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Tara A. Paton, Ph.D. - Publications

Affiliations: 
2004 University of Toronto, Toronto, ON, Canada 
Area:
Zoology Biology, Genetics
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. Npj Genomic Medicine. 4: 26. PMID 31602316 DOI: 10.1038/S41525-019-0098-3  0.337
2019 Sullivan K, Isabel S, Khodai-Booran N, Paton TA, Abdulnoor M, Dipchand AI, Hébert D, Ng VL, Allen UD. Epstein-Barr VIRUS latent gene EBNA-1 genetic diversity among transplant patients compared with patients with infectious mononucleosis. Clinical Transplantation. e13504. PMID 30790353 DOI: 10.1111/Ctr.13504  0.313
2019 Abdulnoor M, Khodai-Booran N, Schechter T, Paton T, Casallo G, Allen UD. 1778. Epstein–Barr Virus Genetic Diversity: Evaluation of BZLF1 Variants among Bone Marrow Transplant Patients and Individuals with Infectious Mononucleosis Open Forum Infectious Diseases. 6: S655-S655. DOI: 10.1093/Ofid/Ofz360.1641  0.368
2017 Cohn I, Paton TA, Marshall CR, Basran R, Stavropoulos DJ, Ray PN, Monfared N, Hayeems RZ, Meyn MS, Bowdin S, Scherer SW, Cohn RD, Ito S. Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study. Npj Genomic Medicine. 2: 19. PMID 29263831 DOI: 10.1038/S41525-017-0021-8  0.369
2017 Farrell SA, Sodhi S, Marshall CR, Guerin A, Slavotinek A, Paton T, Chong K, Sirkin WL, Scherer SW, Bérubé-Simard FA, Pilon N. HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia. American Journal of Medical Genetics. Part A. PMID 28898547 DOI: 10.1002/Ajmg.A.38354  0.37
2017 C Yuen RK, Merico D, Bookman M, L Howe J, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, Pellecchia G, Buchanan JA, Walker S, Marshall CR, Uddin M, ... ... Paton T, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nature Neuroscience. PMID 28263302 DOI: 10.1038/Nn.4524  0.413
2017 Lok S, Paton TA, Wang Z, Kaur G, Walker S, Yuen RK, Sung WW, Whitney J, Buchanan JA, Trost B, Singh N, Apresto B, Chen N, Coole M, Dawson TJ, et al. De novo genome and transcriptome assembly of the Canadian beaver (Castor canadensis). G3 (Bethesda, Md.). PMID 28087693 DOI: 10.1534/G3.116.038208  0.32
2017 Allen U, Abdulnoor M, Khodai-Booran N, Paton T, Dipchand A, Hebert D, Ng V, Solomon M. Genetic Diversity of Epstein–Barr Virus Lytic Gene BZLF-1 among Patients with and Without Post-transplant Lymphoproliferative Disorder Open Forum Infectious Diseases. 4: S733-S733. DOI: 10.1093/Ofid/Ofx163.1976  0.319
2015 Allen UD, Hu P, Pereira SL, Robinson JL, Paton TA, Beyene J, Khodai-Booran N, Dipchand A, Hébert D, Ng V, Nalpathamkalam T, Read S. The genetic diversity of Epstein-Barr virus in the setting of transplantation relative to non-transplant settings: A feasibility study. Pediatric Transplantation. PMID 26578436 DOI: 10.1111/Petr.12610  0.353
2015 Marshall CR, Scherer SW, Zariwala MA, Lau L, Paton TA, Stockley T, Jobling RK, Ray PN, Knowles MR, Hall DA, Dell SD, Kim RH. Whole Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. G3 (Bethesda, Md.). PMID 26139845 DOI: 10.1534/G3.115.019851  0.372
2015 Marshall CR, Farrell SA, Cushing D, Paton T, Stockley TL, Stavropoulos DJ, Ray PN, Szego M, Lau L, Pereira SL, Cohn RD, Wintle RF, Abuzenadah AM, Abu-Elmagd M, Scherer SW. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. Bmc Genomics. 16: S12. PMID 25923536 DOI: 10.1186/1471-2164-16-S1-S12  0.314
2015 Ammar R, Paton TA, Torti D, Shlien A, Bader GD. Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes. F1000research. 4: 17. PMID 25901276 DOI: 10.12688/F1000Research.6037.1  0.344
2015 Jobling RK, Assoum M, Gakh O, Blaser S, Raiman JA, Mignot C, Roze E, Dürr A, Brice A, Lévy N, Prasad C, Paton T, Paterson AD, Roslin NM, Marshall CR, et al. PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia. Brain : a Journal of Neurology. 138: 1505-17. PMID 25808372 DOI: 10.1093/Brain/Awv057  0.318
2015 Al-Maawali A, Dupuis L, Blaser S, Heon E, Tarnopolsky M, Al-Murshedi F, Marshall CR, Paton T, Scherer SW, Roelofsen J, van Kuilenburg AB, Mendoza-Londono R. Prenatal growth restriction, retinal dystrophy, diabetes insipidus and white matter disease: expanding the spectrum of PRPS1-related disorders. European Journal of Human Genetics : Ejhg. 23: 310-6. PMID 24961627 DOI: 10.1038/Ejhg.2014.112  0.347
2014 Aïssi D, Dennis J, Ladouceur M, Truong V, Zwingerman N, Rocanin-Arjo A, Germain M, Paton TA, Morange PE, Gagnon F, Trégouët DA. Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation. Plos One. 9: e108087. PMID 25265411 DOI: 10.1371/Journal.Pone.0108087  0.302
2012 Andrade DM, Paton T, Turnbull J, Marshall CR, Scherer SW, Minassian BA. Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy. Pediatric Neurology. 47: 205-8. PMID 22883287 DOI: 10.1016/J.Pediatrneurol.2012.05.004  0.329
2012 Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Paton T, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301  0.331
2010 Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Paton T, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307  0.339
2010 Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Paton T, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146  0.348
2007 Baker AJ, Pereira SL, Paton TA. Phylogenetic relationships and divergence times of Charadriiformes genera: multigene evidence for the Cretaceous origin of at least 14 clades of shorebirds. Biology Letters. 3: 205-9. PMID 17284401 DOI: 10.1098/Rsbl.2006.0606  0.524
2006 Paton TA, Baker AJ. Sequences from 14 mitochondrial genes provide a well-supported phylogeny of the Charadriiform birds congruent with the nuclear RAG-1 tree. Molecular Phylogenetics and Evolution. 39: 657-67. PMID 16531074 DOI: 10.1016/J.Ympev.2006.01.011  0.538
2004 Nakabayashi K, Makino S, Minagawa S, Smith AC, Bamforth JS, Stanier P, Preece M, Parker-Katiraee L, Paton T, Oshimura M, Mill P, Yoshikawa Y, Hui CC, Monk D, Moore GE, et al. Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues. Journal of Medical Genetics. 41: 601-8. PMID 15286155 DOI: 10.1136/Jmg.2003.014142  0.314
2004 Kahr WH, Li L, Traivaree C, Christensen H, Paton T, Butchard SE, Curtin J, Blanchette VS. Congenital Macrothrombocytopenia and Defective Localization of the Nonmuscle Myosin Heavy Chain IIA in Leukocytes and Megakaryocytes with a Normal MYH9 Gene. Blood. 104: 3032-3032. DOI: 10.1182/Blood.V104.11.3032.3032  0.33
2003 Paton TA, Baker AJ, Groth JG, Barrowclough GF. RAG-1 sequences resolve phylogenetic relationships within Charadriiform birds. Molecular Phylogenetics and Evolution. 29: 268-78. PMID 13678682 DOI: 10.1016/S1055-7903(03)00098-8  0.514
2003 van Tuinen M, Paton T, Haddrath O, Baker A. ‘Big bang’ for Tertiary birds? A reply Trends in Ecology & Evolution. 18: 442-443. DOI: 10.1016/S0169-5347(03)00212-X  0.422
2002 Paton T, Haddrath O, Baker AJ. Complete mitochondrial DNA genome sequences show that modern birds are not descended from transitional shorebirds. Proceedings. Biological Sciences / the Royal Society. 269: 839-46. PMID 11958716 DOI: 10.1098/Rspb.2002.1961  0.524
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