Andrea L Vincent (Andrea Vincent)

ResearcherID Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 28

Top Topics

Intellectual Disability

Optical Coherence Tomography

Diabetic Retinopathy

Top Venues

Ophthalmic genetics

Clinical & experimental ophthalmology

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

Publications

Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, Erica G M Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard Heinrich Friedrich Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Francesca Simonelli, Tamar Ben-Yosef, Damjan Glavač, G Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P Szaflik, Anna Matynia, Michael B Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfriede De Baere, Carel B Hoyng, Catherina H Z Li, Caroline C W Klaver, Chris F Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L Vincent, Lisa Roberts, Rajkumar Ramesar, Giovanna Sartor, Elena Luppi, Susan M Downes, L Ingeborgh van den Born, Terri L McLaren, John N De Roach, Tina M Lamey, Jennifer A Thompson, Fred K Chen, Anna M Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J Bolz, Hülya Kayserili, Susanne Roosing, Frans P M Cremers
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. Biomolecules 14 (3) (2024)
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, Erica G M Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard Heinrich Friedrich Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Francesca Simonelli, Tamar Ben-Yosef, Damjan Glavač, G Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P Szaflik, Anna Matynia, Michael B Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfriede De Baere, Carel B Hoyng, Catherina H Z Li, Caroline C W Klaver, Chris F Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L Vincent, Lisa Roberts, Rajkumar Ramesar, Giovanna Sartor, Elena Luppi, Susan M Downes, L Ingeborgh van den Born, Terri L McLaren, John N De Roach, Tina M Lamey, Jennifer A Thompson, Fred K Chen, Anna M Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J Bolz, Hülya Kayserili, Susanne Roosing, Frans P M Cremers
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. Biomolecules 14 (3) (2024)
Austin D Igelman, Elizabeth White, Alaa Tayyib, Lesley A Everett, Ajoy Vincent, Elise Heon, Christina Zeitz, Michel Michaelides, Omar A Mahroo, Mohamed Katta, Andrew Webster, Markus Preising, Birgit Lorenz, Samer Khateb, Eyal Banin, Dror Sharon, Shahar Luski, Filip Van Den Broeck, Bart Peter Leroy, Elfride De Baere, Sophie Walraedt, Katarina Stingl, Laura Kuehlewein, Susanne Kohl, Milda Reith, Anne Fulton, Aparna Raghuram, Isabelle Meunier, Hélène Dollfus, Tomas S Aleman, Emma C Bedoukian, Erin C O'Neil, Emily Krauss, Andrea L Vincent, Charlotte Jordan, Alessandro Iannaccone, Parveen Sen, Srilekha Sundaramurthy, Soumittra Nagasamy, Irina Balikova, Ingele Casteels, Shyamanga Borooah, Shaden Yassin, Aaron Nagiel, Hillary Schwartz, Xavier Zanlonghi, Irene Gottlob, Rebecca J McLean, Francis L Munier, Andrew Stephenson, Robert Sisk, Robert Koenekoop, Lorri B Wilson, Douglas Fredrick, Dongseok Choi, Paul Yang, Mark Edward Pennesi
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study. The British journal of ophthalmology (2024)
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, Erica G M Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard Heinrich Friedrich Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Francesca Simonelli, Tamar Ben-Yosef, Damjan Glavač, G Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P Szaflik, Anna Matynia, Michael B Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfriede De Baere, Carel B Hoyng, Catherina H Z Li, Caroline C W Klaver, Chris F Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L Vincent, Lisa Roberts, Rajkumar Ramesar, Giovanna Sartor, Elena Luppi, Susan M Downes, L Ingeborgh van den Born, Terri L McLaren, John N De Roach, Tina M Lamey, Jennifer A Thompson, Fred K Chen, Anna M Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J Bolz, Hülya Kayserili, Susanne Roosing, Frans P M Cremers
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. Biomolecules 14 (3) (2024)
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, Erica G M Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard Heinrich Friedrich Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Francesca Simonelli, Tamar Ben-Yosef, Damjan Glavač, G Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P Szaflik, Anna Matynia, Michael B Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfriede De Baere, Carel B Hoyng, Catherina H Z Li, Caroline C W Klaver, Chris F Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L Vincent, Lisa Roberts, Rajkumar Ramesar, Giovanna Sartor, Elena Luppi, Susan M Downes, L Ingeborgh van den Born, Terri L McLaren, John N De Roach, Tina M Lamey, Jennifer A Thompson, Fred K Chen, Anna M Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J Bolz, Hülya Kayserili, Susanne Roosing, Frans P M Cremers
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. Biomolecules 14 (3) (2024)
Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, Erica G M Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard Heinrich Friedrich Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Francesca Simonelli, Tamar Ben-Yosef, Damjan Glavač, G Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P Szaflik, Anna Matynia, Michael B Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfriede De Baere, Carel B Hoyng, Catherina H Z Li, Caroline C W Klaver, Chris F Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L Vincent, Lisa Roberts, Rajkumar Ramesar, Giovanna Sartor, Elena Luppi, Susan M Downes, L Ingeborgh van den Born, Terri L McLaren, John N De Roach, Tina M Lamey, Jennifer A Thompson, Fred K Chen, Anna M Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J Bolz, Hülya Kayserili, Susanne Roosing, Frans P M Cremers
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. Biomolecules 14 (3) (2024)
Pushkar Raj Silwal, Arier C Lee, David Squirrell, Jinfeng Zhao, Matire Harwood, Andrea L Vincent, Rinki Murphy, Shanthi Ameratunga, Jacqueline Ramke
Use of public sector diabetes eye services in New Zealand 2006-2019: Analysis of national routinely collected datasets. PloS one 18 (5) (2023)
Alexis Ceecee Britten-Jones, Heather G Mack, Andrea L Vincent, Lisa J Hill, Thomas L Edwards, Lauren N Ayton
Genetic testing and gene therapy in retinal diseases: Knowledge and perceptions of optometrists in Australia and New Zealand. Clinical genetics (2023)
Pushkar Raj Silwal, Arier C Lee, David Squirrell, Jinfeng Zhao, Matire Harwood, Andrea L Vincent, Rinki Murphy, Shanthi Ameratunga, Jacqueline Ramke
Use of public sector diabetes eye services in New Zealand 2006-2019: Analysis of national routinely collected datasets. PloS one 18 (5) (2023)
Pushkar Raj Silwal, Arier C Lee, David Squirrell, Jinfeng Zhao, Matire Harwood, Andrea L Vincent, Rinki Murphy, Shanthi Ameratunga, Jacqueline Ramke
Use of public sector diabetes eye services in New Zealand 2006-2019: Analysis of national routinely collected datasets. PloS one 18 (5) (2023)
Shilpa E Kuruvilla, Eileen Song, Naz Raoof, Katherine van Bysterveldt, Verity F Oliver, Sheng Chiong Hong, Rasha Al-Taie, Graham A Wilson, Andrea L Vincent
Genotypic and phenotypic characterisation of RP2- and RPGR-associated X-linked inherited retinal dystrophy, including female manifestations. Clinical & experimental ophthalmology (2023)
Shilpa E Kuruvilla, Eileen Song, Naz Raoof, Katherine van Bysterveldt, Verity F Oliver, Sheng Chiong Hong, Rasha Al Taie, Graham A Wilson, Andrea L Vincent
Genotypic and phenotypic characterisation of RP2- and RPGR- associated X-linked inherited retinal dystrophy, including female manifestations. Clinical & experimental ophthalmology (2023)
Pushkar Raj Silwal, Arier C Lee, David Squirrell, Jinfeng Zhao, Matire Harwood, Andrea L Vincent, Rinki Murphy, Shanthi Ameratunga, Jacqueline Ramke
Use of public sector diabetes eye services in New Zealand 2006-2019: Analysis of national routinely collected datasets. PloS one 18 (5) (2023)
Cam Loveridge-Easther, Gulunay Kiray, Sarah Hull, Andrea L Vincent
Harboyan syndrome with biallelic SLC4A11 pathogenic variants misdiagnosed as congenital CMV infection. Ophthalmic genetics 43 (5) (2022)
Bernd Wissinger, Britta Baumann, Elena Buena-Atienza, Zeinab Ravesh, Artur V Cideciyan, Katarina Stingl, Isabelle Audo, Isabelle Meunier, Béatrice Bocquet, Elias I Traboulsi, Alison J Hardcastle, Jessica C Gardner, Michel Michaelides, Kari E Branham, Thomas Rosenberg, Sten Andreasson, Hélène Dollfus, David Birch, Andrea L Vincent, Loreto Martorell, Jaume Catala, Ulrich Kellner, Klaus Rüther, Birgit Lorenz, Markus N Preising, Emanuela Manfredini, Yuri A Zarate, Raymon Vijzelaar, Eberhart Zrenner, Samuel G Jacobson, Susanne Kohl
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America 119 (27) (2022)
Aaron P C Ong, Jie Zhang, Andrea L Vincent, Charles N J Mcghee
Megalocornea, anterior megalophthalmos, keratoglobus and associated anterior segment disorders: A review. Clinical & experimental ophthalmology 49 (5) (2021)
Benjamin M Nash, Christopher J G Watson, Edward Hughes, Alec L Hou, To Ha Loi, Bruce Bennetts, Diana Jelovic, Philip J Polkinghorne, Mark Gorbatov, John R B Grigg, Andrea L Vincent, Robyn V Jamieson
Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachment. European journal of human genetics : EJHG 29 (5) (2021)
Natasha Spiteri, Nino Hirnschall, Katherine van Bysterveldt, Alec Lin Hou, Gregory Moloney, Matthew Ball, Andrea L Vincent
Impact of TCF4 Repeat Number on Resolution of Corneal Edema after Descemet's Stripping Only in Fuchs Dystrophy: A Pilot Study. Vision (Basel, Switzerland) 5 (4) (2021)
Corina M Chilibeck, Shaheen Shah, Heather C Russell, Andrea L Vincent
The presence and progression of choroidal neurofibromas in a predominantly pediatric population with neurofibromatosis type-1. Ophthalmic genetics 42 (3) (2021)
Haya H Al-Ani, Leo Sheck, Andrea L Vincent
Peripheral pigmented lesions in ABCA4-associated retinopathy. Ophthalmic genetics 42 (4) (2021)
Kent W Small, Lee M Jampol, Benjamin Bakall, Leslie Small, Robert Wiggins, Steven Agemy, Nitin Udar, Jessica Avetisjan, Andrea L Vincent, Fadi S Shaya
Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1). Ophthalmic genetics (2021)
Su Ann Tay, Andrea L Vincent
Senior-Løken syndrome and intracranial hypertension. Ophthalmic genetics 41 (4) (2020)
Corina M Chilibeck, Emma E Glamuzina, Casey Y-J Ung, Emma L Blakely, Robert W Taylor, Andrea L Vincent
Albinism and a mitochondrial DNA deletion. Ophthalmic genetics 41 (3) (2020)
Jamie E Craig, Xikun Han, Ayub Qassim, Mark M Hassall, Jessica N Cooke Bailey, Tyler G Kinzy, Anthony P Khawaja, Jiyuan An, Henry Marshall, Puya Gharahkhani, Robert P Igo, Stuart L Graham, Paul R Healey, Jue-Sheng Ong, Tiger Zhou, Owen M Siggs, Matthew H Law, Emmanuelle Souzeau, Bronwyn Ridge, Pirro G Hysi, Kathryn P Burdon, Richard A Mills, John Landers, Jonathan B Ruddle, Ashish Agar, Anna Galanopoulos, Andrew J R White, Colin Eric Willoughby, Nicholas H Andrew, Stephen Best, Andrea L Vincent, Ivan Goldberg, Graham L Radford-Smith, Nicholas G Martin, Grant W Montgomery, Veronique Vitart, Rene Hoehn, Robert Wojciechowski, Jost Bruno Jonas, Tin Aung, Louis R Pasquale, Angela Jane Cree, Sobha Sivaprasad, Neeru A Vallabh, null null, null null, Ananth C Viswanathan, Francesca Pasutto, Jonathan L Haines, Caroline C W Klaver, Cornelia M van Duijn, Robert J Casson, Paul J Foster, Peng Tee Khaw, Christopher J Hammond, David A Mackey, Paul Mitchell, Andrew John Lotery, Janey L Wiggs, Alex W Hewitt, Stuart Macgregor
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature genetics 52 (2) (2020)
Jacqueline Ramke, Vanessa Jordan, Andrea L Vincent, Matire Harwood, Rinki Murphy, Shanthi Ameratunga
Diabetic eye disease and screening attendance by ethnicity in New Zealand: A systematic review. Clinical & experimental ophthalmology 47 (7) (2019)
Andrea L Vincent, Nandoun Abeysekera, Katherine A van Bysterveldt, Verity F Oliver, Jamie M Ellingford, Stephanie Barton, Graeme Cm Black
Next-generation sequencing targeted disease panel in rod-cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation. Clinical & experimental ophthalmology 45 (9) (2017)
Naz Raoof, Andrea L Vincent
Novel gene mutation in a patient with Bietti crystalline dystrophy without corneal deposits. Clinical & experimental ophthalmology 45 (4) (2017)
Katherine A van Bysterveldt, Rasha Al Taie, Will Ikink, Verity F Oliver, Andrea L Vincent
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians. Ophthalmic genetics 38 (6) (2017)