Nancy F. Hansen

27.3k citations

49 papers · 2.3k indexed · h-index 24

Co-authors: James C. Mullikin Hans Christian Andersen Settara C. Chandrasekharappa Michael O’Donovan Jeremy P. Cheadle Jehannine Austin Peter J. Oefner Bastiaan Hoogendoorn
Topics: Genomics and Phylogenetic Studies (7 papers)Cancer Genomics and Diagnostics (5 papers)CRISPR and Genetic Engineering (4 papers)
Cited by: Cancer Research Molecular Biology Genetics
Journals: Proceedings of the National Academy of Sciences The Journal of Chemical Physics Nature Genetics
Partner nations: United States Canada United Kingdom

In The Last Decade

Nancy F. Hansen

49 papers receiving 2.2k citations

Peers

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

#	Work	Indexed citations
1	Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans 2020 ·PLoS ONE ·Zhi Liu,Daniel Shriner,Nancy F. Hansen,Charles N. Rotimi,James C. Mullikin,(unknown)	8
2	Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas 2019 ·Neuro-Oncology ·Alexander Pemov,Nancy F. Hansen,Sivasish Sindiri,Rajesh Patidar,Christine S. Higham,Eva Dombi,Markku Miettinen,Patricia Fetsch,Hilde Brems,Settara C. Chandrasekharappa,Kristine Jones,Bin Zhu,Jun S. Wei,James C. Mullikin,Margaret R. Wallace,Javed Khan,Eric Legius,Brigitte C. Widemann,Douglas R. Stewart	69
3	Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep 2017 ·PLoS Genetics ·Susan T Harbison,Yazmin L. Serrano Negron,Nancy F. Hansen,(unknown)	38
4	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 2017 ·BMC Cancer ·(unknown),Ramita Dewan,Alexander Pemov,(unknown),Evgenia Pak,Nancy A. Edwards,Abhik Ray‐Chaudhury,Nancy F. Hansen,Settara C. Chandrasekharappa,James C. Mullikin,Ashok R. Asthagiri,John D. Heiss,Douglas R. Stewart,Anand V. Germanwala	13
5	Neuroanatomic, epigenetic and genetic differences in monozygotic twins discordant for attention deficit hyperactivity disorder 2017 ·Molecular Psychiatry ·Yee‐Chun Chen,Gustavo Sudre,Wendy Sharp,Frank X. Donovan,Settara C. Chandrasekharappa,Nancy F. Hansen,Laura Elnitski,Philip Shaw	42
6	The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas 2017 ·Oncogene ·Alexander Pemov,(unknown),Rajesh Patidar,Nancy F. Hansen,Sivasish Sindiri,Stephen W. Hartley,Jun S. Wei,Abdel Elkahloun,Settara C. Chandrasekharappa,(unknown),Joseph F. Boland,Sara Bass,James C. Mullikin,Javed Khan,Brigitte C. Widemann,Margaret R. Wallace,Douglas R. Stewart	72
7	Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencing 2017 ·Cancer ·Matthieu Le Gallo,Meghan L. Rudd,Mary Ellen Urick,Nancy F. Hansen,Suiyuan Zhang,(unknown),Fred Lozy,Dennis C. Sgroi,August Vidal,Xavier Matías‐Guiu,Russell R. Broaddus,Karen H. Lu,Douglas A. Levine,David G. Mutch,Paul J. Goodfellow,Helga B. Salvesen,James C. Mullikin,Daphne W. Bell	63
8	The FOXA2 transcription factor is frequently somatically mutated in uterine carcinosarcomas and carcinomas 2017 ·Cancer ·Matthieu Le Gallo,Meghan L. Rudd,Mary Ellen Urick,Nancy F. Hansen,Maria J. Merino,David G. Mutch,Paul J. Goodfellow,James C. Mullikin,Daphne W. Bell	28
9	Variant Calling From Next Generation Sequence Data 2016 ·Methods in molecular biology ·Nancy F. Hansen	8
10	The transcription factors Ets1 and Sox10 interact during murine melanocyte development 2015 ·Developmental Biology ·(unknown),Erasmo M. Perera,Dawn E. Watkins‐Chow,Nancy F. Hansen,Meghana Vemulapalli,James C. Mullikin,NISC Comparative Sequencing Program,William J. Pavan,Lidia Kos	15
11	Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1 2014 ·BMC Cancer ·Meghan L. Rudd,Hassan Mohamed,Jessica C. Price,Andrea O’Hara,Matthieu Le Gallo,Mary Ellen Urick,(unknown),Pedro Cruz,Suiyuan Zhang,Nancy F. Hansen,Andrew K. Godwin,Dennis C. Sgroi,Tyra G. Wolfsberg,James C. Mullikin,Maria J. Merino,Daphne W. Bell	12
12	Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans 2014 ·PLoS Genetics ·Amy R. Bentley,Guanjie Chen,Daniel Shriner,Ayo P. Doumatey,Jie Zhou,Hanxia Huang,James C. Mullikin,Robert W. Blakesley,Nancy F. Hansen,Gerard G. Bouffard,Praveen F. Cherukuri,Baishali Maskeri,Alice C. Young,Adebowale Adeyemo,Charles N. Rotimi	28
13	Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma Genomes 2012 ·PLoS Genetics ·Stephen C.J. Parker,Jared J. Gartner,(unknown),Xiaomu Wei,Hatice Özel Abaan,Subramanian S. Ajay,Nancy F. Hansen,Lingyun Song,Umesh Bhanot,J. Keith Killian,Yevgeniy Gindin,Robert L. Walker,Paul S. Meltzer,James C. Mullikin,Terrence S. Furey,Gregory E. Crawford,Steven A. Rosenberg,Yardena Samuels,Elliott H. Margulies	8
14	Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL Association 2012 ·Molecular Syndromology ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Donald W. Hadley,Nancy F. Hansen,(unknown),Frank X. Donovan,Settara C. Chandrasekharappa,Sung‐Kook Hong,Erich Roessler,James C. Mullikin,(unknown)	15
15	Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration 2011 ·European Journal of Human Genetics ·(unknown),Tyler Mark Pierson,Dimitre R. Simeonov,Murat Sincan,David A. Adams,Thomas C. Markello,Gretchen Golas,(unknown),Nancy F. Hansen,Praveen F. Cherukuri,Pedro Cruz,(unknown),Cynthia J. Tifft,Cornelius F. Boerkoel,William A. Gahl	44
16	Personalized genomic medicine: Lessons from the exome 2011 ·Molecular Genetics and Metabolism ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Donald W. Hadley,NISC Comparative Sequencing Program,Jamie K. Teer,Praveen F. Cherukuri,Nancy F. Hansen,Pedro Cruz,Alice Young,Robert W. Blakesley,Brendan C. Lanpher,(unknown),Murat Sincan,Settara C. Chandrasekharappa,James C. Mullikin	11
17	Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate 2010 ·The American Journal of Human Genetics ·Jennifer J. Johnston,Jamie K. Teer,Praveen F. Cherukuri,Nancy F. Hansen,Stacie K. Loftus,Karen Chong,James C. Mullikin,Leslie G. Biesecker	120
18	Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing 2010 ·Genome Research ·Jamie K. Teer,Lori L. Bonnycastle,Peter S. Chines,Nancy F. Hansen,Natsuyo Aoyama,Amy J. Swift,Hatice Özel Abaan,Thomas J. Albert,(unknown),Elliott H. Margulies,Eric D. Green,Francis S. Collins,James C. Mullikin,Leslie G. Biesecker	155
19	Light whole genome sequence for SNP discovery across domestic cat breeds 2010 ·BMC Genomics ·James C. Mullikin,Nancy F. Hansen,Lei Shen,Heather Ebling,William F. Donahue,Wei Tao,(unknown),(unknown),Marc Rubenfield,Alice Young,Pedro Cruz,(unknown),Carlos A. Driscoll,Victor A. David,Samer W.K. Al-Murrani,Mary Locniskar,Mitchell S. Abrahamsen,Stephen J. O’Brien,Andrew R. Smith,Jeffrey A. Brockman	42
20	Modified representational difference analysis: isolation of differentially expressed mRNAs from rare cell populations 2004 ·Analytical Biochemistry ·Edward O’Hara,Marna Williams,Lusijah Rott,(unknown),Nancy F. Hansen,Ted Jones,(unknown),Nancy A. Federspiel,Eugene C. Butcher	5

About Nancy F. Hansen

Nancy F. Hansen is a scholar working on Aging, Obstetrics and Gynecology and Genetics, having authored 49 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (7 papers), Cancer Genomics and Diagnostics (5 papers) and CRISPR and Genetic Engineering (4 papers). The work is most often cited by research in Cancer Research (319 citations), Molecular Biology (1.3k citations) and Genetics (497 citations). Nancy F. Hansen has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include James C. Mullikin, Hans Christian Andersen, Settara C. Chandrasekharappa, Michael O’Donovan, Jeremy P. Cheadle, Jehannine Austin, Peter J. Oefner, Bastiaan Hoogendoorn, Jamie K. Teer and Meghan L. Rudd. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Journal of Chemical Physics and Nature Genetics.

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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