Ellen Taub

620 total citations
12 papers, 446 citations indexed

About

Ellen Taub is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Ellen Taub has authored 12 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in Ellen Taub's work include Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Ellen Taub is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Ellen Taub collaborates with scholars based in Israel, United States and Australia. Ellen Taub's co-authors include Nurit Magal, Lina Basel‐Vanagaite, Valerie Drasinover, Mordechai Shohat, Bella Davidov, Gabrielle J. Halpern, Mordechai Shohat, Hagit Toledano‐Alhadef, Lisa G. Shaffer and Idit Maya and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Ellen Taub

12 papers receiving 430 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ellen Taub Israel 8 263 207 121 88 31 12 446
Marie‐Christine de Blois France 8 352 1.3× 182 0.9× 96 0.8× 63 0.7× 20 0.6× 10 455
Deborah Barbouth United States 11 412 1.6× 285 1.4× 183 1.5× 85 1.0× 22 0.7× 32 678
Tiziana Filippi Italy 9 374 1.4× 207 1.0× 67 0.6× 157 1.8× 27 0.9× 10 539
Valerie Drasinover Israel 8 214 0.8× 172 0.8× 114 0.9× 42 0.5× 35 1.1× 8 374
Aneek Das Bhowmik India 13 179 0.7× 179 0.9× 68 0.6× 50 0.6× 23 0.7× 36 428
Sureni V. Mullegama United States 15 308 1.2× 315 1.5× 65 0.5× 31 0.4× 31 1.0× 27 564
Angela Peron Italy 18 365 1.4× 261 1.3× 127 1.0× 73 0.8× 24 0.8× 54 827
Marzia Pollazzon Italy 14 494 1.9× 368 1.8× 143 1.2× 43 0.5× 48 1.5× 31 692
F Ballesta Spain 14 249 0.9× 246 1.2× 47 0.4× 83 0.9× 23 0.7× 28 547
Eric Crawford United States 7 343 1.3× 260 1.3× 192 1.6× 57 0.6× 10 0.3× 12 609

Countries citing papers authored by Ellen Taub

Since Specialization
Citations

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

Fields of papers citing papers by Ellen Taub

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellen Taub

This figure shows the co-authorship network connecting the top 25 collaborators of Ellen Taub. A scholar is included among the top collaborators of Ellen Taub 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 Ellen Taub. Ellen Taub is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Hubshman, Monika Weisz, Lina Basel‐Vanagaite, Aviva C. Krauss, et al.. (2016). Homozygous deletion of RAG1, RAG2 and 5′ region TRAF6 causes severe immune suppression and atypical osteopetrosis. Clinical Genetics. 91(6). 902–907. 6 indexed citations
2.
Borck, Guntram, Katrin Friedrich, Ellen Taub, et al.. (2011). High frequency of autosomal‐recessive DFNB59 hearing loss in an isolated Arab population in Israel. Clinical Genetics. 82(3). 271–276. 19 indexed citations
3.
Maya, Idit, Bella Davidov, Liron Gershovitz, et al.. (2010). Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting. Prenatal Diagnosis. 30(12-13). 1131–1137. 61 indexed citations
4.
Basel‐Vanagaite, Lina, Ellen Taub, Valerie Drasinover, et al.. (2008). Genetic Carrier Screening for Spinal Muscular Atrophy and Spinal Muscular Atrophy with Respiratory Distress 1 in an Isolated Population in Israel. Genetic Testing. 12(1). 53–56. 22 indexed citations
5.
Basel‐Vanagaite, Lina, Rachel Straussberg, Metsada Pasmanik‐Chor, et al.. (2006). Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis. Annals of Neurology. 60(2). 214–222. 92 indexed citations
6.
Basel‐Vanagaite, Lina, Ellen Taub, Gabrielle J. Halpern, et al.. (2006). Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel. European Journal of Human Genetics. 15(2). 250–253. 31 indexed citations
7.
Weintrob, Naomi, Jacques Drouin, Sophie Vallette-Kasic, et al.. (2006). Low Estriol Levels in the Maternal Triple-Marker Screen as a Predictor of Isolated Adrenocorticotropic Hormone Deficiency Caused by a New Mutation in the TPIT Gene. PEDIATRICS. 117(2). e322–e327. 26 indexed citations
8.
Avigad, Smadar, Dan Peleg, Noa Ben-Baruch, et al.. (2004). Prenatal Diagnosis in Li-Fraumeni Syndrome. Journal of Pediatric Hematology/Oncology. 26(9). 541–545. 6 indexed citations
9.
Basel‐Vanagaite, Lina, Nufar Marcus, Gil Klinger, et al.. (2003). New syndrome of simplified gyral pattern, micromelia, dysmorphic features and early death. American Journal of Medical Genetics Part A. 119A(2). 200–206. 5 indexed citations
10.
Toledano‐Alhadef, Hagit, Lina Basel‐Vanagaite, Nurit Magal, et al.. (2001). Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel. The American Journal of Human Genetics. 69(2). 351–360. 159 indexed citations
11.
Drasinover, Valerie, Nurit Magal, Ellen Taub, et al.. (2000). Increased transmission of intermediate alleles of theFMR1 gene compared with normal alleles among female heterozygotes. American Journal of Medical Genetics. 93(2). 155–157. 14 indexed citations
12.
Shohat, Mordechai, Yakov Sivan, Ellen Taub, & Shmuel Davidson. (1992). Autosomal dominant congenital laryngomalacia. American Journal of Medical Genetics. 42(6). 813–814. 5 indexed citations

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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