Marzia Pollazzon

1.5k total citations
31 papers, 692 citations indexed

About

Marzia Pollazzon is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Marzia Pollazzon has authored 31 papers receiving a total of 692 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 16 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Marzia Pollazzon's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (4 papers). Marzia Pollazzon is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (4 papers). Marzia Pollazzon collaborates with scholars based in Italy, Switzerland and United States. Marzia Pollazzon's co-authors include Alessandra Renieri, Francesca Mari, Maria Antonietta Mencarelli, Joussef Hayek, Francesca Ariani, Rosangela Artuso, Sabrina Buoni, Ilaria Longo, Ilaria Meloni and Michele Zappella and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Experimental Eye Research.

In The Last Decade

Marzia Pollazzon

30 papers receiving 686 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marzia Pollazzon Italy	14	494	368	143	48	43	31	692
Bhooma Thiruvahindrapuram Canada	14	500 1.0×	420 1.1×	147 1.0×	41 0.9×	123 2.9×	47	880
Yaping Yang United States	17	440 0.9×	485 1.3×	48 0.3×	54 1.1×	61 1.4×	35	843
Krzysztof Szczałuba Poland	15	369 0.7×	328 0.9×	67 0.5×	37 0.8×	69 1.6×	57	638
Deborah Barbouth United States	11	412 0.8×	285 0.8×	183 1.3×	22 0.5×	85 2.0×	32	678
Melissa T. Carter Canada	16	326 0.7×	320 0.9×	103 0.7×	25 0.5×	75 1.7×	34	616
Gladys Ho Australia	19	855 1.7×	778 2.1×	219 1.5×	25 0.5×	67 1.6×	43	1.4k
H. Smeets Netherlands	11	360 0.7×	785 2.1×	88 0.6×	47 1.0×	76 1.8×	21	1.1k
Megan T. Cho United States	20	462 0.9×	508 1.4×	79 0.6×	30 0.6×	65 1.5×	27	838
Alexandra Afenjar France	16	621 1.3×	521 1.4×	69 0.5×	27 0.6×	113 2.6×	42	1.0k
Rossella Caselli Italy	15	607 1.2×	401 1.1×	139 1.0×	55 1.1×	68 1.6×	20	796

Countries citing papers authored by Marzia Pollazzon

Since Specialization

Citations

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

Fields of papers citing papers by Marzia Pollazzon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marzia Pollazzon

This figure shows the co-authorship network connecting the top 25 collaborators of Marzia Pollazzon. A scholar is included among the top collaborators of Marzia Pollazzon 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 Marzia Pollazzon. Marzia Pollazzon 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

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Carlotta Spagnoli, et al.. (2023). Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant – A Case Report and a Brief Review of the Literature. Molecular Syndromology. 15(1). 63–70. 2 indexed citations

Pollazzon, Marzia, Cecilia Mancini, Simone Pizzi, et al.. (2023). Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures. Frontiers in Neurology. 14. 1207176–1207176. 3 indexed citations

Bernardini, Laura, Marzia Pollazzon, Maria Grazia Giuffrida, et al.. (2023). Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes. 14(8). 1526–1526. 2 indexed citations

Bonasoni, Maria Paola, Giuseppina Comitini, Stefano Giuseppe Caraffi, et al.. (2023). Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings. Fetal and Pediatric Pathology. 42(6). 979–989. 1 indexed citations

Spagnoli, Carlotta, Daniele Frattini, Stefano Giuseppe Caraffi, et al.. (2023). Expanding Phenotype of SYT1-Related Neurodevelopmental Disorder: Case Report and Literature Review. Molecular Syndromology. 14(6). 493–497. 2 indexed citations

Rosato, Simonetta, Sheila Unger, Belinda Campos‐Xavier, et al.. (2022). Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features. Genes. 13(2). 261–261. 9 indexed citations

Caraffi, Stefano Giuseppe, Francesca Clementina Radio, Sabina Barresi, et al.. (2021). Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White–Sutton Syndrome: Case Report and Review of the Literature. Genes. 12(7). 950–950. 3 indexed citations

Pollazzon, Marzia, Stefano Giuseppe Caraffi, Silvia Faccioli, et al.. (2021). Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis. Genes. 13(1). 29–29. 10 indexed citations

Errichiello, Edoardo, Stefano Giuseppe Caraffi, Simonetta Rosato, et al.. (2020). Improving the phenotype description of Basel-Vanagaite-Smirin-Yosef syndrome, MED25-related: polymicrogyria as a distinctive neuroradiological finding. Neurogenetics. 22(1). 19–25. 1 indexed citations

10.

Caraffi, Stefano Giuseppe, Ivan Ivanovski, Marzia Pollazzon, et al.. (2019). Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6. Genes. 10(10). 799–799. 15 indexed citations

11.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Elisa Magnani, et al.. (2019). Alazami syndrome: the first case of papillary thyroid carcinoma. Journal of Human Genetics. 65(2). 133–141. 15 indexed citations

12.

Ivanovski, Ivan, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.. (2018). Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes. American Journal of Medical Genetics Part A. 176(5). 1166–1174. 13 indexed citations

13.

Ivanovski, Ivan, Olivera Djurić, Stefano Giuseppe Caraffi, et al.. (2018). Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 34–34. 4 indexed citations

14.

Pollazzon, Marzia, Simonetta Rosato, Ivan Ivanovski, et al.. (2018). Complex cranio-vertebral malformation: disruption sequence or iniencephaly?. Clinical Dysmorphology. 27(3). 105–108.

15.

Artuso, Rosangela, Filomena Tiziana Papa, Elisa Grillo, et al.. (2011). Investigation of modifier genes within copy number variations in Rett syndrome. Journal of Human Genetics. 56(7). 508–515. 27 indexed citations

16.

Katzaki, Eleni, Gilles Morin, Marzia Pollazzon, et al.. (2010). Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients. American Journal of Medical Genetics Part A. 152A(7). 1711–1717. 19 indexed citations

17.

Pollazzon, Marzia, Salvatore Grosso, Filomena Tiziana Papa, et al.. (2009). A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb. European Journal of Medical Genetics. 52(2-3). 131–133. 16 indexed citations

18.

Pollazzon, Marzia, Tiina Suominen, Sini Penttilä, et al.. (2009). The first Italian family with tibial muscular dystrophy caused by a novel titin mutation. Journal of Neurology. 257(4). 575–579. 40 indexed citations

19.

Ariani, Francesca, Joussef Hayek, Rosangela Artuso, et al.. (2008). FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome. The American Journal of Human Genetics. 83(1). 89–93. 297 indexed citations

20.

Mencarelli, Maria Antonietta, Eleni Katzaki, Filomena Tiziana Papa, et al.. (2008). Private inherited microdeletion/microduplications: Implications in clinical practice. European Journal of Medical Genetics. 51(5). 409–416. 53 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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