David E Gray
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Explore the profile of David E Gray including associated specialties, affiliations and a list of published articles.
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12
Citations
329
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Recent Articles
1.
Lemke A, Thompson M, Gimpel E, McNamara K, Rich C, Finnila C, et al.
J Pers Med
. 2023 Jul;
13(7).
PMID: 37511639
Background: It is critical to understand the wide-ranging clinical and non-clinical effects of genome sequencing (GS) for parents in the NICU context. We assessed parents' experiences with GS as a...
2.
Bowling K, Thompson M, Finnila C, Hiatt S, Latner D, Amaral M, et al.
Genet Med
. 2021 Dec;
24(4):851-861.
PMID: 34930662
Purpose: SouthSeq is a translational research study that undertook genome sequencing (GS) for infants with symptoms suggestive of a genetic disorder. Recruitment targeted racial/ethnic minorities and rural, medically underserved areas...
3.
Hiatt S, Lawlor J, Handley L, Ramaker R, Rogers B, Partridge E, et al.
HGG Adv
. 2021 May;
2(2).
PMID: 33937879
Exome and genome sequencing have proven to be effective tools for the diagnosis of neurodevelopmental disorders (NDDs), but large fractions of NDDs cannot be attributed to currently detectable genetic variation....
4.
Childerhose J, Rich C, East K, Kelley W, Simmons S, Finnila C, et al.
AJOB Empir Bioeth
. 2021 Apr;
12(3):179-189.
PMID: 33843487
The desire of parents to obtain a genetic diagnosis for their child with intellectual disability and associated symptoms has long been framed as a diagnostic odyssey, an arduous and sometimes...
5.
Bowling K, Thompson M, Gray D, Lawlor J, Williams K, East K, et al.
Genet Med
. 2020 Sep;
23(2):280-288.
PMID: 32989269
Purpose: To evaluate the effectiveness and specificity of population-based genomic screening in Alabama. Methods: The Alabama Genomic Health Initiative (AGHI) has enrolled and evaluated 5369 participants for the presence of...
6.
Cochran J, McKinley E, Cochran M, Amaral M, Moyers B, Lasseigne B, et al.
Cold Spring Harb Mol Case Stud
. 2019 Dec;
5(6).
PMID: 31836585
We assessed the results of genome sequencing for early-onset dementia. Participants were selected from a memory disorders clinic. Genome sequencing was performed along with repeat expansion testing. All returned sequencing...
7.
Hiatt S, Thompson M, Prokop J, Lawlor J, Gray D, Bebin E, et al.
Am J Hum Genet
. 2019 Mar;
104(4):701-708.
PMID: 30879638
Developmental delay and intellectual disability (DD and ID) are heterogeneous phenotypes that arise in many rare monogenic disorders. Because of this rarity, developing cohorts with enough individuals to robustly identify...
8.
Thompson M, Finnila C, Bowling K, Brothers K, Neu M, Amaral M, et al.
Genet Med
. 2018 May;
20(12):1635-1643.
PMID: 29790872
Purpose: Clinically relevant secondary variants were identified in parents enrolled with a child with developmental delay and intellectual disability. Methods: Exome/genome sequencing and analysis of 789 "unaffected" parents was performed....
9.
Sanghvi R, Buhay C, Powell B, Tsai E, Dorschner M, Hong C, et al.
Genet Med
. 2017 Nov;
20(8):855-866.
PMID: 29144510
Purpose: As massively parallel sequencing is increasingly being used for clinical decision making, it has become critical to understand parameters that affect sequencing quality and to establish methods for measuring...
10.
Bowling K, Thompson M, Amaral M, Finnila C, Hiatt S, Engel K, et al.
Genome Med
. 2017 May;
9(1):43.
PMID: 28554332
Background: Developmental disabilities have diverse genetic causes that must be identified to facilitate precise diagnoses. We describe genomic data from 371 affected individuals, 309 of which were sequenced as proband-parent...