| A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects C Marshall, D Howrigan, D Merico, B Thiruvahindrapuram, W Wu, D Greer, ... Nature Genetics 49 (11), 27–35, 2016 | 996* | 2016 |
| Paternally inherited cis-regulatory structural variants are associated with autism WM Brandler, D Antaki, M Gujral, ML Kleiber, J Whitney, MS Maile, ... Science 360 (6386), 327-331, 2018 | 219 | 2018 |
| Common variants in left/right asymmetry genes and pathways are associated with relative hand skill WM Brandler, AP Morris, DM Evans, TS Scerri, JP Kemp, NJ Timpson, ... PLoS genetics 9 (9), e1003751, 2013 | 180 | 2013 |
| The genetic relationship between handedness and neurodevelopmental disorders WM Brandler, S Paracchini Trends in molecular medicine 20 (2), 83-90, 2014 | 178 | 2014 |
| PCSK6 is associated with handedness in individuals with dyslexia TS Scerri, WM Brandler, S Paracchini, AP Morris, SM Ring, AJ Richardson, ... Human molecular genetics 20 (3), 608-614, 2011 | 166 | 2011 |
| Genome‐wide screening for DNA variants associated with reading and language traits A Gialluisi, DF Newbury, EG Wilcutt, RK Olson, JC DeFries, WM Brandler, ... Genes, Brain and Behavior 13 (7), 686-701, 2014 | 147 | 2014 |
| Frequency and complexity of de novo structural mutation in autism WM Brandler, D Antaki, M Gujral, A Noor, G Rosanio, TR Chapman, ... The American Journal of Human Genetics 98 (4), 667-679, 2016 | 118 | 2016 |
| Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia A Gialluisi, TFM Andlauer, N Mirza-Schreiber, K Moll, J Becker, ... Translational psychiatry 9 (1), 77, 2019 | 110 | 2019 |
| Autism risk in offspring can be assessed through quantification of male sperm mosaicism MW Breuss, D Antaki, RD George, M Kleiber, KN James, LL Ball, O Hong, ... Nature Medicine 26 (1), 143-150, 2020 | 92 | 2020 |
| SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes D Antaki, WM Brandler, J Sebat Bioinformatics 34 (10), 1774-1777, 2018 | 56 | 2018 |
| From de novo mutations to personalized therapeutic interventions in autism WM Brandler, J Sebat Annual review of medicine 66 (1), 487-507, 2015 | 53 | 2015 |
| Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia NH Simpson, L Addis, WM Brandler, V Slonims, A Clark, J Watson, ... Developmental Medicine & Child Neurology 56 (4), 346-353, 2014 | 51 | 2014 |
| The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts R Shore, L Covill, KA Pettigrew, WM Brandler, R Diaz, Y Xu, JA Tello, ... Human Molecular Genetics 25 (9), 1771-1779, 2016 | 10 | 2016 |
| Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions EA Maury, MA Sherman, G Genovese, TG Gilgenast, T Kamath, SJ Burris, ... Cell genomics 3 (8), 2023 | 9 | 2023 |
| The Genetic Revolution: Implications for our health, children, and gym attendance: Science Communication Competition Winning Article W Brandler The Biochemist 33 (4), 42-44, 2011 | 1 | 2011 |
| Advancements in somatic variant calling from UG100 whole genome and whole exome sequencing data D Shem-Tov, M Levy, G Hornung, I Soifer, H Benjamin, A Jaimovich, ... Cancer Research 84 (6_Supplement), 4926-4926, 2024 | | 2024 |
| Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia G Alessandro, AT FM, MS Nazanin, K Moll, J Becker, P Hoffmann, ... Translational Psychiatry 9 (1), 2019 | | 2019 |
| Methods for assessing risk of or diagnosing genetic defects by identifying de novo mutations or somatic mosaic variants in sperm or somatic tissues J Gleeson, M Breuss, J Kiely, J Sebat, M Kleiber, D Antaki, W Brandler | | 2018 |
| SV2: Accurate Structural Variation Genotyping andDe NovoMutation Detection from Whole Genomes D Antaki, WM Brandler, J Sebat | | 2017 |
Silvia ParacchiniProfessor, University of St Andrews在 st-andrews.ac.uk 的电子邮件经过验证
