Rina Schmidt

572 citations
20 papers · 430 indexed · h-index 12
    • Congenital limb and hand anomalies 4
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities 5
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetic Syndromes and Imprinting 2
    • Genetics and Neurodevelopmental Disorders 2
    • Prenatal Screening and Diagnostics 5
    • Genomic variations and chromosomal abnormalities 5
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetic Syndromes and Imprinting 2
    • Genetics and Neurodevelopmental Disorders 2
  • Anatomy top 10%
    • Hedgehog Signaling Pathway Studies 2
    • RNA modifications and cancer 2

Rina Schmidt

18 papers receiving 391 citations

Peers

Rina Schmidt
Comparison fields: 5 of 58
  • Developmental Biology 39
  • Genetics 257
  • Pediatrics, Perinatology and Child Health 109
  • Genetics 32
  • Anatomy 4
Replace G. R. Stalder with:
G. R. Stalder Switzerland
L Y Hsu United States
Berta Santesson Sweden
Jürgen Herrmann United States
I D Young United Kingdom
Jean‐Louis Taillemite France
R. Rauskolb Germany
Drew Duckett United Kingdom
G. Bourrouillou France
P Colombiès France
Rina Schmidt relative to G. R. Stalder Switzerland G. R. Stalder's profile →
Citations per field
00.5×
G. R. Stalder · 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-authorship network

The 25 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

20 of 20 papers shown
#Work
1 199913
2 198722
3 19840
4 198135
5 198111
6 197828
7 197812
8 197734
9 197711
10 197621
11 19768
12 197627
13 197535
14 19741
15 197210
16 19729
17
Familial de Lange syndrome with chromosome abnormalities.
196680
18 196672
19 19661
20
[THE MUSCULI LUMBRICALES OF THE HUMAN FOOT].
19630

About Rina Schmidt

Rina Schmidt is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Hematology, having authored 20 papers that have together received 430 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Congenital limb and hand anomalies (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers), Hedgehog Signaling Pathway Studies (2 papers), RNA modifications and cancer (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Developmental Biology (39 citations), Genetics (257 citations), Pediatrics, Perinatology and Child Health (109 citations), Genetics (32 citations) and Anatomy (4 citations). Rina Schmidt has collaborated with scholars based in United States, Israel and Denmark. Frequent co-authors include George A. Jervis, Arthur Falek, Harold M. Nitowsky, Hanna Dar, Ichiro Sekine, Lydia Eviatar, M Pajewski, M Rosenblatt, Marty Kwok‐Shing Wong and Norman E. Leeds. Their work appears in journals such as Journal of Medical Genetics, Pediatric Research, Clinical Genetics, PEDIATRICS and JAMA.

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.

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