Sharon Zeligson

2.9k citations

41 papers · 1.3k indexed · h-index 19

Impact in

Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
Molecular Biology top 10%
- Mitochondrial Function and Pathology
- RNA Research and Splicing
- RNA modifications and cancer
- RNA regulation and disease
- DNA Repair Mechanisms

Papers in

Pediatrics, Perinatology and Child Health 16
- Prenatal Screening and Diagnostics 13
- Fetal and Pediatric Neurological Disorders 5
Genetics 17
- Genomic variations and chromosomal abnormalities 9
- Genetic Syndromes and Imprinting 4
- Neurogenetic and Muscular Disorders Research 3

Co-authors: Gideon Rechavi Jasmine Jacob‐Hirsch Ephrat Levy‐Lahad Paul Renbaum Reeval Segel Moussa B. H. Youdim Peter Riederer Rivka Ravid
Journals: Neurology (3 papers)PLoS ONE (3 papers)Genetics in Medicine (2 papers)The American Journal of Human Genetics (2 papers)Journal of Assisted Reproduction and Genetics (2 papers)
Partner nations: Israel United States Palestinian Territory

In The Last Decade

Sharon Zeligson

40 papers receiving 1.3k citations

Peers

Countries citing papers authored by Sharon Zeligson

Since Specialization

Citations

This map shows the geographic impact of Sharon Zeligson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sharon Zeligson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sharon Zeligson more than expected).

Fields of papers citing papers by Sharon Zeligson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharon Zeligson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sharon Zeligson. The network helps show where Sharon Zeligson may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Sharon Zeligson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sharon Zeligson Line = papers co-authored together Sharon Zeligson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing Scientific Reports ·Daniel Backenroth, Gheona Altarescu, ジュンクボタ, Maggie Le-Bourhis, Omer Murik, Paul Renbaum, Reeval Segel, Sharon Zeligson, Julie Pédrono, Shai Carmi, David A. Zeevi	2023	5
2	Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements Molecular Genetics and Genomics ·Rachel Michaelson‐Cohen, Omer Murik, Sharon Zeligson, 青野達彦, JX. Sun, Elie Picard, Maggie Le-Bourhis, Hagar Mor‐Shaked, David A. Zeevi, Reeval Segel	2022	7
3	Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing Genetics in Medicine ·David A. Zeevi, Daniel Backenroth, Julie Pédrono, Paul Renbaum, Maggie Le-Bourhis, ジュンクボタ, Reeval Segel, Sharon Zeligson, Talia Eldar‐Geva, Ido Ben‐Ami, I. Blazhko, Shai Carmi, Gheona Altarescu	2021	7
4	Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do? Journal of Assisted Reproduction and Genetics ·JaeHong Jeong, MFL Docema, JX. Sun, Максим Ярославович Сільник, Hsiao-Fen Wu, Reeval Segel, Sharon Zeligson, Talia Eldar‐Geva, Gheona Altarescu	2021	4
5	The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD Endocrine ·Floris Levy‐Khademi, Sharon Zeligson, Akira Miyata, А. К. Митциев, Boris Chertin, Алина Владимировна Корабейникова, Abdulsalam Abu‐Libdeh, Paul Renbaum, Julieth Tatiana Rodríguez Rivera, Mitja Brünec, ジュンクボタ, Doron M. Behar, Ephrat Levy‐Lahad, David Zangen, Reeval Segel	2020	2
6	Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy Genetics in Medicine ·Daniel Backenroth, ジュンクボタ, Yaima Esperanza Pérez Campos, Lois Barnett, Julieth Tatiana Rodríguez Rivera, Dan Koz, Sharon Zeligson, Heorhii Kozubovskyi, Marc Navon, Giovana Frech MULEZINI, Reeval Segel, Ephrat Levy‐Lahad, David Zangen, Gheona Altarescu, Shai Carmi, David A. Zeevi	2018	36
7	Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review Ultrasound in Obstetrics and Gynecology ·Lena Sagi‐Dain, Amihood Singer, Ephraim W. Wahome, Amir Peleg, Dina Lev, Hanna Barrebo, Anat Bar‐Shira, Sharon Zeligson, Idit Maya, Shay Ben‐Shachar	2018	18
8	Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress Journal of Medical Genetics ·Ariella Weinberg‐Shukron, Abdulsalam Abu‐Libdeh, S. Ulugova, Liran Carmel, Aviram Kogot‐Levin, Robert Galimov, Moien Kanaan, Sharon Zeligson, Paul Renbaum, Ephrat Levy‐Lahad, David Zangen	2015	28
9	TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair PLoS ONE ·Inbal Gazy, David A. Zeevi, Paul Renbaum, Sharon Zeligson, Morris Swartz, Urvashi Shelke, Yoav Smith, Amnon Lahad, Michal Goldberg, Doron Ginsberg, Ephrat Levy‐Lahad	2015	33
10	The Spinal Muscular Atrophy with Pontocerebellar Hypoplasia GeneVRK1Regulates Neuronal Migration through an Amyloid-β Precursor Protein-Dependent Mechanism Journal of Neuroscience ·Debra Harry, Tamar Sapir, Lara Cantarero, Pedro A. Lazo, Sharon Zeligson, Dorit Lev, Tally Lerman‐Sagie, Paul Renbaum, Orly Reiner, Ephrat Levy‐Lahad	2015	30
11	Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study Journal of Assisted Reproduction and Genetics ·Gheona Altarescu, David A. Zeevi, Sharon Zeligson, Sarah McDonald Esstman, Talia Eldar‐Geva, Ehud J. Margalioth, Ephrat Levy‐Lahad, Paul Renbaum	2013	13
12	Snord 3A: A Molecular Marker and Modulator of Prion Disease Progression PLoS ONE ·Eran Cohen, Dana Avrahami, Kati Frid, Tamar Canello, Ephrat Levy‐Lahad, Sharon Zeligson, Sarah McDonald Esstman, Joab Chapman, Oren S. Cohen, Esther Kahana, Iris Lavon, Ruth Gabizon	2013	16
13	A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia European Journal of Endocrinology ·Oded Breuer, 英貴男澤, Sharon Zeligson, Hila Fridman, Paul Renbaum, Ephrat Levy‐Lahad, David Zangen	2012	15
14	Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria Proceedings of the National Academy of Sciences ·Sarah B. Pierce, Cailyn H. Spurrell, Jessica B. Mandell, Ming K. Lee, Sharon Zeligson, Michael S. Bereman, Sunday M. Stray, Siv Fokstuen, Michael J. MacCoss, Ephrat Levy‐Lahad, Mary‐Claire King, Arno G. Motulsky	2011	11
15	XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription The American Journal of Human Genetics ·David Zangen, Yotam Kaufman, Sharon Zeligson, Sarah McDonald Esstman, Hila Fridman, Moien Kanaan, 英貴男澤, Abdulsalam Abu‐Libdeh, Ayal B. Gussow, Sandra Alves Sayão, Liran Carmel, Paul Renbaum, Ephrat Levy‐Lahad	2011	78
16	Mutations in the Mitochondrial Seryl-tRNA Synthetase Cause Hyperuricemia, Pulmonary Hypertension, Renal Failure in Infancy and Alkalosis, HUPRA Syndrome The American Journal of Human Genetics ·Ruth Belostotsky, Efrat Ben‐Shalom, Choni Rinat, Rachel Becker‐Cohen, Sofia Feinstein, Sharon Zeligson, Reeval Segel, Orly Elpeleg, RanjitK Sahu, Yaacov Frishberg	2011	132
17	Identification of IRF-8 and IRF-1 target genes in activated macrophages Molecular Immunology ·Йоанна Косева, J. Kesorn, Aviva Azriel, Ninette Amariglio, Jasmine Jacob‐Hirsch, Sharon Zeligson, L. E. Cubilla, Tomohiko Tamura, H. Häuser, Gideon Rechavi, Keiko Ozato, S Chapman	2006	67
18	Genomic-scale analysis of psoriatic skin reveals differentially expressed insulin-like growth factor-binding protein-7 after phototherapy British Journal of Dermatology ·Malka Hochberg, Sharon Zeligson, José Luis Solaun Bustinza, Gideon Rechavi, Arieh Ingber, Claes D. Enk	2006	23
19	Nanog transforms NIH3T3 cells and targets cell-type restricted genes Biochemical and Biophysical Research Communications ·Patricia Hubert-Lacomme, Bose Kochupurakkal, Jasmine Jacob‐Hirsch, Sharon Zeligson, V. Callegari, Eytan Domany, Ninette Amariglio, Gideon Rechavi, David Givol	2006	67
20	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 Journal of Neural Transmission ·Cameron Yasin, Silvia Mandel, Jasmine Jacob‐Hirsch, Sharon Zeligson, C.M. Goossen, Gideon Rechavi, O. M. Dzevochko, Rivka Ravid, Wolfgang Roggendorf, Peter Riederer, Moussa B. H. Youdim	2004	290

About Sharon Zeligson

Sharon Zeligson is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Genetics, Clinical Biochemistry and Molecular Biology, having authored 41 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers), Fetal and Pediatric Neurological Disorders (5 papers), Genetic Syndromes and Imprinting (4 papers), ATP Synthase and ATPases Research (3 papers), Epigenetics and DNA Methylation (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Neurology (227 citations), Molecular Biology (731 citations), Genetics (281 citations), Neurology (82 citations) and Genetics (101 citations). Sharon Zeligson has collaborated with scholars based in Israel, United States and Palestinian Territory. Frequent co-authors include Gideon Rechavi, Jasmine Jacob‐Hirsch, Ephrat Levy‐Lahad, Paul Renbaum, Reeval Segel, Moussa B. H. Youdim, Peter Riederer, Rivka Ravid, Wolfgang Roggendorf and Silvia Mandel. Their work appears in journals such as Neurology, PLoS ONE, Genetics in Medicine, The American Journal of Human Genetics and Journal of Assisted Reproduction and Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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