Zobrazeno 1 - 10
of 259
pro vyhledávání: '"L. Bonham"'
Autor:
Benjamin L. L. Réant, Fraser J. Mackintosh, Gemma K. Gransbury, Carlo Andrea Mattei, Barak Alnami, Benjamin E. Atkinson, Katherine L. Bonham, Jack Baldwin, Ashley J. Wooles, Iñigo J. Vitorica-Yrezabal, Daniel Lee, Nicholas F. Chilton, Stephen T. Liddle, David P. Mills
Publikováno v:
JACS Au, Vol 4, Iss 7, Pp 2695-2711 (2024)
Externí odkaz:
https://doaj.org/article/17d8c09f13904d7197b11b1ac80617b7
Autor:
Faeben Wossenseged, Kristina Franklin, Talya Gordon, Ashley Buscetta, Gwenyth R. Wallen, Vence L. Bonham, Nicole Farmer
Publikováno v:
Health Equity, Vol 8, Iss 1, Pp 238-248 (2024)
Introduction: In the United States, sickle cell disease (SCD)?the homozygous inheritance of a point mutation within the beta-globin chain of hemoglobin?affects between 80,000 and 100,000 people. Adequate nutrition can influence the pathophysiology of
Externí odkaz:
https://doaj.org/article/b3a245e433724a49bd84d2d6a117f438
Autor:
Ashley J. Buscetta, Khadijah E. Abdallah, K. Jameson Floyd, Faeben S. Wossenseged, Corinne A. Conn, Hasmin C. Ramirez, Vence L. Bonham
Publikováno v:
BMC Psychology, Vol 10, Iss 1, Pp 1-10 (2022)
Abstract Background The COVID-19 pandemic has impacted the physical and mental health of people worldwide including those living with genetic conditions. Sickle cell disease (SCD) is a hematologic chronic disease that causes multisystem damage and mo
Externí odkaz:
https://doaj.org/article/46824cebc97f4f6c9a6a5712d4323b2d
This is a timely and vital resource for new and seasoned gerontology nurses responsible for coordinating care and advocacy for their patients as health care shifts from hospital-based to community-based care. Comprehensive and organized for quick acc
Autor:
Jamal M. Jefferson, Wynton M. Sims, Nkeiruka Umeh, Yen Ji Julia Byeon, Khadijah E. Abdallah, Vence L. Bonham, Rakhi P. Naik, Kim Smith‐Whitley
Publikováno v:
eJHaem, Vol 2, Iss 3, Pp 585-600 (2021)
Abstract Sickle cell trait (SCT), a commonly asymptomatic condition, has many associated clinical complications that upon presentation, can be very difficult to attribute to SCT. The effects of SCT on the spleen, for example, are not completely under
Externí odkaz:
https://doaj.org/article/1bae4397c8cf42e0a15883b54f51ae4a
Autor:
Shameka P. Thomas, Kiana Amini, K. Jameson Floyd, Rachele Willard, Faeben Wossenseged, Madison Keller, Jamil B. Scott, Khadijah E. Abdallah, Ashley Buscetta, Vence L. Bonham
Publikováno v:
HGG Advances, Vol 2, Iss 4, Pp 100052- (2021)
Summary: The diversity of the U.S. population is currently not reflected in the genomic workforce and across the greater scientific enterprise. Although diversity and inclusion efforts have focused on increasing the number of individuals from underre
Externí odkaz:
https://doaj.org/article/1ab54d78f1c143fd8c066b94441173c0
Publikováno v:
American Journal of Preventive Medicine. 64:477-482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4684058f73ea77bf2b92c1d53b25fa72
https://doi.org/10.1016/j.amepre.2022.10.019
https://doi.org/10.1016/j.amepre.2022.10.019
Publikováno v:
Prenatal Diagnosis. 43:435-442
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cb952d764dedbd567f8f57bdc86a601
https://doi.org/10.1002/pd.6338
https://doi.org/10.1002/pd.6338
Autor:
Vence L. Bonham, Nkeiruka I. Umeh, Brooke A. Cunningham, Khadijah E. Abdallah, Sherrill L. Sellers, Lisa A. Cooper
Publikováno v:
Health Equity, Vol 1, Iss 1, Pp 118-126 (2017)
Purpose: The clinical utility of race and ethnicity has been debated. It is important to understand if and how race and ethnicity are communicated and collected in clinical settings. We investigated physicians' self-reported methods of collecting a p
Externí odkaz:
https://doaj.org/article/e892577c3e384b708c84be1eaa59ce33
Autor:
Paul S, Appelbaum, Wylie, Burke, Erik, Parens, David A, Zeevi, Laura, Arbour, Nanibaa' A, Garrison, Vence L, Bonham, Wendy K, Chung
Publikováno v:
Am J Hum Genet
The underrepresentation of non-European ancestry groups in current genomic databases complicates interpretation of their genetic test results, yielding a much higher prevalence of variants of uncertain significance (VUSs). Such VUS findings can frust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae7610ac51ab7b5f7f22a2c5da6226a
https://doi.org/10.1016/j.ajhg.2022.04.012
https://doi.org/10.1016/j.ajhg.2022.04.012