Peter Hechtman
Impact in
- Physiology top 5%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Physiology 33
- Lysosomal Storage Disorders Research 33
- Biochemistry 11
- Amino Acid Enzymes and Metabolism 11
- Co-authors
- Feige Kaplan (18 shared papers)Janet K. Bayleran (7 shared papers)Charles R. Scriver (9 shared papers)Bruce A. Gordon (2 shared papers)Pierre Ledoux (2 shared papers)N.M.K. Ng Ying Kin (1 shared paper)Marc De Braekeleer (3 shared papers)E. Andermann (3 shared papers)
- Journals
- Pediatric Research (4 papers)Biochemical Journal (3 papers)Journal of Biological Chemistry (3 papers)Clinical Genetics (2 papers)Human Mutation (2 papers)
- Partner nations
- CanadaUnited StatesFrance
In The Last Decade
Peter Hechtman
49 papers receiving 881 citations
Peers
Comparison fields: 5 of 62
- Physiology 574
- Clinical Biochemistry 90
- Biochemistry 76
- Genetics 114
- Biotechnology 17
Countries citing papers authored by Peter Hechtman
This map shows the geographic impact of Peter Hechtman'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 Peter Hechtman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Hechtman more than expected).
Fields of papers citing papers by Peter Hechtman
This network shows the impact of papers produced by Peter Hechtman. 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 Peter Hechtman. The network helps show where Peter Hechtman may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Hechtman, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 78 | |
| 2 | 1982 | 58 | |
| 3 | 2003 | 49 | |
| 4 | More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians. | 1990 | 46 |
| 5 | 1977 | 45 | |
| 6 | 1993 | 45 | |
| 7 | 1997 | 42 | |
| 8 | 1977 | 35 | |
| 9 | Expression and molecular analysis of mutations in prolidase deficiency. | 1996 | 35 |
| 10 | 1992 | 33 | |
| 11 | 1992 | 29 | |
| 12 | 1989 | 28 | |
| 13 | 1992 | 28 | |
| 14 | Four novel PEPD alleles causing prolidase deficiency. | 1994 | 27 |
| 15 | 1983 | 26 | |
| 16 | 2000 | 25 | |
| 17 | A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs disease. | 1987 | 24 |
| 18 | 1992 | 23 | |
| 19 | Tay-Sachs disease with hexosaminidase A: characterization of the defective enzyme in two patients. | 1987 | 22 |
| 20 | 1992 | 21 |
About Peter Hechtman
Peter Hechtman is a scholar working on Physiology, Biochemistry, Clinical Biochemistry, Genetics and Toxicology, having authored 51 papers that have together received 971 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (33 papers), Amino Acid Enzymes and Metabolism (11 papers), Metabolism and Genetic Disorders (7 papers), Bacterial Genetics and Biotechnology (3 papers), Glycosylation and Glycoproteins Research (3 papers), Bioactive Compounds and Antitumor Agents (2 papers), Sphingolipid Metabolism and Signaling (2 papers) and Thyroid Disorders and Treatments (2 papers). The work is most often cited by research in Physiology (574 citations), Clinical Biochemistry (90 citations), Biochemistry (76 citations), Genetics (114 citations) and Biotechnology (17 citations). Peter Hechtman has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Feige Kaplan, Janet K. Bayleran, Charles R. Scriver, Bruce A. Gordon, Pierre Ledoux, N.M.K. Ng Ying Kin, Marc De Braekeleer, E. Andermann, Andréa Richter and Don J. Mahuran. Their work appears in journals such as Pediatric Research, Biochemical Journal, Journal of Biological Chemistry, Clinical Genetics and Human Mutation.
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.