Sharon Zeligson

Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 33 publications

Resolving Genomic Mysteries with Long-read Sequencing

Resolving Genomic Mysteries with Long-read Sequencing

Journal: Harefuah

Published: March 09, 2026

SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing.

SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing.

Journal: Scientific reports

Published: June 15, 2023

Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements.

Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements.

Journal: Molecular genetics and genomics : MGG

Published: September 19, 2021

A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome.

A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome.

Journal: Clinical dysmorphology

Published: July 07, 2021

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome.

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome.

Journal: Journal of medical genetics

Published: April 06, 2021

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.

Journal: Journal of medical genetics

Published: April 04, 2021

Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing.

Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 06, 2021

Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?

Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?

Journal: Journal of assisted reproduction and genetics

Published: September 21, 2020

The yield of chromosomal microarray testing for cases of abnormal fetal head circumference.

The yield of chromosomal microarray testing for cases of abnormal fetal head circumference.

Journal: Journal of perinatal medicine

Published: July 29, 2020

A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures.

A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures.

Journal: Neurogenetics

Published: March 05, 2020

The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD.

The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD.

Journal: Endocrine

Published: January 23, 2020

Is fetal isolated double renal collecting system an indication for chromosomal microarray?

Is fetal isolated double renal collecting system an indication for chromosomal microarray?

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: April 30, 2019

Showing 1-12 of 33

Last Updated: 09/26/2026