Thomas M. Morgan
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 6
- BRCA gene mutations in cancer 5
- Genetic Associations and Epidemiology 5
- Genomics and Rare Diseases 3
- Co-authors
- Richard P. LiftonHarlan M. KrumholzJohn A. SpertusMatthew W. StateAmi KlinMurat GünelKatarzyna ChawarskaA. Gulhan Ercan‐Sencicek
- Journals
- PEDIATRICS (2 papers)The American Journal of Human Genetics (2 papers)The Journal of Law Medicine & Ethics (2 papers)European Journal of Human Genetics (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomTürkiye
In The Last Decade
Thomas M. Morgan
42 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 130
- Genetics 716
- Cognitive Neuroscience 322
- Molecular Biology 662
- Cardiology and Cardiovascular Medicine 196
- Cell Biology 114
Countries citing papers authored by Thomas M. Morgan
This map shows the geographic impact of Thomas M. Morgan'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 Thomas M. Morgan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas M. Morgan more than expected).
Fields of papers citing papers by Thomas M. Morgan
This network shows the impact of papers produced by Thomas M. Morgan. 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 Thomas M. Morgan. The network helps show where Thomas M. Morgan may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas M. Morgan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 53 | |
| 2 | 2019 | 5 | |
| 3 | 2018 | 2 | |
| 4 | 2017 | 88 | |
| 5 | 2015 | 149 | |
| 6 | 2014 | 6 | |
| 7 | 2014 | 56 | |
| 8 | 2012 | 41 | |
| 9 | 2011 | 25 | |
| 10 | 2011 | 9 | |
| 11 | 2011 | 12 | |
| 12 | 2008 | 397 | |
| 13 | 2008 | 45 | |
| 14 | 2008 | 15 | |
| 15 | 2007 | 197 | |
| 16 | 2007 | 8 | |
| 17 | 2004 | 32 | |
| 18 | The education and medical practice of Dr. James McCune Smith (1813-1865), first black American to hold a medical degree. | 2003 | 7 |
| 19 | 2003 | 22 | |
| 20 | 2003 | 53 |
About Thomas M. Morgan
Thomas M. Morgan is a scholar working on Transplantation, Genetics, Software, Clinical Biochemistry and Obstetrics and Gynecology, having authored 42 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), BRCA gene mutations in cancer (5 papers), Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (3 papers), Congenital heart defects research (3 papers), Acute Myocardial Infarction Research (3 papers) and Birth, Development, and Health (3 papers). The work is most often cited by research in Genetics (716 citations), Cognitive Neuroscience (322 citations), Molecular Biology (662 citations), Cardiology and Cardiovascular Medicine (196 citations) and Cell Biology (114 citations). Thomas M. Morgan has collaborated with scholars based in United States, United Kingdom and Türkiye. Frequent co-authors include Richard P. Lifton, Harlan M. Krumholz, John A. Spertus, Matthew W. State, Ami Klin, Murat Günel, Katarzyna Chawarska, A. Gulhan Ercan‐Sencicek, Abha R. Gupta and Collen Masimirembwa. Their work appears in journals such as PEDIATRICS, The American Journal of Human Genetics, The Journal of Law Medicine & Ethics, European Journal of Human Genetics and European Journal of Medical 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.