Samuel P. Strom

4.0k total citations · 1 hit paper
28 papers, 1.7k citations indexed

About

Samuel P. Strom is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Samuel P. Strom has authored 28 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 17 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Samuel P. Strom's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Retinal Development and Disorders (5 papers). Samuel P. Strom is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Retinal Development and Disorders (5 papers). Samuel P. Strom collaborates with scholars based in United States, Switzerland and Canada. Samuel P. Strom's co-authors include Vincent Funari, Phillip Fleshner, Marla C. Dubinsky, Jordan Brown, Christopher N. Reyes, Dermot McGovern, Kent D. Taylor, Gordon D. Brown, Quoclinh Nguyen and Iliyan D. Iliev and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Samuel P. Strom

28 papers receiving 1.7k 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.

Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis

2012 827 citations Iliyan D. Iliev, Vincent Funari et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Samuel P. Strom United States	16	1.0k	553	360	200	197	28	1.7k
Nathalie Daniel France	22	893 0.9×	577 1.0×	333 0.9×	159 0.8×	140 0.7×	67	1.9k
Arvind Batra Germany	15	476 0.5×	371 0.7×	104 0.3×	506 2.5×	356 1.8×	20	1.4k
Sameet Mehta United States	21	1.5k 1.5×	224 0.4×	173 0.5×	382 1.9×	194 1.0×	38	2.2k
Zbigniew Mikulski United States	24	950 0.9×	174 0.3×	219 0.6×	1.1k 5.6×	225 1.1×	53	2.3k
Sandro Orrù Italy	23	725 0.7×	310 0.6×	91 0.3×	515 2.6×	127 0.6×	84	1.8k
Zhongde Ye United States	21	761 0.7×	90 0.2×	164 0.5×	575 2.9×	157 0.8×	26	1.6k
Ramakrishna Sompallae United States	23	899 0.9×	166 0.3×	470 1.3×	475 2.4×	334 1.7×	42	2.0k
Kyoji Hioki Japan	19	830 0.8×	441 0.8×	180 0.5×	874 4.4×	187 0.9×	63	2.6k
Matthew L. Wheeler United States	14	875 0.9×	93 0.2×	233 0.6×	572 2.9×	220 1.1×	17	1.6k

Countries citing papers authored by Samuel P. Strom

Since Specialization

Citations

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

Fields of papers citing papers by Samuel P. Strom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuel P. Strom

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

Bleyer, Anthony J., Jing Xie, Michelle S. Bloom, et al.. (2022). Genetic Etiologies for Chronic Kidney Disease Revealed through Next-Generation Renal Gene Panel. American Journal of Nephrology. 53(4). 297–306. 28 indexed citations

Matynia, Anna, Jun Wang, Sangbae Kim, et al.. (2022). Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients. Translational Vision Science & Technology. 11(3). 33–33. 6 indexed citations

Hossain, Waheeda A., et al.. (2022). Next‐generation sequencing and analysis of consecutive patients referred for connective tissue disorders. American Journal of Medical Genetics Part A. 188(10). 3016–3023. 2 indexed citations

Strom, Samuel P., Waheeda A. Hossain, Melina Grigorian, et al.. (2021). A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics. Frontiers in Genetics. 12. 608889–608889. 17 indexed citations

Strom, Samuel P., et al.. (2020). Prenatal presentation and diagnosis of Baraitser‐Winter syndrome using exome sequencing. American Journal of Medical Genetics Part A. 182(9). 2124–2128. 4 indexed citations

Adegbola, Abidemi, Richard E. Lutz, Elina Nikkola, et al.. (2020). Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia. SHILAP Revista de lepidopterología. 1(1). 100007–100007. 9 indexed citations

Strom, Samuel P.. (2018). Fundamentals of RNA Analysis on Biobanked Specimens. Methods in molecular biology. 1897. 345–357. 3 indexed citations

Mullegama, Sureni V., Chen Li, Naghmeh Dorrani, et al.. (2017). Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED 13L haploinsufficiency syndromes. Clinical Case Reports. 5(6). 833–840. 4 indexed citations

Mullegama, Sureni V., Steven D. Klein, T. Niroshini Senaratne, et al.. (2017). De novo loss‐of‐function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies. American Journal of Medical Genetics Part A. 173(5). 1319–1327. 36 indexed citations

10.

Strom, Samuel P., Michael J. Clark, Sarah Garcia, et al.. (2016). De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa. PLoS ONE. 11(3). e0150944–e0150944. 31 indexed citations

11.

Seksenyan, Akop, Ann E. Walts, Brian de la Torre, et al.. (2015). TOX3 is expressed in mammary ER+ epithelial cells and regulates ER target genes in luminal breast cancer. BMC Cancer. 15(1). 22–22. 31 indexed citations

12.

Arboleda, Valerie A., Hane Lee, Naghmeh Dorrani, et al.. (2015). De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay. The American Journal of Human Genetics. 96(3). 498–506. 92 indexed citations

13.

Kansal, Rina, Xinmin Li, Joseph Shen, et al.. (2015). An infant with MLH3 variants, FOXG1‐duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing study. Genes Chromosomes and Cancer. 55(2). 131–142. 4 indexed citations

14.

Strom, Samuel P., Reymundo Lozano, Hane Lee, et al.. (2014). De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing. BMC Medical Genetics. 15(1). 49–49. 44 indexed citations

15.

Ortube, Maria Carolina, et al.. (2014). Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophy. BMC Medical Genetics. 15(1). 11–11. 7 indexed citations

16.

Strom, Samuel P., Hane Lee, Kingshuk Das, et al.. (2014). Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory. Genetics in Medicine. 16(7). 510–515. 95 indexed citations

17.

Iliev, Iliyan D., Vincent Funari, Kent D. Taylor, et al.. (2012). Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis. Science. 336(6086). 1314–1317. 827 indexed citations breakdown →

18.

Strom, Samuel P., Zugen Chen, Stanley F. Nelson, et al.. (2012). Molecular diagnosis of putative Stargardt disease probands by exome sequencing. BMC Medical Genetics. 13(1). 67–67. 26 indexed citations

19.

Day, Allen, Jun Dong, Vincent Funari, et al.. (2009). Disease Gene Characterization through Large-Scale Co-Expression Analysis. PLoS ONE. 4(12). e8491–e8491. 19 indexed citations

20.

Strom, Samuel P., Jennifer Stone, Jason Bosch, et al.. (2009). High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. Molecular Psychiatry. 15(10). 996–1005. 51 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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