Wayne Gottlieb
Home Office(GB)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Sperm and Testicular Function, Reproductive Biology and Fertility, Prenatal Screening and Diagnostics, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints(1999)281 cited
- → The Frequency of Uniparental Disomy in Prader-Willi Syndrome(1992)260 cited
- → Ultrastructural studies of the early events of the human sperm acrosome reaction as initiated by human follicular fluid(1988)149 cited
- → Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome(1992)67 cited
- → The Mr115 kd fiber cell-specific protein is a component of the lens cytoskeleton(1989)64 cited
- → Partial characterization of a fraction from human follicular fluid that initiates the human sperm acrosome reaction in vitro(1988)41 cited
- → Cytogenetic and molecular analysis in Angelman syndrome(1993)40 cited
- → Biochemical Studies of Metalloendoprotease Activity in the Spermatozoa of Three Mammalian Species(1987)29 cited
- → A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region(1994)6 cited
- Chromosome breakage in Prader-Willi and Angelman syndrome deletions may involve recombination between a repeat at the proximal and distal breakpoints(1994)