DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration A Vig, JA Poulter, D Ottaviani, E Tavares, K Toropova, AM Tracewska, ... Genetics in Medicine 22 (12), 2041-2051, 2020 | 42 | 2020 |
Biomarkers of agitation and aggression in Alzheimer's disease: a systematic review M Ruthirakuhan, KL Lanctôt, M Di Scipio, M Ahmed, N Herrmann Alzheimer's & Dementia 14 (10), 1344-1376, 2018 | 38 | 2018 |
Phenotype driven analysis of whole genome sequencing identifies deep intronic variants that cause retinal dystrophies by aberrant exonization M Di Scipio, E Tavares, S Deshmukh, I Audo, K Green-Sanderson, ... Investigative ophthalmology & visual science 61 (10), 36-36, 2020 | 23 | 2020 |
CDC42 regulates the expression of superficial zone molecules in part through the actin cytoskeleton and myocardin‐related transcription factor‐A E Delve, J Parreno, V Co, PH Wu, J Chong, M Di Scipio, RA Kandel Journal of Orthopaedic Research® 36 (9), 2421-2430, 2018 | 15 | 2018 |
Comparative natural history of visual function from patients with biallelic variants in BBS1 and BBS10 MKG Pechhacker, SG Jacobson, AV Drack, M Di Scipio, I Strubbe, ... Investigative ophthalmology & visual science 62 (15), 26-26, 2021 | 13 | 2021 |
A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets M Di Scipio, M Khan, S Mao, M Chong, C Judge, N Pathan, N Perrot, ... Nature Communications 14 (1), 5196, 2023 | 8 | 2023 |
CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency MK Grudzinska Pechhacker, M Di Scipio, A Vig, A Tumber, N Roslin, ... Ophthalmic Genetics 41 (5), 457-464, 2020 | 4 | 2020 |
Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa A Dvaladze, E Tavares, M Di Scipio, G Nimmo, ... Clinical Genetics 102 (6), 524-529, 2022 | 2 | 2022 |
COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage S Tabbarah, E Tavares, J Charish, A Vincent, A Paterson, M Di Scipio, ... Scientific Reports 10 (1), 21269, 2020 | 2 | 2020 |
What Causes Premature Coronary Artery Disease? A Le, H Peng, D Golinsky, M Di Scipio, R Lali, G Paré Current Atherosclerosis Reports 26 (6), 189-203, 2024 | 1 | 2024 |
Genetic Determinants of Vascular Dementia N Pathan, MK Kharod, S Nawab, M Di Scipio, G Paré, M Chong Canadian Journal of Cardiology, 2024 | 1 | 2024 |
The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions A Man, M Di Scipio, S Grewal, Y Suk, E Trinari, R Ejaz, R Whitney Genes 15 (3), 332, 2024 | 1 | 2024 |
A method to estimate the contribution of rare coding variants to complex trait heritability N Pathan, WQ Deng, M Di Scipio, M Khan, S Mao, RW Morton, R Lali, ... Nature Communications 15 (1), 1245, 2024 | 1 | 2024 |
P311: Use of a DNA methylation signature for the diagnosis of TET3-related Beck-Fahrner syndrome and expansion of its related phenotype A Man, M Di Scipio, R Hough, H McConkey, E Diehl, C Marshall, ... Genetics in Medicine Open 2, 2024 | | 2024 |
Contribution of rare coding variants to complex trait heritability N Pathan, WQ Deng, M Khan, M Di Scipio, S Mao, RW Morton, R Lali, ... | | 2022 |
A Versatile, Fast, and Unbiased Method for Estimation of Gene-by-environment Interaction Effects on Biobank-Scale Datasets M Di Scipio, M Khan, S Mao, M Chong, N Pathan, C Judge, N Perrot, ... GENETIC EPIDEMIOLOGY 46 (7), 490-490, 2022 | | 2022 |
Natural history study of visual function in patients with BBS1-and BBS10-related retinal degeneration. MG Pechhacker, SG Jacobson, AV Drack, M Di Scipio, I Stubbe, ... Investigative Ophthalmology & Visual Science 62 (8), 3284-3284, 2021 | | 2021 |
A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets M Khan, M Di Scipio, C Judge, N Perrot, M Chong, S Mao, S Di, W Nelson, ... medRxiv, 2021.04. 24.21255884, 2021 | | 2021 |
CRB1-related retinopathy superimposed on a S-adenosylhomocysteine hydrolase deficiency phenotype M Di Scipio, MK Pechhacker, A Vig, A Anupreet, E Tavares, A Vincent, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 186-187, 2020 | | 2020 |
Proteoglycan 4 expression by superficial zone chondrocytes is regulated in part by JNK and P38 in vitro E Delve, M Di Scipio, R Kandel Osteoarthritis and Cartilage 28, S106, 2020 | | 2020 |