Ortal Barel

2.4k citations

64 papers · 897 · h-index 16

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Immunology
- Immunodeficiency and Autoimmune Disorders

Papers in

Molecular Biology 21
- RNA modifications and cancer 8
- Congenital heart defects research 4
Genetics 19
- Genomics and Rare Diseases 7
- Blood disorders and treatments 5
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Ohad S. Birk (3 shared papers)Rivka Ofir (2 shared papers)Zamir Shorer (2 shared papers)Gal Finer (2 shared papers)Gideon Rechavi (13 shared papers)Eran Eyal (12 shared papers)Raz Somech (24 shared papers)Atar Lev (21 shared papers)
Journals: Frontiers in Immunology (5 papers)European Journal of Medical Genetics (4 papers)Clinical & Experimental Immunology (3 papers)Clinical Genetics (3 papers)European Journal of Human Genetics (3 papers)
Partner nations: Israel United States Italy

In The Last Decade

Ortal Barel

60 papers receiving 893 citations

Peers

Countries citing papers authored by Ortal Barel

Since Specialization

Citations

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

Fields of papers citing papers by Ortal Barel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ortal Barel. 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 Ortal Barel. The network helps show where Ortal Barel may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 64 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 The American Journal of Human Genetics ·Ortal Barel, Stavit A. Shalev, Rivka Ofir, Asi Cohen, Joël Zlotogora, Zamir Shorer, Galia Mazor, Gal Finer, Shareef Khateeb, Noam Zilberberg, Ohad S. Birk	2008	137
2	Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ The American Journal of Human Genetics ·Ortal Barel, Zamir Shorer, Hagit Flusser, Rivka Ofir, Ginat Narkis, Gal Finer, Hanah Shalev, A El Nasasra, Ann Saada, Ohad S. Birk	2008	95
3	Somatic NRAS mutation in patient with generalized lymphatic anomaly Angiogenesis ·Eugenia Manevitz-Mendelson, Gil S. Leichner, Ortal Barel, Inbal Davidi-Avrahami, Limor Ziv-Strasser, Eran Eyal, Itai M. Pessach, Uri Rimon, Aviv Barzilai, Abraham Hirshberg, Keren Chechekes, Ninette Amariglio, Gideon Rechavi, Karina Yaniv, Shoshana Greenberger	2018	61
4	Disruption of Thrombocyte and T Lymphocyte Development by a Mutation in ARPC1B The Journal of Immunology ·Raz Somech, Atar Lev, Yu Nee Lee, Amos J. Simon, Ortal Barel, Ginette Schiby, Camila Avivi, Iris Barshack, Michele Rhodes, Jiejing Yin, Minshi Wang, Yibin Yang, Jennifer Rhodes, Nufar Marcus, Ben-Zion Garty, Jerry Stein, Ninette Amariglio, Gideon Rechavi, David L. Wiest, Yong Zhang	2017	56
5	SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum Clinical Genetics ·Gali Heimer, Dina Marek‐Yagel, Eran Eyal, Ortal Barel, Dikla Levi, (unknown), Elizabeth K. Ruzzo, Esther Ganelin‐Cohen, Doron Lancet, Elon Pras, Gideon Rechavi, Andreea Nissenkorn, Yair Anikster, David B. Goldstein, Bruria Ben Zeev	2015	45
6	Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations European Journal of Human Genetics ·Joshi Stephen, Thierry Vilboux, Yael Haberman, Hadass Pri‐Chen, Ben Pode‐Shakked, Sina Mazaheri, Dina Marek‐Yagel, Ortal Barel, Ayelet Di Segni, Eran Eyal, Goni Hout‐Siloni, Avishay Lahad, Tzippora Shalem, Gideon Rechavi, May Christine V. Malicdan, Batia Weiss, William A. Gahl, Yair Anikster	2016	36
7	Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families Frontiers in Genetics ·Lior Greenbaum, Ben Pode‐Shakked, Shlomit Eisenberg‐Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik‐Wolf, Hana Poran, Amihai Rigbi, Ortal Barel, Aida M. Bertoli‐Avella, Peter Bauer, Miriam Regev, Annick Raas‐Rothschild, Elon Pras, Michal Berkenstadt	2019	32
8	Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire Journal of Clinical Immunology ·Shirly Frizinsky, Erez Rechavi, Ortal Barel, Rose H. Najeeb, Shoshana Greenberger, Yu Nee Lee, Amos J. Simon, Atar Lev, Chi A., Guangping Sun, Sarah A. Blackstone, Joshua D. Milner, Raz Somech, Tali Stauber	2019	27
9	Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community Clinical Immunology ·Amos J. Simon, Adi Cohen Golan, Atar Lev, Tali Stauber, Ortal Barel, Ido Somekh, Christoph Klein, Omar AbuZaitun, Eran Eyal, Nitzan Kol, Ekrem Ünal, Ninette Amariglio, Gideon Rechavi, Raz Somech	2020	24
10	Expanding the molecular diversity and phenotypic spectrum of glycerol 3‐phosphate dehydrogenase 1 deficiency Journal of Inherited Metabolic Disease ·Carlo Dionisi‐Vici, Eyal Shteyer, Marcello Niceta, Cristiano Rizzo, Ben Pode‐Shakked, Giovanni Chillemi, Alessandro Bruselles, Michela Semeraro, Ortal Barel, Eran Eyal, Nitzan Kol, Yael Haberman, Avishai Lahad, Francesca Diomedi‐Camassei, Dina Marek‐Yagel, Gideon Rechavi, Marco Tartaglia, Yair Anikster	2016	22
11	BRPF1‐associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family Molecular Genetics & Genomic Medicine ·Naomi Pode‐Shakked, Ortal Barel, Ben Pode‐Shakked, Aviva Eliyahu, Amihood Singer, Omri Nayshool, Nitzan Kol, Annick Raas‐Rothschild, Elon Pras, Mordechai Shohat	2019	22
12	Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy Clinical Genetics ·Ben Pode‐Shakked, Hila Barash, Limor Ziv, Karen W. Gripp, Elisabetta Flex, Ortal Barel, Karinne Spirandelli Carvalho, Mena Scavina, Giovanni Chillemi, Marcello Niceta, Eran Eyal, Nitzan Kol, Bruria Ben‐Zeev, Omer Bar‐Yosef, Dina Marek‐Yagel, Enrico Bertini, Angela L. Duker, Yair Anikster, Marco Tartaglia, Annick Raas‐Rothschild	2016	22
13	RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing features Frontiers in Immunology ·Mutaz Sultan, Mohammad Adawi, Nitzan Kol, Blake McCourt, Ihda Adawi, Liran Baram, Noa Tal, Lael Werner, Atar Lev, Scott B. Snapper, Ortal Barel, Liza Konnikova, Raz Somech, Dror S. Shouval	2022	18
14	T and B cell clonal expansion in Ras-associated lymphoproliferative disease (RALD) as revealed by next-generation sequencing Clinical & Experimental Immunology ·Sarina Levy‐Mendelovich, Atar Lev, Erez Rechavi, Ortal Barel, Hana Golan, Bella Bielorai, Yoram Neumann, Amos J. Simon, Raz Somech	2017	17
15	G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures BMC Genomics ·Oz Solomon, Vered Kunik, Amos J. Simon, Nitzan Kol, Ortal Barel, Atar Lev, Ninette Amariglio, Raz Somech, Gidi Rechavi, Eran Eyal	2016	16
16	Four patients with D-bifunctional protein (DBP) deficiency: Expanding the phenotypic spectrum of a highly variable disease Molecular Genetics and Metabolism Reports ·Yuval E. Landau, Gali Heimer, Ortal Barel, Nechama Shalva, Dina Marek‐Yagel, Alvit Veber, Elisheva Javasky, Aya Shilon, Andreea Nissenkorn, Bruria Ben‐Zeev, Yair Anikster	2020	15
17	Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome American Journal of Medical Genetics Part A ·Orna Staretz‐Chacham, Rachel Shukrun, Ortal Barel, Ben Pode‐Shakked, Oren Pleniceanu, Yair Anikster, Nechama Shalva, Carlos R. Ferreira, Admit Ben‐Haim Kadosh, Justin Richardson, Shrikant Mane, Friedhelm Hildebrandt, Asaf Vivante	2019	14
18	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature BMC Medical Genetics ·Ben Pode‐Shakked, Asaf Vivante, Ortal Barel, Shai Padeh, Dina Marek‐Yagel, Alvit Veber, Shachar Abudi, Aviva Eliyahu, Irit Tirosh, Shiri Shpilman, Shirlee Shril, Friedhelm Hildebrandt, Mordechai Shohat, Yair Anikster	2019	13
19	Clinical significance of E148Q heterozygous variant in paediatric familial Mediterranean fever Lara D. Veeken ·Irit Tirosh, Yonatan Yacobi, Asaf Vivante, Ortal Barel, Yishay Ben‐Moshe, Ortal Erez Granat, Shiri Spielman, Rotem Semo Oz, Yael Shinar, Maya Gerstein	2021	13
20	Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay Frontiers in Pediatrics ·Aviva Eliyahu, Ortal Barel, Lior Greenbaum, Gal Zaks Hoffer, Yael Goldberg, Annick Raas‐Rothschild, Amihood Singer, Ifat Bar-Joseph, Vered Kunik, Elisheva Javasky, Orna Staretz‐Chacham, Naomi Pode‐Shakked, Lily Bazak, Noa Ruhrman‐Shahar, Elon Pras, Moshe Frydman, Mordechai Shohat, Ben Pode‐Shakked	2022	11

About Ortal Barel

Ortal Barel is a scholar working on Molecular Biology, Genetics, Immunology, Epidemiology and Surgery, having authored 64 papers that have together received 897 indexed citations. Recurring topics across this work include Immunodeficiency and Autoimmune Disorders (12 papers), RNA modifications and cancer (8 papers), Genomics and Rare Diseases (7 papers), Blood disorders and treatments (5 papers), Immune Cell Function and Interaction (5 papers), Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Clinical Biochemistry (74 citations), Immunology (172 citations), Genetics (219 citations), Biochemistry (46 citations) and Molecular Biology (412 citations). Ortal Barel has collaborated with scholars based in Israel, United States and Italy. Frequent co-authors include Ohad S. Birk, Rivka Ofir, Zamir Shorer, Gal Finer, Gideon Rechavi, Eran Eyal, Raz Somech, Atar Lev, Ben Pode‐Shakked and Amos J. Simon. Their work appears in journals such as Frontiers in Immunology, European Journal of Medical Genetics, Clinical & Experimental Immunology, Clinical Genetics and European Journal of Human 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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