| Functional impact of global rare copy number variation in autism spectrum disorders D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ... Nature 466 (7304), 368-372, 2010 | 2324 | 2010 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1654 | 2007 |
| A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009 | 798 | 2009 |
| A genome-wide scan for common alleles affecting risk for autism R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ... Human molecular genetics 19 (20), 4072-4082, 2010 | 727 | 2010 |
| A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium Human Molecular Genetics 7 (3), 571-578, 1998 | 504 | 1998 |
| Individual common variants exert weak effects on the risk for autism spectrum disorders R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ... Human molecular genetics 21 (21), 4781-4792, 2012 | 452 | 2012 |
| 224th ENMC International Workshop:: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016 Y Allenbach, AL Mammen, O Benveniste, W Stenzel, A Amato, A Aussey, ... Neuromuscular disorders 28 (1), 87-99, 2018 | 449 | 2018 |
| A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia SE Fisher, AJ Marlow, J Lamb, E Maestrini, DF Williams, AJ Richardson, ... The American journal of human genetics 64 (1), 146-156, 1999 | 415 | 1999 |
| A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p International Molecular Genetic Study of Autism Consortium The American Journal of Human Genetics 69 (3), 570-581, 2001 | 411 | 2001 |
| FOXP2 is not a major susceptibility gene for autism or specific language impairment DF Newbury, E Bonora, JA Lamb, SE Fisher, CSL Lai, G Baird, L Jannoun, ... The American Journal of Human Genetics 70 (5), 1318-1327, 2002 | 371 | 2002 |
| A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12 JE Asher, JA Lamb, D Brocklebank, JB Cazier, E Maestrini, L Addis, ... The American Journal of Human Genetics 84 (2), 279-285, 2009 | 302 | 2009 |
| The EuroMyositis registry: an international collaborative tool to facilitate myositis research JB Lilleker, J Vencovsky, G Wang, LR Wedderburn, LP Diederichsen, ... Annals of the rheumatic diseases 77 (1), 30-39, 2018 | 249 | 2018 |
| A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ... Human genetics 131, 565-579, 2012 | 229 | 2012 |
| Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT G Barnby, A Abbott, N Sykes, A Morris, DE Weeks, R Mott, J Lamb, ... The American Journal of Human Genetics 76 (6), 950-966, 2005 | 216 | 2005 |
| 239th ENMC international workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018 AL Mammen, Y Allenbach, W Stenzel, O Benveniste, J De Bleecker, ... Neuromuscular Disorders 30 (1), 70-92, 2020 | 214 | 2020 |
| Autism: recent molecular genetic advances JA Lamb, J Moore, A Bailey, AP Monaco Human Molecular Genetics 9 (6), 861-868, 2000 | 212 | 2000 |
| Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08 PK Gregersen, R Kosoy, AT Lee, J Lamb, J Sussman, D McKee, ... Annals of neurology 72 (6), 927-935, 2012 | 189 | 2012 |
| Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic … S Rothwell, RG Cooper, IE Lundberg, FW Miller, PK Gregersen, J Bowes, ... Annals of the rheumatic diseases 75 (8), 1558-1566, 2016 | 168 | 2016 |
| High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility E Maestrini, AT Pagnamenta, JA Lamb, E Bacchelli, NH Sykes, I Sousa, ... Molecular psychiatry 15 (9), 954-968, 2010 | 165 | 2010 |
| Molecular findings from 537 individuals with inherited retinal disease JM Ellingford, S Barton, S Bhaskar, J O'Sullivan, SG Williams, JA Lamb, ... Journal of medical genetics 53 (11), 761-767, 2016 | 162 | 2016 |
