Daniel Amram

1.4k total citations
9 papers, 421 citations indexed

About

Daniel Amram is a scholar working on Molecular Biology, Surgery and Pathology and Forensic Medicine. According to data from OpenAlex, Daniel Amram has authored 9 papers receiving a total of 421 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Surgery and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Daniel Amram's work include RNA and protein synthesis mechanisms (2 papers), Reconstructive Surgery and Microvascular Techniques (1 paper) and RNA modifications and cancer (1 paper). Daniel Amram is often cited by papers focused on RNA and protein synthesis mechanisms (2 papers), Reconstructive Surgery and Microvascular Techniques (1 paper) and RNA modifications and cancer (1 paper). Daniel Amram collaborates with scholars based in France, United Kingdom and Germany. Daniel Amram's co-authors include Rupert Handgretinger, Nicolas Sévenet, Pascale Schneider, Olivier Delattre, Jean‐Luc Faillie, Dominique Hillaire‐Buys, Jean‐Luc Puel, Alain Uziel, Y Nordmann and Rémy Pujol and has published in prestigious journals such as Brain, The American Journal of Human Genetics and Pediatric Research.

In The Last Decade

Daniel Amram

9 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Amram France 6 340 176 60 46 46 9 421
Leah W. Burke United States 13 182 0.5× 49 0.3× 105 1.8× 41 0.9× 31 0.7× 22 552
Gail D. Wenger United States 11 187 0.6× 72 0.4× 56 0.9× 6 0.1× 33 0.7× 14 406
K. Kapinas Greece 6 68 0.2× 351 2.0× 80 1.3× 29 0.6× 105 2.3× 9 546
Olga Dratviman‐Storobinsky Israel 15 214 0.6× 18 0.1× 32 0.5× 57 1.2× 33 0.7× 31 509
Delphine Larrieu‐Ciron France 11 151 0.4× 70 0.4× 98 1.6× 14 0.3× 14 0.3× 21 364
Cheryl L. Khanna United States 10 124 0.4× 119 0.7× 85 1.4× 19 0.4× 10 0.2× 32 515
Cecilie F. Rustad Norway 11 210 0.6× 62 0.4× 170 2.8× 13 0.3× 20 0.4× 18 491
Johan Mellergård Sweden 10 88 0.3× 215 1.2× 63 1.1× 17 0.4× 145 3.2× 22 394
Anastasie Dunn‐Pirio United States 7 73 0.2× 58 0.3× 71 1.2× 7 0.2× 55 1.2× 18 341
Armando Flor United States 6 48 0.1× 183 1.0× 91 1.5× 12 0.3× 88 1.9× 8 315

Countries citing papers authored by Daniel Amram

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Amram

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Amram

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

All Works

9 of 9 papers shown
1.
Chopra, Maya, Richard Caswell, Giulia Barcia, et al.. (2022). Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1. European Journal of Human Genetics. 30(8). 960–966. 1 indexed citations
2.
Piard, Juliette, George K. E. Umanah, Frederike L. Harms, et al.. (2017). A homozygous ATAD1 mutation impairs postsynaptic AMPA receptor trafficking and causes a lethal encephalopathy. Brain. 141(3). 651–661. 35 indexed citations
3.
Sinico, Martine, Guillaume Bassez, Claudine Touboul, et al.. (2010). Excess of Neuromuscular Spindles in a Fetus with Costello Syndrome: A Clinicopathological Report. Pediatric and Developmental Pathology. 14(3). 218–223. 5 indexed citations
4.
Hillaire‐Buys, Dominique, et al.. (2008). Möbius Syndrome in a Neonate After Mifepristone and Misoprostol Elective Abortion Failure. Annals of Pharmacotherapy. 42(6). 888–892. 23 indexed citations
5.
Guitton, Matthieu J., et al.. (2006). Early Maturation of Evoked Otoacoustic Emissions and Medial Olivocochlear Reflex in Preterm Neonates. Pediatric Research. 59(2). 305–308. 21 indexed citations
6.
Amram, Daniel, et al.. (1999). Le chylothorax de découverte anténatale. Archives de Pédiatrie. 6(8). 867–871. 6 indexed citations
7.
Sévenet, Nicolas, et al.. (1999). Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers. The American Journal of Human Genetics. 65(5). 1342–1348. 312 indexed citations
8.
Nordmann, Y, et al.. (1990). Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease). Journal of Inherited Metabolic Disease. 13(5). 687–691. 17 indexed citations
9.
Larchet, M, et al.. (1988). [Pneumococcal pneumonia and septic shock in the newborn infant].. PubMed. 43(6). 515–8. 1 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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