Irén Haltrich

696 citations
33 papers · 239 · h-index 9

Impact in

    • Acute Myeloid Leukemia Research
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Congenital heart defects research 4
    • Genomics and Chromatin Dynamics 3
    • Genomic variations and chromosomal abnormalities 10
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • Genetics and Neurodevelopmental Disorders 5
    • Genomics and Rare Diseases 4

Irén Haltrich

28 papers receiving 236 citations

Peers

Irén Haltrich
Comparison fields: 5 of 59
  • Hematology 43
  • Genetics 93
  • Cognitive Neuroscience 33
  • Cancer Research 25
  • Genetics 16
Replace Jun‐ichi Nagai with:
Jun‐ichi Nagai Japan
Frédérique Sloan‐Béna Switzerland
Lauryl M. J. Nutter Canada
Thomas Smol France
Kari Casas United States
Outi Kuismin Finland
Chloë Marden United Kingdom
Dyane Auclair Australia
Elisabeth Syk Lundberg Sweden
Kathrin S. Precht United States
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Citations per field
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Jun‐ichi Nagai · 1×
Citations per year

Countries citing papers authored by Irén Haltrich

Since Specialization
Citations

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

Fields of papers citing papers by Irén Haltrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Irén Haltrich, 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 Irén Haltrich Line = papers co-authored together Irén Haltrich links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201353
2 201242
3 201317
4 200317
5 201211
6 20199
7 20059
8 20219
9 20179
10 20058
11 20127
12 20156
13 20205
14 20205
15 20145
16 20194
17 20063
18 20203
19 20193
20 20153

About Irén Haltrich

Irén Haltrich is a scholar working on Molecular Biology, Genetics, Hematology, Pulmonary and Respiratory Medicine and Public Health, Environmental and Occupational Health, having authored 33 papers that have together received 239 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Acute Myeloid Leukemia Research (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (4 papers), Genomics and Rare Diseases (4 papers), Acute Lymphoblastic Leukemia research (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Hematology (43 citations), Genetics (93 citations), Cognitive Neuroscience (33 citations), Cancer Research (25 citations) and Genetics (16 citations). Irén Haltrich has collaborated with scholars based in Hungary, Sweden and Germany. Frequent co-authors include György Fekete, G. Fekete, Tatjana Bierhals, Georg Rosenberger, Inga Nagel, Kerstin Kutsche, Hengameh Abdollahpour, Balázs Győrffy, István Likó and Zoltán Szállási. Their work appears in journals such as Molecular Cytogenetics, BMC Pediatrics, Endocrinology, Stem Cell Research and European Journal of Medical Genetics.

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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