Lauren Bartik
Overview
Explore the profile of Lauren Bartik 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
6
Citations
46
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Banks E, Francis V, Lin S, Kharfallah F, Fonov V, Levesque M, et al.
Nat Commun
. 2024 Aug;
15(1):7239.
PMID: 39174524
Developmental and epileptic encephalopathies (DEEs) feature altered brain development, developmental delay and seizures, with seizures exacerbating developmental delay. Here we identify a cohort with biallelic variants in DENND5A, encoding a...
2.
Banks E, Francis V, Lin S, Kharfallah F, Fonov V, Levesque M, et al.
medRxiv
. 2024 Feb;
PMID: 38352438
Developmental and epileptic encephalopathies (DEEs) are a heterogenous group of epilepsies in which altered brain development leads to developmental delay and seizures, with the epileptic activity further negatively impacting neurodevelopment....
3.
Zion T, Berrios C, Cohen A, Bartik L, Cross L, Engleman K, et al.
Genet Med
. 2023 Jan;
25(5):100020.
PMID: 36718845
Purpose: This study aimed to assess the amount and types of clinical genetic testing denied by insurance and the rate of diagnostic and candidate genetic findings identified through research in...
4.
Kolvenbach C, Felger T, Schierbaum L, Thiffault I, Pastinen T, Szczepanska M, et al.
J Med Genet
. 2022 Nov;
60(6):587-596.
PMID: 36379543
Background: is thought to play an important role in cytoskeletal modification and development of the early nervous system. Previously, single-nucleotide variants (SNVs) or copy number variations (CNVs) in have been...
5.
Cadieux-Dion M, Farrow E, Thiffault I, Cohen A, Welsh H, Bartik L, et al.
Clin Genet
. 2022 May;
102(2):136-141.
PMID: 35533077
Loss of function variants in JARID2 were recently reported in 16 patients with a neurodevelopmental disorder characterized by delays, intellectual and learning disability, autism, behavioral abnormalities, and dysmorphic features. Most...
6.
Cohen A, Farrow E, Abdelmoity A, Alaimo J, Amudhavalli S, Anderson J, et al.
Genet Med
. 2022 Mar;
24(6):1336-1348.
PMID: 35305867
Purpose: This study aimed to provide comprehensive diagnostic and candidate analyses in a pediatric rare disease cohort through the Genomic Answers for Kids program. Methods: Extensive analyses of 960 families...