Samuel P. Strom

4.0k citations

28 papers · 1.7k indexed · 1 hit paper · h-index 16

Co-authors: Vincent Funari Phillip Fleshner Marla C. Dubinsky Jordan Brown Christopher N. Reyes Dermot McGovern Kent D. Taylor Gordon D. Brown
Topics: Genomics and Rare Diseases (9 papers)Genomic variations and chromosomal abnormalities (6 papers)Retinal Development and Disorders (5 papers)
Cited by: Genetics Infectious Diseases Molecular Biology
Journals: ScienceSHILAP Revista de lepidopterologíaPLoS ONE
Partner nations: United States Switzerland Canada

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

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

#	Work	Indexed citations
1	Genetic Etiologies for Chronic Kidney Disease Revealed through Next-Generation Renal Gene Panel 2022 ·American Journal of Nephrology ·Anthony J. Bleyer,(unknown),Jing Xie,Michelle S. Bloom,(unknown),(unknown),Frederick S. Jones,Miklos Z. Molnar,Wayne Kotzker,Prince Mohan,Stanislav Kmoch,Yuan Chao Xue,Samuel P. Strom,Sumit Punj,Zachary Demko,Hossein Tabriziani,Paul R. Billings,(unknown)	28
2	Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients 2022 ·Translational Vision Science & Technology ·Anna Matynia,Jun Wang,Sangbae Kim,Yumei Li,(unknown),Zhichun Jiang,Jane Hu,Samuel P. Strom,Roxana A. Radu,Rui Chen,Michael B. Gorin	6
3	Next‐generation sequencing and analysis of consecutive patients referred for connective tissue disorders 2022 ·American Journal of Medical Genetics Part A ·(unknown),Waheeda A. Hossain,Olivia J. Veatch,Samuel P. Strom,Merlin G. Butler	2
4	A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics 2021 ·Frontiers in Genetics ·Samuel P. Strom,Waheeda A. Hossain,Melina Grigorian,(unknown),(unknown),William A. Scaringe,Hai-Yun Yen,(unknown),(unknown),Harry Gao,Merlin G. Butler	17
5	Prenatal presentation and diagnosis of Baraitser‐Winter syndrome using exome sequencing 2020 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Samuel P. Strom,(unknown),(unknown),(unknown)	4
6	Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia 2020 ·SHILAP Revista de lepidopterología ·Abidemi Adegbola,Richard E. Lutz,Elina Nikkola,Samuel P. Strom,Jonathan Picker,Anthony Wynshaw‐Boris	9
7	Fundamentals of RNA Analysis on Biobanked Specimens 2018 ·Methods in molecular biology ·Samuel P. Strom	3
8	Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED 13L haploinsufficiency syndromes 2017 ·Clinical Case Reports ·Sureni V. Mullegama,(unknown),Chen Li,Naghmeh Dorrani,Sibel Kantarci,Bruce Blumberg,Wayne W. Grody,Samuel P. Strom	4
9	De novo loss‐of‐function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies 2017 ·American Journal of Medical Genetics Part A ·Sureni V. Mullegama,Steven D. Klein,(unknown),T. Niroshini Senaratne,Kathryn Singh,(unknown),Natalie M. Gallant,Samuel P. Strom,Shahnaz Ghahremani,Nagesh Rao,Julián A. Martínez-Agosto	36
10	De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa 2016 ·PLoS ONE ·Samuel P. Strom,Michael J. Clark,(unknown),Sarah Garcia,(unknown),Anna Matynia,Suhag Parikh,Lori S. Sullivan,Sara J. Bowne,Stephen P. Daiger,Michael B. Gorin	31
11	TOX3 is expressed in mammary ER+ epithelial cells and regulates ER target genes in luminal breast cancer 2015 ·BMC Cancer ·Akop Seksenyan,(unknown),Ann E. Walts,Brian de la Torre,Dror Berel,Samuel P. Strom,Parinaz Aliahmad,Vincent Funari,Jonathan Kaye	31
12	De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay 2015 ·The American Journal of Human Genetics ·Valerie A. Arboleda,Hane Lee,Naghmeh Dorrani,Neda Zadeh,Mary Willis,Colleen Macmurdo,Melanie A. Manning,Andrea Kwan,Louanne Hudgins,Florian Barthélémy,M. Carrie Miceli,Fabiola Quintero‐Rivera,Sibel Kantarci,Samuel P. Strom,Joshua L. Deignan,Wayne W. Grody,Éric Vilain,Stanley F. Nelson	92
13	An infant with MLH3 variants, FOXG1‐duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing study 2015 ·Genes Chromosomes and Cancer ·Rina Kansal,Xinmin Li,Joseph Shen,David Samuel,Fred H. Laningham,Hane Lee,Gagan B. Panigrahi,Andrew Y. Shuen,Sibel Kantarci,Naghmeh Dorrani,Jean Reiss,Peter Shintaku,Joshua L. Deignan,Samuel P. Strom,Christopher E. Pearson,Éric Vilain,Wayne W. Grody	4
14	De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing 2014 ·BMC Medical Genetics ·Samuel P. Strom,Reymundo Lozano,Hane Lee,Naghmeh Dorrani,John Mann,(unknown),Nicole Mans,Joshua L. Deignan,Éric Vilain,Stanley F. Nelson,Wayne W. Grody,Fabiola Quintero‐Rivera	44
15	Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophy 2014 ·BMC Medical Genetics ·Maria Carolina Ortube,Samuel P. Strom,Stanley F. Nelson,Steven Nusinowitz,(unknown),Michael B. Gorin	7
16	Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory 2014 ·Genetics in Medicine ·Samuel P. Strom,Hane Lee,Kingshuk Das,Éric Vilain,Stanley F. Nelson,Wayne W. Grody,Joshua L. Deignan	95
17	Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitisbreakdown → 2012 ·Science ·Iliyan D. Iliev,Vincent Funari,Kent D. Taylor,Quoclinh Nguyen,Christopher N. Reyes,Samuel P. Strom,Jordan Brown,Courtney Becker,Phillip Fleshner,Marla C. Dubinsky,Jerome I. Rotter,Hanlin L. Wang,Dermot McGovern,Gordon D. Brown,David M. Underhill	827
18	Molecular diagnosis of putative Stargardt disease probands by exome sequencing 2012 ·BMC Medical Genetics ·Samuel P. Strom,(unknown),(unknown),(unknown),Zugen Chen,Stanley F. Nelson,Steven Nusinowitz,Debora B. Farber,Michael B. Gorin	26
19	Disease Gene Characterization through Large-Scale Co-Expression Analysis 2009 ·PLoS ONE ·Allen Day,Jun Dong,Vincent Funari,(unknown),Samuel P. Strom,D.H. Cohn,Stanley F. Nelson	19
20	High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene 2009 ·Molecular Psychiatry ·Samuel P. Strom,Jennifer Stone,Jason Bosch,Barry Merriman,Rita M. Cantor,Daniel H. Geschwind,Stan F. Nelson	51

About Samuel P. Strom

Samuel P. Strom is a scholar working on Genetics, Ophthalmology and Cancer Research, having authored 28 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Retinal Development and Disorders (5 papers). The work is most often cited by research in Genetics (553 citations), Infectious Diseases (360 citations) and Molecular Biology (1.0k citations). Samuel P. Strom has collaborated with scholars based in United States, Switzerland and Canada. Frequent 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. Their work appears in journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

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