| Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ... Nature 515 (7526), 209-215, 2014 | 2945 | 2014 |
| Mapping genomic loci implicates genes and synaptic biology in schizophrenia V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ... Nature 604 (7906), 502-508, 2022 | 1794 | 2022 |
| The UK10K project identifies rare variants in health and disease Statistics group Ciampi Antonio 8 Greenwood Celia MT (co-chair) 7 8 14 19 ... Nature 526 (7571), 82-90, 2015 | 1134 | 2015 |
| Brain charts for the human lifespan RAI Bethlehem, J Seidlitz, SR White, JW Vogel, KM Anderson, ... Nature 604 (7906), 525-533, 2022 | 1112 | 2022 |
| Timing, rates and spectra of human germline mutation R Rahbari, A Wuster, SJ Lindsay, RJ Hardwick, LB Alexandrov, S Al Turki, ... Nature genetics 48 (2), 126-133, 2016 | 960 | 2016 |
| Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ... Nature neuroscience 19 (4), 571-577, 2016 | 456 | 2016 |
| Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ... Nature communications 6 (1), 8111, 2015 | 444 | 2015 |
| The genetic basis of non-syndromic intellectual disability: a review L Kaufman, M Ayub, JB Vincent Journal of neurodevelopmental disorders 2, 182-209, 2010 | 412 | 2010 |
| A roadmap to increase diversity in genomic studies S Fatumo, T Chikowore, A Choudhury, M Ayub, AR Martin, ... Nature medicine 28 (2), 243-250, 2022 | 394 | 2022 |
| INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse M Jacoby, JJ Cox, S Gayral, DJ Hampshire, M Ayub, M Blockmans, ... Nature genetics 41 (9), 1027-1031, 2009 | 377 | 2009 |
| Suicide, self-harm and suicidal ideation during COVID-19: a systematic review S Farooq, J Turnmore, W Ali, M Ayub Psychiatry Research, 2021 | 359 | 2021 |
| Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan KJ Carss, E Stevens, AR Foley, S Cirak, M Riemersma, S Torelli, ... The American Journal of Human Genetics 93 (1), 29-41, 2013 | 253 | 2013 |
| Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability MA Khan, MA Rafiq, A Noor, S Hussain, JV Flores, V Rupp, AK Vincent, ... The American Journal of Human Genetics 90 (5), 856-863, 2012 | 245 | 2012 |
| An international adult guideline for making clozapine titration safer by using six ancestry-based personalized dosing titrations, CRP, and clozapine levels J De Leon, G Schoretsanitis, RL Smith, E Molden, A Solismaa, N Seppälä, ... Pharmacopsychiatry 55 (02), 73-86, 2022 | 222 | 2022 |
| Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ... Molecular psychiatry 23 (4), 973-984, 2018 | 196 | 2018 |
| Identification of mutations in TRAPPC9, which encodes the NIK-and IKK-β-binding protein, in nonsyndromic autosomal-recessive mental retardation A Mir, L Kaufman, A Noor, MM Motazacker, T Jamil, M Azam, K Kahrizi, ... The American Journal of Human Genetics 85 (6), 909-915, 2009 | 187 | 2009 |
| Barriers to using clozapine in treatment-resistant schizophrenia: systematic review S Farooq, A Choudry, D Cohen, F Naeem, M Ayub BJPsych bulletin 43 (1), 8-16, 2019 | 169 | 2019 |
| Prevalence and psychosocial risk factors of PTSD: 18 months after Kashmir earthquake in Pakistan F Naeem, M Ayub, K Masood, H Gul, M Khalid, A Farrukh, A Shaheen, ... Journal of affective disorders 130 (1-2), 268-274, 2011 | 130 | 2011 |
| CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa A Noor, C Windpassinger, M Patel, B Stachowiak, A Mikhailov, M Azam, ... The American Journal of Human Genetics 82 (4), 1011-1018, 2008 | 125 | 2008 |
| Screen use and mental health symptoms in Canadian children and youth during the COVID-19 pandemic X Li, LM Vanderloo, CDG Keown-Stoneman, KT Cost, A Charach, ... JAMA network open 4 (12), e2140875-e2140875, 2021 | 123 | 2021 |
Farooq NaeemUniversity of Toronto, Toronto, ON, CanadaVerifierad e-postadress på camh.ca