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Role of Histone Methyltransferase G9a in CpG Methylation of the Prader-Willi Syndrome Imprinting Center

The Journal of biological chemistry, 2003-04, Vol.278 (17), p.14996-15000

2003

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Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein

The Journal of biological chemistry, 2004-09, Vol.279 (39), p.41208-41217

2004

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Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome

Neurobiology of disease, 2005-11, Vol.20 (2), p.471-478

2005

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Cell-free DNA is more sensitive than cell-free mRNA as a marker for evaluation of fetal-maternal hemorrhage

Clinical chemistry (Baltimore, Md.), 2006-11, Vol.52 (11), p.2121-2123

2006

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UBE3A/E6-AP mutations cause Angelman syndrome

Nature genetics, 1997-01, Vol.15 (1), p.70-73

1997

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Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

Neurobiology of disease, 2002-03, Vol.9 (2), p.149-159

2002

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Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes

Genomics (San Diego, Calif.), 1998-01, Vol.47 (1), p.101-107

1998

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A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus

Nature (London), 1993-07, Vol.364 (6436), p.448-450

1993

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Parent-Specific Complementary Patterns of Histone H3 Lysine 9 and H3 Lysine 4 Methylation at the Prader-Willi Syndrome Imprinting Center

American journal of human genetics, 2001-12, Vol.69 (6), p.1389-1394

2001

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Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

Neurobiology of disease, 2002-03, Vol.9 (2), p.149-159

2002

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Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene

The Lancet (British edition), 1992-02, Vol.339 (8789), p.366-367

1992

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Effects of a low dose of melatonin on sleep in children with Angelman syndrome

Journal of Pediatric Endocrinology and Metabolism, 1999-01, Vol.12 (1), p.57

1999

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SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome

Human genetics, 2004-05, Vol.114 (6), p.553-561

2004

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Mutation Analysis of UBE3A in Angelman Syndrome Patients

American journal of human genetics, 1998-06, Vol.62 (6), p.1353-1360

1998

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Genomic organization of the UBE3A/E6-AP gene and related pseudogenes

Genomics (San Diego, Calif.), 1998, Vol.47 (1), p.101-107

1998

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Genetics beyond Mendel: Understanding nontraditional inheritance patterns

Postgraduate medicine, 2000-09, Vol.108 (3), p.131-138

Wagstaff, Joseph

2000

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A familial balanced 3:9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings

American journal of human genetics, 1995, Vol.56 (1), p.302-309

1995

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Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

Nucleic acids research, 2005-01, Vol.33 (13), p.3976-3984

2005

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Meiosis in Haploid Yeast

Proceedings of the National Academy of Sciences - PNAS, 1982-05, Vol.79 (9), p.2986-2990

1982

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Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABA A receptor β 3 -subunit gene

The Lancet (British edition), 1992-02, Vol.339 (8789), p.366

1992

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OA1 Mutations and Deletions in X-Linked Ocular Albinism

American journal of human genetics, 1998-04, Vol.62 (4), p.800-809

1998

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FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader–Willi syndrome chromosomal regions

Human molecular genetics, 1993-02, Vol.2 (2), p.183-189

1993

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High-resolution mapping of the γ-aminobutyric acid receptor subunit β3 and α5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients

American journal of human genetics, 1993, Vol.52 (6), p.1216-1229

1993

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Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3

American journal of human genetics, 1997-03, Vol.60 (3), p.574-580

1997

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Phenotypic variability in X-linked ocular albinism : relationship to linkage genotypes

American journal of human genetics, 1994-09, Vol.55 (3), p.484-496

1994

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Role of Histone Methyltransferase G9a in CpG Methylation of the Prader-Willi Syndrome Imprinting Center

Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein

Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome

Cell-free DNA is more sensitive than cell-free mRNA as a marker for evaluation of fetal-maternal hemorrhage

UBE3A/E6-AP mutations cause Angelman syndrome

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes

A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus

Parent-Specific Complementary Patterns of Histone H3 Lysine 9 and H3 Lysine 4 Methylation at the Prader-Willi Syndrome Imprinting Center

Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene

Effects of a low dose of melatonin on sleep in children with Angelman syndrome

SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome

Mutation Analysis of UBE3A in Angelman Syndrome Patients

Genomic organization of the UBE3A/E6-AP gene and related pseudogenes

Genetics beyond Mendel: Understanding nontraditional inheritance patterns

A familial balanced 3:9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings

Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

Meiosis in Haploid Yeast

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABA A receptor β 3 -subunit gene

OA1 Mutations and Deletions in X-Linked Ocular Albinism

FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader–Willi syndrome chromosomal regions

High-resolution mapping of the γ-aminobutyric acid receptor subunit β3 and α5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3

Phenotypic variability in X-linked ocular albinism : relationship to linkage genotypes

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