Genetics, Fetal Care
Perinatal Outcomes of Fetuses and Infants Diagnosed with Trisomy 13 or Trisomy 18. Journal of Pediatrics. 2022; 247:116-123.e5.
Experiences of reproductive genetic counselors with abortion regulations in Ohio. Journal of Genetic Counseling. 2022; 31:641-652.
Alobar holoprosencephaly: Exploring mothers' perspectives on prenatal decision-making and prognostication. Prenatal Diagnosis. 2022; 42:617-627.
Beyond Diagnostic Yield: Prenatal Exome Sequencing Results in Maternal, Neonatal, and Familial Clinical Management Changes. Obstetrical and Gynecological Survey. 2021; 76:663-664.
Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes. Genetics in Medicine. 2021; 23:909-917.
eP372 Experience of targeted exome analyses of 130 patients with diverse inborn error of immunity phenotypes. Molecular Genetics and Metabolism. 2021; 132.
Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes. Birth Defects Research. 2020; 112:1733-1737.
Aneuploid embryo transfer: clinical policies and provider opinions at United States fertility clinics. Fertility and Sterility. 2020; 114:110-117.
The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1). Journal of Clinical Immunology. 2019; 39:857-859.
Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population: Who, When, How, and at What Cost?. Journal of Pediatrics. 2019; 213:211-217.e4.
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