| Strong association of de novo copy number mutations with sporadic schizophrenia B Xu, JL Roos, S Levy, EJ Van Rensburg, JA Gogos, M Karayiorgou Nature genetics 40 (7), 880-885, 2008 | 970 | 2008 |
| Exome sequencing supports a de novo mutational paradigm for schizophrenia B Xu, JL Roos, P Dexheimer, B Boone, B Plummer, S Levy, JA Gogos, ... Nature genetics 43 (9), 864-868, 2011 | 541 | 2011 |
| De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia B Xu, I Ionita-Laza, JL Roos, B Boone, S Woodrick, Y Sun, S Levy, ... Nature genetics 44 (12), 1365-1369, 2012 | 490 | 2012 |
| 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 | 489 | 2007 |
| Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia H Liu, SC Heath, C Sobin, JL Roos, BL Galke, ML Blundell, M Lenane, ... Proceedings of the National Academy of Sciences 99 (6), 3717-3722, 2002 | 424 | 2002 |
| Meta-analysis of 32 genome-wide linkage studies of schizophrenia MYM Ng, DF Levinson, SV Faraone, BK Suárez, LE DeLisi, T Arinami, ... Molecular psychiatry 14 (8), 774-785, 2009 | 373 | 2009 |
| Genetic variation in the 22q11 locus and susceptibility to schizophrenia H Liu, GR Abecasis, SC Heath, A Knowles, S Demars, YJ Chen, JL Roos, ... Proceedings of the National Academy of Sciences 99 (26), 16859-16864, 2002 | 241 | 2002 |
| Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene A Takata, B Xu, I Ionita-Laza, JL Roos, JA Gogos, M Karayiorgou Neuron 82 (4), 773-780, 2014 | 212 | 2014 |
| Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies S Service, J DeYoung, M Karayiorgou, JL Roos, H Pretorious, G Bedoya, ... Nature genetics 38 (5), 556-560, 2006 | 179 | 2006 |
| Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans B Xu, A Woodroffe, L Rodriguez-Murillo, JL Roos, EJ van Rensburg, ... Proceedings of the National Academy of Sciences 106 (39), 16746-16751, 2009 | 172 | 2009 |
| Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1 GR Abecasis, RA Burt, D Hall, S Bochum, KF Doheny, SL Lundy, ... The American Journal of Human Genetics 74 (3), 403-417, 2004 | 98 | 2004 |
| Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13. 3 as a susceptibility gene for schizophrenia and autism I Ionita-Laza, B Xu, V Makarov, JD Buxbaum, JL Roos, JA Gogos, ... Proceedings of the National Academy of Sciences 111 (1), 343-348, 2014 | 85 | 2014 |
| Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches R Hsu, A Woodroffe, WS Lai, MN Cook, J Mukai, JP Dunning, ... PloS one 2 (11), e1234, 2007 | 80 | 2007 |
| Aberrant function of the C-terminal tail of HIST1H1E accelerates cellular senescence and causes premature aging E Flex, S Martinelli, A Van Dijck, A Ciolfi, S Cecchetti, E Coluzzi, ... The American Journal of Human Genetics 105 (3), 493-508, 2019 | 69 | 2019 |
| Heterogeneity of the axon initial segment in interneurons and pyramidal cells of rodent visual cortex F Höfflin, A Jack, C Riedel, J Mack-Bucher, J Roos, C Corcelli, C Schultz, ... Frontiers in cellular neuroscience 11, 332, 2017 | 69 | 2017 |
| Medical students on the value of role models for developing'soft skills'-" That's the way you do it PM Joubert, C Krüger, AM Bergh, GE Pickworth, CW Van Staden, JL Roos, ... African Journal of Psychiatry 9 (1), 28-32, 2006 | 65 | 2006 |
| Medical students' perceptions of their development of 'soft skills' : part II : the development of 'soft skills' through 'guiding and growing' AM Bergh, CW Van Staden, PM Joubert, C Kruger, GE Pickworth, JL Roos, ... South African Family Practice 48 (8), 1, 2006 | 48 | 2006 |
| Assessment of the frequency of the 22q11 deletion in Afrikaner schizophrenic patients GJ Wiehahn, GP Bosch, RR Du Preez, HW Pretorius, M Karayiorgou, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 129 …, 2004 | 44 | 2004 |
| Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database M Karayiorgou, M Torrington, GR Abecasis, H Pretorius, B Robertson, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 124 …, 2004 | 44 | 2004 |
| Prevalence and clinical characteristics of obsessive-compulsive disorder and obsessive compulsive symptoms in Afrikaner schizophrenia and schizoaffective disorder patients F Seedat, JL Roos, HW Pretorius, M Karayiorgou, B Nel African Journal of Psychiatry 10 (4), 219-224, 2007 | 43 | 2007 |
