Megan P Hall
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Explore the profile of Megan P Hall including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
1174
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Recent Articles
1.
Industry engagement: Accelerating discovery, application, and adoption through industry partnerships
Peralta P, Hall M, Bhan S, Brown K, Parton M, Yeshwant K, et al.
Cancer
. 2022 Feb;
128 Suppl 4:918-926.
PMID: 35133660
No abstract available.
2.
Razavi P, Li B, Brown D, Jung B, Hubbell E, Shen R, et al.
Nat Med
. 2019 Nov;
25(12):1928-1937.
PMID: 31768066
Accurate identification of tumor-derived somatic variants in plasma circulating cell-free DNA (cfDNA) requires understanding of the various biological compartments contributing to the cfDNA pool. We sought to define the technical...
3.
Samango-Sprouse C, Kirkizlar E, Hall M, Lawson P, Demko Z, Zneimer S, et al.
PLoS One
. 2016 Aug;
11(8):e0161045.
PMID: 27512996
Background: X&Y chromosomal aneuploidies are among the most common human whole-chromosomal copy number changes, but the population-based incidence and prevalence in the child-bearing population is unclear. Methods: This retrospective analysis...
4.
Wapner R, Babiarz J, Levy B, Stosic M, Zimmermann B, Sigurjonsson S, et al.
Am J Obstet Gynecol
. 2014 Dec;
212(3):332.e1-9.
PMID: 25479548
Objective: The purpose of this study was to estimate the performance of a single-nucleotide polymorphism (SNP)-based noninvasive prenatal test for 5 microdeletion syndromes. Study Design: Four hundred sixty-nine samples (358...
5.
Curnow K, Wilkins-Haug L, Ryan A, Kirkizlar E, Stosic M, Hall M, et al.
Am J Obstet Gynecol
. 2014 Dec;
212(1):79.e1-9.
PMID: 25447960
Objective: We sought to determine the ability of single-nucleotide polymorphism-based noninvasive prenatal testing (NIPT) to identify triploid, unrecognized twin, and vanishing twin pregnancies. Study Design: The study included 30,795 consecutive...
6.
Dar P, Curnow K, Gross S, Hall M, Stosic M, Demko Z, et al.
Am J Obstet Gynecol
. 2014 Aug;
211(5):527.e1-527.e17.
PMID: 25111587
Objective: We sought to report on laboratory and clinical experience following 6 months of clinical implementation of a single-nucleotide polymorphism-based noninvasive prenatal aneuploidy test in high- and low-risk women. Study...
7.
Pergament E, Cuckle H, Zimmermann B, Banjevic M, Sigurjonsson S, Ryan A, et al.
Obstet Gynecol
. 2014 Jul;
124(2 Pt 1):210-218.
PMID: 25004354
Objective: To estimate performance of a single-nucleotide polymorphism-based noninvasive prenatal screen for fetal aneuploidy in high-risk and low-risk populations on single venopuncture. Methods: One thousand sixty-four maternal blood samples from...
8.
Levy B, Sigurjonsson S, Pettersen B, Maisenbacher M, Hall M, Demko Z, et al.
Obstet Gynecol
. 2014 Jul;
124(2 Pt 1):202-209.
PMID: 25004334
Objective: To report the full cohort of identifiable anomalies, regardless of known clinical significance, in a large-scale cohort of postmiscarriage products-of-conception samples analyzed using a high-resolution single-nucleotide polymorphism (SNP)-based microarray...
9.
Hall M, Hill M, Zimmermann B, Sigurjonsson S, Westemeyer M, Saucier J, et al.
PLoS One
. 2014 May;
9(5):e96677.
PMID: 24805989
Purpose: To determine how a single nucleotide polymorphism (SNP)- and informatics-based non-invasive prenatal aneuploidy test performs in detecting trisomy 13. Methods: Seventeen trisomy 13 and 51 age-matched euploid samples, randomly...
10.
Samango-Sprouse C, Banjevic M, Ryan A, Sigurjonsson S, Zimmermann B, Hill M, et al.
Prenat Diagn
. 2013 May;
33(7):643-9.
PMID: 23712453
Objective: This study aimed to develop a single-nucleotide polymorphism-based and informatics-based non-invasive prenatal test that detects sex chromosome aneuploidies early in pregnancy. Methods: Sixteen aneuploid samples, including thirteen 45,X, two...