Sara Chandros Hull
Overview
Explore the profile of Sara Chandros Hull including associated specialties, affiliations and a list of published articles.
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55
Citations
958
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Recent Articles
11.
Sullivan H, Bayefsky M, Wakim P, Huddleston K, Biesecker B, Hull S, et al.
Obstet Gynecol
. 2019 Feb;
133(3):525-532.
PMID: 30741804
Objective: To assess pregnant women's views and preferences on noninvasive prenatal whole genome sequencing. Methods: A survey was offered to 805 pregnant women receiving prenatal care in practices affiliated with...
12.
Walajahi H, Wilson D, Hull S
Genet Med
. 2019 Jan;
21(8):1744-1750.
PMID: 30662065
Purpose: Direct-to-consumer (DTC) genetic ancestry companies have rapidly increased in popularity, with top testing services maintaining genetic databases of several million consumers. While genetic ancestry tests are often characterized as...
13.
Splinter K, Hull S, Holm I, McDonough T, Wise A, Ramoni R
Clin Transl Sci
. 2017 Sep;
11(1):28-31.
PMID: 28945957
No abstract available.
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Chen S, Berkman B, Hull S
Genet Med
. 2017 Jan;
19(8):883-889.
PMID: 28125076
Purpose: Facilitating genomic research may require the use of samples and data collected via consent processes that did not include specific descriptions of secondary uses. We explore whether a waiver...
17.
Bayefsky M, White A, Wakim P, Hull S, Wasserman D, Chen S, et al.
Prenat Diagn
. 2016 Nov;
36(13):1250-1256.
PMID: 27862072
Objective: Given public demand for genetic information, the potential to perform prenatal whole-genome sequencing (PWGS) non-invasively in the future, and decreasing costs of whole-genome sequencing, it is likely that OB/GYN...
18.
Ortiz R, Hull S, Colloca L
BMJ Open
. 2016 Apr;
6(4):e011012.
PMID: 27044586
Objectives: To examine qualitative responses regarding the use of placebo treatments in medical care in a sample of US patients.Survey studies suggest a deliberate clinical use of placebos by physicians,...
19.
Koretzky M, Bonham V, Berkman B, Kruszka P, Adeyemo A, Muenke M, et al.
Genet Med
. 2016 Mar;
18(11):1069-1074.
PMID: 26963283
An important gap exists in textbooks (or atlases) of dysmorphology used by health-care professionals to help diagnose genetic syndromes. The lack of varied phenotypic images in available atlases limits the...
20.
Darnell A, Austin H, Bluemke D, Cannon 3rd R, Fischbeck K, Gahl W, et al.
Am J Hum Genet
. 2016 Mar;
98(3):435-441.
PMID: 26942283
Human genome and exome sequencing are powerful research tools that can generate secondary findings beyond the scope of the research. Most secondary genomic findings are of low importance, but some...