|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
|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
|Specific Language Impairment in families|
JF Flax, T Realpe-Bonilla, LS Hirsch, LM Brzustowicz, CW Bartlett, ...
Journal of Speech, Language, and Hearing Research, 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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|Defining the genetic architecture of human developmental language impairment|
N Li, CW Bartlett
Life sciences 90 (13-14), 469-475, 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
|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
|GeneŚ gene interaction in shared etiology of autism and specific language impairment|
CW Bartlett, JF Flax, Z Fermano, A Hare, L Hou, SA Petrill, S Buyske, ...
Biological psychiatry 72 (8), 692-699, 2012
|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
|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
|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