| Large recurrent microdeletions associated with schizophrenia H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ... nature 455 (7210), 232-236, 2008 | 3691* | 2008 |
| Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivičres, ... Nature 520 (7546), 224-229, 2015 | 882 | 2015 |
| Meta-analysis and imputation refines the association of 15q25 with smoking quantity JZ Liu, F Tozzi, DM Waterworth, SG Pillai, P Muglia, L Middleton, ... Nature genetics 42 (5), 436-440, 2010 | 738 | 2010 |
| The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ... Brain imaging and behavior 8, 153-182, 2014 | 707 | 2014 |
| The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 687 | 2020 |
| A genome-wide investigation of SNPs and CNVs in schizophrenia AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ... PLoS genetics 5 (2), e1000373, 2009 | 572 | 2009 |
| α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking W Berrettini, X Yuan, F Tozzi, K Song, C Francks, H Chilcoat, ... Molecular psychiatry 13 (4), 368-373, 2008 | 543 | 2008 |
| ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries PM Thompson, N Jahanshad, CRK Ching, LE Salminen, SI Thomopoulos, ... Translational psychiatry 10 (1), 100, 2020 | 538 | 2020 |
| 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 |
| LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ... Molecular psychiatry 12 (12), 1129-1139, 2007 | 493 | 2007 |
| Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function MS Artigas, DW Loth, LV Wain, SA Gharib, M Obeidat, W Tang, G Zhai, ... Nature genetics 43 (11), 1082-1090, 2011 | 483 | 2011 |
| A genomewide scan for loci involved in attention-deficit/hyperactivity disorder SE Fisher, C Francks, JT McCracken, JJ McGough, AJ Marlow, ... The American Journal of Human Genetics 70 (5), 1183-1196, 2002 | 448 | 2002 |
| Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia SE Fisher, C Francks, AJ Marlow, IL MacPhie, DF Newbury, LR Cardon, ... Nature genetics 30 (1), 86-91, 2002 | 388 | 2002 |
| Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium XZ Kong, SR Mathias, T Guadalupe, ENIGMA Laterality Working Group, ... Proceedings of the National Academy of Sciences 115 (22), E5154-E5163, 2018 | 366 | 2018 |
| Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry LJ Scott, P Muglia, XQ Kong, W Guan, M Flickinger, R Upmanyu, F Tozzi, ... Proceedings of the National Academy of Sciences 106 (18), 7501-7506, 2009 | 363 | 2009 |
| The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration S Paracchini, A Thomas, S Castro, C Lai, M Paramasivam, Y Wang, ... Human molecular genetics 15 (10), 1659-1666, 2006 | 363 | 2006 |
| Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism SL Smalley, V Kustanovich, SL Minassian, JL Stone, MN Ogdie, ... The American Journal of Human Genetics 71 (4), 959-963, 2002 | 349 | 2002 |
| On the other hand: including left-handers in cognitive neuroscience and neurogenetics RM Willems, LV der Haegen, SE Fisher, C Francks Nature reviews neuroscience 15 (3), 193-201, 2014 | 344 | 2014 |
| Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts P Muglia, F Tozzi, NW Galwey, C Francks, R Upmanyu, XQ Kong, ... Molecular psychiatry 15 (6), 589-601, 2010 | 336 | 2010 |
| A 77-kilobase region of chromosome 6p22. 2 is associated with dyslexia in families from the United Kingdom and from the United States C Francks, S Paracchini, SD Smith, AJ Richardson, TS Scerri, LR Cardon, ... The American Journal of Human Genetics 75 (6), 1046-1058, 2004 | 333 | 2004 |
Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsVerified email at mpi.nl
