M. T. Vanier
Impact in
- Physiology top 0.5%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
- Cell Biology top 2%
- Cellular transport and secretion
Papers in
- Physiology 41
- Lysosomal Storage Disorders Research 39
- Epidemiology 15
- Trypanosoma species research and implications 5
- Traumatic Brain Injury Research 5
- Co-authors
- Lars Svennerholm (4 shared papers)J.‐E. Månsson (2 shared papers)Peter G. Pentchev (6 shared papers)Howard S. Kruth (4 shared papers)Marcella Comly (4 shared papers)Eugene D. Carstea (2 shared papers)J D Butler (4 shared papers)Claire Rodriguez‐Lafrasse (3 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (3 papers)Journal of Biological Chemistry (3 papers)Human Molecular Genetics (2 papers)Biochimie (2 papers)Clinical Genetics (2 papers)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
M. T. Vanier
57 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 105
- Physiology 1.8k
- Physiology 255
- Cell Biology 573
- Organic Chemistry 491
- Hematology 149
Countries citing papers authored by M. T. Vanier
This map shows the geographic impact of M. T. Vanier'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 M. T. Vanier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. T. Vanier more than expected).
Fields of papers citing papers by M. T. Vanier
This network shows the impact of papers produced by M. T. Vanier. 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 M. T. Vanier. The network helps show where M. T. Vanier may publish in the future.
Co-authors
The 25 scholars most cited alongside M. T. Vanier, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1980 | 272 | |
| 2 | Genetic heterogeneity in Niemann-Pick C disease: a study using somatic cell hybridization and linkage analysis. | 1996 | 183 |
| 3 | 1987 | 160 | |
| 4 | 1986 | 138 | |
| 5 | 1997 | 137 | |
| 6 | 1986 | 106 | |
| 7 | 2006 | 103 | |
| 8 | 1994 | 103 | |
| 9 | 2006 | 100 | |
| 10 | 1973 | 92 | |
| 11 | 1990 | 88 | |
| 12 | 2010 | 79 | |
| 13 | 2003 | 75 | |
| 14 | 2005 | 72 | |
| 15 | 2007 | 69 | |
| 16 | 1991 | 56 | |
| 17 | 1998 | 49 | |
| 18 | Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk. | 1992 | 44 |
| 19 | 2004 | 43 | |
| 20 | 1999 | 40 |
About M. T. Vanier
M. T. Vanier is a scholar working on Physiology, Epidemiology, Molecular Biology, Cell Biology and Organic Chemistry, having authored 57 papers that have together received 2.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (39 papers), Cellular transport and secretion (9 papers), Carbohydrate Chemistry and Synthesis (7 papers), Autoimmune and Inflammatory Disorders Research (7 papers), Biomedical Research and Pathophysiology (5 papers), Trypanosoma species research and implications (5 papers), Traumatic Brain Injury Research (5 papers) and Glycosylation and Glycoproteins Research (4 papers). The work is most often cited by research in Physiology (1.8k citations), Physiology (255 citations), Cell Biology (573 citations), Organic Chemistry (491 citations) and Hematology (149 citations). M. T. Vanier has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Lars Svennerholm, J.‐E. Månsson, Peter G. Pentchev, Howard S. Kruth, Marcella Comly, Eugene D. Carstea, J D Butler, Claire Rodriguez‐Lafrasse, Sylvie Duthel and David A. Wenger. Their work appears in journals such as Journal of Inherited Metabolic Disease, Journal of Biological Chemistry, Human Molecular Genetics, Biochimie and Clinical 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.