Charles M. Strom

3.7k total citations · 1 hit paper
75 papers, 2.4k citations indexed

About

Charles M. Strom is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Charles M. Strom has authored 75 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Pediatrics, Perinatology and Child Health, 20 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in Charles M. Strom's work include Prenatal Screening and Diagnostics (28 papers), Cystic Fibrosis Research Advances (14 papers) and Genomic variations and chromosomal abnormalities (8 papers). Charles M. Strom is often cited by papers focused on Prenatal Screening and Diagnostics (28 papers), Cystic Fibrosis Research Advances (14 papers) and Genomic variations and chromosomal abnormalities (8 papers). Charles M. Strom collaborates with scholars based in United States, Poland and Russia. Charles M. Strom's co-authors include Yury Verlinsky, Norman Ginsberg, Aaron Lifchez, Svetlana Rechitsky, Weimin Sun, Jacob Moise, Anver Kuliev, J. Valle, Joy B. Redman and Franklin Quan and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Clinical Oncology.

In The Last Decade

Charles M. Strom

71 papers receiving 2.2k 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.

Eater, a Transmembrane Protein Mediating Phagocytosis of Bacterial Pathogens in Drosophila

2005 307 citations Charles M. Strom et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles M. Strom United States	26	1.2k	688	556	376	318	75	2.4k
Luigi F. Bernini Netherlands	31	549 0.5×	640 0.9×	858 1.5×	117 0.3×	224 0.7×	107	3.1k
Erik C. Thorland United States	28	843 0.7×	2.1k 3.1×	1.8k 3.2×	129 0.3×	324 1.0×	61	4.2k
Faith Kung United States	25	332 0.3×	87 0.1×	478 0.9×	429 1.1×	116 0.4×	49	1.8k
Fernando Regla Vargas Brazil	24	204 0.2×	480 0.7×	805 1.4×	444 1.2×	47 0.1×	83	2.0k
Yoshihide Ueda Japan	29	183 0.2×	742 1.1×	2.8k 5.1×	115 0.3×	288 0.9×	122	4.6k
Masato Tsukahara Japan	22	299 0.3×	557 0.8×	477 0.9×	236 0.6×	77 0.2×	97	1.4k
Laird G. Jackson United States	30	1.0k 0.9×	866 1.3×	1.6k 2.8×	163 0.4×	162 0.5×	71	3.0k
P Rubinstein United States	33	249 0.2×	1.1k 1.6×	805 1.4×	417 1.1×	1.4k 4.3×	139	4.7k
Luis E. Figuera Mexico	23	126 0.1×	622 0.9×	637 1.1×	110 0.3×	159 0.5×	134	1.8k
Anne E. O’Connor Australia	30	319 0.3×	489 0.7×	1.1k 1.9×	591 1.6×	234 0.7×	76	2.2k

Countries citing papers authored by Charles M. Strom

Since Specialization

Citations

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

Fields of papers citing papers by Charles M. Strom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles M. Strom

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

Strom, Charles M., et al.. (2024). Machine perfusion organ preservation: Highlights from the American Transplant Congress 2023. Artificial Organs. 48(7). 794–799. 3 indexed citations

Hemmat, Morteza, Weina Chen, Arturo Anguiano, et al.. (2014). Submicroscopic deletion of 5q involving tumor suppressor genes (CTNNA1, HSPA9) and copy neutral loss of heterozygosity associated with TET2 and EZH2 mutations in a case of MDS with normal chromosome and FISH results. Molecular Cytogenetics. 7(1). 35–35. 8 indexed citations

Hemmat, Morteza, Xiaojing Yang, Arturo Anguiano, et al.. (2014). Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay. Molecular Cytogenetics. 7(1). 50–50. 6 indexed citations

Strom, Charles M., Vladimira Sulcova, David Tsao, et al.. (2013). DNA Combing Assay for Detection of Contraction-Dependent Facioscapulohumeral Muscular Dystrophy (FSHD1) (PD3.005). Neurology. 80(7_supplement). 1 indexed citations

Strom, Charles M., Beryl Crossley, Ke Zhang, et al.. (2012). Testing for variants in CYP2C19: population frequencies and testing experience in a clinical laboratory. Genetics in Medicine. 14(1). 95–100. 64 indexed citations

Anguiano, Arturo, Fatih Z Boyar, Mary Haddadin, et al.. (2012). Spectral Karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory. Molecular Cytogenetics. 5(1). 3–3. 11 indexed citations

Hantash, Feras, et al.. (2009). Apparent Homozygosity of a Novel Frame Shift Mutation in the CFTR Gene Because of a Large Deletion. Journal of Molecular Diagnostics. 11(3). 253–256. 14 indexed citations

Hantash, Feras, Aubrey Milunsky, Zhenyuan Wang, et al.. (2006). A large deletion in the CFTR gene in CBAVD. Genetics in Medicine. 8(2). 93–95. 25 indexed citations

Strom, Charles M., et al.. (2006). Technical Validation of a Tm Biosciences Luminex-Based Multiplex Assay for Detecting the American College of Medical Genetics Recommended Cystic Fibrosis Mutation Panel. Journal of Molecular Diagnostics. 8(3). 371–375. 19 indexed citations

10.

Brown, Nicholas M., Victoria M. Pratt, Arlene Buller, et al.. (2005). Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results. Genetics in Medicine. 7(4). 278–282. 16 indexed citations

11.

Strom, Charles M., Richard Janeczko, Ben Anderson, et al.. (2005). Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descent. Genetics in Medicine. 7(9). 633–639. 13 indexed citations

12.

Hantash, Feras, Joy B. Redman, Ben Anderson, et al.. (2005). Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening. Human Genetics. 119(1-2). 126–136. 37 indexed citations

13.

Buller, Arlene, Susan C. Olson, Joy B. Redman, et al.. (2004). Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T. Genetics in Medicine. 6(2). 108–109. 11 indexed citations

14.

Strom, Charles M., Beryl Crossley, Joy B. Redman, et al.. (2004). Molecular screening for diseases frequent in Ashkenazi Jews: Lessons learned from more than 100,000 tests performed in a commercial laboratory. Genetics in Medicine. 6(3). 145–152. 28 indexed citations

15.

Strom, Charles M., Donghui Huang, Christina Chen, et al.. (2003). Extensive sequencing of the cystic fibrosis transmembrane regulator gene: Assay validation and unexpected benefits of developing a comprehensive test. Genetics in Medicine. 5(1). 9–14. 44 indexed citations

16.

Strom, Charles M., Norman Ginsberg, Svetlana Rechitsky, et al.. (1998). Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis. American Journal of Obstetrics and Gynecology. 178(6). 1298–1306. 29 indexed citations

17.

Strom, Charles M., Svetlana Rechitsky, Norman Ginsberg, Oleg Verlinsky, & Yury Verlinsky. (1996). Prenatal paternity testing with deoxyribonucleic acid techniques. American Journal of Obstetrics and Gynecology. 174(6). 1849–1854. 9 indexed citations

18.

Verlinsky, Yury, Svetlana Rechitsky, Michael Freidine, et al.. (1996). Birth of a healthy girl after preimplantation gender determination using a combination of polymerase chain reaction and fluorescent in situ hybridization analysis. Fertility and Sterility. 65(2). 358–360. 17 indexed citations

19.

Ginsberg, Norman, et al.. (1992). Term birth after midtrimester hysterotomy and selective delivery of an acardiac twin. American Journal of Obstetrics and Gynecology. 167(1). 33–37. 49 indexed citations

20.

Verlinsky, Yury, Eugene Pergament, & Charles M. Strom. (1990). The preimplantation genetic diagnosis of genetic diseases. Journal of Assisted Reproduction and Genetics. 7(1). 1–5. 25 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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