Sarah Guterman
Hôpital Necker-Enfants Malades(FR)Assistance Publique – Hôpitaux de Paris(FR)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Congenital heart defects research, Birth, Development, and Health, Prenatal Screening and Diagnostics, Infant Nutrition and Health
Most-Cited Works
- → Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France(2019)43 cited
- → 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients(2022)33 cited
- → Intervention to Decrease Glyburide Use in Elderly Patients With Renal Insufficiency(2011)30 cited
- → Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renal-hepatic-pancreatic dysplasia(2020)26 cited
- → Autoimmune disorders but not heparin are associated with cell-free fetal DNA test failure(2018)25 cited
- → Laparoscopy in the second and third trimesters of pregnancy for abdominal surgical emergencies(2017)25 cited
- → Prenatal findings in 1p36 deletion syndrome: New cases and a literature review(2019)20 cited
- → First prenatal diagnosis of a ‘pure’ 9q34.3 deletion (Kleefstra syndrome): A case report and literature review(2017)11 cited
- → 174: Is extending the second stage of labor in women with an occiput-posterior position beneficial and safe?(2018)1 cited
- → OP01.09: Prediction of birthweight in SGA at 11–13+6 weeks using maternal history, LMP, ultrasound and biochemistry(2017)