Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fabien, Delahaye"'
Autor:
Natalia Pervjakova, Gunn-Helen Moen, Maria-Carolina Borges, Teresa Ferreira, James P Cook, Catherine Allard, Robin N Beaumont, Mickaël Canouil, Gad Hatem, Anni Heiskala, Anni Joensuu, Ville Karhunen, Soo Heon Kwak, Frederick T J Lin, Jun Liu, Sheryl Rifas-Shiman, Claudia H Tam, Wing Hung Tam, Gudmar Thorleifsson, Toby Andrew, Juha Auvinen, Bishwajit Bhowmik, Amélie Bonnefond, Fabien Delahaye, Ayse Demirkan, Philippe Froguel, Kadri Haller-Kikkatalo, Hildur Hardardottir, Sandra Hummel, Akhtar Hussain, Eero Kajantie, Elina Keikkala, Amna Khamis, Jari Lahti, Tove Lekva, Sanna Mustaniemi, Christine Sommer, Aili Tagoma, Evangelia Tzala, Raivo Uibo, Marja Vääräsmäki, Pia M Villa, Kåre I Birkeland, Luigi Bouchard, Cornelia M Duijn, Sarah Finer, Leif Groop, Esa Hämäläinen, Geoffrey M Hayes, Graham A Hitman, Hak C Jang, Marjo-Riitta Järvelin, Anne Karen Jenum, Hannele Laivuori, Ronald C Ma, Olle Melander, Emily Oken, Kyong Soo Park, Patrice Perron, Rashmi B Prasad, Elisabeth Qvigstad, Sylvain Sebert, Kari Stefansson, Valgerdur Steinthorsdottir, Tiinamaija Tuomi, Marie-France Hivert, Paul W Franks, Mark I McCarthy, Cecilia M Lindgren, Rachel M Freathy, Deborah A Lawlor, Andrew P Morris, Reedik Mägi
Publikováno v:
Hum Mol Genet
Pervjakova, N, Moen, G H, Borges, M C, Ferreira, T, Lawlor, D A & Mägi, R 2022, ' Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes ', Human Molecular Genetics, vol. 31, no. 19, ddac050, pp. 3377-3391 . https://doi.org/10.1093/hmg/ddac050
Hum. Mol. Genet. 31, 3377–3391 (2022)
Human Molecular Genetics, 31(19), 3377-3391. Oxford University Press
Human Molecular Genetics
Pervjakova, N, Moen, G H, Borges, M C, Ferreira, T, Lawlor, D A & Mägi, R 2022, ' Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes ', Human Molecular Genetics, vol. 31, no. 19, ddac050, pp. 3377-3391 . https://doi.org/10.1093/hmg/ddac050
Hum. Mol. Genet. 31, 3377–3391 (2022)
Human Molecular Genetics, 31(19), 3377-3391. Oxford University Press
Human Molecular Genetics
Gestational diabetes mellitus (GDM) is associated with increased risk of pregnancy complications and adverse perinatal outcomes. GDM often reoccurs and is associated with increased risk of subsequent diagnosis of type 2 diabetes (T2D). To improve our
Autor:
Alexandre Pelletier, Arnaud Carrier, Yongmei Zhao, Mickaël Canouil, Mehdi Derhourhi, Emmanuelle Durand, Lionel Berberian-Ferrato, John Greally, Francine Hughes, Philippe Froguel, Amélie Bonnefond, Fabien Delahaye
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 13; Pages: 7323
Excessive fetal growth is associated with DNA methylation alterations in human hematopoietic stem and progenitor cells (HSPC), but their functional impact remains elusive. We implemented an integrative analysis combining single-cell epigenomics, sing
Publikováno v:
Biomolecules, Vol 10, Iss 1359, p 1359 (2020)
Biomolecules
Biomolecules
Worldwide, the number of people with diabetes has quadrupled since 1980 reaching 422 million in 2014 (World Health Organization). This distressing rise in diabetes also affects pregnant women and thus, in regard to early programming of adult diseases
Autor:
Marion Ouidir, Tsegaselassie Workalemahu, Fabien Delahaye, Xuehuo Zeng, Ronald J. Wapner, Cuilin Zhang, Fasil Tekola-Ayele
Publikováno v:
Clinical Epigenetics
Background Birthweight marks an important milestone of health across the lifespan, including cardiometabolic disease risk in later life. The placenta, a transient organ at the maternal-fetal interface, regulates fetal growth. Identifying genetic loci
Autor:
Yu Kong, Benjamin Tycko, Martha Salas, Fabien Delahaye, Francine Hughes, Catherine Do, Ronald J. Wapner, Remi Ashkar
Publikováno v:
PLoS Genetics, Vol 14, Iss 11, p e1007785 (2018)
PLoS Genetics
PLoS Genetics
From genomic association studies, quantitative trait loci analysis, and epigenomic mapping, it is evident that significant efforts are necessary to define genetic-epigenetic interactions and understand their role in disease susceptibility and progres
Autor:
Ronald J. Wapner, Martha Salas, Ben Tycko, Remi Ashkar, Catherine Do, Yu Kong, Fabien Delahaye, Francine Hughes
Publikováno v:
PLoS Genetics, Vol 15, Iss 4, p e1008118 (2019)
[This corrects the article DOI: 10.1371/journal.pgen.1007785.].
Autor:
J Tozour, John M. Greally, N A Wijetunga, Marien Pascual, M Adeyeye, A W Wolkoff, Amit Verma, M Alani, Fabien Delahaye
Publikováno v:
Oncogene
The predisposition of patients with Hepatitis C virus (HCV) infection to hepatocellular carcinoma (HCC) involves components of viral infection, inflammation and time. The development of multifocal, genetically distinct tumours is suggestive of a fiel
Publikováno v:
American Journal of Obstetrics and Gynecology. 214:S136-S137
Autor:
Andrew D. Johnston, N. Ari Wijetunga, Netha Ulahannan, Kami Kim, Ryo Maekawa, John M. Greally, Fabien Delahaye
Publikováno v:
BMC Bioinformatics
Background The molecular assays that test gene expression, transcriptional, and epigenetic regulation are increasingly diverse and numerous. The information generated by each type of assay individually gives an insight into the state of the cells tes