Richard P. Lifton
Impact in
- Endocrinology, Diabetes and Metabolism top 0.02%
- Hormonal Regulation and Hypertension
- Nephrology top 0.1%
- Renal function and acid-base balance
Papers in
-
- Ion Transport and Channel Regulation 92
- Ion channel regulation and function 33
- Congenital heart defects research 10
-
- Hormonal Regulation and Hypertension 51
- Co-authors
- Carol Nelson‐Williams (49 shared papers)David B. Simon (13 shared papers)David S. Geller (9 shared papers)Ali G. Gharavi (10 shared papers)Kristopher T. Kahle (31 shared papers)Richard A. Shimkets (9 shared papers)Sami A. Sanjad (7 shared papers)Xavier Jeunemaı̂tre (9 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (44 papers)Nature Genetics (20 papers)The American Journal of Human Genetics (9 papers)Journal of Biological Chemistry (9 papers)The Journal of Clinical Endocrinology & Metabolism (8 papers)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Richard P. Lifton
274 papers receiving 34.8k citations
Richard P. Lifton's Hit Papers
Peers
Comparison fields: 5 of 168
- Endocrinology, Diabetes and Metabolism 8.6k
- Nephrology 2.9k
- Molecular Biology 19.4k
- Nutrition and Dietetics 3.3k
- Cardiology and Cardiovascular Medicine 4.3k
Countries citing papers authored by Richard P. Lifton
This map shows the geographic impact of Richard P. Lifton'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 Richard P. Lifton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard P. Lifton more than expected).
Fields of papers citing papers by Richard P. Lifton
This network shows the impact of papers produced by Richard P. Lifton. 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 Richard P. Lifton. The network helps show where Richard P. Lifton may publish in the future.
Co-authors
The 25 scholars most cited alongside Richard P. Lifton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 277 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular basis of human hypertension: Role of angiotensinogen Hit paper breakdown → | 1992 | 1490 |
| 2 | Molecular Mechanisms of Human Hypertension Hit paper breakdown → | 2001 | 1221 |
| 3 | High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5 Hit paper breakdown → | 2002 | 1205 |
| 4 | Human Hypertension Caused by Mutations in WNK Kinases Hit paper breakdown → | 2001 | 1120 |
| 5 | Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel Hit paper breakdown → | 1994 | 969 |
| 6 | Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter Hit paper breakdown → | 1996 | 900 |
| 7 | Genetic diagnosis by whole exome capture and massively parallel DNA sequencing Hit paper breakdown → | 2009 | 892 |
| 8 | Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg 2+ Resorption Hit paper breakdown → | 1999 | 819 |
| 9 | A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension Hit paper breakdown → | 1992 | 815 |
| 10 | K + Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension Hit paper breakdown → | 2011 | 694 |
| 11 | Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2 Hit paper breakdown → | 1996 | 661 |
| 12 | Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK Hit paper breakdown → | 1996 | 614 |
| 13 | Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1 Hit paper breakdown → | 1996 | 600 |
| 14 | Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndrome Hit paper breakdown → | 1995 | 584 |
| 15 | Rare independent mutations in renal salt handling genes contribute to blood pressure variation Hit paper breakdown → | 2008 | 548 |
| 16 | 1996 | 486 | |
| 17 | 2007 | 462 | |
| 18 | 2000 | 457 | |
| 19 | Vaccine Breakthrough Infections with SARS-CoV-2 Variants Hit paper breakdown → | 2021 | 444 |
| 20 | 2008 | 399 |
About Richard P. Lifton
Richard P. Lifton is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism, Genetics, Surgery and Pulmonary and Respiratory Medicine, having authored 277 papers that have together received 35.5k indexed citations. Recurring topics across this work include Ion Transport and Channel Regulation (92 papers), Hormonal Regulation and Hypertension (51 papers), Ion channel regulation and function (33 papers), Magnesium in Health and Disease (21 papers), Electrolyte and hormonal disorders (15 papers), Renal Diseases and Glomerulopathies (11 papers), Renal function and acid-base balance (11 papers) and Congenital heart defects research (10 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (8.6k citations), Nephrology (2.9k citations), Molecular Biology (19.4k citations), Nutrition and Dietetics (3.3k citations) and Cardiology and Cardiovascular Medicine (4.3k citations). Richard P. Lifton has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Carol Nelson‐Williams, David B. Simon, David S. Geller, Ali G. Gharavi, Kristopher T. Kahle, Richard A. Shimkets, Sami A. Sanjad, Xavier Jeunemaı̂tre, Anita Farhi and Fiona E. Karet. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics, The American Journal of Human Genetics, Journal of Biological Chemistry and The Journal of Clinical Endocrinology & Metabolism.
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.