Natasha T. Strande

5.3k citations

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

Genetics top 5%
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 9
- Neurogenetic and Muscular Disorders Research 3
Genetics top 10%
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 9
- Neurogenetic and Muscular Disorders Research 3
Molecular Biology top 10%
- DNA Repair Mechanisms 8
- Genomics and Chromatin Dynamics 4
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics 3
Cancer Research
- Cancer Genomics and Diagnostics 8
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 3

Co-authors: Dale A. Ramsden Jonathan S. Berg Steven A. Roberts Christina Strom Martin D. Burkhalter John M. Pryor Jody M. Havener Paul Hasty
Cited by: Genetics Molecular Biology
Journals: Nature (1 paper)Proceedings of the National Academy of Sciences (2 papers)JAMA (1 paper)
Partner nations: United States United Kingdom

In The Last Decade

Natasha T. Strande

34 papers receiving 1.3k citations

Hit Papers

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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

The 25 scholars most cited alongside Natasha T. Strande, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Natasha T. Strande Line = papers co-authored together Natasha T. Strande links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing Genetics in Medicine ·Marissa W Mitchel,Matthew T. Oetjens,Alexander S. F. Berry,Alicia Johns,Andrés Moreno-De-Luca,Rebecca I. Torene,Natasha T. Strande,Marina T. DiStefano,Lindsay Havens Dyer,Tracy Brandt,Brenda Finucane,David H. Ledbetter,Kyle Retterer,Christa Lese Martin,Scott M. Myers	2025	2
2	Genomic Screening at a Single Health System JAMA Network Open ·Juliann M. Savatt,Melissa Kelly,Amy C. Sturm,Cara Z. McCormick,Marc S. Williams,Michelle Pistner Nixon,David D.K. Rolston,Natasha T. Strande,Karen E. Wain,Huntington F. Willard,W. Andrew Faucett,David H. Ledbetter,Adam H. Buchanan,Alastair J. Martin	2025	5
3	Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening Journal of the American Heart Association ·Samuel S. Gidding,H. Lester Kirchner,Andrew Brangan,William H. Howard,Melissa Kelly,Kelly D. Myers,Kelly Morgan,Matthew T. Oetjens,Timothy C. Shuey,David Staszak,Natasha T. Strande,Nicole Walters,Kristen Yu,Katherine Wilemon,Marc S. Williams,Amy C. Sturm,Laney K. Jones	2023	7
4	The Phenotypic Spectrum of COL4A3 Heterozygotes 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	2023	18
5	Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants Human Genetics and Genomics Advances ·Kelvin C. de Andrade,Natasha T. Strande,Jung Kim,Jeremy S. Haley,Jessica N. Hatton,Megan N. Frone,Payal P. Khincha,Gretchen M. Thone,Uyenlinh L. Mirshahi,Cindy Schneider,Heena Desai,James Dove,Diane T. Smelser,Arnold J. Levine,Kara N. Maxwell,Douglas R. Stewart,David J. Carey,Sharon A. Savage	2023	6
6	A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System Frontiers in Genetics ·Laney K. Jones,Natasha T. Strande,Evan M. Calvo,Jingheng Chen,Gabriela Rodriguez,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	2022	13
7	An approach to integrating exome sequencing for fetal structural anomalies into clinical practice Genetics in Medicine ·Neeta L. Vora,Kelly L. Gilmore,Alicia Brandt,Chelsea Gustafson,Natasha T. Strande,Lori Ramkissoon,Emily Hardisty,Ann Katherine M. Foreman,Kirk C. Wilhelmsen,Phillips Owen,Karen E. Weck,Jonathan S. Berg,Cynthia M. Powell,Bradford C. Powell	2020	51
8	Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients 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	2020	27
9	An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening The Journal of Pediatrics ·Laura V. Milko,Julianne O’Daniel,Daniela M. DeCristo,Stephanie B. Crowley,Ann Katherine M. Foreman,Kathleen Wallace,Lonna Mollison,Natasha T. Strande,Zahra S. Girnary,Lacey Boshe,Arthur S. Aylsworth,Müge Güçsavaş‐Çalıkoğlu,Dianne M. Frazier,Neeta L. Vora,Myra I. Roche,Bradford C. Powell,Cynthia M. Powell,Jonathan S. Berg	2019	44
10	Navigating the nuances of clinical sequence variant interpretation in Mendelian disease Genetics in Medicine ·Natasha T. Strande,Sarah E. Brnich,Tamara S. Roman,Jonathan S. Berg	2018	34
11	“Possibly positive or certainly uncertain?”: participants’ responses to uncertain diagnostic results from exome sequencing 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	2018	35
12	Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case Molecular Case Studies ·Gloria Haskell,Mari Mori,Cynthia M. Powell,Timothy J. Amrhein,Gillian Rice,Lauren A. Bailey,Natasha T. Strande,Karen E. Weck,James P. Evans,Jonathan S. Berg,Priya S. Kishnani	2018	4
13	Increasing the diagnostic yield of exome sequencing by copy number variant analysis PLoS ONE ·Daniel S. Marchuk,Kristy Crooks,Natasha T. Strande,Kathleen Kaiser‐Rogers,Laura V. Milko,Alicia Brandt,Alexandra Arreola,Christian R. Tilley,Chris Bizon,Neeta L. Vora,Kirk C. Wilhelmsen,James P. Evans,Jonathan S. Berg	2018	49
14	ClinGen Allele Registry links information about genetic variants Human Mutation ·Piotr Pawliczek,Ronak Y. Patel,Lillian Ashmore,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	2018	25
15	Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges 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,Jason Reilly,Phil Owen,Cynthia M. Powell,Debra Skinner,Christine Rini,Anne Drapkin Lyerly,Kim Boggess,Karen E. Weck,Jonathan S. Berg,James P. Evans	2017	105
16	Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair 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	2015	131
17	Nonhomologous end joining: A good solution for bad ends DNA repair ·Crystal A. Waters,Natasha T. Strande,David W. Wyatt,John M. Pryor,Dale A. Ramsden	2014	95
18	The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining Nature Communications ·Crystal A. Waters,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	2014	68
19	Specificity of the dRP/AP Lyase of Ku Promotes Nonhomologous End Joining (NHEJ) Fidelity at Damaged Ends Journal of Biological Chemistry ·Natasha T. Strande,Steven A. Roberts,Sehyun Oh,Eric A. Hendrickson,Dale A. Ramsden	2012	46
20	UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways Current Genetics ·Margery L. Evans,Lindsey J. Bostelman,Ashley M. Albrecht,Andrew Keller,Natasha T. Strande,Jeffrey S. Thompson	2008	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), DNA Repair Mechanisms (8 papers), Cancer Genomics and Diagnostics (8 papers), Genomics and Chromatin Dynamics (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genetic factors in colorectal cancer (3 papers) and Prenatal Screening and Diagnostics (3 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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