Researcher profile · Semantic Scholar

S. Noblin

h-index: 12
Works: 24
Citations: 530

Most-cited papers

NSGC Practice Guideline: Prenatal Screening and Diagnostic Testing Options for Chromosome Aneuploidy
K. L. Wilson, Jennifer L. Czerwinski, J. Hoskovec, S. Noblin +6 more
2013Journal of Genetic Counseling147 citations
Semantic Scholar
2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling
D. Doyle, Rawan I. Awwad, J. Austin, Bonnie J. Baty +16 more
2016Journal of Genetic Counseling59 citations Open access
Semantic Scholar
Indications for genetic referral: a guide for healthcare providers
B. Pletcher, H. Toriello, S. Noblin, L. Seaver +3 more
2007Genetics in Medicine57 citations Open access
Semantic Scholar
The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Individuals with Li-Fraumeni Syndrome
J. Ross, J. Bojadzieva, S. Peterson, S. Noblin +3 more
2017Genetics in Medicine47 citations Open access
Semantic Scholar
Exploring the Role of Religiosity and Spirituality in Amniocentesis Decision-Making Among Latinas
S. G. Seth, Thomas J. Goka, Andrea Harbison, L. Hollier +3 more
2011Journal of Genetic Counseling38 citations Open access
Semantic Scholar
Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States
Ginger J. Tsai, C. Cameron, Jennifer L. Czerwinski, H. Mendez-Figueroa +2 more
2017Journal of Genetic Counseling25 citations Open access
Semantic Scholar
Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas.
Georgiann Garza, Priscila Hodges-Delgado, J. Hoskovec, G. Palos +3 more
2020Journal of Genetic Counseling18 citations
Semantic Scholar
Undergraduate Student Perceptions and Awareness of Genetic Counseling
A. Gerard, S. Noblin, S. S. Hashmi, Andrew J. Bean +4 more
2018Journal of Genetic Counseling17 citations
Semantic Scholar
Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model
S. Thompson, S. Noblin, J. Lemons, S. Peterson +2 more
2015Journal of Genetic Counseling17 citations Open access
Semantic Scholar
Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1)
Kayla Rosnau, S. S. Hashmi, H. Northrup, J. Slopis +2 more
2017Journal of Genetic Counseling16 citations Open access
Semantic Scholar
National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions
L. Senter, R. Bennett, A. Madeo, S. Noblin +5 more
2018Journal of Genetic Counseling13 citations
Semantic Scholar
First Neonatal Demise with Travel-Associated Zika Virus Infection in the United States of America
N. Zacharias, J. Whitty, S. Noblin, S. Tsakiri +6 more
2017American Journal of Perinatology Reports13 citations Open access
Semantic Scholar
The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers
Leslie Durham, R. Papanna, B. Stevens, S. Noblin +3 more
2019Prenatal Diagnosis12 citations Open access
Semantic Scholar
Genetic Testing Practices of Genetic Counselors, Geneticists, and Pediatric Neurologists With Regard to Childhood-Onset Neurogenetic Conditions
Sara Wofford, S. Noblin, Jessica M. Davis, L. Farach +3 more
2019Journal of Child Neurology12 citations
Semantic Scholar
Evaluating the NCCN Clinical Criteria for Recommending BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.
Caiqian Cropper, A. Woodson, B. Arun, C. Barcenas +5 more
2017The Journal of the National Comprehensive Cancer Network12 citations Open access
Semantic Scholar
Is it all Lynch Syndrome? An assessment of family history in individuals with mismatch repair deficient tumors
Katherine M. Dempsey, R. Broaddus, Y. You, S. Noblin +5 more
2014Genetics in Medicine11 citations Open access
Semantic Scholar
Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices
Danielle Williams, E. Vilar, S. S. Hashmi, Meagan G Choates +2 more
2020Journal of Genetic Counseling6 citations
Semantic Scholar
Fetal trisomy 21 and the risk of preeclampsia
Jennifer A. Defant, M. Gambello, M. Monga, P. Langlois +2 more
2009Journal of Maternal-Fetal & Neonatal Medicine6 citations
Semantic Scholar
Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents
Amy Wells, H. Northrup, S. Crandell, T. King +4 more
2009Genetics in Medicine5 citations Open access
Semantic Scholar
AN ASSESSMENT OF KNOWLEDGE AND ATTITUDES OF GENETIC COUNSELING SERVICES IN U.S. HTCs
Brad Rolf, Deborah L. Brown, M. Escobar, S. Hashmi +3 more
20131 citations
Semantic Scholar
eP303: A tale of two tests: A PGT-M and expanded carrier screening clinical experience study
A. Wolfe, M. Maisenbacher, C. Palsuledesai, M. Pastrick +11 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar
ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME
Allie Copeland, Louise C. Strong, Michelle Jackson, S. Hashmi +3 more
20200 citations
Semantic Scholar
Patients with unexplained mismatch repair deficiency are interested in updated genetic testing
J. Omark, E. Vilar, Y. You, L. Dunnington +3 more
2020Hereditary Cancer in Clinical Practice0 citations Open access
Semantic Scholar
Latinas’ Amniocentesis Decision-Making Process Semi-Structured Interview Guide
S. G. Seth, Goka Tj, Andrea Harbison, L. Hollier +3 more
20150 citations
Semantic Scholar

B. Stevens

×3

M. Mork×3

Jennifer L. Czerwinski×2

J. Hoskovec×2

K. Ormond×2

H. Toriello×2

R. Bennett×2

S. G. Seth×2