S. Rienstein

发表

Epidermal growth factor receptor gene amplification and expression in disseminated pediatric low-grade gliomas.

N. Amariglio, G. Rechavi, S. Izraeli, 2005, Journal of neurosurgery.

Chromosomal aberrations and gene expression profiles in non-small cell lung cancer.

M. Bittner, Z. Yakhini, A. Ben-Dor, 2007, Lung cancer.

Proximal 19q Trisomy: A New Syndrome of Morbid Obesity and Mental Retardation

A. Zung, Z. Zadik, S. Rienstein, 2006, Hormone Research in Paediatrics.

Time dependency of hematopoietic growth factor coupled to chronotoxicity of carboplatin

I. Ashkenazi, L. Peleg, I. Ron, 1998, Cancer Chemotherapy and Pharmacology.

Abnormal nuchal translucency followed by normal microarray analysis is associated with placental pathology‐related complications

Y. Yinon, S. Rienstein, A. Shemer, 2021, Prenatal diagnosis.

Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.

M. Frydman, E. Pras, E. Pras, 2006, Investigative ophthalmology & visual science.

Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas.

Z. Rappaport, Z. Ram, E. Friedman, 2001, Cancer genetics and cytogenetics.

True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: Clinical features, cytogenetic findings, and literature review

J. Meyerovitch, D. Modan-Moses, S. Rienstein, 2003, American journal of medical genetics. Part A.

Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier’s embryos- preliminary observations of two robertsonian translocation carrier families

E. Pras, H. Yonath, J. Levron, 2010, Journal of Assisted Reproduction and Genetics.

Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1q

J. Itskovitz‐Eldor, H. Reznik‐Wolf, M. Amit, 2012, European Journal of Human Genetics.

Caudal dysplasia sequence with penile enlargement: case report and a potential pathogenic hypothesis.

R. Gershoni-baruch, M. Epelman, T. Paperna, 2001, American journal of medical genetics.

Chromosomal integrity of human preimplantation embryos at different days post fertilization

H. Yonath, A. Hourvitz, S. Rienstein, 2013, Journal of Assisted Reproduction and Genetics.

Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinoma.

E. Friedman, W. Gotlieb, S. Mahmud, 2009, Cancer genetics and cytogenetics.

Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGH.

E. Friedman, W. Gotlieb, O. Israeli, 2003, Gynecologic oncology.

In silico chromosomal clustering of genes displaying altered expression patterns in ovarian cancer.

E. Friedman, O. Israeli, S. Rienstein, 2005, Cancer genetics and cytogenetics.

Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia

B. Pode-Shakked, Y. Anikster, E. Pras, 2012, Human Genetics.

Comparative genomic hybridization analysis of craniopharyngiomas.

E. Friedman, S. Rienstein, B. Goldman, 2003, Journal of neurosurgery.

Post-childhood Presentation and Diagnosis of DiGeorge Syndrome

R. Somech, Yonatan Yeshayahu, S. Rienstein, 2016, Clinical pediatrics.

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney

A. Frumkin, R. Segel, L. Sagi‐Dain, 2018, Journal of perinatal medicine.

Do human embryos have the ability of self-correction?

H. Shani, S. Rienstein, R. Orvieto, 2020, Reproductive Biology and Endocrinology.

Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

D. Goldstein, E. Heinzen, V. Aggarwal, 2020, Journal of Human Genetics.

Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa Anomalies

H. Yonath, E. Katorza, L. Sagi‐Dain, 2021, Neurology: Genetics.

Genomic analyses of primary and metastatic serous epithelial ovarian cancer.

E. Friedman, W. Gotlieb, O. Israeli, 2004, Cancer genetics and cytogenetics.

Alterations of Circadian Rhythms in Mice Induced by Anti-Cancer Drugs

I. Ashkenazi, L. Peleg, I. Ron, 1998 .

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?

H. Yonath, L. Sagi‐Dain, A. Singer, 2020, Acta obstetricia et gynecologica Scandinavica.

Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

D. Goldstein, E. Heinzen, V. Aggarwal, 2020, Journal of Human Genetics.

Daily rhythms in male mice meiosis.

I. Ashkenazi, L. Avivi, A. Dotan, 1998, Chronobiology international.

Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia

B. Pode-Shakked, Y. Anikster, E. Pras, 2012, Human Genetics.