Balram Gangaram
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Explore the profile of Balram Gangaram including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
58
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Recent Articles
1.
Gangaram B, Lee V, Slavotinek A
Am J Med Genet A
. 2024 Feb;
194(7):e63567.
PMID: 38389298
Biallelic variants in the OTUD6B gene have been reported in the literature in association with an intellectual developmental disorder featuring dysmorphic facies, seizures, and distal limb abnormalities. Physical differences described...
2.
Stanley H, White B, LaRosa C, Cocalis M, Gaynor J, Strong A, et al.
Am J Med Genet A
. 2023 Dec;
194(4):e63500.
PMID: 38071433
Patent ductus arteriosus (PDA) and coarctation of the aorta (CoA) are relatively common congenital heart defects. Pathogenic variants in PRDM6, which encodes a smooth-muscle-cell-specific transcription factor, have now been etiologically...
3.
Priestley J, Deshwar A, Murthy H, DAgostino M, Dupuis L, Gangaram B, et al.
Genet Med
. 2023 May;
25(8):100863.
PMID: 37125634
Purpose: Bone morphogenic proteins (BMPs) regulate gene expression that is related to many critical developmental processes, including osteogenesis for which they are named. In addition, BMP2 is widely expressed in...
4.
Adamo C, Beyens A, Schiavinato A, Keene D, Tufa S, Morgelin M, et al.
Am J Hum Genet
. 2022 Nov;
109(12):2230-2252.
PMID: 36351433
EMILIN1 (elastin-microfibril-interface-located-protein-1) is a structural component of the elastic fiber network and localizes to the interface between the fibrillin microfibril scaffold and the elastin core. How EMILIN1 contributes to connective...
5.
Gangaram B, Devine W, Slavotinek A
Eur J Med Genet
. 2022 Apr;
65(6):104496.
PMID: 35398350
Pathogenic variants in the OFD1 gene have been classically associated with the Orofaciodigital syndrome type 1 in females, a condition previously considered to be X-linked dominant with male embryonic lethality....
6.
Sheppard S, Campbell I, Harr M, Gold N, Li D, Bjornsson H, et al.
Am J Med Genet A
. 2021 Mar;
185(6):1649-1665.
PMID: 33783954
Wiedemann-Steiner syndrome (WSS) is an autosomal dominant disorder caused by monoallelic variants in KMT2A and characterized by intellectual disability and hypertrichosis. We performed a retrospective, multicenter, observational study of 104...
7.
Cohen L, MacLaren J, Demore M, Fortson B, Friedman A, Lim C, et al.
Clin J Pain
. 2009 Jun;
25(6):490-4.
PMID: 19542796
Objectives: The purpose of this study was to evaluate the effectiveness of vapocoolant for preschoolers' immunization injection pain relief. Methods: Fifty-seven 4 to 6-year-old children were randomized into vapocoolant alone...
8.
Cohen L, MacLaren J, Fortson B, Friedman A, Demore M, Lim C, et al.
Pain
. 2006 Jun;
125(1-2):165-71.
PMID: 16781075
Distraction has been shown to be an effective technique for managing pain in children; however, few investigations have examined the utility of this technique with infants. The goal of the...