John Chamberlin

412 total citations
16 papers, 288 citations indexed

About

John Chamberlin is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, John Chamberlin has authored 16 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in John Chamberlin's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (3 papers) and Cancer-related molecular mechanisms research (3 papers). John Chamberlin is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (3 papers) and Cancer-related molecular mechanisms research (3 papers). John Chamberlin collaborates with scholars based in United States, South Korea and Ethiopia. John Chamberlin's co-authors include R.E. Magenis, E.W. Lovrien, Timothy F. Brady, D. James Harris, Michael L. Begleiter, Janice S. Lee, Michelle Angrish, Younghee Lee, Bonnie R. Joubert and Timothy A. Donlon and has published in prestigious journals such as Genome Research, Human Genetics and Frontiers in Oncology.

In The Last Decade

John Chamberlin

14 papers receiving 265 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John Chamberlin United States	8	161	110	107	74	19	16	288
Philip Tedder United Kingdom	6	102 0.6×	45 0.4×	198 1.9×	30 0.4×	19 1.0×	7	276
Kathy Klinger United States	5	159 1.0×	149 1.4×	84 0.8×	69 0.9×	17 0.9×	5	265
José Ramón Hernández Mora Spain	13	78 0.5×	86 0.8×	234 2.2×	85 1.1×	20 1.1×	15	345
Congjian Xu China	9	76 0.5×	76 0.7×	107 1.0×	38 0.5×	70 3.7×	18	221
Osamu Miyoshi Japan	11	116 0.7×	74 0.7×	176 1.6×	37 0.5×	16 0.8×	22	278
Anna Ruggeri Italy	10	197 1.2×	255 2.3×	122 1.1×	31 0.4×	45 2.4×	13	402
R.H. Martin Canada	9	253 1.6×	125 1.1×	167 1.6×	149 2.0×	18 0.9×	11	435
James H. Crichton United Kingdom	9	88 0.5×	68 0.6×	270 2.5×	109 1.5×	16 0.8×	10	363
Liangwen Zhong China	9	77 0.5×	30 0.3×	210 2.0×	38 0.5×	33 1.7×	14	321
S Dhanjal United Kingdom	8	198 1.2×	258 2.3×	80 0.7×	30 0.4×	8 0.4×	10	354

Countries citing papers authored by John Chamberlin

Since Specialization

Citations

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

Fields of papers citing papers by John Chamberlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Chamberlin

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

All Works

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16 of 16 papers shown

Chamberlin, John, Austin E. Gillen, & Aaron R. Quinlan. (2024). Improved characterization of 3′ single-cell RNA-seq libraries with paired-end avidity sequencing. NAR Genomics and Bioinformatics. 6(4). lqae175–lqae175.

Carswell, Gleta, John Chamberlin, Brian D. Bennett, Pierre R. Bushel, & Brian N. Chorley. (2024). Persistent gene expression and DNA methylation alterations linked to carcinogenic effects of dichloroacetic acid. Frontiers in Oncology. 14. 1389634–1389634.

Chamberlin, John, Younghee Lee, Gábor Marth, & Aaron R. Quinlan. (2024). Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experiments. Genome Research. 34(2). 179–188. 3 indexed citations

Jin, Young‐Joo, et al.. (2020). Differential alternative splicing between hepatocellular carcinoma with normal and elevated serum alpha-fetoprotein. BMC Medical Genomics. 13(S11). 194–194. 6 indexed citations

Jin, Young‐Joo, Seonggyun Han, John Chamberlin, et al.. (2019). Differential alternative splicing regulation among hepatocellular carcinoma with different risk factors. BMC Medical Genomics. 12(S8). 175–175. 13 indexed citations

Mortensen, Holly M., John Chamberlin, Bonnie R. Joubert, et al.. (2018). Leveraging human genetic and adverse outcome pathway (AOP) data to inform susceptibility in human health risk assessment. Mammalian Genome. 29(1-2). 190–204. 22 indexed citations

Chamberlin, John, et al.. (2017). The Impact of Virtualized Technology on Undergraduate Computer Networking Education. 109–114. 6 indexed citations

Chamberlin, John, et al.. (1993). Mitigating rate impacts of DSM programs. The Electricity Journal. 6(9). 46–56. 4 indexed citations

Harris, D. James, et al.. (1982). Parental trisomy 21 mosaicism.. PubMed. 34(1). 125–33. 31 indexed citations

10.

Magenis, Ellen, Michael G. Brown, John Chamberlin, et al.. (1981). Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: Confirmation of suspected 12p12.3 intraband by deletion dosage effect of LDHB. American Journal of Medical Genetics. 9(2). 95–103. 25 indexed citations

11.

Chamberlin, John & R.E. Magenis. (1980). Parental origin of de novo chromosome rearrangements. Human Genetics. 53(3). 343–347. 59 indexed citations

12.

Chamberlin, John, et al.. (1979). The 8p- syndrome. Human Genetics. 47(2). 135–140. 19 indexed citations

13.

Magenis, R.E., et al.. (1978). Exclusion of glutathione reductase from 8pter→8p22 and localization to 8p21. Cytogenetic and Genome Research. 22(1-6). 446–448. 7 indexed citations

14.

Magenis, R.E., et al.. (1978). Linkage relationships of HLA and a familial chromosome 6 inversion (pter→p23::q23→p23::q23→qter): lack of dose effect in duplication-deficient offspring. Cytogenetic and Genome Research. 22(1-6). 418–420. 5 indexed citations

15.

Magenis, R.E., et al.. (1977). Parental origin of the extra chromosome in Down's syndrome. Human Genetics. 37(1). 7–16. 65 indexed citations

16.

Magenis, R.E., et al.. (1976). Cytogenetic darkroom magic: now you see them, now you don't.. PubMed. 28(4). 417–9. 23 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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