Walter Just

3.1k citations
55 papers · 1.6k · h-index 24

Impact in

  • Genetics top 2%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic diversity and population structure
    • Animal Genetics and Reproduction
    • Sexual Differentiation and Disorders

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 21
    • Genetic diversity and population structure 5
    • Sexual Differentiation and Disorders 10
    • Glycosylation and Glycoproteins Research 6

Walter Just

55 papers receiving 1.6k citations

Peers

Walter Just
Comparison fields: 5 of 99
  • Genetics 827
  • Molecular Biology 816
  • Reproductive Medicine 92
  • Cell Biology 188
  • Neurology 151
Replace Peter G. Farlie with:
Peter G. Farlie Australia
Eric Bellefroid Belgium
Wilbur R. Harrison United States
Mario R. Capecchi United States
Giorgio Bernardi France
Brian A. Parr United States
Michel Cohen‐Tannoudji France
Paul J. Scotting United Kingdom
Angela Maria Vianna‐Morgante Brazil
Catherine Ziller France
Walter Just relative to Peter G. Farlie Australia Peter G. Farlie's profile →
Citations per field
00.5×3.9×
Peter G. Farlie · 1×
Citations per year

Countries citing papers authored by Walter Just

Since Specialization
Citations

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

Fields of papers citing papers by Walter Just

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1999119
2 1991115
3 1995103
4 199393
5 199592
6 200064
7 200062
8 200756
9 201556
10 199852
11 199748
12 202046
13 201346
14 199945
15 199543
16 200740
17 201634
18 199332
19 201332
20 199627

About Walter Just

Walter Just is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Neurology, having authored 55 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Sexual Differentiation and Disorders (10 papers), Chromosomal and Genetic Variations (8 papers), Glycosylation and Glycoproteins Research (6 papers), Head and Neck Anomalies (6 papers), Amyotrophic Lateral Sclerosis Research (5 papers), Proteoglycans and glycosaminoglycans research (5 papers) and Genetic diversity and population structure (5 papers). The work is most often cited by research in Genetics (827 citations), Molecular Biology (816 citations), Reproductive Medicine (92 citations), Cell Biology (188 citations) and Neurology (151 citations). Walter Just has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Walther Vogel, H. Hameister, I. Reisert, U. Vetter, Marian F. Young, Larry W. Fisher, Christof Pilgrim, Annette Baumstark, John D. Termine and Anne‐Marie Heegaard. Their work appears in journals such as Human Genetics, Chromosome Research, Human Molecular Genetics, Hereditas and Mammalian Genome.

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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