J.A. Böök

1.8k citations
48 papers · 1.2k · h-index 18

Impact in

  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Associations and Epidemiology

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
    • Genomic variations and chromosomal abnormalities 4
    • Yeasts and Rust Fungi Studies 2

J.A. Böök

45 papers receiving 941 citations

Peers

J.A. Böök
Comparison fields: 5 of 117
  • Developmental Biology 42
  • Genetics 535
  • Psychiatry and Mental health 150
  • Pediatrics, Perinatology and Child Health 184
  • Biological Psychiatry 20
Replace Beverly J. White with:
Beverly J. White United States
Amanda Collins United Kingdom
Jennifer A. Donald Australia
Charles P. Miles United States
Ute Moog Germany
Johannes Nielsen Denmark
J Feingold France
S. Walker United Kingdom
Akira Morishima United States
S G Ratcliffe United Kingdom
J.A. Böök relative to Beverly J. White United States Beverly J. White's profile →
Citations per field
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Beverly J. White · 1×
Citations per year

Countries citing papers authored by J.A. Böök

Since Specialization
Citations

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

Fields of papers citing papers by J.A. Böök

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1960178
2 1978111
3 195397
4 196083
5
A genetic and neuropsychiatric investigation of a North-Swedish population. with special regard to schizophrenia and mental deficiency.
195366
6 195757
7 196153
8 195343
9 195643
10 195142
11 195942
12 196339
13 196429
14 196129
15 196227
16 196222
17 196122
18 197320
19 196916
20 197515

About J.A. Böök

J.A. Böök is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Pediatrics, Perinatology and Child Health, having authored 48 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers), Botanical Research and Chemistry (4 papers), Chromosomal and Genetic Variations (4 papers), Congenital Anomalies and Fetal Surgery (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Gestational Trophoblastic Disease Studies (3 papers) and Yeasts and Rust Fungi Studies (2 papers). The work is most often cited by research in Developmental Biology (42 citations), Genetics (535 citations), Psychiatry and Mental health (150 citations), Pediatrics, Perinatology and Child Health (184 citations) and Biological Psychiatry (20 citations). J.A. Böök has collaborated with scholars based in Sweden, Poland and Israel. Frequent co-authors include Berta Santesson, Lennart Wetterberg, PER ZETTERQVIST, M. Fraccaro, B. Kjessler, ALBERT LEVAN, Arthur Robinson, D.G. Harnden, E.H.Y. Chu and David A. Hungerford. Their work appears in journals such as Hereditas, Human Heredity, Acta Paediatrica, The Lancet and Clinical Genetics.

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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