Mark D. Pertile
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 39
- Fetal and Pediatric Neurological Disorders 13
- Genetics 26
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 7
- Mesenchymal stem cell research 5
- Co-authors
- H.W.G. Baker (2 shared papers)Mohamed Abumaree (6 shared papers)Bill Kalionis (6 shared papers)Gina D. Kusuma (6 shared papers)C. Stern (1 shared paper)Lyndon Hale (1 shared paper)Lisa Hui (8 shared papers)Shaun P. Brennecke (4 shared papers)
- Journals
- Prenatal Diagnosis (10 papers)Ultrasound in Obstetrics and Gynecology (3 papers)Human Reproduction (3 papers)European Journal of Human Genetics (2 papers)Placenta (2 papers)
- Partner nations
- AustraliaUnited StatesSaudi Arabia
In The Last Decade
Mark D. Pertile
49 papers receiving 1.3k citations
Mark D. Pertile's Hit Papers
Peers
Comparison fields: 5 of 69
- Pediatrics, Perinatology and Child Health 826
- Genetics 564
- Reproductive Medicine 142
- Cancer Research 246
- Obstetrics and Gynecology 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 127 | |
| 2 | 2017 | 108 | |
| 3 | 2020 | 88 | |
| 4 | 1997 | 84 | |
| 5 | 2011 | 64 | |
| 6 | 2016 | 63 | |
| 7 | Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies Hit paper breakdown → | 2023 | 58 |
| 8 | 2008 | 58 | |
| 9 | 2006 | 45 | |
| 10 | 2015 | 44 | |
| 11 | 2016 | 42 | |
| 12 | 2020 | 41 | |
| 13 | 2009 | 41 | |
| 14 | 2019 | 36 | |
| 15 | 2019 | 36 | |
| 16 | 2006 | 36 | |
| 17 | 2016 | 35 | |
| 18 | 2014 | 33 | |
| 19 | 2003 | 30 | |
| 20 | 2021 | 30 |
About Mark D. Pertile
Mark D. Pertile is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Cancer Research and Infectious Diseases, having authored 51 papers that have together received 1.4k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (39 papers), Genomic variations and chromosomal abnormalities (16 papers), Fetal and Pediatric Neurological Disorders (13 papers), Genetic Syndromes and Imprinting (7 papers), Parvovirus B19 Infection Studies (7 papers), Cancer Genomics and Diagnostics (6 papers), Mesenchymal stem cell research (5 papers) and MicroRNA in disease regulation (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (826 citations), Genetics (564 citations), Reproductive Medicine (142 citations), Cancer Research (246 citations) and Obstetrics and Gynecology (110 citations). Mark D. Pertile has collaborated with scholars based in Australia, United States and Saudi Arabia. Frequent co-authors include H.W.G. Baker, Mohamed Abumaree, Bill Kalionis, Gina D. Kusuma, C. Stern, Lyndon Hale, Lisa Hui, Shaun P. Brennecke, Martin B. Delatycki and Darcy Vavrek. Their work appears in journals such as Prenatal Diagnosis, Ultrasound in Obstetrics and Gynecology, Human Reproduction, European Journal of Human Genetics and Placenta.
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.