Luc Lemli

1.1k citations
12 papers · 808 · 1 hit paper · h-index 9

Impact in

Papers in

    • RNA modifications and cancer 2
    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 2
    • Genetics and Neurodevelopmental Disorders 1
    • Digestive system and related health 1
    • Genetic Syndromes and Imprinting 1

Luc Lemli

12 papers receiving 734 citations

Luc Lemli's Hit Papers

A newly recognized syndromeof multiple congenital anomalies 1964 · 517 citations
5170+20+41Years since publication100200300400500

Peers

Luc Lemli
Comparison fields: 5 of 70
  • Developmental Biology 23
  • Surgery 404
  • Genetics 221
  • Biochemistry 54
  • Molecular Biology 462
Replace A Munnich with:
A Munnich France
Patrice Eydoux Canada
Markus Bussen Germany
E. Vámos Belgium
G Fanconi Germany
Heather M. Stringham United States
M. Rivière Belgium
Shigeto Takeuchi Japan
Victoria Parker United Kingdom
Luc Lemli relative to A Munnich France A Munnich's profile →
Citations per field
00.5×1.5×2.3×
A Munnich · 1×
Citations per year

Countries citing papers authored by Luc Lemli

Since Specialization
Citations

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

Fields of papers citing papers by Luc Lemli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 17 scholars most cited alongside Luc Lemli, 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 Luc Lemli Line = papers co-authored together Luc Lemli links everyone, so they are left out of the graph.

All Works

12 of 12 papers shown
#Work
1
A newly recognized syndromeof multiple congenital anomalies
Hit paper breakdown →
1964517
2 1963146
3 196338
4 197724
5 196320
6 196417
7 200816
8 196310
9
Partial duplication of the long arm of chromosome 22 (22q 13) with complete 22 trisomy phenotype.
198010
10
Minimal dysmorphic stigmata in 9q deletion of paternal origin.
19924
11
Smith-Lemli-Optiz syndrome without failure to thrive.
19784
12 19642

About Luc Lemli

Luc Lemli is a scholar working on Molecular Biology, Genetics, Surgery, Rheumatology and Endocrinology, Diabetes and Metabolism, having authored 12 papers that have together received 808 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), RNA modifications and cancer (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Hyperglycemia and glycemic control in critically ill and hospitalized patients (1 paper), Digestive system and related health (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Developmental Biology (23 citations), Surgery (404 citations), Genetics (221 citations), Biochemistry (54 citations) and Molecular Biology (462 citations). Luc Lemli has collaborated with scholars based in United States and Belgium. Frequent co-authors include David W. Smith, John M. Opitz, Ludwig Gutmann, David W. Smith, David W. Smith, Francis de Zegher, Koenraad Devriendt, Harry A. Waisman, Theo Gerritsen and Louis J. Ptáček. Their work appears in journals such as The Journal of Pediatrics, PEDIATRICS, PubMed, Archives of Neurology and Hormone Research.

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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