Bradford C. Powell

2.8k citations

37 papers · 1.2k indexed · 1 hit paper · h-index 15

Molecular Biology
Genetics top 5%
Cardiology and Cardiovascular Medicine top 10%
Cell Biology top 5%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Jonathan S. Berg Richard E. Cheney Ann Katherine M. Foreman James P. Evans Cynthia M. Powell Natasha T. Strande Neeta L. Vora Kirk C. Wilhelmsen
Topics: Genomics and Rare Diseases (21 papers)Genomic variations and chromosomal abnormalities (12 papers)BRCA gene mutations in cancer (9 papers)
Cited by: Cell Biology Genetics Cardiology and Cardiovascular Medicine
Journals: JAMASHILAP Revista de lepidopterologíaCancer Research
Partner nations: United States

In The Last Decade

Bradford C. Powell

35 papers receiving 1.2k 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.

A Millennial Myosin Census

2001 592 citations Jonathan S. Berg, Bradford C. Powell et al. profile →

Peers

Countries citing papers authored by Bradford C. Powell

Since Specialization

Citations

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

Fields of papers citing papers by Bradford C. Powell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bradford C. Powell. 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 Bradford C. Powell. The network helps show where Bradford C. Powell may publish in the future.

Co-authorship network of co-authors of Bradford C. Powell

This figure shows the co-authorship network connecting the top 25 collaborators of Bradford C. Powell. A scholar is included among the top collaborators of Bradford C. Powell 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 Bradford C. Powell. Bradford C. Powell 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	Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalities 2023 ·Genetics in Medicine ·(unknown),(unknown),Kelly L. Gilmore,(unknown),Bradford C. Powell,Karen E. Weck,Erica E. Davis,Neeta L. Vora	8
2	Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial 2023 ·Patient Education and Counseling ·Margaret Waltz,(unknown),R. Jean Cadigan,(unknown),(unknown),Jeannette T. Bensen,(unknown),Chad Haldeman‐Englert,Laura Farnan,Ann Katherine M. Foreman,(unknown),(unknown),Feng‐Chang Lin,(unknown),Julianne O’Daniel,Suzanne C. O’Neill,(unknown),Bradford C. Powell,Jonathan S. Berg,Christine Rini	6
3	P379: Characterizing research on the diagnostic odyssey in the United States: A systematic mapping review* 2023 ·SHILAP Revista de lepidopterología ·(unknown),Margaret Waltz,Jonathan S. Berg,Bradford C. Powell,Michael Adams,Anna R. Kahkoska,Kristen Hassmiller Lich	1
4	Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience 2022 ·Human Genetics and Genomics Advances ·(unknown),Laura M. Amendola,Tia L. Kauffman,Kathleen F. Mittendorf,Jeannette T. Bensen,Flavia Chen,Richard Green,Bradford C. Powell,Mark Kvale,Frank Angelo,Laura Farnan,Stephanie M. Fullerton,Jill O. Robinson,Tianran Li,(unknown),James M.J. Lawlor,Jeffrey Ou,Lucia A. Hindorff,Gail P. Jarvik,David R. Crosslin	6
5	Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing 2022 ·Genome Medicine ·Kevin M. Bowling,Michelle L. Thompson,Melissa Kelly,Sarah Scollon,Anne Slavotinek,Bradford C. Powell,Brian Kirmse,Laura G. Hendon,Kyle B. Brothers,Bruce R. Korf,Gregory M. Cooper,John M. Greally,Anna Hurst	10
6	Testing and extending strategies for identifying genetic disease–related encounters in pediatric patients 2022 ·Genetics in Medicine ·Lisa P. Spees,(unknown),Michael C. C. Adams,Laura Farnan,Jeannette T. Bensen,Donna Gilleskie,Jonathan S. Berg,Bradford C. Powell,Kristen Hassmiller Lich	0
7	Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial 2021 ·Trials ·(unknown),Laura V. Milko,Margaret Waltz,(unknown),(unknown),(unknown),Laura Farnan,Myra I. Roche,(unknown),Alexandra F. Lightfoot,Ann Katherine M. Foreman,Julianne O’Daniel,Suzanne C. O’Neill,Feng‐Chang Lin,Tamara S. Roman,Alicia Brandt,Bradford C. Powell,Christine Rini,Jonathan S. Berg,Jeannette T. Bensen	6
8	Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making 2021 ·Genome Medicine ·(unknown),Laura V. Milko,Julianne O’Daniel,Ann Katherine M. Foreman,(unknown),Bradford C. Powell,Cynthia M. Powell,Jonathan S. Berg	18
9	Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty 2020 ·Journal of Genetic Counseling ·Margaret Waltz,Anya E. R. Prince,Julianne O’Daniel,Ann Katherine M. Foreman,Bradford C. Powell,Jonathan S. Berg	5
10	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
11	Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels 2019 ·Genome Medicine ·Dona Kanavy,Shannon McNulty,(unknown),Sarah E. Brnich,Chris Bizon,Bradford C. Powell,Jonathan S. Berg	33
12	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
13	Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings 2018 ·Genetics in Medicine ·Kurt D. Christensen,Barbara A. Bernhardt,Gail P. Jarvik,Lucia A. Hindorff,Jeffrey Ou,Sawona Biswas,Bradford C. Powell,Robert W. Grundmeier,Kalotina Machini,Dean Karavite,Jeffrey W. Pennington,Ian D. Krantz,Jonathan S. Berg,Katrina A.B. Goddard	5
14	Factors influencing NCGENES research participants- requests for non-medically actionable secondary findings 2018 ·Genetics in Medicine ·Myra I. Roche,(unknown),Cynthia M. Khan,Elizabeth Moore,Feng‐Chang Lin,Julianne O’Daniel,Ann Katherine M. Foreman,Kristy Lee,Bradford C. Powell,Jonathan S. Berg,James P. Evans,Gail E. Henderson,Christine Rini	10
15	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
16	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
17	The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study 2017 ·Genetics in Medicine ·Christine Rini,Cynthia M. Khan,Elizabeth Moore,Myra I. Roche,James P. Evans,Jonathan S. Berg,Bradford C. Powell,Giselle Corbie‐Smith,Ann Katherine M. Foreman,(unknown),Kristy Lee,Julianne O’Daniel,Gail E. Henderson	20
18	Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs 2016 ·Pharmacogenetics and Genomics ·(unknown),(unknown),Rajarshi Ghosh,Bradford C. Powell,Stephanie C. Hicks,Marek Kimmel,Qingchang Meng,Deborah Ritter,David A. Wheeler,Richard A. Gibbs,Francis Tsai,Sharon E. Plon	2
19	Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing 2012 ·Pediatric Blood & Cancer ·Bradford C. Powell,Lichun Jiang,Donna M. Muzny,Lisa R. Treviño,ZoAnn E. Dreyer,Louise C. Strong,David A. Wheeler,Richard A. Gibbs,Sharon E. Plon	35
20	Tracking the evolution of alternatively spliced exons within the Dscam family 2006 ·BMC Evolutionary Biology ·(unknown),Bradford C. Powell,Todd Vision,Morgan C. Giddings	44

About Bradford C. Powell

Bradford C. Powell is a scholar working on Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (21 papers), Genomic variations and chromosomal abnormalities (12 papers) and BRCA gene mutations in cancer (9 papers). The work is most often cited by research in Cell Biology (239 citations), Genetics (387 citations) and Cardiology and Cardiovascular Medicine (275 citations). Bradford C. Powell has collaborated with scholars based in United States. Frequent co-authors include Jonathan S. Berg, Richard E. Cheney, Ann Katherine M. Foreman, James P. Evans, Cynthia M. Powell, Natasha T. Strande, Neeta L. Vora, Kirk C. Wilhelmsen, Julianne O’Daniel and Chris Bizon. Their work appears in journals such as JAMA, SHILAP Revista de lepidopterología and Cancer Research.

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