Hannah Wand
Overview
Explore the profile of Hannah Wand including associated specialties, affiliations and a list of published articles.
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Articles
20
Citations
568
Followers
0
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Recent Articles
1.
Hull L, Aday A, Bui Q, Luzum J, Muchira J, Wand H, et al.
Circulation
. 2025 Mar;
PMID: 40079117
Despite insufficient evidence to support direct-to-consumer genetic testing in routine clinical care, cardiovascular clinicians increasingly face questions about its utility and interpretation because individuals can purchase these tests directly from...
2.
Christian S, Dzwiniel T, Baker A, Biesecker B, Borle K, Mostafavi R, et al.
J Genet Couns
. 2024 Dec;
34(2):e1995.
PMID: 39620251
The rising demand for genetic counseling has prompted the implementation of various innovative service delivery models, such as patient webinars, videos, chatbots, and the integration of genetic testing into mainstream...
3.
Martschenko D, Wand H, Young J, Wojcik G
Nat Genet
. 2023 May;
55(6):895-900.
PMID: 37202500
No abstract available.
4.
Reddi H, Wand H, Funke B, Zimmermann M, Lebo M, Qian E, et al.
Genet Med
. 2023 Mar;
25(5):100804.
PMID: 36971772
No abstract available.
5.
Abu-El-Haija A, Reddi H, Wand H, Rose N, Mori M, Qian E, et al.
Genet Med
. 2023 Mar;
25(5):100803.
PMID: 36920474
No abstract available.
6.
Wand H, Martschenko D, Smitherman A, Michelson S, Pun T, Witte J, et al.
J Community Genet
. 2023 Feb;
14(5):459-469.
PMID: 36765027
As genomic technologies rapidly develop, polygenic scores (PGS) are entering into a growing conversation on how to improve precision in public health and prevent chronic disease. While the integration of...
7.
Wand H, Kalia S, Helm B, Suckiel S, Brockman D, Vriesen N, et al.
J Genet Couns
. 2023 Jan;
32(3):558-575.
PMID: 36617640
Polygenic scores (PGS) are primed for use in personalized risk assessments for common, complex conditions and population health screening. Although there is growing evidence supporting the clinical validity of these...
8.
Preston C, Wright M, Madhavrao R, Harrison S, Goldstein J, Luo X, et al.
Genome Med
. 2022 Jan;
14(1):6.
PMID: 35039090
Background: Identification of clinically significant genetic alterations involved in human disease has been dramatically accelerated by developments in next-generation sequencing technologies. However, the infrastructure and accessible comprehensive curation tools necessary...
9.
Chora J, Iacocca M, Tichy L, Wand H, Kurtz C, Zimmermann H, et al.
Genet Med
. 2021 Dec;
24(2):293-306.
PMID: 34906454
Purpose: In 2015, the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) published consensus standardized guidelines for sequence-level variant classification in Mendelian disorders....
10.
OSullivan J, Shcherbina A, Justesen J, Turakhia M, Perez M, Wand H, et al.
Circ Genom Precis Med
. 2021 May;
14(3):e003168.
PMID: 34029116
Background: Atrial fibrillation (AF) is associated with a five-fold increased risk of ischemic stroke. A portion of this risk is heritable; however, current risk stratification tools (CHADS-VASc) do not include...