Tally Lerman‐Sagie

12.0k total citations
240 papers, 5.8k citations indexed

About

Tally Lerman‐Sagie is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Tally Lerman‐Sagie has authored 240 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 100 papers in Pediatrics, Perinatology and Child Health, 95 papers in Molecular Biology and 41 papers in Genetics. Recurrent topics in Tally Lerman‐Sagie's work include Fetal and Pediatric Neurological Disorders (73 papers), Prenatal Screening and Diagnostics (42 papers) and Mitochondrial Function and Pathology (39 papers). Tally Lerman‐Sagie is often cited by papers focused on Fetal and Pediatric Neurological Disorders (73 papers), Prenatal Screening and Diagnostics (42 papers) and Mitochondrial Function and Pathology (39 papers). Tally Lerman‐Sagie collaborates with scholars based in Israel, United States and France. Tally Lerman‐Sagie's co-authors include Dorit Lev, G. Malinger, Nathan Watemberg, Esther Leshinsky‐Silver, Liat Ben‐Sira, Sara Kivity, Bruria Ben‐Zeev, Lubov Blumkin, Z. Leibovitz and Andreea Nissenkorn and has published in prestigious journals such as Journal of Neuroscience, Neurology and PEDIATRICS.

In The Last Decade

Tally Lerman‐Sagie

232 papers receiving 5.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tally Lerman‐Sagie Israel 42 2.2k 1.8k 1.3k 1.0k 957 240 5.8k
Oebele F. Brouwer Netherlands 44 1.7k 0.8× 1.8k 1.0× 1.7k 1.3× 1.1k 1.0× 1.2k 1.2× 154 5.2k
Federico Vigevano Italy 41 2.1k 0.9× 1.1k 0.6× 4.0k 3.0× 1.3k 1.2× 1.4k 1.4× 289 6.2k
Jean Aicardi France 49 2.6k 1.2× 2.3k 1.3× 2.8k 2.1× 1.8k 1.7× 1.6k 1.6× 188 7.7k
Leena Valanne Finland 38 756 0.3× 1.4k 0.8× 823 0.6× 614 0.6× 420 0.4× 121 4.3k
Tiziana Granata Italy 39 1.9k 0.9× 1.5k 0.9× 2.9k 2.2× 864 0.8× 2.0k 2.1× 142 5.9k
Isabelle Desguerre France 46 665 0.3× 3.6k 2.1× 724 0.5× 1.2k 1.2× 711 0.7× 212 7.1k
Kazuyoshi Watanabe Japan 40 3.0k 1.4× 631 0.4× 2.2k 1.6× 397 0.4× 833 0.9× 294 5.6k
Nicola Specchio Italy 38 1.8k 0.8× 1.3k 0.7× 3.6k 2.7× 1.5k 1.4× 1.4k 1.5× 234 6.3k
Makiko Ōsawa Japan 36 882 0.4× 2.4k 1.3× 1.5k 1.1× 818 0.8× 1.1k 1.1× 196 4.9k
Wang‐Tso Lee Taiwan 34 701 0.3× 977 0.6× 761 0.6× 422 0.4× 588 0.6× 199 3.9k

Countries citing papers authored by Tally Lerman‐Sagie

Since Specialization
Citations

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

Fields of papers citing papers by Tally Lerman‐Sagie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tally Lerman‐Sagie. 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 Tally Lerman‐Sagie. The network helps show where Tally Lerman‐Sagie may publish in the future.

Co-authorship network of co-authors of Tally Lerman‐Sagie

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

All Works

20 of 20 papers shown
1.
Lev, Dorit, et al.. (2024). Parental magnetic resonance imaging for the evaluation of fetuses with brain anomalies. Developmental Medicine & Child Neurology. 67(4). 463–474. 3 indexed citations
2.
Weissbach, Tal, B. Messing, R. Birnbaum, et al.. (2024). Prenatal Sonographic Features of Rubinstein–Taybi Syndrome—A Small Case Series of a Rare Syndrome. Prenatal Diagnosis. 44(12). 1502–1508. 2 indexed citations
3.
Tzadok, Michal, Yael Michaeli, Tal Gilboa, et al.. (2023). Real-Life Experience With Purified Cannabidiol Treatment for Refractory Epilepsy: A Multicenter Retrospective Study. Pediatric Neurology. 150. 91–96. 10 indexed citations
4.
Garel, Cathérine, Z. Leibovitz, Stéphanie Valence, et al.. (2023). Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation. American Journal of Neuroradiology. 44(3). 334–340.
5.
Haratz, Karina Krajden, G. Malinger, Liat Ben‐Sira, et al.. (2022). Spectrum of brain malformations in fetuses with mild tubulinopathy. Ultrasound in Obstetrics and Gynecology. 61(6). 740–748. 10 indexed citations
6.
Zerem, Ayelet, Liat Ben‐Sira, Z. Leibovitz, et al.. (2021). White matter abnormalities and iron deposition in prenatal mucolipidosis IV- fetal imaging and pathology. Metabolic Brain Disease. 36(7). 2155–2167. 8 indexed citations
7.
Michelson, Marina, Emanuela Argilli, Keren Yosovich, et al.. (2021). Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders. Journal of Human Genetics. 67(2). 95–101. 2 indexed citations
8.
Viñals, Fernando Nuez, et al.. (2020). Agenesis of the septum pellucidum: Prenatal diagnosis and outcome. Prenatal Diagnosis. 40(6). 674–680. 7 indexed citations
9.
Ben‐Sira, Liat, Keren Yosovich, Adeline Vanderver, et al.. (2019). Brain white matter abnormalities associated with copy number variants. American Journal of Medical Genetics Part A. 182(1). 93–103. 6 indexed citations
10.
Sapir, Tamar, Tahsin Stefan Barakat, Mercedes F. Paredes, et al.. (2019). Building Bridges Between the Clinic and the Laboratory: A Meeting Review – Brain Malformations: A Roadmap for Future Research. Frontiers in Cellular Neuroscience. 13. 434–434. 3 indexed citations
11.
Shinar, Shiri, Tally Lerman‐Sagie, Fernando Nuez Viñals, et al.. (2018). Fetal pericallosal lipomas – Clues to diagnosis in the second trimester. European Journal of Paediatric Neurology. 22(6). 929–934. 6 indexed citations
12.
Haratz, Karina Krajden, Z. Leibovitz, Dina Lev, et al.. (2018). Fourth ventricle index: sonographic marker for severe fetal vermian dysgenesis/agenesis. Ultrasound in Obstetrics and Gynecology. 53(3). 390–395. 8 indexed citations
13.
Leibovitz, Z., Laurent Guibaud, Cathérine Garel, et al.. (2018). The cerebellar “tilted telephone receiver sign” enables prenatal diagnosis of PHACES syndrome. European Journal of Paediatric Neurology. 22(6). 900–909. 12 indexed citations
14.
Hamanaka, Kohei, Satoko Miyatake, Ayelet Zerem, et al.. (2018). Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic. Journal of Human Genetics. 63(12). 1223–1229. 14 indexed citations
15.
16.
Shinar, Shiri, G. Malinger, Z. Leibovitz, et al.. (2016). Familial Brain Periventricular Pseudocysts. Fetal Diagnosis and Therapy. 42(1). 42–47. 5 indexed citations
17.
Haratz, Karina Krajden, Z. Leibovitz, Ran Svirsky, et al.. (2016). The ‘Brain Shadowing Sign': A Novel Marker of Fetal Craniosynostosis. Fetal Diagnosis and Therapy. 40(4). 277–284. 8 indexed citations
18.
Watemberg, Nathan, et al.. (2007). Developmental coordination disorder in children with attention‐deficit–hyperactivity disorder and physical therapy intervention. Developmental Medicine & Child Neurology. 49(12). 920–925. 110 indexed citations
19.
Malinger, G., Dorit Lev, Nathan Watemberg, et al.. (2003). Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findings.. American Journal of Neuroradiology. 24(1). 28–32. 146 indexed citations
20.
Wallace, Robyn H., Ingrid E. Scheffer, Shaun Barnett, et al.. (2001). Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus. The American Journal of Human Genetics. 68(4). 859–865. 272 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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