Erika Tavares
University of Toronto
H-index: 19
North America-Canada
Top articles of Erika Tavares
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Characterization of the Retinal Phenotype in PYGM-related McArdle Disease | Investigative Ophthalmology & Visual Science | Alaa Tayyib Rowaida Hussein Anupreet Tumber Kashif Ahmed Erika Tavares | 2023/6/1 |
Factors associated with research participation in a large primary care practice-based pediatric cohort: Results from the TARGet Kids! longitudinal cohort study | Plos one | Xuedi Li Charles DG Keown-Stoneman Cornelia M Borkhoff Peter D Wong Dana Arafeh | 2023/4/11 |
Randomized controlled trial evaluating a virtual parenting intervention for young children at risk of obesity: study protocol for Parenting Addressing Early Years Intervention … | Trials | Sarah Rae Jonathon Maguire Mary Aglipay Melanie Barwick Karoon Danavan | 2023/1/4 |
Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa | Clinical Genetics | Anna Dvaladze Erika Tavares Matteo Di Scipio Graeme Nimmo Monika K Grudzinska‐Pechhacker | 2022/12 |
Genetic structure in the nonbreeding range of rufa Red Knots suggests distinct Arctic breeding populations | The Condor | Yvonne I Verkuil Erika Tavares Patricia M González Kristen Choffe Oliver Haddrath | 2022/2/1 |
Unilateral cataract and congenital stationary night blindness in a child with novel variants in TRPM1 | Journal of American Association for Pediatric Ophthalmology and Strabismus | Eman Saleh Monika Grudzinska Pechhacker Anjali Vig Maanik Mehta Jason Maynes | 2022/8/1 |
Underweight in the first 2 years of life and growth in later childhood | JAMA Network Open | Courtney A South Charles DG Keown-Stoneman Catherine S Birken Vasanti S Malik Stanley H Zlotkin | 2022/7/1 |
Prevalence of choroidal abnormalities and lisch nodules in children meeting clinical and molecular diagnosis of neurofibromatosis type 1 | Translational Vision Science & Technology | Mariana Flores Pimentel Anna Heath Michael J Wan Rowaida Hussein Kate E Leahy | 2022/2/1 |
Natural history study of visual function in patients with BBS1-and BBS10-related retinal degeneration. | Investigative Ophthalmology & Visual Science | Monika Grudzinska Pechhacker Samuel G Jacobson Arlene V Drack Matteo Di Scipio Ine Stubbe | 2021/6/21 |
Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness | Genes | Kate E Leahy Tom Wright Monika K Grudzinska Pechhacker Isabelle Audo Anupreet Tumber | 2021/2/25 |
Comparative natural history of visual function from patients with biallelic variants in BBS1 and BBS10 | Investigative ophthalmology & visual science | Monika K Grudzinska Pechhacker Samuel G Jacobson Arlene V Drack Matteo Di Scipio Ine Strubbe | 2021/12/1 |
Parent engagement in co-design of clinical trials: the PARENT trial | Trials | Leigh M Vanderloo Shelley M Vanderhout Erika Tavares Jonathon Maguire Sharon Straus | 2021/12 |
Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing … | Genes | Zhuo Shao Ikuo Masuho Anupreet Tumber Jason T Maynes Erika Tavares | 2021/8/29 |
The Role of Extended Phenotyping and Functional Testing in Variant Interpretation of a Complex Patient with Overlapping Traits | Investigative Ophthalmology & Visual Science | Zhuo Shao Ikuo Masuho Anupreet Tumber Jason Maynes Erika Tavares | 2021/6/21 |
Cow’s Milk Fat Obesity pRevention Trial (CoMFORT): a primary care embedded randomised controlled trial protocol to determine the effect of cow’s milk fat on child adiposity | BMJ open | Shelley M Vanderhout Mary Aglipay Catherine Birken Patricia Li Deborah L O'Connor | 2020/5/1 |
CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency | Ophthalmic Genetics | Monika K Grudzinska Pechhacker Matteo Di Scipio Anjali Vig Anupreet Tumber Nicole Roslin | 2020/9/2 |
Phenotype driven analysis of whole genome sequencing identifies deep intronic variants that cause retinal dystrophies by aberrant exonization | Investigative ophthalmology & visual science | Matteo Di Scipio Erika Tavares Shriya Deshmukh Isabelle Audo Kit Green-Sanderson | 2020/8/3 |
Taxonomic status of the extinct Canary Islands Oystercatcher Haematopus meadewaldoi | Ibis | Tereza Senfeld Thomas J Shannon Hein Van Grouw Dane M Paijmans Erika S Tavares | 2019 |
COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage | Scientific Reports | Sami Tabbarah Erika Tavares Jason Charish Ajoy Vincent Andrew Paterson | 2020/12/4 |
Discovery of novel disease-causing mutations in inherited retinal dystrophies–an application to retinitis pigmentosa | Investigative Ophthalmology & Visual Science | W Yu Caberry Erika Tavares Vaishnavi Batmanabane Ajoy Vincent Elise Heon | 2020/6/10 |
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