Lionel Van Maldergem
Lionel Van Maldergem publishes mostly in Molecular Biology, Genetics and Cell Biology, on topics such as Genomic variations and chromosomal abnormalities, Connective tissue disorders research and Genetics and Neurodevelopmental Disorders.
- World rank
- #210,669 of 7,710,434 ranked researchers
- Rank in France
- #13,393 of 324,115
- Works
- 332
- Citations
- 18k
- Citations per work
- 53.4
What does Lionel Van Maldergem research?
Lionel Van Maldergem's work is mostly in Biochemistry, Genetics and Molecular Biology (55%), Medicine (10%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences18254.7%
- Everything else11935.8%
- Health Sciences329.5%
- Medicine329.5%
- 1Molecular Biology26% of their works
- 2Genetics25% of their works
- 3Cell Biology4% of their works
- 4Pediatrics, Perinatology and Child Health4% of their works
- 5Surgery3% of their works
- 6Rheumatology3% of their works
Research topics
Which keywords describe Lionel Van Maldergem's research?
The keywords of their largest research topics: Copy Number Variation, Ehlers-Danlos Syndrome, Genomic Rearrangements, Marfan Syndrome, DNA Methylation, Fragile X Syndrome, Rett Syndrome and Genetic Variants.
- Epigenetic Reprogramming
- Nucleocytoplasmic Transport
- Genomic Imprinting
- Biochemical Genetics
- Genetic Variants
- Fragile X Syndrome
- Marfan Syndrome
- Ehlers-Danlos Syndrome
- Copy Number Variation
- Genomic Rearrangements
- DNA Methylation
- Rett Syndrome
- Sequence Interpretation
- Metabolic Disorders
- Nuclear Pore Complex
- Parental Influence
- Histone Modification
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most.
All 17 words, with their numbers
- Copy Number Variation361 topic
- Ehlers-Danlos Syndrome361 topic
- Genomic Rearrangements361 topic
- Marfan Syndrome361 topic
- DNA Methylation332 topics
- Fragile X Syndrome311 topic
- Rett Syndrome311 topic
- Genetic Variants281 topic
- Sequence Interpretation281 topic
- Biochemical Genetics211 topic
- Metabolic Disorders211 topic
- Genomic Imprinting171 topic
- Nuclear Pore Complex171 topic
- Nucleocytoplasmic Transport171 topic
- Parental Influence171 topic
- Epigenetic Reprogramming161 topic
- Histone Modification161 topic
Where does Lionel Van Maldergem work?
Lionel Van Maldergem's main affiliation in the publication record is Université de Franche-Comté, France.
How many publications and citations does Lionel Van Maldergem have?
OpenAlex counts 332 works and 17,734 citations for Lionel Van Maldergem, an h-index of 72, ranking #210,669 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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