James Harraway

2.4k total citations · 1 hit paper
26 papers, 1.5k citations indexed

About

James Harraway is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, James Harraway has authored 26 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Pediatrics, Perinatology and Child Health and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in James Harraway's work include Prenatal Screening and Diagnostics (10 papers), Cancer Genomics and Diagnostics (5 papers) and Genetic factors in colorectal cancer (3 papers). James Harraway is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Cancer Genomics and Diagnostics (5 papers) and Genetic factors in colorectal cancer (3 papers). James Harraway collaborates with scholars based in Australia, New Zealand and United States. James Harraway's co-authors include Parry Guilford, Anthony E. Reeve, Andrew Miller, Peter M. George, Murray L. Barclay, Richard B. Gearry, Mark P. Smith, Rebecca L Roberts, Chris Florkowski and Vicki Gibbs and has published in prestigious journals such as Nature, Clinical Chemistry and Human Reproduction.

In The Last Decade

James Harraway

25 papers receiving 1.5k 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.

E-cadherin germline mutations in familial gastric cancer

1998 1.2k citations Parry Guilford, James Harraway et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James Harraway Australia	12	850	452	448	297	283	26	1.5k
Cindy A. Eads United States	9	2.2k 2.5×	337 0.7×	361 0.8×	243 0.8×	321 1.1×	10	2.6k
Elvis Terci Valera Brazil	18	725 0.9×	118 0.3×	141 0.3×	144 0.5×	86 0.3×	108	1.4k
Kandelaria M. Rumilla United States	21	339 0.4×	282 0.6×	220 0.5×	190 0.6×	229 0.8×	38	1.2k
Adrian A. Suarez United States	20	560 0.7×	418 0.9×	138 0.3×	151 0.5×	134 0.5×	72	1.6k
Karey Shumansky Canada	15	495 0.6×	345 0.8×	114 0.3×	268 0.9×	87 0.3×	20	1.3k
Hironori Tashiro Japan	21	572 0.7×	129 0.3×	198 0.4×	117 0.4×	125 0.4×	37	1.4k
Sheila N.J. Sait United States	20	510 0.6×	178 0.4×	65 0.1×	127 0.4×	181 0.6×	72	1.2k
W. Michael Hogan United States	18	254 0.3×	151 0.3×	304 0.7×	164 0.6×	200 0.7×	33	1.3k
Hanna Rennert United States	14	462 0.5×	218 0.5×	214 0.5×	240 0.8×	139 0.5×	25	1.0k
Laura De Gregorio Italy	17	1.1k 1.3×	154 0.3×	80 0.2×	213 0.7×	446 1.6×	38	1.7k

Countries citing papers authored by James Harraway

Since Specialization

Citations

This map shows the geographic impact of James Harraway'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 James Harraway with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James Harraway more than expected).

Fields of papers citing papers by James Harraway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James Harraway. 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 James Harraway. The network helps show where James Harraway may publish in the future.

Co-authorship network of co-authors of James Harraway

This figure shows the co-authorship network connecting the top 25 collaborators of James Harraway. A scholar is included among the top collaborators of James Harraway 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 James Harraway. James Harraway 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

Sousa, Sunita M C De, Timothy M. E. Davis, James Harraway, et al.. (2025). Australian and New Zealand joint society consensus statement on genetic testing for monogenic diabetes in adults. The Medical Journal of Australia. 223(9). 484–491. 2 indexed citations

Flynn, Maria, et al.. (2023). IDH1 p.R132C mutation in prostatic carcinoma with psammomatous calcifications: report of two cases. Pathology. 56(3). 419–421. 1 indexed citations

Anderson, Erin M., James Harraway, Anna Stewart, et al.. (2022). WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review. Pediatric Nephrology. 37(10). 2369–2374. 3 indexed citations

Thomas, Joseph, et al.. (2021). Non‐invasive prenatal testing: clinical utility and ethical concerns about recent advances. The Medical Journal of Australia. 214(4). 168–168. 7 indexed citations

Kim, Roger H., Anna Lapuk, James Harraway, et al.. (2020). Prevalence of the EGFR T790M and other resistance mutations in the Australian population and histopathological correlation in a small subset of cases. Pathology. 52(4). 410–420. 2 indexed citations

Lee, Eric, et al.. (2020). Reduced sensitivity for EGFR T790M mutations using the Idylla EGFR Mutation Test. Journal of Clinical Pathology. 74(1). 43–47. 17 indexed citations

Matsika, Admire, Mark Williams, Gareth Price, et al.. (2019). DNA extraction from placental, fetal and neonatal tissue at autopsy: what organ to sample for DNA in the genomic era?. Pathology. 51(7). 705–710. 3 indexed citations

Hui, Lisa, Anthea Lindquist, Mark D. Pertile, et al.. (2019). OC01.03: State‐wide performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study. Ultrasound in Obstetrics and Gynecology. 54(S1). 1–2. 2 indexed citations

Halliday, Jane, Anthea Lindquist, Fabrício da Silva Costa, et al.. (2019). Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio‐economic status in Victoria, Australia: A population‐based cohort study from 2015 to 2016. Prenatal Diagnosis. 39(13). 1254–1261.

10.

Armes, Jane E., Mark Williams, Gareth Price, et al.. (2017). Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death. Pediatric and Developmental Pathology. 21(1). 54–67. 18 indexed citations

11.

Liu, Cheng, et al.. (2016). Ovarian Microcystic Stromal Tumor: A Rare Clinical Manifestation of Familial Adenomatous Polyposis. International Journal of Gynecological Pathology. 35(6). 561–565. 24 indexed citations

12.

Harraway, James. (2015). Non-Invasive Prenatal Testing. Journal of Turgut Ozal Medical Center. 22(2). 735–739. 24 indexed citations

13.

Thomas, Joseph, et al.. (2014). Complete Penoscrotal Transposition: Case Report and Review of the Literature. Fetal Diagnosis and Therapy. 37(1). 70–74. 9 indexed citations

14.

Kamien, Benjamin, James Harraway, Ben Lundie, et al.. (2013). Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy. American Journal of Medical Genetics Part A. 164(3). 782–788. 33 indexed citations

15.

Laurie, Andrew D., James Harraway, Andrew Fellowes, et al.. (2010). Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches. Journal of Thrombosis and Haemostasis. 8(4). 783–789. 28 indexed citations

16.

Harraway, James, Mark P. Smith, & Peter M. George. (2006). A highly informative, multiplexed assay for the indirect detection of hemophilia A using five‐linked microsatellites. Journal of Thrombosis and Haemostasis. 4(3). 587–590. 16 indexed citations

17.

Harraway, James & Peter M. George. (2005). Use of Fully Denaturing HPLC for UGT1A1 Genotyping in Gilbert Syndrome. Clinical Chemistry. 51(11). 2183–2185. 12 indexed citations

18.

Gearry, Richard B., Murray L. Barclay, Rebecca L Roberts, et al.. (2005). Thiopurine methyltransferase and 6‐thioguanine nucleotide measurement: early experience of use in clinical practice. Internal Medicine Journal. 35(10). 580–585. 51 indexed citations

19.

Harraway, James, et al.. (2005). Dual porphyria with mutations in both the UROD and HMBS genes. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 43(1). 80–82. 8 indexed citations

20.

Guilford, Parry, et al.. (1998). E-cadherin germline mutations in familial gastric cancer. Nature. 392(6674). 402–405. 1217 indexed citations breakdown →

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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