Shobana Kubendran
Overview
Explore the profile of Shobana Kubendran including associated specialties, affiliations and a list of published articles.
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10
Citations
142
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0
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Recent Articles
1.
Wong J, Butler K, Shapiro L, Thelin J, Mattison K, Garber K, et al.
Front Pharmacol
. 2021 Dec;
12:748415.
PMID: 34867351
Numerous mutations have been identified, of which, the majority are missense variants. Most mutations result in epileptic encephalopathy; however, some are associated with less severe phenotypes. Mouse models generated by...
2.
Kubendran S, Duong J, Dong F, Lueking A, Farley D
Perm J
. 2018 Jul;
22:17-204.
PMID: 30010531
Context: Results from chromosome testing after spontaneous abortion (SAB) or intrauterine fetal demise (IUFD) are useful in patient counseling; however, results can be inconclusive when cell cultures for chromosomes are...
3.
Stoll K, Kubendran S, Cohen S
Am J Med Genet C Semin Med Genet
. 2018 Mar;
178(1):24-37.
PMID: 29512888
Precision medicine aims to approach disease treatment and prevention with consideration of the variability in genes, environment, and lifestyle for each person. This focus on the individual is also key...
4.
Kubendran S, Sivamurthy S, Schaefer G
Genet Med
. 2017 May;
19(11):1260-1267.
PMID: 28471436
PurposeOur aim was to improve access to genetic services in an underserved region by developing a collaborative telegenetic service delivery model with a pediatrician, medical geneticist, and genetics counselor (GC).MethodsProtocols...
5.
Narayanaswamy J, Moily N, Kubendran S, Reddy Y, Jain S
Med Hypotheses
. 2014 Jul;
83(3):387-90.
PMID: 25066100
Background: Bipolar disorder (BD) is characterized by recurrent episodes of mood dysregulations and depression is considered as the most frequent form of relapse. However, there is some evidence that in...
6.
Bear K, Solomon B, Roessler E, Alvarez D, Kubendran S, OHara M, et al.
Clin Dysmorphol
. 2012 Feb;
21(3):148-151.
PMID: 22354285
No abstract available.
7.
Anbazhagan P, Purushottam M, Kiran Kumar H, Kubendran S, Mukherjee O, Brahmachari S, et al.
Bioinformation
. 2008 Oct;
2(10):471-4.
PMID: 18841245
The chromosome 18q22-23 region has been shown to be implicated in bipolar disorder (BPAD) by several studies. PHLPP1 gene, in the locus (chromosome 18q22-23), is involved in circadian pathways and...
8.
Kiran Kumar H, Purushottam M, Kubendran S, Gayathri P, Mukherjee O, Murthy A, et al.
Psychiatr Genet
. 2007 Aug;
17(5):253-60.
PMID: 17728663
Background: Altered serotonergic function is implicated in the aetiology and pathogenesis of a host of psychiatric disorders, and structural variations/polymorphisms in genes encoding the serotonin transporter and various serotonin receptor...
9.
Verma R, Kubendran S, Das S, Jain S, Brahmachari S
J Hum Genet
. 2005 Oct;
50(12):635-40.
PMID: 16215643
Chromosome 22q11-13 is one of the most consistent linkage regions for schizophrenia (SCZ) and bipolar disorder (BPAD). The SYNGR1 gene, which is associated with presynaptic vesicles in neuronal cells, is...
10.
Verma R, Mukerji M, Grover D, B-Rao C, Das S, Kubendran S, et al.
Biol Psychiatry
. 2005 Jul;
58(1):16-22.
PMID: 15992519
Background: Chromosome 22q13 has shown linkage with schizophrenia (SCZ) and bipolar affective disorder (BPAD). A missense mutation in MLC1 (putative cation-channel gene on 22q13) co-segregating with periodic catatonic schizophrenia has...