Marian L. Rivas
- Urology top 5%
- Biotechnology top 10%
- Enzyme Production and Characterization 3
- Nephrology top 10%
- Renal Diseases and Glomerulopathies 3
- Periodontics top 10%
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- Salivary Gland Disorders and Functions 3
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- Complement system in diseases 3
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- Metabolism and Genetic Disorders 2
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- Pancreatitis Pathology and Treatment 2
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- Amino Acid Enzymes and Metabolism 1
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- Genomics and Rare Diseases 1
- Co-authors
- A.D. MerrittRobert WyattH. Norman NoeJoseph PeedenR. C. NewellDavid BixlerP.M. ConneallyJewell C. Ward
- Cited by
- UrologyBiotechnologyNephrology
- Journals
- Cytogenetic and Genome Research (4 papers)The Journal of Pediatrics (3 papers)The Journal of Urology (1 paper)
- Partner nations
- United StatesItaly
In The Last Decade
Marian L. Rivas
22 papers receiving 491 citations
Peers
Comparison fields: 5 of 81
- Urology 103
- Biotechnology 59
- Nephrology 48
- Pediatrics, Perinatology and Child Health 124
- Periodontics 19
Countries citing papers authored by Marian L. Rivas
This map shows the geographic impact of Marian L. Rivas'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 Marian L. Rivas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marian L. Rivas more than expected).
Fields of papers citing papers by Marian L. Rivas
This network shows the impact of papers produced by Marian L. Rivas. 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 Marian L. Rivas. The network helps show where Marian L. Rivas may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Marian L. Rivas, 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 | 1996 | 19 | |
| 2 | 1995 | 7 | |
| 3 | 1992 | 14 | |
| 4 | 1992 | 108 | |
| 5 | 1991 | 7 | |
| 6 | 1990 | 20 | |
| 7 | 1990 | 4 | |
| 8 | 1990 | 31 | |
| 9 | 1989 | 9 | |
| 10 | RISK-XLR: A Microcomputer-Based Genetic Risk Program for X-Linked Recessive Traits | 1987 | 1 |
| 11 | Regionalization in hereditary IgA nephropathy. | 1987 | 24 |
| 12 | 1980 | 40 | |
| 13 | 1980 | 4 | |
| 14 | 1978 | 12 | |
| 15 | 1978 | 8 | |
| 16 | Genetic studies of human acidic salivary protein (Pa). | 1975 | 37 |
| 17 | Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. | 1973 | 29 |
| 18 | Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. | 1973 | 85 |
| 19 | Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci. | 1972 | 41 |
| 20 | 1965 | 0 |
About Marian L. Rivas
Marian L. Rivas is a scholar working on Nephrology, Biotechnology and Clinical Biochemistry, having authored 23 papers that have together received 545 indexed citations. Recurring topics across this work include Renal Diseases and Glomerulopathies (3 papers), Salivary Gland Disorders and Functions (3 papers), Complement system in diseases (3 papers), Enzyme Production and Characterization (3 papers), Metabolism and Genetic Disorders (2 papers), Pancreatitis Pathology and Treatment (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Urology (103 citations), Biotechnology (59 citations) and Nephrology (48 citations). Marian L. Rivas has collaborated with scholars based in United States and Italy. Frequent co-authors include A.D. Merritt, Robert Wyatt, H. Norman Noe, Joseph Peeden, R. C. Newell, David Bixler, P.M. Conneally, Jewell C. Ward, E.W. Lovrien and Richard D. Friedman. Their work appears in journals such as Cytogenetic and Genome Research, The Journal of Pediatrics, The Journal of Urology, Journal of Dental Research and Human 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.