A. M. Rose

发表

CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance

Amna Z. Shah, C. Rivolta, S. Bhattacharya, 2012, PLoS genetics.

Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis

P. Luthert, S. Coupland, C. Jayasena, 2018, BMC Cancer.

Junk DNA and Cancer: Why the Trash in Your Cells is Very Important

A. M. Rose, 2018, Front. Young Minds..

Late presentation to hospital services necessitates greater community-based care for malnourished children.

A. M. Rose, 2015, Journal of tropical pediatrics.

Epistasis: the key to understanding immunological disease?

A. M. Rose, N. Mitchison, N. Avrion Mitchison, 2011, European journal of immunology.

A Study into the Evolutionary Divergence of the Core Promoter Elements of PRPF31 and TFPT

Amna Z. Shah, S. Bhattacharya, G. Alfano, 2013, Journal of Molecular and Genetic Medicine.

A Rare Case of Orbital Haemangiopericytoma Arising in Childhood

A. M. Rose, G. Rose, J. Kabiru, 2013, Orbit.

Primary Orbital Melanoma: Presentation, Treatment, and Long-term Outcomes for 13 Patients

P. Luthert, C. Jayasena, A. M. Rose, 2017, Front. Oncol..

Presentation, Treatment, and Prognosis of Secondary Melanoma within the Orbit

C. Jayasena, A. M. Rose, D. Verity, 2017, Front. Oncol..

Epistasis and immunity: the role of genetic interactions in autoimmune diseases

A. M. Rose, L. Bell, 2012, Immunology.

Aetiology and management of malnutrition in HIV-positive children

A. M. Rose, N. Martinez-Alier, C. Hall, 2014, Archives of Disease in Childhood.

Dominant PRPF31 Mutations Are Hypostatic to a Recessive CNOT3 Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of “Linked Trans-Acting Epistasis”

Amna Z. Shah, C. Rivolta, S. Bhattacharya, 2013, Annals of human genetics.

Gene of the month: PRPF31

S. Bhattacharya, A. M. Rose, Rong Luo, 2017, Journal of Clinical Pathology.

Variant haploinsufficiency and phenotypic non‐penetrance in PRPF31‐associated retinitis pigmentosa

S. Bhattacharya, A. M. Rose, S.S. Bhattacharya, 2016, Clinical genetics.

Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa

Amna Z. Shah, A. Chakravarti, C. Rivolta, 2016, Scientific Reports.

A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosa.

S. Bhattacharya, A. Webster, N. Waseem, 2011, Investigative ophthalmology & visual science.

Multiple primary malignancies and prolonged survival in a patient with widespread metastatic cutaneous melanoma

P. Luthert, S. Coupland, C. Jayasena, 2018, Melanoma research.

MSR1 repeats modulate gene expression and affect risk of breast and prostate cancer

Amna Z. Shah, A. Chakravarti, S. Chambers, 2018, Annals of oncology : official journal of the European Society for Medical Oncology.

Induction of the alternative lengthening of telomeres pathway by trapping of proteins on DNA

R. Gibbons, A. M. Rose, David Clynes, 2023, Nucleic acids research.

Expression of PRPF31 and TFPT: regulation in health and retinal disease.

Amna Z. Shah, S. Bhattacharya, G. Alfano, 2012, Human molecular genetics.

Alveolar soft-part sarcoma of the orbit.

A. M. Rose, G. Rose, J. Kabiru, 2011, African journal of paediatric surgery : AJPS.

Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis

P. Luthert, S. Coupland, C. Jayasena, 2018, BMC Cancer.

Risk and Lag-time for Development of Lacrimal Gland Carcinoma Expleomorphic Adenoma: Observations and Conjectural Study

A. M. Rose, G. Rose, K. Vahdani, 2022, Ophthalmic Plastic and Reconstructive Surgery.

Diverse clinical phenotypes associated with a nonsense mutation in FAM161A

S. Bhattacharya, P. Sergouniotis, A. Webster, 2015, Eye.