R F Mueller
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics 5
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Developmental Biology top 10%
- Congenital limb and hand anomalies 3
- Molecular Biology top 10%
- RNA regulation and disease 3
- Connexins and lens biology 2
- Endocrine and Autonomic Systems top 10%
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- Urological Disorders and Treatments 5
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- Pediatric Urology and Nephrology Studies 2
- Co-authors
- Anna MiddletonJenny HewisonJulian R. SampsonKaren OliverJames A. CookPer Halkjær NielsenGraham R. TaylorGulshan Karbani
- Journals
- Applied and Environmental Microbiology (1 paper)The American Journal of Human Genetics (3 papers)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesIreland
In The Last Decade
R F Mueller
27 papers receiving 1.4k citations
Hit Papers
Peers
Comparison fields: 5 of 130
- Sensory Systems 234
- Genetics 487
- Developmental Biology 27
- Molecular Biology 751
- Endocrine and Autonomic Systems 67
Countries citing papers authored by R F Mueller
This map shows the geographic impact of R F Mueller'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 R F Mueller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R F Mueller more than expected).
Fields of papers citing papers by R F Mueller
This network shows the impact of papers produced by R F Mueller. 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 R F Mueller. The network helps show where R F Mueller may publish in the future.
Co-authorship network
The 25 scholars most cited alongside R F Mueller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 16 | |
| 2 | 2002 | 41 | |
| 3 | 1999 | 37 | |
| 4 | 1999 | 51 | |
| 5 | 1998 | 126 | |
| 6 | 1998 | 14 | |
| 7 | Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild. | 1997 | 16 |
| 8 | 1997 | 31 | |
| 9 | 1997 | 4 | |
| 10 | 1997 | 8 | |
| 11 | 1997 | 91 | |
| 12 | 1997 | 1 | |
| 13 | 1996 | 37 | |
| 14 | A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. | 1996 | 37 |
| 15 | 1996 | 1 | |
| 16 | 1993 | 91 | |
| 17 | 1992 | 33 | |
| 18 | 1989 | 13 | |
| 19 | 1988 | 33 | |
| 20 | 1966 | 1 |
About R F Mueller
R F Mueller is a scholar working on Developmental Biology, Sensory Systems and Urology, having authored 28 papers that have together received 1.5k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), Urological Disorders and Treatments (5 papers), Congenital limb and hand anomalies (3 papers), RNA regulation and disease (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Connexins and lens biology (2 papers) and Pediatric Urology and Nephrology Studies (2 papers). The work is most often cited by research in Sensory Systems (234 citations), Genetics (487 citations) and Developmental Biology (27 citations). R F Mueller has collaborated with scholars based in United Kingdom, United States and Ireland. Frequent co-authors include Anna Middleton, Jenny Hewison, Julian R. Sampson, Karen Oliver, James A. Cook, Per Halkjær Nielsen, Graham R. Taylor, Gulshan Karbani, A. Caine and Nicholas Lench. Their work appears in journals such as Applied and Environmental Microbiology, The American Journal of Human Genetics and Human Molecular 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.