Adele A Mitchell
Overview
Explore the profile of Adele A Mitchell 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
24
Citations
631
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Goutman S, Goyal N, Payne K, Paisan-Ruiz C, Kupelian V, Kang M, et al.
Ann Clin Transl Neurol
. 2024 Jul;
11(8):2201-2211.
PMID: 39044379
Objective: To report initial results from the Amyotrophic Lateral Sclerosis (ALS) Identified genetic testing (GT) program on characteristics of individuals tested and frequency of reported disease-causing variants. Methods: ALS Identified...
2.
Benatar M, Wuu J, Andersen P, Bucelli R, Andrews J, Otto M, et al.
Neurotherapeutics
. 2022 Sep;
19(5):1686.
PMID: 36175782
No abstract available.
3.
Benatar M, Wuu J, Andersen P, Bucelli R, Andrews J, Otto M, et al.
Neurotherapeutics
. 2022 May;
19(4):1248-1258.
PMID: 35585374
Despite extensive research, amyotrophic lateral sclerosis (ALS) remains a progressive and invariably fatal neurodegenerative disease. Limited knowledge of the underlying causes of ALS has made it difficult to target upstream...
4.
Bodea C, Mitchell A, Bloemendal A, Day-Williams A, Runz H, Sunyaev S
Genome Biol
. 2018 Oct;
19(1):173.
PMID: 30359302
Functional characterization of the noncoding genome is essential for biological understanding of gene regulation and disease. Here, we introduce the computational framework PINES (Phenotype-Informed Noncoding Element Scoring), which predicts the...
5.
Gormley P, Kurki M, Hiekkala M, Veerapen K, Happola P, Mitchell A, et al.
Neuron
. 2018 Sep;
99(5):1098.
PMID: 30189203
No abstract available.
6.
Gormley P, Kurki M, Hiekkala M, Veerapen K, Happola P, Mitchell A, et al.
Neuron
. 2018 May;
98(4):743-753.e4.
PMID: 29731251
Complex traits, including migraine, often aggregate in families, but the underlying genetic architecture behind this is not well understood. The aggregation could be explained by rare, penetrant variants that segregate...
7.
Kornreich D, Mitchell A, Webb B, Cristian I, Jabs E
Cleft Palate Craniofac J
. 2014 Dec;
53(1):126-31.
PMID: 25489769
Objective: Comparison of global versus landmark analyses of facial asymmetry using three-dimensional photogrammetry to establish a precise method for evaluating facial asymmetry. Design: The landmark-based approach utilized anthropometric data points....
8.
Ostojic L, Klempner S, Patel R, Mitchell A, Axler-DiPerte G, Wurmbach E
Electrophoresis
. 2014 Aug;
35(21-22):3165-72.
PMID: 25098234
Fingerprints and touched items are important sources of DNA for STR profiling, since this evidence can be recovered in a wide variety of criminal offenses. However, there are some fundamental...
9.
Wang D, Shah K, Um S, Eng L, Zhou B, Lin Y, et al.
Forensic Sci Int
. 2014 Mar;
237:90-9.
PMID: 24631775
Sudden unexplained deaths (SUD) in apparently healthy individuals, for which the causes of deaths remained undetermined after comprehensive forensic investigations and autopsy, present vexing challenges to medical examiners and coroners....
10.
Mulle J, Pulver A, McGrath J, Wolyniec P, Dodd A, Cutler D, et al.
Biol Psychiatry
. 2013 Jul;
75(5):371-7.
PMID: 23871472
Background: Several copy number variants (CNVs) have been implicated as susceptibility factors for schizophrenia (SZ). Some of these same CNVs also increase risk for autism spectrum disorders, suggesting an etiologic...