Kevin Gregory-Evans
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Explore the profile of Kevin Gregory-Evans including associated specialties, affiliations and a list of published articles.
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49
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943
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Recent Articles
1.
Gregory-Evans K, Kolawole O, Molday R, Gregory-Evans C
Ophthalmologica
. 2024 Jul;
247(4):231-240.
PMID: 39043154
Introduction: Conclusive molecular genetic diagnoses in inherited retinal diseases remains a major challenge due to the large number of variants of uncertain significance (VUS) identified in genetic testing. Here, we...
2.
Lammers M, Young E, Yanai A, Viringipurampeer I, Le T, Straatman L, et al.
J Otolaryngol Head Neck Surg
. 2024 Jun;
53:19160216241258431.
PMID: 38888945
Importance: Mesenchymal stem cells (MSCs) have the capability of providing ongoing paracrine support to degenerating tissues. Since MSCs can be extracted from a broad range of tissues, their specific surface...
3.
Stephenson K, Paton K, Gregory-Evans C, Gregory-Evans K
Ophthalmic Genet
. 2024 Jun;
45(5):494-498.
PMID: 38853699
Introduction: In addition to sensorineural hearing loss, Waardenburg Syndrome (WS) may present with variable pigmentation of skin and choroid, which may simulate other life-threating conditions (e.g. melanoma). Case Report: Two...
4.
Kolawole O, Gregory-Evans C, Bikoo R, Huang A, Gregory-Evans K
Mol Vis
. 2024 Jan;
29:329-337.
PMID: 38264610
Purpose: Autosomal recessive cone and cone-rod dystrophies (CD/CRD) are inherited forms of vison loss. Here, we report on and correlate the clinical phenotypes with the underlying genetic mutations. Methods: Clinical...
5.
Kolawole O, Huang A, Gregory-Evans C, Shunmugam M, Weaver T, Gregory-Evans K
Can J Ophthalmol
. 2023 Sep;
59(5):e575-e581.
PMID: 37678418
Objective: To evaluate the success of diagnostic genetic testing in inherited retinal dystrophy (IRD) patients in the clinical setting. Design: Retrospective cohort analysis. Participants: A total of 446 consecutive participants...
6.
Wang X, Shan X, Gregory-Evans K, Gregory-Evans C
Precis Clin Med
. 2022 Jun;
3(2):113-126.
PMID: 35692607
Leber congenital amaurosis (LCA) is a severe, genetically heterogeneous recessive eye disease in which ~ 35% of gene mutations are in-frame nonsense mutations coding for loss-of-function premature termination codons (PTCs)...
7.
Gregory-Evans K
Handb Clin Neurol
. 2021 Apr;
178:1-11.
PMID: 33832671
Diseases of the retina are common and numerous, with causes ranging over inherited, inflammatory, vascular, infectious, neoplastic, traumatic, toxic, and idiopathic etiologies. A key issue in the diagnosis of retinal...
8.
Viringipurampeer I, Yanai A, Nizamudheen V, Gregory-Evans C, Gregory-Evans K
J Tissue Eng Regen Med
. 2021 Mar;
15(6):556-566.
PMID: 33779072
Cell replacement therapy is emerging as an important approach in novel treatments for neurodegenerative diseases. Many problems remain, in particular improvements are needed in the survival of transplanted cells and...
9.
ALSomiry A, Gregory-Evans C, Gregory-Evans K
Hum Genet
. 2019 May;
138(8-9):865-880.
PMID: 31073883
Ocular coloboma is an uncommon, but often severe, sight-threatening condition that can be identified from birth. This congenital anomaly is thought to be caused by maldevelopment of optic fissure closure...
10.
Gregory-Evans C, Wang X, Gregory-Evans K
Hum Genet
. 2019 Jan;
138(8-9):1019-1026.
PMID: 30603775
Over the last three decades, genetic studies have made great strides toward the identification of genes and genetic mechanisms underlying congenital disorders of the eye. However, despite the vast knowledge...