Daniel Halpérin

1.5k citations
43 papers · 1.1k · h-index 18

Impact in

  • Hematology top 5%
    • Erythropoietin and Anemia Treatment
  • Genetics top 10%
    • Hemoglobinopathies and Related Disorders

Papers in

    • Ion channel regulation and function 5
    • RNA modifications and cancer 3
    • RNA Research and Splicing 2
    • Hemoglobinopathies and Related Disorders 3

Daniel Halpérin

42 papers receiving 1.0k citations

Peers

Daniel Halpérin
Comparison fields: 5 of 114
  • Hematology 152
  • Genetics 130
  • Biochemistry 71
  • Physiology 191
  • Clinical Psychology 130
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Citations per field
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Citations per year

Countries citing papers authored by Daniel Halpérin

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Halpérin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Daniel Halpérin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniel Halpérin Line = papers co-authored together Daniel Halpérin links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1990147
2 2008126
3 1996124
4
Diamond-blackfan anemia: etiology, pathophysiology, and treatment.
198991
5 201775
6 201272
7 201245
8 199340
9 201931
10 199931
11 201830
12 202329
13 199727
14 202124
15 201821
16 200221
17 199121
18 201718
19 201714
20 201713

About Daniel Halpérin

Daniel Halpérin is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Physiology and Epidemiology, having authored 43 papers that have together received 1.1k indexed citations. Recurring topics across this work include Ion channel regulation and function (5 papers), Adipose Tissue and Metabolism (3 papers), Hemoglobinopathies and Related Disorders (3 papers), Hereditary Neurological Disorders (3 papers), RNA modifications and cancer (3 papers), Neurological diseases and metabolism (2 papers), RNA Research and Splicing (2 papers) and Child Abuse and Trauma (2 papers). The work is most often cited by research in Hematology (152 citations), Genetics (130 citations), Biochemistry (71 citations), Physiology (191 citations) and Clinical Psychology (130 citations). Daniel Halpérin has collaborated with scholars based in Israel, United States and Switzerland. Frequent co-authors include Peter Tontonoz, MH Freedman, Kye Won Park, Pierre Wacker, Marinette Wyss, G Lacourt, Matti Aapro, Ohad S. Birk, Paul Bouvier and Yonatan Perez. Their work appears in journals such as Journal of Pediatric Hematology/Oncology, Journal of Medical Genetics, CHEST Journal, Clinical Genetics and Acta Psychiatrica Scandinavica.

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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