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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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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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From Electrophysiology to Chromatin: A Bottom-Up Approach to Angelman Syndrome

Annals of the New York Academy of Sciences, 2004-12, Vol.1030 (1), p.599-611

2004

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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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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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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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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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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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Evidence for two pathways of meiotic intrachromosomal recombination in yeast

Proceedings of the National Academy of Sciences - PNAS, 1989-09, Vol.86 (18), p.7072-7076

1989

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Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiency

The Journal of pediatrics, 1991, Vol.118 (4), p.569-572

1991

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A cluster of three GABA sub(A) 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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A cluster of three GABA A 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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Wolbachia depletion blocks transmission of lymphatic filariasis by preventing chitinase-dependent parasite exsheathment

Proceedings of the National Academy of Sciences - PNAS, 2022-04, Vol.119 (15), p.e2120003119-e2120003119

2022

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Apalutamide Treatment and Metastasis-free Survival in Prostate Cancer

The New England journal of medicine, 2018-04, Vol.378 (15), p.1408-1418

2018

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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

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

From Electrophysiology to Chromatin: A Bottom-Up Approach to Angelman Syndrome

UBE3A/E6-AP mutations cause Angelman syndrome

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

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

Mutation Analysis of UBE3A in Angelman Syndrome Patients

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

Evidence for two pathways of meiotic intrachromosomal recombination in yeast

Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiency

A cluster of three GABA sub(A) receptor subunit genes is deleted in a neurological mutant of the mouse p locus

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

Wolbachia depletion blocks transmission of lymphatic filariasis by preventing chitinase-dependent parasite exsheathment

Apalutamide Treatment and Metastasis-free Survival in Prostate Cancer

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