M. Siniscalco
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Hemoglobinopathies and Related Disorders 11
- Genomic variations and chromosomal abnormalities 10
- Virus-based gene therapy research 8
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Hemoglobinopathies and Related Disorders 11
- Genomic variations and chromosomal abnormalities 10
- Virus-based gene therapy research 8
- Hematology top 5%
-
- Neonatal Health and Biochemistry 12
- Clinical Biochemistry top 5%
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- Biochemical and Molecular Research 10
- CRISPR and Genetic Engineering 9
- Co-authors
- Cedric A. B. SmithG FilippiB LatteLuigi F. BerniniA RinaldiBecky AlhadeffSergio PiomelliP. Meera Khan
- Cited by
- GeneticsHematology
- Journals
- Cytogenetic and Genome Research (13 papers)Nature (8 papers)Proceedings of the National Academy of Sciences (8 papers)
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
M. Siniscalco
102 papers receiving 2.3k citations
Hit Papers
Peers
Comparison fields: 5 of 142
- Genetics 1.1k
- Genetics 316
- Hematology 294
- Pediatrics, Perinatology and Child Health 406
- Clinical Biochemistry 115
Countries citing papers authored by M. Siniscalco
This map shows the geographic impact of M. Siniscalco'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 M. Siniscalco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Siniscalco more than expected).
Fields of papers citing papers by M. Siniscalco
This network shows the impact of papers produced by M. Siniscalco. 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 M. Siniscalco. The network helps show where M. Siniscalco may publish in the future.
Co-authorship network
The 25 scholars most cited alongside M. Siniscalco, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 92 | |
| 2 | 2010 | 5 | |
| 3 | 2001 | 29 | |
| 4 | 1999 | 12 | |
| 5 | 1996 | 10 | |
| 6 | 1996 | 1 | |
| 7 | 1995 | 6 | |
| 8 | 1994 | 16 | |
| 9 | 1993 | 17 | |
| 10 | 1992 | 5 | |
| 11 | 1991 | 14 | |
| 12 | 1988 | 6 | |
| 13 | 1987 | 21 | |
| 14 | 1987 | 1 | |
| 15 | Abstracts of papers presented at the 51st Cold Spring Harbor Symposium on Quantitative Biology : molecular biology of Homo sapiens, May 28-June 4, 1986 | 1986 | 1 |
| 16 | Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes. | 1984 | 14 |
| 17 | 1967 | 32 | |
| 18 | 1964 | 100 | |
| 19 | 1963 | 0 | |
| 20 | 1962 | 5 |
About M. Siniscalco
M. Siniscalco is a scholar working on Genetics, Genetics and Horticulture, having authored 104 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (20 papers), Neonatal Health and Biochemistry (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Hemoglobinopathies and Related Disorders (11 papers), Biochemical and Molecular Research (10 papers), Genomic variations and chromosomal abnormalities (10 papers), CRISPR and Genetic Engineering (9 papers) and Virus-based gene therapy research (8 papers). The work is most often cited by research in Genetics (1.1k citations), Genetics (316 citations) and Hematology (294 citations). M. Siniscalco has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include Cedric A. B. Smith, G Filippi, B Latte, Luigi F. Bernini, A Rinaldi, Becky Alhadeff, Sergio Piomelli, P. Meera Khan, Michele Purrello and Karl‐Heinz Grzeschik. Their work appears in journals such as Cytogenetic and Genome Research, Nature, Proceedings of the National Academy of Sciences, Annals of Human Genetics and Human Heredity.
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.