Lisa C Burnett
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Explore the profile of Lisa C Burnett including associated specialties, affiliations and a list of published articles.
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7
Citations
211
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0
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Recent Articles
1.
Eddiry S, Diene G, Molinas C, Salles J, Auriol F, Gennero I, et al.
Genet Med
. 2021 May;
23(9):1664-1672.
PMID: 34040195
Purpose: Prader-Willi syndrome (PWS) is a neurodevelopmental disorder with hypothalamic dysfunction due to deficiency of imprinted genes located on the 15q11-q13 chromosome. Among them, the SNORD116 gene appears critical for...
2.
Wang L, Liu Y, Stratigopoulos G, Panigrahi S, Sui L, Zhang Y, et al.
J Clin Invest
. 2021 Feb;
131(8).
PMID: 33630762
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder caused by mutations in genes encoding components of the primary cilium and is characterized by hyperphagic obesity. To investigate the molecular...
3.
Chen H, Victor A, Klein J, Fon Tacer K, Tai D, de Esch C, et al.
JCI Insight
. 2020 Sep;
5(17).
PMID: 32879135
Prader-Willi syndrome (PWS) is a developmental disorder caused by loss of maternally imprinted genes on 15q11-q13, including melanoma antigen gene family member L2 (MAGEL2). The clinical phenotypes of PWS suggest...
4.
Skowronski A, LeDuc C, Foo K, Goffer Y, Burnett L, Egli D, et al.
Sci Transl Med
. 2020 Jan;
12(524).
PMID: 31894105
Leptin plays a role in central nervous system developmental programs and intercurrent physiological processes related to body fat regulation. The timing and neuromolecular mechanisms for these effects are relevant to...
5.
Burnett L, LeDuc C, Sulsona C, Paull D, Rausch R, Eddiry S, et al.
J Clin Invest
. 2016 Dec;
127(1):293-305.
PMID: 27941249
Prader-Willi syndrome (PWS) is caused by a loss of paternally expressed genes in an imprinted region of chromosome 15q. Among the canonical PWS phenotypes are hyperphagic obesity, central hypogonadism, and...
6.
Burnett L, LeDuc C, Sulsona C, Paull D, Eddiry S, Levy B, et al.
Stem Cell Res
. 2016 Oct;
17(3):526-530.
PMID: 27789403
Prader-Willi syndrome (PWS) is a syndromic obesity caused by loss of paternal gene expression in an imprinted interval on 15q11.2-q13. Induced pluripotent stem cells were generated from skin cells of...
7.
Heymsfield S, Avena N, Baier L, Brantley P, Bray G, Burnett L, et al.
Obesity (Silver Spring)
. 2014 Feb;
22 Suppl 1:S1-S17.
PMID: 24574081
Objective: Hyperphagia is a central feature of inherited disorders (e.g., Prader-Willi Syndrome) in which obesity is a primary phenotypic component. Hyperphagia may also contribute to obesity as observed in the...