G. Nocera

536 total citations
11 papers, 152 citations indexed

About

G. Nocera is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, G. Nocera has authored 11 papers receiving a total of 152 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in G. Nocera's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (2 papers). G. Nocera is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (2 papers). G. Nocera collaborates with scholars based in Italy. G. Nocera's co-authors include Leda Dalprà, M.G. Tibiletti, Gabriele Vignati, Luciano Bovicelli, Paolo Beck‐Peccoz, Luca Persani, Maria Carla Pittalis, Francesca Torricelli, N. Rizzo and E Cariati and has published in prestigious journals such as Human Reproduction, European Journal of Human Genetics and American Journal of Medical Genetics.

In The Last Decade

G. Nocera

10 papers receiving 145 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Nocera Italy	6	85	72	39	30	21	11	152
Stephanie Harris United States	9	15 0.2×	48 0.7×	45 1.2×	10 0.3×	15 0.7×	11	169
Heleen Schuring‐Blom Netherlands	7	113 1.3×	117 1.6×	42 1.1×	13 0.4×		8	178
David M. deKretser Australia	6	34 0.4×	133 1.8×	117 3.0×	28 0.9×	4 0.2×	10	278
Verónica Seidel Spain	5	77 0.9×	51 0.7×	87 2.2×	23 0.8×		9	191
Beata Stasiewicz‐Jarocka Poland	7	52 0.6×	107 1.5×	68 1.7×	11 0.4×	2 0.1×	16	195
Karen David United States	6	105 1.2×	130 1.8×	42 1.1×	44 1.5×		9	183
Aurélie Coussement France	7	38 0.4×	67 0.9×	40 1.0×	33 1.1×	1 0.0×	16	141
J. Lespinasse France	12	162 1.9×	195 2.7×	69 1.8×	16 0.5×		25	310
Céline Pebrel‐Richard France	7	39 0.5×	91 1.3×	69 1.8×	26 0.9×		20	138
Mitsukazu Mamada Japan	6	42 0.5×	158 2.2×	104 2.7×	97 3.2×		11	259

Countries citing papers authored by G. Nocera

Since Specialization

Citations

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

Fields of papers citing papers by G. Nocera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Nocera

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

All Works

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11 of 11 papers shown

Giardino, Daniela, et al.. (2004). Unbalanced segregation of a complex four-break 5q23–31 insertion in the 5p13 band in a malformed child. European Journal of Human Genetics. 12(6). 455–459. 3 indexed citations

Castorina, Pierangela, Ornella Rodeschini, G. Nocera, & Lidia Larizza. (2000). Reproductive follow-up of carriers of familial reciprocal balanced translocations involving chromosome 9 and comparison with predicted outcome.. PubMed. 11(3). 229–39. 1 indexed citations

Vignati, Gabriele, et al.. (1999). Thyroid hemiagenesis and elevated thyrotropin levels in a child with Williams syndrome. American Journal of Medical Genetics. 85(5). 491–494. 31 indexed citations

Doneda, Luisa, et al.. (1998). A Rare Chromosome 5 Heterochromatic Variant Derived from Insertion of 9qh Satellite 3 Sequences. Chromosome Research. 6(5). 411–414. 4 indexed citations

Pittalis, Maria Carla, Leda Dalprà, Francesca Torricelli, et al.. (1994). The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods. Prenatal Diagnosis. 14(4). 267–278. 58 indexed citations

Dalprà, Leda, et al.. (1993). ‘Late’ chorionic villus sampling: Cytogenetic aspects. Prenatal Diagnosis. 13(4). 239–246. 6 indexed citations

Tozzi, Alberto Eugenio, Luciano Bovicelli, Leda Dalprà, et al.. (1993). Transverse limb reduction defects after chorion villus sampling: A retrospective Cohort study. Prenatal Diagnosis. 13(11). 1051–1056. 18 indexed citations

Dalprà, Leda, et al.. (1986). Technical aspects and diagnostic problems of direct chromosome analysis using chorionic villus sampling in the first trimester. Human Reproduction. 1(2). 103–106. 3 indexed citations

Nocera, G., et al.. (1985). Five cases of prenatally diagnosed sex chromosome mosaicism. Prenatal Diagnosis. 5(3). 169–174. 2 indexed citations

10.

Archidiacono, Nicoletta, Vanna Pecile, Mariano Rocchi, et al.. (1984). A rare non‐heterochromatic 9p+ variant in two amniotic fluid cell cultures. Prenatal Diagnosis. 4(3). 231–233. 11 indexed citations

11.

Dalprà, Leda, et al.. (1983). SCE analysis in children exposed to lead emission from a smelting plant. Mutation Research Letters. 120(4). 249–256. 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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