D E Rooney

796 citations
15 papers · 673 · h-index 10

Impact in

    • Prenatal Screening and Diagnostics
    • Fetal and Pediatric Neurological Disorders
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

D E Rooney

14 papers receiving 637 citations

Peers

D E Rooney
Comparison fields: 5 of 72
  • Pediatrics, Perinatology and Child Health 236
  • Genetics 266
  • Hematology 67
  • Genetics 42
  • Developmental Biology 8
Replace Rolf‐Dieter Wegner with:
Rolf‐Dieter Wegner Germany
Nataline B. Kardon United States
J.D. Singer United Kingdom
Silvana Guerneri Italy
Paolo Guanciali Franchi Italy
Sara Kaffe United States
Elena Kolomietz Canada
E. Orye Belgium
H. D. Hager Germany
Lydia E. McMorrow United States
D E Rooney relative to Rolf‐Dieter Wegner Germany Rolf‐Dieter Wegner's profile →
Citations per field
00.5×1.6×
Rolf‐Dieter Wegner · 1×
Citations per year

Countries citing papers authored by D E Rooney

Since Specialization
Citations

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

Fields of papers citing papers by D E Rooney

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D E Rooney. 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 D E Rooney. The network helps show where D E Rooney may publish in the future.

Co-authors

The 19 scholars most cited alongside D E Rooney, 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 D E Rooney Line = papers co-authored together D E Rooney links everyone, so they are left out of the graph.

All Works

15 of 15 papers shown
#Work
1
Human cytogenetics : a practical approach
1986317
2 1994112
3 200154
4 199135
5 198935
6 199923
7 199121
8
Human Chromosome Preparation: Essential Techniques
199719
9
Malignancy and acquired abnormalities
199217
10 198916
11
Human cytogenetics : essential data
19949
12 19929
13 20105
14
Constitutional analysis : a practical approach
20011
15
Malignancy and acquired abnormalities : a practical approach
20010

About D E Rooney

D E Rooney is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Surgery, Molecular Biology and Infectious Diseases, having authored 15 papers that have together received 673 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers), Congenital Anomalies and Fetal Surgery (3 papers), Genetic Syndromes and Imprinting (3 papers), Genomics and Chromatin Dynamics (1 paper), Acute Myeloid Leukemia Research (1 paper), Epigenetics and DNA Methylation (1 paper) and Acute Lymphoblastic Leukemia research (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (236 citations), Genetics (266 citations), Hematology (67 citations), Genetics (42 citations) and Developmental Biology (8 citations). D E Rooney has collaborated with scholars based in United Kingdom, Canada and Saudi Arabia. Frequent co-authors include Barbara Czepulkowski, Jackie Wolstenholme, E. V. Davison, F. E. Loeffler, R. W. Beard, George Rebello, D. V. Coleman, Charlie Gray, Gerald Hackett and JA Smith. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, American Journal of Medical Genetics, Medical Entomology and Zoology and BMJ.

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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