Reuven Sharony

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Journal: Clinical genetics

Published: May 04, 2020

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Journal: European journal of medical genetics

Published: February 18, 2020

Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor.

Journal: European journal of human genetics : EJHG

Published: March 06, 2019

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Journal: Ophthalmic genetics

Published: April 21, 2018

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

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: February 20, 2018

The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Published: February 02, 2018

The impact of third-trimester genetic counseling.

Journal: Archives of gynecology and obstetrics

Published: October 23, 2017

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.

Journal: Journal of perinatal medicine

Published: October 17, 2017

The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally †.

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: October 13, 2017

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.

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

Published: February 23, 2017

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor.

Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor.

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.

The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.

The impact of third-trimester genetic counseling.

The impact of third-trimester genetic counseling.

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.

The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally †.

The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally †.

The magnitude of elevated maternal serum human chorionic gonadotropin and pregnancy complications.

The magnitude of elevated maternal serum human chorionic gonadotropin and pregnancy complications.

The mid-gestation triple test profile among women diagnosed with vasa previa.

The mid-gestation triple test profile among women diagnosed with vasa previa.

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.