Jessica L Bell
Overview
Explore the profile of Jessica L Bell 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
40
Citations
1539
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Degner K, Bell J, Jones S, Won H
Cell Insight
. 2024 Dec;
4(1):100214.
PMID: 39618480
The human genome is largely noncoding, yet the field is still grasping to understand how noncoding variants impact transcription and contribute to disease etiology. The massively parallel reporter assay (MPRA)...
2.
Bond M, Quiroga-Barber I, DCosta S, Wu Y, Bell J, McAfee J, et al.
medRxiv
. 2024 Oct;
PMID: 39371155
Genome-wide association studies have identified loci associated with Alzheimer's Disease (AD), but identifying the exact causal variants and genes at each locus is challenging due to linkage disequilibrium and their...
3.
McAfee J, Lee S, Lee J, Bell J, Krupa O, Davis J, et al.
Cell Genom
. 2023 Oct;
3(10):100404.
PMID: 37868037
Genome-wide association studies (GWASs) have successfully identified 145 genomic regions that contribute to schizophrenia risk, but linkage disequilibrium makes it challenging to discern causal variants. We performed a massively parallel...
4.
Poursani E, Mercatelli D, Raninga P, Bell J, Saletta F, Kohane F, et al.
Cell Biosci
. 2023 Jul;
13(1):132.
PMID: 37480151
Background: Metastatic cancer cells exploit Epithelial-mesenchymal-transition (EMT) to enhance their migration, invasion, and resistance to treatments. Recent studies highlight that elevated levels of copper are implicated in cancer progression and...
5.
Tenney A, Di Gioia S, Webb B, Chan W, de Boer E, Garnai S, et al.
Nat Genet
. 2023 Jun;
55(7):1149-1163.
PMID: 37386251
Hereditary congenital facial paresis type 1 (HCFP1) is an autosomal dominant disorder of absent or limited facial movement that maps to chromosome 3q21-q22 and is hypothesized to result from facial...
6.
Allan K, Astore M, Kardia E, Wong S, Fawcett L, Bell J, et al.
Front Mol Biosci
. 2023 Jun;
10:1148501.
PMID: 37325471
Cystic fibrosis (CF) is caused by a wide spectrum of mutations in the CF transmembrane conductance regulator () gene, with some leading to non-classical clinical presentations. We present an integrated...
7.
Hagemann S, Misiak D, Bell J, Fuchs T, Lederer M, Bley N, et al.
Mol Cancer
. 2023 May;
22(1):88.
PMID: 37246217
Background: Neuroblastoma is the most common solid tumor in infants accounting for approximately 15% of all cancer-related deaths. Over 50% of high-risk neuroblastoma relapse, emphasizing the need of novel drug...
8.
McAfee J, Bell J, Krupa O, Matoba N, Stein J, Won H
J Neurodev Disord
. 2022 Sep;
14(1):50.
PMID: 36085003
A growing number of variants associated with risk for neurodevelopmental disorders have been identified by genome-wide association and whole genome sequencing studies. As common risk variants often fall within large...
9.
Vemula S, Kim S, Muvavarirwa T, Bell J, Whitman M
Invest Ophthalmol Vis Sci
. 2022 Sep;
63(10):4.
PMID: 36083589
Purpose: To determine if extraocular muscles (EOMs) from mice with nystagmus show abnormalities in myofiber composition and innervation, as seen in EOMs from human nystagmus patients, and to determine when...
10.
Whitman M, Gilette N, Bell J, Kim S, Tischfield M, Engle E
Dev Biol
. 2022 Aug;
490:126-133.
PMID: 35944701
Heterozygous loss of function mutations in TWIST1 cause Saethre-Chotzen syndrome, which is characterized by craniosynostosis, facial asymmetry, ptosis, strabismus, and distinctive ear appearance. Individuals with syndromic craniosynostosis have high rates...