Ursula L. Harper

1.1k total citations
14 papers, 723 citations indexed

About

Ursula L. Harper is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ursula L. Harper has authored 14 papers receiving a total of 723 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ursula L. Harper's work include Epigenetics and DNA Methylation (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). Ursula L. Harper is often cited by papers focused on Epigenetics and DNA Methylation (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). Ursula L. Harper collaborates with scholars based in United States, Australia and United Kingdom. Ursula L. Harper's co-authors include Paul S. Meltzer, Sean Davis, Robert L. Walker, Yidong Chen, Arthur A. Glatfelter, Cristina R. Antonescu, Paul H. Duray, Kristin Baird, Laura M. Yudt and Pamela M. Pollock and has published in prestigious journals such as PLoS ONE, Cancer Research and Oncogene.

In The Last Decade

Ursula L. Harper

14 papers receiving 718 citations

Peers

Countries citing papers authored by Ursula L. Harper

Since Specialization

Citations

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

Fields of papers citing papers by Ursula L. Harper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ursula L. Harper. 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 Ursula L. Harper. The network helps show where Ursula L. Harper may publish in the future.

Co-authorship network of co-authors of Ursula L. Harper

This figure shows the co-authorship network connecting the top 25 collaborators of Ursula L. Harper. A scholar is included among the top collaborators of Ursula L. Harper 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 Ursula L. Harper. Ursula L. Harper is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development 2021 ·Blood Advances ·Erica Bresciani, Blake Carrington, Kai Yu, (unknown), Tao Zhen, (unknown), (unknown), Kevin Bishop, Martha Kirby, Ursula L. Harper, Stephen Wincovitch, Stefania Dell’Orso, Vittorio Sartorelli, Raman Sood, Paul Liu	12
2	Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1 2020 ·Disease Models & Mechanisms ·Jorge L. Rodriguez‐Gil, Dawn E. Watkins‐Chow, Laura L. Baxter, Gene Elliot, Ursula L. Harper, Stephen Wincovitch, (unknown), Arturo Incao, Mylene Huebecker, Frederick J. Boehm, William S. Garver, Forbes D. Porter, Karl W. Broman, Frances M. Platt, William J. Pavan	20
3	Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility 2018 ·PLoS Genetics ·(unknown), Blake Carrington, Mukundhan Ramaswami, Kevin Bishop, (unknown), MaryPat Jones, Ursula L. Harper, (unknown), (unknown), Raman Sood, Settara C. Chandrasekharappa	48
4	Highly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection 2017 ·G3 Genes Genomes Genetics ·Dawn E. Watkins‐Chow, Gaurav K. Varshney, Lisa Garrett, Zelin Chen, Erin Jimenez, Cecilia Rivas, Kevin Bishop, Raman Sood, Ursula L. Harper, William J. Pavan, Shawn M. Burgess	20
5	CRISPR-Mediated Triple Knockout of SLAMF1, SLAMF5 and SLAMF6 Supports Positive Signaling Roles in NKT Cell Development 2016 ·PLoS ONE ·Bonnie Huang, Julio Gómez‐Rodríguez, Silvia Preite, Lisa Garrett, Ursula L. Harper, Pamela L. Schwartzberg	18
6	Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia 2016 ·Human Mutation ·Frank X. Donovan, (unknown), Yonghwan Kim, Francis P. Lach, Ursula L. Harper, Aparna A. Kamat, MaryPat Jones, Erica Sanborn, (unknown), John E. Wagner, Margaret L. MacMillan, Elaine A. Ostrander, Arleen D. Auerbach, Agata Smogorzewska, Settara C. Chandrasekharappa	7
7	Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease 2012 ·Molecular Psychiatry ·Jorge I. Vélez, Settara C. Chandrasekharappa, Eliana Henao, (unknown), Ursula L. Harper, M. G. K. Jones, Benjamin D. Solomon, Liliana López, Gloria García, Daniel Camilo Aguirre–Acevedo, Natalia Acosta‐Baena, Juan Carlos Correa, (unknown), (unknown), Diego Rivera, Kenneth S. Kosik, Nicholas J. Schork, James M. Swanson, Francisco Lopera, Mauricio Arcos‐Burgos	29
8	GWAS reveals new recessive loci associated with non-syndromic facial clefting 2012 ·European Journal of Medical Genetics ·Maurício Camargo, (unknown), Lina M. Moreno, Andrew C. Lidral, Ursula L. Harper, MaryPat Jones, Benjamin D. Solomon, Erich Roessler, Jorge I. Vélez, Ariel F. Martinez, Settara C. Chandrasekharappa, Mauricio Arcos‐Burgos	26
9	Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering 2011 ·Molecular Genetics and Metabolism ·Thomas C. Markello, Sangwoo T. Han, Hannah Carlson-Donohoe, (unknown), Ursula L. Harper, MaryPat Jones, Settara C. Chandrasekharappa, Yair Anikster, David R. Adams, NISC Comparative Sequencing Program, (unknown), Cornelius F. Boerkoel	11
10	Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22 2011 ·International Journal of Cancer ·Cheryl D. Cropp, Claire L. Simpson, Tiina Wahlfors, (unknown), (unknown), MaryPat Jones, Ursula L. Harper, (unknown), (unknown), Teuvo L.J. Tammela, Joan E. Bailey‐Wilson, Johanna Schleutker	16
11	Loss-of-Function Fibroblast Growth Factor Receptor-2 Mutations in Melanoma 2009 ·Molecular Cancer Research ·Michael G. Gartside, Huaibin Chen, Omar A. Ibrahimi, Sara A. Byron, (unknown), Candice L. Wellens, (unknown), Laura M. Yudt, Anna V. Eliseenkova, Jinghong Ma, John A. Curtin, (unknown), Ursula L. Harper, Erica L. Riedesel, Graham J. Mann, Jeffrey M. Trent, Boris C. Bastian, Paul S. Meltzer, Moosa Mohammadi, Pamela M. Pollock	102
12	Gene Expression Profiling of Human Sarcomas: Insights into Sarcoma Biology 2005 ·Cancer Research ·Kristin Baird, Sean Davis, Cristina R. Antonescu, Ursula L. Harper, Robert L. Walker, Yidong Chen, Arthur A. Glatfelter, Paul H. Duray, Paul S. Meltzer	277
13	Identification of FGFR2 as a novel melanoma oncogene 2005 ·Cancer Research ·Michael G. Gartside, (unknown), Laura M. Yudt, Ursula L. Harper, (unknown), Sandra Pavey, Ralph J. Tuthill, Boris C. Bastian, Paul S. Meltzer, Pamela M. Pollock	1
14	Microarray expression profiling in melanoma reveals a BRAF mutation signature 2004 ·Oncogene ·Sandra Pavey, Peter A. Johansson, Leisl Packer, Jennifer M. Taylor, Mitchell Stark, Pamela M. Pollock, Graeme J. Walker, Glen M. Boyle, Ursula L. Harper, Sarah‐Jane Cozzi, Katherine Hansen, Laura M. Yudt, Christopher Schmidt, Peter Hersey, K.A.O. Ellem, Michael G. E. OʼRourke, Peter G. Parsons, Paul Meltzer, Markus Ringnér, Nicholas K. Hayward	136

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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