| A copy number variation map of the human genome M Zarrei, JR MacDonald, D Merico, SW Scherer Nature reviews genetics 16 (3), 172-183, 2015 | 946 | 2015 |
| Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ... Nature neuroscience 20 (4), 602-611, 2017 | 785 | 2017 |
| Whole-genome sequencing of quartet families with autism spectrum disorder RKC Yuen, B Thiruvahindrapuram, D Merico, S Walker, K Tammimies, ... Nature Medicine 21 (2), 185-191, 2015 | 588 | 2015 |
| Genome-wide characteristics of de novo mutations in autism RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ... NPJ Genomic Medicine 1, 16027-1, 2016 | 237 | 2016 |
| Clinically relevant copy number variations detected in cerebral palsy M Oskoui, MJ Gazzellone, B Thiruvahindrapuram, M Zarrei, J Andersen, ... Nature Communications 6, 2015 | 159 | 2015 |
| Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors ND Anderson, R de Borja, MD Young, F Fuligni, A Rosic, ND Roberts, ... Science 361 (6405), eaam8419, 2018 | 153 | 2018 |
| A large data resource of genomic copy number variation across neurodevelopmental disorders M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ... NPJ genomic medicine 4 (1), 26, 2019 | 147 | 2019 |
| Genomic architecture of autism from comprehensive whole-genome sequence annotation B Trost, B Thiruvahindrapuram, AJS Chan, W Engchuan, ... Cell 185 (23), 4409-4427. e18, 2022 | 98 | 2022 |
| De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy M Zarrei, DL Fehlings, K Mawjee, L Switzer, B Thiruvahindrapuram, ... Genetics in Medicine 20 (2), 172-180, 2018 | 94 | 2018 |
| Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology R Mello-Silva, DYAC Santos, MLF Salatino, LB Motta, MB Cattai, D Sasaki, ... Annals of Botany 108 (1), 87-102, 2011 | 85 | 2011 |
| Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation M Zarrei, MJ Gazzellone, CL Burton, S Walker, M Uddin, SM Shaheen, ... American Society of Human Genetics - ASHG 2016, 2016 | 75* | 2016 |
| Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation M Gazzellone, M Zarrei, SW Scherer J Neurodev Disord 8, 36, 2016 | 75 | 2016 |
| Molecular systematics of Gagea and Lloydia (Liliaceae; Liliales): implications of analyses of nuclear ribosomal and plastid DNA sequences for infrageneric classification M Zarrei, P Wilkin, MF Fay, MJ Ingrouille, S Zarre, MW Chase Annals of Botany, mcp103, 2009 | 65 | 2009 |
| Whole-genome sequencing suggests schizophrenia risk mechanisms in humans with 22q11. 2 deletion syndrome D Merico, M Zarrei, G Costain, L Ogura, B Alipanahi, MJ Gazzellone, ... G3: Genes, Genomes, Genetics 5 (11), 2453-2461, 2015 | 60 | 2015 |
| Systematic revision of the genus Gagea Salisb. (Liliaceae) in Iran M Zarrei, S Zarre, P Wilkin, M Rix Botanical Journal of the Linnean Society 154 (4), 559-588, 2007 | 48 | 2007 |
| Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly M Woodbury-Smith, E Deneault, RKC Yuen, S Walker, M Zarrei, ... Molecular autism 8, 1-10, 2017 | 45 | 2017 |
| Pollen morphology of the genus Gagea (Liliaceae) in Iran M Zarrei, S Zarre Flora-morphology, distribution, functional ecology of plants 200 (1), 96-108, 2005 | 45 | 2005 |
| Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes M Woodbury-Smith, R Nicolson, M Zarrei, RKC Yuen, S Walker, J Howe, ... NPJ genomic medicine 2 (1), 17, 2017 | 44 | 2017 |
| Intratumoral genetic and functional heterogeneity in pediatric glioblastoma M Hoffman, AH Gillmor, DJ Kunz, MJ Johnston, A Nikolic, K Narta, ... Cancer research 79 (9), 2111-2123, 2019 | 42 | 2019 |
| Indexing effects of copy number variation on genes involved in developmental delay M Uddin, G Pellecchia, B Thiruvahindrapuram, L D’Abate, D Merico, ... Scientific reports 6 (1), 28663, 2016 | 40 | 2016 |
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of Toronto在 sickkids.ca 的电子邮件经过验证
