Hagar Mor‐Shaked

646 citations

32 papers · 267 indexed · h-index 10

Genetics
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 3
- Blood disorders and treatments 2
Cognitive Neuroscience
- Autism Spectrum Disorder Research 3
Molecular Biology
- Epigenetics and DNA Methylation 4
Cellular and Molecular Neuroscience
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3
Cell Biology
- Cellular transport and secretion 4

Co-authors: Rachel Eiges Silvina Epsztejn‐Litman Tamar Harel Orly Elpeleg Vardiella Meiner Paul Renbaum Gheona Altarescu Talia Eldar‐Geva
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Partner nations: Israel United States Germany

In The Last Decade

Hagar Mor‐Shaked

28 papers receiving 267 citations

Peers

Countries citing papers authored by Hagar Mor‐Shaked

Since Specialization

Citations

This map shows the geographic impact of Hagar Mor‐Shaked'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 Hagar Mor‐Shaked with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hagar Mor‐Shaked more than expected).

Fields of papers citing papers by Hagar Mor‐Shaked

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hagar Mor‐Shaked. 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 Hagar Mor‐Shaked. The network helps show where Hagar Mor‐Shaked may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hagar Mor‐Shaked, 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 Hagar Mor‐Shaked Line = papers co-authored together Hagar Mor‐Shaked links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics Rivka Birnbaum,Maya Slovik,Shamir Zenvirt,Ilana Livyatan,I. B. Altman,Samuel Gershon,Jonathan Rips,Hagit Daum,Chaggai Rosenbluh,Orly Elpeleg,Vardiella Meiner,Ayala Frumkin,Hagar Mor‐Shaked,Tamar Harel	2025	0
2	A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF Zippora Brownstein,Lara Kamal,Shir Mishan-Montefiori,Yoav Hoffman,Dina Fine,Yoel Hirsch,Tzvi Weiden,Rivka Birnbaum,Hagar Mor‐Shaked,Bella Davidov,Yuval Yaron,Karen B. Avraham	2025	0
3	Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome Shiyu Luo,Valérie Gailus-Durner,Bobbi McGivern,Qifei Li,Jessica Kottmeier,Mai‐Lan Ho,Hagar Mor‐Shaked,Orly Elpeleg,Erfan Aref‐Eshghi,Amanda C Brodeur,Klaus Schmitz‐Abe,Casie A. Genetti,Jonathan Picker,Jiahai Shi,Reem Ibrahim Bux,Tawfeg Ben‐Omran,Helmut Fuchs,Tamar Harel,Martin Hrabě de Angelis,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2025	0
4	A neurodevelopmental disorder associated with a loss-of-function missense mutation in RAB35 Adriana Aguila,Somaya Salah,Gopinath Kulasekaran,Moatasem Shweiki,Nava Shaul-Lotan,Hagar Mor‐Shaked,Muhannad Daana,Tamar Harel,Peter S. McPherson	2024	0
5	A recurrent de novo variant in NUSAP1 escapes nonsense‐mediated decay and leads to microcephaly, epilepsy, and developmental delay Alisa Mo,Emuna Paz‐Ebstein,Shira Yanovsky‐Dagan,Abbe Lai,Hagar Mor‐Shaked,Tal Gilboa,Edward Yang,Diane D. Shao,Christopher A. Walsh,Tamar Harel	2023	6
6	Exome sequencing for structurally normal fetuses—yields and ethical issues Hagit Daum,Tamar Harel,Talya Millo,Avital Eilat,Duha Fahham,Shiri Gershon-Naamat,Adily Basal,Chaggai Rosenbluh,N. Yanai,Shay Porat,Doron Kabiri,Simcha Yagel,D. V. Valsky,Orly Elpeleg,Vardiella Meiner,Hagar Mor‐Shaked	2022	12
7	Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements Rachel Michaelson‐Cohen,Omer Murik,Sharon Zeligson,Orit Lobel,Omri Weiss,Elie Picard,Tzvia Mann,Hagar Mor‐Shaked,David A. Zeevi,Reeval Segel	2022	7
8	Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delay Hagar Mor‐Shaked,Somaya Salah,Shira Yanovsky‐Dagan,Vardiella Meiner,Osama Atawneh,Bassam Abu‐Libdeh,Orly Elpeleg,Tamar Harel	2021	12
9	Levodopa-responsive dystonia caused by biallelic PRKN exon inversion invisible to exome sequencing Hagar Mor‐Shaked,Emuna Paz‐Ebstein,Adily Basal,Simona Ben‐Haim,Hanna Grobe,Sami Heymann,Zvi Israel,Montaser Namnah,Anat Nitzan,Chaggai Rosenbluh,Ann Saada,Tomer Tzur,Shira Yanovsky‐Dagan,Ronen Zaidel‐Bar,Tamar Harel,David Arkadir	2021	9
10	Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosis Ehud Even‐Or,Gali Schiesel,Natalia Simanovsky,Adeeb NaserEddin,Irina Zaidman,Orly Elpeleg,Hagar Mor‐Shaked,Polina Stepensky	2021	7
11	The Clinical Aspect of Adaptor Molecules in T Cell Signaling: Lessons Learnt From Inborn Errors of Immunity Yael Dinur-Schejter,Irina Zaidman,Hagar Mor‐Shaked,Polina Stepensky	2021	7
12	Homozygous variant in MADD, encoding a Rab guanine nucleotide exchange factor, results in pleiotropic effects and a multisystemic disorder Bassam Abu‐Libdeh,Hagar Mor‐Shaked,Amir A. Atawna,David Gillis,Orli Halstuk,Nava Shaul-Lotan,Mordechai Slae,Mutaz Sultan,Vardiella Meiner,Orly Elpeleg,Tamar Harel	2021	6
13	Characterization of a L136P mutation in Formin-like 2 (FMNL2) from a patient with chronic inflammatory bowel disease Raphael Trefzer,Orly Elpeleg,Tatyana V. Gabrusskaya,Polina Stepensky,Hagar Mor‐Shaked,Robert Grosse,Dominique T. Brandt	2021	7
14	Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation Montaser Namnah,Max Bauer,Hagar Mor‐Shaked,Susan Bressman,Deborah Raymond,Laurie J. Ozelius,David Arkadir	2020	6
15	Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia Alex Gileles‐Hillel,Hagar Mor‐Shaked,David Shoseyov,Joel Reiter,Reuven Tsabari,Avigdor Hevroni,Malena Cohen‐Cymberknoh,Israel Amirav,Shuli Brammli‐Greenberg,Amjad Horani,Eitan Kerem,Oded Breuer	2020	15
16	A human case of GIMAP6 deficiency: a novel primary immune deficiency Bella Shadur,Nathalie Asherie,Shlomit Kfir‐Erenfeld,Taly Dubnikov,Adeeb NaserEddin,Yael Dinur Schejter,Orly Elpeleg,Hagar Mor‐Shaked,Polina Stepensky	2020	7
17	Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected child Hagar Mor‐Shaked,Jonathan Rips,Shiri Gershon Naamat,Avichai Reich,Orly Elpeleg,Vardiella Meiner,Tamar Harel	2020	8
18	Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome Hagar Mor‐Shaked,Rachel Eiges	2018	18
19	The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA Manar Abu Diab,Hagar Mor‐Shaked,Eliora Cohen,Yaara Cohen‐Hadad,Oren Ram,Silvina Epsztejn‐Litman,Rachel Eiges	2018	22
20	FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells Michal Avitzour,Hagar Mor‐Shaked,Shira Yanovsky‐Dagan,Shira Aharoni,Gheona Altarescu,Paul Renbaum,Talia Eldar‐Geva,Oshrat Schonberger,Ephrat Levy‐Lahad,Silvina Epsztejn‐Litman,Rachel Eiges	2014	51

About Hagar Mor‐Shaked

Hagar Mor‐Shaked is a scholar working on Genetics, Cell Biology and Molecular Biology, having authored 32 papers that have together received 267 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers), Epigenetics and DNA Methylation (4 papers), Cellular transport and secretion (4 papers), Autism Spectrum Disorder Research (3 papers), Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Blood disorders and treatments (2 papers). The work is most often cited by research in Genetics (145 citations), Cognitive Neuroscience (49 citations) and Molecular Biology (154 citations). Hagar Mor‐Shaked has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Rachel Eiges, Silvina Epsztejn‐Litman, Tamar Harel, Orly Elpeleg, Vardiella Meiner, Paul Renbaum, Gheona Altarescu, Talia Eldar‐Geva, Oshrat Schonberger and Ephrat Levy‐Lahad.

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