Dorit Lev

11.4k total citations
188 papers, 4.9k citations indexed

About

Dorit Lev is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Dorit Lev has authored 188 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 70 papers in Pediatrics, Perinatology and Child Health and 43 papers in Genetics. Recurrent topics in Dorit Lev's work include Fetal and Pediatric Neurological Disorders (56 papers), Prenatal Screening and Diagnostics (40 papers) and Mitochondrial Function and Pathology (35 papers). Dorit Lev is often cited by papers focused on Fetal and Pediatric Neurological Disorders (56 papers), Prenatal Screening and Diagnostics (40 papers) and Mitochondrial Function and Pathology (35 papers). Dorit Lev collaborates with scholars based in Israel, United States and Germany. Dorit Lev's co-authors include Tally Lerman‐Sagie, G. Malinger, Esther Leshinsky‐Silver, Liat Ben‐Sira, Nathan Watemberg, Lubov Blumkin, Sharon E. Plon, Murali Chintagumpala, Moise L. Levy and Maureen Rogers and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Dorit Lev

183 papers receiving 4.7k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Dorit Lev	2.0k	1.6k	1.0k	642	441	188	4.9k
B. Chabrol	1.6k 0.8×	480 0.3×	701 0.7×	400 0.6×	683 1.5×	235	3.9k
G Ponsot	1.5k 0.7×	708 0.4×	458 0.4×	630 1.0×	501 1.1×	147	3.8k
Paolo Balestri	944 0.5×	725 0.5×	835 0.8×	383 0.6×	249 0.6×	109	2.8k
P. Landrieu	1.1k 0.5×	574 0.4×	333 0.3×	586 0.9×	204 0.5×	117	3.2k
Françoise Goutières	1.4k 0.7×	525 0.3×	579 0.6×	407 0.6×	356 0.8×	76	3.2k
Thomas S. Jacques	2.1k 1.0×	367 0.2×	487 0.5×	547 0.9×	134 0.3×	148	5.8k
Rachel Straussberg	1.1k 0.5×	400 0.2×	559 0.5×	461 0.7×	131 0.3×	122	2.7k
Kenjiro Kosaki	2.7k 1.3×	591 0.4×	1.8k 1.8×	239 0.4×	103 0.2×	363	5.2k
Michael A. Morris	2.1k 1.0×	427 0.3×	1.7k 1.6×	284 0.4×	148 0.3×	118	4.8k
Marc De Braekeleer	1.9k 0.9×	986 0.6×	1.7k 1.6×	382 0.6×	276 0.6×	235	5.6k

Countries citing papers authored by Dorit Lev

Since Specialization

Citations

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

Fields of papers citing papers by Dorit Lev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorit Lev

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

All Works

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20 of 20 papers shown

Leibovitz, Z., Letizia Schreiber, Dvora Kidron, et al.. (2025). Parental counselling and autopsy results: A retrospective diagnostic cohort study at a multidisciplinary fetal neurology clinic. Developmental Medicine & Child Neurology. 68(3). 441–452.

Michelson, Marina, et al.. (2024). Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical Genetics. 105(6). 671–675.

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

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.

Pavlova, Elena, Dorit Lev, Marina Michelson, et al.. (2022). Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A. Human Mutation. 43(12). 2265–2278. 10 indexed citations

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

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

Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations

Haratz, Karina Krajden, A. Peled, L. Gindes, et al.. (2017). Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRI. Fetal Diagnosis and Therapy. 43(1). 53–60. 5 indexed citations

10.

Shinar, Shiri, G. Malinger, Z. Leibovitz, et al.. (2016). Familial Brain Periventricular Pseudocysts. Fetal Diagnosis and Therapy. 42(1). 42–47. 5 indexed citations

11.

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

12.

Blumkin, Lubov, Teisha Y. Bradshaw, Marina Michelson, et al.. (2015). Molecular and functional studies of retinal degeneration as a clinical presentation of SACS-related disorder. European Journal of Paediatric Neurology. 19(4). 472–476. 10 indexed citations

13.

Lev, Dorit, et al.. (2014). Pathways Mediating the Interaction between Endothelial Progenitor Cells (EPCs) and Platelets. PLoS ONE. 9(6). e95156–e95156. 19 indexed citations

14.

Hoffmann, Chen, Liat Ben‐Sira, Dorit Lev, et al.. (2011). Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?. Prenatal Diagnosis. 31(4). 360–366. 55 indexed citations

15.

Zeev, Bruria Ben, Dorit Lev, Dan Su, et al.. (2010). Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy. The American Journal of Human Genetics. 87(4). 538–544. 107 indexed citations

16.

Lev, Dorit, et al.. (2006). Hypomyelinating leukoencephalopathy with paroxysmal tonic upgaze and absence of psychomotor development. Movement Disorders. 22(2). 226–230. 12 indexed citations

17.

Lev, Dorit, et al.. (2005). Automatic Scanning of Interphase FISH for Prenatal Diagnosis in Uncultured Amniocytes. Genetic Testing. 9(1). 41–47. 14 indexed citations

18.

Malinger, G., Liat Ben‐Sira, Dorit Lev, et al.. (2004). Fetal brain imaging: a comparison between magnetic resonance imaging and dedicated neurosonography. Ultrasound in Obstetrics and Gynecology. 23(4). 333–340. 125 indexed citations

19.

Figer, Arié, Alexander Kaplan, Moshe Frydman, et al.. (2002). Germline mutations in the PTEN gene in Israeli patients with Bannayan–Riley–Ruvalcaba syndrome and women with familial breast cancer. Clinical Genetics. 62(4). 298–302. 15 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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