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Characterizing sleep disorders in an autism-specific collection of electronic health records

Sleep medicine, 2022-04, Vol.92, p.88-95

2022

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Allelic Heterogeneity at the Serotonin Transporter Locus ( SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors

American journal of human genetics, 2005-08, Vol.77 (2), p.265-279

2005

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Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration

Journal of inflammation research, 2024-01, Vol.17, p.2169-2172

2024

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Human Serotonin Transporter Variants Display Altered Sensitivity to Protein Kinase G and p38 Mitogen-Activated Protein Kinase

Proceedings of the National Academy of Sciences - PNAS, 2005-08, Vol.102 (32), p.11545-11550

2005

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0028 SHORTER SLEEP DURATION IS ASSOCIATED WITH SOCIAL IMPAIRMENT AND PSYCHIATRIC COMORBIDITIES IN AUTISM

Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A10-A11

2017

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Analysis of the RELN gene as a genetic risk factor for autism

Molecular psychiatry, 2005-06, Vol.10 (6), p.563-571

2005

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene ( UBE3A ) in Angelman syndrome

Nature genetics, 1997-01, Vol.15 (1), p.74-77

1997

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Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation

Neurology, 2001-12, Vol.57 (12), p.2265-2272

2001

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Imprinted expression of the murine Angelman syndrome gene, Ube3a , in hippocampal and Purkinje neurons

Nature genetics, 1997-09, Vol.17 (1), p.75-78

1997

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Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Human genetics, 2015-02, Vol.134 (2), p.191-201

2015

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A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-11, Vol.131B (1), p.51-59

2004

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Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-05, Vol.127B (1), p.104-112

2004

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Exploratory Subsetting of Autism Families Based on Savant Skills Improves Evidence of Genetic Linkage to 15q11-q13

Journal of the American Academy of Child and Adolescent Psychiatry, 2003-07, Vol.42 (7), p.856-863

2003

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

BMC medical genetics, 2005-01, Vol.6 (1), p.1-1, Article 1

2005

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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

Nature genetics, 1994-09, Vol.8 (1), p.52-58

1994

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Oestradiol attenuates the cognitive deficit induced by acute phencyclidine treatment in mature female hooded-Lister rats

Journal of psychopharmacology (Oxford), 2008-11, Vol.22 (8), p.918-922

2008

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Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families

Genomics (San Diego, Calif.), 2001-09, Vol.77 (1-2), p.105-113

2001

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Cell, 1991-12, Vol.67 (6), p.1047-1058

1991

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Genetics of Childhood Disorders: XLVII. Autism, Part 6: Duplication and Inherited Susceptibility of Chromosome 15q11-q13 Genes in Autism

Journal of the American Academy of Child and Adolescent Psychiatry, 2003-02, Vol.42 (2), p.253-256

2003

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Lack of Association Between Autism and SLC25A12

The American journal of psychiatry, 2006-05, Vol.163 (5), p.929-931

2006

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The spectrum of mutations in UBE3A causing Angelman syndrome

Human molecular genetics, 1999, Vol.8 (1), p.129-135

1999

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Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the LGI1 Gene

Epilepsia (Copenhagen), 2004-03, Vol.45 (3), p.218-222

2004

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Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism

Molecular psychiatry, 2003-01, Vol.8 (6), p.624-634

2003

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Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes

Neuroscience letters, 2004-12, Vol.372 (3), p.209-214

2004

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Characterizing sleep disorders in an autism-specific collection of electronic health records

Allelic Heterogeneity at the Serotonin Transporter Locus ( SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors

Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration

Human Serotonin Transporter Variants Display Altered Sensitivity to Protein Kinase G and p38 Mitogen-Activated Protein Kinase

0028 SHORTER SLEEP DURATION IS ASSOCIATED WITH SOCIAL IMPAIRMENT AND PSYCHIATRIC COMORBIDITIES IN AUTISM

Analysis of the RELN gene as a genetic risk factor for autism

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene ( UBE3A ) in Angelman syndrome

Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation

Imprinted expression of the murine Angelman syndrome gene, Ube3a , in hippocampal and Purkinje neurons

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

Exploratory Subsetting of Autism Families Based on Savant Skills Improves Evidence of Genetic Linkage to 15q11-q13

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

Oestradiol attenuates the cognitive deficit induced by acute phencyclidine treatment in mature female hooded-Lister rats

Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Genetics of Childhood Disorders: XLVII. Autism, Part 6: Duplication and Inherited Susceptibility of Chromosome 15q11-q13 Genes in Autism

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Lack of Association Between Autism and SLC25A12

The spectrum of mutations in UBE3A causing Angelman syndrome

Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the LGI1 Gene

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes

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