Peter Tsang
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Hematology top 5%
Papers in
- Hematology 11
- Iron Metabolism and Disorders 3
- Platelet Disorders and Treatments 2
- Genetics 10
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 4
- Hemoglobinopathies and Related Disorders 3
- Myeloproliferative Neoplasms: Diagnosis and Treatment 2
- Co-authors
- N. Alice Yamada (7 shared papers)Laurakay Bruhn (7 shared papers)Nick Sampas (5 shared papers)Stephen Laderman (3 shared papers)Zohar Yakhini (3 shared papers)Amir Ben‐Dor (3 shared papers)Anya Tsalenko (6 shared papers)Robert A. Ach (3 shared papers)
- Journals
- Cytogenetic and Genome Research (2 papers)Human Molecular Genetics (2 papers)Blood (2 papers)The American Journal of Human Genetics (2 papers)American Journal of Perinatology (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Peter Tsang
33 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 116
- Genetics 812
- Hematology 218
- Biochemistry 73
- Molecular Biology 765
- Genetics 106
Countries citing papers authored by Peter Tsang
This map shows the geographic impact of Peter Tsang'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 Tsang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Tsang more than expected).
Fields of papers citing papers by Peter Tsang
This network shows the impact of papers produced by Peter Tsang. 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 Tsang. The network helps show where Peter Tsang may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Tsang, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 289 | |
| 2 | 2008 | 273 | |
| 3 | 2007 | 180 | |
| 4 | 2013 | 128 | |
| 5 | 2013 | 123 | |
| 6 | 2003 | 110 | |
| 7 | 2004 | 108 | |
| 8 | 2010 | 104 | |
| 9 | 2012 | 92 | |
| 10 | 2011 | 65 | |
| 11 | 2010 | 64 | |
| 12 | 1996 | 40 | |
| 13 | The effect of factor V Leiden carriage on maternal and fetal health. | 2002 | 36 |
| 14 | 1982 | 31 | |
| 15 | 2006 | 27 | |
| 16 | 2008 | 24 | |
| 17 | 2010 | 22 | |
| 18 | 2006 | 14 | |
| 19 | 2020 | 13 | |
| 20 | 2010 | 9 |
About Peter Tsang
Peter Tsang is a scholar working on Hematology, Genetics, Genetics, Rheumatology and Molecular Biology, having authored 33 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers), Genomics and Rare Diseases (4 papers), Systemic Lupus Erythematosus Research (3 papers), Hemoglobinopathies and Related Disorders (3 papers), Iron Metabolism and Disorders (3 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers) and Platelet Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (812 citations), Hematology (218 citations), Biochemistry (73 citations), Molecular Biology (765 citations) and Genetics (106 citations). Peter Tsang has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include N. Alice Yamada, Laurakay Bruhn, Nick Sampas, Stephen Laderman, Zohar Yakhini, Amir Ben‐Dor, Anya Tsalenko, Robert A. Ach, Dag H. Yasui and Janine M. LaSalle. Their work appears in journals such as Cytogenetic and Genome Research, Human Molecular Genetics, Blood, The American Journal of Human Genetics and American Journal of Perinatology.
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.