Vishal Singh Guleria

Title(s)	Postdoctoral Scholar - Research Associate
School	Keck School of Medicine of Usc
Address	10182 Telesis Court, 3rd Floor Off Campus San Diego CA 92121
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Bibliographic

Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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Early insights into the role of Exoc6B associated with spondyloepimetaphyseal dysplasia with joint laxity type 3 in primary ciliogenesis and chondrogenic differentiation in vitro. Mol Biol Rep. 2024 Feb 02; 51(1):274. Guleria VS, Quadri N, Prasad K, Das R, Upadhyai P. PMID: 38305850.

View in: PubMed Mentions: Fields:
Mol Molecular Biology
Translation:Cells
Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3. Hum Mutat. 2022 12; 43(12):2116-2129. Simsek-Kiper PO, Jacob P, Upadhyai P, Taskiran ZE, Guleria VS, Karaosmanoglu B, Imren G, Gocmen R, Bhavani GS, Kausthubham N, Shah H, Utine GE, Boduroglu K, Girisha KM. PMID: 36150098; PMCID: PMC7615863.

View in: PubMed Mentions: 5 Fields:
Gen Genetics
Translation:Humans
The intraflagellar transport protein IFT52 associated with short-rib thoracic dysplasia is essential for ciliary function in osteogenic differentiation in vitro and for sensory perception in Drosophila. Exp Cell Res. 2022 09 15; 418(2):113273. Guleria VS, Parit R, Quadri N, Das R, Upadhyai P. PMID: 35839863.

View in: PubMed Mentions: 2 Fields:
Cel Cell Biology
Translation:Humans Animals Cells
Biallelic deep intronic variant c.5457+81T>A in TRIP11 causes loss of function and results in achondrogenesis 1A. Hum Mutat. 2021 08; 42(8):1005-1014. Upadhyai P, Radhakrishnan P, Guleria VS, Kausthubham N, Nayak SS, Superti-Furga A, Girisha KM. PMID: 34057271.

View in: PubMed Mentions: 3 Fields:
Gen Genetics
Translation:Humans
Bi-allelic missense variant, p.Ser35Leu in EXOSC1 is associated with pontocerebellar hypoplasia. Clin Genet. 2021 04; 99(4):594-600. Somashekar PH, Kaur P, Stephen J, Guleria VS, Kadavigere R, Girisha KM, Bielas S, Upadhyai P, Shukla A. PMID: 33463720; PMCID: PMC9990822.

View in: PubMed Mentions: 8 Fields:
Gen Genetics
Translation:Humans Cells
Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiation. PeerJ. 2020; 8:e9799. Upadhyai P, Guleria VS, Udupa P. PMID: 32884864; PMCID: PMC7444507.

View in: PubMed Mentions: 5 Fields:
Bio Biology Env Environmental Health Med Medicine (General)
Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature. Clin Dysmorphol. 2020 Jul; 29(3):127-131. Upadhyai P, Amiri EF, Guleria VS, Bielas SL, Girisha KM, Shukla A. PMID: 32459673; PMCID: PMC8555865.

View in: PubMed Mentions: 3 Fields:
Ter Teratology
Translation:Humans Cells