J. Amos

1.1k citations
21 papers · 814 · h-index 12

Impact in

Papers in

J. Amos

21 papers receiving 777 citations

Peers

J. Amos
Comparison fields: 5 of 65
  • Pulmonary and Respiratory Medicine 363
  • Genetics 86
  • Sensory Systems 39
  • Genetics 189
  • Pediatrics, Perinatology and Child Health 105
Replace John E. Mickle with:
John E. Mickle United States
Joy B. Redman United States
Thomas A. Maher United States
Valère Cacheux France
Uta Grieshammer United States
Christopher R. Futtner United States
Olaf Rittinger Austria
Karin Writzl Slovenia
Nathalie Collot France
Junko Kanno Japan
J. Amos relative to John E. Mickle United States John E. Mickle's profile →
Citations per field
00.5×1.5×1.9×
John E. Mickle · 1×
Citations per year

Countries citing papers authored by J. Amos

Since Specialization
Citations

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

Fields of papers citing papers by J. Amos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside J. Amos, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J. Amos Line = papers co-authored together J. Amos links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1993335
2
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.
1992143
3 199590
4
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.
199153
5
Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling.
198927
6 199326
7
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
198825
8 200424
9 199122
10 201616
11 199116
12 197814
13 19808
14 19585
15
Correlation of the level of full-length CFTR transcript with pulmonary phenotype in patients carrying R117H and 1342-1,-2delAG mutations
19942
16 19912
17
DNA analysis of cystic fibrosis genotypes in relatives with equivocal sweat test results.
19902
18
Uniparental disomy (UPD) for fra(X) in a 47,XXY male
19941
19
[Polymorphism of restriction fragment length in the detection of the precise status of monosomy 21 in a deformed retarded girl].
19881
20 19601

About J. Amos

J. Amos is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Genetics, Physiology and Plant Science, having authored 21 papers that have together received 814 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (5 papers), Tracheal and airway disorders (4 papers), Neonatal Respiratory Health Research (3 papers), Tuberous Sclerosis Complex Research (3 papers), Genetic factors in colorectal cancer (2 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers), Plant Reproductive Biology (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (363 citations), Genetics (86 citations), Sensory Systems (39 citations), Genetics (189 citations) and Pediatrics, Perinatology and Child Health (105 citations). J. Amos has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include John E. Mickle, Robert D. Oates, Aubrey Milunsky, W. Edward Highsmith, Garry R. Cutting, C.S. Chu, Colin A. Graham, Siobhan M. Cashman, Ronald G. Crystal and David R. Witt. Their work appears in journals such as Annals of the New York Academy of Sciences, The American Journal of Human Genetics, Journal of Clinical Pathology, British Journal of Cancer and Nature 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.

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