Search Results - "Flax, Judy"

Common genetic risk factors in ASD and ADHD co-occurring families by Zhou, Anbo, Cao, Xiaolong, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W., Flax, Judy F., Brzustowicz, Linda M., Xing, Jinchuan

“…Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) are two major neurodevelopmental disorders that frequently co-occur…”
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Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments by Alibutud, Rohan, Hansali, Sammy, Cao, Xiaolong, Zhou, Anbo, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W, Flax, Judy F, Brzustowicz, Linda M, Xing, Jinchuan

“…Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restrictive interests and/or repetitive behaviors and deficits in social…”
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Functional connectivity of the sensorimotor area in naturally sleeping infants by Liu, Wen-Ching, Flax, Judy F, Guise, Kevin G, Sukul, Vishad, Benasich, April A

“…Abstract Patterns of cortical functional connectivity in normal infants were examined during natural sleep by observing the time course of very low frequency…”
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MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders by Wong, Anthony, Zhou, Anbo, Cao, Xiaolong, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W, Flax, Judy F, Brzustowicz, Linda M, Xing, Jinchuan

“…Autism spectrum disorder (ASD) is a childhood neurodevelopmental disorder with a complex and heterogeneous genetic etiology. MicroRNA (miRNA), a class of small…”
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A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment by Bartlett, Christopher W., Hou, Liping, Flax, Judy F., Hare, Abby, Cheong, Soo Yeon, Fermano, Zena, Zimmerman-Bier, Barbie, Cartwright, Charles, Azaro, Marco A., Buyske, Steven, Brzustowicz, Linda M.

“…A study of 79 families with one child with autism and at least one child with a language impairment revealed a possible genetic connection between autism in…”
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The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait by Petrill, Stephen A, Klamer, Brett G, Buyske, Steven, Willcutt, Erik G, Gruen, Jeffrey R, Francis, David J, Flax, Judy F, Brzustowicz, Linda M, Bartlett, Christopher W

“…Genetics researchers increasingly combine data across many sources to increase power and to conduct analyses that cross multiple individual studies. However,…”
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Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses by Connacher, Robert, Williams, Madeline, Prem, Smrithi, Yeung, Percy L., Matteson, Paul, Mehta, Monal, Markov, Anna, Peng, Cynthia, Zhou, Xiaofeng, McDermott, Courtney R., Pang, Zhiping P., Flax, Judy, Brzustowicz, Linda, Lu, Che-Wei, Millonig, James H., DiCicco-Bloom, Emanuel

“…Neural precursor cell (NPC) dysfunction has been consistently implicated in autism. Induced pluripotent stem cell (iPSC)-derived NPCs from two autism groups…”
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5.20 DIAGNOSING SOCIAL PRAGMATIC COMMUNICATION DISORDER AND GENDER DIFFERENCES by Fradkin, Yuli, MD, Flax, Judy, PhD, Majmundar, Parth, Wilson, Sherry, Gwin, Chrisitine, Brzustowicz, Linda, MD

“…Objectives: The objective of this presentation is to explore whether higher-order language abnormalities are associated with social pragmatic communication…”
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Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment by Bartlett, Christopher W, Flax, Judy F, Fermano, Zena, Hare, Abby, Hou, Liping, Petrill, Stephen A, Buyske, Steven, Brzustowicz, Linda M

“…Background To examine the relationship between autism spectrum disorders (ASD) and specific language impairment (SLI), family studies typically take a…”
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Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index by Hare-Harris, Abby E, Mitchel, Marissa W, Myers, Scott M, Mitchel, Aaron D, King, Brian R, Ruocco, Brittany G, Martin, Christa Lese, Flax, Judy F, Brzustowicz, Linda M

“…Qualitatively atypical language development characterized by non-sequential skill acquisition within a developmental domain, which has been called…”
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Gene x Gene Interaction in Shared Etiology of Autism and Specific Language Impairment by BARTLETT, Christopher W, FLAX, Judy F, FERMANO, Zena, HARE, Abby, LIPING HOU, PETRILL, Stephen A, BUYSKE, Steven, BRZUSTOWICZ, Linda M

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Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds by Bruni, Matthew, Flax, Judy F., Buyske, Steven, Shindhelm, Amber D., Witton, Caroline, Brzustowicz, Linda M., Bartlett, Christopher W.

“…Auditory detection thresholds for certain frequencies of both amplitude modulated (AM) and frequency modulated (FM) dynamic auditory stimuli are associated…”
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Assessment of functional development in normal infant brain using arterial spin labeled perfusion MRI by Wang, Ze, Fernández-Seara, María, Alsop, David C., Liu, Wen-Ching, Flax, Judy F., Benasich, April A., Detre, John A.

“…Arterial spin labeled (ASL) perfusion MRI provides a noninvasive approach for longitudinal imaging of regional brain function in infants. In the present study,…”
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Using Early Standardized Language Measures to Predict Later Language and Early Reading Outcomes in Children at High Risk for Language-Learning Impairments by Flax, Judy F., Realpe-Bonilla, Teresa, Roesler, Cynthia, Choudhury, Naseem, Benasich, April

“…The aim of the study was to examine the profiles of children with a family history (FH+) of language-learning impairments (LLI) and a control group of children…”
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A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21 by Bartlett, Christopher W., Flax, Judy F., Logue, Mark W., Vieland, Veronica J., Bassett, Anne S., Tallal, Paula, Brzustowicz, Linda M.

“…Children who fail to develop language normally—in the absence of explanatory factors such as neurological disorders, hearing impairment, or lack of adequate…”
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Specific Language Impairment in Families: Evidence for Co-Occurrence with Reading Impairments by Flax, Judy F, Realpe-Bonilla, Teresa, Hirsch, Linda S, Brzustowicz, Linda M, Bartlett, Christopher W, Tallal, Paula

“…Two family aggregation studies involving 25 children (ages 5-10) with specific language impairment (SLI) report the occurrence and co-occurrence of oral…”
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Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families by Simmons, Tabatha R, Flax, Judy F, Azaro, Marco A, Hayter, Jared E, Justice, Laura M, Petrill, Stephen A, Bassett, Anne S, Tallal, Paula, Brzustowicz, Linda M, Bartlett, Christopher W

“…While advances in network and pathway analysis have flourished in the era of genome-wide association analysis, understanding the genetic mechanism of…”
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Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci by Flax, Judy F, Hare, Abby, Azaro, Marco A, Vieland, Veronica J, Brzustowicz, Linda M

“…Using behavioral and genetic information from the Autism Genetics Resource Exchange (AGRE) data set we developed phenotypes and investigated linkage and…”
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Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment by Bartlett, Christopher W, Flax, Judy F, Logue, Mark W, Smith, Brett J, Vieland, Veronica J, Tallal, Paula, Brzustowicz, Linda M

“…Specific language impairment is a neurodevelopmental disorder characterized by impairments essentially restricted to the domain of language and language…”
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Familial Aggregation in Specific Language Impairment by Tallal, Paula, Hirsch, Linda S, Realpe-Bonilla, Teresa, Miller, Steve, Brzustowicz, Linda M, Bartlett, Christopher, Flax, Judy F

“…A case-control family study design examined the current language-related abilities of all biological, primary relatives of probands (N=22) with specific…”
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