Rita Mingarelli
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Developmental Biology top 5%
Papers in
- Genetics 62
- Genomic variations and chromosomal abnormalities 27
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Congenital Ear and Nasal Anomalies 8
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- Congenital heart defects research 25
- Hedgehog Signaling Pathway Studies 6
- Co-authors
- Bruno Dallapiccola (91 shared papers)M. Cristina Digilio (18 shared papers)Anna Sárközy (9 shared papers)Antonio Pizzuti (7 shared papers)Bruno Marino (8 shared papers)Giuseppe Novelli (19 shared papers)Aldo Giannotti (23 shared papers)Marco Castori (5 shared papers)
- Journals
- Clinical Genetics (9 papers)Journal of Medical Genetics (9 papers)Human Genetics (8 papers)European Journal of Human Genetics (7 papers)Human Mutation (5 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Rita Mingarelli
112 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 107
- Genetics 1.0k
- Developmental Biology 62
- Rheumatology 295
- Molecular Biology 1.3k
- Immunology 372
Countries citing papers authored by Rita Mingarelli
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
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-authors
The 25 scholars most cited alongside Rita Mingarelli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 113 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 272 | |
| 2 | 2005 | 145 | |
| 3 | 1995 | 94 | |
| 4 | 2006 | 87 | |
| 5 | 2009 | 86 | |
| 6 | 2004 | 81 | |
| 7 | 1993 | 78 | |
| 8 | 1998 | 74 | |
| 9 | 2001 | 74 | |
| 10 | 2002 | 74 | |
| 11 | Widening of a Y-chromosome interval-6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to the RBM1 and DAZ genes. | 1996 | 53 |
| 12 | 2013 | 50 | |
| 13 | 2005 | 47 | |
| 14 | 1998 | 47 | |
| 15 | 1996 | 45 | |
| 16 | 2009 | 41 | |
| 17 | 1994 | 41 | |
| 18 | 1995 | 40 | |
| 19 | Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome. | 1996 | 39 |
| 20 | 2004 | 38 |
About Rita Mingarelli
Rita Mingarelli is a scholar working on Genetics, Molecular Biology, Epidemiology, Pulmonary and Respiratory Medicine and Surgery, having authored 113 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Congenital heart defects research (25 papers), Congenital Heart Disease Studies (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Chromosomal and Genetic Variations (11 papers), Prenatal Screening and Diagnostics (10 papers), Congenital Ear and Nasal Anomalies (8 papers) and Hedgehog Signaling Pathway Studies (6 papers). The work is most often cited by research in Genetics (1.0k citations), Developmental Biology (62 citations), Rheumatology (295 citations), Molecular Biology (1.3k citations) and Immunology (372 citations). Rita Mingarelli has collaborated with scholars based in Italy, United States and Germany. Frequent 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. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Human Genetics, European Journal of Human Genetics and Human Mutation.
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.