Barbara Kellam

1.5k citations
14 papers · 993 · 1 hit paper · h-index 11

Impact in

  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Genomics and Rare Diseases 5
    • Genetics and Neurodevelopmental Disorders 4
    • Autism Spectrum Disorder Research 3
    • Hearing Loss and Rehabilitation 1

Barbara Kellam

14 papers receiving 962 citations

Barbara Kellam's Hit Papers

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder 2017 · 617 citations
6170+3+6Years since publication200400600

Peers

Barbara Kellam
Comparison fields: 5 of 92
  • Genetics 554
  • Cognitive Neuroscience 339
  • Aging 12
  • Molecular Biology 399
  • Pediatrics, Perinatology and Child Health 87
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Barbara Kellam relative to Daniel J. Weiner United States Daniel J. Weiner's profile →
Citations per field
00.5×2×2.8×
Daniel J. Weiner · 1×
Citations per year

Countries citing papers authored by Barbara Kellam

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Kellam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

14 of 14 papers shown
#Work
1
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Hit paper breakdown →
2017617
2 2019130
3 201842
4 200839
5 201937
6 201822
7 202121
8 201719
9 201418
10 200113
11 202011
12 20209
13 20198
14 20087

About Barbara Kellam

Barbara Kellam is a scholar working on Genetics, Cognitive Neuroscience, Pharmacy, Molecular Biology and Cancer Research, having authored 14 papers that have together received 993 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers), Epigenetics and DNA Methylation (2 papers), Congenital heart defects research (2 papers), Infant Development and Preterm Care (1 paper) and Hearing Loss and Rehabilitation (1 paper). The work is most often cited by research in Genetics (554 citations), Cognitive Neuroscience (339 citations), Aging (12 citations), Molecular Biology (399 citations) and Pediatrics, Perinatology and Child Health (87 citations). Barbara Kellam has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include Jatinder J. S. Bhatia, Stephen W. Scherer, Dimitri James Stavropoulos, Susan D. Walker, Jill Hamilton, Matthew J. Gazzellone, Rosanna Weksberg, Jeremy R Parr, Cheryl S. Cytrynbaum and Thanuja Selvanayagam. Their work appears in journals such as Journal of Pediatric Nursing, Brain, Human Genetics, Journal of Neurodevelopmental Disorders and npj Genomic Medicine.

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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