List of works - Valerie Greger

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes ⬇️

scientific article published on June 15, 1992

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene ⬇️

scientific article published on December 1, 1992

Carrier screening by next-generation sequencing: health benefits and cost effectiveness.

scientific article published on 29 January 2016

Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.

scientific article

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus

scientific article published on 01 July 1987

Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus

scientific article published on 01 February 1987

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

scientific article published on 01 November 1994

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

scientific article published in May 1994

Mapping of the Angelman and Prader-Willi syndromes.

scientific article published on January 1993

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene

scientific article published on 01 December 1993

Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening

scientific article

Next-generation carrier screening

scientific article published on 13 June 2013

No evidence for linkage between lipoprotein(a) (LPA) and esterase D (ESD)

scientific article published on 01 January 1988

Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinoma

scientific article published on 01 November 1990

The critical region for Angelman syndrome lies between D15S122 and D15S113

The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation ⬇️

scientific article published on March 20, 1995

Truncating variants in the majority of the cytoplasmic domain of PCDH15 are unlikely to cause Usher syndrome 1F.

scientific article published in November 2014

Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families

scientific article published on 01 February 1990

Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing.

scientific article

List of works by Valerie Greger

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes ⬇️

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene ⬇️

Carrier screening by next-generation sequencing: health benefits and cost effectiveness.

Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus

Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

Mapping of the Angelman and Prader-Willi syndromes.

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene

Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening

Next-generation carrier screening

No evidence for linkage between lipoprotein(a) (LPA) and esterase D (ESD)

Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinoma

The critical region for Angelman syndrome lies between D15S122 and D15S113

The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation ⬇️

Truncating variants in the majority of the cytoplasmic domain of PCDH15 are unlikely to cause Usher syndrome 1F.

Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families

Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing.