Jean Amos

1.9k total citations
24 papers, 1.3k citations indexed

About

Jean Amos is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Jean Amos has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pulmonary and Respiratory Medicine, 7 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Jean Amos's work include Cystic Fibrosis Research Advances (13 papers), Tracheal and airway disorders (5 papers) and Genomics and Rare Diseases (4 papers). Jean Amos is often cited by papers focused on Cystic Fibrosis Research Advances (13 papers), Tracheal and airway disorders (5 papers) and Genomics and Rare Diseases (4 papers). Jean Amos collaborates with scholars based in United States, United Kingdom and Russia. Jean Amos's co-authors include Aubrey Milunsky, Robert D. Oates, Christopher F. Hoth, Clinton T. Baldwin, Elias O. Da‐Silva, Michael Dean, Marga Belle White, Mark Leppert, Bernard Gerrard and Claudia Stewart and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Jean Amos

24 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jean Amos United States 11 565 487 418 123 95 24 1.3k
John E. Mickle United States 11 499 0.9× 841 1.7× 161 0.4× 92 0.7× 94 1.0× 12 1.4k
Lucia Bartoloni Italy 19 724 1.3× 814 1.7× 834 2.0× 80 0.7× 191 2.0× 38 1.9k
Marie Legendre France 23 741 1.3× 503 1.0× 583 1.4× 65 0.5× 97 1.0× 82 1.6k
Paolo Simi Italy 22 633 1.1× 201 0.4× 571 1.4× 127 1.0× 138 1.5× 82 1.4k
Shalini N. Jhangiani United States 25 1.1k 1.9× 128 0.3× 801 1.9× 116 0.9× 115 1.2× 80 2.0k
Güven Lüleci Türkiye 21 750 1.3× 99 0.2× 808 1.9× 166 1.3× 286 3.0× 110 1.7k
Edmond G. Lemire Canada 14 240 0.4× 142 0.3× 202 0.5× 66 0.5× 76 0.8× 42 616
Naomi Fitch Canada 22 479 0.8× 81 0.2× 585 1.4× 95 0.8× 186 2.0× 44 1.1k
Corinne Gehrig Switzerland 19 983 1.7× 175 0.4× 648 1.6× 17 0.1× 157 1.7× 28 1.7k
Thomas A. Maher United States 13 270 0.5× 137 0.3× 147 0.4× 30 0.2× 58 0.6× 23 586

Countries citing papers authored by Jean Amos

Since Specialization
Citations

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

Fields of papers citing papers by Jean Amos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean Amos

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

All Works

20 of 20 papers shown
1.
Patnaik, Madhumita, Jeffrey S. Dlott, Robert N. Fontaine, et al.. (2004). Detection of Genomic Polymorphisms Associated with Venous Thrombosis Using the Invader Biplex Assay. Journal of Molecular Diagnostics. 6(2). 137–144. 25 indexed citations
2.
Amos, Jean, et al.. (2004). Development and integration of molecular genetic tests into clinical practice: the US experience. Expert Review of Molecular Diagnostics. 4(4). 465–477. 10 indexed citations
3.
Amos, Jean, et al.. (2003). Cystic Fibrosis. PubMed. 120(suppl_1). S3–S13. 5 indexed citations
4.
Amos, Jean, et al.. (2002). Commercial molecular diagnostics in the U.S.: The Human Genome Project to the clinical laboratory. Human Mutation. 19(4). 324–333. 31 indexed citations
5.
Richards, Carolyn Sue, Linda Bradley, Jean Amos, et al.. (2002). Standards and Guidelines for CFTR Mutation Testing. Genetics in Medicine. 4(5). 379–391. 90 indexed citations
6.
Amos, Jean & Bert Gold. (1998). Testing environment for single-gene disorders in U.S. reference laboratories. Human Mutation. 12(5). 293–300. 10 indexed citations
7.
Sawyer, Susan M., et al.. (1996). Pulmonary Function and Clinical Observations in Men With Congenital Bilateral Absence of the Vas Deferens. CHEST Journal. 110(2). 440–445. 39 indexed citations
8.
Oates, Robert D. & Jean Amos. (1994). The Genetic Basis of Congenital Bilateral Absence of the Vas Deferens and Cystic Fibrosis. Journal of Andrology. 15(1). 1–8. 140 indexed citations
9.
Risch, Neil, Bernard Lerer, Richard E. Straub, et al.. (1993). Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigrees. Nature Genetics. 3(1). 49–55. 121 indexed citations
10.
Milunsky, Aubrey, et al.. (1993). 46,XY/47,XYY male with the fragile X syndrome: Cytogenetic and molecular studies. American Journal of Medical Genetics. 45(5). 589–593. 5 indexed citations
11.
Baldwin, Clinton T., Christopher F. Hoth, Jean Amos, Elias O. Da‐Silva, & Aubrey Milunsky. (1992). An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature. 355(6361). 637–638. 385 indexed citations
12.
Dean, Michael, Marga Belle White, Bernard Gerrard, Aubrey Milunsky, & Jean Amos. (1992). A 22-bp deletion in the coding region of the cystic fibrosis gene. Genomics. 13(1). 235–236. 7 indexed citations
13.
Milunsky, Aubrey, et al.. (1991). Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probes. American Journal of Obstetrics and Gynecology. 164(3). 751–755. 1 indexed citations
14.
Dean, Michael, Bernard Gerrard, Claudia Stewart, et al.. (1991). Identification of Cystic Fibrosis Mutations. Advances in experimental medicine and biology. 290. 45–51. 6 indexed citations
15.
Bejjani, Bassem A., et al.. (1991). The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD). Clinical Genetics. 39(4). 245–252. 3 indexed citations
16.
White, Marga Belle, et al.. (1990). A frame-shift mutation in the cystic fibrosis gene. Nature. 344(6267). 665–667. 92 indexed citations
17.
Dean, Michael, Marga Belle White, Jean Amos, et al.. (1990). Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients. Cell. 61(5). 863–870. 287 indexed citations
18.
Dean, Michael, P. O’Connell, Mark Leppert, et al.. (1987). Three additional DNA polymorphisms in the met gene and D7S8 locus: Use in prenatal diagnosis of cystic fibrosis. The Journal of Pediatrics. 111(4). 490–495. 29 indexed citations
19.
Amos, Jean, et al.. (1984). Relative argininosuccinate synthetase mRNA levels and gene copy number in canavanine-resistant lymphoblasts. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 782(3). 247–253. 10 indexed citations
20.
Amos, Jean. (1977). Anther culture and regeneration studies in four Arabidopsis species /. OhioLink ETD Center (Ohio Library and Information Network). 1 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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