Alice E Davidson (Alice Davidson)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Machine Learning

Top Venues

European journal of human genetics : EJHG

Journal of clinical medicine

NAR genomics and bioinformatics

This page only lists publications with an associated author ORCID identifier.

Publications

Freddie L Braddock, Jessica C Gardner, Nihar Bhattacharyya, Beatriz Sanchez-Pintado, Marcos Costa, Christina Zarouchlioti, Anita Szabo, Petra Lišková, Michael E Cheetham, Robert D Young, Caroline M H Thaung, Alice E Davidson, Stephen J Tuft, Alison J Hardcastle
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant. European journal of human genetics : EJHG (2024)
Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, Amanda N Sadan, Anita Szabo, Christina Zarouchlioti, Jana Jedlickova, Szi Kay Leung, Tianyi Liao, Lubica Dudakova, Pavlina Skalicka, Mohit Parekh, Ismail Moghul, Aaron R Jeffries, Michael E Cheetham, Kirithika Muthusamy, Alison J Hardcastle, Nikolas Pontikos, Petra Liskova, Stephen J Tuft, Alice E Davidson
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease. PLoS genetics 20 (5) (2024)
Freddie L Braddock, Jessica C Gardner, Nihar Bhattacharyya, Beatriz Sanchez-Pintado, Marcos Costa, Christina Zarouchlioti, Anita Szabo, Petra Lišková, Michael E Cheetham, Robert D Young, Caroline M H Thaung, Alice E Davidson, Stephen J Tuft, Alison J Hardcastle
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant. European journal of human genetics : EJHG (2024)
Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, Amanda N Sadan, Anita Szabo, Christina Zarouchlioti, Jana Jedlickova, Szi Kay Leung, Tianyi Liao, Lubica Dudakova, Pavlina Skalicka, Mohit Parekh, Ismail Moghul, Aaron R Jeffries, Michael E Cheetham, Kirithika Muthusamy, Alison J Hardcastle, Nikolas Pontikos, Petra Liskova, Stephen J Tuft, Alice E Davidson
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease. PLoS genetics 20 (5) (2024)
Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, Amanda N Sadan, Anita Szabo, Christina Zarouchlioti, Jana Jedlickova, Szi Kay Leung, Tianyi Liao, Lubica Dudakova, Pavlina Skalicka, Mohit Parekh, Ismail Moghul, Aaron R Jeffries, Michael E Cheetham, Kirithika Muthusamy, Alison J Hardcastle, Nikolas Pontikos, Petra Liskova, Stephen J Tuft, Alice E Davidson
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease. PLoS genetics 20 (5) (2024)
Alysha S Taylor, Dinis Barros, Nastassia Gobet, Thierry Schuepbach, Branduff McAllister, Lorene Aeschbach, Emma L Randall, Evgeniya Trofimenko, Eleanor R Heuchan, Paula Barszcz, Marc Ciosi, Joanne Morgan, Nathaniel J Hafford-Tear, Alice E Davidson, Thomas H Massey, Darren G Monckton, Lesley Jones, Registry Investigators Of The European Huntington's Disease Network, Ioannis Xenarios, Vincent Dion
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing. NAR genomics and bioinformatics 4 (4) (2022)
Pavlina Skalicka, Jana Jedlickova, Ales Horinek, Marie Trkova, Alice E Davidson, Stephen J Tuft, Lubica Dudakova, Petra Liskova
Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant. Journal of clinical medicine 11 (17) (2022)
Lubica Dudakova, Viktor Stranecky, Lenka Piherová, Tomas Palecek, Nikolas Pontikos, Stanislav Kmoch, Pavlina Skalicka, Manuela Vaneckova, Alice E Davidson, Petra Liskova
Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles. Genes 12 (5) (2021)
Howard Maile, Ji-Peng Olivia Li, Daniel Gore, Marcello Leucci, Pádraig J Mulholland, Scott C Hau, Anita Szabo, Ismail Moghul, Konstantinos Balaskas, Kaoru Fujinami, Pirro G Hysi, Alice E Davidson, Petra Liskova, Alison J Hardcastle, Stephen J Tuft, Nikolas Pontikos
Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review. JMIR medical informatics 9 (12) (2021)
Alison J Hardcastle, Petra Liskova, Yelena Bykhovskaya, Bennet J McComish, Alice E Davidson, Chris F Inglehearn, Xiaohui Li, Helene Choquet, Mahmoud Habeeb, Sionne E M Lucas, Srujana Sahebjada, Nikolas Pontikos, Karla E Rojas Lopez, Anthony P Khawaja, Manir Ali, Lubica Dudakova, Pavlina Skalicka, Bart T H Van Dooren, Annette J M Geerards, Christoph Walter Haudum, Valeria Lo Faro, Abi Tenen, Mark J Simcoe, Karina Patasova, Darioush Yarrand, Jie Yin, Salina Siddiqui, Aine Rice, Layal Abi Farraj, Yii-Der Ida Chen, Jugnoo S Rahi, Ronald M Krauss, Elisabeth Theusch, Jac C Charlesworth, Loretta Szczotka-Flynn, Carmel Toomes, Magda A Meester-Smoor, Andrea J Richardson, Paul A Mitchell, Kent D Taylor, Ronald B Melles, Anthony J Aldave, Richard A Mills, Ke Cao, Elsie Chan, Mark D Daniell, Jie Jing Wang, Jerome I Rotter, Alex W Hewitt, Stuart Macgregor, Caroline C W Klaver, Wishal D Ramdas, Jamie E Craig, Sudha K Iyengar, David O'Brart, Eric Jorgensen, Paul N Baird, Yaron S Rabinowitz, Kathryn P Burdon, Christopher J Hammond, Stephen J Tuft, Pirro G Hysi
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Communications biology 4 (1) (2021)
Alice E Davidson, Nathaniel J Hafford-Tear, Lubica Dudakova, Amanda N Sadan, Nikolas Pontikos, Alison J Hardcastle, Stephen J Tuft, Petra Liskova
CUGC for posterior polymorphous corneal dystrophy (PPCD). European journal of human genetics : EJHG 28 (1) (2019)
Nathaniel J Hafford-Tear, Yu-Chih Tsai, Amanda N Sadan, Beatriz Sanchez-Pintado, Christina Zarouchlioti, Geoffrey J Maher, Petra Liskova, Stephen J Tuft, Alison J Hardcastle, Tyson A Clark, Alice E Davidson
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat. Genetics in medicine : official journal of the American College of Medical Genetics 21 (9) (2019)