Marie Doherty

1.2k citations
8 papers · 804 · 1 hit paper · h-index 6

Impact in

  • Hematology top 5%
    • Hemophilia Treatment and Research
    • Blood Coagulation and Thrombosis Mechanisms
  • Genetics top 10%
    • Hemoglobinopathies and Related Disorders
    • Animal Genetics and Reproduction

Papers in

Marie Doherty

8 papers receiving 766 citations

Marie Doherty's Hit Papers

An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences 1987 · 676 citations
6760+13+26Years since publication200400600

Peers

Marie Doherty
Comparison fields: 5 of 93
  • Hematology 204
  • Genetics 117
  • Genetics 201
  • Molecular Biology 384
  • Transplantation 9
Replace Floor Weerkamp with:
Floor Weerkamp Netherlands
L d'Auriol France
Shivkumar Venkatasubrahmanyam United States
M. J. Hobart United Kingdom
Shigeki Mitsunaga Japan
J. H. Stimpfling United States
Kevin Macon United States
James P.S. Yang United States
Joanne Luider Canada
Véronique Pancré France
Marie Doherty relative to Floor Weerkamp Netherlands Floor Weerkamp's profile →
Citations per field
00.5×4.5×
Floor Weerkamp · 1×
Citations per year

Countries citing papers authored by Marie Doherty

Since Specialization
Citations

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

Fields of papers citing papers by Marie Doherty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 17 scholars most cited alongside Marie Doherty, 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 Marie Doherty Line = papers co-authored together Marie Doherty links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1
An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences
Hit paper breakdown →
1987676
2 198752
3 197136
4 198813
5 197712
6 198811
7 20073
8 20091

About Marie Doherty

Marie Doherty is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Hematology, Surgery and Genetics, having authored 8 papers that have together received 804 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (2 papers), Hemophilia Treatment and Research (1 paper), Nursing education and management (1 paper), Nursing Diagnosis and Documentation (1 paper), Cancer-related gene regulation (1 paper), Streptococcal Infections and Treatments (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Congenital Anomalies and Fetal Surgery (1 paper). The work is most often cited by research in Hematology (204 citations), Genetics (117 citations), Genetics (201 citations), Molecular Biology (384 citations) and Transplantation (9 citations). Marie Doherty has collaborated with scholars based in United States and Italy. Frequent co-authors include Scott C. Kogan, Jane Gitschier, Nicholas L. Petrakis, T Tuveri, Antonio Cao, R. Galanello, Mario Pirastu, Yuet Wai Kan, Jane Gitschier and Sophie Smith. Their work appears in journals such as Obstetrical & Gynecological Survey, Proceedings of the National Academy of Sciences, New England Journal of Medicine, Acta Haematologica and Journal for Nurses in Staff Development.

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