Jules G. Leroy

4.7k total citations
89 papers, 2.6k citations indexed

About

Jules G. Leroy is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jules G. Leroy has authored 89 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 31 papers in Genetics and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jules G. Leroy's work include Lysosomal Storage Disorders Research (14 papers), Connective tissue disorders research (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Jules G. Leroy is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Connective tissue disorders research (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Jules G. Leroy collaborates with scholars based in Belgium, United States and France. Jules G. Leroy's co-authors include Robert DeMars, John S. O’Brien, Geert Mortier, Mae Wan Ho, Jürgen W. Spranger, Jack Jacob, K Zielke, Allen C. Crocker, Murray Feingold and John M. Opitz and has published in prestigious journals such as Science, New England Journal of Medicine and PEDIATRICS.

In The Last Decade

Jules G. Leroy

84 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jules G. Leroy Belgium 29 1.2k 716 616 395 273 89 2.6k
George E. Tiller United States 22 884 0.7× 709 1.0× 829 1.3× 316 0.8× 176 0.6× 46 2.4k
Maja Di Rocco Italy 34 1.5k 1.2× 1.2k 1.6× 860 1.4× 498 1.3× 232 0.8× 147 3.6k
Marianne Rohrbach Switzerland 26 631 0.5× 897 1.3× 1.0k 1.7× 253 0.6× 143 0.5× 81 2.4k
W A Grasser United States 23 1.4k 1.1× 286 0.4× 313 0.5× 328 0.8× 195 0.7× 33 3.0k
Hiroshi Kawame Japan 23 1.1k 0.9× 239 0.3× 634 1.0× 208 0.5× 259 0.9× 66 2.1k
Alexander Lossos Israel 30 656 0.5× 397 0.6× 327 0.5× 125 0.3× 276 1.0× 110 2.9k
H. Scott Boswell United States 29 1.6k 1.3× 273 0.4× 459 0.7× 246 0.6× 183 0.7× 63 3.6k
Kiyomi Mizugishi Japan 21 1.5k 1.2× 296 0.4× 223 0.4× 397 1.0× 160 0.6× 30 2.2k
Amittha Wickrema United States 38 1.8k 1.4× 1.0k 1.4× 198 0.3× 224 0.6× 192 0.7× 111 3.9k
Christine M. Eng United States 26 871 0.7× 3.0k 4.1× 513 0.8× 884 2.2× 108 0.4× 40 3.9k

Countries citing papers authored by Jules G. Leroy

Since Specialization
Citations

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

Fields of papers citing papers by Jules G. Leroy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jules G. Leroy. 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 Jules G. Leroy. The network helps show where Jules G. Leroy may publish in the future.

Co-authorship network of co-authors of Jules G. Leroy

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

All Works

20 of 20 papers shown
1.
Louie, Raymond J., Michael J. Friez, Jaime L. Frías, et al.. (2018). Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations. Clinical Case Reports. 6(11). 2252–2255. 7 indexed citations
2.
Bolar, Nikhita, Arnaud Vanlander, Nathalie Van der Aa, et al.. (2013). Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy. Human Molecular Genetics. 22(13). 2590–2602. 90 indexed citations
3.
Isidor, Bertrand, Olivier Pichon, Richard Redon, et al.. (2010). Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13. The American Journal of Human Genetics. 87(1). 95–100. 31 indexed citations
4.
Leroy, Jules G., Lieve Nuytinck, Jo Lambert, J.M. Naeyaert, & Geert Mortier. (2007). Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene. American Journal of Medical Genetics Part A. 143A(24). 3144–3149. 18 indexed citations
5.
Goriely, Alain, et al.. (2006). Toy models: The jumping pendulum. American Journal of Physics. 74(9). 784–788. 3 indexed citations
6.
Leroy, Jules G., Raili Seppälä, Marjan Huizing, et al.. (2001). Dominant Inheritance of Sialuria, an Inborn Error of Feedback Inhibition. The American Journal of Human Genetics. 68(6). 1419–1427. 41 indexed citations
7.
Vanhaesebrouck, Piet, J. Kint, Marc Dhont, Claudine De Praeter, & Jules G. Leroy. (1994). Aminoterminal Propeptide of Type III Procollagen in Cord Blood and Amniotic Fluid of Appropriate-for-Gestational-Age Infants: A Predictor of Age-Related Fetal Growth Rate. Pediatric Research. 36(1 Pt 1). 64–70. 9 indexed citations
8.
9.
Viljoen, Denis, et al.. (1992). Putative monosomy 21 in two patients: clinical findings and investigation using fluorescence in situ hybridization. Clinical Genetics. 42(3). 105–109. 23 indexed citations
10.
Speleman, Frank, et al.. (1991). Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps?. Genes Chromosomes and Cancer. 3(4). 318–319. 16 indexed citations
11.
Leroy, Jules G., et al.. (1982). Les peintures des couvents du Ouadi Natroun. 4 indexed citations
12.
Waheed, Abdül, et al.. (1982). Deficiency of UDP-N-acetylglucosamine: Lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients. Biochemical and Biophysical Research Communications. 105(3). 1052–1058. 124 indexed citations
13.
Leroy, Jules G., et al.. (1981). Cerebro-costo-mandibular syndrome with autosomal dominant inheritance. The Journal of Pediatrics. 99(3). 441–443. 26 indexed citations
14.
Leroy, Jules G.. (1976). A. Grabar, Les Revêtements en or et en argent des icônes byzantines du moyen âge. Bibliothèque de l'Institut hellénique d'études byzantines et postbyzantines de Venise, n. 7, Venise 1975.. Persée (Ministère de lEnseignement supérieur et de la Recherche). 1 indexed citations
15.
Leroy, Jules G.. (1974). Les manuscrits coptes et coptes-arabes illustrés. 7 indexed citations
16.
Leroy, Jules G., et al.. (1973). L'Éthiopie : archéologie et culture. Desclée de Brouwer eBooks. 1 indexed citations
17.
Leroy, Jules G., et al.. (1973). Iris dysplasia, orbital hypertelorism, and psychomotor retardation: A dominantly inherited developmental syndrome. The Journal of Pediatrics. 82(4). 679–681. 34 indexed citations
18.
Leroy, Jules G., Jürgen W. Spranger, Murray Feingold, John M. Opitz, & Allen C. Crocker. (1971). I-cell disease: A clinical picture. The Journal of Pediatrics. 79(3). 360–365. 128 indexed citations
19.
Leroy, Jules G.. (1964). Les manuscrits syriaques à peintures conservés dans les bibliothèques d'Europe et d'Orient. 6 indexed citations
20.
Leroy, Jules G.. (1955). Un nouveau manuscrit arabe-chrétien illustré du roman de Baarlam et Joasaph. Syria. 32(1). 101–122. 1 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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