Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Amelia Li Min Tan"'
Autor:
Griffin M Weber, Harrison G Zhang, Sehi L'Yi, Clara-Lea Bonzel, Chuan Hong, Paul Avillach, Alba Gutiérrez-Sacristán, Nathan P Palmer, Amelia Li Min Tan, Xuan Wang, William Yuan, Nils Gehlenborg, Anna Alloni, Danilo F Amendola, Antonio Bellasi, Riccardo Bellazzi, Michele Beraghi, Mauro Bucalo, Luca Chiovato, Kelly Cho, Arianna Dagliati, Hossein Estiri, Robert W Follett, Noelia García Barrio, David A Hanauer, Darren W Henderson, Yuk-Lam Ho, John H Holmes, Meghan R Hutch, Ramakanth Kavuluru, Katie Kirchoff, Jeffrey G Klann, Ashok K Krishnamurthy, Trang T Le, Molei Liu, Ne Hooi Will Loh, Sara Lozano-Zahonero, Yuan Luo, Sarah Maidlow, Adeline Makoudjou, Alberto Malovini, Marcelo Roberto Martins, Bertrand Moal, Michele Morris, Danielle L Mowery, Shawn N Murphy, Antoine Neuraz, Kee Yuan Ngiam, Marina P Okoshi, Gilbert S Omenn, Lav P Patel, Miguel Pedrera Jiménez, Robson A Prudente, Malarkodi Jebathilagam Samayamuthu, Fernando J Sanz Vidorreta, Emily R Schriver, Petra Schubert, Pablo Serrano Balazote, Byorn WL Tan, Suzana E Tanni, Valentina Tibollo, Shyam Visweswaran, Kavishwar B Wagholikar, Zongqi Xia, Daniela Zöller, Isaac S Kohane, Tianxi Cai, Andrew M South, Gabriel A Brat
Publikováno v:
Journal of Medical Internet Research, Vol 23, Iss 11, p e34625 (2021)
Externí odkaz:
https://doaj.org/article/bb7b0815f77948b3b5652a6b5c0cc28b
Autor:
Griffin M Weber, Harrison G Zhang, Sehi L'Yi, Clara-Lea Bonzel, Chuan Hong, Paul Avillach, Alba Gutiérrez-Sacristán, Nathan P Palmer, Amelia Li Min Tan, Xuan Wang, William Yuan, Nils Gehlenborg, Anna Alloni, Danilo F Amendola, Antonio Bellasi, Riccardo Bellazzi, Michele Beraghi, Mauro Bucalo, Luca Chiovato, Kelly Cho, Arianna Dagliati, Hossein Estiri, Robert W Follett, Noelia García Barrio, David A Hanauer, Darren W Henderson, Yuk-Lam Ho, John H Holmes, Meghan R Hutch, Ramakanth Kavuluru, Katie Kirchoff, Jeffrey G Klann, Ashok K Krishnamurthy, Trang T Le, Molei Liu, Ne Hooi Will Loh, Sara Lozano-Zahonero, Yuan Luo, Sarah Maidlow, Adeline Makoudjou, Alberto Malovini, Marcelo Roberto Martins, Bertrand Moal, Michele Morris, Danielle L Mowery, Shawn N Murphy, Antoine Neuraz, Kee Yuan Ngiam, Marina P Okoshi, Gilbert S Omenn, Lav P Patel, Miguel Pedrera Jiménez, Robson A Prudente, Malarkodi Jebathilagam Samayamuthu, Fernando J Sanz Vidorreta, Emily R Schriver, Petra Schubert, Pablo Serrano Balazote, Byorn WL Tan, Suzana E Tanni, Valentina Tibollo, Shyam Visweswaran, Kavishwar B Wagholikar, Zongqi Xia, Daniela Zöller, Isaac S Kohane, Tianxi Cai, Andrew M South, Gabriel A Brat
Publikováno v:
Journal of Medical Internet Research, Vol 23, Iss 10, p e31400 (2021)
BackgroundMany countries have experienced 2 predominant waves of COVID-19–related hospitalizations. Comparing the clinical trajectories of patients hospitalized in separate waves of the pandemic enables further understanding of the evolving epidemi
Externí odkaz:
https://doaj.org/article/27ff5270bd1848529bda8ca6d11637ce
Autor:
Marie Pereira, Jeong-Hun Ko, John Logan, Hayley Protheroe, Kee-Beom Kim, Amelia Li Min Tan, Peter I Croucher, Kwon-Sik Park, Maxime Rotival, Enrico Petretto, JH Duncan Bassett, Graham R Williams, Jacques Behmoaras
Publikováno v:
eLife, Vol 9 (2020)
Functional characterisation of cell-type-specific regulatory networks is key to establish a causal link between genetic variation and phenotype. The osteoclast offers a unique model for interrogating the contribution of co-regulated genes to in vivo
Externí odkaz:
https://doaj.org/article/3598a6a41082456e82266d54eb35c4ad
Autor:
Esteban J. Parra, E-Shyong Tai, Habiba Alsafar, Enrico Petretto, Jirong Long, Amelia Li Min Tan, Xueling Sim, Yik Ying Teo, Miguel Cruz, Huimei Chen, Qiuju Ding
Publikováno v:
Journal of Human Genetics. 65:411-420
Genome-wide association studies (GWASs) have identified many genetic variations associated with type 2 diabetes mellitus (T2DM) in Asians, but understanding the functional genetic variants that influence traits is often a complex process. In this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15aa7cc40d6fada864559fbe74165016
https://doi.org/10.1038/s10038-019-0720-3
https://doi.org/10.1038/s10038-019-0720-3
Autor:
John G. Logan, Hayley Protheroe, Jeong-Hun Ko, Kee-Beom Kim, Graham R. Williams, Kwon-Sik Park, Jacques Behmoaras, Peter I. Croucher, J. H. Duncan Bassett, Enrico Petretto, Marie Pereira, Maxime Rotival, Amelia Li Min Tan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991238fd233053d2d127caa6b62108de
https://doi.org/10.7554/elife.55549.sa2
https://doi.org/10.7554/elife.55549.sa2
Autor:
John G. Logan, Jeong-Hun Ko, J. H. Duncan Bassett, Hayley Protheroe, Kee-Beom Kim, Graham R. Williams, Enrico Petretto, Jacques Behmoaras, Kwon-Sik Park, Marie Pereira, Maxime Rotival, Amelia Li Min Tan
Functional characterisation of cell-type specific regulatory networks is key to establish a causal link between genetic variation and phenotype. The osteoclast offers a unique model for interrogating the contribution of co-regulated genes to in vivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b468be37181e0e32edc4b7f9980457a
https://doi.org/10.1101/2020.02.13.947705
https://doi.org/10.1101/2020.02.13.947705
Autor:
Jacques Behmoaras, Marie Pereira, Enrico Petretto, Peter I. Croucher, Amelia Li Min Tan, Kwon-Sik Park, Graham R. Williams, J. H. Duncan Bassett, Maxime Rotival, Jeong-Hun Ko, Hayley Protheroe, Kee-Beom Kim, John G. Logan
Publikováno v:
eLife
eLife, 2020, 9, pp.e55549. ⟨10.7554/eLife.55549⟩
eLife, Vol 9 (2020)
eLife, 2020, 9, pp.e55549. ⟨10.7554/eLife.55549⟩
eLife, Vol 9 (2020)
International audience; Functional characterisation of cell-type-specific regulatory networks is key to establish a causal link between genetic variation and phenotype. The osteoclast offers a unique model for interrogating the contribution of co-reg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::493a34e7e75296bafede564fed28020a
https://pubmed.ncbi.nlm.nih.gov/32553114
https://pubmed.ncbi.nlm.nih.gov/32553114
Publikováno v:
COSMOS. 10:25-38
Advances in medical research have shed light on the genetic cause of many human diseases. Gene therapy is a promising approach which can be used to deliver therapeutic genes to treat genetic diseases at its most fundamental level. In general, nonvira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42fbffc33d97fa0796bfa62cdef830ec
https://doi.org/10.1142/s0219607714400059
https://doi.org/10.1142/s0219607714400059
Autor:
Weber, Griffin M.1 (AUTHOR), Zhang, Harrison G.1 (AUTHOR), L'Yi, Sehi1 (AUTHOR), Bonzel, Clara-Lea1 (AUTHOR), Chuan Hong1 (AUTHOR), Avillach, Paul1 (AUTHOR), Gutiérrez-Sacristán, Alba1 (AUTHOR), Palmer, Nathan P.1 (AUTHOR), Amelia Li Min Tan1 (AUTHOR), Xuan Wang1 (AUTHOR), Yuan, William1 (AUTHOR), Gehlenborg, Nils1 (AUTHOR), Alloni, Anna2 (AUTHOR), Amendola, Danilo F.3 (AUTHOR), Bellasi, Antonio4 (AUTHOR), Bellazzi, Riccardo5 (AUTHOR), Beraghi, Michele6 (AUTHOR), Bucalo, Mauro2 (AUTHOR), Chiovato, Luca7 (AUTHOR), Cho, Kelly8 (AUTHOR)
Publikováno v:
Journal of Medical Internet Research. Nov2021, Vol. 23 Issue 11, p1-3. 3p.
Publikováno v:
COSMOS. Dec2014, Vol. 10 Issue 1, p25-38. 14p.