L Moschini

477 total citations
9 papers, 239 citations indexed

About

L Moschini is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, L Moschini has authored 9 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Endocrinology, Diabetes and Metabolism, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in L Moschini's work include Thyroid Disorders and Treatments (5 papers), Congenital heart defects research (3 papers) and Genetic Syndromes and Imprinting (2 papers). L Moschini is often cited by papers focused on Thyroid Disorders and Treatments (5 papers), Congenital heart defects research (3 papers) and Genetic Syndromes and Imprinting (2 papers). L Moschini collaborates with scholars based in Italy. L Moschini's co-authors include Luca Chiovato, Mariangiola Baserga, Paolo Emidio Macchia, Gianfranco Fenzi, Roberto Di Lauro, Cristina Fazzini, M Sorcini, Paola Lapi, Anna Perri and A Pinchera and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Thyroid and Acta Paediatrica.

In The Last Decade

L Moschini

9 papers receiving 226 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L Moschini Italy	6	163	140	89	32	25	9	239
Keith Usiskin United States	5	49 0.3×	149 1.1×	60 0.7×	21 0.7×	25 1.0×	5	267
J. B. McAteer United States	6	103 0.6×	73 0.5×	146 1.6×	17 0.5×	75 3.0×	7	252
E Topper Israel	6	53 0.3×	47 0.3×	64 0.7×	8 0.3×	15 0.6×	13	152
Matthias Viemann Germany	7	217 1.3×	160 1.1×	80 0.9×	9 0.3×	40 1.6×	10	269
F Kurtz France	4	92 0.6×	71 0.5×	52 0.6×	6 0.2×	10 0.4×	6	155
V. Lyssenko Sweden	5	86 0.5×	70 0.5×	135 1.5×	21 0.7×	91 3.6×	7	239
Stine M. Præstholm Denmark	5	71 0.4×	43 0.3×	39 0.4×	34 1.1×	16 0.6×	6	169
V. Beauloye Belgium	6	45 0.3×	128 0.9×	28 0.3×	10 0.3×	16 0.6×	8	216
Angela K. Chua United States	8	62 0.4×	48 0.3×	88 1.0×	14 0.4×	9 0.4×	8	389
Athanasia Stoupa France	9	161 1.0×	197 1.4×	92 1.0×	4 0.1×	18 0.7×	23	261

Countries citing papers authored by L Moschini

Since Specialization

Citations

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

Fields of papers citing papers by L Moschini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Moschini

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

All Works

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9 of 9 papers shown

1.

Dentice, Monica, Viviana Cordeddu, Annamaria Rosica, et al.. (2006). Missense Mutation in the Transcription Factor NKX2–5: A Novel Molecular Event in the Pathogenesis of Thyroid Dysgenesis. The Journal of Clinical Endocrinology & Metabolism. 91(4). 1428–1433. 121 indexed citations

2.

Tonacchera, Massimo, Paola Lapi, Caterina Di Cosmo, et al.. (2004). Genetic Analysis of TTF-2 Gene in Children with Congenital Hypothyroidism and Cleft Palate, Congenital Hypothyroidism, or Isolated Cleft Palate. Thyroid. 14(8). 584–588. 20 indexed citations

3.

Lapi, Paola, Paolo Emidio Macchia, Luca Chiovato, et al.. (1997). Mutations in the Gene EncodingThyroid Transcription Factor-1 (TTF-1) Are Not a Frequent Cause of Congenital Hypothyroidism (CH) with Thyroid Dysgenesis. Thyroid. 7(3). 383–387. 59 indexed citations

4.

Moschini, L, et al.. (1994). [2 cases of Beckwith-Wiedemann syndrome. Morphogenetic characteristics, cardiac involvement and current diagnostic possibilities].. PubMed. 46(11). 509–15. 1 indexed citations

5.

Moschini, L, et al.. (1994). [The instrumental and clinical laboratory follow-up of congenital hypothyroidism].. PubMed. 30(3). 335–8. 2 indexed citations

6.

Moschini, L, et al.. (1986). Longitudinal assessment of children with congenital hypothyroidism detected by neonatal screening.. PubMed. 41(5). 415–24. 20 indexed citations

7.

Sorcini, M, L Moschini, Lucia Fiore, et al.. (1982). Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidism. Journal of Endocrinological Investigation. 5(1). 21–25. 5 indexed citations

8.

Midulla, M, L Businco, & L Moschini. (1972). SOME EFFECTS OF RUBELLA VACCINATION ON IMMUNOLOGIC RESPONSIVENESS1. Acta Paediatrica. 61(5). 609–611. 10 indexed citations

9.

Midulla, M, et al.. (1971). [Jeune's thoracic dystrophy].. PubMed. 23(1). 19–29. 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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