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Frontiers in Pharmacology|May 28, 2020
Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With EpilepsyCarlos Alberto Calderon-Ospina, Jubby Marcela Galvez, Claudia López-Cabra, et al.
Scientific Reports|January 14, 2016
Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsiaAurélien Ducat, Ludivine Doridot, Rosamaria Calicchio, et al.
Plos One|March 20, 2012
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian FailureSandrine Caburet, Petra Zavadakova, Ziva Ben-Neriah, et al.
Human Genomics|June 18, 2015
Success stories in genomic medicine from resource-limited countriesKonstantinos Mitropoulos, Hayat Al Jaibeji, Diego A Forero, et al.
Human Genetics|October 24, 2019
Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysisDora Janeth Fonseca, Luz Adriana Caro, Diana Carolina Sierra-Díaz, et al.
Hypertension (Dallas, Tex. : 1979)|November 8, 2006
Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsiaSonia T Chelbi, Françoise Mondon, Hélène Jammes, et al.
European Journal of Endocrinology|April 29, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failurePaul Laissue, Sophie Christin-Maitre, Philippe Touraine, et al.
Pregnancy Hypertension|October 15, 2020
Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencingKaren Marcela Jiménez, Adrien Morel, Laura Parada-Niño, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 20, 2012
CITED2 mutations potentially cause idiopathic premature ovarian failureDora Janeth Fonseca, Diego Ojeda, Besma Lakhal, et al.
Open Biology|November 3, 2016
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humansPaul Laissue, Besma Lakhal, Magalie Vatin, et al.
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