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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.
Molecular Medicine (Cambridge, Mass.)|August 10, 2019
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsiaPaula Quintero-Ronderos, Karen Marcela Jiménez, Clara Esteban-Pérez, 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.
Journal of Personalized Medicine|June 2, 2021
A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel TherapyMariana Angulo-Aguado, Karen Panche, Caroll Andrea Tamayo-Agudelo, et al.
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