Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ora, Gordon"'
Autor:
Lindsay Dickey, Ben Gronowski, Kyle Jones, J. B. Rinaldi, Kate Emery, Jon Clemens, Ora Gordon, Keri Vartanian
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Genomics has the potential to transform medicine by identifying genetic risk factors that predispose people to certain illnesses. Use of genetic screening is rapidly expanding and shifting towards screening all patients regardless of kn
Externí odkaz:
https://doaj.org/article/dbadf87366f143e29007ae25aac4e8c6
Autor:
Elisha Hughes, Susanne Wagner, Dmitry Pruss, Ryan Bernhisel, Braden Probst, Victor Abkevich, Timothy Simmons, Brooke Hullinger, Thaddeus Judkins, Eric Rosenthal, Benjamin Roa, Susan M. Domchek, Charis Eng, Judy Garber, Monique Gary, Jennifer Klemp, Semanti Mukherjee, Kenneth Offit, Olufunmilayo I. Olopade, Joseph Vijai, Jeffrey N. Weitzel, Pat Whitworth, Lamis Yehia, Ora Gordon, Holly Pederson, Allison Kurian, Thomas P. Slavin, Alexander Gutin, Jerry S. Lanchbury
Publikováno v:
JCO Precision Oncology.
PURPOSE Polygenic risk scores (PRSs) for breast cancer (BC) risk stratification have been developed primarily in women of European ancestry. Their application to women of non-European ancestry has lagged because of the lack of a formal approach to in
Autor:
Elisha Hughes, Braden Probst, Holly Jane Pederson, Timothy Simmons, Brian Morris, Susan M. Domchek, Charis Eng, Monique Gary, Ora Gordon, Jennifer R. Klemp, Semanti Mukherjee, Kenneth Offit, Olufunmilayo I. Olopade, Mark E. Robson, Joseph Vijai, Pat W. Whitworth, Susanne Wagner, Jerry Lanchbury, Thomas Paul Slavin, Alexander Gutin
Publikováno v:
Journal of Clinical Oncology. 40:557-557
557 Background: BC risk assessment is important for guiding personalized screening and risk-reducing interventions. TCv8 is used to estimate BC risk based on age, breast density, family cancer history and other clinical factors. Accuracy may be impro
Autor:
Lorenzo Cohen, Suzanne Danhauer, David Ira Rosenthal, Mark Steven Chambers, M. Kay Garcia, Andrew Cusimano, Mark Brown, Emily Van Meter Dressler, Jewel Ochoa, Peiying Yang, Joseph S Chiang, Ora Gordon, Rhonda Crutcher, Jung K Kim, Michael P. Russin, Joshua Lukenbill, Mercedes Porosnicu, Kathleen J Yost, Kathryn E. Weaver, Glenn Jay Lesser
Publikováno v:
Journal of Clinical Oncology. 40:12004-12004
12004 Background: The majority of head/neck (HN) patients who undergo radiotherapy develop RIX. Unfortunately, existing treatments are of limited benefit and have side effects. Initial small studies suggest acupuncture may treat chronic RIX. A multic
Autor:
Stephanie Meek, Placede Tiemeny, Jennifer R. Klemp, Alexander Gutin, Shannon Gallagher, Jeffrey N. Weitzel, Olufunmilayo I. Olopade, Susanne Wagner, Jerry S. Lanchbury, Charis Eng, Elisha Hughes, Thomas P. Slavin, Holly J. Pederson, Ora Gordon, Monique Gary, Pat Whitworth, Lamis Yehia
Publikováno v:
Journal of Clinical Oncology. 39:10502-10502
10502 Background: BC risk is influenced by single-nucleotide polymorphisms (SNPs) with small effects that can be aggregated into polygenic risk scores (PRSs). PRSs have primarily been developed and validated for populations of European descent. To ma
Publikováno v:
The Breast Journal. 21:596-603
To evaluate the expression of insulin-like growth factor II mRNA-binding protein (IMP3), CK8/18, and CK14 in BRCA mutated and sporadic invasive breast carcinoma. Immunohistochemistry for IMP3, CK8/18, and CK14 was performed on 39 cases of invasive br
Autor:
Charlotte A. Brown, Carol A. Crowe, Ora Gordon, Carla Grosmann, Viola F. Gnocchi, Ismail A. Khatri, Matthew Bower, Erynn S. Gordon, Kevin J. Felice, Alexander Asamoah, Juliet A. Ellis, Peter S. Zammit, Diana M. Escolar, Susan T. Iannaccone, Matthew N. Meriggioli, Jerry R. Mendell, Juergen Scharner
Publikováno v:
Human Mutation; Vol 32
Mutations in LMNA cause a variety of diseases affecting striated muscle including autosomal Emery-Dreifuss muscular dystrophy (EDMD), LMNA-associated congenital muscular dystrophy (L-CMD), and limb-girdle muscular dystrophy type 1B (LGMD1B). Here, we
Autor:
Tali Geva, Ora Gordon
Publikováno v:
AMA Journal of Ethics. 11:690-696
Family history is important to patient care. Virtual Mentor is a monthly bioethics journal published by the American Medical Association.
Autor:
Christopher J. O'Donnell, Benjamin S. Wilfond, Steven A. Lubitz, Deborah A. Nickerson, William M. Grady, Robert J. Desnick, Brian H. Shirts, Andrew D. Johnson, Carlos J. Gallego, Melissa A. Kelly, Michael J. Bamshad, Daniel Seung Kim, Heidi L. Rehm, C. Ronald Scott, Kathleen A. Leppig, Matthew C. Dulik, Ora Gordon, Nancy B. Spinner, Lesli A. Kiedrowski, Ella R. Jarvik, Tom Walsh, Jerry H. Kim, Elisabeth A. Rosenthal, Laura K. Conlin, Robin L. Bennett, Jennifer Schleit, Kristy Lee, Colin C. Pritchard, Fuki M. Hisama, Stephanie M. Fullerton, Mari Tokita, Laura M. Amendola, Amber A. Burt, Peter H. Byers, Wendy H. Raskind, Seema M. Jamal, Kalotina Machini, Surabhi Mulchandani, Jerome I. Rotter, Daniel S. Herman, Yaoping Yang, Kent D. Taylor, James P. Evans, Ragan Hart, Peggy D. Robertson, Xiuqing Guo, David R. Crosslin, Gail P. Jarvik, Michael O. Dorschner, Leslie J. Raffel, James T. Bennett, Virginia P. Sybert, Leslie G. Biesecker, Jonathan S. Berg, Mitzi L. Murray, Kristy Crooks, Thomas D. Bird, Holly K. Tabor, Emily H. Turner, C. Sue Richards, Arno G. Motulsky, Steven Joffe, Jenica L. Abrudan, Wylie Burke, Danielle R. Metterville, Avni Santani, Ann Katherine M. Foreman, Stephen S. Rich, Joseph Salama, Kelly L. Jones, Jane E. Ranchalis, Andy Itsara, Greg M. Cooper
Publikováno v:
Genome research, vol 25, iss 3
Recommendations for laboratories to report incidental findings from genomic tests have stimulated interest in such results. In order to investigate the criteria and processes for assigning the pathogenicity of specific variants and to estimate the fr
Autor:
Patricia Y. Fechner, Emmanuèle Délot, Leigh Ramos-Platt, Margaret P. Adam, Hayk Barseghyan, Renee Bargman, Valerie A. Arboleda, Hane Lee, Heather J. Stalker, Anna Pawlikowska-Haddal, Catherine E. Keegan, Revi P. Mathew, Eric Vilain, Ora Gordon, Ruth M. Baxter, Stanley F. Nelson, Roberto T. Zori, Louanne Hudgins, Ascia Eskin, Sharon Travers, Susan Schelley
Publikováno v:
The Journal of clinical endocrinology and metabolism. 100(2)
Context: Disorders of sex development (DSD) are clinical conditions where there is a discrepancy between the chromosomal sex and the phenotypic (gonadal or genital) sex of an individual. Such conditions can be stressful for patients and their familie