Anna Maria Nardone

905 total citations
38 papers, 552 citations indexed

About

Anna Maria Nardone is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anna Maria Nardone has authored 38 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 22 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anna Maria Nardone's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Anna Maria Nardone is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Anna Maria Nardone collaborates with scholars based in Italy, United States and Poland. Anna Maria Nardone's co-authors include Giuseppe Novelli, F Gullotta, Maria Rosaria D’Apice, Giovanna Lattanzi, Marta Columbaro, Gioacchino Scarano, Elisabetta Mattioli, Nadir M. Maraldi, Federica Sangiuolo and Silvia Biocca and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Anna Maria Nardone

36 papers receiving 520 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Maria Nardone Italy	13	380	213	55	35	33	38	552
Laura A. Crinnion United Kingdom	13	274 0.7×	160 0.8×	45 0.8×	22 0.6×	50 1.5×	26	413
Emma Hobson United Kingdom	9	213 0.6×	256 1.2×	37 0.7×	40 1.1×	33 1.0×	24	405
Filomena Tiziana Papa Italy	14	182 0.5×	257 1.2×	37 0.7×	41 1.2×	19 0.6×	26	412
Kelly E. Jackson United States	8	204 0.5×	211 1.0×	40 0.7×	50 1.4×	11 0.3×	15	375
Simone Schiller Germany	6	307 0.8×	393 1.8×	65 1.2×	34 1.0×	34 1.0×	8	507
Claas Wodarczyk Italy	8	353 0.9×	300 1.4×	28 0.5×	33 0.9×	27 0.8×	9	565
M. Crippa Italy	12	203 0.5×	145 0.7×	40 0.7×	43 1.2×	14 0.4×	37	396
María Palomares‐Bralo Spain	13	339 0.9×	364 1.7×	55 1.0×	105 3.0×	19 0.6×	38	540
Jim Mullikin United States	10	245 0.6×	195 0.9×	96 1.7×	68 1.9×	31 0.9×	14	379
Cornelia Daumer‐Haas Germany	8	245 0.6×	264 1.2×	62 1.1×	73 2.1×	16 0.5×	10	451

Countries citing papers authored by Anna Maria Nardone

Since Specialization

Citations

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

Fields of papers citing papers by Anna Maria Nardone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Maria Nardone. 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 Anna Maria Nardone. The network helps show where Anna Maria Nardone may publish in the future.

Co-authorship network of co-authors of Anna Maria Nardone

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

All Works

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20 of 20 papers shown

Dahan, Idit, Sarah Vergult, Marta Vidal‐García, et al.. (2022). HDAC9structural variants disruptingTWIST1transcriptional regulation lead to craniofacial and limb malformations. Genome Research. 32(7). 1242–1253. 11 indexed citations

Lonardo, Fortunato, M. Cristina Digilio, Daniela Rogaia, et al.. (2021). Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American Journal of Medical Genetics Part A. 185(4). 1204–1210. 5 indexed citations

Recalcati, Maria Paola, Maria Teresa Bonati, Isabella Mammi, et al.. (2017). Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature. European Journal of Medical Genetics. 61(3). 173–180. 2 indexed citations

Pitzianti, Mariabernarda, Diana Postorivo, Anna Maria Nardone, et al.. (2017). A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype. Cytogenetic and Genome Research. 153(1). 22–28. 2 indexed citations

Acquaviva, Fabio, Maria Elena Sana, Matteo Della Monica, et al.. (2016). First evidence of Smith–Magenis syndrome in mother and daughter due to a novel RAI mutation. American Journal of Medical Genetics Part A. 173(1). 231–238. 26 indexed citations

Pietropolli, Adalgisa, Stefania Zampatti, Anna Maria Nardone, et al.. (2013). Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis. The Journal of Maternal-Fetal & Neonatal Medicine. 27(16). 1656–1660. 2 indexed citations

Alesi, Viola, Marta Bertoli, Giuseppe Barrano, et al.. (2012). 335.4kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features. Gene. 505(2). 384–387. 11 indexed citations

Columbaro, Marta, Elisabetta Mattioli, Nadir M. Maraldi, et al.. (2012). Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(3). 411–420. 21 indexed citations

Spielmann, Malte, Francesco Brancati, Peter Krawitz, et al.. (2012). Homeotic Arm-to-Leg Transformation Associated with Genomic Rearrangements at the PITX1 Locus. The American Journal of Human Genetics. 91(4). 629–635. 83 indexed citations

10.

Lo‐Castro, Adriana, Cinzia Galasso, Alberto Verrotti, et al.. (2011). De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems. European Journal of Medical Genetics. 54(3). 329–332. 13 indexed citations

11.

Giacomozzi, Claudio, et al.. (2010). Premature ovarian failure, absence of pubic and axillary hair with de novo 46,X,t(X;15)(q24;q26.3). American Journal of Medical Genetics Part A. 152A(5). 1305–1309. 9 indexed citations

12.

Giardina, Emiliano, Raffaella Cascella, Valeria Foti Cuzzola, et al.. (2009). A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7. Electrophoresis. 30(11). 2008–2011. 4 indexed citations

13.

Chiriacò, Maria Serena, Gigliola Di Matteo, Emiliano Giardina, et al.. (2009). Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. Genetic Testing and Molecular Biomarkers. 13(6). 785–789. 7 indexed citations

14.

Galasso, Cinzia, et al.. (2006). Interstitial deletion of a proximal 3p: A clinically recognisable syndrome. Brain and Development. 29(5). 312–316. 10 indexed citations

15.

Salehi, Leila, Oronzo Scarciolla, Anna Maria Nardone, et al.. (2006). Identification of a novel mutation in the SRY gene in a 46, XY female patient. European Journal of Medical Genetics. 49(6). 494–498. 9 indexed citations

16.

Filesi, Ilaria, F Gullotta, Giovanna Lattanzi, et al.. (2005). Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy. Physiological Genomics. 23(2). 150–158. 104 indexed citations

17.

D’Apice, Maria Rosaria, Stefano Gambardella, Silvia Russo, et al.. (2004). Segregation analysis in cystic fibrosis at‐risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism. Prenatal Diagnosis. 24(12). 981–983. 2 indexed citations

18.

Contino, Gianmarco, Francesca Amati, Sabina Pucci, et al.. (2004). Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. Gene. 328. 69–74. 22 indexed citations

19.

D’Apice, Maria Rosaria, Stefano Gambardella, Mario Bengala, et al.. (2004). Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy. BMC Medical Genetics. 5(1). 8–8. 20 indexed citations

20.

Sangiuolo, Federica, Emanuela M. Bruscia, Annalucia Serafino, et al.. (2002). In vitrocorrection of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique. BMC Medical Genetics. 3(1). 8–8. 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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