Aviva Eliyahu

706 total citations
6 papers, 51 citations indexed

About

Aviva Eliyahu is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Aviva Eliyahu has authored 6 papers receiving a total of 51 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Aviva Eliyahu's work include Genetics and Neurodevelopmental Disorders (2 papers), Congenital limb and hand anomalies (1 paper) and Genomics and Rare Diseases (1 paper). Aviva Eliyahu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Congenital limb and hand anomalies (1 paper) and Genomics and Rare Diseases (1 paper). Aviva Eliyahu collaborates with scholars based in Israel and United States. Aviva Eliyahu's co-authors include Ben Pode‐Shakked, Ortal Barel, Naomi Pode‐Shakked, Mordechai Shohat, Amihood Singer, Annick Raas‐Rothschild, Elon Pras, Nitzan Kol, Friedhelm Hildebrandt and Asaf Vivante and has published in prestigious journals such as Prenatal Diagnosis, American Journal of Medical Genetics Part A and Frontiers in Pediatrics.

In The Last Decade

Aviva Eliyahu

5 papers receiving 51 citations

Peers

Countries citing papers authored by Aviva Eliyahu

Since Specialization

Citations

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

Fields of papers citing papers by Aviva Eliyahu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aviva Eliyahu

This figure shows the co-authorship network connecting the top 25 collaborators of Aviva Eliyahu. A scholar is included among the top collaborators of Aviva Eliyahu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aviva Eliyahu. Aviva Eliyahu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Prenatal Sonographic Features of Rubinstein–Taybi Syndrome—A Small Case Series of a Rare Syndrome 2024 ·Prenatal Diagnosis ·(unknown), Tal Weissbach, B. Messing, R. Birnbaum, L. Gindes, Michal Levy, Tally Lerman‐Sagie, (unknown), Aviva Eliyahu, (unknown), Eran Kassif	2
2	White epidermal nevus as an early sign of tuberous sclerosis complex—A case series 2023 ·Pediatric Dermatology ·Ayelet Ollech, (unknown), Michal Tzadok, (unknown), (unknown), Aviva Eliyahu, Aviv Barzilai, Shoshana Greenberger	0
3	Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay 2022 ·Frontiers in Pediatrics ·Aviva Eliyahu, Ortal Barel, Lior Greenbaum, (unknown), (unknown), Annick Raas‐Rothschild, Amihood Singer, Ifat Bar-Joseph, Vered Kunik, (unknown), Orna Staretz‐Chacham, Naomi Pode‐Shakked, Lily Bazak, Noa Ruhrman‐Shahar, Elon Pras, Moshe Frydman, Mordechai Shohat, Ben Pode‐Shakked	10
4	Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux–Lamy syndrome (MPS VI) 2021 ·American Journal of Medical Genetics Part A ·Dina Marek‐Yagel, Aviva Eliyahu, (unknown), Nechama Shalva, (unknown), Ortal Barel, (unknown), Ben Pode‐Shakked, Neta Loewenthal, Yair Anikster, Orna Staretz‐Chacham	4
5	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature 2019 ·BMC Medical Genetics ·Ben Pode‐Shakked, Asaf Vivante, Ortal Barel, Shai Padeh, Dina Marek‐Yagel, (unknown), (unknown), Aviva Eliyahu, Irit Tirosh, (unknown), Shirlee Shril, Friedhelm Hildebrandt, Mordechai Shohat, Yair Anikster	13
6	BRPF1‐associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family 2019 ·Molecular Genetics & Genomic Medicine ·Naomi Pode‐Shakked, Ortal Barel, Ben Pode‐Shakked, Aviva Eliyahu, Amihood Singer, (unknown), Nitzan Kol, Annick Raas‐Rothschild, Elon Pras, Mordechai Shohat	22

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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