Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Samantha L. Rosenthal"'
Autor:
Jenna C. Carlson, Mohanraj Krishnan, Samantha L. Rosenthal, Emily M. Russell, Jerry Z. Zhang, Nicola L. Hawley, Jaye Moors, Hong Cheng, Nicola Dalbeth, Janak R. de Zoysa, Huti Watson, Muhammad Qasim, Rinki Murphy, Take Naseri, Muagututi’a Sefuiva Reupena, Satupa‘itea Viali, Lisa K. Stamp, John Tuitele, Erin E. Kershaw, Ranjan Deka, Stephen T. McGarvey, Tony R. Merriman, Daniel E. Weeks, Ryan L. Minster
Publikováno v:
HGG Advances, Vol 4, Iss 1, Pp 100155- (2023)
Summary: Current understanding of lipid genetics has come mainly from studies in European-ancestry populations; limited effort has focused on Polynesian populations, whose unique population history and high prevalence of dyslipidemia may provide insi
Externí odkaz:
https://doaj.org/article/733af63f641347d89dd47716fcd3a8aa
Autor:
Jitendra S Kanshana, Polly E Mattila, Michael C Ewing, Ashlee N Wood, Gabriele Schoiswohl, Anna C Meyer, Aneta Kowalski, Samantha L Rosenthal, Sebastien Gingras, Brett A Kaufman, Ray Lu, Daniel E Weeks, Stephen T McGarvey, Ryan L Minster, Nicola L Hawley, Erin E Kershaw
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0251895 (2021)
Obesity and diabetes have strong heritable components, yet the genetic contributions to these diseases remain largely unexplained. In humans, a missense variant in Creb3 regulatory factor (CREBRF) [rs373863828 (p.Arg457Gln); CREBRFR457Q] is strongly
Externí odkaz:
https://doaj.org/article/89877e3193b84a7a9605cc11de25289c
Autor:
Jenna C. Carlson, Mohanraj Krishnan, Samantha L. Rosenthal, Emily M. Russell, Jerry Z. Zhang, Nicola L. Hawley, Jaye Moors, Hong Cheng, Nicola Dalbeth, Janak R. de Zoysa, Huti Watson, Muhammad Qasim, Rinki Murphy, Take Naseri, Muagututi’a Sefuiva Reupena, Satupa‘itea Viali, Lisa K. Stamp, John Tuitele, Erin E. Kershaw, Ranjan Deka, Stephen T. McGarvey, Tony R. Merriman, Daniel E. Weeks, Ryan L. Minster.
Current understanding of lipid genetics has come mainly from studies in European-ancestry populations; limited effort has focused on Polynesian populations, whose unique population history and high prevalence of dyslipidemia may provide insight into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8aa27ad3708294c09d5d2b029a76653
https://doi.org/10.1101/2022.06.22.22276448
https://doi.org/10.1101/2022.06.22.22276448
Autor:
Jenna C, Carlson, Mohanraj, Krishnan, Samantha L, Rosenthal, Emily M, Russell, Jerry Z, Zhang, Nicola L, Hawley, Jaye, Moors, Hong, Cheng, Nicola, Dalbeth, Janak R, de Zoysa, Huti, Watson, Muhammad, Qasim, Rinki, Murphy, Take, Naseri, Muagututi'a Sefuiva, Reupena, Satupa'itea, Viali, Lisa K, Stamp, John, Tuitele, Erin E, Kershaw, Ranjan, Deka, Stephen T, McGarvey, Tony R, Merriman, Daniel E, Weeks, Ryan L, Minster
Publikováno v:
HGG advances. 4(1)
Current understanding of lipid genetics has come mainly from studies in European-ancestry populations; limited effort has focused on Polynesian populations, whose unique population history and high prevalence of dyslipidemia may provide insight into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3faf413a35ba8a44ff880a3f7fd68ec0
https://pubmed.ncbi.nlm.nih.gov/36340932
https://pubmed.ncbi.nlm.nih.gov/36340932
Autor:
M. Ilyas Kamboh, Eleanor Feingold, Kang-Hsien Fan, F. Yesim Demirci, Oscar L. Lopez, Samantha L. Rosenthal, Mary Ganguli
Publikováno v:
J Alzheimers Dis
The genetics of late-onset Alzheimer's disease (AD) is complex due to the heterogeneous nature of the disorder. APOE*4 is the strongest genetic risk factor for AD. Genome-wide association studies have identified more than 30 additional loci, each hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aad15e74e94612a79ca492f2b36b6d7
https://doi.org/10.3233/jad-200037
https://doi.org/10.3233/jad-200037
Autor:
Nicola L. Hawley, Ray Lu, Stephen T. McGarvey, Anna C. Meyer, Polly E. Mattila, Gabriele Schoiswohl, Michael Ewing, Sebastien Gingras, Erin E. Kershaw, Daniel E. Weeks, Ashlee N Wood, Aneta Kowalski, Brett A. Kaufman, Ryan L. Minster, Samantha L. Rosenthal, Jitendra S. Kanshana
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 9, p e0251895 (2021)
PLoS ONE, Vol 16, Iss 9, p e0251895 (2021)
Obesity and diabetes have strong heritable components, yet the genetic contributions to these diseases remain largely unexplained. In humans, a missense variant in Creb3 regulatory factor (CREBRF) [rs373863828 (p.Arg457Gln); CREBRFR457Q] is strongly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::903e3f3413f4aa8bf2b5a92c80c296a6
http://europepmc.org/articles/PMC8439463
http://europepmc.org/articles/PMC8439463
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e95152 (2014)
Late-onset Alzheimer's disease (LOAD) is a multifactorial disorder with over twenty loci associated with disease risk. Given the number of genome-wide significant variants that fall outside of coding regions, it is possible that some of these variant
Externí odkaz:
https://doaj.org/article/623033e9ca72455b85f5ec18843261f1
Autor:
Jitendra S. Kanshana, Erin E. Kershaw, Samantha L. Rosenthal, Nicola L. Hawley, Dan E Weeks, Ashlee N Wood, Aneta Kowalski, Ray Lu, Sebastien Gingras, Brett A. Kaufman, Gabriele Schoiswohl, Polly E. Mattila, Stephen T. McGarvey, Michael Ewing, Anna C. Meyer, Ryan L. Minster
Obesity and diabetes have strong heritable components, yet the genetic contributions to these diseases remain largely unexplained. In humans, a missense variant in Creb3 regulatory factor (CREBRF) [rs373863828 (p.Arg457Gln); CREBRFR457Q] is strongly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff9d2a33c29065a617f3a523df014f35
https://doi.org/10.1101/2021.05.06.442909
https://doi.org/10.1101/2021.05.06.442909
Autor:
John Tuitele, Daniel E. Weeks, Ranjan Deka, Stephen T. McGarvey, Hong Cheng, Samantha L. Rosenthal, Take Naseri, Muagututi‘a Sefuiva Reupena, Emily M. Russell, Guangyun Sun, Nicola L. Hawley, Ryan L. Minster, Jenna C. Carlson
Publikováno v:
Am J Hum Biol
ObjectivesStudies have demonstrated that rs373863828, a missense mutation in CREBRF, is associated with a number of anthropometric traits including body mass index (BMI), obesity, percent body fat, hip circumference, and abdominal circumference. Give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::290c10437b4b51780b8014bde00eb0d2
https://doi.org/10.1002/ajhb.23414
https://doi.org/10.1002/ajhb.23414
Autor:
Viali Lameko, Folla Unasa, Lupesina Vesi, Nicola L. Hawley, Courtney C Choy, Muagututia Sefuiva Reupena, Corina Penaia, Seipepa Unasa, Sophie B. To, Christina Soti-Ulberg, Ranjan Deka, Angela T Prescott, Gloria Siufaga, Scott E. Crouter, Lauren C LaMonica, Rachel L. Duckham, Tracy Fatu, Jenna C. Carlson, Vaimoana Lupematisila, Stephen T. McGarvey, Zsolt Urban, Ryan L. Minster, Samantha L. Rosenthal, Alysa Pomer, Take Naseri, Susan Redline, Daniel E. Weeks, Erin E. Kershaw, Abigail I. Wetzel, Anna C Rivara, Kima Faasalele-Savusa, Melania Selu
Publikováno v:
JMIR Research Protocols
JMIR Research Protocols, Vol 9, Iss 7, p e17329 (2020)
JMIR Research Protocols, Vol 9, Iss 7, p e17329 (2020)
Background The prevalence of obesity and diabetes in Samoa, like many other Pacific Island nations, has reached epidemic proportions. Although the etiology of these conditions can be largely attributed to the rapidly changing economic and nutritional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a64c88772b5963ab1dc738203b93449
https://doi.org/10.2196/17329
https://doi.org/10.2196/17329