F. J. Dill

1.3k citations
24 papers · 868 · h-index 15

Impact in

    • Prenatal Screening and Diagnostics
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Genomic variations and chromosomal abnormalities 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
    • Genetics and Neurodevelopmental Disorders 4
    • Genetic Syndromes and Imprinting 2
    • Sexual Differentiation and Disorders 2

F. J. Dill

24 papers receiving 786 citations

Peers

F. J. Dill
Comparison fields: 5 of 69
  • Pediatrics, Perinatology and Child Health 440
  • Genetics 528
  • Developmental Biology 28
  • Obstetrics and Gynecology 43
  • Hematology 43
Replace Avirachan T. Tharapel with:
Avirachan T. Tharapel United States
B. Rafael Elejalde United States
Walter Fuhrmann Germany
M. G. J. Jahoda Netherlands
M. Ray Canada
Isabel Lorda‐Sánchez Spain
Kamal K. Naguib Kuwait
Franz Binkert Switzerland
Kenneth L. Garver United States
Janice Matsuura United States
F. J. Dill relative to Avirachan T. Tharapel United States Avirachan T. Tharapel's profile →
Citations per field
00.5×1.5×
Avirachan T. Tharapel · 1×
Citations per year

Countries citing papers authored by F. J. Dill

Since Specialization
Citations

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

Fields of papers citing papers by F. J. Dill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. J. Dill. 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 F. J. Dill. The network helps show where F. J. Dill may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1983279
2 1987115
3 198148
4 198047
5 200141
6 198739
7 197939
8 198739
9 196428
10 198728
11 197628
12
Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos.
198122
13 198621
14 198018
15 199315
16 199213
17 200811
18 197011
19 199210
20 19736

About F. J. Dill

F. J. Dill is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Plant Science, having authored 24 papers that have together received 868 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (4 papers), Assisted Reproductive Technology and Twin Pregnancy (3 papers), Sexual Differentiation and Disorders (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (440 citations), Genetics (528 citations), Developmental Biology (28 citations), Obstetrics and Gynecology (43 citations) and Hematology (43 citations). F. J. Dill has collaborated with scholars based in Canada, United States and Tunisia. Frequent co-authors include DK Kalousek, Dagmar K. Kalousek, Barbara McGillivray, Betty J. Poland, Tapio Pantzar, R. Douglas Wilson, Siu Li Yong, Diana S. Herbst, Stephen Wood and James R. Miller. Their work appears in journals such as Human Genetics, The Journal of Pediatrics, Science, Clinical Genetics and Obstetrical & Gynecological Survey.

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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