Alobar holoprosencephaly: Exploring mothers' perspectives on prenatal decision-making and prognostication.
Elfarawi, H; Tolusso, L; McGowan, ML; Cortezzo, DM; Vawter-Lee, M.
Prenatal Diagnosis.
2022;
42:617-627.
Perinatal Outcomes of Fetuses and Infants Diagnosed with Trisomy 13 or Trisomy 18.
Cortezzo, DE; Tolusso, LK; Swarr, DT.
Journal of Pediatrics.
2022.
eP248: Impact of DNA methylation signature exploration for variants of uncertain significance within epigenetic syndromes.
Gittens, O; Qu'd, D; Tolusso, L; Brightman, D; Kerkhof, J; Owens, J; Saal, H; Ayala, SS; Shillington, A; Widmeyer, K; et al.
Genetics in Medicine.
2022;
24:s157-s158.
Experiences of reproductive genetic counselors with abortion regulations in Ohio.
Heuerman, AC; Bessett, D; Matheny Antommaria, AH; Tolusso, LK; Smith, N; Norris, AH; McGowan, ML.
Journal of Genetic Counseling.
2021.
Beyond Diagnostic Yield: Prenatal Exome Sequencing Results in Maternal, Neonatal, and Familial Clinical Management Changes.
Tolusso, LK; Hazelton, P; Wong, B; Swarr, DT.
Obstetrical and Gynecological Survey.
2021;
76:663-664.
Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes.
Tolusso, LK; Hazelton, P; Wong, B; Swarr, DT.
Genetics in Medicine.
2021;
23:909-917.
eP372 Experience of targeted exome analyses of 130 patients with diverse inborn error of immunity phenotypes.
Sun, M; Tolusso, L; Dawson, B; Zhang, WZ; Zhang, K; Bleesing, J; Marsh, R.
Molecular Genetics and Metabolism.
2021;
132.
Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes.
Abell, K; Tolusso, L; Smith, N; Hopkin, R; Vawter-Lee, M; Habli, M; Riddle, S; Calvo-Garcia, MA; Guan, Q; Bierbrauer, K; et al.
Birth Defects Research.
2020;
112:1733-1737.
Aneuploid embryo transfer: clinical policies and provider opinions at United States fertility clinics.
McGowan, R; Pilipenko, V; Smolarek, TA; West, E; Tolusso, LK.
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).
Kellner, ES; Rathbun, PA; Marshall, GS; Tolusso, LK; Smolarek, TA; Sun, M; Chandra, S; Bleesing, J; Marsh, RA.
Journal of Clinical Immunology.
2019;
39:857-859.