Chris Amos

3.6k total citations · 1 hit paper
20 papers, 1.6k citations indexed

About

Chris Amos is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Chris Amos has authored 20 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Chris Amos's work include Hepatitis C virus research (3 papers), DNA Repair Mechanisms (2 papers) and Chronic Lymphocytic Leukemia Research (2 papers). Chris Amos is often cited by papers focused on Hepatitis C virus research (3 papers), DNA Repair Mechanisms (2 papers) and Chronic Lymphocytic Leukemia Research (2 papers). Chris Amos collaborates with scholars based in United States, Lebanon and United Kingdom. Chris Amos's co-authors include Jennifer M. Bailey, David W. Stockton, Olga Zhuchenko, Penelope E. Bonnen, Huda Y. Zoghbi, Tetsuo Ashizawa, Cheng Chi Lee, S. H. Subramony, William B. Dobyns and Sherri J. Bale and has published in prestigious journals such as Nature Genetics, PLoS ONE and Cancer.

In The Last Decade

Chris Amos

20 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

1997 1.2k citations Olga Zhuchenko, Jennifer M. Bailey et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chris Amos United States	11	1.1k	1.1k	421	225	140	20	1.6k
Peter Sillevis Smitt Netherlands	22	636 0.6×	705 0.7×	1.5k 3.6×	478 2.1×	103 0.7×	48	2.4k
Vesa Juvonen Finland	22	433 0.4×	1.2k 1.1×	244 0.6×	137 0.6×	132 0.9×	43	1.7k
Kathleen A. Leppig United States	23	507 0.5×	662 0.6×	310 0.7×	681 3.0×	95 0.7×	57	2.0k
Bastien Joubert France	28	500 0.5×	415 0.4×	2.0k 4.8×	352 1.6×	79 0.6×	104	2.6k
Cécile Cazeneuve France	24	314 0.3×	975 0.9×	518 1.2×	115 0.5×	69 0.5×	44	1.9k
Jean‐Christophe Antoine France	25	454 0.4×	302 0.3×	1.7k 4.1×	327 1.5×	98 0.7×	64	2.1k
B. de Leeuw Netherlands	16	368 0.3×	532 0.5×	742 1.8×	297 1.3×	150 1.1×	26	1.5k
Loreto Martorell Spain	22	735 0.7×	1.0k 0.9×	333 0.8×	366 1.6×	55 0.4×	73	1.4k
Roberta Vitaliani Italy	15	383 0.4×	301 0.3×	1.8k 4.2×	394 1.8×	62 0.4×	27	1.9k
L. J. Rubinstein United States	21	267 0.2×	550 0.5×	480 1.1×	74 0.3×	70 0.5×	32	1.6k

Countries citing papers authored by Chris Amos

Since Specialization

Citations

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

Fields of papers citing papers by Chris Amos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chris Amos

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

All Works

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20 of 20 papers shown

Kuo, Dick, Lorraine R. Reitzel, Susan Parker, et al.. (2024). Self-Collection for Primary HPV Testing: Acceptability in a Large Urban Emergency Department. Annals of Emergency Medicine. 85(3). 249–257. 1 indexed citations

McDonald, Malcolm F., Ethan B. Ludmir, Shlomit Yust‐Katz, et al.. (2023). Prevalence of pathogenic germline variants in adult-type diffuse glioma. Neuro-Oncology Practice. 10(5). 482–490. 1 indexed citations

Kanwal, Fasiha, Sumeet K. Asrani, Aaron P. Thrift, et al.. (2022). The Texas collaborative center for hepatocellular cancer: Reducing liver cancer mortality in Texas through coordination, collaboration and advocacy. Frontiers in Oncology. 12. 953933–953933. 1 indexed citations

Seguin‐Fowler, Rebecca A., Chris Amos, Bettina M. Beech, et al.. (2022). The Texas Community-Engagement Research Alliance Against COVID-19 in Disproportionately Affected Communities (TX CEAL) Consortium. Journal of Clinical and Translational Science. 6(1). e64–e64. 9 indexed citations

Channa, Roomasa, Kyungmoo Lee, Kristen A. Staggers, et al.. (2021). Detecting retinal neurodegeneration in people with diabetes: Findings from the UK Biobank. PLoS ONE. 16(9). e0257836–e0257836. 13 indexed citations

Oluyomi, Abiodun, et al.. (2021). COVID-19 Community Incidence and Associated Neighborhood-Level Characteristics in Houston, Texas, USA. International Journal of Environmental Research and Public Health. 18(4). 1495–1495. 20 indexed citations

Whitworth, Kristina W., Chris Amos, Marisa Estarlich, et al.. (2021). Air pollution, residential greenness and metabolic dysfunction during early pregnancy in the INfancia y Medio Ambiente (INMA) Cohort. ISEE Conference Abstracts. 2021(1). 1 indexed citations

Havrda, Matthew C., Myung Chang Lee, Linton T. Evans, et al.. (2019). Characterizing the heterogeneity in 5-aminolevulinic acid–induced fluorescence in glioblastoma. Journal of neurosurgery. 132(6). 1706–1714. 13 indexed citations

Bayraktar, Soley, Laura M. Amendola, Angelica M. Gutierrez‐Barrera, et al.. (2014). Clinicopathologic characteristics of breast cancer in BRCA-carriers and non-carriers in women 35 years of age or less. The Breast. 23(6). 770–774. 20 indexed citations

10.

Eyre, Stephen, John Bowes, Anne Barton, et al.. (2012). Fine mapping in over 14,000 rheumatoid arthritis cases and 18,500 controls refines associations to known loci, indicates multiple independent affects and reveals novel associations. Lara D. Veeken. 51. 50–50. 1 indexed citations

11.

Liu, Qian, Jinyun Chen, Chris Amos, et al.. (2010). Abstract B52: MicroRNAs and SEL1L gene regulation in human pancreatic ductal adenocarcinoma. Cancer Prevention Research. 3(1_Supplement). B52–B52. 1 indexed citations

12.

Uyei, Anne, Susan K. Peterson, Julie Erlichman, et al.. (2006). Association between clinical characteristics and risk‐reduction interventions in women who underwent BRCA1 and BRCA2 testing. Cancer. 107(12). 2745–2751. 57 indexed citations

13.

Derom, Cathérine, Damini Jawaheer, Wei V. Chen, et al.. (2005). Genome-wide linkage scan for spontaneous DZ twinning. European Journal of Human Genetics. 14(1). 117–122. 15 indexed citations

14.

Bosken, Carol H., Ying‐Chin Ko, Sanjay Shete, et al.. (2001). Adaptations of Linkage and Association Methods for the Study of Asthma, A Complex Trait. Genetic Epidemiology. 21(S1). S89–96. 2 indexed citations

15.

Cash, Joseph M., et al.. (1998). Familial clustering of rheumatoid arthritis with other autoimmune diseases. Human Genetics. 103(4). 475–482. 105 indexed citations

16.

Zhuchenko, Olga, Jennifer M. Bailey, Penelope E. Bonnen, et al.. (1997). Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel. Nature Genetics. 15(1). 62–69. 1240 indexed citations breakdown →

17.

Duvic, Madeleine, et al.. (1995). Analysis of HLA-D Locus Alleles in Alopecia Areata Patients and Families. Journal of Investigative Dermatology. 104(5). 5–6. 38 indexed citations

18.

Rubin, Laurence A., Chris Amos, Judith A. Wade, et al.. (1994). Investigating the genetic basis for ankylosing spondylitis. Linkage studies with the major histocompatibility complex region. Arthritis & Rheumatism. 37(8). 1212–1220. 76 indexed citations

19.

Caporaso, Neil E., Jean Whitehouse, Pablo Bertín, et al.. (1991). A 20 Year Clinical and Laboratory Study of Familial B-Chronic Lymphocytic Leukemia in a Single Kindred. Leukemia & lymphoma. 3(5-6). 331–342. 9 indexed citations

20.

George, Varghese, et al.. (1987). Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree. Genetic Epidemiology. 4(4). 267–275. 19 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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