Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kimberly A, Schahl"'
Autor:
Ronald S. Go, Michael John Hovan, Ralitza M Gavrilova, Roshini S. Abraham, Erik C. Thorland, Margot A. Cousin, Katherine S. Hunt, Ann M. Reed, Michael J. Ackerman, Jennifer L. Kemppainen, David R. Linden, Scott A. Beck, Dimitar Gavrilov, Eric W. Klee, Eric D. Wieben, Konstantinos N. Lazaridis, Noralane M. Lindor, David R. Deyle, Michael C. Stephens, Matthew J. Ferber, Timothy B. Niewold, Geoffrey J. Beek, Gianrico Farrugia, Douglas L. Riegert-Johnson, Teresa M. Kruisselbrink, Jennifer B. McCormick, Stephen N. Thibodeau, Kimberly J. Guthrie, Brooke M. McLaughlin, Pavel N. Pichurin, Devin Oglesbee, Elizabeth J. Atkinson, Marine I. Murphree, Kimberly A. Schahl, Linnea M. Baudhuin, Tammy M. McAllister, Dusica Babovic-Vuksanovic, Myra J. Wick, Jennifer L. Hand
Publikováno v:
Mayo Clinic Proceedings. 91:297-307
Objective To describe the experience and outcome of performing whole-exome sequencing (WES) for resolution of patients on a diagnostic odyssey in the first 18 months of an individualized medicine clinic (IMC). Patients and Methods The IMC offered WES
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ede495e39ea5a5d0555dc5c1c25dd456
https://doi.org/10.1016/j.mayocp.2015.12.018
https://doi.org/10.1016/j.mayocp.2015.12.018
Autor:
Alexander Fiksdal, Kara A. Mensink, Matthew J. Ferber, Yuan Ji, Douglas L. Riegert-Johnson, Kelly E. Ormond, Eric W. Klee, W. Edward Highsmith, Kimberly A. Schahl, Jennifer B. McCormick, John L. Black, Eric D. Wieben, Tammy M. McAllister, Umut Aypar, Noralane M. Lindor, Gianrico Farrugia, Stephen N. Thibodeau, Rondell P. Graham, Kiley J. Johnson, Vivek Sarangi, Katherine S. Hunt
Publikováno v:
Mayo Clinic Proceedings. 90:1327-1337
Objective To understand motivations, educational needs, and concerns of individuals contemplating whole-exome sequencing (WES) and determine what amount of genetic information might be obtained by sequencing a generally healthy cohort so as to more e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1e19eb7bf7dbe5f51e533b15b02ab3f
https://doi.org/10.1016/j.mayocp.2015.05.021
https://doi.org/10.1016/j.mayocp.2015.05.021
Autor:
Katie N. Jones, Xiaojia Tang, Jason P. Sinnwell, Daniel W. Visscher, Hugues Sicotte, Richard Gray, Richard M. Weinshilboum, Vera J. Suman, James N. Ingle, Donald W. Northfelt, Judy C. Boughey, Sarah A. McLaughlin, Michelle McDonough, Matthew P. Goetz, Amy Lynn Conners, Kimberly A. Schahl, Eric D. Wieben, Marissa S. Ellingson, Sara J. Felten, Alvaro Moreno-Aspitia, Peter T. Vedell, Poulami Barman, Krishna R. Kalari, Jeanette E. Eckel-Passow, Kevin J. Thompson, Steven N. Hart, Ann M. Moyer, Liewei Wang, Travis J. Dockter
Publikováno v:
Breast Cancer Research and Treatment
When sequencing blood and tumor samples to identify targetable somatic variants for cancer therapy, clinically relevant germline variants may be uncovered. We evaluated the prevalence of deleterious germline variants in cancer susceptibility genes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cebe595249f0412b6849528b64e4875
https://doi.org/10.1007/s10549-015-3545-6
https://doi.org/10.1007/s10549-015-3545-6
Autor:
Konstantinos N. Lazaridis, Matthew J. Ferber, Gianrico Farrugia, Mitesh J. Borad, Douglas L. Riegert-Johnson, Tammy M. McAllister, Rafael Fonseca, Kimberly A. Schahl, Jennifer B. McCormick, Alan H. Bryce, Cloann G. Schultz, Alexander S. Parker, George C Then, Carolyn R. Rohrer Vitek, Keith Stewart, Dusica Babovic-Vuksanovic, Scott A. Beck, Eric W. Klee, Kiley J. Johnson, Robert R. McWilliams, Asher Chanan-Khan, Eric D. Wieben, Noralane M. Lindor
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 166:15-23
There is increasing recognition that genomic medicine as part of individualized medicine has a defined role in patient care. Rapid advances in technology and decreasing cost combine to bring genomic medicine closer to the clinical practice. There is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91b403c3930fb68630f8752f967bf9d7
https://doi.org/10.1002/ajmg.c.31387
https://doi.org/10.1002/ajmg.c.31387
Autor:
Konstantinos N, Lazaridis, Kimberly A, Schahl, Margot A, Cousin, Dusica, Babovic-Vuksanovic, Douglas L, Riegert-Johnson, Ralitza H, Gavrilova, Tammy M, McAllister, Noralane M, Lindor, Roshini S, Abraham, Michael J, Ackerman, Pavel N, Pichurin, David R, Deyle, Dimitar K, Gavrilov, Jennifer L, Hand, Eric W, Klee, Michael C, Stephens, Myra J, Wick, Elizabeth J, Atkinson, David R, Linden, Matthew J, Ferber, Eric D, Wieben, Gianrico, Farrugia, Erik C, Thorland
Publikováno v:
Mayo Clinic proceedings. 91(3)
To describe the experience and outcome of performing whole-exome sequencing (WES) for resolution of patients on a diagnostic odyssey in the first 18 months of an individualized medicine clinic (IMC).The IMC offered WES to physicians of Mayo Clinic pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::75a88e8de4de11d894dfd95aa000b149
https://pubmed.ncbi.nlm.nih.gov/26944241
https://pubmed.ncbi.nlm.nih.gov/26944241
Autor:
Mitesh J. Borad, Maitray D. Patel, Jonathan Adkins, Keith C. Bible, Alvin C. Silva, Ann E. McCullough, Rafael Fonseca, Robert R. McWilliams, Sara Nasser, Daniel D. Von Hoff, Scott W. Young, Ahmet Kurdoglu, Benjamin R. Kipp, Konstantinos N. Lazaridis, Yan W. Asmann, Rachel M. Condjella, Katherine S. Hunt, Alexis Christoforides, Alan H. Bryce, Pamela Placek, Mia D. Champion, Michael T. Barrett, Pamela E. Harris, Emily G. Barr Fritcher, Jaysheel D. Bhavsar, Jackie McDonald, Tyler Izatt, Stephen D. Mastrian, Jessica Aldrich, Winnie S. Liang, Asha Nair, Eric W. Klee, Matthew S. Block, Jan B. Egan, Kimberly A. Schahl, Lori Phillips, John D. Carpten, David Craig, Irene Cherni, Gavin R. Oliver, Haiyong Han, Jean Pierre A. Kocher, A. Keith Stewart, Janine LoBello, Rebecca Reiman, Aprill Watanabe, Joseph M. Collins, Angela Baker, Sumit Middha
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 10, Iss 2, p e1004135 (2014)
PLoS Genetics, Vol 10, Iss 2, p e1004135 (2014)
Advanced cholangiocarcinoma continues to harbor a difficult prognosis and therapeutic options have been limited. During the course of a clinical trial of whole genomic sequencing seeking druggable targets, we examined six patients with advanced chola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b42524fd39d8caead646c436382bc1bb
http://europepmc.org/articles/PMC3923676
http://europepmc.org/articles/PMC3923676
Autor:
Kiley J. Johnson, Konstantinos N. Lazaridis, Jennifer B. McCormick, Gianrico Farrugia, Mitesh J. Borad, Joseph A. Murray, Alan H. Bryce, Richard R. Sharp, Alexander S. Parker, Robert R. McWilliams, Matthew J. Ferber, Kimberly A. Schahl, Dusica Babovic-Vuksanovic, Eric D. Wieben, Noralane M. Lindor, Richard J. Caselli
Publikováno v:
Mayo Clinic proceedings. 89(6)
M.J.B., ter for Mayo .S.P.). I n March 2013, the American College of Medical Genetics and Genomics (ACMG) released recommendations on how to handle incidental findings (IFs) for the clinical application of whole exome or whole genome sequencing (WES/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69e022cb02dfb2ba7698e86a42c8baf2
https://pubmed.ncbi.nlm.nih.gov/23788249
https://pubmed.ncbi.nlm.nih.gov/23788249
Autor:
Jessie H. Conta, Katrina E. Kotzer, McKinsey L. Goodenberger, Claire M. Anderson, Jacquelyn D. Riley, Kimberly A. Schahl
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 427
Laboratory genetic counselors within hospital laboratories and genetic testing laboratories have an important role in increasing the appropriate utilization of genetic tests. This service is becoming more important as genetic testing becomes more com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77b31bc1da549e8f02ba091167583425
https://pubmed.ncbi.nlm.nih.gov/24084506
https://pubmed.ncbi.nlm.nih.gov/24084506