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S. Zeligson · SciRah

Researcher profile · Semantic Scholar

S. Zeligson

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S. Zeligson — researcher profile on SciRah

h-index: 24
Works: 59
Citations: 2,802

Most-cited papers

Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.
Paulina Navon Elkan, S. Pierce, R. Segel, T. Walsh +31 more
2014New England Journal of Medicine628 citations
Semantic Scholar
Gene expression profiling of parkinsonian substantia nigra pars compacta; alterations in ubiquitin-proteasome, heat shock protein, iron and oxidative stress regulated proteins, cell adhesion/cellular matrix and vesicle trafficking genes
E. Grünblatt, S. Mandel, J. Jacob-Hirsch, S. Zeligson +7 more
2004Journal of neural transmission360 citations
Semantic Scholar
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group.
L. Hertzberg, E. Vendramini, I. Ganmore, G. Cazzaniga +21 more
2010Blood353 citations Open access
Semantic Scholar
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.
Ruth Belostotsky, Efrat Ben-Shalom, Choni Rinat, R. Becker-Cohen +6 more
2011American Journal of Human Genetics183 citations Open access
Semantic Scholar
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
D. Zangen, Yotam Kaufman, S. Zeligson, Shira Perlberg +9 more
2011American Journal of Human Genetics106 citations Open access
Semantic Scholar
Copy number variations in cryptogenic cerebral palsy
R. Segel, H. Ben-Pazi, S. Zeligson, A. Fatal-Valevski +9 more
2015Neurology97 citations
Semantic Scholar
Identification of IRF-8 and IRF-1 target genes in activated macrophages.
N. Dror, Michal Alter-Koltunoff, A. Azriel, N. Amariglio +8 more
2007Molecular Immunology94 citations Open access
Semantic Scholar
CD133‐Positive Hematopoietic Stem Cell “Stemness” Genes Contain Many Genes Mutated or Abnormally Expressed in Leukemia
A. Toren, B. Bielorai, J. Jacob-Hirsch, T. Fisher +10 more
2005Stem Cells92 citations
Semantic Scholar
Essential Role of BRCA2 in Ovarian Development and Function
A. Weinberg-Shukron, M. Rachmiel, P. Renbaum, S. Gulsuner +13 more
2018New England Journal of Medicine85 citations Open access
Semantic Scholar
A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis.
A. Weinberg-Shukron, P. Renbaum, R. Kalifa, S. Zeligson +11 more
2015Journal of Clinical Investigation83 citations Open access
Semantic Scholar
Nanog transforms NIH3T3 cells and targets cell-type restricted genes.
D. Piestun, B. Kochupurakkal, J. Jacob-Hirsch, S. Zeligson +5 more
2006Biochemical and Biophysical Research Communications - BBRC75 citations
Semantic Scholar
Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy
D. Backenroth, F. Zahdeh, Y. Kling, Aharon Peretz +12 more
2018Genetics in Medicine44 citations Open access
Semantic Scholar
The Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Gene VRK1 Regulates Neuronal Migration through an Amyloid-β Precursor Protein-Dependent Mechanism
Hadar Vinograd-Byk, Tamar Sapir, L. Cantarero, P. Lazo +6 more
2015Journal of Neuroscience41 citations Open access
Semantic Scholar
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair
I. Gazy, David A. Zeevi, P. Renbaum, S. Zeligson +7 more
2015PLoS ONE38 citations Open access
Semantic Scholar
Mechanisms Operative in the Antitumor Activity of Temozolomide in Glioblastoma Multiforme
T. Fisher, Gil Galanti, G. Lavie, J. Jacob-Hirsch +7 more
2007Cancer Journal38 citations
Semantic Scholar
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection
A. Aran, N. Rosenfeld, R. Jaron, P. Renbaum +16 more
2016Neurology33 citations Open access
Semantic Scholar
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy
Michal Yechieli, S. Gulsuner, H. Ben-Pazi, A. Fattal +18 more
2021Journal of Medical Genetics32 citations
Semantic Scholar
Mitochondrial PITRM1 peptidase loss-of-function in childhood cerebellar atrophy
Yeshaya Langer, A. Aran, S. Gulsuner, B. Abu-Libdeh +17 more
2018Journal of Medical Genetics32 citations Open access
Semantic Scholar
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress
A. Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, L. Carmel +7 more
2015Journal of Medical Genetics32 citations
Semantic Scholar
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome
A. Aran, R. Segel, Kaneshige Kota, S. Gulsuner +12 more
2017Neurology31 citations Open access
Semantic Scholar
Genomic‐scale analysis of psoriatic skin reveals differentially expressed insulin‐like growth factor‐binding protein‐7 after phototherapy
M. Hochberg, S. Zeligson, N. Amariglio, G. Rechavi +2 more
2007British Journal of Dermatology28 citations
Semantic Scholar
Evolutionary regulation of the blind subterranean mole rat, Spalax, revealed by genome-wide gene expression.
L. Brodsky, J. Jacob-Hirsch, A. Avivi, L. Trakhtenbrot +7 more
2005Proceedings of the National Academy of Sciences of the United States of America27 citations Open access
Semantic Scholar
Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review
L. Sagi-Dain, A. Singer, S. Josefsberg, A. Peleg +6 more
2019Ultrasound in Obstetrics and Gynecology24 citations Open access
Semantic Scholar
Snord 3A: A Molecular Marker and Modulator of Prion Disease Progression
E. Cohen, D. Avrahami, Kati Frid, T. Canello +8 more
2013PLoS ONE24 citations Open access
Semantic Scholar
P2X4 is Up-regulated in Gingival Fibroblasts after Periodontal Surgery
I. Binderman, H. Bahar, J. Jacob-Hirsch, S. Zeligson +4 more
2007Journal of dentistry research24 citations
Semantic Scholar
Expanding the phenotype of CRB2 mutations – A new ciliopathy syndrome?
R. Jaron, N. Rosenfeld, F. Zahdeh, S. Carmi +8 more
2016Clinical Genetics22 citations
Semantic Scholar
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria
S. Pierce, Cailyn H. Spurrell, Jessica B. Mandell, Ming K. Lee +8 more
2011Proceedings of the National Academy of Sciences of the United States of America22 citations Open access
Semantic Scholar
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.
O. Breuer, Maha Abdulhadi-Atwan, S. Zeligson, Hila Fridman +3 more
2012European Journal of Endocrinology18 citations
Semantic Scholar
What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
I. Maya, A. Singer, H. Yonath, A. Reches +4 more
2020Acta Obstetricia et Gynecologica Scandinavica17 citations
Semantic Scholar
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures
R. Segel, A. Aran, S. Gulsuner, Hiroki Nakamura +11 more
2020Neurogenetics16 citations
Semantic Scholar
Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study
G. Altarescu, D. Zeevi, S. Zeligson, Shira Perlberg +4 more
2013Journal of Assisted Reproduction and Genetics15 citations Open access
Semantic Scholar
A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD)
Z. Ben‐Neriah, R. Michaelson-Cohen, M. Inbar-Feigenberg, M. Nadjari +5 more
2011American Journal of Medical Genetics. Part A13 citations
Semantic Scholar
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements
R. Michaelson-Cohen, Omer Murik, S. Zeligson, Orit Lobel +6 more
2022Zeitschrift für Induktive Abstammungs- und Vererbungslehre11 citations
Semantic Scholar
Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing
David A. Zeevi, D. Backenroth, Elinor Hakam-Spector, P. Renbaum +9 more
2021Genetics in Medicine10 citations Open access
Semantic Scholar
The yield of chromosomal microarray testing for cases of abnormal fetal head circumference
Y. Pasternak, A. Singer, I. Maya, L. Sagi-Dain +6 more
2020Journal of Perinatal Medicine10 citations
Semantic Scholar
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing
D. Backenroth, G. Altarescu, F. Zahdeh, Tzvia Mann +7 more
2023Scientific Reports9 citations Open access
Semantic Scholar
Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?
K. Rotshenker-Olshinka, Naama Srebnik Moshe, O. Weiss, S. Shaviv +5 more
2021Journal of Assisted Reproduction and Genetics8 citations Open access
Semantic Scholar
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader‐Willi male
T. Eldar-Geva, V. Gross-Tsur, H. Hirsch, G. Altarescu +5 more
2018Molecular Genetics & Genomic Medicine6 citations Open access
Semantic Scholar
DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.
L. Hertzberg, E. Vendramini, I. Ganmore, G. Cazzaniga +21 more
20096 citations Open access
Semantic Scholar
Is fetal isolated double renal collecting system an indication for chromosomal microarray?
A. Singer, I. Maya, A. Frumkin, S. Zeligson +4 more
2019Journal of Maternal-Fetal & Neonatal Medicine5 citations
Semantic Scholar
Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis
S. Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, G. Altarescu +6 more
2015PLoS ONE5 citations Open access
Semantic Scholar
Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome
H. Daum, R. Segel, V. Meiner, Y. Goldberg +7 more
2022Journal of Medical Genetics3 citations
Semantic Scholar
Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 Deletion
T. Gilboa, R. Segel, S. Zeligson, Gheona Alterescu +1 more
2018Journal of Child Neurology3 citations
Semantic Scholar
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD
Floris Levy-Khademi, S. Zeligson, E. Lavi, T. Klopstock +11 more
2020Endocrine2 citations
Semantic Scholar
A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome
Hagit Goldenstein, Sara Beni Shrem, O. Weiss, S. Zeligson +3 more
2021Clinical Dysmorphology1 citations
Semantic Scholar
Array-Comparative-Genomic-Hybridization (Acgh) Based Preimplantation-Genetic-Diagnosis (PGD) for Balanced Translocation Carriers Improves both Diagnostic and Pregnancy Rates Compared to Fluorescent-In-Situ-Hybridization (FISH) and Polymerase-Chain-Reaction (PCR) Based PGD
T. Mishael, T. Eldar-Geva, S. Zeligson, R. Beeri +8 more
20151 citations Open access
Semantic Scholar
OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN)
E. Levy-Lahad, P. Elkan-Navon, R. Segel, S. Pierce +25 more
2013Pediatric Rheumatology Online Journal1 citations Open access
Semantic Scholar
Effect of allicin and its derivatives on vascular endothelial cell functions and glutathione level
Limor Horev-Azaria, D. Mirelman, T. Miron, J. Jacob-Hirsch +3 more
20061 citations
Semantic Scholar
[Resolving Genomic Mysteries with Long-read Sequencing].
Omer Murik, D. Zeevi, Tzvia Mann, R. Beeri +10 more
2026Harefuah0 citations
Semantic Scholar
SHaploseek: A sequencing-only high-resolution implementation of comprehensive preimplantation genetic testing
D. Backenroth, G. Altarescu, F. Zahdeh, Tzvia Mann +7 more
2023medRxiv0 citations Open access
Semantic Scholar

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