Mark D. Pertile
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Papers in
-
- Prenatal Screening and Diagnostics 39
- Fetal and Pediatric Neurological Disorders 7
- Genetics 20
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 6
- Mesenchymal stem cell research 3
- Co-authors
- H.W.G. Baker (2 shared papers)Nicola Flowers (11 shared papers)Lyndon Hale (1 shared paper)C. Stern (1 shared paper)Bill Kalionis (6 shared papers)Gina D. Kusuma (6 shared papers)Mohamed Abumaree (6 shared papers)Lisa Hui (8 shared papers)
- Journals
- Prenatal Diagnosis (10 papers)Human Reproduction (3 papers)Ultrasound in Obstetrics and Gynecology (3 papers)Placenta (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Mark D. Pertile
51 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 70
- Pediatrics, Perinatology and Child Health 853
- Genetics 472
- Cancer Research 217
- Obstetrics and Gynecology 96
- Reproductive Medicine 110
Countries citing papers authored by Mark D. Pertile
This map shows the geographic impact of Mark D. Pertile'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 D. Pertile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark D. Pertile more than expected).
Fields of papers citing papers by Mark D. Pertile
This network shows the impact of papers produced by Mark D. Pertile. 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 D. Pertile. The network helps show where Mark D. Pertile may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark D. Pertile, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 149 | |
| 2 | 2017 | 122 | |
| 3 | 1997 | 91 | |
| 4 | 2020 | 91 | |
| 5 | 2011 | 70 | |
| 6 | 2016 | 66 | |
| 7 | 2008 | 63 | |
| 8 | 2023 | 61 | |
| 9 | 2006 | 53 | |
| 10 | 2003 | 48 | |
| 11 | 2006 | 46 | |
| 12 | 2015 | 45 | |
| 13 | 2020 | 44 | |
| 14 | 2009 | 44 | |
| 15 | 2016 | 43 | |
| 16 | 2019 | 41 | |
| 17 | 2010 | 40 | |
| 18 | 2016 | 39 | |
| 19 | 2019 | 38 | |
| 20 | 2014 | 34 |
About Mark D. Pertile
Mark D. Pertile is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Cancer Research and Surgery, having authored 53 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (39 papers), Genomic variations and chromosomal abnormalities (12 papers), Fetal and Pediatric Neurological Disorders (7 papers), Genetic Syndromes and Imprinting (6 papers), Cancer Genomics and Diagnostics (4 papers), Parvovirus B19 Infection Studies (4 papers), Chromosomal and Genetic Variations (3 papers) and Mesenchymal stem cell research (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (853 citations), Genetics (472 citations), Cancer Research (217 citations), Obstetrics and Gynecology (96 citations) and Reproductive Medicine (110 citations). Mark D. Pertile has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include H.W.G. Baker, Nicola Flowers, Lyndon Hale, C. Stern, Bill Kalionis, Gina D. Kusuma, Mohamed Abumaree, Lisa Hui, Martin B. Delatycki and Shaun P. Brennecke. Their work appears in journals such as Prenatal Diagnosis, Human Reproduction, Ultrasound in Obstetrics and Gynecology, Placenta and European 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.