| A review of trisomy X (47, XXX) NR Tartaglia, S Howell, A Sutherland, R Wilson, L Wilson Orphanet journal of rare diseases 5, 1-9, 2010 | 397 | 2010 |
| 48, XXYY, 48, XXXY and 49, XXXXY syndromes: not just variants of Klinefelter syndrome N Tartaglia, N Ayari, S Howell, C D’Epagnier, P Zeitler Acta paediatrica 100 (6), 851-860, 2011 | 224 | 2011 |
| The spectrum of the behavioral phenotype in boys and adolescents 47, XXY (Klinefelter syndrome) N Tartaglia, L Cordeiro, S Howell, R Wilson, J Janusz Pediatric endocrinology reviews: PER 8 (0 1), 151, 2010 | 125 | 2010 |
| Advances in the interdisciplinary care of children with Klinefelter syndrome S Davis, S Howell, R Wilson, T Tanda, J Ross, P Zeitler, N Tartaglia Advances in pediatrics 63 (1), 15-46, 2016 | 97 | 2016 |
| Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis K Wigby, C D'Epagnier, S Howell, A Reicks, R Wilson, L Cordeiro, ... American journal of medical genetics Part A 170 (11), 2870-2881, 2016 | 95 | 2016 |
| Clinical developmental, neuropsychological, and social–emotional features of Turner syndrome C Hutaff‐Lee, E Bennett, S Howell, N Tartaglia American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2019 | 71 | 2019 |
| Timing of diagnosis of 47, XXY and 48, XXYY: a survey of parent experiences J Visootsak, N Ayari, S Howell, J Lazarus, N Tartaglia American Journal of Medical Genetics Part A 161 (2), 268-272, 2013 | 50 | 2013 |
| The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy N Tartaglia, S Howell, R Wilson, J Janusz, R Boada, S Martin, JB Frazier, ... Journal of Multidisciplinary Healthcare, 323-334, 2015 | 44 | 2015 |
| Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors … N Tartaglia, S Howell, S Davis, K Kowal, T Tanda, M Brown, C Boada, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2020 | 42 | 2020 |
| “How should I tell my child?” Disclosing the diagnosis of sex chromosome aneuploidies A Dennis, S Howell, L Cordeiro, N Tartaglia Journal of genetic counseling 24, 88-103, 2015 | 38 | 2015 |
| Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies T Thompson, S Howell, S Davis, R Wilson, J Janusz, R Boada, L Pyle, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2020 | 26 | 2020 |
| Evaluation of prognostic risk models for postoperative pulmonary complications in adult patients undergoing major abdominal surgery: a systematic review and international … O Kouli, V Murray, S Bhatia, WA Cambridge, M Kawka, S Shafi, SR Knight, ... The Lancet Digital Health 4 (7), e520-e531, 2022 | 23 | 2022 |
| A mixed methods study of physical activity and quality of life in adolescents with Turner syndrome T Thompson, B Zieba, S Howell, W Karakash, S Davis American Journal of Medical Genetics Part A 182 (2), 386-396, 2020 | 20 | 2020 |
| Diminished ovarian reserve in girls and adolescents with trisomy X syndrome SM Davis, K Soares, S Howell, M Cree-Green, E Buyers, J Johnson, ... Reproductive Sciences 27, 1985-1991, 2020 | 17 | 2020 |
| A review of trisomy X (47, XXX) Orphanet J Rare Dis. 2010; 5: 8. doi: 10.1186 NR Tartaglia, S Howell, A Sutherland, R Wilson, L Wilson Europe PMC free article][Abstract][CrossRef][Google Scholar], 0 | 16 | |
| Executive function in XXY: comparison of performance‐based measures and rating scales J Janusz, C Harrison, C Boada, L Cordeiro, S Howell, N Tartaglia, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2020 | 14 | 2020 |
| Clinical phenotype and management of individuals with mosaic monosomy X with Y chromosome material stratified by genital phenotype L Guzewicz, S Howell, CE Crerand, H Umbaugh, NJ Nokoff, J Barker, ... American Journal of Medical Genetics Part A 185 (5), 1437-1447, 2021 | 12 | 2021 |
| Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey T Thompson, S Davis, J Janusz, E Frith, L Pyle, S Howell, R Boada, ... Journal of school psychology 93, 28-40, 2022 | 8 | 2022 |
| Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies K Hager, K Jennings, S Hosono, S Howell, JR Gruen, SA Rivkees, ... International Journal of Pediatric Endocrinology 2012, 1-10, 2012 | 7 | 2012 |
| Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome T Dowlut-McElroy, S Davis, S Howell, I Gutmark-Little, V Bamba, ... American journal of obstetrics and gynecology 227 (6), 862-870, 2022 | 6 | 2022 |
