenbrink, Alicia Villacampa, Silvio Weging, Chris Wolverton, Sarah E. Wyatt, Luis Zea, Sylvain V. Costes, Jonathan M. Galazka
Publikováno v:
iScience, Vol 24, Iss 4, Pp 102361- (2021)
Summary: With the development of transcriptomic technologies, we are able to quantify precise changes in gene expression profiles from astronauts and other organisms exposed to spaceflight. Members of NASA GeneLab and GeneLab-associated analysis work
Externí odkaz:
https://doaj.org/article/db05f4c13f9d4050b634492f121e3d68
Autor:
Maximilian Diehn, Ash A. Alizadeh, Joseph C. Liao, Mandy L.Y. Sin, Barzin Y. Nabet, Helio A. Costa, Harumi Lim, Chih Long Liu, Henning Stehr, Aadel A. Chaudhuri, Jacob J. Chabon, Dharati Trivedi, Mohammad S. Esfahani, Simon B. Chen, William Y. Shi, Daniel V. Lazzareschi, Joseph Schroers-Martin, Jonathan C. Dudley
Supplemental Figures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5bcfbb1cb23e976565fa82373056e8
https://doi.org/10.1158/2159-8290.22532998
https://doi.org/10.1158/2159-8290.22532998
Autor:
Maximilian Diehn, Ash A. Alizadeh, Joseph C. Liao, Mandy L.Y. Sin, Barzin Y. Nabet, Helio A. Costa, Harumi Lim, Chih Long Liu, Henning Stehr, Aadel A. Chaudhuri, Jacob J. Chabon, Dharati Trivedi, Mohammad S. Esfahani, Simon B. Chen, William Y. Shi, Daniel V. Lazzareschi, Joseph Schroers-Martin, Jonathan C. Dudley
Supplemental Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65d03cd713f3fa1d092b5a412f4f2abe
https://doi.org/10.1158/2159-8290.22532992.v1
https://doi.org/10.1158/2159-8290.22532992.v1
Autor:
Fiona Senchyna, Dora Y. Ho, Hayden T. Schwenk, Niaz Banaei, Aruna Subramanian, Catherine A. Hogan, Indre Budvytiene, Angel Moreno, Saurabh Gombar, Kanagavel Murugesan, Helio A. Costa
Publikováno v:
Clinical Infectious Diseases. 73:1677-1684
Background Invasive fungal infection (IFI) is a growing cause of morbidity and mortality in oncology and transplant patients. Diagnosis of IFI is often delayed due to need for invasive biopsy and low sensitivity of conventional diagnostic methods. Fu
Autor:
Carlos Bustamante, James L. Zehnder, Richard E. Green, Brandon J. Rice, Ramesh Ramakrishnan, Sameed Siddiqui, Marco Blanchette, Nicholas H. Putnam, Christopher J. Troll, Paul D. Hartley, Christian A. Kunder, Martin P. Powers, Javkhlan-Ochir Ganbat, Helio A. Costa
Publikováno v:
The Journal of Molecular Diagnostics. 21:375-383
The clinical management and therapy of many solid tumor malignancies depends on detection of medically actionable or diagnostically relevant genetic variation. However, a principal challenge for genetic assays from tumors is the fragmented and chemic
Autor:
Helio A. Costa, William Shi, Chih Long Liu, Mohammad Shahrokh Esfahani, Dharati Trivedi, Henning Stehr, Harumi Lim, Maximilian Diehn, Aadel A. Chaudhuri, Simon B. Chen, Barzin Y. Nabet, Jonathan C. Dudley, Joseph G Schroers-Martin, Jacob J. Chabon, Ash A. Alizadeh, Daniel Lazzareschi, Mandy L. Y. Sin, Joseph C. Liao
Publikováno v:
Cancer Discovery. 9:500-509
Current regimens for the detection and surveillance of bladder cancer are invasive and have suboptimal sensitivity. Here, we present a novel high-throughput sequencing (HTS) method for detection of urine tumor DNA (utDNA) called utDNA CAPP-Seq (uCAPP
Autor:
Meredith A. Mills, George W. Sledge, Helio A. Costa, Christina Curtis, Rochelle Reyes, Carlos Suárez, James L. Zehnder, James M. Ford
Publikováno v:
JCO Precision Oncology. :1-4
Gene‐specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel
Autor:
Kathleen S. Hruska, Joanne Ngeow, Rajarshi Ghosh, Madhuri Hegde, Robert Huether, Sharon E. Plon, Liying Zhang, Charis Eng, Jessica L. Mester, Helio A. Costa, Laura V. Milko, Jill S. Barnholtz-Sloan, Katherine Lachlan, Tina Pesaran, Felicia Hernandez, Rachid Karam, Kaitlin Sesock
Publikováno v:
Human Mutation. 39:1581-1592
The ClinGen PTEN Expert Panel was organized by the ClinGen Hereditary Cancer Clinical Domain Working Group to assemble clinicians, researchers, and molecular diagnosticians with PTEN expertise to develop specifications to the 2015 ACMG/AMP Sequence V
Autor:
Dalton K, Preston Cg, Steven M. Harrison, Lawrence J. Babb, Bryan Wulf, Heidi L. Rehm, Selina S. Dwight, Jimmy Zhen, J. M. Cherry, Deborah I. Ritter, Kristy Lee, Erin Rooney Riggs, Madhavrao R, Cheng S, Jessica L. Mester, Ronak Y. Patel, Matthew Wright, Tong H, Jennifer L. Goldstein, Carlos Bustamante, Julianne M. O’Daniel, Xi Luo, Hannah Wand, Cheung G, Helio A. Costa, Zastrow Db, Jonathan S. Berg, Mandell Me, Sai Lakshmi Subramanian, Sharon E. Plon, Alice B. Popejoy, Arturo Lopez Pineda, Michael A. Iacocca, Marina T. DiStefano, Aleksandar Milosavljevic
Publikováno v:
Genome Medicine
Genome Medicine, Vol 14, Iss 1, Pp 1-12 (2022)
Genome Medicine, Vol 14, Iss 1, Pp 1-12 (2022)
Background Identification of clinically significant genetic alterations involved in human disease has been dramatically accelerated by developments in next-generation sequencing technologies. However, the infrastructure and accessible comprehensive c