Nicholas Pachter

3.4k total citations
30 papers, 578 citations indexed

About

Nicholas Pachter is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Nicholas Pachter has authored 30 papers receiving a total of 578 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Nicholas Pachter's work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (7 papers) and Genetic factors in colorectal cancer (6 papers). Nicholas Pachter is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (7 papers) and Genetic factors in colorectal cancer (6 papers). Nicholas Pachter collaborates with scholars based in Australia, United States and United Kingdom. Nicholas Pachter's co-authors include Ingrid Winship, Anthony J. Gill, Peter Earls, Adele Clarkson, Roderick Clifton‐Bligh, Stewart Fleming, Diana E. Benn, Barbara Young, Angela Chou and Bruce G. Robinson and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and International Journal of Cancer.

In The Last Decade

Nicholas Pachter

29 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicholas Pachter Australia	14	233	210	123	121	86	30	578
Carles Zafón Spain	18	252 1.1×	139 0.7×	86 0.7×	77 0.6×	179 2.1×	73	968
Marco Salvatore Italy	13	264 1.1×	170 0.8×	94 0.8×	151 1.2×	45 0.5×	50	631
Jessica Clague United States	13	396 1.7×	255 1.2×	113 0.9×	269 2.2×	50 0.6×	18	775
Julie Richer Canada	13	202 0.9×	399 1.9×	80 0.7×	55 0.5×	46 0.5×	34	670
Yiola Marcou Cyprus	11	243 1.0×	137 0.7×	75 0.6×	109 0.9×	29 0.3×	23	536
Isabelle Coupier France	14	255 1.1×	274 1.3×	108 0.9×	275 2.3×	275 3.2×	35	834
Talat Mushtaq United Kingdom	14	216 0.9×	131 0.6×	71 0.6×	36 0.3×	80 0.9×	36	653
Stanley Hooker United States	16	187 0.8×	310 1.5×	224 1.8×	118 1.0×	40 0.5×	26	735
Suzanne P. MacFarland United States	13	187 0.8×	89 0.4×	58 0.5×	74 0.6×	73 0.8×	45	527
En Yun Loy Singapore	12	130 0.6×	166 0.8×	98 0.8×	37 0.3×	65 0.8×	17	528

Countries citing papers authored by Nicholas Pachter

Since Specialization

Citations

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

Fields of papers citing papers by Nicholas Pachter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicholas Pachter

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

Collins, Felicity, Susan M. White, Mathew Wallis, et al.. (2024). Assessing the unmet needs of genomic testing in Australia: a geospatial exploration. European Journal of Human Genetics. 33(4). 496–503. 1 indexed citations

Gupta, Surabhi, Cassandra Nichols, Jessica Phillips, et al.. (2021). Lynch syndrome associated endometrial carcinomas in Western Australia: an analysis of universal screening by mismatch repair protein immunohistochemistry. International Journal of Gynecological Cancer. 31(6). 846–851. 1 indexed citations

O’Sullivan, Sarah, et al.. (2021). Patient Satisfaction with Private Genetic Counselling for Familial Cancer in Western Australia: A Prospective Audit. Asian Pacific Journal of Cancer Prevention. 22(10). 3253–3259. 1 indexed citations

Meiser, Bettina, Rachel Austin, Cassandra Nichols, et al.. (2021). Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study. Journal of Community Genetics. 13(1). 59–73. 1 indexed citations

Tiller, Jane, Rebecca Macintosh, Sarah O’Sullivan, et al.. (2020). Disclosing genetic information to family members without consent: Five Australian case studies. European Journal of Medical Genetics. 63(11). 104035–104035. 8 indexed citations

Beecroft, Sarah J., Kyle S. Yau, Richard J. N. Allcock, et al.. (2020). Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience. Annals of Clinical and Translational Neurology. 7(3). 353–362. 24 indexed citations

Ong, Royston, Samantha Edwards, Denise Howting, et al.. (2019). Study protocol of a multicentre cohort pilot study implementing an expanded preconception carrier-screening programme in metropolitan and regional Western Australia. BMJ Open. 9(6). e028209–e028209. 5 indexed citations

Nichols, Cassandra, et al.. (2019). Uptake of testing for germline BRCA mutations in patients with non-mucinous epithelial ovarian cancers in Western Australia: a comparison of different genetic counseling methods. International Journal of Gynecological Cancer. 29(6). 1038–1042. 13 indexed citations

Pathak, Gopal P., Dimitar N. Azmanov, Erin B. Taylor, et al.. (2019). Tricho-hepatic-enteric syndrome (THES) without intractable diarrhoea. Gene. 699. 110–114. 12 indexed citations

10.

Morrow, April, Emily Hogden, Yoon‐Jung Kang, et al.. (2019). Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol. Trials. 20(1). 373–373. 16 indexed citations

11.

Beilby, John, Nicholas Pachter, Gareth Baynam, et al.. (2019). Genomic Testing for Human Health and Disease Across the Life Cycle: Applications and Ethical, Legal, and Social Challenges. Frontiers in Public Health. 7. 40–40. 45 indexed citations

12.

Stewart, Colin J.R., et al.. (2019). Incidence of germline BRCA1/2 mutations in women with tubo-ovarian high-grade serous carcinomas with and without serous tubal intra-epithelial carcinomas. International Journal of Gynecological Cancer. 30(1). 94–99. 1 indexed citations

13.

Song, Yong, Jing Guo, Belinda J. Hales, et al.. (2018). Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children. Journal of Translational Medicine. 16(1). 42–42. 37 indexed citations

14.

Lan, N., Michael Fietz, Nicholas Pachter, Vincent Paul, & David Playford. (2018). A case of vascular Ehlers-Danlos Syndrome with a cardiomyopathy and multi-system involvement. Cardiovascular Pathology. 35. 48–51. 7 indexed citations

15.

Mascarenhas, Lyon, Susan Shanley, Gillian Mitchell, et al.. (2018). Current mismatch repair deficiency tumor testing practices and capabilities: A survey of Australian pathology providers. Asia-Pacific Journal of Clinical Oncology. 14(6). 417–425. 9 indexed citations

16.

Baynam, Gareth, Nicholas Pachter, Lyn Schofield, et al.. (2017). 3-Dimensional Facial Analysis—Facing Precision Public Health. Frontiers in Public Health. 5. 31–31. 9 indexed citations

17.

Baynam, Gareth, Caron Molster, Emma Kowal, et al.. (2017). Indigenous Genetics and Rare Diseases: Harmony, Diversity and Equity. Advances in experimental medicine and biology. 1031. 511–520. 18 indexed citations

18.

Cohen, Paul A., et al.. (2016). Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing. International Journal of Gynecological Cancer. 26(5). 892–897. 20 indexed citations

19.

Baynam, Gareth, Nicholas Pachter, F. Ellis McKenzie, et al.. (2015). AB002. The rare and undiagnosed diseases diagnostic service. Annals of Translational Medicine. 4(2). 3–3.

20.

Gill, Anthony J., Nicholas Pachter, Angela Chou, et al.. (2011). Renal Tumors Associated With Germline SDHB Mutation Show Distinctive Morphology. The American Journal of Surgical Pathology. 35(10). 1578–1585. 138 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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