Bernard Weisskopf

518 citations
21 papers · 386 indexed · h-index 12
Topics
Genomic variations and chromosomal abnormalities (3 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers)Fetal and Pediatric Neurological Disorders (3 papers)

In The Last Decade

Bernard Weisskopf

21 papers receiving 347 citations

Peers

Bernard Weisskopf
Comparison fields: 5 of 72
  • Genetics 161
  • Molecular Biology 127
  • Pediatrics, Perinatology and Child Health 116
  • Psychiatry and Mental health 38
  • Epidemiology 33
Replace W. Rosendahl with:
W. Rosendahl Germany
S Collyer United Kingdom
J.M. Limal France
LyttI. Gardner United States
R Prager-Lewin Israel
Johannes Nielsen Denmark
Dolores Saavedra Mexico
Brian Turner Armenia
Frank J. Gareis United States
W Zaleski Canada
Bernard Weisskopf relative to W. Rosendahl Germany W. Rosendahl's profile →
Citations per field
00.5×3.3×
W. Rosendahl · 1×
Citations per year

Countries citing papers authored by Bernard Weisskopf

Since Specialization
Citations

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

Fields of papers citing papers by Bernard Weisskopf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Weisskopf

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard Weisskopf. A scholar is included among the top collaborators of Bernard Weisskopf based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bernard Weisskopf. Bernard Weisskopf is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 5
2 2
3 29
4 1
5 22
6 11
7 17
8 77
9 17
10 11
11 10
12 31
13 6
14 26
15 16
16 4
17 28
18 16
19 4
20 41

About Bernard Weisskopf

Bernard Weisskopf is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 21 papers that have together received 386 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). The work is most often cited by research in Developmental Biology (13 citations), Pediatrics, Perinatology and Child Health (116 citations) and Genetics (161 citations). Bernard Weisskopf has collaborated with scholars based in United States, Qatar and Germany. Frequent co-authors include Joseph H. Hersh, George E. Rogers, Nuhad D. Dinno, Kenneth R. Swiatek, Marvin Cornblath, William C. Edwards, Laura Russell, Jane F. Donat, J. Edwin Seegmiller and Andrew W. Zimmerman. Their work appears in journals such as PEDIATRICS, Journal of the American Academy of Child & Adolescent Psychiatry and The Journal of Pediatrics.

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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