Benjamin Kamien
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
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- Mitochondrial Function and Pathology 2
- Glycosylation and Glycoproteins Research 1
- Genetics 8
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 3
- Co-authors
- Michael T. Gabbett (2 shared papers)Tracy Dudding‐Byth (3 shared papers)Rani Sachdev (1 shared paper)Janice M. Fullerton (1 shared paper)Jenny Morton (1 shared paper)Michael Cardamone (1 shared paper)Louise Brueton (1 shared paper)Dominic McMullan (1 shared paper)
- Journals
- Birth Defects Research Part A Clinical and Molecular Teratology (1 paper)Neurology (1 paper)Genes (1 paper)BMJ Open (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Benjamin Kamien
19 papers receiving 228 citations
Peers
Comparison fields: 5 of 47
- Genetics 121
- Pediatrics, Perinatology and Child Health 35
- Molecular Biology 115
- Clinical Biochemistry 10
- Genetics 11
Countries citing papers authored by Benjamin Kamien
This map shows the geographic impact of Benjamin Kamien'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 Benjamin Kamien with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Benjamin Kamien more than expected).
Fields of papers citing papers by Benjamin Kamien
This network shows the impact of papers produced by Benjamin Kamien. 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 Benjamin Kamien. The network helps show where Benjamin Kamien may publish in the future.
Co-authors
The 25 scholars most cited alongside Benjamin Kamien, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 50 | |
| 2 | 2013 | 34 | |
| 3 | 2018 | 33 | |
| 4 | 2017 | 19 | |
| 5 | 2012 | 19 | |
| 6 | 2020 | 14 | |
| 7 | 2010 | 12 | |
| 8 | 2015 | 9 | |
| 9 | 2014 | 9 | |
| 10 | 2018 | 9 | |
| 11 | 2007 | 7 | |
| 12 | 2015 | 7 | |
| 13 | 2019 | 5 | |
| 14 | 2009 | 5 | |
| 15 | 2022 | 3 | |
| 16 | 2024 | 3 | |
| 17 | 2023 | 2 | |
| 18 | 2023 | 2 | |
| 19 | 2019 | 1 | |
| 20 | 2025 | 0 |
About Benjamin Kamien
Benjamin Kamien is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Genetics, having authored 20 papers that have together received 243 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), Prenatal Screening and Diagnostics (2 papers) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (121 citations), Pediatrics, Perinatology and Child Health (35 citations), Molecular Biology (115 citations), Clinical Biochemistry (10 citations) and Genetics (11 citations). Benjamin Kamien has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Michael T. Gabbett, Tracy Dudding‐Byth, Rani Sachdev, Janice M. Fullerton, Jenny Morton, Michael Cardamone, Louise Brueton, Dominic McMullan, John A. Lawson and Nicola Brunetti‐Pierri. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Neurology, Genes, BMJ Open and European Journal of Human Genetics.
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.