Mark C. Lanasa
Impact in
- Genetics top 1%
- Chronic Lymphocytic Leukemia Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
- Immune Cell Function and Interaction
Papers in
- Genetics 48
- Chronic Lymphocytic Leukemia Research 48
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Immunology 27
- Immunodeficiency and Autoimmune Disorders 19
- Co-authors
- W. Allen Hogge (6 shared papers)Tait D. Shanafelt (8 shared papers)Urvashi Surti (2 shared papers)J. Brice Weinberg (21 shared papers)Paolo Ghia (5 shared papers)Andy C. Rawstron (4 shared papers)Eric P. Hoffman (4 shared papers)Ola Landgren (2 shared papers)
- Journals
- Blood (19 papers)Journal of Clinical Oncology (12 papers)Leukemia (4 papers)Annals of Oncology (4 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesUnited KingdomSouth Korea
In The Last Decade
Mark C. Lanasa
74 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 86
- Genetics 798
- Immunology 812
- Pathology and Forensic Medicine 536
- Oncology 771
- Hematology 169
Countries citing papers authored by Mark C. Lanasa
This map shows the geographic impact of Mark C. Lanasa'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 Mark C. Lanasa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark C. Lanasa more than expected).
Fields of papers citing papers by Mark C. Lanasa
This network shows the impact of papers produced by Mark C. Lanasa. 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 Mark C. Lanasa. The network helps show where Mark C. Lanasa may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark C. Lanasa, 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 158 | |
| 2 | 2010 | 143 | |
| 3 | 2012 | 138 | |
| 4 | 2018 | 114 | |
| 5 | 2003 | 109 | |
| 6 | 1997 | 107 | |
| 7 | 2011 | 103 | |
| 8 | 2019 | 81 | |
| 9 | 2010 | 73 | |
| 10 | 2013 | 72 | |
| 11 | 2019 | 68 | |
| 12 | 2020 | 67 | |
| 13 | 1999 | 60 | |
| 14 | 2018 | 52 | |
| 15 | 2017 | 51 | |
| 16 | 2001 | 49 | |
| 17 | 2009 | 49 | |
| 18 | 2019 | 43 | |
| 19 | 2015 | 41 | |
| 20 | 2019 | 38 |
About Mark C. Lanasa
Mark C. Lanasa is a scholar working on Genetics, Immunology, Pathology and Forensic Medicine, Oncology and Genetics, having authored 76 papers that have together received 2.3k indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (48 papers), Lymphoma Diagnosis and Treatment (23 papers), Immunodeficiency and Autoimmune Disorders (19 papers), PARP inhibition in cancer therapy (8 papers), Cancer Immunotherapy and Biomarkers (7 papers), Advanced Breast Cancer Therapies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Acute Lymphoblastic Leukemia research (6 papers). The work is most often cited by research in Genetics (798 citations), Immunology (812 citations), Pathology and Forensic Medicine (536 citations), Oncology (771 citations) and Hematology (169 citations). Mark C. Lanasa has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include W. Allen Hogge, Tait D. Shanafelt, Urvashi Surti, J. Brice Weinberg, Paolo Ghia, Andy C. Rawstron, Eric P. Hoffman, Ola Landgren, Jon P. Gockerman and Alicia D. Volkheimer. Their work appears in journals such as Blood, Journal of Clinical Oncology, Leukemia, Annals of Oncology and The American Journal of 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.