Christina Corsello
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Explore the profile of Christina Corsello including associated specialties, affiliations and a list of published articles.
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20
Citations
3453
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Recent Articles
1.
Antaki D, Guevara J, Maihofer A, Klein M, Gujral M, Grove J, et al.
Nat Genet
. 2022 Jun;
54(8):1259.
PMID: 35768728
No abstract available.
2.
Haine-Schlagel R, Corsello C, Caplan B, Gould H, Brookman-Frazee L
J Autism Dev Disord
. 2022 Jun;
54(3):1221-1230.
PMID: 35665870
Families of children with autism spectrum disorder (ASD) face challenges engaging in services following diagnosis. This study: (1) developed and implemented a toolkit to tailor ASD evaluation feedback to families'...
3.
Antaki D, Guevara J, Maihofer A, Klein M, Gujral M, Grove J, et al.
Nat Genet
. 2022 Jun;
54(9):1284-1292.
PMID: 35654974
The genetic etiology of autism spectrum disorder (ASD) is multifactorial, but how combinations of genetic factors determine risk is unclear. In a large family sample, we show that genetic loads...
4.
Qiu Y, Arbogast T, Lorenzo S, Li H, Tang S, Richardson E, et al.
Cell Rep
. 2019 Sep;
28(13):3320-3328.e4.
PMID: 31553903
A copy-number variant (CNV) of 16p11.2 encompassing 30 genes is associated with developmental and psychiatric disorders, head size, and body mass. The genetic mechanisms that underlie these associations are not...
5.
Brandler W, Antaki D, Gujral M, Kleiber M, Whitney J, Maile M, et al.
Science
. 2018 Apr;
360(6386):327-331.
PMID: 29674594
The genetic basis of autism spectrum disorder (ASD) is known to consist of contributions from de novo mutations in variant-intolerant genes. We hypothesize that rare inherited structural variants in cis-regulatory...
6.
Meerschaut I, Rochefort D, Revencu N, Petre J, Corsello C, Rouleau G, et al.
J Med Genet
. 2017 Jul;
54(9):613-623.
PMID: 28735298
Background: Mutations in forkhead box protein P1 () cause intellectual disability (ID) and specific language impairment (SLI), with or without autistic features (MIM: 613670). Despite multiple case reports no specific...
7.
Brandler W, Antaki D, Gujral M, Noor A, Rosanio G, Chapman T, et al.
Am J Hum Genet
. 2016 Mar;
98(4):667-79.
PMID: 27018473
Genetic studies of autism spectrum disorder (ASD) have established that de novo duplications and deletions contribute to risk. However, ascertainment of structural variants (SVs) has been restricted by the coarse...
8.
Jones R, Risi S, Wexler D, Anderson D, Corsello C, Pickles A, et al.
J Child Psychol Psychiatry
. 2014 Sep;
56(5):577-85.
PMID: 25243378
Background: Caregiver report is crucial for the diagnosis of childhood onset psychiatric disorders, particularly autism. Three experiments were conducted to determine whether caregiver reports of past and current behaviors are...
9.
Paul L, Corsello C, Kennedy D, Adolphs R
Brain
. 2014 Apr;
137(Pt 6):1813-29.
PMID: 24771497
The corpus callosum, with its ∼200 million axons, remains enigmatic in its contribution to cognition and behaviour. Agenesis of the corpus callosum is a congenital condition in which the corpus...
10.
Michaelson J, Shi Y, Gujral M, Zheng H, Malhotra D, Jin X, et al.
Cell
. 2012 Dec;
151(7):1431-42.
PMID: 23260136
De novo mutation plays an important role in autism spectrum disorders (ASDs). Notably, pathogenic copy number variants (CNVs) are characterized by high mutation rates. We hypothesize that hypermutability is a...