Natasha T. Strande

5.3k citations

37 papers · 1.3k indexed · 1 hit paper · h-index 19

Molecular Biology top 10%
Genetics top 5%
Oncology
Pediatrics, Perinatology and Child Health top 10%
Cancer Research

Co-authors: Dale A. Ramsden Jonathan S. Berg Steven A. Roberts Christina Strom Martin D. Burkhalter John M. Pryor Jody M. Havener Paul Hasty
Topics: Genomics and Rare Diseases (16 papers)Genomic variations and chromosomal abnormalities (9 papers)DNA Repair Mechanisms (8 papers)
Cited by: Genetics Molecular Biology
Journals: Nature Proceedings of the National Academy of Sciences JAMA
Partner nations: United States United Kingdom

In The Last Decade

Natasha T. Strande

34 papers receiving 1.3k 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.

Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population

2023 113 citations Uyenlinh L. Mirshahi, Jung Kim et al. profile →

Peers

Countries citing papers authored by Natasha T. Strande

Since Specialization

Citations

This map shows the geographic impact of Natasha T. Strande'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 Natasha T. Strande with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natasha T. Strande more than expected).

Fields of papers citing papers by Natasha T. Strande

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natasha T. Strande. 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 Natasha T. Strande. The network helps show where Natasha T. Strande may publish in the future.

Co-authorship network of co-authors of Natasha T. Strande

This figure shows the co-authorship network connecting the top 25 collaborators of Natasha T. Strande. A scholar is included among the top collaborators of Natasha T. Strande 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 Natasha T. Strande. Natasha T. Strande 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	Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing 2025 ·Genetics in Medicine ·(unknown),Matthew T. Oetjens,Alexander S. F. Berry,(unknown),Andrés Moreno-De-Luca,Rebecca I. Torene,Natasha T. Strande,Marina T. DiStefano,(unknown),Tracy Brandt,Brenda Finucane,David H. Ledbetter,Kyle Retterer,Christa Lese Martin,Scott M. Myers	2
2	Genomic Screening at a Single Health System 2025 ·JAMA Network Open ·Juliann M. Savatt,Melissa Kelly,Amy C. Sturm,Cara Z. McCormick,Marc S. Williams,(unknown),David D.K. Rolston,Natasha T. Strande,Karen E. Wain,Huntington F. Willard,W. Andrew Faucett,(unknown),Adam H. Buchanan,Alastair J. Martin	5
3	Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening 2023 ·Journal of the American Heart Association ·Samuel S. Gidding,H. Lester Kirchner,(unknown),William H. Howard,Melissa Kelly,Kelly D. Myers,(unknown),Matthew T. Oetjens,(unknown),(unknown),Natasha T. Strande,(unknown),(unknown),Katherine Wilemon,Marc S. Williams,Amy C. Sturm,Laney K. Jones	7
4	The Phenotypic Spectrum of COL4A3 Heterozygotes 2023 ·Kidney International Reports ·Kaushal Solanki,Yirui Hu,Bryn S. Moore,Vida Abedi,Venkatesh Avula,Tooraj Mirshahi,Natasha T. Strande,Ion D. Bucaloiu,Alex R. Chang	18
5	Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants 2023 ·Human Genetics and Genomics Advances ·Kelvin C. de Andrade,Natasha T. Strande,Jung Kim,Jeremy S. Haley,(unknown),Megan N. Frone,Payal P. Khincha,(unknown),Uyenlinh L. Mirshahi,Cindy Schneider,(unknown),James Dove,Diane T. Smelser,Arnold J. Levine,Kara N. Maxwell,Douglas R. Stewart,David J. Carey,Sharon A. Savage	6
6	A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System 2022 ·Frontiers in Genetics ·Laney K. Jones,Natasha T. Strande,(unknown),(unknown),(unknown),Cara Z. McCormick,Miranda L. G. Hallquist,Juliann M. Savatt,Heather Rocha,Marc S. Williams,Amy C. Sturm,Adam H. Buchanan,Russell E. Glasgow,Christa Lese Martin,Alanna Kulchak Rahm	13
7	An approach to integrating exome sequencing for fetal structural anomalies into clinical practice 2020 ·Genetics in Medicine ·Neeta L. Vora,Kelly L. Gilmore,Alicia Brandt,(unknown),Natasha T. Strande,Lori Ramkissoon,Emily Hardisty,Ann Katherine M. Foreman,Kirk C. Wilhelmsen,Phillips Owen,(unknown),Jonathan S. Berg,Cynthia M. Powell,Bradford C. Powell	51
8	Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients 2020 ·PLoS ONE ·Matthew T. Oetjens,Jonathan Z. Luo,Alex R. Chang,Joseph B. Leader,Dustin N. Hartzel,Bryn S. Moore,Natasha T. Strande,H. Lester Kirchner,David H. Ledbetter,Anne E. Justice,David J. Carey,Tooraj Mirshahi	27
9	An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening 2019 ·The Journal of Pediatrics ·Laura V. Milko,Julianne O’Daniel,(unknown),Stephanie B. Crowley,Ann Katherine M. Foreman,Kathleen Wallace,(unknown),Natasha T. Strande,(unknown),(unknown),Arthur S. Aylsworth,Müge Güçsavaş‐Çalıkoğlu,Dianne M. Frazier,Neeta L. Vora,Myra I. Roche,Bradford C. Powell,Cynthia M. Powell,Jonathan S. Berg	44
10	Navigating the nuances of clinical sequence variant interpretation in Mendelian disease 2018 ·Genetics in Medicine ·Natasha T. Strande,Sarah E. Brnich,Tamara S. Roman,Jonathan S. Berg	34
11	“Possibly positive or certainly uncertain?”: participants’ responses to uncertain diagnostic results from exome sequencing 2018 ·Genetics in Medicine ·Debra Skinner,Myra I. Roche,Karen E. Weck,Kelly Raspberry,Ann Katherine M. Foreman,Natasha T. Strande,Jonathan S. Berg,James P. Evans,Gail E. Henderson	35
12	Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case 2018 ·Molecular Case Studies ·Gloria Haskell,Mari Mori,Cynthia M. Powell,Timothy J. Amrhein,Gillian Rice,(unknown),Natasha T. Strande,(unknown),James P. Evans,Jonathan S. Berg,Priya S. Kishnani	4
13	Increasing the diagnostic yield of exome sequencing by copy number variant analysis 2018 ·PLoS ONE ·Daniel S. Marchuk,Kristy Crooks,Natasha T. Strande,Kathleen Kaiser‐Rogers,Laura V. Milko,Alicia Brandt,Alexandra Arreola,(unknown),Chris Bizon,Neeta L. Vora,Kirk C. Wilhelmsen,James P. Evans,Jonathan S. Berg	49
14	ClinGen Allele Registry links information about genetic variants 2018 ·Human Mutation ·(unknown),Ronak Y. Patel,(unknown),Andrew R. Jackson,Chris Bizon,Tristan Nelson,Bradford C. Powell,Robert R. Freimuth,Natasha T. Strande,Neethu Shah,Sameer Paithankar,Matt W. Wright,Selina S. Dwight,Jimmy Zhen,Melissa Landrum,Peter B. McGarvey,Lawrence Babb,Sharon E. Plon,Aleksandar Milosavljevic	25
15	Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges 2017 ·Genetics in Medicine ·Neeta L. Vora,Bradford C. Powell,Alicia Brandt,Natasha T. Strande,Emily Hardisty,Kelly L. Gilmore,Ann Katherine M. Foreman,Kirk C. Wilhelmsen,Chris Bizon,(unknown),Phil Owen,Cynthia M. Powell,Debra Skinner,Christine Rini,Anne Drapkin Lyerly,Kim Boggess,Karen E. Weck,Jonathan S. Berg,James P. Evans	105
16	Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair 2015 ·Proceedings of the National Academy of Sciences ·Dylan A. Reid,Sarah Keegan,Alejandra Leo‐Macías,Go Watanabe,Natasha T. Strande,Howard H. Chang,Betül Akgöl Oksuz,David Fenyö,Michael R. Lieber,Dale A. Ramsden,Eli Rothenberg	131
17	Nonhomologous end joining: A good solution for bad ends 2014 ·DNA repair ·(unknown),Natasha T. Strande,David W. Wyatt,John M. Pryor,Dale A. Ramsden	95
18	The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining 2014 ·Nature Communications ·(unknown),Natasha T. Strande,John M. Pryor,Christina Strom,Piotr A. Mieczkowski,Martin D. Burkhalter,Sehyun Oh,Bahjat F. Qaqish,Dominic T. Moore,Eric A. Hendrickson,Dale A. Ramsden	68
19	Specificity of the dRP/AP Lyase of Ku Promotes Nonhomologous End Joining (NHEJ) Fidelity at Damaged Ends 2012 ·Journal of Biological Chemistry ·Natasha T. Strande,Steven A. Roberts,Sehyun Oh,Eric A. Hendrickson,Dale A. Ramsden	46
20	UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways 2008 ·Current Genetics ·Margery L. Evans,(unknown),(unknown),Andrew Keller,Natasha T. Strande,Jeffrey S. Thompson	14

About Natasha T. Strande

Natasha T. Strande is a scholar working on Genetics, Cancer Research and Genetics, having authored 37 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (9 papers) and DNA Repair Mechanisms (8 papers). The work is most often cited by research in Genetics (488 citations), Genetics (115 citations) and Molecular Biology (736 citations). Natasha T. Strande has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Dale A. Ramsden, Jonathan S. Berg, Steven A. Roberts, Christina Strom, Martin D. Burkhalter, John M. Pryor, Jody M. Havener, Paul Hasty, Ann Katherine M. Foreman and James P. Evans. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and JAMA.

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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