R Pallotta

1.3k total citations
30 papers, 914 citations indexed

About

R Pallotta is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R Pallotta has authored 30 papers receiving a total of 914 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R Pallotta's work include Ocular Disorders and Treatments (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Prenatal Screening and Diagnostics (4 papers). R Pallotta is often cited by papers focused on Ocular Disorders and Treatments (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Prenatal Screening and Diagnostics (4 papers). R Pallotta collaborates with scholars based in Italy, United States and United Kingdom. R Pallotta's co-authors include Bruno Dallapiccola, Paolo Sbraccia, Antoine Muchir, Giuseppe Novelli, Maria Rosaria D’Apice, Luciano Merlini, Francesca Capon, Federica Sangiuolo, Gisèle Bonne and Renato Lauro and has published in prestigious journals such as Radiology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

R Pallotta

30 papers receiving 895 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R Pallotta Italy 11 633 369 88 83 75 30 914
K Imaizumi Japan 15 566 0.9× 404 1.1× 88 1.0× 143 1.7× 50 0.7× 27 885
Stephanie Spranger Germany 14 509 0.8× 606 1.6× 80 0.9× 70 0.8× 46 0.6× 34 860
Muriel Rigolet France 12 662 1.0× 347 0.9× 170 1.9× 70 0.8× 125 1.7× 24 948
Yangzhu Du United States 13 611 1.0× 366 1.0× 54 0.6× 76 0.9× 90 1.2× 20 979
J G Lesko United States 12 383 0.6× 274 0.7× 308 3.5× 93 1.1× 55 0.7× 15 805
Shu C. Yau United Kingdom 10 399 0.6× 335 0.9× 270 3.1× 79 1.0× 93 1.2× 15 719
Ana Elisa C. Billerbeck Brazil 23 1.1k 1.7× 747 2.0× 67 0.8× 108 1.3× 34 0.5× 53 1.5k
Cathy Holding United Kingdom 12 599 0.9× 180 0.5× 147 1.7× 79 1.0× 89 1.2× 38 878
Ghazala Mirza United Kingdom 18 552 0.9× 714 1.9× 120 1.4× 47 0.6× 70 0.9× 20 1.1k
B. Rafael Elejalde United States 15 357 0.6× 467 1.3× 230 2.6× 122 1.5× 29 0.4× 39 833

Countries citing papers authored by R Pallotta

Since Specialization
Citations

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

Fields of papers citing papers by R Pallotta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Pallotta

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

All Works

20 of 20 papers shown
1.
Loke, Johnny, Alexander Pearlman, Orietta Radi, et al.. (2013). Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling. Human Molecular Genetics. 23(4). 1073–1083. 64 indexed citations
2.
Avnet, Sofia, R Pallotta, Francesca Perut, et al.. (2011). Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(7). 711–718. 27 indexed citations
3.
Pallotta, R, et al.. (2007). A case of multiple vertebral segmentation defects, unilateral renal agenesis, and an unusual ‘Cooley-like’ hand appearance. Clinical Dysmorphology. 16(3). 157–161. 1 indexed citations
4.
Domizio, Silvia Di, R Pallotta, Angela Romanelli, et al.. (2006). A Case of Smith-Lemli-Opitz Syndrome, Defect of Cholesterol Biosynthesis. International Journal of Immunopathology and Pharmacology. 19(2). 439–442. 2 indexed citations
5.
Celentano, Claudio, Raffaella Zannolli, Sabrina Buoni, et al.. (2005). Classical lissencephaly associated with dolichocephaly, hair and nail defect. Brain and Development. 28(6). 392–394. 1 indexed citations
6.
Pallotta, R, Ines Bucci, Claudio Celentano, Marco Liberati, & U Bellati. (2004). The ‘skipped generation’ phenomenon in a family with renal agenesis. Ultrasound in Obstetrics and Gynecology. 24(5). 586–587. 6 indexed citations
7.
Novelli, Giuseppe, Antoine Muchir, Federica Sangiuolo, et al.. (2002). Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C. The American Journal of Human Genetics. 71(2). 426–431. 402 indexed citations
8.
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
9.
Pallotta, R, et al.. (2000). Occurrence of Dandy-Walker anomaly in a familial case of distal arthogryposis type IIB. American Journal of Medical Genetics. 95(5). 477–481. 9 indexed citations
10.
Zollino, Marcella, Cristina Di Stefano, Giuseppe Zampino, et al.. (2000). Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. American Journal of Medical Genetics. 94(3). 254–261. 125 indexed citations
11.
Pallotta, R, et al.. (1999). Kyphomelic Dysplasia: Clinical and Radiologic Long-term Follow-up of One Case and Review of the Literature. Radiology. 212(3). 847–852. 8 indexed citations
12.
Sabatino, Giuseppe, Alberto Verrotti, Maria De Martino, et al.. (1999). Neonatal suppurative parotitis: a study of five cases. European Journal of Pediatrics. 158(4). 312–314. 45 indexed citations
13.
Verrotti, Alberto, L. Lobefalo, Francesco Chiarelli, et al.. (1997). Lipids and lipoproteins in diabetic adolescents and young adults with retinopathy. Eye. 11(6). 876–881. 9 indexed citations
14.
Pallotta, R, et al.. (1996). Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome. Clinical Genetics. 50(5). 411–416. 4 indexed citations
15.
Ramer, Jeanette C., Angela E. Lin, William B. Dobyns, et al.. (1995). Previously apparently undescribed syndrome: Shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation. American Journal of Medical Genetics. 57(3). 403–409. 82 indexed citations
16.
Pallotta, R. (1991). Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.. Journal of Medical Genetics. 28(5). 342–344. 12 indexed citations
17.
Pallotta, R, et al.. (1989). Dermatoglyphics in von Recklinghausen neurofibromatosis. American Journal of Medical Genetics. 34(2). 233–236. 8 indexed citations
18.
Pallotta, R, et al.. (1988). The Unreliability of Metacarpo-Phalangeal Profile (MPP) in the Diagnosis of Achondroplasia. PubMed. 48. 179–181. 1 indexed citations
19.
Pallotta, R. (1985). Genetic counseling in anophthalmia. Ophthalmic Paediatrics and Genetics. 6(1-2). 99–102. 3 indexed citations
20.
Pallotta, R & Bruno Dallapiccola. (1984). A syndrome with true anophthalmia, hand-foot defects and mental retardation. Ophthalmic Paediatrics and Genetics. 4(1). 19–23. 10 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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