Mark D. Pertile

2.5k total citations · 1 hit paper
51 papers, 1.4k citations indexed

About

Mark D. Pertile is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Mark D. Pertile has authored 51 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Pediatrics, Perinatology and Child Health, 26 papers in Genetics and 10 papers in Molecular Biology. Recurrent topics in Mark D. Pertile's work include Prenatal Screening and Diagnostics (39 papers), Genomic variations and chromosomal abnormalities (16 papers) and Fetal and Pediatric Neurological Disorders (13 papers). Mark D. Pertile is often cited by papers focused on Prenatal Screening and Diagnostics (39 papers), Genomic variations and chromosomal abnormalities (16 papers) and Fetal and Pediatric Neurological Disorders (13 papers). Mark D. Pertile collaborates with scholars based in Australia, United States and Saudi Arabia. Mark D. Pertile's co-authors include H.W.G. Baker, Gina D. Kusuma, Bill Kalionis, Mohamed Abumaree, Lyndon Hale, C. Stern, Shaun P. Brennecke, Lisa Hui, Martin B. Delatycki and Darcy Vavrek and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Mark D. Pertile

49 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2023 58 citations Lisa Hui, Katie Ellis et al. Prenatal Diagnosis profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Mark D. Pertile Australia	23	826	564	383	246	188	51	1.4k
Georgia Kokkali Greece	21	1.1k 1.3×	378 0.7×	324 0.8×	58 0.2×	135 0.7×	35	1.5k
Francesco Fiorentino Italy	30	2.5k 3.1×	1.1k 1.9×	548 1.4×	144 0.6×	278 1.5×	58	2.9k
Diane Van Opstal Netherlands	28	2.0k 2.5×	1.2k 2.2×	457 1.2×	75 0.3×	285 1.5×	97	2.6k
Avirachan T. Tharapel United States	19	881 1.1×	976 1.7×	443 1.2×	39 0.2×	162 0.9×	61	1.5k
Laird Jackson United States	15	547 0.7×	343 0.6×	360 0.9×	76 0.3×	161 0.9×	27	1.2k
Zhihong Yang United States	11	532 0.6×	188 0.3×	566 1.5×	53 0.2×	133 0.7×	22	1.2k
Iris Bartels Germany	20	738 0.9×	643 1.1×	305 0.8×	21 0.1×	130 0.7×	69	1.3k
Hiroaki Okae Japan	26	1.1k 1.3×	546 1.0×	1.5k 3.9×	137 0.6×	80 0.4×	49	2.3k
JDA Delhanty United Kingdom	17	531 0.6×	399 0.7×	285 0.7×	139 0.6×	171 0.9×	30	1.2k
Ashleigh Murch Australia	20	293 0.4×	135 0.2×	291 0.8×	49 0.2×	105 0.6×	42	936

Countries citing papers authored by Mark D. Pertile

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mark D. Pertile

This figure shows the co-authorship network connecting the top 25 collaborators of Mark D. Pertile. A scholar is included among the top collaborators of Mark D. Pertile based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mark D. Pertile. Mark D. Pertile is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hui, Lisa, et al.. (2024). Disparities in integrating non-invasive prenatal testing into antenatal healthcare in Australia: a survey of healthcare professionals. BMC Pregnancy and Childbirth. 24(1). 355–355. 3 indexed citations

Hui, Lisa, Katie Ellis, Mark D. Pertile, et al.. (2023). 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. Prenatal Diagnosis. 43(7). 814–828. 58 indexed citations breakdown →

Cifuentes, Marta, et al.. (2023). “It becomes your whole life”—Exploring experiences of reciprocal translocation carriers and their partners. Journal of Genetic Counseling. 32(5). 1057–1068. 1 indexed citations

Pertile, Mark D., et al.. (2022). Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy. Prenatal Diagnosis. 43(2). 226–234. 22 indexed citations

Greytak, Sarah R., Kelly B. Engel, Sonya Parpart-Li, et al.. (2020). Harmonizing Cell-Free DNA Collection and Processing Practices through Evidence-Based Guidance. Clinical Cancer Research. 26(13). 3104–3109. 88 indexed citations

Palomaki, Glenn E., Rossa W. K. Chiu, Mark D. Pertile, et al.. (2020). International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies. Prenatal Diagnosis. 41(10). 1222–1232. 41 indexed citations

Burgess, Trent, et al.. (2020). Genome-wide noninvasive prenatal screening for carriers of balanced reciprocal translocations. Genetics in Medicine. 22(12). 1944–1955. 16 indexed citations

Bowman‐Smart, Hilary, Julian Savulescu, Christopher Gyngell, et al.. (2019). ‘Is it better not to know certain things?’: views of women who have undergone non-invasive prenatal testing on its possible future applications. Journal of Medical Ethics. 45(4). 231–238. 36 indexed citations

Kan, Anita Sik Yau, et al.. (2018). A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin. Journal of obstetrics and gynaecology research. 44(5). 955–959. 4 indexed citations

10.

Amsterdam, Karin Huijsdens–van, Ida Vogel, Else Marie Vestergaard, et al.. (2018). Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome. European Journal of Human Genetics. 26(10). 1490–1496. 14 indexed citations

11.

Kusuma, Gina D., Rishika A. Pace, Sandra Isenmann, et al.. (2016). Establishment and characterization of fetal and maternal mesenchymal stem/stromal cell lines from the human term placenta. Placenta. 39. 134–146. 35 indexed citations

12.

Murphy, Nicholas M., Matthew J. Burton, David Powell, et al.. (2016). Haplotyping the human leukocyte antigen system from single chromosomes. Scientific Reports. 6(1). 30381–30381. 6 indexed citations

13.

Kusuma, Gina D., Danijela Menicanin, Stan Gronthos, et al.. (2015). Ectopic Bone Formation by Mesenchymal Stem Cells Derived from Human Term Placenta and the Decidua. PLoS ONE. 10(10). e0141246–e0141246. 44 indexed citations

14.

Liu, Haiying, Padma Murthi, Gina D. Kusuma, et al.. (2014). A Novel Combination of Homeobox Genes Is Expressed in Mesenchymal Chorionic Stem/Stromal Cells in First Trimester and Term Pregnancies. Reproductive Sciences. 21(11). 1382–1394. 13 indexed citations

15.

Coman, David, R. J McKinlay Gardner, Mark D. Pertile, & Pekka Kannus. (2010). Trisomy 16 Mosaicism at Chorionic Villus Sampling and Amniocentesis with a Normal Physical and Intellectual Outcome. Fetal Diagnosis and Therapy. 28(2). 117–118. 24 indexed citations

16.

Pertile, Mark D., et al.. (2009). Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stability. Genome Research. 19(12). 2202–2213. 41 indexed citations

17.

Wong, Nicholas C., Boris Novakovic, Roberta Andronikos, et al.. (2008). Methylation of the adenomatous polyposis coli (APC) gene in human placenta and hypermethylation in choriocarcinoma cells. Cancer Letters. 268(1). 56–62. 58 indexed citations

18.

Bruno, Damien L., Trent Burgess, Hua Ren, et al.. (2006). High‐throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy. American Journal of Medical Genetics Part A. 140A(24). 2786–2793. 45 indexed citations

19.

O’Donnell, Colm P., et al.. (2004). Monozygotic twins with discordant karyotypes: a case report. The Journal of Pediatrics. 145(3). 406–408. 21 indexed citations

20.

Daniel, Art, Neil Athayde, Robert Ogle, et al.. (2003). Prospective ranking of the sonographic markers for aneuploidy: Data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound. Australian and New Zealand Journal of Obstetrics and Gynaecology. 43(1). 16–26. 30 indexed citations

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.

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