B. Biederman

411 citations
18 papers · 292 · h-index 11

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetics and Neurodevelopmental Disorders
    • Animal Genetics and Reproduction
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Chromosomal and Genetic Variations

Papers in

    • Genomic variations and chromosomal abnormalities 10
    • Animal Genetics and Reproduction 3
    • Genetic Mapping and Diversity in Plants and Animals 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Chromosomal and Genetic Variations 8

B. Biederman

17 papers receiving 260 citations

Peers

B. Biederman
Comparison fields: 5 of 43
  • Genetics 256
  • Plant Science 139
  • Pediatrics, Perinatology and Child Health 56
  • Developmental Biology 5
  • Molecular Biology 132
Replace Malcolm Parslow with:
Malcolm Parslow New Zealand
C.-L. Richer Canada
H.E. Wyandt United States
R H Smythe New Zealand
Carolyn Trunca United States
Christine A Joyce United Kingdom
M. Pierluigi Italy
Catherine Ozilou France
D R Romain New Zealand
Julie Leana‐Cox United States
B. Biederman relative to Malcolm Parslow New Zealand Malcolm Parslow's profile →
Citations per field
00.5×1.5×
Malcolm Parslow · 1×
Citations per year

Countries citing papers authored by B. Biederman

Since Specialization
Citations

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

Fields of papers citing papers by B. Biederman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 22 scholars most cited alongside B. Biederman, 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 B. Biederman Line = papers co-authored together B. Biederman links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 198055
2 197841
3 197729
4 198325
5
The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.
198525
6 197624
7 197819
8 198019
9 198014
10
Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect.
197610
11 198210
12 19827
13 19785
14 19813
15 19773
16 19792
17 19791
18 19760

About B. Biederman

B. Biederman is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 18 papers that have together received 292 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers), Prenatal Screening and Diagnostics (5 papers), Animal Genetics and Reproduction (3 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromatin Remodeling and Cancer (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (256 citations), Plant Science (139 citations), Pediatrics, Perinatology and Child Health (56 citations), Developmental Biology (5 citations) and Molecular Biology (132 citations). B. Biederman has collaborated with scholars based in Canada, United States and New Zealand. Frequent co-authors include Phyllis E. Bowen, Peter Bowen, Cheng‐Chieh Lin, A. B. Hawthorne, Robert B. Church, John M. Opitz, Ching‐Shwun Lin, Charlene M.T. Robertson, David Schiff and P. H. Fitzgerald. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Cancer, Journal of Intellectual Disability Research and Journal of Heredity.

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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