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Tim Morgan

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Articles 47
Citations 742
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Recent Articles
1.
John R, Williams G, Morgan T, George M, Reynolds R, Acton J
Ophthalmic Physiol Opt . 2024 Nov; 45(1):308-314. PMID: 39485049
Background: The certificate of vision impairment has an important role in enabling access to support for people with vision impairment (VI) and the provision of epidemiological data regarding sight loss....
2.
Wade E, Goodin E, Morgan T, Pereira S, Woolley A, Jenkins Z, et al.
Eur J Clin Invest . 2024 Aug; 54(12):e14308. PMID: 39215762
Introduction: The filamins are cytoskeletal binding proteins that dynamically crosslink actin into orthogonal networks or bundle it into stress fibres. The domain structure of filamin proteins is very well characterised,...
3.
Barnard Giustini A, Patel A, Cheung R, Nobbe A, Perumalswami P, Johnson R, et al.
Liver Transpl . 2024 Jun; 30(11):E48-E49. PMID: 38920367
No abstract available.
4.
Bullen K, Lovell P, Morgan T
BMJ Support Palliat Care . 2024 Jun; 15(1):58. PMID: 38918049
No abstract available.
5.
Wade E, Morgan T, Gimenez G, Jenkins Z, Titheradge H, ODonnell M, et al.
Am J Med Genet A . 2024 Jun; 194(10):e63779. PMID: 38853608
Pathogenic variants in FLNA cause a diversity of X-linked developmental disorders associated with either preserved or diminished levels of filamin A protein and are conceptualized dichotomously as relating to underlying...
6.
Dobson K, Blore K, Henke J, Hung K, Morgan T, Posey T, et al.
J Am Mosq Control Assoc . 2023 Apr; 39(1):12-17. PMID: 37043605
Mosquito suppression strategies based on "rear and release" of male mosquitoes are attracting renewed interest from governments, municipalities, and private businesses. These include irradiation-based sterile insect technique, Wolbachia-based technologies, and...
7.
Wade E, Goodin E, Wang Y, Morgan T, Callon K, Watson M, et al.
Bone Rep . 2023 Mar; 18:101668. PMID: 36909664
Mutations in , which encodes the cytoskeletal protein FLNA, cause a spectrum of sclerosing skeletal dysplasias. Although many of these genetic variants are recurrent and cluster within the gene, the...
8.
Morgan T, Ryan B
Ophthalmic Physiol Opt . 2021 Nov; 42(1):4-7. PMID: 34786759
No abstract available.
9.
Wade E, Jenkins Z, Morgan T, Gimenez G, Gibson H, Peng H, et al.
Am J Med Genet A . 2021 Jul; 185(12):3675-3682. PMID: 34272929
Pathogenic variation in the X-linked gene FLNA causes a wide range of human developmental phenotypes. Loss-of-function is usually male embryonic-lethal, and most commonly results in a neuronal migration disorder in...
10.
Wade E, Parthasarathy P, Mi J, Morgan T, Wollnik B, Robertson S, et al.
Eur J Hum Genet . 2021 May; 30(4):480-484. PMID: 33967277
Pulmonary acinar hypoplasia (PAH) and lacrimo-auriculo-dento-digital (LADD) syndrome have both been associated with loss-of-function variants in, or deletions of FGF10. Here we report a multi-generational family with seven members manifesting...