M. Volodarsky

发表

Fetal acid–base balance after betamethasone administration: relation to fetal heart rate variability

S. Shenhav, M. Volodarsky, E. Anteby, 2008, Archives of Gynecology and Obstetrics.

Genetic and epigenetic profiling of BRCA1/2 in ovarian tumors reveals additive diagnostic yield and evidence of a genomic BRCA1/2 DNA methylation signature

P. Ainsworth, B. Sadikovic, M. Volodarsky, 2020, Journal of Human Genetics.

Is there a survival advantage in diagnosing endometrial cancer in asymptomatic postmenopausal patients? An Israeli Gynecology Oncology Group study

M. Volodarsky, O. Gemer, O. Raban, 2018, American journal of obstetrics and gynecology.

Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase

G. Narkis, D. Landau, K. Elbedour, 2013, European Journal of Human Genetics.

Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients

M. Tarnopolsky, P. Ainsworth, B. Sadikovic, 2020, Journal of Medical Genetics.

Midtrimester triple test levels in women with severe preeclampsia and HELLP syndrome

S. Shenhav, M. Volodarsky, O. Gemer, 2003, Acta obstetricia et gynecologica Scandinavica.

Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.

O. Birk, M. Volodarsky, U. Zilberman, 2015, Archives of oral biology.

Mid‐trimester triple test levels in early and late onset severe pre‐eclampsia

R. Peled, S. Shenhav, M. Volodarsky, 2002, Prenatal diagnosis.

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome

G. Rutter, R. Zarivach, O. Birk, 2017, Brain : a journal of neurology.

CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay.

O. Birk, Y. Perez, R. Shaco‐Levy, 2015, Human molecular genetics.

A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta

D. Landau, O. Birk, B. Markus, 2013, Human mutation.

The oncological safety of hysteroscopy in the diagnosis of early-stage endometrial cancer: An Israel gynecologic oncology group study.

M. Volodarsky, O. Gemer, O. Raban, 2019, European journal of obstetrics, gynecology, and reproductive biology.

Laparoscopic Management of an Invasive Mole Perforating the Uterus.

M. Volodarsky, E. Anteby, O. Gemer, 2017, Journal of minimally invasive gynecology.

The diagnosis of endometrial cancer in women with asymptomatic endometrial polyp does not increase survival rates: an israel gynecologic oncology group study.

M. Volodarsky, O. Gemer, Z. Vaknin, 2021, Maturitas.

Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario

V. Siu, C. Campbell, B. Sadikovic, 2020, Journal of Human Genetics.

A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex

O. Birk, M. Volodarsky, Yshaia Langer, 2014, BMC Medical Genetics.

Is intrauterine device a risk factor for failure of conservative management in patients with tubo-ovarian abscess? An observational retrospective study

M. Volodarsky, E. Anteby, O. Gemer, 2018, Archives of Gynecology and Obstetrics.

Controlled ovarian hyperstimulation: are we monitoring the appropriate sex-steroid hormones?

M. Volodarsky, R. Homburg, R. Orvieto, 2008, Fertility and sterility.

Age is an independent predictor of outcome in endometrial cancer patients: An Israeli Gynecology Oncology Group cohort study

M. Volodarsky, O. Gemer, O. Raban, 2020, Acta obstetricia et gynecologica Scandinavica.

Are Ultrasonographic Findings Suggestive of Ovarian Stromal Edema Associated with Ischemic Adnexal Torsion?

M. Volodarsky, E. Anteby, O. Gemer, 2015, Gynecologic and Obstetric Investigation.

Controlled ovarian hyperstimulation using multi-dose gonadotropin-releasing hormone (GnRH) antagonist results in less systemic inflammation than the GnRH-agonist long protocol

M. Volodarsky, E. Anteby, R. Homburg, 2007, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN

O. Birk, R. Birnbaum, Y. Perez, 2015, Journal of Medical Genetics.

ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size

O. Birk, B. Markus, T. Harel, 2016, PLoS genetics.

Mosaic embryo transfer—first report of a live born with nonmosaic partial aneuploidy and uniparental disomy 15

E. Strong, M. Volodarsky, M. Steinraths, 2022, F&S reports.

Increased ultrasonographic endometrial thickness is associated with poor survival in patients with endometrial cancer: An Israel gynecologic oncology group study.

M. Volodarsky, O. Gemer, O. Raban, 2020, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach

P. Ainsworth, B. Sadikovic, M. Volodarsky, 2021, Frontiers in Genetics.

Laparoscopic Management of Uterine Rupture After Early Second-Trimester Medical Abortion in a Patient With a Prior Cesarean Section.

M. Volodarsky, E. Anteby, O. Gemer, 2016, Journal of minimally invasive gynecology.

Genetic and epigenetic profiling of BRCA1/2 in ovarian tumors reveals additive diagnostic yield and evidence of a genomic BRCA1/2 DNA methylation signature

P. Ainsworth, B. Sadikovic, M. Volodarsky, 2020, Journal of Human Genetics.

Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.

O. Birk, M. Volodarsky, U. Zilberman, 2015, Archives of oral biology.