| Consensus paper: pathological role of the cerebellum in autism SH Fatemi, KA Aldinger, P Ashwood, ML Bauman, CD Blaha, GJ Blatt, ... The Cerebellum 11, 777-807, 2012 | 785 | 2012 |
| A human cell atlas of fetal gene expression J Cao, DR O’day, HA Pliner, PD Kingsley, M Deng, RM Daza, MA Zager, ... Science 370 (6518), eaba7721, 2020 | 491 | 2020 |
| Population genetic study of the brain-derived neurotrophic factor (BDNF) gene TL Petryshen, PC Sabeti, KA Aldinger, B Fry, JB Fan, SF Schaffner, ... Molecular psychiatry 15 (8), 810-815, 2010 | 292 | 2010 |
| A human cell atlas of fetal chromatin accessibility S Domcke, AJ Hill, RM Daza, J Cao, DR O’Day, HA Pliner, KA Aldinger, ... Science 370 (6518), eaba7612, 2020 | 283 | 2020 |
| FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation KA Aldinger, OJ Lehmann, L Hudgins, VV Chizhikov, AG Bassuk, ... Nature genetics 41 (9), 1037-1042, 2009 | 266 | 2009 |
| Support for involvement of neuregulin 1 in schizophrenia pathophysiology TL Petryshen, FA Middleton, A Kirby, KA Aldinger, S Purcell, AR Tahl, ... Molecular psychiatry 10 (4), 366-374, 2005 | 238 | 2005 |
| Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies KA Aldinger, G Sokoloff, DM Rosenberg, AA Palmer, KJ Millen PloS one 4 (3), e4729, 2009 | 171 | 2009 |
| Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia TL Petryshen, FA Middleton, AR Tahl, GN Rockwell, S Purcell, ... Molecular psychiatry 10 (12), 1074-1088, 2005 | 154 | 2005 |
| Lissencephaly: expanded imaging and clinical classification N Di Donato, S Chiari, GM Mirzaa, K Aldinger, E Parrini, C Olds, ... American journal of medical genetics Part A 173 (6), 1473-1488, 2017 | 146 | 2017 |
| Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development AL Lennox, ML Hoye, R Jiang, BL Johnson-Kerner, LA Suit, ... Neuron 106 (3), 404-420. e8, 2020 | 142 | 2020 |
| Patterns of risk for multiple co‐occurring medical conditions replicate across distinct cohorts of children with autism spectrum disorder KA Aldinger, CJ Lane, J Veenstra‐VanderWeele, P Levitt Autism Research 8 (6), 771-781, 2015 | 135 | 2015 |
| Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem VV Chizhikov, AG Lindgren, Y Mishima, RW Roberts, KA Aldinger, ... Proceedings of the National Academy of Sciences 107 (23), 10725-10730, 2010 | 135 | 2010 |
| A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair KW Gripp, KA Aldinger, JT Bennett, L Baker, J Tusi, N Powell‐Hamilton, ... American journal of medical genetics Part A 170 (9), 2237-2247, 2016 | 126 | 2016 |
| Amyoplasia revisited JG Hall, KA Aldinger, KI Tanaka American journal of medical genetics Part A 164 (3), 700-730, 2014 | 120 | 2014 |
| Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly N Di Donato, AE Timms, KA Aldinger, GM Mirzaa, JT Bennett, S Collins, ... Genetics in Medicine 20 (11), 1354-1364, 2018 | 116 | 2018 |
| Association and mutation analyses of 16p11. 2 autism candidate genes RA Kumar, CR Marshall, JA Badner, TD Babatz, Z Mukamel, KA Aldinger, ... PloS one 4 (2), e4582, 2009 | 115 | 2009 |
| Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum P Haldipur, KA Aldinger, S Bernardo, M Deng, AE Timms, LM Overman, ... Science 366 (6464), 454-460, 2019 | 107 | 2019 |
| Spatial and cell type transcriptional landscape of human cerebellar development KA Aldinger, Z Thomson, IG Phelps, P Haldipur, M Deng, AE Timms, ... Nature neuroscience 24 (8), 1163-1175, 2021 | 101 | 2021 |
| Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy KA Aldinger, SJ Mosca, M Tétreault, JC Dempsey, GE Ishak, T Hartley, ... The American Journal of Human Genetics 95 (2), 227-234, 2014 | 97 | 2014 |
| Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex DM Werling, S Pochareddy, J Choi, JY An, B Sheppard, M Peng, Z Li, ... Cell reports 31 (1), 2020 | 93 | 2020 |
