Blake C Ballif
Overview
Explore the profile of Blake C Ballif 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
83
Citations
4073
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
21.
Shaffer L, Dabell M, Fisher A, Coppinger J, Bandholz A, Ellison J, et al.
Prenat Diagn
. 2012 Aug;
32(10):976-85.
PMID: 22865506
Objective: To demonstrate the usefulness of microarray testing in prenatal diagnosis based on our laboratory experience. Methods: Prenatal samples received from 2004 to 2011 for a variety of indications (n...
22.
Shaffer L, Rosenfeld J, Dabell M, Coppinger J, Bandholz A, Ellison J, et al.
Prenat Diagn
. 2012 Aug;
32(10):986-95.
PMID: 22847778
Objective: The aim of this study is to understand the diagnostic utility of comparative genomic hybridization (CGH)-based microarrays for pregnancies with abnormal ultrasound findings. Methods: We performed a retrospective analysis...
23.
Lamb A, Rosenfeld J, Coppinger J, Dodge E, Dabell M, Torchia B, et al.
Genet Med
. 2012 Jul;
14(11):914-21.
PMID: 22766610
Purpose: To understand the ability of microarray-based comparative genomic hybridization to detect copy-number variation in the presence of maternal cell contamination. Methods: To simulate maternal cell contamination, normal female DNA...
24.
Shaffer L, Dabell M, Rosenfeld J, Neill N, Ballif B, Coppinger J, et al.
Prenat Diagn
. 2012 May;
32(6):611.
PMID: 22622835
No abstract available.
25.
Shaffer L, Dabell M, Rosenfeld J, Neill N, Ballif B, Coppinger J, et al.
Prenat Diagn
. 2012 Apr;
32(4):344-50.
PMID: 22467165
Objective: To understand the prenatal referral patterns from the United States, Canada, and Israel for two whole-genome microarray platforms, each with a different resolution. Method: Physicians selected one of the...
26.
Shaffer L, Schultz R, Ballif B
Curr Opin Genet Dev
. 2012 Feb;
22(3):264-71.
PMID: 22336526
The cytogenetic evaluation of hematologic disease can confirm a diagnosis, determine treatment options, and provide prognostic information to the patient. Among the potential cytogenetic aberrations that can be identified are...
27.
Rosenfeld J, Traylor R, Schaefer G, McPherson E, Ballif B, Klopocki E, et al.
Eur J Hum Genet
. 2012 Feb;
20(7):754-61.
PMID: 22317977
Chromosomal band 1q21.1 can be divided into two distinct regions, proximal and distal, based on segmental duplications that mediate recurrent rearrangements. Microdeletions and microduplications of the distal region within 1q21.1,...
28.
Lamb A, Rosenfeld J, Neill N, Talkowski M, Blumenthal I, Girirajan S, et al.
Hum Mutat
. 2012 Feb;
33(4):728-40.
PMID: 22290657
SOX5 encodes a transcription factor involved in the regulation of chondrogenesis and the development of the nervous system. Despite its important developmental roles, SOX5 disruption has yet to be associated...
29.
Rosenfeld J, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, et al.
Neurogenetics
. 2012 Jan;
13(1):31-47.
PMID: 22218741
Interstitial deletions of 6q are associated with variable phenotypes, including growth retardation, dysmorphic features, upper limb malformations, and Prader-Willi (PW)-like features. Only a minority of cases in the literature have...
30.
Kolquist K, Schultz R, Furrow A, Brown T, Han J, Campbell L, et al.
Cancer Genet
. 2011 Dec;
204(11):603-28.
PMID: 22200086
The myelodysplastic syndromes (MDS) are a heterogeneous group of clonal disorders characterized by ineffective hematopoiesis, cytopenias, and a risk of transformation to acute myeloid leukemia (AML). However, only approximately 50%...