| Mapping autism risk loci using genetic linkage and chromosomal rearrangements P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ... Nature genetics 39 (3), 319, 2007 | 1443 | 2007 |
| A major susceptibility locus for specific language impairment is located on 13q21 CW Bartlett, JF Flax, MW Logue, VJ Vieland, AS Bassett, P Tallal, ... The American Journal of Human Genetics 71 (1), 45-55, 2002 | 303 | 2002 |
| Specific Language Impairment in families JF Flax, T Realpe-Bonilla, LS Hirsch, LM Brzustowicz, CW Bartlett, ... Journal of Speech, Language, and Hearing Research, 2003 | 214 | 2003 |
| The search for autism disease genes TH Wassink, LM Brzustowicz, CW Bartlett, P Szatmari Mental retardation and developmental disabilities research reviews 10 (4 …, 2004 | 153 | 2004 |
| Familial aggregation in specific language impairment P Tallal, LS Hirsch, T Realpe-Bonilla, S Miller, LM Brzustowicz, C Bartlett, ... Journal of Speech, Language, and hearing research, 2001 | 142 | 2001 |
| Who is afraid of math? Two sources of genetic variance for mathematical anxiety Z Wang, SA Hart, Y Kovas, S Lukowski, B Soden, LA Thompson, R Plomin, ... Journal of child psychology and psychiatry 55 (9), 1056-1064, 2014 | 129 | 2014 |
| Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment CW Bartlett, JF Flax, MW Logue, BJ Smith, VJ Vieland, P Tallal, ... Human heredity 57 (1), 10-20, 2004 | 124 | 2004 |
| Three autism candidate genes: a synthesis of human genetic analysis with other disciplines CW Bartlett, N Gharani, JH Millonig, LM Brzustowicz International Journal of developmental neuroscience 23 (2-3), 221-234, 2005 | 100 | 2005 |
| Evaluation of the chromosome 2q37. 3 gene CENTG2 as an autism susceptibility gene TH Wassink, J Piven, VJ Vieland, L Jenkins, R Frantz, CW Bartlett, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 136 …, 2005 | 80 | 2005 |
| Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set CW Bartlett, R Goedken, VJ Vieland The American Journal of Human Genetics 76 (4), 688-695, 2005 | 47 | 2005 |
| A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications VJ Vieland, Y Huang, C Bartlett, TF Davies, Y Tomer The American Journal of Human Genetics 82 (6), 1349-1356, 2008 | 41 | 2008 |
| A genome scan for loci shared by autism spectrum disorder and language impairment CW Bartlett, L Hou, JF Flax, A Hare, SY Cheong, Z Fermano, ... American Journal of Psychiatry 171 (1), 72-81, 2014 | 32 | 2014 |
| Empirically based profiles of the early literacy skills of children with language impairment in early childhood special education L Justice, J Logan, J Kaderavek, MB Schmitt, V Tompkins, C Bartlett Journal of Learning Disabilities 48 (5), 482-494, 2015 | 30 | 2015 |
| Defining the genetic architecture of human developmental language impairment N Li, CW Bartlett Life sciences 90 (13-14), 469-475, 2012 | 30 | 2012 |
| The role of candidate‐gene CNTNAP2 in childhood apraxia of speech and specific language impairment TM Centanni, JN Sanmann, JR Green, J Iuzzini‐Seigel, C Bartlett, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015 | 26 | 2015 |
| Collection and extraction of saliva DNA for next generation sequencing MR Goode, SY Cheong, N Li, WC Ray, CW Bartlett JoVE (Journal of Visualized Experiments), e51697, 2014 | 24 | 2014 |
| Understanding developmental language disorder-the Helsinki longitudinal SLI study (HelSLI): a study protocol M Laasonen, S Smolander, P Lahti-Nuuttila, M Leminen, HR Lajunen, ... BMC psychology 6 (1), 1-13, 2018 | 23 | 2018 |
| Heritability across the distribution: An application of quantile regression JAR Logan, SA Petrill, SA Hart, C Schatschneider, LA Thompson, ... Behavior genetics 42 (2), 256-267, 2012 | 23 | 2012 |
| Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families TR Simmons, JF Flax, MA Azaro, JE Hayter, LM Justice, SA Petrill, ... Human heredity 70 (4), 232-244, 2010 | 23 | 2010 |
| Catechol‐O‐methyltransferase Val158met polymorphism interacts with early experience to predict executive functions in early childhood C Blair, M Sulik, M Willoughby, R Mills‐Koonce, S Petrill, C Bartlett, ... Developmental psychobiology 57 (7), 833-841, 2015 | 22 | 2015 |
