Benjamin Kamien

1.0k total citations
19 papers, 228 citations indexed

About

Benjamin Kamien is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Benjamin Kamien has authored 19 papers receiving a total of 228 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Benjamin Kamien's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Benjamin Kamien is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Benjamin Kamien collaborates with scholars based in Australia, United Kingdom and Canada. Benjamin Kamien's co-authors include Tracy Dudding‐Byth, Michael T. Gabbett, Vicki Gibbs, Janice M. Fullerton, John A. Lawson, James Harraway, Rani Sachdev, Michael Cardamone, Anna Heath and Ben Lundie and has published in prestigious journals such as Neurology, BMJ Open and Genetics in Medicine.

In The Last Decade

Benjamin Kamien

18 papers receiving 215 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Benjamin Kamien Australia 9 128 124 42 20 14 19 228
Yannis Duffourd France 7 201 1.6× 125 1.0× 38 0.9× 13 0.7× 15 1.1× 8 266
Konstantina Kosma Greece 10 137 1.1× 130 1.0× 37 0.9× 21 1.1× 21 1.5× 30 288
Riina Žordania Estonia 12 140 1.1× 182 1.5× 66 1.6× 16 0.8× 15 1.1× 25 350
Yoko Hiraki Japan 10 131 1.0× 97 0.8× 22 0.5× 21 1.1× 14 1.0× 17 219
Elaine M. Pereira United States 8 100 0.8× 68 0.5× 35 0.8× 18 0.9× 12 0.9× 24 191
Yannis Duffourd France 10 132 1.0× 115 0.9× 24 0.6× 17 0.8× 8 0.6× 25 221
Tracy Dudding‐Byth Australia 10 146 1.1× 147 1.2× 37 0.9× 17 0.8× 24 1.7× 18 272
Juliette Piard France 10 121 0.9× 151 1.2× 16 0.4× 15 0.8× 16 1.1× 24 253
Dhanya Lakshmi Narayanan India 10 88 0.7× 135 1.1× 22 0.5× 19 0.9× 8 0.6× 42 261
Magdalena Bartnik Poland 10 168 1.3× 140 1.1× 56 1.3× 8 0.4× 19 1.4× 23 266

Countries citing papers authored by Benjamin Kamien

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Benjamin Kamien

This figure shows the co-authorship network connecting the top 25 collaborators of Benjamin Kamien. A scholar is included among the top collaborators of Benjamin Kamien 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 Benjamin Kamien. Benjamin Kamien is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Barnett, Christopher F., Mary‐Louise Freckmann, Matthew F. Hunter, et al.. (2024). Critically unwell infants and children with mitochondrial disorders diagnosed by ultrarapid genomic sequencing. Genetics in Medicine. 27(1). 101293–101293. 1 indexed citations
2.
Steel, Dora, Federica Rachele Danti, Benjamin Kamien, et al.. (2023). Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants. Neurology. 100(21). e2214–e2223. 1 indexed citations
3.
Misceo, Doriana, Inger‐Lise Mero, Arvind Y. M. Sundaram, et al.. (2023). Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome. Genes. 14(11). 1985–1985. 1 indexed citations
4.
Kamien, Benjamin, Joshua S. Clayton, Elyshia McNamara, et al.. (2022). Bi-allelic MYH3 loss-of-function variants cause a lethal form of contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B. Neuromuscular Disorders. 32(5). 445–449. 3 indexed citations
5.
Li, Dong, Rebecca C. Ahrens‐Nicklas, Janice Baker, et al.. (2020). The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?. American Journal of Medical Genetics Part A. 182(9). 2058–2067. 14 indexed citations
6.
Ong, Royston, Samantha Edwards, Denise Howting, et al.. (2019). Study protocol of a multicentre cohort pilot study implementing an expanded preconception carrier-screening programme in metropolitan and regional Western Australia. BMJ Open. 9(6). e028209–e028209. 5 indexed citations
7.
Vilain, Ricardo E., et al.. (2019). Fatal Exsanguination Following Rupture of an Iliac Artery Aneurysm in an Infant With Menkes Disease. Pediatric and Developmental Pathology. 22(5). 486–491.
8.
Kamien, Benjamin, Anne Ronan, Gemma Poke, et al.. (2018). A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing. Molecular Syndromology. 9(2). 70–82. 32 indexed citations
9.
Kamien, Benjamin, et al.. (2018). A sibling study of isolated optic neuropathy associated with novel variants in the ACO2 gene. Ophthalmic Genetics. 39(5). 648–651. 9 indexed citations
10.
Beygo, Jasmin, Benjamin Kamien, Jill Clayton‐Smith, et al.. (2017). Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literature. American Journal of Medical Genetics Part A. 173(3). 753–757. 18 indexed citations
11.
Wong, Keith, Randal X. Moldrich, Matthew F. Hunter, et al.. (2015). A familial 7q36.3 duplication associated with agenesis of the corpus callosum. American Journal of Medical Genetics Part A. 167(9). 2201–2208. 7 indexed citations
12.
Kamien, Benjamin, M. Cristina Digilio, Antonio Novelli, et al.. (2015). Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions. European Journal of Medical Genetics. 58(11). 629–633. 6 indexed citations
13.
Brueton, Louise, Jenny Morton, Dominic McMullan, et al.. (2015). Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders. European Journal of Human Genetics. 24(3). 373–380. 48 indexed citations
14.
Kamien, Benjamin, et al.. (2014). Outfoxed by RBFOX1‐A caution about ascertainment bias. American Journal of Medical Genetics Part A. 164(6). 1411–1418. 9 indexed citations
15.
Kamien, Benjamin, James Harraway, Ben Lundie, et al.. (2013). Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy. American Journal of Medical Genetics Part A. 164(3). 782–788. 33 indexed citations
16.
Kamien, Benjamin, Michael Cardamone, John A. Lawson, & Rani Sachdev. (2012). A genetic diagnostic approach to infantile epileptic encephalopathies. Journal of Clinical Neuroscience. 19(7). 934–941. 19 indexed citations
17.
Kamien, Benjamin, Andreas Zankl, & Michael T. Gabbett. (2010). Septo‐optic dysplasia and associations with amyoplasia and gastroschisis. Birth Defects Research Part A Clinical and Molecular Teratology. 88(6). 497–501. 12 indexed citations
18.
Kamien, Benjamin & Michael T. Gabbett. (2009). Aicardi syndrome associated with hepatoblastoma and pulmonary sequestration. American Journal of Medical Genetics Part A. 149A(8). 1850–1852. 4 indexed citations
19.
Kamien, Benjamin & Linda Harris. (2007). Twin troubles – rickets causing myelofibrosis. Journal of Paediatrics and Child Health. 43(7-8). 573–575. 6 indexed citations

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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