L Alison McInnes
Overview
Explore the profile of L Alison McInnes including associated specialties, affiliations and a list of published articles.
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19
Citations
934
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Recent Articles
1.
McInnes L, Marton T, Qian J
J Affect Disord
. 2024 Feb;
352:199-200.
PMID: 38350540
No abstract available.
2.
Hietamies T, McInnes L, Klise A, Worley M, Qian J, Williams L, et al.
J Affect Disord
. 2023 May;
335:484-492.
PMID: 37201900
Introduction: Ketamine intravenous therapy (KIT) appears effective for treating depression in controlled trials testing a short series of infusions. A rapidly proliferating number of clinics offer KIT for depression and...
3.
McInnes L, Qian J, Gargeya R, DeBattista C, Heifets B
J Affect Disord
. 2022 Jan;
301:486-495.
PMID: 35027209
Background: Outcomes of ketamine intravenous therapy (KIT) for depression in real-world care settings have been minimally evaluated. We set out to quantify treatment response to KIT in a large sample...
4.
Eisendrath S, Gillung E, Delucchi K, Segal Z, Nelson J, McInnes L, et al.
Psychother Psychosom
. 2016 Jan;
85(2):99-110.
PMID: 26808973
Background: Due to the clinical challenges of treatment-resistant depression (TRD), we evaluated the efficacy of mindfulness-based cognitive therapy (MBCT) relative to a structurally equivalent active comparison condition as adjuncts to...
5.
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, et al.
Am J Hum Genet
. 2014 Apr;
94(5):677-94.
PMID: 24768552
Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in...
6.
Sakurai T, Dorr N, Takahashi N, McInnes L, Elder G, Buxbaum J
Autism Res
. 2011 Feb;
4(1):28-39.
PMID: 21328569
Identifying genes involved in social behavior is important for autism research. Williams-Beuren syndrome (WBS) is a developmental syndrome with unique neurocognitive features, including low IQ, deficits in visuospatial and visual-motor...
7.
McInnes L, Nakamine A, Pilorge M, Brandt T, Gonzalez P, Fallas M, et al.
Mol Autism
. 2010 Aug;
1(1):5.
PMID: 20678247
Background: The 15q24 microdeletion syndrome has been recently described as a recurrent, submicroscopic genomic imbalance found in individuals with intellectual disability, typical facial appearance, hypotonia, and digital and genital abnormalities....
8.
Lauriat T, Shiue L, Haroutunian V, Verbitsky M, Ares Jr M, Ospina L, et al.
J Neurosci Res
. 2007 Oct;
86(4):785-96.
PMID: 17918747
Decreased expression of oligodendrocyte/myelin-related (OMR) genes, including quaking (QKI), is a consistent finding in gene expression studies of post-mortem brain from subjects with schizophrenia, and these changes are most prominent...
9.
Bartz J, McInnes L
Bioessays
. 2007 Aug;
29(9):837-41.
PMID: 17688286
The peptide hormone oxytocin plays a critical role in regulating affiliative behaviors including mating, pair-bond formation, maternal/parenting behavior, social recognition, separation distress and other aspects of attachment. Jin and colleagues...
10.
Nakamine A, Ouchanov L, Jimenez P, Manghi E, Esquivel M, Monge S, et al.
Am J Med Genet A
. 2007 Mar;
146A(5):636-43.
PMID: 17334992
Duplications of 17(p11.2p11.2) have been associated with various behavioral manifestations including attention deficits, obsessive-compulsive symptoms, autistic traits, and language delay. We are conducting a genetic study of autism and are...