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Skalicka, Pavlina, Porter, Louise F ORCID: 0000-0002-7406-0319, Brejchova, Kristyna, Malinka, Frantisek, Dudakova, Lubica and Liskova, Petra (2020) Brittle cornea syndrome: Disease-causing mutations in <i>ZNF469</i> and two novel variants identified in a patient followed for 26 years. BIOMEDICAL PAPERS-OLOMOUC, 164 (2). pp. 183-188.

Saptarshi, Neil, Green, Daniel, Cree, Angela, Lotery, Andrew, Paraoan, Luminita ORCID: 0000-0001-7568-7116 and Porter, Louise F ORCID: 0000-0002-7406-0319 (2021) Epigenetic Age Acceleration Is Not Associated with Age-Related Macular Degeneration. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 22 (24). 13457-.

Dhirachaikulpanich, Dhanach ORCID: 0000-0003-2234-1837, Li, Xin, Porter, Louise F ORCID: 0000-0002-7406-0319 and Paraoan, Luminita ORCID: 0000-0001-7568-7116 (2020) Integrated Microarray and RNAseq Transcriptomic Analysis of Retinal Pigment Epithelium/Choroid in Age-Related Macular Degeneration. Frontiers in Cell and Developmental Biology, 8. 808-.

Saptarshi, Neil, Porter, Louise F and Paraoan, Luminita ORCID: 0000-0001-7568-7116 (2022) PERK/EIF2AK3 integrates endoplasmic reticulum stress-induced apoptosis, oxidative stress and autophagy responses in immortalised retinal pigment epithelial cells. SCIENTIFIC REPORTS, 12 (1). 13324-.

Walkden, Andrew, Porter, Louise F ORCID: 0000-0002-7406-0319, Morarji, Jiten, Kelly, Simon P and Sioras, Evangelos (2017) Pseudophakic cystoid macular edema and spectral-domain optical coherence tomography-detectable central macular thickness changes with perioperative prostaglandin analogs. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 43 (8). pp. 1027-1030.

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Porter, Louise F ORCID: 0000-0002-7406-0319, Saptarshi, Neil, Fang, Yongxiang ORCID: 0000-0002-4514-5292, Rathi, Sonika, den Hollander, Anneke I, de Jong, Eiko K, Clark, Simon J, Bishop, Paul N, Olsen, Timothy W, Liloglou, Triantafillos ORCID: 0000-0003-0460-1404 et al (show 2 more authors) , Chavali, Venkata RM and Paraoan, Luminita ORCID: 0000-0001-7568-7116 (2019) Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes. Clinical epigenetics, 11 (1). p. 6.

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Khaled, Mariam Lofty, Bykhovskaya, Yelena, Gu, Chunfang, Liu, Alice, Drewry, Michelle D, Chen, Zhong, Mysona, Barbara A, Parker, Emily, McNabb, Ryan P, Yu, Hongfang et al (show 15 more authors) , Lu, Xiaowen, Wang, Jing, Li, Xiaohui, Al-Muammar, Abdulrahman, Rotter, Jerome I, Porter, Louise F ORCID: 0000-0002-7406-0319, Estes, Amy, Watsky, Mitchell A, Smith, Sylvia B, Xu, Hongyan, Abu-Amero, Khaled K, Kuo, Anthony, Shears, Stephen B, Rabinowitz, Yaron S and Liu, Yutao (2019) <i>PPIP5K2</i> and <i>PCSK1</i> are Candidate Genetic Contributors to Familial Keratoconus. SCIENTIFIC REPORTS, 9 (1). 19406-.