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Neurons derived from patients with bipolar disorder divide into intrinsically different sub-populations of neurons, predicting the patients’ responsiveness to lithium

Molecular psychiatry, 2018-06, Vol.23 (6), p.1453-1465

2018

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Science (American Association for the Advancement of Science), 2009-02, Vol.323 (5918), p.1205-1208

2009

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Posttranslational modifications & lithium’s therapeutic effect—Potential biomarkers for clinical responses in psychiatric & neurodegenerative disorders

Neuroscience and biobehavioral reviews, 2021-08, Vol.127, p.424-445

2021

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Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

Journal of medical genetics, 2009-02, Vol.46 (2), p.112-114

2009

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Alpha galactosidase A activity in Parkinson's disease

Neurobiology of disease, 2018-04, Vol.112, p.85-90

2018

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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Molecular psychiatry, 2011-03, Vol.16 (3), p.238-239

2011

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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Molecular psychiatry, 2011-08, Vol.16 (8), p.867-880

2011

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Risk Factors for Suicide Completion in Major Depression: A Case-Control Study of Impulsive and Aggressive Behaviors in Men

The American journal of psychiatry, 2005-11, Vol.162 (11), p.2116-2124

2005

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Exploring cesium properties internal to the LANSCE H- ion source using resonant absorption spectroscopy

Journal of instrumentation, 2023-06, Vol.18 (6), p.C06005

2023

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Patterns of gene expression in the limbic system of suicides with and without major depression

Molecular psychiatry, 2007-07, Vol.12 (7), p.640-655

2007

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Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures

Clinical genetics, 2017-03, Vol.91 (3), p.470-475

2017

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Molecular mechanisms underlying polyalanine diseases

Neurobiology of disease, 2009-06, Vol.34 (3), p.397-405

2009

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Aven recognition of RNA G-quadruplexes regulates translation of the mixed lineage leukemia protooncogenes

eLife, 2015-08, Vol.4

2015

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Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors

Molecular psychiatry, 2018-10, Vol.23 (10), p.2050-2056

2018

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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations

Neurology, 2012-05, Vol.78 (19), p.1519-1526

2012

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Mutations in FUS cause FALS and SALS in French and French Canadian populations

Neurology, 2009-10, Vol.73 (15), p.1176-1179

2009

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Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia

Translational psychiatry, 2011-11, Vol.1 (11), p.e55-e55

2011

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An intubation technique using hyperangulated video laryngoscopy and a DuCanto suction catheter preloaded with a bougie: A case report with a video demonstration

Journal of the American College of Emergency Physicians Open, 2024-08, Vol.5 (4), p.e13238-n/a

2024

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A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

Clinical genetics, 2015-07, Vol.88 (1), p.E1-E4

2015

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The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

Journal of Medical Genetics, 2005-07, Vol.42 (7), p.540-546

2005

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Novel integrative genomic tool for interrogating lithium response in bipolar disorder

Translational psychiatry, 2015-02, Vol.5 (2), p.e504-e504

2015

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Tension Pneumomediastinum and Coronary Artery Thrombosis Following a Motorcycle Accident: A Case Report

Clinical practice and cases in emergency medicine, 2023-05, Vol.7 (2), p.97-100

2023

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Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

Human molecular genetics, 2000-09, Vol.9 (15), p.2321-2328

2000

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Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

NPJ Parkinson's Disease, 2019-05, Vol.5 (1), p.8, Article 8

2019

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Neurons derived from patients with bipolar disorder divide into intrinsically different sub-populations of neurons, predicting the patients’ responsiveness to lithium

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Posttranslational modifications & lithium’s therapeutic effect—Potential biomarkers for clinical responses in psychiatric & neurodegenerative disorders

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

Alpha galactosidase A activity in Parkinson's disease

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Risk Factors for Suicide Completion in Major Depression: A Case-Control Study of Impulsive and Aggressive Behaviors in Men

Exploring cesium properties internal to the LANSCE H- ion source using resonant absorption spectroscopy

Patterns of gene expression in the limbic system of suicides with and without major depression

Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures

Molecular mechanisms underlying polyalanine diseases

Aven recognition of RNA G-quadruplexes regulates translation of the mixed lineage leukemia protooncogenes

Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations

Mutations in FUS cause FALS and SALS in French and French Canadian populations

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia

An intubation technique using hyperangulated video laryngoscopy and a DuCanto suction catheter preloaded with a bougie: A case report with a video demonstration

A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

Novel integrative genomic tool for interrogating lithium response in bipolar disorder

Tension Pneumomediastinum and Coronary Artery Thrombosis Following a Motorcycle Accident: A Case Report

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

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