Nancy F. Hansen

27.3k total citations
49 papers, 2.3k citations indexed

About

Nancy F. Hansen is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Nancy F. Hansen has authored 49 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Nancy F. Hansen's work include Genomics and Phylogenetic Studies (7 papers), Cancer Genomics and Diagnostics (5 papers) and CRISPR and Genetic Engineering (4 papers). Nancy F. Hansen is often cited by papers focused on Genomics and Phylogenetic Studies (7 papers), Cancer Genomics and Diagnostics (5 papers) and CRISPR and Genetic Engineering (4 papers). Nancy F. Hansen collaborates with scholars based in United States, Canada and United Kingdom. Nancy F. Hansen's co-authors include James C. Mullikin, Hans Christian Andersen, Settara C. Chandrasekharappa, Bastiaan Hoogendoorn, Michael O’Donovan, Peter J. Oefner, Jeremy P. Cheadle, Jehannine Austin, Jamie K. Teer and Daphne W. Bell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Chemical Physics and Nature Genetics.

In The Last Decade

Nancy F. Hansen

49 papers receiving 2.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nancy F. Hansen United States	24	1.3k	497	319	227	191	49	2.3k
Marie‐Laure Yaspo Germany	27	2.9k 2.2×	970 2.0×	737 2.3×	241 1.1×	161 0.8×	70	4.7k
Benjamin C. Hitz United States	14	3.1k 2.4×	1.1k 2.1×	580 1.8×	247 1.1×	154 0.8×	16	4.3k
Bret Barnes United Kingdom	14	2.3k 1.7×	1.0k 2.1×	588 1.8×	228 1.0×	101 0.5×	21	3.2k
Kathy Boon United States	25	1.8k 1.4×	384 0.8×	304 1.0×	182 0.8×	77 0.4×	40	2.8k
Pratyush Kumar Das United States	14	2.5k 1.9×	386 0.8×	391 1.2×	200 0.9×	129 0.7×	17	3.3k
Wanding Zhou United States	24	1.8k 1.4×	421 0.8×	414 1.3×	162 0.7×	103 0.5×	60	2.4k
Roy Navon Israel	10	2.1k 1.6×	409 0.8×	750 2.4×	161 0.7×	183 1.0×	20	3.2k
Kai Tan United States	36	2.8k 2.1×	436 0.9×	389 1.2×	193 0.9×	99 0.5×	98	3.9k
Michael Lush United Kingdom	14	1.2k 0.9×	476 1.0×	255 0.8×	127 0.6×	124 0.6×	22	2.3k
J Dausset France	24	1.3k 1.0×	706 1.4×	138 0.4×	211 0.9×	188 1.0×	148	3.9k

Countries citing papers authored by Nancy F. Hansen

Since Specialization

Citations

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

Fields of papers citing papers by Nancy F. Hansen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy F. Hansen. 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 Nancy F. Hansen. The network helps show where Nancy F. Hansen may publish in the future.

Co-authorship network of co-authors of Nancy F. Hansen

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy F. Hansen. A scholar is included among the top collaborators of Nancy F. Hansen 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 Nancy F. Hansen. Nancy F. Hansen 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

Jain, Chirag, Arang Rhie, Nancy F. Hansen, Sergey Koren, & Adam M. Phillippy. (2022). Long-read mapping to repetitive reference sequences using Winnowmap2. Nature Methods. 19(6). 705–710. 116 indexed citations

Rudd, Meghan L., Nancy F. Hansen, Xiaolu Zhang, et al.. (2022). KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid endometrial carcinomas. PLoS ONE. 17(1). e0251286–e0251286. 2 indexed citations

Liu, Zhi, et al.. (2020). Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans. PLoS ONE. 15(4). e0232048–e0232048. 8 indexed citations

Pemov, Alexander, Nancy F. Hansen, Sivasish Sindiri, et al.. (2019). Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas. Neuro-Oncology. 21(8). 981–992. 69 indexed citations

Dewan, Ramita, Alexander Pemov, Evgenia Pak, et al.. (2017). First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation. BMC Cancer. 17(1). 127–127. 13 indexed citations

Harbison, Susan T, et al.. (2017). Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep. PLoS Genetics. 13(12). e1007098–e1007098. 38 indexed citations

Chen, Yee‐Chun, Gustavo Sudre, Wendy Sharp, et al.. (2017). Neuroanatomic, epigenetic and genetic differences in monozygotic twins discordant for attention deficit hyperactivity disorder. Molecular Psychiatry. 23(3). 683–690. 42 indexed citations

Hansen, Nancy F.. (2016). Variant Calling From Next Generation Sequence Data. Methods in molecular biology. 1418. 209–224. 8 indexed citations

Perera, Erasmo M., Dawn E. Watkins‐Chow, Nancy F. Hansen, et al.. (2015). The transcription factors Ets1 and Sox10 interact during murine melanocyte development. Developmental Biology. 407(2). 300–312. 15 indexed citations

10.

Rudd, Meghan L., Hassan Mohamed, Jessica C. Price, et al.. (2014). Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1. BMC Cancer. 14(1). 884–884. 12 indexed citations

11.

Bentley, Amy R., Guanjie Chen, Daniel Shriner, et al.. (2014). Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans. PLoS Genetics. 10(3). e1004190–e1004190. 28 indexed citations

12.

Cheng, Linzhao, Nancy F. Hansen, Ling Zhao, et al.. (2012). Low Incidence of DNA Sequence Variation in Human Induced Pluripotent Stem Cells Generated by Nonintegrating Plasmid Expression. Cell stem cell. 10(3). 337–344. 190 indexed citations

13.

Solomon, Benjamin D., Daniel Pineda‐Alvarez, Donald W. Hadley, et al.. (2012). Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL Association. Molecular Syndromology. 4(1-2). 27–31. 15 indexed citations

14.

Pierson, Tyler Mark, David A. Adams, Thomas C. Markello, et al.. (2012). Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM ₁ -gangliosidosis. Neurology. 79(2). 123–126. 23 indexed citations

15.

Pierson, Tyler Mark, Dimitre R. Simeonov, Murat Sincan, et al.. (2011). Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration. European Journal of Human Genetics. 20(4). 476–479. 44 indexed citations

16.

Solomon, Benjamin D., Daniel Pineda‐Alvarez, Donald W. Hadley, et al.. (2011). Personalized genomic medicine: Lessons from the exome. Molecular Genetics and Metabolism. 104(1-2). 189–191. 11 indexed citations

17.

Johnston, Jennifer J., Jamie K. Teer, Praveen F. Cherukuri, et al.. (2010). Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate. The American Journal of Human Genetics. 86(5). 743–748. 120 indexed citations

18.

Teer, Jamie K., Lori L. Bonnycastle, Peter S. Chines, et al.. (2010). Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing. Genome Research. 20(10). 1420–1431. 155 indexed citations

19.

Mullikin, James C., Nancy F. Hansen, Lei Shen, et al.. (2010). Light whole genome sequence for SNP discovery across domestic cat breeds. BMC Genomics. 11(1). 406–406. 42 indexed citations

20.

O’Hara, Edward, Marna Williams, Lusijah Rott, et al.. (2004). Modified representational difference analysis: isolation of differentially expressed mRNAs from rare cell populations. Analytical Biochemistry. 336(2). 221–230. 5 indexed citations

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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