Priscilla M.K. Poon

3.2k total citations · 2 hit papers
29 papers, 2.5k citations indexed

About

Priscilla M.K. Poon is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Priscilla M.K. Poon has authored 29 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Priscilla M.K. Poon's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (4 papers). Priscilla M.K. Poon is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (4 papers). Priscilla M.K. Poon collaborates with scholars based in Hong Kong, China and United States. Priscilla M.K. Poon's co-authors include James S. Wainscoat, N M Hjelm, Yuk Ming Dennis Lo, Philip E. Johnson, Tze Kin Lau, Allan Chang, Tse Ngong Leung, Mark Tein, Christopher J. Haines and Michael Murphy and has published in prestigious journals such as New England Journal of Medicine, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Priscilla M.K. Poon

29 papers receiving 2.4k 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.

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

1998 1.3k citations Yuk Ming Dennis Lo, Mark Tein et al. The American Journal of Human Genetics profile →
Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

1998 534 citations N M Hjelm, Priscilla M.K. Poon et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Priscilla M.K. Poon Hong Kong	14	1.5k	788	707	550	320	29	2.5k
Theodore B. Moore United States	26	250 0.2×	692 0.9×	276 0.4×	245 0.4×	403 1.3×	99	2.0k
R. Finn United Kingdom	22	200 0.1×	413 0.5×	99 0.1×	459 0.8×	461 1.4×	65	2.2k
Klaus Rieneck Denmark	27	410 0.3×	457 0.6×	375 0.5×	152 0.3×	425 1.3×	64	1.9k
Augustine Rajakumar United States	34	2.0k 1.3×	446 0.6×	316 0.4×	81 0.1×	71 0.2×	73	3.7k
Carlo Carcassi Italy	29	134 0.1×	327 0.4×	97 0.1×	340 0.6×	408 1.3×	115	2.5k
Anastasia Konstantinidou Greece	23	296 0.2×	536 0.7×	120 0.2×	234 0.4×	84 0.3×	81	1.6k
Maurizio Sampietro Italy	31	644 0.4×	663 0.8×	161 0.2×	235 0.4×	1.4k 4.3×	83	3.1k
Nury Steuerwald United States	26	564 0.4×	1.1k 1.4×	57 0.1×	357 0.6×	66 0.2×	86	2.5k
Bertil Glader United States	30	365 0.2×	2.2k 2.7×	358 0.5×	1.6k 2.9×	1.4k 4.4×	131	4.6k
Katia Boven Belgium	23	229 0.2×	578 0.7×	1.6k 2.3×	175 0.3×	125 0.4×	36	2.7k

Countries citing papers authored by Priscilla M.K. Poon

Since Specialization

Citations

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

Fields of papers citing papers by Priscilla M.K. Poon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Priscilla M.K. Poon. 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 Priscilla M.K. Poon. The network helps show where Priscilla M.K. Poon may publish in the future.

Co-authorship network of co-authors of Priscilla M.K. Poon

This figure shows the co-authorship network connecting the top 25 collaborators of Priscilla M.K. Poon. A scholar is included among the top collaborators of Priscilla M.K. Poon 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 Priscilla M.K. Poon. Priscilla M.K. Poon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ichihara, Kiyoshi, Ferruccio Ceriotti, Priscilla M.K. Poon, et al.. (2013). The Asian project for collaborative derivation of reference intervals: (1) strategy and major results of standardized analytes. Clinical Chemistry and Laboratory Medicine (CCLM). 51(7). 1429–42. 56 indexed citations

Ichihara, Kiyoshi, et al.. (2007). Sources of Variation of Commonly Measured Serum Analytes in 6 Asian Cities and Consideration of Common Reference Intervals. Clinical Chemistry. 54(2). 356–365. 70 indexed citations

Wong, Chun Kwok, Priscilla M.K. Poon, Siu‐Po Ip, et al.. (2006). In vitro Immunomodulatory activities of a newly concocted traditional Chinese medicine formula: VI‐28. Phytotherapy Research. 20(10). 883–888. 10 indexed citations

Poon, Priscilla M.K., et al.. (2005). AGG interspersion analysis of the FMR1 CGG repeats in mental retardation of unspecific cause. Clinical Biochemistry. 39(3). 244–248. 1 indexed citations

Lam, Ching‐Wan, et al.. (2005). Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemia. Clinica Chimica Acta. 360(1-2). 167–172. 6 indexed citations

Pang, Chi‐Pui, Man-Wo Tsang, Ching‐Wan Lam, et al.. (2003). Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes. Human Mutation. 21(4). 453–453. 23 indexed citations

Yeung, David K. W., et al.. (2001). Detection of an intense resonance at 2.4 ppm in ¹H MR spectra of patients with severe late‐delayed, radiation‐induced brain injuries. Magnetic Resonance in Medicine. 45(6). 994–1000. 12 indexed citations

Lam, Ching‐Wan, Priscilla M.K. Poon, Sui-Fan Tong, et al.. (2001). Novel Mutation and Polymorphisms of the HMBS Gene Detected by Denaturing HPLC. Clinical Chemistry. 47(2). 343–346. 12 indexed citations

Lam, Ching‐Wan, Kwun Nam Hui, Priscilla M.K. Poon, et al.. (2001). Novel splicing mutation of the PPOX gene (IVS10+1G→A) detected by denaturing high-performance liquid chromatography. Clinica Chimica Acta. 305(1-2). 197–200. 4 indexed citations

10.

Orrico, Alfredo, Ching‐Wan Lam, Lucia Galli, et al.. (2000). MECP2 mutation in male patients with non‐specific X‐linked mental retardation. FEBS Letters. 481(3). 285–288. 183 indexed citations

11.

Lam, C. K., et al.. (2000). Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography. Prenatal Diagnosis. 20(9). 765–768. 33 indexed citations

12.

Poon, Priscilla M.K., et al.. (2000). Rapid Analysis of CGG Repeat Length in the FMR1 Gene. Clinical Chemistry and Laboratory Medicine (CCLM). 38(9). 935–938. 2 indexed citations

13.

Poon, Priscilla M.K., et al.. (1999). FRAXAC1 and DXS548 polymorphisms in the Chinese population. American Journal of Medical Genetics. 84(3). 208–213. 10 indexed citations

14.

Zhong, Nan, Weina Ju, Weimin Xu, et al.. (1999). Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians. American Journal of Medical Genetics. 84(3). 191–194. 31 indexed citations

15.

Baum, Larry, Chi Pui Pang, Dorothy S.P. Fan, et al.. (1999). Run-on mutation and three novel nonsense mutations identified in the PAX6 gene in patients with aniridia. Human Mutation. 14(3). 272–273. 20 indexed citations

16.

Pang, Chi‐Pui, et al.. (1999). Trinucleotide CGG repeat in theFMR1 gene in Chinese mentally retarded patients. American Journal of Medical Genetics. 84(3). 179–183. 24 indexed citations

17.

Poon, Priscilla M.K., et al.. (1998). CGG Repeat Interruptions in the FMR1 Gene in Patients with Infantile Autism. Clinical Chemistry and Laboratory Medicine (CCLM). 36(8). 649–653. 3 indexed citations

18.

Lo, Yuk Ming Dennis, Mark Tein, Tze Kin Lau, et al.. (1998). Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis. The American Journal of Human Genetics. 62(4). 768–775. 1262 indexed citations breakdown →

19.

Ju, Weina, et al.. (1996). A survey ofFRAXE allele sizes in three populations. American Journal of Medical Genetics. 64(2). 415–419. 22 indexed citations

20.

Poon, Priscilla M.K., et al.. (1993). Gas chromatographic-mass fragmentographic determination of serum 1α,25 dihydroxyvitamin D3. Clinical Biochemistry. 26(6). 461–469. 8 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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