Jennifer C Dempsey
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Explore the profile of Jennifer C Dempsey including associated specialties, affiliations and a list of published articles.
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39
Citations
1028
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Recent Articles
1.
Kumar A, Benson L, Wymore E, Phipers J, Dempsey J, Cort L, et al.
Nat Commun
. 2025 Jan;
16(1):824.
PMID: 39827121
Prenatal cannabis use is associated with neurodevelopmental deficits, likely due to exposure to the psychoactive cannabinoid, (-)-Δ-tetrahydrocannabinol, and its active metabolite, (±)-11-OH-Δ-tetrahydrocannabinol. To determine causality, preclinical studies mimicking human fetal...
2.
Ju-Wang J, Dempsey J, Zhang C, Doherty D, Witmans M, Tablizo M, et al.
Ther Adv Respir Dis
. 2025 Jan;
19():17534666241308405.
PMID: 39817683
Background: Joubert syndrome (JS) is an autosomal recessive disorder with a distinctive mid-hindbrain malformation known as the "molar tooth sign" which involves the breathing control center and its connections with...
3.
MacDuffie K, Stein J, Doherty D, Jayadev S, Girault J, Emmons K, et al.
Stem Cell Reports
. 2023 Jun;
18(7):1389-1393.
PMID: 37352851
Debates about the ethics of human brain organoids have proceeded without the input of individuals whose brains are being modeled. Interviews with donors of biospecimens for brain organoid research revealed...
4.
Serpieri V, Mortarini G, Loucks H, Biagini T, Micalizzi A, Palmieri I, et al.
J Med Genet
. 2023 Feb;
60(9):885-893.
PMID: 36788019
Background: Joubert syndrome (JS) is a neurodevelopmental ciliopathy characterised by a distinctive mid-hindbrain malformation, the 'molar tooth sign'. Over 40 JS-associated genes are known, accounting for two-thirds of cases. Methods:...
5.
Van der Sluijs P, Joosten M, Alby C, Attie-Bitach T, Gilmore K, Dubourg C, et al.
Genet Med
. 2023 Feb;
25(2):100004.
PMID: 36745127
No abstract available.
6.
Van der Sluijs P, Joosten M, Alby C, Attie-Bitach T, Gilmore K, Dubourg C, et al.
Genet Med
. 2022 May;
24(8):1753-1760.
PMID: 35579625
Purpose: Genome-wide sequencing is increasingly being performed during pregnancy to identify the genetic cause of congenital anomalies. The interpretation of prenatally identified variants can be challenging and is hampered by...
7.
MacDuffie K, Hyun I, Krogen M, Dempsey J, Murry C, Copp A, et al.
Stem Cell Reports
. 2021 Nov;
16(12):2839-2843.
PMID: 34822773
Research using human fetal tissue has saved millions of lives through vaccines and other advances, but was markedly restricted by federal regulations in 2019. Although the restrictions were partially reversed...
8.
Serpieri V, DAbrusco F, Dempsey J, Cheng Y, Arrigoni F, Baker J, et al.
J Med Genet
. 2021 Oct;
59(9):888-894.
PMID: 34675124
Background: Joubert syndrome (JS) is a recessively inherited ciliopathy characterised by congenital ocular motor apraxia (COMA), developmental delay (DD), intellectual disability, ataxia, multiorgan involvement, and a unique cerebellar and brainstem...
9.
Van der Sluijs P, Alders M, Dingemans A, Parbhoo K, van Bon B, Dempsey J, et al.
Genes (Basel)
. 2021 Aug;
12(8).
PMID: 34440449
is one of the most frequently mutated genes in intellectual disability (~1%). Most variants are readily classified, since they are de novo and are predicted to lead to loss of...
10.
Zheng G, Schreder E, Dempsey J, Uding N, Chu V, Andres G, et al.
Environ Sci Technol
. 2021 May;
55(11):7510-7520.
PMID: 33982557
This is the first study in the last 15 years to analyze per- and polyfluoroalkyl substances (PFAS) in breast milk collected from mothers ( = 50) in the United States,...