Vijaya Ramachandran
Overview
Explore the profile of Vijaya Ramachandran including associated specialties, affiliations and a list of published articles.
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44
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2411
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Recent Articles
1.
Chandler N, Scotchman E, McKay F, Ramachandran V, Chitty L
Prenat Diagn
. 2024 Nov;
45(2):171-177.
PMID: 39586789
Objective: Accurate recurrence risks are essential for genomic counselling and parental reproductive choices. Historically, Sanger sequencing was used to test parental samples, which has a limited sensitivity of ∼ 10%...
2.
Willison C, Ramachandran V, Chandler N, Hillman S, Ashraf T
Prenat Diagn
. 2023 Dec;
43(13):1674-1677.
PMID: 38059661
Trio exome sequencing was performed on a fetus with bilateral mesomelia of the lower limbs with significant angulation of the tibial bones, micrognathia and hypertelorism detected on ultrasound scan at...
3.
Chandler N, Ramachandran V, Beesley C, Otigbah C, Davison J, Ashraf T
Prenat Diagn
. 2023 Nov;
43(12):1567-1569.
PMID: 37964423
Duo exome testing was performed on a fetus conceived via in vitro fertilization with an egg donor. The fetus presented with non-immune hydrops fetalis (NIHF) at 20 + 0 weeks...
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5.
Chandler N, Scotchman E, Mellis R, Ramachandran V, Roberts R, Chitty L
Prenat Diagn
. 2022 May;
42(7):831-844.
PMID: 35506549
Background: Prenatal exome sequencing (ES) for monogenic disorders in fetuses with structural anomalies increases diagnostic yield. In England there is a national trio ES service delivered from two laboratories. To...
6.
Wang Y, Ramachandran V, Sui D, Xu K, Haydu L, Fang S, et al.
J Invest Dermatol
. 2021 Dec;
142(7):2046-2049.e3.
PMID: 34952092
No abstract available.
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Feng R, Wang Y, Ramachandran V, Ma Q, May M, Li M, et al.
J Exp Clin Cancer Res
. 2020 Dec;
39(1):273.
PMID: 33278894
Background: MUC18 is a glycoprotein highly expressed on the surface of melanoma and other cancers which promotes tumor progression and metastasis. However, its mechanism of action and suitability as a...
9.
Yates T, Drucker M, Barnicoat A, Low K, Gerkes E, Fry A, et al.
Hum Mutat
. 2020 Feb;
41(5):1042-1050.
PMID: 32097528
Pathogenic variants in ZMYND11, which acts as a transcriptional repressor, have been associated with intellectual disability, behavioral abnormalities, and seizures. Only 11 affected individuals have been reported to date, and...
10.
Pemberton L, Barker R, Cockell A, Ramachandran V, Haworth A, Homfray T
BMC Med Genet
. 2020 Jan;
21(1):7.
PMID: 31910817
Background: Osteocraniostenosis (OCS) is a rare genetic disorder characterised by premature closure of cranial sutures, gracile bones and perinatal lethality. Previously, diagnosis has only been possible postnatally on clinical and...