Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alex Drong"'
Autor:
Stephanie Shiau, Leishen Wang, Huikun Liu, Yinan Zheng, Alex Drong, Brian T. Joyce, Jun Wang, Weiqin Li, Junhong Leng, Yun Shen, Ru Gao, Gang Hu, Lifang Hou, Andrea A. Baccarelli
Publikováno v:
Epigenetics, Vol 16, Iss 2, Pp 186-195 (2021)
Background: We investigated the association between prenatal GDM exposure and offspring DNA methylation (DNAm) age at 3–10 years of age in the Tianjin GDM Observational Study. Methods: This study included 578 GDM and 578 non-GDM mother-child pairs.
Externí odkaz:
https://doaj.org/article/ed38859407534e27a6e4a719a2e371c9
Autor:
Felix Day, Tugce Karaderi, Michelle R Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Magi, Richa Saxena, Triin Laisk, Margrit Urbanek, M Geoffrey Hayes, Gudmar Thorleifsson, Juan Fernandez-Tajes, Anubha Mahajan, Benjamin H Mullin, Bronwyn G A Stuckey, Timothy D Spector, Scott G Wilson, Mark O Goodarzi, Lea Davis, Barbara Obermayer-Pietsch, André G Uitterlinden, Verneri Anttila, Benjamin M Neale, Marjo-Riitta Jarvelin, Bart Fauser, Irina Kowalska, Jenny A Visser, Marianne Andersen, Ken Ong, Elisabet Stener-Victorin, David Ehrmann, Richard S Legro, Andres Salumets, Mark I McCarthy, Laure Morin-Papunen, Unnur Thorsteinsdottir, Kari Stefansson, andMe Research Team, Unnur Styrkarsdottir, John R B Perry, Andrea Dunaif, Joop Laven, Steve Franks, Cecilia M Lindgren, Corrine K Welt
Publikováno v:
PLoS Genetics, Vol 15, Iss 12, p e1008517 (2019)
[This corrects the article DOI: 10.1371/journal.pgen.1007813.].
Externí odkaz:
https://doaj.org/article/758400ebfc3d4b0da53963dd663aaad5
Autor:
Felix Day, Tugce Karaderi, Michelle R Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Magi, Richa Saxena, Triin Laisk, Margrit Urbanek, M Geoffrey Hayes, Gudmar Thorleifsson, Juan Fernandez-Tajes, Anubha Mahajan, Benjamin H Mullin, Bronwyn G A Stuckey, Timothy D Spector, Scott G Wilson, Mark O Goodarzi, Lea Davis, Barbara Obermayer-Pietsch, André G Uitterlinden, Verneri Anttila, Benjamin M Neale, Marjo-Riitta Jarvelin, Bart Fauser, Irina Kowalska, Jenny A Visser, Marianne Andersen, Ken Ong, Elisabet Stener-Victorin, David Ehrmann, Richard S Legro, Andres Salumets, Mark I McCarthy, Laure Morin-Papunen, Unnur Thorsteinsdottir, Kari Stefansson, andMe Research Team, Unnur Styrkarsdottir, John R B Perry, Andrea Dunaif, Joop Laven, Steve Franks, Cecilia M Lindgren, Corrine K Welt
Publikováno v:
PLoS Genetics, Vol 14, Iss 12, p e1007813 (2018)
Polycystic ovary syndrome (PCOS) is a disorder characterized by hyperandrogenism, ovulatory dysfunction and polycystic ovarian morphology. Affected women frequently have metabolic disturbances including insulin resistance and dysregulation of glucose
Externí odkaz:
https://doaj.org/article/c68abd5b52b94dbab11b2cca436008a6
Autor:
Brian T. Joyce, Alex Drong, Weiqin Li, Leishen Wang, Lifang Hou, Ru Gao, Jun Wang, Yun Shen, Stephanie Shiau, Junhong Leng, Yinan Zheng, Andrea A. Baccarelli, Huikun Liu, Gang Hu
Publikováno v:
Epigenetics
Background: We investigated the association between prenatal GDM exposure and offspring DNA methylation (DNAm) age at 3–10 years of age in the Tianjin GDM Observational Study. Methods: This study included 578 GDM and 578 non-GDM mother-child pairs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e830bb1bcfd48796ebdadba49880026
https://doi.org/10.1080/15592294.2020.1790924
https://doi.org/10.1080/15592294.2020.1790924
Autor:
Sissel Juul, Alex Drong, Xiaoguang Dai, Celine Chen, Ariel Swett, Ronan Chaligne, Irene M. Ghobrial, Scott F. Hickey, Neville Dusaj, Daniel H. Wiseman, Paulina Chamely, Justin Taylor, Tarek H. Mouhieddine, Allegra G. Hawkins, Lloyd Kluegel, Omar Abdel-Wahab, Franco Izzo, John Beaulaurier, Dan A. Landau, Eoghan D. Harrington, Federico Gaiti
Publikováno v:
Blood. 138:145-145
Splicing factor mutations are recurrent genetic alterations in blood disorders, highlighting the importance of alternative splicing regulation in hematopoiesis. Specifically, mutations in splicing factor 3B subunit 1 (SF3B1) are implicated in the pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a76e4f51d5b389bcaeca9695f2837ea
https://doi.org/10.1182/blood-2021-147529
https://doi.org/10.1182/blood-2021-147529
Autor:
Weiqin Li, Leishen Wang, Ru Gao, Brian T. Joyce, Yun Shen, Yinan Zheng, Jun Wang, Drew Nannini, Andrea A. Baccarelli, Junhong Leng, Stephanie Shiau, Gang Hu, Alex Drong, Huikun Liu, Lifang Hou
Publikováno v:
Circulation. 139
Background: Gestational diabetes mellitus (GDM) is a known risk factor for macrosomia, with recent estimates suggesting that between 15-45% of newborns of mothers with GDM are macrosomic (vs. 12% in non-GDM mothers). This study’s objectives were to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0171d53b0dfa708587334de4827ce4b2
https://doi.org/10.1161/circ.139.suppl_1.p073
https://doi.org/10.1161/circ.139.suppl_1.p073