J.A. Böök

1.7k citations
49 papers · 1.3k · 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

J.A. Böök

44 papers receiving 980 citations

Peers

J.A. Böök
Comparison fields: 5 of 119
  • Genetics 568
  • Developmental Biology 43
  • Psychiatry and Mental health 179
  • Pediatrics, Perinatology and Child Health 198
  • Biological Psychiatry 25
Replace N.E. Morton with:
N.E. Morton United States
Charles P. Miles United States
S. Walker United Kingdom
Johannes Nielsen Denmark
Robert Roger Lebel United States
Beate Glaser United Kingdom
Christopher N. Herndon United States
Marlene J. Huggins Canada
Uwe Menzel Sweden
P.A. Jacobs United Kingdom
J.A. Böök relative to N.E. Morton United States N.E. Morton's profile →
Citations per field
00.5×2×3×4.3×
N.E. Morton · 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 49 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1960201
2 1978130
3 1953109
4 196099
5
A genetic and neuropsychiatric investigation of a North-Swedish population. with special regard to schizophrenia and mental deficiency.
195375
6 195764
7 196160
8 195649
9 195347
10 196345
11 195142
12 196136
13 196432
14 196230
15 196225
16 196124
17 197322
18 196918
19 197516
20 197913

About J.A. Böök

J.A. Böök is a scholar working on Genetics, Molecular Biology, Ecology, Evolution, Behavior and Systematics, General Social Sciences and Plant Science, having authored 49 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Botanical Research and Chemistry (4 papers), Prenatal Screening and Diagnostics (3 papers), Gestational Trophoblastic Disease Studies (3 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Bipolar Disorder and Treatment (2 papers). The work is most often cited by research in Genetics (568 citations), Developmental Biology (43 citations), Psychiatry and Mental health (179 citations), Pediatrics, Perinatology and Child Health (198 citations) and Biological Psychiatry (25 citations). J.A. Böök has collaborated with scholars based in Sweden, Poland and Hungary. Frequent co-authors include Berta Santesson, Lennart Wetterberg, PER ZETTERQVIST, M. Fraccaro, B. Kjessler, K. H. Gustavson, P.A. Jacobs, Hermann Joseph Muller, ALBERT LEVAN and T. C. Hsü. Their work appears in journals such as Hereditas, Human Heredity, The Lancet, Clinical Genetics and Acta Paediatrica.

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