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Targeted long-read sequencing captures CRISPR editing and AAV integration outcomes in brain

Molecular therapy, 2023-03, Vol.31 (3), p.760-773

2023

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Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain

Nature medicine, 2021-11, Vol.27 (11), p.1982-1989

2021

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The role of AGG interruptions in the transcription of FMR1 premutation alleles

PloS one, 2011-07, Vol.6 (7), p.e21728

2011

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AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

Journal of neurodevelopmental disorders, 2014-07, Vol.6 (1), p.24-24, Article 24

2014

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FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea

Reproductive biology and endocrinology, 2024-06, Vol.22 (1), p.71-7, Article 71

2024

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AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome

Genetics in medicine, 2012-08, Vol.14 (8), p.729-736

2012

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Screening newborn blood spots for 22q11.2 deletion syndrome using multiplex droplet digital PCR

Clinical chemistry (Baltimore, Md.), 2015-01, Vol.61 (1), p.182-190

2015

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Comparison of Whole-Genome DNA Methylation Patterns in Whole Blood, Saliva, and Lymphoblastoid Cell Lines

Behavior genetics, 2013-03, Vol.43 (2), p.168-176

2013

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Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome

Brain & development (Tokyo. 1979), 2017-06, Vol.39 (6), p.483-492

2017

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CRISPR to the Rescue: Advances in Gene Editing for the FMR1 Gene

Brain sciences, 2019-01, Vol.9 (1), p.17

2019

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Clinical and molecular implications of mosaicism in FMR1 full mutations

Frontiers in genetics, 2014-09, Vol.5, p.318-318

2014

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Genes Controlling Affiliative Behavior as Candidate Genes for Autism

Biological psychiatry (1969), 2008-05, Vol.63 (10), p.911-916

2008

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Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population

Pediatrics (Evanston), 2016-04, Vol.137 (4)

2016

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Macrophage migration inhibitory factor and autism spectrum disorders

Pediatrics (Evanston), 2008-08, Vol.122 (2), p.e438-e445

2008

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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles

American journal of medical genetics. Part A, 2013-04, Vol.161A (4), p.771-778

2013

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Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions

Journal of human genetics, 2013-08, Vol.58 (8), p.553-559

2013

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Differential increases of specific FMR1 mRNA isoforms in premutation carriers

Journal of medical genetics, 2015-01, Vol.52 (1), p.42-52

2015

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Schooling and variation in the COMT gene: the devil is in the details

Journal of child psychology and psychiatry, 2013-10, Vol.54 (10), p.1056-1065

2013

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Gene variants associated with antisocial behaviour: a latent variable approach

Journal of child psychology and psychiatry, 2013-10, Vol.54 (10), p.1074-1085

2013

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Association between Polymorphisms in the Dopamine Transporter Gene and Depression: Evidence for a Gene-Environment Interaction in a Sample of Juvenile Detainees

Psychological science, 2008-01, Vol.19 (1), p.62-69

2008

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Distribution of AGG interruption patterns within nine world populations

Intractable & Rare Diseases Research, 2014/11/30, Vol.3(4), pp.153-161

2014

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Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover

Aggressive behavior, 2010-05, Vol.36 (3), p.158-176

2010

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Twenty-one-base-pair insertion polymorphism creates an enhancer element and potentiates SLC6A1 GABA transporter promoter activity

Pharmacogenetics and genomics, 2009-01, Vol.19 (1), p.53-65

2009

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A balanced t(10;15) translocation in a male patient with developmental language disorder

European journal of medical genetics, 2012-02, Vol.55 (2), p.128-131

2012

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Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension

Development and psychopathology, 2007, Vol.19 (4), p.1089-1103

2007

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Targeted long-read sequencing captures CRISPR editing and AAV integration outcomes in brain

Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain

The role of AGG interruptions in the transcription of FMR1 premutation alleles

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome

Screening newborn blood spots for 22q11.2 deletion syndrome using multiplex droplet digital PCR

Comparison of Whole-Genome DNA Methylation Patterns in Whole Blood, Saliva, and Lymphoblastoid Cell Lines

Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome

CRISPR to the Rescue: Advances in Gene Editing for the FMR1 Gene

Clinical and molecular implications of mosaicism in FMR1 full mutations

Genes Controlling Affiliative Behavior as Candidate Genes for Autism

Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population

Macrophage migration inhibitory factor and autism spectrum disorders

Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles

Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions

Differential increases of specific FMR1 mRNA isoforms in premutation carriers

Schooling and variation in the COMT gene: the devil is in the details

Gene variants associated with antisocial behaviour: a latent variable approach

Association between Polymorphisms in the Dopamine Transporter Gene and Depression: Evidence for a Gene-Environment Interaction in a Sample of Juvenile Detainees

Distribution of AGG interruption patterns within nine world populations

Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover

Twenty-one-base-pair insertion polymorphism creates an enhancer element and potentiates SLC6A1 GABA transporter promoter activity

A balanced t(10;15) translocation in a male patient with developmental language disorder

Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension

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