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Author/Creator McLenachan, Samuel

3. Anti-retinal IgG antibodies in patients with early and advanced type 2 macular telangiectasia. (May 2022)

Authors:
McLenachan, Samuel; Balaratnasingam, Chandrakumar; Heath Jeffery, Rachael C.; Chen, Shang-Chih; Zhang, Dan; Chan, Geoffrey; Dolz-Marco, Rosa; Bacci, Tommaso; Lo, Johnny; Wiffen, Steven; Yannuzzi, Lawrence A.; Chen, Fred K.
Journal:
Experimental eye research
Issue:
Volume 218(2022)
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Record Type:
Journal Article
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4. Characterising splicing defects of ABCA4 variants within exons 13–50 in patient-derived fibroblasts. (December 2022)

Authors:
Huang, Di; Thompson, Jennifer A.; Chen, Shang-Chih; Adams, Abbie; Pitout, Ianthe; Lima, Alanis; Zhang, Dan; Jeffery, Rachael C. Heath; Attia, Mary S.; McLaren, Terri L.; Lamey, Tina M.; De Roach, John N.; McLenachan, Samuel; Aung-Htut, May Thandar; Fletcher, Sue; Wilton, Steve D.; Chen, Fred K.
Journal:
Experimental eye research
Issue:
Volume 225(2022)
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Record Type:
Journal Article
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5. Characterization of CRB1 splicing in retinal organoids derived from a patient with adult‐onset rod‐cone dystrophy caused by the c.1892A>G and c.2548G>A variants. Issue 11 (15th September 2020)

Authors:
Zhang, Xiao; Thompson, Jennifer A.; Zhang, Dan; Charng, Jason; Arunachalam, Sukanya; McLaren, Terri L.; Lamey, Tina M.; De Roach, John N.; Jennings, Luke; McLenachan, Samuel; Chen, Fred K.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 11(2020)
Page Start:
n/a
Record Type:
Journal Article
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6. Characterization of CRB1 splicing in retinal organoids derived from a patient with adult‐onset rod‐cone dystrophy caused by the c.1892A>G and c.2548G>A variants. Issue 11 (15th September 2020)

Authors:
Zhang, Xiao; Thompson, Jennifer A.; Zhang, Dan; Charng, Jason; Arunachalam, Sukanya; McLaren, Terri L.; Lamey, Tina M.; De Roach, John N.; Jennings, Luke; McLenachan, Samuel; Chen, Fred K.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 11(2020)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Deep clinical phenotyping and gene expression analysis in a patient with RCBTB1-associated retinopathy. (4th May 2021)

Authors:
Huang, Zhiqin; Zhang, Dan; Thompson, Jennifer A.; Jamuar, Saumya S.; Roshandel, Danial; Jennings, Luke; Mellough, Carla; Charng, Jason; Chen, Shang-Chih; McLaren, Terri L.; Lamey, Tina M.; Chelva, Enid; De Roach, John N.; Chan, Choi Mun; McLenachan, Samuel; Chen, Fred K.
Journal:
Ophthalmic genetics
Issue:
Volume 42:Number 3(2021)
Page Start:
266
Record Type:
Journal Article
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8. Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy. (2nd January 2021)

Authors:
Roshandel, Danial; Thompson, Jennifer A.; Charng, Jason; Zhang, Dan; Chelva, Enid; Arunachalam, Sukanya; Attia, Mary S.; Lamey, Tina M.; McLaren, Terri L.; De Roach, John N.; Mackey, David A.; Wilton, Steve D.; Fletcher, Sue; McLenachan, Samuel; Chen, Fred K.
Journal:
Ophthalmic genetics
Issue:
Volume 42:Number 1(2021)
Page Start:
1
Record Type:
Journal Article
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9. Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy. (2nd January 2021)

Authors:
Roshandel, Danial; Thompson, Jennifer A.; Charng, Jason; Zhang, Dan; Chelva, Enid; Arunachalam, Sukanya; Attia, Mary S.; Lamey, Tina M.; McLaren, Terri L.; De Roach, John N.; Mackey, David A.; Wilton, Steve D.; Fletcher, Sue; McLenachan, Samuel; Chen, Fred K.
Journal:
Ophthalmic genetics
Issue:
Volume 42:Number 1(2021)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

10. Gene correction of the CLN3 c.175G>A variant in patient‐derived induced pluripotent stem cells prevents pathological changes in retinal organoids. Issue 3 (26th January 2021)

Authors:
Zhang, Xiao; Zhang, Dan; Thompson, Jennifer A.; Chen, Shang‐Chih; Huang, Zhiqin; Jennings, Luke; McLaren, Terri L.; Lamey, Tina M.; De Roach, John N.; Chen, Fred K.; McLenachan, Samuel
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 3(2021)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗