Zobrazeno 1 - 10
of 61
pro vyhledávání: '"D. Kinnamon"'
Publikováno v:
Clinical and Translational Science, Vol 14, Iss 2, Pp 550-557 (2021)
Precision medicine genetics study design requires large, diverse cohorts and thoughtful use of electronic technologies. Involving patients in research design may increase enrollment and engagement, thereby enabling a means to relevant patient outcome
Externí odkaz:
https://doaj.org/article/23d4386b58f44ed2bfb7911a2836a2c1
Autor:
Hanyu Ni, Elizabeth Jordan, Daniel D. Kinnamon, Jinwen Cao, Garrie J. Haas, Mark Hofmeyer, Evan Kransdorf, Gregory A. Ewald, Alanna A. Morris, Anjali Owens, Brian Lowes, Douglas Stoller, W.H. Wilson Tang, Sonia Garg, Barry H. Trachtenberg, Palak Shah, Salpy V. Pamboukian, Nancy K. Sweitzer, Matthew T. Wheeler, Jane E. Wilcox, Stuart Katz, Stephen Pan, Javier Jimenez, Daniel P. Fishbein, Frank Smart, Jessica Wang, Stephen S. Gottlieb, Daniel P. Judge, Charles K. Moore, Gordon S. Huggins, Ray E. Hershberger
Publikováno v:
Journal of the American College of Cardiology. 81:2059-2071
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85ed9eaa5e043cef5ad4a75d21bac488
https://doi.org/10.1016/j.jacc.2023.03.419
https://doi.org/10.1016/j.jacc.2023.03.419
Autor:
Barry H. Trachtenberg, Javier Jimenez, Alanna A. Morris, Evan Kransdorf, Anjali Owens, Daniel P. Fishbein, Elizabeth Jordan, Daniel D. Kinnamon, Jonathan O. Mead, Gordon S. Huggins, Ray E. Hershberger, Garrie Haas, Daniel Fishbein, Stephen S. Gottlieb, Matthew T. Wheeler, Mark Hofmeyer, W. H. Wilson Tang, Anjali T. Owens, Charles K. Moore, Javier Jimenez Carcamo, Barry Trachtenberg, Nancy K. Sweitzer, Palak Shah, Brian Lowes, Douglas Stoller, Frank Smart, Jane Wilcox, Stuart Katz, Gregory A. Ewald, Keith D. Aaronson, Jessica J. Wang, Salpy Pamboukian, Daniel P. Judge, Evan P. Kransdorf, Sonia Garg, Patrice Desvigne-Nickens, James Troendle, Yi-Ping Fu, Lucia Hindorff
Publikováno v:
Genetics in Medicine. 24:1495-1502
The cardiac phenotype of hereditary transthyretin amyloidosis (hTTR) usually presents as a restrictive or hypertrophic cardiomyopathy, and, although rarely observed as dilated cardiomyopathy (DCM), TTR is routinely included in DCM genetic testing pan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c69ccefe6398c6715752be5ee4a6726
https://doi.org/10.1016/j.gim.2022.03.011
https://doi.org/10.1016/j.gim.2022.03.011
Autor:
Wylie Burke, Shelly R. Hovick, Elizabeth Jordan, Hanyu Ni, Daniel D. Kinnamon, Ray E. Hershberger
Publikováno v:
Circ Genom Precis Med
Background: Assuring that relatives are informed about a genetic diagnosis and have appropriate medical follow-up can be challenging. We hypothesize that communal coping (CC)—an approach in which a group views a stressor (such as a new genetic diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5830aa6199b877bf7a4221e77aaa59
https://doi.org/10.1161/circgen.121.003541
https://doi.org/10.1161/circgen.121.003541
Autor:
Garrie J. Haas, Karolina M. Zareba, Hanyu Ni, Erika Bello-Pardo, Gordon S. Huggins, Ray E. Hershberger, Daniel D. Kinnamon, Elizabeth Jordan, Daniel P. Fishbein, Stephen S. Gottlieb, Matthew T. Wheeler, Mark Hofmeyer, W.H. Wilson Tang, Anjali T. Owens, Charles K. Moore, Javier Jimenez, Barry H. Trachtenberg, Nancy K. Sweitzer, Palak Shah, Brian D. Lowes, Douglas Stoller, Frank Smart, Alanna A. Morris, Jane E. Wilcox, Stuart Katz, Stephen Pan, Gregory A. Ewald, Keith D. Aaronson, Jessica J. Wang, Salpy Pamboukian, Daniel P. Judge, Evan P. Kransdorf, Sonia Garg, Patrice Desvigne-Nickens, James Troendle, Yi-Ping Fu, Lucia Hindorff
Publikováno v:
Circulation: Heart Failure. 15
Background: Coronary angiography to identify coronary artery disease has been foundational to distinguish the cause of dilated cardiomyopathy (DCM), including the assignment of idiopathic or ischemic cardiomyopathy. Late gadolinium enhancement (LGE)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bad3e7a07566cf46911304dd9965c61
https://doi.org/10.1161/circheartfailure.121.008877
https://doi.org/10.1161/circheartfailure.121.008877
Publikováno v:
Clinical and Translational Science
Clinical and Translational Science, Vol 14, Iss 2, Pp 550-557 (2021)
Clinical and Translational Science, Vol 14, Iss 2, Pp 550-557 (2021)
Precision medicine genetics study design requires large, diverse cohorts and thoughtful use of electronic technologies. Involving patients in research design may increase enrollment and engagement, thereby enabling a means to relevant patient outcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ffd6cd739f32192838e77189b245910
http://europepmc.org/articles/PMC7993282
http://europepmc.org/articles/PMC7993282
Autor:
Lynn Schoenfield, Silvia Casadei, Meghan J DeBenedictis, Mohamed H. Abdel-Rahman, Ben Kelly, Peter White, Frederick H. Davidorf, Andrew W. Stacey, Daniel D. Kinnamon, Mary Claire King, David M Gordon, Arun D. Singh, James B. Massengill, T. Walsh, Nicholas K. Hayward, Getachew Boru, Klarke M. Sample, James Scarth, Timothy W. Grosel, Ellie Fewings, Colleen M. Cebulla, Peter Johansson, Marc Tischkowitz, Robert Pilarski
Publikováno v:
Ophthalmology
To identify susceptibility genes associated with hereditary predisposition to uveal melanoma (UM) in patients with no detectable germline BAP1 alterations.Retrospective case series from academic referral centers.Cohort of 154 UM patients with high ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5c06225736a8c0b262c47402da19f74
https://doi.org/10.1016/j.ophtha.2019.11.009
https://doi.org/10.1016/j.ophtha.2019.11.009
Autor:
Gordon S, Huggins, Daniel D, Kinnamon, Garrie J, Haas, Elizabeth, Jordan, Mark, Hofmeyer, Evan, Kransdorf, Gregory A, Ewald, Alanna A, Morris, Anjali, Owens, Brian, Lowes, Douglas, Stoller, W H Wilson, Tang, Sonia, Garg, Barry H, Trachtenberg, Palak, Shah, Salpy V, Pamboukian, Nancy K, Sweitzer, Matthew T, Wheeler, Jane E, Wilcox, Stuart, Katz, Stephen, Pan, Javier, Jimenez, Keith D, Aaronson, Daniel P, Fishbein, Frank, Smart, Jessica, Wang, Stephen S, Gottlieb, Daniel P, Judge, Charles K, Moore, Jonathan O, Mead, Hanyu, Ni, Wylie, Burke, Ray E, Hershberger
Publikováno v:
JAMA. 327(5)
Idiopathic dilated cardiomyopathy (DCM) aggregates in families, and early detection in at-risk family members can provide opportunity to initiate treatment prior to late-phase disease. Most studies have included only White patients, yet Black patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400170ed2202b9ca2390f43b126ec30f
https://pubmed.ncbi.nlm.nih.gov/35103786
https://pubmed.ncbi.nlm.nih.gov/35103786
Autor:
M. Hofmeyer, G. Haas, E. Kransdorf, G. Ewald, A. Morris, A. Owens, B. Lowes, D. Stoller, W. Tang, S. Garg, B. Trachtenberg, P. Shah, S. Pamboukian, N. Sweitzer, M. Wheeler, J. Wilcox, S. Katz, S. Pan, J. Jimenez, F. Smart, J. Wang, S. Gottlieb, D. Judge, C. Moore, G. Huggins, E. Jordan, D. Kinnamon, H. Ni, R.E. Hershberger
Publikováno v:
The Journal of Heart and Lung Transplantation. 42:S176
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f844d0ac9273975e1f09e4daf9adc28
https://doi.org/10.1016/j.healun.2023.02.1674
https://doi.org/10.1016/j.healun.2023.02.1674
Autor:
Hanyu Ni, Elizabeth Jordan, Jinwen Cao, Daniel D. Kinnamon, Stephen S. Gottlieb, Mark Hofmeyer, Javier Jimenez, Daniel P. Judge, Evan Kransdorf, Alanna A. Morris, Anjali Owens, Palak Shah, W. H. Wilson Tang, Jessica Wang, Ray E. Hershberger
Publikováno v:
JAMA Cardiology. 8:33
ImportanceCardiovascular disease contributes outsized mortality in patients from underrepresented racial and ethnic groups. Understanding levels of trust in medical researchers and knowledge of genome sequencing may help identify barriers to research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c77684e70059c94d45d47b0c267188b
https://doi.org/10.1001/jamacardio.2022.4132
https://doi.org/10.1001/jamacardio.2022.4132