Thomas A. Maher
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Reproductive Medicine top 10%
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 3
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- Epigenetics and DNA Methylation 2
- RNA regulation and disease 2
- Co-authors
- Jeff M. Milunsky (11 shared papers)Aubrey Milunsky (13 shared papers)Robert Davis Oates (2 shared papers)Geping Zhao (2 shared papers)Virginia V. Michels (1 shared paper)Aida B. Metzenberg (2 shared papers)Masamichi Ito (4 shared papers)Theresa J. McCallum (1 shared paper)
- Journals
- Clinical Genetics (4 papers)American Journal of Obstetrics and Gynecology (2 papers)Fetal Diagnosis and Therapy (1 paper)Diagnostic Molecular Pathology (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- United StatesCanadaUruguay
In The Last Decade
Thomas A. Maher
25 papers receiving 672 citations
Peers
Comparison fields: 5 of 83
- Genetics 180
- Reproductive Medicine 49
- Pulmonary and Respiratory Medicine 151
- Sensory Systems 23
- Molecular Biology 282
Countries citing papers authored by Thomas A. Maher
This map shows the geographic impact of Thomas A. Maher'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 A. Maher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas A. Maher more than expected).
Fields of papers citing papers by Thomas A. Maher
This network shows the impact of papers produced by Thomas A. Maher. 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 A. Maher. The network helps show where Thomas A. Maher may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas A. Maher, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 118 | |
| 2 | Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis. | 1992 | 106 |
| 3 | 2000 | 75 | |
| 4 | 2001 | 68 | |
| 5 | 2018 | 62 | |
| 6 | 2002 | 44 | |
| 7 | 2003 | 33 | |
| 8 | 2003 | 31 | |
| 9 | 2007 | 25 | |
| 10 | 2001 | 19 | |
| 11 | 2000 | 18 | |
| 12 | 2005 | 18 | |
| 13 | 2009 | 17 | |
| 14 | 2010 | 17 | |
| 15 | 2019 | 12 | |
| 16 | 2011 | 9 | |
| 17 | 2005 | 7 | |
| 18 | 2007 | 6 | |
| 19 | 2008 | 5 | |
| 20 | 2010 | 4 |
About Thomas A. Maher
Thomas A. Maher is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cancer Research and Rheumatology, having authored 25 papers that have together received 705 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (3 papers), Epigenetics and DNA Methylation (2 papers), RNA regulation and disease (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Cystic Fibrosis Research Advances (2 papers). The work is most often cited by research in Genetics (180 citations), Reproductive Medicine (49 citations), Pulmonary and Respiratory Medicine (151 citations), Sensory Systems (23 citations) and Molecular Biology (282 citations). Thomas A. Maher has collaborated with scholars based in United States, Canada and Uruguay. Frequent co-authors include Jeff M. Milunsky, Aubrey Milunsky, Robert Davis Oates, Geping Zhao, Virginia V. Michels, Aida B. Metzenberg, Masamichi Ito, Theresa J. McCallum, Doria H. Harris and Claudia Stewart. Their work appears in journals such as Clinical Genetics, American Journal of Obstetrics and Gynecology, Fetal Diagnosis and Therapy, Diagnostic Molecular Pathology and Prenatal Diagnosis.
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.