Harris T Bland
Overview
Explore the profile of Harris T Bland including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
13
Citations
124
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Zayhowski K, Roth S, Westerfield M, Martin M, Blumen K, Bland H, et al.
J Genet Couns
. 2025 Mar;
34(2):e70008.
PMID: 40055970
No abstract available.
2.
Mittendorf K, Bland H, Andujar J, Celaya-Cobbs N, Edwards C, Gerhart M, et al.
Contemp Clin Trials
. 2024 Oct;
148:107714.
PMID: 39395532
Background: Hereditary cancer syndromes cause a high lifetime risk of early, aggressive cancers. Early recognition of individuals at risk can allow risk-reducing interventions that improve morbidity and mortality. Family health...
3.
Clayton E, Bland H, Mittendorf K
JAMA
. 2024 Apr;
331(18):1527-1528.
PMID: 38619831
No abstract available.
4.
Hu J, Korchina V, Zouk H, Harden M, Murdock D, Macbeth A, et al.
BMC Res Notes
. 2024 Mar;
17(1):62.
PMID: 38433186
Objective: Data from DNA genotyping via a 96-SNP panel in a study of 25,015 clinical samples were utilized for quality control and tracking of sample identity in a clinical sequencing...
5.
Hu J, Korchina V, Zouk H, Harden M, Murdock D, Macbeth A, et al.
Res Sq
. 2023 Oct;
PMID: 37790445
Objective: Data from DNA genotyping via a 96-SNP panel in a study of 25,015 clinical samples were utilized for quality control and tracking of sample identity in a clinical sequencing...
6.
Bland H, Gilmore M, Andujar J, Martin M, Celaya-Cobbs N, Edwards C, et al.
J Genet Couns
. 2023 Sep;
33(4):772-785.
PMID: 37667436
A person's phenotypic sex (i.e., endogenous expression of primary, secondary, and endocrinological sex characteristics) can impact crucial aspects of genetic assessment and resulting clinical care recommendations. In studies with genetics...
7.
Connolly J, Berner E, Smith M, Levy S, Terek S, Harr M, et al.
Genet Med
. 2023 May;
25(9):100906.
PMID: 37246632
Polygenic risk scores (PRS) have potential to improve health care by identifying individuals that have elevated risk for common complex conditions. Use of PRS in clinical practice, however, requires careful...
8.
Linder J, Allworth A, Bland H, Caraballo P, Chisholm R, Clayton E, et al.
Genet Med
. 2023 Jan;
25(4):100006.
PMID: 36621880
Purpose: Assessing the risk of common, complex diseases requires consideration of clinical risk factors as well as monogenic and polygenic risks, which in turn may be reflected in family history....
9.
Finn K, Lynch J, Aufox S, Bland H, Chung W, Halverson C, et al.
Am J Med Genet A
. 2022 Sep;
185(2):508-516.
PMID: 36046768
Population-based genomic screening has the potential to improve health outcomes by identifying genetic causes of disease before they occur. While much attention has been paid to supporting the needs of...
10.
Leppig K, Rahm A, Appelbaum P, Aufox S, Bland H, Buchanan A, et al.
Genet Med
. 2022 Feb;
24(5):1130-1138.
PMID: 35216901
Purpose: The goal of Electronic Medical Records and Genomics (eMERGE) Phase III Network was to return actionable sequence variants to 25,084 consenting participants from 10 different health care institutions across...