MARCELLO SINISCALCO
MARCELLO SINISCALCO publishes mostly in Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health, on topics such as Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities and Hemoglobinopathies and Related Disorders.
- World rank
- #953,554 of 7,710,434 ranked researchers
- Rank in United States
- #312,835 of 1,627,098
- Works
- 153
- Citations
- 3.5k
- Citations per work
- 22.7
What does MARCELLO SINISCALCO research?
MARCELLO SINISCALCO's work is mostly in Biochemistry, Genetics and Molecular Biology (52%), Medicine (18%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences7951.6%
- Everything else4730.6%
- Health Sciences2717.8%
- Medicine2717.8%
- 1Molecular Biology28% of their works
- 2Genetics24% of their works
- 3Pediatrics, Perinatology and Child Health7% of their works
- 4Genetics5% of their works
- 5Physiology3% of their works
- 6Hematology3% of their works
Research topics
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Hemoglobinopathies and Related Disorders
- Neonatal Health and Biochemistry
- Biochemical and Molecular Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- CRISPR and Genetic Engineering
- RNA modifications and cancer
Which keywords describe MARCELLO SINISCALCO's research?
The keywords of their largest research topics: Fragile X Syndrome, Rett Syndrome, Copy Number Variation, Genomic Rearrangements, Glucose-6-Phosphate Dehydrogenase Deficiency, Neonatal Jaundice, Sickle-cell Disease and Thalassemia.
- m6A-seq
- RNA-Guided
- X Chromosome Inactivation
- Nucleotide Metabolism
- Thalassemia
- Neonatal Jaundice
- Genomic Rearrangements
- Rett Syndrome
- Fragile X Syndrome
- Copy Number Variation
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Sickle-cell Disease
- Enzyme Regulation
- Sex Determination
- Genome Engineering
- RNA methylation
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.
All 16 words, with their numbers
- Fragile X Syndrome221 topic
- Rett Syndrome221 topic
- Copy Number Variation151 topic
- Genomic Rearrangements151 topic
- Glucose-6-Phosphate Dehydrogenase Deficiency141 topic
- Neonatal Jaundice141 topic
- Sickle-cell Disease141 topic
- Thalassemia141 topic
- Enzyme Regulation131 topic
- Nucleotide Metabolism131 topic
- Sex Determination121 topic
- X Chromosome Inactivation121 topic
- Genome Engineering91 topic
- RNA-Guided91 topic
- RNA methylation81 topic
- m6A-seq81 topic
Where does MARCELLO SINISCALCO work?
MARCELLO SINISCALCO's main affiliation in the publication record is Kettering University, United States.
How many publications and citations does MARCELLO SINISCALCO have?
OpenAlex counts 153 works and 3,475 citations for MARCELLO SINISCALCO, an h-index of 32, ranking #953,554 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised citation excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
Discussion
Ask a question or share a note about MARCELLO SINISCALCO. Keep it to the research: no personal attacks, advertising or links. Any reader can report a post, which collapses it for everyone until it is opened.