Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Stephen B Ellis"'
Autor:
Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, Laura J Rasmussen-Torvik, Luke V Rasmussen, Frederick T J Lin, Mariza de Andrade, Kenneth M Borthwick, Erwin Bottinger, Andrew Cagan, David S Carrell, Joshua C Denny, Stephen B Ellis, Omri Gottesman, James G Linneman, Jyotishman Pathak, Peggy L Peissig, Ning Shang, Gerard Tromp, Annapoorani Veerappan, Maureen E Smith, Rex L Chisholm, Andrew J Gawron, M Geoffrey Hayes, Abel N Kho
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0283553 (2023)
ObjectiveDiverticular disease (DD) is one of the most prevalent conditions encountered by gastroenterologists, affecting ~50% of Americans before the age of 60. Our aim was to identify genetic risk variants and clinical phenotypes associated with DD,
Externí odkaz:
https://doaj.org/article/78f28682110648cfbe41e76d4bf5e28c
Autor:
Jung-Im Shin, Alex R. Chang, Morgan E. Grams, Josef Coresh, Shoshana H. Ballew, Aditya Surapaneni, Kunihiro Matsushita, Henk J.G. Bilo, Juan J. Carrero, Gabriel Chodick, Kenn B. Daratha, Simerjot K. Jassal, Girish N. Nadkarni, Robert G. Nelson, Christoph Nowak, Nikita Stempniewicz, Keiichi Sumida, Jamie P. Traynor, Mark Woodward, Yingying Sang, Ron T. Gansevoort, John Chalmers, Katherine Tuttle, Radica Alicic, Sterling McPherson, Cami Jones, Gurmukteshwar Singh, Jamie Green, H. Lester Kirchner, Varda Shalev, Erwin P. Bottinger, Ruth J.F. Loos, Stephen B. Ellis, John Cuddeback, Elizabeth Ciemins, Emily Carbonara, Stephan Dunning, William C. Knowler, Helen C. Looker, Lyane M. Kieneker, Stephan J.L. Bakker, Hans L. Hillege, Pim van der Harst, Jacklyn Bergstrom, Joachim Ix, Csaba P. Kovesdy, Praveen Potukuchi, Marco Trevisan, Carl Gustaf Elinder, Björn Wettermark, Johan Ärnlöv, Patrick B. Mark, Peter C. Thomson, Colin C. Geddes, Gijs W.D. Landman, Kornelis J.J. van Hateren, Nanne Kleefstra, Orlando Gutierrez, Tsuneo Konta, Andrew S. Levey, Kevan Polkinghorne, Elke Schäffner, Jingsha Chen, Aditya Surapeneni
Publikováno v:
Hypertension
Hypertension (Dallas, Tex. : 1979), 78(4), 1042-1052. LIPPINCOTT WILLIAMS & WILKINS
Hypertension (Dallas, Tex. : 1979), 78(4), 1042-1052. LIPPINCOTT WILLIAMS & WILKINS
Albuminuria is an under-recognized component of chronic kidney disease definition, staging, and prognosis. Guidelines, particularly for hypertension, conflict on recommendations for urine albumin-to-creatinine ratio (ACR) measurement. Separately amon
Autor:
Aniwaa Owusu Obeng, Stuart A. Scott, Tom Kaszemacher, Stephen B. Ellis, Ana Mejia, Alanna Gomez, Rajiv Nadukuru, Noura S. Abul‐Husn, Aida Vega, Eva Waite, Omri Gottesman, Judy Cho, Erwin P. Bottinger
Publikováno v:
Clinical pharmacology and therapeutics.
Pharmacogenetic implementation programs are increasingly feasible due to the availability of clinical guidelines for implementation research. The utilization of these resources has been reported with selected drug-gene pairs; however, little is known
Autor:
Jessica E. Rodriguez, Carol R. Horowitz, Nathaniel M. Pearson, Monisha Sebastin, Dana Watnick, Nicole M. Yelton, Mimsie Robinson, Nehama Teitelman, George A. Diaz, John M. Greally, Kojo Davis, Patricia Kovatch, Bruce D. Gelb, Melissa P. Wasserstein, Gabrielle Bertier, Laurie J. Bauman, Katie Gallagher, Noura S. Abul-Husn, Michelle A. Ramos, Tom Kaszemacher, Nicole Kelly, Eimear E. Kenny, Estefany Maria, Irma Laguerre, Christian Stolte, Stephen B. Ellis, Randi E. Zinberg, Lynne D. Richardson, Jaqueline A. Odgis, Jessenia Lopez, Sabrina A. Suckiel, Faygel Beren
Publikováno v:
Genetics in Medicine
PurposeUse of genomic sequencing is increasing at a pace that requires technological solutions to effectively meet the needs of a growing patient population. We developed GUÍA, a web-based application, to enhance the delivery of genomic results and
Autor:
Muh-Ching Yee, Aniwaa Owusu Obeng, Eimear E. Kenny, Omri Gottesman, Stephen B. Ellis, Matthew A. Levin, Stephane Wenric, Erwin P. Bottinger, Thomas T. Joseph, Janina M. Jeff, Gillian M. Belbin
Publikováno v:
The Pharmacogenomics Journal
BackgroundThe emergence of genomic data in biobanks and health systems offers new ways to derive medically important phenotypes, including acute phenotypes that occur during in-patient clinical care. We hypothesized that there is a genetic underpinni
Autor:
Stephen B. Ellis, H. Quincy Brown
Publikováno v:
Performance Improvement Quarterly. 33:327-347
Autor:
Girish N. Nadkarni, Kezhen Fei, Michelle A. Ramos, Diane Hauser, Emilia Bagiella, Stephen B. Ellis, Saskia Sanderson, Stuart A. Scott, Tatiana Sabin, Ebony Madden, Richard Cooper, Martin Pollak, Neil Calman, Erwin P. Bottinger, Carol R. Horowitz
Publikováno v:
JAMA network open. 5(3)
Risk variants in the apolipoprotein L1 (APOL1 [OMIM 603743]) gene on chromosome 22 are common in individuals of West African ancestry and confer increased risk of kidney failure for people with African ancestry and hypertension. Whether disclosing AP
Autor:
Judy H. Cho, Tielman Van Vleck, Catherine K. Craven, Ron Do, Ruth J. F. Loos, Lili Chan, Girish N. Nadkarni, Joseph L. Kannry, Stephen B. Ellis, Steven G. Coca, Peter A Bonis
Publikováno v:
Int J Med Inform
Objective Electronic health record (EHR) systems contain structured data (such as diagnostic codes) and unstructured data (clinical documentation). Clinical insights can be derived from analyzing both. The use of natural language processing (NLP) alg
Publikováno v:
The Routledge International Handbook of Student-Centered Learning and Teaching in Higher Education ISBN: 9780429259371
This chapter discusses how a US Air Force (USAF) technical training organization shifted instructional strategies to employ student-centered instruction (SCI). Technical training leaders are leaning forward to meet this challenge because they have fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f93c7149967326db9a4425d6f1bef08
https://doi.org/10.4324/9780429259371-32
https://doi.org/10.4324/9780429259371-32
Autor:
Omri Gottesman, Frederick T.J. Lin, James G. Linneman, Mariza de Andrade, Luke V. Rasmussen, Rex L. Chisholm, Joshua C. Denny, Annapoorani Veerappan, Gerard Tromp, Laura J. Rasmussen-Torvik, Kenneth M. Borthwick, Andrew Cagan, Peggy L. Peissig, Jyotishman Pathak, M. Geoffrey Hayes, Ning Shang Shang, Erwin P. Bottinger, William K. Thompson, Jennifer A. Pacheco, Stephen B. Ellis, Andrew J. Gawron, Maureen E. Smith, Yoonjung Yoonie Joo, David Carrell, Abel N. Kho
Background and aimsDiverticular disease is among the most prevalent conditions encountered by gastroenterologists, affecting ∼50% of Americans before the age of 60. Our aim was to identify genetic risk variants and clinical phenotypes associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e08c4c98f1159a3e13441ba2cf0f8b08
https://doi.org/10.1101/2020.06.08.138735
https://doi.org/10.1101/2020.06.08.138735