L Duprez

1.1k total citations
16 papers, 656 citations indexed

About

L Duprez is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Molecular Biology. According to data from OpenAlex, L Duprez has authored 16 papers receiving a total of 656 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Endocrinology, Diabetes and Metabolism, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in L Duprez's work include Thyroid Disorders and Treatments (7 papers), Growth Hormone and Insulin-like Growth Factors (4 papers) and Prenatal Screening and Diagnostics (3 papers). L Duprez is often cited by papers focused on Thyroid Disorders and Treatments (7 papers), Growth Hormone and Insulin-like Growth Factors (4 papers) and Prenatal Screening and Diagnostics (3 papers). L Duprez collaborates with scholars based in Belgium, France and Denmark. L Duprez's co-authors include Jasmine Parma, Marc Abramowicz, G Vassart, Claudine Heinrichs, Gilbert Vassart, J. Van Sande, J.E. Dumont, Massimo Tonacchera, Patrice Rodien and E. Vámos and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and Annals of the New York Academy of Sciences.

In The Last Decade

L Duprez

16 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L Duprez Belgium	14	395	271	190	106	90	16	656
T Sunthornthepvarakul Thailand	12	430 1.1×	302 1.1×	202 1.1×	49 0.5×	57 0.6×	25	694
Ameeta Mehta United Kingdom	10	461 1.2×	270 1.0×	270 1.4×	73 0.7×	90 1.0×	11	682
E Joss Switzerland	13	406 1.0×	279 1.0×	195 1.0×	84 0.8×	48 0.5×	36	643
James Turton United Kingdom	12	484 1.2×	290 1.1×	297 1.6×	68 0.6×	96 1.1×	15	710
C Bancroft United States	14	290 0.7×	249 0.9×	118 0.6×	29 0.3×	44 0.5×	17	525
Roberto Romoli Italy	13	334 0.8×	271 1.0×	187 1.0×	19 0.2×	41 0.5×	18	589
R Keret Israel	12	704 1.8×	306 1.1×	324 1.7×	78 0.7×	117 1.3×	35	856
Laura A. Dollar United States	11	487 1.2×	278 1.0×	126 0.7×	37 0.3×	114 1.3×	12	671
Mariarosaria Lang‐Muritano Switzerland	14	337 0.9×	366 1.4×	375 2.0×	64 0.6×	176 2.0×	35	756
C Y Hayashida Brazil	12	476 1.2×	309 1.1×	295 1.6×	58 0.5×	180 2.0×	18	873

Countries citing papers authored by L Duprez

Since Specialization

Citations

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

Fields of papers citing papers by L Duprez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Duprez

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

All Works

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16 of 16 papers shown

Bugge, Merete, Andrew Collins, Jens Michael Hertz, et al.. (2007). Non-disjunction of chromosome 13. Human Molecular Genetics. 16(16). 2004–2010. 43 indexed citations

Donner, Catherine, Nicole Van Regemorter, L Duprez, et al.. (2005). Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?. Prenatal Diagnosis. 25(7). 567–573. 45 indexed citations

Bugge, Merete, C.D. DeLozier-Blanchet, Mads Bak, et al.. (2004). Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases. American Journal of Medical Genetics Part A. 132A(3). 310–313. 21 indexed citations

Uchino, S., L Duprez, María José Costa, et al.. (2002). Oncogenic mutations in the thyrotropin receptor of autonomously functioning thyroid nodules in the Japanese population. European Journal of Endocrinology. 147(3). 287–291. 22 indexed citations

Vassart, Gilbert, Marc Abramowicz, Pascale Cochaux, et al.. (2002). [Medical genetics service].. PubMed. 23 Suppl 2. 63–7. 2 indexed citations

Bretones, Patricia, L Duprez, Jasmine Parma, et al.. (2001). A Familial Case of Congenital Hypothyroidism Caused by a Homozygous Mutation of the Thyrotropin Receptor Gene. Thyroid. 11(10). 977–980. 32 indexed citations

Heinrichs, Claudine, Neal H. Scherberg, François Delange, et al.. (2000). Congenital Central Isolated Hypothyroidism Caused by a Homozygous Mutation in the TSH-β Subunit Gene. Thyroid. 10(5). 387–391. 38 indexed citations

Duprez, L, et al.. (1999). A Novel Thyrotropin Receptor Mutation in an Infant with Severe Thyrotoxicosis. Thyroid. 9(10). 1005–1010. 40 indexed citations

Duprez, L, et al.. (1999). Pathology of the TSH receptor.. PubMed. 12 Suppl 1. 295–302. 28 indexed citations

10.

Abramowicz, Marc, L Duprez, Jasmine Parma, G Vassart, & Claudine Heinrichs. (1997). Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.. Journal of Clinical Investigation. 99(12). 3018–3024. 173 indexed citations

11.

Duprez, L. (1997). Two Autonomous Nodules of a Patient with Multinodular Goiter Harbor Different Activating Mutations of the Thyrotropin Receptor Gene. The Journal of Clinical Endocrinology & Metabolism. 82(1). 306–308. 19 indexed citations

12.

Tonacchera, Massimo, J. Van Sande, Jasmine Parma, et al.. (1996). TSH receptor and disease. Clinical Endocrinology. 44(6). 621–633. 63 indexed citations

13.

Vassart, Gilbert, J. Van Sande, Jasmine Parma, et al.. (1996). Activating mutations of the TSH receptor gene cause thyroid diseases.. PubMed. 57(1). 50–4. 7 indexed citations

14.

Vassart, G, Frank Désarnaud, L Duprez, et al.. (1995). The G Protein–coupled Receptor Family and One of Its Members, the TSH Receptor^a. Annals of the New York Academy of Sciences. 766(1). 23–30. 14 indexed citations

15.

Abramowicz, Marc, Marc Andrien, E. Dupont, et al.. (1994). Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.. Journal of Clinical Investigation. 94(1). 418–421. 67 indexed citations

16.

Parma, Jasmine, L Duprez, Pascale Cochaux, et al.. (1994). Somatic Mutations in the Thyrotropin Receptor Gene Cause Hyperfunctioning Thyroid Adenomas. The Endocrinologist. 4(2). 152–152. 42 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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