Harold Chen

2.0k total citations
57 papers, 921 citations indexed

About

Harold Chen is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Harold Chen has authored 57 papers receiving a total of 921 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 19 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in Harold Chen's work include Genomic variations and chromosomal abnormalities (11 papers), Genetic Syndromes and Imprinting (6 papers) and Connective tissue disorders research (6 papers). Harold Chen is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetic Syndromes and Imprinting (6 papers) and Connective tissue disorders research (6 papers). Harold Chen collaborates with scholars based in United States, Netherlands and Mexico. Harold Chen's co-authors include Wladimir Wertelecki, John M. Opitz, Cathy M. Tuck‐Müller, Shibo Li, Chung‐Ho Chang, Christine J. Kusyk, Denise Batista, Will R. Blackburn, A. Al Saadi and Eugene V. Perrin and has published in prestigious journals such as JAMA, Journal of the American Academy of Dermatology and Human Genetics.

In The Last Decade

Harold Chen

53 papers receiving 861 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Harold Chen United States 19 514 351 203 158 144 57 921
S A Al-Awadi Kuwait 17 424 0.8× 294 0.8× 239 1.2× 161 1.0× 146 1.0× 66 899
Eric A. Wulfsberg United States 23 768 1.5× 462 1.3× 255 1.3× 81 0.5× 241 1.7× 47 1.2k
Alessandra Carnevale Mexico 20 522 1.0× 377 1.1× 204 1.0× 130 0.8× 184 1.3× 98 1.2k
Diana García‐Cruz Mexico 16 356 0.7× 272 0.8× 112 0.6× 72 0.5× 131 0.9× 81 727
Frank Majewski Germany 16 755 1.5× 579 1.6× 271 1.3× 157 1.0× 200 1.4× 26 1.3k
J. O. Van Hemel Netherlands 21 809 1.6× 457 1.3× 356 1.8× 85 0.5× 109 0.8× 38 1.1k
Fryns Jp Belgium 16 728 1.4× 399 1.1× 297 1.5× 85 0.5× 108 0.8× 106 996
L Koulischer Belgium 19 386 0.8× 276 0.8× 208 1.0× 122 0.8× 154 1.1× 94 1.1k
Talaat I. Farag Kuwait 17 432 0.8× 314 0.9× 213 1.0× 149 0.9× 160 1.1× 64 923
M. H. K. Shokeir Canada 19 355 0.7× 557 1.6× 178 0.9× 175 1.1× 191 1.3× 48 1.3k

Countries citing papers authored by Harold Chen

Since Specialization
Citations

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

Fields of papers citing papers by Harold Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harold Chen

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

All Works

20 of 20 papers shown
1.
Akbari, Maryam, et al.. (2018). Basal cell nevus syndrome (Gorlin syndrome): genetic insights, diagnostic challenges, and unmet milestones. Pathophysiology. 25(2). 77–82. 17 indexed citations
2.
Sankararaman, Senthilkumar, et al.. (2012). Another case of genitopatellar syndrome. Clinical Dysmorphology. 21(4). 226–228. 2 indexed citations
3.
Chen, Harold. (2012). Multiple Pterygium Syndrome. PubMed. 8(6). 1479–1485. 1 indexed citations
4.
Hoffman, William H., Alka Jain, Harold Chen, & Neal S. Fedarko. (2008). Matrix extracellular phosphoglycoprotein (MEPE) correlates with serum phosphorus prior to and during octreotide treatment and following excisional surgery in hypophosphatemic linear sebaceous nevus syndrome. American Journal of Medical Genetics Part A. 146A(16). 2164–2168. 8 indexed citations
5.
Toydemir, Reha M., Harold Chen, Virginia K. Proud, et al.. (2006). Trismus‐pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8. American Journal of Medical Genetics Part A. 140A(22). 2387–2393. 51 indexed citations
6.
Chen, Harold, et al.. (1999). Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility. American Journal of Medical Genetics. 82(3). 215–218. 17 indexed citations
7.
Asamoah, Alexander, et al.. (1998). A case of insertional translocation involving chromosomes 2 and 4. Clinical Genetics. 53(2). 142–146. 2 indexed citations
8.
Li, Shibo, et al.. (1998). Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH). American Journal of Medical Genetics. 80(5). 487–490. 22 indexed citations
9.
Tuck‐Müller, Cathy M., Harold Chen, Shibo Li, et al.. (1995). Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Human Genetics. 96(1). 119–129. 81 indexed citations
10.
Chen, Harold, Will R. Blackburn, & Wladimir Wertelecki. (1995). Fetal akinesia and multiple perinatal fractures. American Journal of Medical Genetics. 55(4). 472–477. 25 indexed citations
11.
Chen, Harold, Cathy M. Tuck‐Müller, Denise Batista, & Wladimir Wertelecki. (1995). Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. American Journal of Medical Genetics. 56(2). 219–223. 20 indexed citations
12.
Tuck‐Müller, Cathy M., Paul Dyken, Shibo Li, et al.. (1995). Translocation 10;18 in a patient with juvenile neuronal ceroid‐lipofuscinosis (Batten disease). American Journal of Medical Genetics. 57(2). 168–171.
13.
King, Judy, et al.. (1995). Neu-Laxova Syndrome: Pathological Evaluation of a Fetus and Review of the Literature. Pediatric Pathology & Laboratory Medicine. 15(1). 57–79. 17 indexed citations
14.
Chen, Harold. (1994). An Approach to Work-up of Dysmorphic Patients: Clinical, Cytogenetic, and Molecular Aspects.. The Keio Journal of Medicine. 43(2). 98–107. 4 indexed citations
15.
16.
Carrington, Patrick R., et al.. (1994). Trichorhinophalangeal syndrome, type I. Journal of the American Academy of Dermatology. 31(2). 331–336. 20 indexed citations
17.
Chen, Harold & Wladimir Wertelecki. (1994). Genetic services in the United States. The Japanese Journal of Human Genetics. 39(2). 275–288. 2 indexed citations
18.
Arn, Pamela, et al.. (1994). SRVX, a sex reversing locus in Xp21.2?p22.11. Human Genetics. 93(4). 389–93. 49 indexed citations
19.
Chen, Harold, Enrique A. González, John M. Opitz, & James F. Reynolds. (1987). Amniotic band sequence and its neurocutaneous manifestations. American Journal of Medical Genetics. 28(3). 661–673. 17 indexed citations
20.
Langer, Leonard O., et al.. (1976). A severe infantile micromelic chondrodysplasia which resembles kniest disease. European Journal of Pediatrics. 123(1). 29–38. 18 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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