Louise Frances Porter

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Louise Frances Porter currently works at the Institute of Ageing & Chronic Disease, University of Liverpool. Louise does research in Ophthalmology, Genetic Epidemiology and Genetics. Their current project is 'Epigenetics in age-related ocular disease'.

Research Interests

Papers共 36 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

Epigenetic Changes of Ageing and Age-Related Macular Degeneration

Louise F. Porter,Neil Saptarshi,Daniel Green,Luminita Paraoan

JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICSno. 8 (2023): A125-A125

Cited0Views0Bibtex

WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects

Adella Karam,Clarisse Delvallee,Alejandro Estrada-Cuzcano,Veronique Geoffroy,Jean-Baptiste Lamouche,Anne-Sophie Leuvrey,Elsa Nourisson,Julien Tarabeux,Corinne Stoetzel,Sophie Scheidecker,Louise Frances Porter,Emmanuelle Genin,Richard Redon,Florian Sandron,Anne Boland,Jean-Francois Deleuze,Nicolas Le May,Helene Dollfus,Jean Muller

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESno. 10 (2023)

Cited0Views0WOSBibtex

PERK/EIF2AK3 Integrates Endoplasmic Reticulum Stress-Induced Apoptosis, Oxidative Stress and Autophagy Responses in Immortalised Retinal Pigment Epithelial Cells

Neil Saptarshi,Louise F. Porter,Luminita Paraoan

Scientific Reports（2022）

Cited11Views0WOSNATUREBibtex

Epigenetic Age Acceleration is Not Associated with Age-Related Macular Degeneration

Neil Saptarshi,Daniel Green,Angela Cree,Andrew Lotery,Luminita Paraoan,Louise F. Porter

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES（2021）

Cited6Views0WOSBibtex

Presence of Active Myocarditis at the 6 Month Follow‐up Appointment for a Severe Form of COVID‐19: a Case Report

Maxence Meyer,Thomas Vogel,Anita Meyer,Florentin Constancias,Louise F. Porter,Georges Kaltenbach,Elise Schmitt,Said Chayer,Floriane Zeyons,Marianne Riou,Samira Fafi-Kremer,Aurelie Velay,Soraya El Ghannudi

ESC Heart Failure（2021）

Cited6Views0WOSBibtex

Atypical Retinal Phenotype in a Patient with Alström Syndrome and Biallelic Novel Pathogenic Variants in ALMS1, Including a De Novo Variation

Laura Mauring,Louise Frances Porter,Valerie Pelletier, Axelle Riehm,Anne-Sophie Leuvrey,Aurelie Gouronc,Fouzia Studer,Corinne Stoetzel,Helene Dollfus,Jean Muller

Frontiers in Genetics (2020)

Cited7Views0WOSBibtex

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Lecturer

Papers共 36 篇Author StatisticsCo-AuthorSimilar Experts