Judy F Flax
Overview
Explore the profile of Judy F Flax including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
16
Citations
332
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Petrill S, Klamer B, Buyske S, Willcutt E, Gruen J, Francis D, et al.
Genes (Basel)
. 2023 Sep;
14(9).
PMID: 37761888
Genetics researchers increasingly combine data across many sources to increase power and to conduct analyses that cross multiple individual studies. However, there is often a lack of alignment on outcome...
2.
Alibutud R, Hansali S, Cao X, Zhou A, Mahaganapathy V, Azaro M, et al.
Int J Mol Sci
. 2023 Sep;
24(17).
PMID: 37686052
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restrictive interests and/or repetitive behaviors and deficits in social interaction and communication. ASD is a multifactorial disease with a complex...
3.
Zhou A, Cao X, Mahaganapathy V, Azaro M, Gwin C, Wilson S, et al.
Hum Genet
. 2022 Oct;
142(2):217-230.
PMID: 36251081
Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) are two major neurodevelopmental disorders that frequently co-occur. However, the genetic mechanism of the co-occurrence remains unclear. The New Jersey Language and...
4.
MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders
Wong A, Zhou A, Cao X, Mahaganapathy V, Azaro M, Gwin C, et al.
Genes (Basel)
. 2022 Jul;
13(8).
PMID: 35893067
Autism spectrum disorder (ASD) is a childhood neurodevelopmental disorder with a complex and heterogeneous genetic etiology. MicroRNA (miRNA), a class of small non-coding RNAs, could regulate ASD risk genes post-transcriptionally...
5.
Hare-Harris A, Mitchel M, Myers S, Mitchel A, King B, Ruocco B, et al.
J Neurodev Disord
. 2019 Sep;
11(1):21.
PMID: 31519145
Background: Qualitatively atypical language development characterized by non-sequential skill acquisition within a developmental domain, which has been called developmental deviance or difference, is a common characteristic of autism spectrum disorder...
6.
Bruni M, Flax J, Buyske S, Shindhelm A, Witton C, Brzustowicz L, et al.
Behav Genet
. 2016 Nov;
47(2):193-201.
PMID: 27826669
Auditory detection thresholds for certain frequencies of both amplitude modulated (AM) and frequency modulated (FM) dynamic auditory stimuli are associated with reading in typically developing and dyslexic readers. We present...
7.
Bartlett C, Hou L, Flax J, Hare A, Cheong S, Fermano Z, et al.
Am J Psychiatry
. 2013 Oct;
171(1):72-81.
PMID: 24170272
Objective: The authors conducted a genetic linkage study of families that have both autism spectrum disorder (ASD) and language-impaired probands to find common communication impairment loci. The hypothesis was that...
8.
Bartlett C, Flax J, Fermano Z, Hare A, Hou L, Petrill S, et al.
Biol Psychiatry
. 2012 Jun;
72(8):692-9.
PMID: 22704665
Background: To examine the relationship between autism spectrum disorders (ASD) and specific language impairment (SLI), family studies typically take a comparative approach where families with one disease are examined for...
9.
Flax J, Hare A, Azaro M, Vieland V, Brzustowicz L
J Neurodev Disord
. 2010 Dec;
2(4):210-223.
PMID: 21125004
Using behavioral and genetic information from the Autism Genetics Resource Exchange (AGRE) data set we developed phenotypes and investigated linkage and association for individuals with and without Autism Spectrum Disorders...
10.
Simmons T, Flax J, Azaro M, Hayter J, Justice L, Petrill S, et al.
Hum Hered
. 2010 Oct;
70(4):232-44.
PMID: 20948219
While advances in network and pathway analysis have flourished in the era of genome-wide association analysis, understanding the genetic mechanism of individual loci on phenotypes is still readily accomplished using...