Christopher w  Bartlett
Christopher w Bartlett
Rutgers, Ohio State, nationwide children's
Verified email at pediatrics.ohio-state.edu
Title
Cited by
Cited by
Year
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
14302007
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
2982002
Specific Language Impairment in families
JF Flax, T Realpe-Bonilla, LS Hirsch, LM Brzustowicz, CW Bartlett, ...
Journal of Speech, Language, and Hearing Research, 2003
2122003
The search for autism disease genes
TH Wassink, LM Brzustowicz, CW Bartlett, P Szatmari
Mental retardation and developmental disabilities research reviews 10 (4 …, 2004
1532004
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
1372001
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
1222014
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
1202004
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
1002005
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
802005
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
462005
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
412008
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
322014
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
302015
Defining the genetic architecture of human developmental language impairment
N Li, CW Bartlett
Life sciences 90 (13-14), 469-475, 2012
292012
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
252015
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
222015
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
222012
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
222012
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
222010
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
212018
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