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Rare Autism-Associated Variants Implicate Syntaxin 1 (STX1 R26Q) Phosphorylation and the Dopamine Transporter (hDAT R51W) in Dopamine Neurotransmission and Behaviors

EBioMedicine, 2015-02, Vol.2 (2), p.135-146

2015

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Synaptic, transcriptional and chromatin genes disrupted in autism

Nature (London), 2014-11, Vol.515 (7526), p.209-215

2014

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature (London), 2012-05, Vol.485 (7397), p.242-245

2012

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Alterations in Body Temperature, Corticosterone, and Behavior Following the Administration of 5-Methoxy-Diisopropyltryptamine ('Foxy') to Adult Rats: a New Drug of Abuse

Neuropsychopharmacology (New York, N.Y.), 2007-06, Vol.32 (6), p.1404-1420

2007

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Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in SLC6A3

Proceedings of the National Academy of Sciences - PNAS, 2019-02, Vol.116 (9), p.3853-3862

2019

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Colocalization and regulated physical association of presynaptic serotonin transporters with A₃ adenosine receptors

Molecular pharmacology, 2011-09, Vol.80 (3), p.458-465

2011

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Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Genomics (San Diego, Calif.), 2013-10, Vol.102 (4), p.270-277

2013

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Zn(2+) reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder

Molecular autism, 2015, Vol.6, p.8-8

2015

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Zn2+ reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder

Molecular autism, 2015-02, Vol.6 (1), Article 8

2015

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Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome

Molecular autism, 2013-08, Vol.4 (1), p.28-28, Article 28

2013

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MDMA administration to pregnant Sprague–Dawley rats results in its passage to the fetal compartment

Neurotoxicology and teratology, 2006-07, Vol.28 (4), p.459-465

2006

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Prenatal 3,4-methylenedioxymethamphetamine (ecstasy) alters exploratory behavior, reduces monoamine metabolism, and increases forebrain tyrosine hydroxylase fiber density of juvenile rats

Neurotoxicology and teratology, 2003-09, Vol.25 (5), p.509-517

2003

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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

Molecular psychiatry, 2013-12, Vol.18 (12), p.1315-1323

2013

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Neonatal 3,4-methylenedioxymethamphetamine (ecstasy) alters dopamine and serotonin neurochemistry and increases brain-derived neurotrophic factor in the forebrain and brainstem of the rat

Brain research. Developmental brain research, 2003-12, Vol.147 (1), p.177-182

2003

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Colocalization and Regulated Physical Association of Presynaptic Serotonin Transporters with A 3 Adenosine Receptors

Molecular pharmacology, 2011-09, Vol.80 (3), p.458-465

2011

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Colocalization and Regulated Physical Association of Presynaptic Serotonin Transporters with A3 Adenosine ReceptorsS

Molecular pharmacology, 2011-09, Vol.80 (3), p.458-465

2011

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The genetics of lignin biosynthesis: connecting genotype to phenotype

Annual review of genetics, 2010-01, Vol.44 (1), p.337-363

2010

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K29-Selective Ubiquitin Binding Domain Reveals Structural Basis of Specificity and Heterotypic Nature of K29 Polyubiquitin

Molecular cell, 2015-04, Vol.58 (1), p.83-94

2015

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Trajectories of Loneliness Among Older Women and Men: Variation by Sexual Identity?

The Gerontologist, 2023-02, Vol.63 (2), p.328-337

2023

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14-3-3 binding to LRRK2 is disrupted by multiple Parkinson's disease-associated mutations and regulates cytoplasmic localization

Biochemical journal, 2010-09, Vol.430 (3), p.393-404

2010

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LRRK2 activation controls the repair of damaged endomembranes in macrophages

The EMBO journal, 2020-09, Vol.39 (18), p.e104494-n/a

2020

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A qualitative study of rural healthcare providers' views of social, cultural, and programmatic barriers to healthcare access

BMC health services research, 2022-04, Vol.22 (1), p.438-438, Article 438

2022

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Rare Autism-Associated Variants Implicate Syntaxin 1 (STX1 R26Q) Phosphorylation and the Dopamine Transporter (hDAT R51W) in Dopamine Neurotransmission and Behaviors

Synaptic, transcriptional and chromatin genes disrupted in autism

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Alterations in Body Temperature, Corticosterone, and Behavior Following the Administration of 5-Methoxy-Diisopropyltryptamine ('Foxy') to Adult Rats: a New Drug of Abuse

Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in SLC6A3

Colocalization and regulated physical association of presynaptic serotonin transporters with A₃ adenosine receptors

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Zn(2+) reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder

Zn2+ reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder

Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome

MDMA administration to pregnant Sprague–Dawley rats results in its passage to the fetal compartment

Prenatal 3,4-methylenedioxymethamphetamine (ecstasy) alters exploratory behavior, reduces monoamine metabolism, and increases forebrain tyrosine hydroxylase fiber density of juvenile rats

De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

Neonatal 3,4-methylenedioxymethamphetamine (ecstasy) alters dopamine and serotonin neurochemistry and increases brain-derived neurotrophic factor in the forebrain and brainstem of the rat

Colocalization and Regulated Physical Association of Presynaptic Serotonin Transporters with A 3 Adenosine Receptors

Colocalization and Regulated Physical Association of Presynaptic Serotonin Transporters with A3 Adenosine ReceptorsS

The genetics of lignin biosynthesis: connecting genotype to phenotype

K29-Selective Ubiquitin Binding Domain Reveals Structural Basis of Specificity and Heterotypic Nature of K29 Polyubiquitin

Trajectories of Loneliness Among Older Women and Men: Variation by Sexual Identity?

14-3-3 binding to LRRK2 is disrupted by multiple Parkinson's disease-associated mutations and regulates cytoplasmic localization

Clinical and biological implications of driver mutations in myelodysplastic syndromes

LRRK2 activation controls the repair of damaged endomembranes in macrophages

Non-BRCA DNA Damage Repair Gene Alterations and Response to the PARP Inhibitor Rucaparib in Metastatic Castration-Resistant Prostate Cancer: Analysis From the Phase II TRITON2 Study

British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults

A qualitative study of rural healthcare providers' views of social, cultural, and programmatic barriers to healthcare access

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