Ashwinikumar Kulkarni
Overview
Explore the profile of Ashwinikumar Kulkarni including associated specialties, affiliations and a list of published articles.
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23
Citations
4369
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Recent Articles
11.
Ayhan F, Kulkarni A, Berto S, Sivaprakasam K, Douglas C, Lega B, et al.
Neuron
. 2021 May;
109(13):2091-2105.e6.
PMID: 34051145
The hippocampus supports many facets of cognition, including learning, memory, and emotional processing. Anatomically, the hippocampus runs along a longitudinal axis, posterior to anterior in primates. The structure, function, and...
12.
Xiao L, Merullo D, Koch T, Cao M, Co M, Kulkarni A, et al.
Nat Commun
. 2021 May;
12(1):2617.
PMID: 33976169
Disruption of the transcription factor FoxP2, which is enriched in the basal ganglia, impairs vocal development in humans and songbirds. The basal ganglia are important for the selection and sequencing...
13.
Berto S, Fontenot M, Seger S, Ayhan F, Caglayan E, Kulkarni A, et al.
Nat Neurosci
. 2021 Mar;
24(4):554-564.
PMID: 33686299
In humans, brain oscillations support critical features of memory formation. However, understanding the molecular mechanisms underlying this activity remains a major challenge. Here, we measured memory-sensitive oscillations using intracranial electroencephalography...
14.
Khandelwal N, Cavalier S, Rybalchenko V, Kulkarni A, Anderson A, Konopka G, et al.
Mol Psychiatry
. 2021 Jan;
26(6):1761-1774.
PMID: 33402705
Heterozygous loss-of-function mutations in the transcription factor FOXP1 are strongly associated with autism. Dopamine receptor 2 expressing (D2) striatal projection neurons (SPNs) in heterozygous Foxp1 (Foxp1) mice have higher intrinsic...
15.
Bjorness T, Kulkarni A, Rybalchenko V, Suzuki A, Bridges C, Harrington A, et al.
Elife
. 2020 Aug;
9.
PMID: 32851972
Neuronal activity and gene expression in response to the loss of sleep can provide a window into the enigma of sleep function. Sleep loss is associated with brain differential gene...
16.
Anderson A, Kulkarni A, Harper M, Konopka G
Cell Rep
. 2020 Mar;
30(9):3051-3066.e7.
PMID: 32130906
The striatum is a critical forebrain structure integrating cognitive, sensory, and motor information from diverse brain regions into meaningful behavioral output. However, the transcriptional mechanisms underlying striatal development at single-cell...
17.
Co M, Hickey S, Kulkarni A, Harper M, Konopka G
Cereb Cortex
. 2019 Nov;
30(3):1855-1870.
PMID: 31711176
Genetic studies have associated FOXP2 variation with speech and language disorders and other neurodevelopmental disorders (NDDs) involving pathology of the cortex. In this brain region, FoxP2 is expressed from development...
18.
Kulkarni A, Anderson A, Merullo D, Konopka G
Curr Opin Biotechnol
. 2019 Apr;
58:129-136.
PMID: 30978643
Single-cell RNA sequencing (scRNA-seq) is a promising approach to study the transcriptomes of individual cells in the brain and the central nervous system (CNS). This technology acts as a bridge...
19.
Usui N, Araujo D, Kulkarni A, Co M, Ellegood J, Harper M, et al.
Genes Dev
. 2017 Nov;
31(20):2039-2055.
PMID: 29138280
The molecular mechanisms driving brain development at risk in autism spectrum disorders (ASDs) remain mostly unknown. Previous studies have implicated the transcription factor FOXP1 in both brain development and ASD...
20.
Araujo D, Toriumi K, Escamilla C, Kulkarni A, Anderson A, Harper M, et al.
J Neurosci
. 2017 Oct;
37(45):10917-10931.
PMID: 28978667
Genetic perturbations of the transcription factor () are causative for severe forms of autism spectrum disorder that are often comorbid with intellectual disability. Recent work has begun to reveal an...