Carole A Samango-Sprouse (Carole Samango-Sprouse)

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 20

Top Topics

Anterior Cruciate Ligament

Replacement Therapy

Traumatic Brain Injury

Top Venues

American journal of medical genetics. Part A

Prenatal diagnosis

Clinical epigenetics

This page only lists publications with an associated author ORCID identifier.

Publications

Mary P Hamzik, Andrea L Gropman, Michaela R Brooks, Sherida Powell, Teresa Sadeghin, Carole A Samango-Sprouse
The Effect of Hormonal Therapy on the Behavioral Outcomes in 47,XXY (Klinefelter Syndrome) between 7 and 12 Years of Age. Genes 14 (7) (2023)
Adrianna K San Roman, Helen Skaletsky, Alexander K Godfrey, Neha V Bokil, Levi Teitz, Isani Singh, Laura V Blanton, Daniel W Bellott, Tatyana Pyntikova, Julian Lange, Natalia Koutseva, Jennifer F Hughes, Laura Brown, Sidaly Phou, Ashley Buscetta, Paul S Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C Lasutschinkow, Colleen Keen, Shanlee M Davis, Angela E Lin, Nicole R Tartaglia, Carole A Samango-Sprouse, Maximilian Muenke, David C Page
The human Y and inactive X chromosomes similarly modulate autosomal gene expression. bioRxiv : the preprint server for biology (2023)
Carole A Samango-Sprouse, Michaela Reiko Brooks, Patricia Lasutchinkow, Teresa Sadeghin, Sherida Powell, Mary Pat Hamzik, Sophia Song, Andrea L Gropman
The effect of early hormonal treatment (EHT) on expressive and receptive language capabilities in boys with 47,XXY (Klinefelter syndrome) during infancy and early childhood. Genetics in medicine : official journal of the American College of Medical Genetics 23 (6) (2021)
Richard S Lee, Sophia Q Song, Henri M Garrison-Desany, Jenny L Carey, Patricia Lasutschinkow, Andrew Zabel, Joseph Bressler, Andrea Gropman, Carole A Samango-Sprouse
DNA methylation and behavioral dysfunction in males with 47,XXY and 49,XXXXY: a pilot study. Clinical epigenetics 13 (1) (2021)
Carole A Samango-Sprouse, Patricia C Lasutschinkow, Michael McLeod, Grace F Porter, Sherida Powell, Jillyan St Laurent, Teresa Sadeghin, Andrea L Gropman
Speech and language development in children with 49,XXXXY syndrome. American journal of medical genetics. Part A 185 (12) (2020)
Carole A Samango-Sprouse, Debra Counts, Andrea Gropman, null null
Insight versus hindsight: What we have learned after 17 years of research with sex chromosome abnormalities. American journal of medical genetics. Part A 185 (3) (2020)
Carole A Samango-Sprouse, Patricia C Lasutschinkow, Francie Mitchell, Grace F Porter, Patricia Hendrie, Sherida Powell, Teresa Sadeghin, Andrea Gropman
49,XXXXY syndrome: A study of neurological function in this uncommon X and Y chromosomal disorder. American journal of medical genetics. Part A 185 (12) (2020)
Patricia C Lasutschinkow, Andrea L Gropman, Grace F Porter, Teresa Sadeghin, Carole A Samango-Sprouse
Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety-related symptoms and intact social awareness. American journal of medical genetics. Part A 182 (5) (2020)
Carole A Samango-Sprouse, Selena L Tran, Patricia C Lasutschinkow, Teresa Sadeghin, Sherida Powell, Francie L Mitchell, Andrea Gropman
Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapy. American journal of medical genetics. Part A 182 (8) (2020)
Andrea L Gropman, Grace F Porter, Patricia C Lasutschinkow, Teresa Sadeghin, Elizabeth S Tipton, Sherida Powell, Carole A Samango-Sprouse
Neurocognitive development and capabilities in boys with 49,XXXXY syndrome. American journal of medical genetics. Part A 185 (12) (2020)
Laura Tosi, Francie Mitchell, Grace F Porter, Leigh Ruland, Andrea Gropman, Patricia C Lasutschinkow, Selena L Tran, Elmer N Rajah, Austin P Gillies, Patricia Hendrie, Rick Peret, Teresa Sadeghin, Carole A Samango-Sprouse
Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY. American journal of medical genetics. Part A 185 (12) (2020)
Carole A Samango-Sprouse, Andrea L Gropman
Introduction: Comprehensive investigation into an international cohort of boys with 49,XXXXY. American journal of medical genetics. Part A 185 (12) (2020)
Debra R Counts, Christine Yu, Patricia C Lasutschinkow, Teresa Sadeghin, Andrea Gropman, Carole A Samango-Sprouse
Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndrome. American journal of medical genetics. Part A 185 (12) (2020)
Selena L Tran, Carole A Samango-Sprouse, Teresa Sadeghin, Sherida Powell, Andrea L Gropman
Hormonal replacement therapy and its potential influence on working memory and competency/adaptive functioning in 47,XXY (Klinefelter syndrome). American journal of medical genetics. Part A 179 (12) (2019)
Carole A Samango-Sprouse, Debra R Counts, Selena L Tran, Patricia C Lasutschinkow, Grace F Porter, Andrea L Gropman
Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome). The application of clinical genetics 12 (2019)
Carole A Samango-Sprouse, Patricia Lasutschinkow, Sherida Powell, Teresa Sadeghin, Andrea Gropman
The incidence of anxiety symptoms in boys with 47,XXY (Klinefelter syndrome) and the possible impact of timing of diagnosis and hormonal replacement therapy. American journal of medical genetics. Part A 179 (3) (2019)
Carole A Samango-Sprouse, Grace F Porter, Patricia C Lasutschinkow, Selena L Tran, Teresa Sadeghin, Andrea L Gropman
Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs). Prenatal diagnosis 40 (4) (2019)
Carole A Samango-Sprouse, Emily Stapleton, Selena Chea, Patrick Lawson, Teresa Sadeghin, Chris Cappello, Leo de Sonneville, Sophie van Rijn
International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences. American journal of medical genetics. Part A 176 (4) (2018)
Carole A Samango-Sprouse, Colleen Keen, Teresa Sadeghin, Andrea L Gropman
The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome). Prenatal diagnosis 37 (5) (2017)
Carole A Samango-Sprouse, Eser Kırkızlar, Megan P Hall, Patrick Lawson, Zachary Demko, Susan M Zneimer, Kirsten J Curnow, Susan Gross, Andrea Gropman
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population. PloS one 11 (8) (2016)