Rita Mingarelli

4.2k total citations
113 papers, 2.6k citations indexed

About

Rita Mingarelli is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Rita Mingarelli has authored 113 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 57 papers in Molecular Biology and 21 papers in Epidemiology. Recurrent topics in Rita Mingarelli's work include Genomic variations and chromosomal abnormalities (28 papers), Congenital heart defects research (25 papers) and Congenital Heart Disease Studies (13 papers). Rita Mingarelli is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Congenital heart defects research (25 papers) and Congenital Heart Disease Studies (13 papers). Rita Mingarelli collaborates with scholars based in Italy, United States and Germany. Rita Mingarelli's co-authors include Bruno Dallapiccola, M. Cristina Digilio, Anna Sárközy, Antonio Pizzuti, Bruno Marino, Giuseppe Novelli, Aldo Giannotti, Marco Castori, Emanuela Conti and Giandomenico Palka and has published in prestigious journals such as Journal of the American College of Cardiology, The American Journal of Human Genetics and The American Journal of Cardiology.

In The Last Decade

Rita Mingarelli

112 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita Mingarelli Italy 28 1.4k 1.1k 419 384 317 113 2.6k
Suvimol Hill United States 37 1.4k 1.0× 875 0.8× 560 1.3× 925 2.4× 268 0.8× 59 4.4k
Peter Meinecke Germany 31 2.5k 1.7× 1.9k 1.7× 306 0.7× 154 0.4× 251 0.8× 105 4.0k
Philippe Duquesnoy France 37 2.1k 1.5× 1.3k 1.2× 735 1.8× 111 0.3× 399 1.3× 71 4.0k
Mark J. Pettenati United States 36 2.1k 1.5× 998 0.9× 397 0.9× 132 0.3× 299 0.9× 148 5.1k
V.J. Hyland Australia 25 893 0.6× 722 0.6× 469 1.1× 259 0.7× 126 0.4× 60 2.1k
Alessandro De Luca Italy 31 1.4k 1.0× 639 0.6× 195 0.5× 356 0.9× 640 2.0× 113 2.9k
Ahmad S. Teebi Canada 31 1.3k 0.9× 1.3k 1.2× 119 0.3× 172 0.4× 226 0.7× 111 3.2k
I D Young United Kingdom 26 1.9k 1.3× 2.1k 1.9× 160 0.4× 336 0.9× 147 0.5× 79 3.6k
Peter D. Turnpenny United Kingdom 35 1.7k 1.2× 1.4k 1.3× 503 1.2× 186 0.5× 303 1.0× 109 4.0k
Hülya Kayserili Türkiye 35 2.8k 1.9× 1.7k 1.5× 177 0.4× 170 0.4× 325 1.0× 152 4.4k

Countries citing papers authored by Rita Mingarelli

Since Specialization
Citations

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

Fields of papers citing papers by Rita Mingarelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Mingarelli

This figure shows the co-authorship network connecting the top 25 collaborators of Rita Mingarelli. A scholar is included among the top collaborators of Rita Mingarelli 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 Rita Mingarelli. Rita Mingarelli 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.
Dallapiccola, Bruno, et al.. (2009). A Nationwide Genetic Testing Survey in Italy, Year 2007. Genetic Testing and Molecular Biomarkers. 14(1). 17–22. 9 indexed citations
2.
Luca, Alessandro De, Anna Sárközy, Federica Consoli, et al.. (2009). Familial transposition of the great arteries caused by multiple mutations in laterality genes. Heart. 96(9). 673–677. 85 indexed citations
3.
Dentici, Maria Lisa, Francesco Brancati, Rita Mingarelli, & Bruno Dallapiccola. (2009). A 6-year-old child with Fryns syndrome: Further delineation of the natural history of the condition in survivors. European Journal of Medical Genetics. 52(6). 421–425. 3 indexed citations
4.
Douzgou, Sofia, Katarina Lehmann, Rita Mingarelli, Stefan Mundlos, & Bruno Dallapiccola. (2008). Compound heterozygosity for GDF5 in Du Pan type chondrodysplasia. American Journal of Medical Genetics Part A. 146A(16). 2116–2121. 15 indexed citations
5.
Bernardini, Laura, Marco Castori, Anna Capalbo, et al.. (2007). Syndromic craniosynostosis due to complex chromosome 5 rearrangement andMSX2gene triplication. American Journal of Medical Genetics Part A. 143A(24). 2937–2943. 27 indexed citations
6.
Sinibaldi, Lorenzo, Laura Bernardini, Roberto De Simone, et al.. (2007). Duplication 18q21.31‐q22.2. American Journal of Medical Genetics Part A. 143A(4). 343–348. 23 indexed citations
7.
Sárközy, Anna, et al.. (2006). Noonan's syndrome and related disorders: Clinical-molecular update and guidelines. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 32(3). 145–155. 3 indexed citations
8.
Castori, Marco, Francesco Brancati, Rosanna Rinaldi, et al.. (2006). Antenatal presentation of the oculo‐auriculo‐vertebral spectrum (OAVS). American Journal of Medical Genetics Part A. 140A(14). 1573–1579. 30 indexed citations
9.
Brancati, Francesco, M. Cristina Digilio, Anna Sárközy, et al.. (2004). KBG syndrome in a cohort of Italian patients. American Journal of Medical Genetics Part A. 131A(2). 144–149. 26 indexed citations
10.
Brancati, Francesco, Rita Mingarelli, & Bruno Dallapiccola. (2003). Recurrent triploidy of maternal origin. European Journal of Human Genetics. 11(12). 972–974. 23 indexed citations
11.
Capon, Francesca, Sabrina Semprini, Giuseppe Novelli, et al.. (2001). Fine Mapping of the PSORS4 Psoriasis Susceptibility Region on Chromosome 1q21. Journal of Investigative Dermatology. 116(5). 728–730. 74 indexed citations
12.
Calabrese, G, Donatella Fantasia, Elisena Morizio, et al.. (2000). Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation. Bone Marrow Transplantation. 26(10). 1125–1127. 7 indexed citations
13.
Palka, Giandomenico, Liborio Stuppia, Paolo Guanciali Franchi, et al.. (2000). Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri–Weill dyschondrosteosis. Clinical Genetics. 57(6). 449–453. 11 indexed citations
14.
Formigari, Roberto, et al.. (1996). Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot. The American Journal of Cardiology. 77(7). 505–508. 45 indexed citations
15.
Digilio, M. Cristina, Bruno Marino, Rita Mingarelli, et al.. (1996). Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11?. Journal of the American College of Cardiology. 27(2). 93–93. 1 indexed citations
16.
Mingarelli, Rita, et al.. (1996). Prenatal ultrasonographic findings of dominant polycystic kidney disease and postnatal renal evolution. American Journal of Medical Genetics. 65(4). 337–341. 7 indexed citations
17.
Mingarelli, Rita, et al.. (1995). Fetal translocation between chromosomes 2, 18, and 21 resolved by fish. Prenatal Diagnosis. 15(3). 278–281. 13 indexed citations
18.
Giannotti, Aldo, M. Cristina Digilio, Giuseppe Albertini, Rita Mingarelli, & Bruno Dallapiccola. (1995). Sporadic trichodental dysplasia with microcephaly and mental retardation. Clinical Dysmorphology. 4(4). 334–337. 2 indexed citations
19.
Mingarelli, Rita, et al.. (1994). Prenatal diagnosis of X‐linked retinitis pigmentosa (RP) in five pregnancies at risk. Prenatal Diagnosis. 14(4). 285–289. 1 indexed citations
20.
Martini, G. A., et al.. (1993). On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome. Prenatal Diagnosis. 13(8). 763–766. 14 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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