Publications by authors named "Tara Paton"

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Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.
Rabiat Adele, Rowaida Hussein, Erika Tavares, Kashif Ahmed, Matteo Di Scipio, Tara A Paton

JCI Insight· December 2024

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Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomics.
Si Lok, Timothy N H Lau, Brett Trost, Amy H Y Tong, Tara Paton

Sci Rep· September 2024

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novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC.
Saima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah, Muhammad Ansar, Tara Paton

Int J Neurosci· June 2024

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Analysis of prognostic germline polymorphisms in patients with advanced hepatocellular carcinoma.
Michael Herman, Benjamin H Lok, Steven Gallinger, Laura Dawson, Raymond Kim, Tara Paton

Transl Gastroenterol Hepatol· October 2023

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Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non-syndromic retinitis pigmentosa.
Anna Dvaladze, Erika Tavares, Matteo Di Scipio, Graeme Nimmo, Monika K Grudzinska-Pechhacker, Tara Paton

Clin Genet· December 2022

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Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, Worrawat Engchuan, Edward J Higginbotham, Tara Paton

Cell· November 2022

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BCOR Internal Tandem Duplication Associated Uterine Sarcoma: Expanding the Clinicopathologic Spectrum.
Sakinah A Thiryayi, Helen Ettler, Emily A Goebel, Michel Prefontaine, Tara A Paton

Int J Gynecol Pathol· September 2022

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Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting.
Iris Cohn, Roozbeh Manshaei, Eriskay Liston, John B A Okello, Reem Khan, Tara A Paton

JAMA Netw Open· May 2021

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DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration.
Anjali Vig, James A Poulter, Daniele Ottaviani, Erika Tavares, Katerina Toropova, Tara Paton

Genet Med· December 2020

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A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Tara Paton

NPJ Genom Med· October 2019

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Epstein-Barr virus latent gene EBNA-1 genetic diversity among transplant patients compared with patients with infectious mononucleosis.
Katie Sullivan, Sandra Isabel, Nasser Khodai-Booran, Tara A Paton, Mariana Abdulnoor

Clin Transplant· April 2019

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Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND Network.
Danielle A Baribeau, Annie Dupuis, Tara A Paton, Christopher Hammill, Stephen W Scherer

Transl Psychiatry· February 2019

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The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
Miriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, Joe Whitney, Iris Cohn, Tara A Paton

CMAJ· February 2018

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HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia.
Sandra A Farrell, Sandi Sodhi, Christian R Marshall, Andrea Guerin, Anne Slavotinek, Tara Paton

Am J Med Genet A· November 2017

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Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders.
Danielle A Baribeau, Annie Dupuis, Tara A Paton, Stephen W Scherer, Russell J Schachar

Sci Rep· September 2017

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Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study.
Iris Cohn, Tara A Paton, Christian R Marshall, Raveen Basran, Dimitri J Stavropoulos

NPJ Genom Med· May 2017

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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Tara Paton

Nat Neurosci· April 2017

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Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression.
Daniel R Evans, Jane S Green, Gordon J Johnson, Jeremy Schwartzentruber, Jacek Majewski, Tara A Paton

Invest Ophthalmol Vis Sci· March 2017

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Genome and Transcriptome Assembly of the Canadian Beaver ().
Si Lok, Tara A Paton, Zhuozhi Wang, Gaganjot Kaur, Susan Walker

G3 (Bethesda)· February 2017

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Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network.
Nardin Samuel, Gavin Wilson, Badr Id Said, Anna Pan, Genevieve Deblois, Tara Paton

Oncotarget· August 2016

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Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L.
Grace Yoon, Zeenat Malam, Tara Paton, Christian R Marshall, Ella Hyatt

J Pediatr· April 2016

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The genetic diversity of Epstein-Barr virus in the setting of transplantation relative to non-transplant settings: A feasibility study.
Upton D Allen, Pingzhao Hu, Sergio L Pereira, Joan L Robinson, Tara A Paton

Pediatr Transplant· February 2016

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Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome.
Christian R Marshall, Sandra A Farrell, Donna Cushing, Tara Paton, Tracy L Stockley

BMC Genomics· January 2016

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GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis.
Gregory S Day, Harald Prüss, Susanne M Benseler, Tara A Paton, Andrew D Paterson

Neurol Neuroimmunol Neuroinflamm· October 2015

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Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia.
Christian R Marshall, Stephen W Scherer, Maimoona A Zariwala, Lynette Lau, Tara A Paton

G3 (Bethesda)· July 2015

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