Rina Schmidt

492 citations
19 papers · 410 · h-index 11

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Dermatoglyphics and Human Traits
    • Genomics and Rare Diseases
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Genomic variations and chromosomal abnormalities 7
    • Dermatoglyphics and Human Traits 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genomics and Rare Diseases 1
    • Prenatal Screening and Diagnostics 3

Rina Schmidt

17 papers receiving 338 citations

Peers

Rina Schmidt
Comparison fields: 5 of 45
  • Developmental Biology 28
  • Genetics 258
  • Pediatrics, Perinatology and Child Health 61
  • Psychiatry and Mental health 35
  • Hematology 24
Replace G Filippi with:
G Filippi Italy
Kenneth W. Dumars United States
Elisabeth G. Kaveggia United States
Kimberly Grace United States
Grange S. Coffin United States
Allan Caine United Kingdom
Hironao Numabe Japan
Gordon S. Stephen United Kingdom
Marianne Verjaal Netherlands
Drew Duckett United Kingdom
Rina Schmidt relative to G Filippi Italy G Filippi's profile →
Citations per field
00.5×1.5×2.2×
G Filippi · 1×
Citations per year

Countries citing papers authored by Rina Schmidt

Since Specialization
Citations

This map shows the geographic impact of Rina Schmidt'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 Rina Schmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rina Schmidt more than expected).

Fields of papers citing papers by Rina Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rina Schmidt. 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 Rina Schmidt. The network helps show where Rina Schmidt may publish in the future.

Co-authors

The 23 scholars most cited alongside Rina Schmidt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rina Schmidt Line = papers co-authored together Rina Schmidt links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1 196694
2 197538
3 198137
4 197736
5 197631
6 197829
7 199929
8 197623
9 198721
10 197813
11 198112
12 197711
13 197210
14 19729
15 19768
16 19777
17 19661
18 19741
19 19840

About Rina Schmidt

Rina Schmidt is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Developmental Biology and Immunology, having authored 19 papers that have together received 410 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Dermatoglyphics and Human Traits (3 papers), Prenatal Screening and Diagnostics (3 papers), Down syndrome and intellectual disability research (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Reproductive System and Pregnancy (2 papers), Genomics and Rare Diseases (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Developmental Biology (28 citations), Genetics (258 citations), Pediatrics, Perinatology and Child Health (61 citations), Psychiatry and Mental health (35 citations) and Hematology (24 citations). Rina Schmidt has collaborated with scholars based in United States and Israel. Frequent co-authors include Harold M. Nitowsky, Hanna Dar, George A. Jervis, Arthur Falek, Ichiro Sekine, Lydia Eviatar, M Pajewski, Michael A. Pollack, Gerald S. Golden and Edna H. Sobel. Their work appears in journals such as Journal of Medical Genetics, Pediatric Research, Clinical Genetics, PEDIATRICS and The Lancet.

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.

Explore authors with similar magnitude of impact