Michael E. Talkowski
Impact in
Papers in
- Genetics 60
- Genomic variations and chromosomal abnormalities 30
- Genomics and Rare Diseases 22
- Genetics and Neurodevelopmental Disorders 14
- Genetic Associations and Epidemiology 11
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- CRISPR and Genetic Engineering 13
- Congenital heart defects research 8
- Co-authors
- James F. Gusella (27 shared papers)Harrison Brand (16 shared papers)Ryan L. Collins (16 shared papers)Serkan Erdin (24 shared papers)Ashok Ragavendran (9 shared papers)Kiran Musunuru (3 shared papers)Chad A. Cowan (3 shared papers)Vishwajit L. Nimgaonkar (13 shared papers)
- Journals
- The American Journal of Human Genetics (10 papers)European Neuropsychopharmacology (7 papers)Schizophrenia Bulletin (6 papers)Nature Communications (5 papers)Human Molecular Genetics (4 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Michael E. Talkowski
100 papers receiving 4.4k citations
Michael E. Talkowski's Hit Papers
Peers
Comparison fields: 5 of 132
- Aging 138
- Genetics 1.8k
- Business and International Management 119
- Molecular Biology 2.6k
- Biological Psychiatry 59
Countries citing papers authored by Michael E. Talkowski
This map shows the geographic impact of Michael E. Talkowski'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 Michael E. Talkowski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael E. Talkowski more than expected).
Fields of papers citing papers by Michael E. Talkowski
This network shows the impact of papers produced by Michael E. Talkowski. 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 Michael E. Talkowski. The network helps show where Michael E. Talkowski may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael E. Talkowski, 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 104 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 397 | |
| 2 | Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9 Hit paper breakdown → | 2014 | 395 |
| 3 | 2012 | 283 | |
| 4 | 2017 | 257 | |
| 5 | 2018 | 239 | |
| 6 | 2014 | 234 | |
| 7 | 2016 | 180 | |
| 8 | 2012 | 130 | |
| 9 | 2011 | 126 | |
| 10 | 2003 | 117 | |
| 11 | 2007 | 114 | |
| 12 | 2014 | 90 | |
| 13 | 2004 | 87 | |
| 14 | 2017 | 83 | |
| 15 | 2019 | 68 | |
| 16 | 2016 | 55 | |
| 17 | 2014 | 54 | |
| 18 | 2013 | 54 | |
| 19 | 2021 | 54 | |
| 20 | 2024 | 51 |
About Michael E. Talkowski
Michael E. Talkowski is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Plant Science, having authored 104 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Genomics and Rare Diseases (22 papers), Genetics and Neurodevelopmental Disorders (14 papers), CRISPR and Genetic Engineering (13 papers), Genetic Associations and Epidemiology (11 papers), Congenital heart defects research (8 papers), Autism Spectrum Disorder Research (8 papers) and Chromosomal and Genetic Variations (8 papers). The work is most often cited by research in Aging (138 citations), Genetics (1.8k citations), Business and International Management (119 citations), Molecular Biology (2.6k citations) and Biological Psychiatry (59 citations). Michael E. Talkowski has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include James F. Gusella, Harrison Brand, Ryan L. Collins, Serkan Erdin, Ashok Ragavendran, Kiran Musunuru, Chad A. Cowan, Vishwajit L. Nimgaonkar, Kodavali V. Chowdari and Alexei Stortchevoi. Their work appears in journals such as The American Journal of Human Genetics, European Neuropsychopharmacology, Schizophrenia Bulletin, Nature Communications and Human Molecular 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.