Martina Putzová
Martina Putzová publishes mostly in Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology, on topics such as Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities and Neurogenetic and Muscular Disorders Research.
- World rank
- #6,594,148 of 7,710,434 ranked researchers
- Rank in Czechia
- #28,562 of 39,303
- Works
- 31
- Citations
- 236
- Citations per work
- 7.6
What does Martina Putzová research?
Martina Putzová's work is mostly in Medicine (37%), Biochemistry, Genetics and Molecular Biology (32%).
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
- Health Sciences1237.1%
- Medicine1237.1%
- Life Sciences1032.0%
- Everything else1030.9%
- 1Pediatrics, Perinatology and Child Health26% of their works
- 2Genetics14% of their works
- 3Molecular Biology13% of their works
- 4Genetics6% of their works
- 5Cancer Research5% of their works
- 6Public Health, Environmental and Occupational Health5% of their works
Research topics
- Prenatal Screening and Diagnostics
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Cancer Genomics and Diagnostics
- Hereditary Neurological Disorders
- Fetal and Pediatric Neurological Disorders
- Gestational Trophoblastic Disease Studies
- Genetic Syndromes and Imprinting
Which keywords describe Martina Putzová's research?
The keywords of their largest research topics: Prenatal Diagnosis, Cell-Free DNA, Aneuploidy Screening, Maternal Plasma DNA Sequencing, Copy Number Variation, Genomic Rearrangements, SMN1 and Spinal Muscular Atrophy.
- Parental Influence
- Mutational Signatures
- Hereditary Spastic Paraplegia
- Fetal MRI
- Cerebral Development
- Spinal Muscular Atrophy
- Genomic Rearrangements
- Maternal Plasma DNA Sequencing
- Cell-Free DNA
- Prenatal Diagnosis
- Aneuploidy Screening
- Copy Number Variation
- SMN1
- Cancer Genomics
- Charcot-Marie-Tooth Disease
- Gestational Trophoblastic Disease
- Hydatidiform Mole
- Genomic Imprinting
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.
All 18 words, with their numbers
- Prenatal Diagnosis223 topics
- Cell-Free DNA192 topics
- Aneuploidy Screening161 topic
- Maternal Plasma DNA Sequencing161 topic
- Copy Number Variation81 topic
- Genomic Rearrangements81 topic
- SMN151 topic
- Spinal Muscular Atrophy51 topic
- Cancer Genomics31 topic
- Cerebral Development31 topic
- Charcot-Marie-Tooth Disease31 topic
- Fetal MRI31 topic
- Gestational Trophoblastic Disease31 topic
- Hereditary Spastic Paraplegia31 topic
- Hydatidiform Mole31 topic
- Mutational Signatures31 topic
- Genomic Imprinting21 topic
- Parental Influence21 topic
Where does Martina Putzová work?
Martina Putzová's main affiliation in the publication record is Biopticka Laborator (Czechia), Czechia.
How many publications and citations does Martina Putzová have?
OpenAlex counts 31 works and 236 citations for Martina Putzová, an h-index of 7, ranking #6,594,148 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised 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.
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