Christine M. Eng

5.4k total citations · 1 hit paper
40 papers, 3.9k citations indexed

About

Christine M. Eng is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Christine M. Eng has authored 40 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Physiology, 14 papers in Molecular Biology and 14 papers in Epidemiology. Recurrent topics in Christine M. Eng's work include Lysosomal Storage Disorders Research (23 papers), Trypanosoma species research and implications (13 papers) and Cellular transport and secretion (10 papers). Christine M. Eng is often cited by papers focused on Lysosomal Storage Disorders Research (23 papers), Trypanosoma species research and implications (13 papers) and Cellular transport and secretion (10 papers). Christine M. Eng collaborates with scholars based in United States, Israel and Japan. Christine M. Eng's co-authors include Robert J. Desnick, Dominique P. Germain, Philip Lee, Nathalie Guffon, William R. Wilcox, Gabor E. Linthorst, Louis R. Caplan, Kenneth H. Astrin, Grace A. Ashley and David F. Bishop and has published in prestigious journals such as New England Journal of Medicine, JAMA and Journal of Clinical Investigation.

In The Last Decade

Christine M. Eng

37 papers receiving 3.8k 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.

Safety and Efficacy of Recombinant Human α-Galactosidase A Replacement Therapy in Fabry's Disease

2001 1.1k citations Christine M. Eng, Nathalie Guffon et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christine M. Eng United States	26	3.0k	1.6k	914	900	884	40	3.9k
Roseline Froissart France	27	2.1k 0.7×	781 0.5×	494 0.5×	646 0.7×	657 0.7×	90	2.8k
Maja Di Rocco Italy	34	1.2k 0.4×	512 0.3×	350 0.4×	778 0.9×	498 0.6×	147	3.6k
Marianne Rohrbach Switzerland	26	897 0.3×	381 0.2×	238 0.3×	638 0.7×	253 0.3×	81	2.4k
Jules G. Leroy Belgium	29	716 0.2×	227 0.1×	235 0.3×	259 0.3×	395 0.4×	89	2.6k
Edward H. Bossen United States	23	604 0.2×	253 0.2×	130 0.1×	530 0.6×	113 0.1×	53	2.0k
Catherine Rehder United States	24	694 0.2×	162 0.1×	194 0.2×	384 0.4×	64 0.1×	75	1.9k
C Borrone Italy	24	613 0.2×	165 0.1×	129 0.1×	169 0.2×	159 0.2×	86	1.7k
Lara Fallon United States	21	191 0.1×	323 0.2×	170 0.2×	625 0.7×	302 0.3×	62	2.4k
Gary S. Gottesman United States	20	369 0.1×	224 0.1×	55 0.1×	451 0.5×	139 0.2×	55	1.6k
Carlos R. Ferreira United States	22	336 0.1×	127 0.1×	74 0.1×	300 0.3×	200 0.2×	101	2.1k

Countries citing papers authored by Christine M. Eng

Since Specialization

Citations

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

Fields of papers citing papers by Christine M. Eng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine M. Eng. 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 Christine M. Eng. The network helps show where Christine M. Eng may publish in the future.

Co-authorship network of co-authors of Christine M. Eng

This figure shows the co-authorship network connecting the top 25 collaborators of Christine M. Eng. A scholar is included among the top collaborators of Christine M. Eng 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 Christine M. Eng. Christine M. Eng 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

Zhao, Sen, Shenglan Li, Jill A. Rosenfeld, et al.. (2025). The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. The American Journal of Human Genetics. 112(11). 2578–2590.

Ben‐Omran, Tawfeg, Basil T. Darras, Sanjay P. Prabhu, et al.. (2013). Clinical Application of Whole-Exome Sequencing. JAMA Neurology. 70(6). 788–788. 14 indexed citations

Nakao, Shoichiro, Toshihiro Takenaka, Akihiro Tanaka, et al.. (2003). Fabry disease: Detection of undiagnosed hemodialysis patients and identification of a “renal variant” phenotype1. Kidney International. 64(3). 801–807. 319 indexed citations

Eng, Christine M. & Robert J. Desnick. (2001). 22. Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases. Advances in genetics. 44. 275–296. 10 indexed citations

Ashley, Grace A., Junaid Shabbeer, Makiko Yasuda, Christine M. Eng, & Robert J. Desnick. (2001). Fabry disease: twenty novel α-galactosidase A mutations causing the classical phenotype. Journal of Human Genetics. 46(4). 192–196. 52 indexed citations

Eng, Christine M., Nathalie Guffon, William R. Wilcox, et al.. (2001). Safety and Efficacy of Recombinant Human α-Galactosidase A Replacement Therapy in Fabry's Disease. New England Journal of Medicine. 345(1). 9–16. 1133 indexed citations breakdown →

Dong, Jianli, David R. Katz, Christine M. Eng, Ruth Kornreich, & Robert J. Desnick. (2001). Nonradioactive Detection of the Common Connexin 26 167delT and 35delG Mutations and Frequencies among Ashkenazi Jews. Molecular Genetics and Metabolism. 73(2). 160–163. 18 indexed citations

Frustaci, Andrea, Cristina Chimenti, Roberta Ricci, et al.. (2001). Improvement in Cardiac Function in the Cardiac Variant of Fabry's Disease with Galactose-Infusion Therapy. New England Journal of Medicine. 345(1). 25–32. 233 indexed citations

Ashley, Grace A., et al.. (1999). Twenty Novel Mutations in the α-Galactosidase A Gene Causing Fabry Disease. Molecular Medicine. 5(12). 806–811. 64 indexed citations

10.

Weston, Ainsley, Ira J. Bleiweiss, Leslie D. McCurdy, et al.. (1998). Frequency and Carrier Risk Associated with Common BRCA1 and BRCA2 Mutations in Ashkenazi Jewish Breast Cancer Patients. The American Journal of Human Genetics. 63(1). 45–51. 167 indexed citations

11.

Brown, Lee K., et al.. (1997). Pulmonary Involvement in Fabry Disease. American Journal of Respiratory and Critical Care Medicine. 155(3). 1004–1010. 66 indexed citations

12.

Caggana, Michele, Grace A. Ashley, Robert J. Desnick, & Christine M. Eng. (1997). Fabry disease: Molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1. American Journal of Medical Genetics. 71(3). 329–335. 17 indexed citations

13.

Eng, Christine M.. (1997). Prenatal Genetic Carrier Testing Using Triple Disease Screening. JAMA. 278(15). 1268–1268. 59 indexed citations

14.

Medintz, Igor L., Louis Levine, Leslie D. McCurdy, et al.. (1997). HLA-DQA1 and Polymarker Allele Frequencies in Two New York City Jewish Populations. Journal of Forensic Sciences. 42(5). 919–922. 7 indexed citations

15.

Eng, Christine M., Susan A. Slaugenhaupt, Anat Blumenfeld, et al.. (1995). Prenatal diagnosis of familial dysautonomia by analysis of linked CA‐repeat polymorphisms on chromosome 9q31–q33. American Journal of Medical Genetics. 59(3). 349–355. 9 indexed citations

16.

Sherman, Jeffrey B., Nina Raben, Zohar Argov, et al.. (1994). Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.. PubMed. 55(2). 305–13. 53 indexed citations

17.

Sakuraba, Hitoshi, Christine M. Eng, Robert J. Desnick, & David F. Bishop. (1992). Invariant exon skipping in the human α-galactosidase A pre-mRNA: A g+1 to t substitution in a 5′-splice site causing Fabry disease. Genomics. 12(4). 643–650. 45 indexed citations

18.

Fisher, Edward A., Robert J. Desnick, Ronald E. Gordon, et al.. (1992). Fabry Disease: An Unusual Cause of Severe Coronary Disease in a Young Man. Annals of Internal Medicine. 117(3). 221–223. 26 indexed citations

19.

Scheidt, Wolfgang von, Christine M. Eng, Thomas Fitzmaurice, et al.. (1991). An Atypical Variant of Fabry's Disease with Manifestations Confined to the Myocardium. New England Journal of Medicine. 324(6). 395–399. 297 indexed citations

20.

Rubin, Steven E., et al.. (1989). Medical Management of Orbital Subperiosteal Abscess in Children/Discussion. Journal of Pediatric Ophthalmology & Strabismus. 26(1). 21–27. 56 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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