M. Clementi

891 total citations
12 papers, 412 citations indexed

About

M. Clementi is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Molecular Biology. According to data from OpenAlex, M. Clementi has authored 12 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in M. Clementi's work include Congenital Anomalies and Fetal Surgery (6 papers), Prenatal Screening and Diagnostics (5 papers) and Pregnancy and Medication Impact (2 papers). M. Clementi is often cited by papers focused on Congenital Anomalies and Fetal Surgery (6 papers), Prenatal Screening and Diagnostics (5 papers) and Pregnancy and Medication Impact (2 papers). M. Clementi collaborates with scholars based in France, Italy and Spain. M. Clementi's co-authors include Claude Stoll, Ester Garne, Romana Gjergja Juraški, Martin Haeusler, Ingeborg Barišić, C. De Vigan, E Cariati, Neus Baena, Míriam Guitart and M.R. Caballı́n and has published in prestigious journals such as Neurology, The Journal of Pediatrics and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

M. Clementi

12 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Clementi France	9	240	182	126	111	67	12	412
Stefanie B. Kasperski United States	9	152 0.6×	109 0.6×	57 0.5×	81 0.7×	40 0.6×	18	284
Elizabeth A. Leeth United States	8	115 0.5×	108 0.6×	143 1.1×	46 0.4×	103 1.5×	11	287
Shuichiro Yoshimura Japan	8	95 0.4×	143 0.8×	66 0.5×	65 0.6×	29 0.4×	14	254
Anne Massez Belgium	8	131 0.5×	189 1.0×	59 0.5×	29 0.3×	46 0.7×	15	285
Elspeth McPherson United States	9	55 0.2×	61 0.3×	97 0.8×	29 0.3×	114 1.7×	13	277
M. Molho France	8	75 0.3×	197 1.1×	72 0.6×	29 0.3×	43 0.6×	15	305
Keiji Goishi Japan	12	227 0.9×	72 0.4×	66 0.5×	157 1.4×	58 0.9×	28	416
R. Wimalasundera United Kingdom	15	101 0.4×	460 2.5×	55 0.4×	43 0.4×	48 0.7×	22	601
Sheau‐Wen Jan Taiwan	12	160 0.7×	168 0.9×	75 0.6×	15 0.1×	31 0.5×	22	290
J. L. J. Gaillard Netherlands	11	358 1.5×	51 0.3×	21 0.2×	204 1.8×	43 0.6×	17	433

Countries citing papers authored by M. Clementi

Since Specialization

Citations

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

Fields of papers citing papers by M. Clementi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Clementi

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

All Works

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12 of 12 papers shown

Trevisson, Eva, Monica Forzan, Leonardo Salviati, & M. Clementi. (2013). Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism. Clinical Genetics. 85(4). 386–389. 5 indexed citations

Winterfeld, Ursula, Alice Panchaud, Paul Merlob, et al.. (2011). Pregnancy Outcome Following Maternal Exposure To Statins: A Multicenter Prospective Study. IRIS. 1 indexed citations

Clementi, M., Elena Di Gianantonio, Luca Fabris, et al.. (2007). Inheritance of hyperbilirubinemia: Evidence for a major autosomal recessive gene. Digestive and Liver Disease. 39(4). 351–355. 19 indexed citations

Botta, Annalisa, Alessandra Tacconelli, Emiliano Giardina, et al.. (2005). Transmission ratio distortion in the spinal muscular atrophy locus. Neurology. 65(10). 1631–1635. 10 indexed citations

Baena, Neus, C. De Vigan, E Cariati, et al.. (2004). Turner syndrome: Evaluation of prenatal diagnosis in 19 European registries. American Journal of Medical Genetics Part A. 129A(1). 16–20. 58 indexed citations

Wellesley, Diana, C. De Vigan, Neus Baena, et al.. (2004). Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers. Annales de Génétique. 47(4). 373–380. 9 indexed citations

Baena, Neus, C. De Vigan, E Cariati, et al.. (2003). Prenatal detection of rare chromosomal autosomal abnormalities in Europe. American Journal of Medical Genetics Part A. 118A(4). 319–327. 31 indexed citations

Garne, Ester, Martin Haeusler, Ingeborg Barišić, et al.. (2002). Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions. Ultrasound in Obstetrics and Gynecology. 19(4). 329–333. 146 indexed citations

Vigan, C. De, Neus Baena, E Cariati, M. Clementi, & Claude Stoll. (2001). Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Annales de Génétique. 44(4). 209–217. 48 indexed citations

10.

Stoll, Claude, et al.. (2000). Evaluation of the prenatal diagnosis of limb reduction deficiencies. Prenatal Diagnosis. 20(10). 811–818. 49 indexed citations

11.

Mastroiacovo, P, Antonio Addis, P. Carlier, et al.. (1999). High vitamin A intake in early pregnancy and major malformations: A multicenter prospective controlled study. Teratology. 59(1). 7–11. 3 indexed citations

12.

Laverda, A. M., O.S. Saia, Paola Drigo, et al.. (1984). Chorioretinal coloboma and joubert syndrome: A nonrandom association. The Journal of Pediatrics. 105(2). 282–284. 33 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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