Laura Roos

996 citations
19 papers · 382 · h-index 9

Impact in

Papers in

    • Genetic Syndromes and Imprinting 2
    • Ocular Disorders and Treatments 2
    • Genetics and Neurodevelopmental Disorders 1
    • Nutrition, Genetics, and Disease 1
    • BRCA gene mutations in cancer 1
    • Prenatal Screening and Diagnostics 3

Laura Roos

18 papers receiving 371 citations

Peers

Laura Roos
Comparison fields: 5 of 61
  • Obstetrics and Gynecology 48
  • Pediatrics, Perinatology and Child Health 104
  • Reproductive Medicine 27
  • Genetics 91
  • Ophthalmology 20
Replace Mahmoud Aarabi with:
Mahmoud Aarabi United States
Sunayna Best United Kingdom
M. L. Martínez‐Frías Spain
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Estelle Dubruc Switzerland
J Battin France
Naohiro Kanayama Japan
Bojana Brajenović‐Milić Croatia
Elliott G. Richards United States
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Citations per field
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Citations per year

Countries citing papers authored by Laura Roos

Since Specialization
Citations

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

Fields of papers citing papers by Laura Roos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Laura Roos, 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 Laura Roos Line = papers co-authored together Laura Roos links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1 2018183
2 200828
3 201325
4 201624
5 201823
6 202319
7 202017
8 201711
9 20189
10 20158
11 20218
12 20227
13 20216
14 20205
15 20223
16 20213
17 20192
18
[Preimplantation genetic testing for aneuploidy].
20191
19 20250

About Laura Roos

Laura Roos is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Molecular Biology and Pathology and Forensic Medicine, having authored 19 papers that have together received 382 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers), Ocular Disorders and Treatments (2 papers), Ectopic Pregnancy Diagnosis and Management (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Nutrition, Genetics, and Disease (1 paper), BRCA gene mutations in cancer (1 paper) and Neuroendocrine Tumor Research Advances (1 paper). The work is most often cited by research in Obstetrics and Gynecology (48 citations), Pediatrics, Perinatology and Child Health (104 citations), Reproductive Medicine (27 citations), Genetics (91 citations) and Ophthalmology (20 citations). Laura Roos has collaborated with scholars based in Denmark, Germany and Italy. Frequent co-authors include C. K. Ekelund, Line Elmerdahl Frederiksen, Andreas Ernst, L Lauridsen, Cecilia Høst Ramlau‐Hansen, Nis Brix, Karen Grønskov, Zeynep Tümer, Hanne Jensen and Line Kessel. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Acta Obstetricia Et Gynecologica Scandinavica, Journal of Cataract & Refractive Surgery and Ultrasound in Obstetrics and Gynecology.

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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