J. Flax

发表

A major susceptibility locus for specific language impairment is located on 13q21.

V. Vieland, P. Tallal, A. Bassett, 2002, American journal of human genetics.

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci

V. Vieland, L. Brzustowicz, J. Flax, 2010, Journal of Neurodevelopmental Disorders.

Common genetic risk factors in ASD and ADHD co-occurring families

Jinchuan Xing, S. Buyske, C. Bartlett, 2022, Human Genetics.

Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses

J. Millonig, Z. Pang, L. Brzustowicz, 2022, Stem cell reports.

Familial aggregation in specific language impairment.

P. Tallal, C. Bartlett, T. Realpe-Bonilla, 1989, Journal of speech, language, and hearing research : JSLHR.

A genome scan for loci shared by autism spectrum disorder and language impairment.

S. Buyske, C. Bartlett, C. Cartwright, 2014, The American journal of psychiatry.

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders

Jinchuan Xing, S. Buyske, C. Bartlett, 2022, Genes.

Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses

J. Millonig, Z. Pang, L. Brzustowicz, 2022, Stem cell reports.

Gene x gene Interactio in Shared Etiology of Autism and Specific Language Impairment

S. Petrill, S. Buyske, C. Bartlett, 2012 .

Associations between the size of the amygdala in infancy and language abilities during the preschool years in normally developing children

P. Ellen Grant, April A. Benasich, Silvia Ortiz-Mantilla, 2010, NeuroImage.

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds

Amber D Shindhelm, S. Buyske, C. Bartlett, 2016, Behavior Genetics.

Auditory event-related responses in children with semi-lobar holoprosencephaly

A. Benasich, H. Jing, Cynthia Roesler, 2006, Brain and Development.

The Carter Neurocognitive Assessment for children with severely compromised expressive language and motor skills.

A. Benasich, H. Leevers, Cynthia Roesler, 2005, Journal of child psychology and psychiatry, and allied disciplines.

Links between abnormal brain structure and cognition in holoprosencephaly.

S. Paterson, J. Hahn, A. Benasich, 2006, Pediatric neurology.

Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

S. Petrill, S. Buyske, C. Bartlett, 2012, Biological Psychiatry.

Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language-Impaired Families

Stephen A. Petrill, Christopher W. Bartlett, Laura M. Justice, 2010, Human Heredity.

Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment

V. Vieland, P. Tallal, C. Bartlett, 2004, Human Heredity.

Specific language impairment in families: evidence for co-occurrence with reading impairments.

P. Tallal, C. Bartlett, T. Realpe-Bonilla, 2003, Journal of speech, language, and hearing research : JSLHR.

Relations between prosodic variables and communicative functions

A Boothroyd, K. Harris, A. Boothroyd, 1991, Journal of Child Language.

The use of spontaneous language measures as criteria for identifying children with specific language impairment: an attempt to reconcile clinical and research incongruence.

M. Sliwinski, M. Dunn, D. Aram, 1996, Journal of speech and hearing research.

Functional connectivity of the sensorimotor area in naturally sleeping infants

Kevin G. Guise, Vishad Sukul, April A. Benasich, 2008, Brain Research.

Assessment of functional development in normal infant brain using arterial spin labeled perfusion MRI

David C. Alsop, John A. Detre, Wen-Ching Liu, 2008, NeuroImage.

Social (Pragmatic) Communication Disorder: Another name for the Broad Autism Phenotype?

S. Buyske, L. Brzustowicz, J. Flax, 2019, Autism : the international journal of research and practice.

Using Early Standardized Language Measures to Predict Later Language and Early Reading Outcomes in Children at High Risk for Language-Learning Impairments

A. Benasich, T. Realpe-Bonilla, Cynthia Roesler, 2009, Journal of learning disabilities.

Look who's talking: a prospective study of familial transmission of language impairments.

P Tallal, P. Tallal, A. Benasich, 1997, Journal of speech, language, and hearing research : JSLHR.

The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

E. Willcutt, S. Petrill, S. Buyske, 2023, Genes.

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds

Amber D Shindhelm, S. Buyske, C. Bartlett, 2016, Behavior Genetics.

Genetic Covariation Underlying Reading, Language and Related Measures in a Sample Selected for Specific Language Impairment

Jessica A. R. Logan, L. Justice, S. Petrill, 2011, Behavior genetics.

Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments

Jinchuan Xing, S. Buyske, C. Bartlett, 2023, International journal of molecular sciences.

Autism Spectrum Disorder and Language Impairment

Steven Buyske, Christopher W. Bartlett, Liping Hou, 2013 .

Familial aggregation in specific language impairment.

P. Tallal, S. Curtiss, R. Ross, 2001, The Journal of speech and hearing disorders.