Hon Fong L. Mark

906 total citations
54 papers, 668 citations indexed

About

Hon Fong L. Mark is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Hon Fong L. Mark has authored 54 papers receiving a total of 668 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 22 papers in Molecular Biology and 14 papers in Plant Science. Recurrent topics in Hon Fong L. Mark's work include Genomic variations and chromosomal abnormalities (22 papers), Chromosomal and Genetic Variations (14 papers) and Prenatal Screening and Diagnostics (11 papers). Hon Fong L. Mark is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Chromosomal and Genetic Variations (14 papers) and Prenatal Screening and Diagnostics (11 papers). Hon Fong L. Mark collaborates with scholars based in United States, Hong Kong and Germany. Hon Fong L. Mark's co-authors include Alaa Afify, Kirby I. Bland, Bruce A. Werness, Douglas R. Gnepp, Iman Hanna, David Feldman, Robert Sokolic, Stephen Brown, Bkc Chow and Yvonne Mark and has published in prestigious journals such as Genetics, Genomics and Breast Cancer Research and Treatment.

In The Last Decade

Hon Fong L. Mark

54 papers receiving 647 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hon Fong L. Mark United States	15	263	237	179	112	107	54	668
Christian Herens Belgium	16	275 1.0×	295 1.2×	101 0.6×	67 0.6×	101 0.9×	35	877
Susi Scappaticci Italy	18	374 1.4×	262 1.1×	124 0.7×	67 0.6×	65 0.6×	47	784
Ilse Chudoba Germany	16	436 1.7×	410 1.7×	71 0.4×	149 1.3×	171 1.6×	36	858
Sandra Hing United Kingdom	16	408 1.6×	211 0.9×	181 1.0×	97 0.9×	242 2.3×	24	916
Kumi Nakazaki Japan	10	543 2.1×	315 1.3×	154 0.9×	151 1.3×	58 0.5×	34	996
Oľga Østrup Denmark	18	619 2.4×	216 0.9×	115 0.6×	208 1.9×	81 0.8×	61	1.0k
Irmgard Verdorfer Austria	17	370 1.4×	136 0.6×	172 1.0×	215 1.9×	188 1.8×	46	849
Marion C. Baker United Kingdom	17	469 1.8×	310 1.3×	206 1.2×	250 2.2×	236 2.2×	27	1.2k
J. L. M. Beck Netherlands	12	433 1.6×	292 1.2×	176 1.0×	211 1.9×	111 1.0×	17	934
Barbara K. Hecht United States	16	498 1.9×	272 1.1×	231 1.3×	117 1.0×	57 0.5×	37	1.1k

Countries citing papers authored by Hon Fong L. Mark

Since Specialization

Citations

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

Fields of papers citing papers by Hon Fong L. Mark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hon Fong L. Mark. 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 Hon Fong L. Mark. The network helps show where Hon Fong L. Mark may publish in the future.

Co-authorship network of co-authors of Hon Fong L. Mark

This figure shows the co-authorship network connecting the top 25 collaborators of Hon Fong L. Mark. A scholar is included among the top collaborators of Hon Fong L. Mark 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 Hon Fong L. Mark. Hon Fong L. Mark 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

Mark, Hon Fong L., et al.. (2005). Constitutional partial 1q trisomy mosaicism and Wilms tumor. Cancer Genetics and Cytogenetics. 162(2). 166–171. 7 indexed citations

Alter, David A. & Hon Fong L. Mark. (2000). Cytogenetic Study of a Patient with Infant Acute Lymphoblastic Leukemia Using GTG-Banding and Chromosome Painting. Experimental and Molecular Pathology. 69(2). 152–158. 2 indexed citations

Mark, Hon Fong L., et al.. (2000). Hypotetraploidy in a Patient with Small Cell Carcinoma. Experimental and Molecular Pathology. 68(1). 70–76. 2 indexed citations

Abuelo, Dianne, et al.. (2000). Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting. American Journal of Medical Genetics. 94(5). 392–399. 18 indexed citations

Mark, Hon Fong L., et al.. (1999). Study of Chromosome 12 Copy Number in Breast Cancer Using Fluorescence In Situ Hybridization. Cancer Genetics and Cytogenetics. 108(1). 26–31. 6 indexed citations

Mark, Hon Fong L., et al.. (1999). Trisomy 9 in a Patient with Secondary Acute Myelogenous Leukemia Detected by Fluorescent in situ Hybridization. Pathobiology. 67(2). 111–114. 3 indexed citations

Mark, Hon Fong L., et al.. (1999). Abnormal Chromosome 8 Copy Number in Stage I to Stage IV Breast Cancer Studied by Fluorescence In Situ Hybridization. Cancer Genetics and Cytogenetics. 108(1). 1–5. 16 indexed citations

Mark, Hon Fong L., David Feldman, & Mark Sigman. (1999). Conventional and Molecular Cytogenetic Identification of a Variant Klinefelter Syndrome Patient with a Deleted X Chromosome. Pathobiology. 67(1). 55–58. 6 indexed citations

Mark, Hon Fong L., et al.. (1999). A Variant Klinefelter Syndrome Patient with an XXY/XX/XY Karyotype Studied by GTG-Banding and Fluorescence in Situ Hybridization. Experimental and Molecular Pathology. 67(1). 50–56. 16 indexed citations

10.

Mark, Hon Fong L., et al.. (1999). A Multimodal Approach in the Diagnosis of Patients with Hematopoietic Disorders. Cancer Genetics and Cytogenetics. 109(1). 14–20. 10 indexed citations

11.

Mark, Hon Fong L., et al.. (1999). Assessment of Chromosomal Trisomies in Prostate Cancer Using Fluorescent in Situ Hybridization. Experimental and Molecular Pathology. 67(2). 109–117. 9 indexed citations

12.

Mark, Hon Fong L., et al.. (1998). Fluorescent in situ Hybridization Detection of HER-2/neu Gene Amplification in Rhabdomyosarcoma. Pathobiology. 66(2). 59–63. 26 indexed citations

13.

Mark, Hon Fong L., et al.. (1998). Fluorescence In Situ Hybridization Analysis of Single-Cell Trisomies for Determination of Clonality. Cancer Genetics and Cytogenetics. 102(1). 1–5. 10 indexed citations

14.

Mark, Hon Fong L., et al.. (1997). Stage I and Stage II Infiltrating Ductal Carcinoma of the Breast Analyzed for Chromosome 8 Copy Number Using Fluorescent in situ Hybridization. Pathobiology. 65(4). 184–189. 21 indexed citations

15.

Mark, Hon Fong L., et al.. (1997). Translocation 2; 19 in a Patient with Probable Relapsed Acute Myeloid Leukemia. Pathobiology. 65(4). 223–228. 4 indexed citations

16.

Afify, Alaa & Hon Fong L. Mark. (1997). Fluorescence in situ hybridization assessment of chromosome 8 copy number in stage i and stage ii infiltrating ductal carcinoma of the breast. Cancer Genetics and Cytogenetics. 97(2). 101–105. 24 indexed citations

17.

Afify, Alaa, Kirby I. Bland, & Hon Fong L. Mark. (1996). Fluorescentin situ hybridization assessment of chromosome 8 copy number in breast cancer. Breast Cancer Research and Treatment. 38(2). 201–208. 40 indexed citations

18.

Mark, Hon Fong L., et al.. (1995). Constitutional trisomy 8 mosaicism and gestational trophoblastic disease. Cancer Genetics and Cytogenetics. 80(2). 150–154. 26 indexed citations

19.

Mark, Hon Fong L., et al.. (1993). A study of homologous chromosomes using a morphometric approach. Genome. 36(5). 1003–1006. 3 indexed citations

20.

Hansen, Katrine, et al.. (1992). Undifferentiated Small Cell Hepatoblastoma with a Unique Chromosomal Translocation: A Case Report. Pediatric Pathology. 12(3). 457–462. 14 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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