Leandra Tolusso.

Leandra K. Tolusso, MS, LGC


  • Genetic Counselor, Division of Human Genetics

About

Publications

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.