L. Dalpr�

448 total citations
9 papers, 317 citations indexed

About

L. Dalpr� is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, L. Dalpr� has authored 9 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in L. Dalpr�'s work include Chromosomal and Genetic Variations (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (2 papers). L. Dalpr� is often cited by papers focused on Chromosomal and Genetic Variations (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (2 papers). L. Dalpr� collaborates with scholars based in Italy and Netherlands. L. Dalpr�'s co-authors include Maria Luisa Tenchini, Romina Combi, Luigi Ferini‐Strambi, Monica Miozzo, A. Conti, Paola Riva, Lidia Larizza, Giuseppe Simoni, F. Rossella and W. Keijzer and has published in prestigious journals such as International Journal of Cancer, Human Genetics and Journal of Neurology.

In The Last Decade

L. Dalpr�

9 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. Dalpr� Italy	8	128	118	100	83	47	9	317
Jean-Marc Pinard France	11	119 0.9×	57 0.5×	47 0.5×	76 0.9×	14 0.3×	16	311
B.E. Reus United States	7	695 5.4×	459 3.9×	245 2.5×	184 2.2×	92 2.0×	8	860
Anders Heuck Denmark	8	212 1.7×	65 0.6×	77 0.8×	41 0.5×	15 0.3×	12	370
João Ramalheira Portugal	10	122 1.0×	64 0.5×	215 2.1×	51 0.6×	7 0.1×	23	386
Núria Setó‐Salvia United Kingdom	7	141 1.1×	99 0.8×	23 0.2×	137 1.7×	10 0.2×	10	466
Clara DM van Karnebeek Canada	7	190 1.5×	49 0.4×	40 0.4×	105 1.3×	15 0.3×	7	349
J. P. Newman Israel	8	48 0.4×	56 0.5×	23 0.2×	59 0.7×	27 0.6×	10	238
Anne Koy Germany	14	114 0.9×	105 0.9×	115 1.1×	59 0.7×	30 0.6×	40	535
Patrick Thierry France	7	206 1.6×	152 1.3×	39 0.4×	62 0.7×	10 0.2×	8	310
Dichen Zhao China	11	176 1.4×	241 2.0×	42 0.4×	61 0.7×	19 0.4×	23	397

Countries citing papers authored by L. Dalpr�

Since Specialization

Citations

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

Fields of papers citing papers by L. Dalpr�

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Dalpr�

This figure shows the co-authorship network connecting the top 25 collaborators of L. Dalpr�. A scholar is included among the top collaborators of L. Dalpr� 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. Dalpr�. L. Dalpr� 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.

Combi, Romina, L. Dalpr�, Maria Luisa Tenchini, & Luigi Ferini‐Strambi. (2004). Autosomal dominant nocturnal frontal lobe epilepsy. Journal of Neurology. 251(8). 923–34. 169 indexed citations

2.

Ferrarese, Carlo, Lucio Tremolizzo, Miriam Rigoldi, et al.. (2001). Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease. Neurological Sciences. 22(1). 65–66. 28 indexed citations

3.

Pallotta, R, et al.. (2001). A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency. American Journal of Medical Genetics. 104(4). 282–286. 16 indexed citations

4.

Dalpr�, L., et al.. (1999). First cytogenetic study of a recurrent familial chordoma of the clivus. International Journal of Cancer. 81(1). 24–30. 49 indexed citations

5.

Russo, Silvia, Angelo Selicorni, Maria Francesca Bedeschi, et al.. (1998). Molecular characterization of FRAXE-positive subjects with mental impairment in two unrelated Italian families. American Journal of Medical Genetics. 75(3). 304–308. 4 indexed citations

6.

Stefanini, Miria, W. Keijzer, L. Dalpr�, et al.. (1980). Differences in the levels of UV repair and in clinical symptoms in two sibs affected by xeroderma pigmentosum. Human Genetics. 54(2). 177–182. 18 indexed citations

7.

Simoni, Giuseppe, L. Dalpr�, G. L. Terzoli, F. Rossella, & M.G. Tibiletti. (1980). The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31). Human Genetics. 55(2). 199–202. 9 indexed citations

8.

Sacchi, Nicoletta, et al.. (1980). A duplication-deficiency X chromosome in a girl with severe mental retardation. Human Genetics. 54(2). 279–281. 9 indexed citations

9.

Simoni, Giuseppe, et al.. (1979). Ring chromosome 10 Associated with multiple congenital malformations. Human Genetics. 51(2). 117–121. 15 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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