Michelle Steinraths
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 1
- Digestive system and related health 1
- Genetic Syndromes and Imprinting 1
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- Renal cell carcinoma treatment 1
- Co-authors
- Jie Xu (2 shared papers)Judy Chernos (2 shared papers)Josée N. Lavoie (2 shared papers)Jean McGowan‐Jordan (2 shared papers)Shashirekha Shetty (1 shared paper)Hilary Vallance (1 shared paper)A. George F. Davidson (1 shared paper)Kamilla Schlade‐Bartusiak (2 shared papers)
- Journals
- Clinical Genetics (2 papers)Prenatal Diagnosis (1 paper)European Journal of Human Genetics (1 paper)Cytogenetic and Genome Research (1 paper)Current Oncology (1 paper)
- Partner nations
- CanadaUnited StatesNetherlands
In The Last Decade
Michelle Steinraths
12 papers receiving 146 citations
Peers
Comparison fields: 5 of 30
- Genetics 89
- Pediatrics, Perinatology and Child Health 47
- Pulmonary and Respiratory Medicine 22
- Molecular Biology 42
- Clinical Biochemistry 3
Countries citing papers authored by Michelle Steinraths
This map shows the geographic impact of Michelle Steinraths'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 Michelle Steinraths with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michelle Steinraths more than expected).
Fields of papers citing papers by Michelle Steinraths
This network shows the impact of papers produced by Michelle Steinraths. 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 Michelle Steinraths. The network helps show where Michelle Steinraths may publish in the future.
Co-authors
The 25 scholars most cited alongside Michelle Steinraths, 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 | 2010 | 39 | |
| 2 | 2011 | 28 | |
| 3 | 2022 | 20 | |
| 4 | 2009 | 18 | |
| 5 | 2007 | 15 | |
| 6 | 2017 | 15 | |
| 7 | 2010 | 13 | |
| 8 | Delays in diagnosing cystic fibrosis: can we find ways to diagnose it earlier? | 2008 | 11 |
| 9 | 2011 | 7 | |
| 10 | 2023 | 2 | |
| 11 | 2017 | 2 | |
| 12 | 2015 | 1 |
About Michelle Steinraths
Michelle Steinraths is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Molecular Biology, Cardiology and Cardiovascular Medicine and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 171 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Congenital heart defects research (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (2 papers), Genomics and Rare Diseases (1 paper), Renal cell carcinoma treatment (1 paper), Digestive system and related health (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (89 citations), Pediatrics, Perinatology and Child Health (47 citations), Pulmonary and Respiratory Medicine (22 citations), Molecular Biology (42 citations) and Clinical Biochemistry (3 citations). Michelle Steinraths has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Jie Xu, Judy Chernos, Josée N. Lavoie, Jean McGowan‐Jordan, Shashirekha Shetty, Hilary Vallance, A. George F. Davidson, Kamilla Schlade‐Bartusiak, Constadina Panagiotopoulos and James E. Potts. Their work appears in journals such as Clinical Genetics, Prenatal Diagnosis, European Journal of Human Genetics, Cytogenetic and Genome Research and Current Oncology.
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.