Vishal Singh Guleria

Title(s)Postdoctoral Scholar - Research Associate
SchoolKeck School of Medicine of Usc
Address10182 Telesis Court, 3rd Floor
Off Campus
San Diego CA 92121
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    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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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. 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:    Translation:Cells
    2. 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:    Translation:Humans
    3. 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:    Translation:HumansAnimalsCells
    4. 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:    Translation:Humans
    5. 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:    Translation:HumansCells
    6. 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:    
    7. 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:    Translation:HumansCells
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