Nathan Anderson

1.1k total citations
10 papers, 606 citations indexed

About

Nathan Anderson is a scholar working on Genetics, Molecular Biology and General Health Professions. According to data from OpenAlex, Nathan Anderson has authored 10 papers receiving a total of 606 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 1 paper in General Health Professions. Recurrent topics in Nathan Anderson's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Nathan Anderson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Nathan Anderson collaborates with scholars based in United States, Sweden and Italy. Nathan Anderson's co-authors include Eric S. Lander, Jill P. Mesirov, Elinor K. Karlsson, Edward J. Kulbokas, Claire M. Wade, Olle Kämpe, Åke Hedhammar, Tara Biagi, Göran Andersson and Kerstin Lindblad‐Toh and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Nathan Anderson

9 papers receiving 592 citations

Peers

Countries citing papers authored by Nathan Anderson

Since Specialization

Citations

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

Fields of papers citing papers by Nathan Anderson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nathan Anderson. 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 Nathan Anderson. The network helps show where Nathan Anderson may publish in the future.

Co-authorship network of co-authors of Nathan Anderson

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	An Analysis of Teaching Menstrual Care Skills Using Single-Subject Methodology: A Systematic Literature Review 2024 ·Journal of Autism and Developmental Disorders ·(unknown), (unknown), Nathan Anderson, (unknown)	0
2	Proteolytic activation of human-specific Olduvai domains by the furin protease 2022 ·International Journal of Biological Macromolecules ·(unknown), Aaron Issaian, Jonathan M. Davis, Nathan Anderson, Travis Nemkov, (unknown), Morkos A. Henen, Beat Vögeli, James M. Sikela, Kirk C. Hansen	3
3	DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores 2014 ·Human Genetics ·(unknown), (unknown), Nathan Anderson, Jonathon Keeney, Armin Raznahan, L. John Horwood, David M. Fergusson, Martin A. Kennedy, Jay N. Giedd, James M. Sikela	22
4	DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism 2014 ·PLoS Genetics ·Jonathan M. Davis, (unknown), Nathan Anderson, Jonathon Keeney, Laura Dumas, James M. Sikela	39
5	Exome sequencing and arrayCGH detection of gene sequence and copy number variation between ILS and ISS mouse strains 2014 ·Mammalian Genome ·Laura Dumas, C. Michael Dickens, Nathan Anderson, Jonathan M. Davis, Beth Bennett, Richard A. Radcliffe, James M. Sikela	5
6	Generation of Mice Lacking DUF1220 Protein Domains: Effects on Fecundity and Hyperactivity 2014 ·Mammalian Genome ·Jonathon Keeney, Majesta O’Bleness, Nathan Anderson, J M Davis, (unknown), Nicolas Busquet, Wallace S. Chick, Jan Rozman, Sabine M. Hölter, Lillian Garrett, Marion Horsch, Johannes Beckers, Wolfgang Wurst, Martin Klingenspor, Diego Restrepo, Martin Hrabě de Angelis, James M. Sikela	2
7	Abstract A258: The PARP inhibitor niraparib demonstrates synergy with chemotherapy in treatment of patient derived Ewing's sarcoma tumorGraft models. 2013 ·Molecular Cancer Therapeutics ·Keith Wilcoxen, David G. Brooks, Dhanrajan Tiruchinapalli, Nathan Anderson, (unknown), (unknown), (unknown), Tin Oo Khor, Bin Lü, Elizabeth De Oliveira, (unknown), Elizabeth Bruckheimer	7
8	Convergent and divergent evolution of genomic imprinting in the marsupial Monodelphis domestica 2012 ·BMC Genomics ·Radhika Das, Nathan Anderson, Mary Ellen Koran, Jennifer Weidman, Tarjei S. Mikkelsen, Michael Kamal, Susan K. Murphy, (unknown), John M. Greally, Randy L. Jirtle	25
9	DUF1220-Domain Copy Number Implicated in Human Brain-Size Pathology and Evolution 2012 ·The American Journal of Human Genetics ·Laura Dumas, Majesta O’Bleness, Jonathan M. Davis, C. Michael Dickens, Nathan Anderson, Jonathon Keeney, J. Brooks Jackson, (unknown), Armin Raznahan, Jay N. Giedd, Judith L. Rapoport, (unknown), Ayelet Erez, Nicola Brunetti‐Pierri, (unknown), James R. Lupski, Tasha E. Fingerlin, Sau Wai Cheung, James M. Sikela	91
10	Efficient mapping of mendelian traits in dogs through genome-wide association 2007 ·Nature Genetics ·Elinor K. Karlsson, (unknown), Claire M. Wade, (unknown), Michael C. Zody, Nathan Anderson, Tara Biagi, (unknown), Gerli Pielberg, Edward J. Kulbokas, Kenine E. Comstock, Evan T. Keller, Jill P. Mesirov, Henrik von Euler, Olle Kämpe, Åke Hedhammar, Eric S. Lander, Göran Andersson, Leif Andersson, Kerstin Lindblad‐Toh	412

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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