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Researcher · Reproductive Genetics Institute · United States

Yury Verlinsky

Yury Verlinsky 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 Assisted Reproductive Technology and Twin Pregnancy.

OpenAlex
World rank
#1,075,557
of 7,710,434 ranked researchers
Rank in United States
#348,812
of 1,627,098
Works
237
Citations
8.7k
Citations per work
36.7
h-index
53
i10-index 132Top 1.6% in Pediatrics, Perinatology and Child Health
Yury Verlinsky

What does Yury Verlinsky research?

Yury Verlinsky's work is mostly in Medicine (52%), Biochemistry, Genetics and Molecular Biology (29%).

Health Sciences: 122 works · 51.5% of their workMedicine: 122 works · 51.5% of their workPediatrics, Perinatology and Child Health: 88 works · 37.3% of their workPublic Health, Environmental and Occupational Health: 15 works · 6.4% of their workSurgery: 14 works · 5.9% of their workGenetics: 5 works · 1.9% of their workLife Sciences: 70 works · 29.4% of their workBiochemistry, Genetics and Molecular Biology: 70 works · 29.4% of their workGenetics: 38 works · 16.2% of their workMolecular Biology: 31 works · 13.2% of their workEverything else: 45 works · 19.1% of their workTHEIR WORKYury Verlinsky237works
Life Sciences29%Health Sciences52%

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
    1. Medicine12251.5%
    1. Biochemistry, Genetics and Molecular Biology7029.4%
  3. Everything else4519.1%
  1. 1Pediatrics, Perinatology and Child Health37% of their works
  2. 2Genetics16% of their works
  3. 3Molecular Biology13% of their works
  4. 4Public Health, Environmental and Occupational Health6% of their works
  5. 5Surgery6% of their works
  6. 6Genetics2% of their works

Research topics

Which keywords describe Yury Verlinsky's research?

The keywords of their largest research topics: Prenatal Diagnosis, Aneuploidy Screening, Maternal Plasma DNA Sequencing, Copy Number Variation, Genomic Rearrangements, Congenital Anomalies, Assisted Reproductive Technology and In Vitro Fertilization.

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 19 words, with their numbers
  1. Prenatal Diagnosis1952 topics
  2. Aneuploidy Screening1671 topic
  3. Maternal Plasma DNA Sequencing1671 topic
  4. Copy Number Variation521 topic
  5. Genomic Rearrangements521 topic
  6. Congenital Anomalies482 topics
  7. Assisted Reproductive Technology471 topic
  8. In Vitro Fertilization471 topic
  9. Pluripotent Stem Cells422 topics
  10. Genomic Imprinting351 topic
  11. Parental Influence351 topic
  12. Fertility Preservation331 topic
  13. Ovarian Tissue Cryopreservation331 topic
  14. Gastroschisis281 topic
  15. Omphalocele281 topic
  16. Embryonic Stem Cells221 topic
  17. Induced Pluripotent Stem Cells221 topic
  18. Kidney Organoids201 topic
  19. Nephrogenesis201 topic

Where does Yury Verlinsky work?

Yury Verlinsky's main affiliation in the publication record is Reproductive Genetics Institute, United States.

How many publications and citations does Yury Verlinsky have?

OpenAlex counts 237 works and 8,699 citations for Yury Verlinsky, an h-index of 53, ranking #1,075,557 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.

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