Luc Lemli

1.1k total citations · 1 hit paper
12 papers, 822 citations indexed

About

Luc Lemli is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Luc Lemli has authored 12 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Luc Lemli's work include Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (2 papers) and Genomics and Rare Diseases (2 papers). Luc Lemli is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (2 papers) and Genomics and Rare Diseases (2 papers). Luc Lemli collaborates with scholars based in United States and Belgium. Luc Lemli's co-authors include David W. Smith, John M. Opitz, Ludwig Gutmann, Francis de Zegher, Koenraad Devriendt, David W. Smith, David W. Smith, Theo Gerritsen, Harry A. Waisman and Louis J. Ptáček and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Archives of Neurology.

In The Last Decade

Luc Lemli

12 papers receiving 745 citations

Hit Papers

A newly recognized syndromeof multiple congenital anomalies 1964 2026 1984 2005 1964 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luc Lemli United States 9 500 407 243 64 62 12 822
Rosanna N. Chute United States 12 221 0.4× 272 0.7× 130 0.5× 40 0.6× 21 0.3× 28 575
Patricia A. Short United States 11 451 0.9× 161 0.4× 146 0.6× 80 1.3× 29 0.5× 15 808
Markus Bussen Germany 7 625 1.3× 290 0.7× 210 0.9× 49 0.8× 22 0.4× 7 930
J.R. Korenberg United States 10 385 0.8× 52 0.1× 155 0.6× 45 0.7× 74 1.2× 19 590
Noémi Polgár Hungary 17 385 0.8× 96 0.2× 216 0.9× 70 1.1× 106 1.7× 30 751
W H Lai Canada 13 520 1.0× 88 0.2× 64 0.3× 35 0.5× 54 0.9× 18 840
M O Ott France 7 573 1.1× 251 0.6× 280 1.2× 27 0.4× 29 0.5× 7 766
Nobuyuki Itoh Japan 8 859 1.7× 121 0.3× 140 0.6× 54 0.8× 24 0.4× 9 1.0k
Robert J. Vosatka United States 10 359 0.7× 125 0.3× 60 0.2× 56 0.9× 39 0.6× 12 678
Rebecca C.J. Twells United Kingdom 14 439 0.9× 178 0.4× 294 1.2× 55 0.9× 123 2.0× 18 788

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-authorship network of co-authors of Luc Lemli

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

All Works

12 of 12 papers shown
1.
Devriendt, Koenraad, et al.. (1995). Growth Hormone Deficiency and Premature Thelarche in a Female Infant with Kabuki Makeup Syndrome. Hormone Research. 43(6). 303–306. 31 indexed citations
2.
Kleczkowska, A, J. P. Fryns, Luc Lemli, & Herman Van den Berghe. (1992). Minimal dysmorphic stigmata in 9q deletion of paternal origin.. PubMed. 3(1). 49–52. 4 indexed citations
3.
Jp, Fryns, et al.. (1980). Partial duplication of the long arm of chromosome 22 (22q 13) with complete 22 trisomy phenotype.. PubMed. 33(2). 125–7. 10 indexed citations
4.
Jeanty, Philippe, Dominique Delbeke, Luc Lemli, & Harry Dorchy. (1978). Smith-Lemli-Optiz syndrome without failure to thrive.. PubMed. 30(3). 175–8. 4 indexed citations
5.
Lemli, Luc. (1977). Fibrous dysplasia of bone. The Journal of Pediatrics. 91(6). 947–949. 24 indexed citations
6.
Smith, David W., Luc Lemli, & John M. Opitz. (1964). A newly recognized syndromeof multiple congenital anomalies. The Journal of Pediatrics. 64(2). 210–217. 516 indexed citations breakdown →
7.
Lemli, Luc, et al.. (1964). The action of Depo-Provera in 3 girls with idiopathic isosexual precocity: Decrease in estrogen effect without urinary gonadotropin reduction. The Journal of Pediatrics. 65(6). 888–894. 17 indexed citations
8.
Lemli, Luc, et al.. (1964). The action of depo-provera in 3 girls with idiopathic isosexual precocity: Decrease in estrogen effect without urinary gonadotrophin reduction. The Journal of Pediatrics. 65(1). 110–110. 2 indexed citations
9.
Lemli, Luc & David W. Smith. (1963). The XO syndrome: A study of the differentiated phenotype in 25 patients. The Journal of Pediatrics. 63(4). 577–588. 146 indexed citations
10.
Gerritsen, Theo, Luc Lemli, Louis J. Ptáček, & Harry A. Waisman. (1963). THE PRESENCE OF LACTULOSE IN THE URINE OF INFANTS WITH LACTOSURIA. PEDIATRICS. 32(6). 1033–1038. 10 indexed citations
11.
Lemli, Luc, et al.. (1963). Zinc glucagon in the managementof idiopathic hypoglycemia. The Journal of Pediatrics. 63(6). 1111–1115. 20 indexed citations
12.
Gutmann, Ludwig & Luc Lemli. (1963). Ataxia-Telangiectasia Associated with Hypogammaglobulinemia. Archives of Neurology. 8(3). 318–327. 38 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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