Nathan Harmston

2.0k citations

37 papers · 1.2k indexed · h-index 17

Impact in

Molecular Biology top 10%
- Wnt/β-catenin signaling in development and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- RNA Research and Splicing
- RNA modifications and cancer
Cancer Research

Papers in ⓘ

Aging 1
Molecular Biology 32
- Wnt/β-catenin signaling in development and cancer 9
- Cancer-related gene regulation 8
- RNA Research and Splicing 5
- RNA modifications and cancer 5
- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 5
- Genomics and Phylogenetic Studies 3
- Pluripotent Stem Cells Research 3

Co-authors: Boris Lenhard (4 shared papers)Enrico Petretto (17 shared papers)David M. Virshup (12 shared papers)Babita Madan (10 shared papers)Malcolm Perry (2 shared papers)Elizabeth Ing‐Simmons (2 shared papers)Anja Barešić (2 shared papers)Ge Tan (1 shared paper)
Journals: Nature Communications (3 papers)Journal of Clinical Investigation (3 papers)Scientific Reports (2 papers)Cell Reports (2 papers)Cells (2 papers)
Partner nations: Singapore United Kingdom United States

In The Last Decade

Nathan Harmston

34 papers receiving 1.2k citations

Peers

Countries citing papers authored by Nathan Harmston

Since Specialization

Citations

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

Fields of papers citing papers by Nathan Harmston

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Nathan Harmston, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nathan Harmston Line = papers co-authored together Nathan Harmston links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Wnt addiction of genetically defined cancers reversed by PORCN inhibition Oncogene ·Babita Madan, Zhanbo Ke, Nathan Harmston, Soo Yei Ho, A O Frois, Jenefer Alam, Duraiswamy A. Jeyaraj, Vishal Pendharkar, Kaustuv Ghosh, Isaac Virshup, Vithya Manoharan, Esther Ong, Kanda Sangthongpitag, Jeffrey Hill, Enrico Petretto, Thomas H. Keller, M.-A. Lee, A. Matter, David M. Virshup	2015	271
2	Topologically associating domains are ancient features that coincide with Metazoan clusters of extreme noncoding conservation Nature Communications ·Nathan Harmston, Elizabeth Ing‐Simmons, Ge Tan, Malcolm Perry, Matthias Merkenschlager, Boris Lenhard	2017	111
3	Chromatin and epigenetic features of long-range gene regulation Nucleic Acids Research ·Nathan Harmston, Boris Lenhard	2013	81
4	Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease Proceedings of the National Academy of Sciences ·Costanza Ferrari Bardile, Marta Garcia‐Miralles, Nicholas S. Caron, Nirmala Arul Rayan, Sarah R. Langley, Nathan Harmston, Ana Maria Rondelli, Roy Tang Yi Teo, Sabine Waltl, Lisa M. Anderson, Han‐Gyu Bae, Sangyong Jung, Anna Williams, Shyam Prabhakar, Enrico Petretto, Michael R. Hayden, Mahmoud A. Pouladi	2019	75
5	Changes in macrophage transcriptome associate with systemic sclerosis and mediate GSDMA contribution to disease risk Annals of the Rheumatic Diseases ·Aida Moreno‐Moral, Marta Bagnati, Surya Koturan, Jeong‐Hun Ko, Carmen Fonseca, Nathan Harmston, Laurence Gamé, Javier Martı́n, Voon H Ong, David Abraham, Christopher P. Denton, Jacques Behmoaras, Enrico Petretto	2018	59
6	Wnt proteins synergize to activate β-catenin signaling Journal of Cell Science ·Anshula Alok, Zhengdeng Lei, N. Suhas Jagannathan, Simran Kaur, Nathan Harmston, Steve Rozen, Lisa Tucker‐Kellogg, David M. Virshup	2017	57
7	Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length Effects Cell Reports ·Jolene Ooi, Sarah R. Langley, Xiaohong Xu, Kagistia Hana Utami, Bernice Sim, Yihui Huang, Nathan Harmston, Yi Lin Tay, Amin Ziaei, Ruizhu Zeng, Donovan Low, Folefac Aminkeng, Radoslaw M. Sobota, Florent Ginhoux, Enrico Petretto, Mahmoud A. Pouladi	2019	55
8	Temporal dynamics of Wnt-dependent transcriptome reveal an oncogenic Wnt/MYC/ribosome axis Journal of Clinical Investigation ·Babita Madan, Nathan Harmston, Gahyathiri Nallan, Alex Montoya, Peter Faull, Enrico Petretto, David M. Virshup	2018	51
9	The mystery of extreme non-coding conservation Philosophical Transactions of the Royal Society B Biological Sciences ·Nathan Harmston, Anja Barešić, Boris Lenhard	2013	45
10	In Vivo Generation of Post-infarct Human Cardiac Muscle by Laminin-Promoted Cardiovascular Progenitors Cell Reports ·Lynn Yap, Jiong‐Wei Wang, Aida Moreno‐Moral, Li Yen Chong, Yi Sun, Nathan Harmston, Xiaoyuan Wang, Suet Yen Chong, Konstantinos Vanezis, Miina K. Öhman, Heming Wei, Ralph M. Bunte, Sujoy Gosh, Stuart A. Cook, Outi Hovatta, Dominique P.V. de Kleijn, Enrico Petretto, Karl Tryggvason	2019	41
11	GenomicInteractions: An R/Bioconductor package for manipulating and investigating chromatin interaction data BMC Genomics ·Nathan Harmston, Elizabeth Ing‐Simmons, Malcolm Perry, Anja Barešić, Boris Lenhard	2015	37
12	The Functional Landscape of Patient-Derived RNF43 Mutations Predicts Sensitivity to Wnt Inhibition Cancer Research ·Jia Yu, Permeen A. Mohamed Yusoff, Daniëlle T.J. Woutersen, Pamela Goh, Nathan Harmston, Ron Smits, David Epstein, David M. Virshup, Babita Madan	2020	33
13	What the papers say: Text mining for genomics and systems biology Human Genomics ·Nathan Harmston, Wendy Filsell, Michael P. H. Stumpf	2010	31
14	WNT inhibition creates a BRCA‐like state in Wnt‐addicted cancer EMBO Molecular Medicine ·Amanpreet Kaur, Jun Yi Stanley Lim, Sugunavathi Sepramaniam, Siddhi Patnaik, Nathan Harmston, May Ann Lee, Enrico Petretto, David M. Virshup, Babita Madan	2021	30
15	A p300/GATA6 axis determines differentiation and Wnt dependency in pancreatic cancer models Journal of Clinical Investigation ·Zheng Zhong, Nathan Harmston, Kris C. Wood, Babita Madan, David M. Virshup	2022	26
16	Biologically relevant laminin as chemically defined and fully human platform for human epidermal keratinocyte culture Nature Communications ·Monica Suryana Tjin, Alvin Wen Choong Chua, Aida Moreno‐Moral, Li Yen Chong, Po Yin Tang, Nathan Harmston, Zuhua Cai, Enrico Petretto, Bien‐Keem Tan, Karl Tryggvason	2018	26
17	Widespread Repression of Gene Expression in Cancer by a Wnt/β-Catenin/MAPK Pathway Cancer Research ·Nathan Harmston, Jun Yi Stanley Lim, Oriol Arqués, Héctor G. Pálmer, Enrico Petretto, David M. Virshup, Babita Madan	2020	21
18	Wnt-regulated lncRNA discovery enhanced by in vivo identification and CRISPRi functional validation Genome Medicine ·Shiyang Liu, Nathan Harmston, Trudy Lee Glaser, Yunka Wong, Zheng Zhong, Babita Madan, David M. Virshup, Enrico Petretto	2020	14
19	Combining stem cell rejuvenation and senescence targeting to synergistically extend lifespan Aging ·Prameet Kaur, Agimaa Otgonbaatar, Anupriya Ramamoorthy, Ellora Hui Zhen Chua, Nathan Harmston, Jan Gruber, Nicholas S. Tolwinski	2022	14
20	Whole-Genome Sequencing of Finnish Type 1 Diabetic Siblings Discordant for Kidney Disease Reveals DNA Variants associated with Diabetic Nephropathy Journal of the American Society of Nephrology ·Jing Guo, Owen J. L. Rackham, Niina Sandholm, Bing He, Anne-May Österholm, Erkka Valo, Valma Harjutsalo, Carol Forsblom, Iiro Toppila, Maija Parkkonen, Qibin Li, Wenjuan Zhu, Nathan Harmston, Sonia Chothani, Miina K. Öhman, Eudora Eng, Yang Sun, Enrico Petretto, Per‐Henrik Groop, Karl Tryggvason	2020	13

About Nathan Harmston

Nathan Harmston is a scholar working on Aging, Molecular Biology, Cellular and Molecular Neuroscience, Geriatrics and Gerontology and Cancer Research, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Wnt/β-catenin signaling in development and cancer (9 papers), Cancer-related gene regulation (8 papers), RNA Research and Splicing (5 papers), RNA modifications and cancer (5 papers), Genomics and Chromatin Dynamics (5 papers), Epigenetics and DNA Methylation (5 papers), Genomics and Phylogenetic Studies (3 papers) and Pluripotent Stem Cells Research (3 papers). The work is most often cited by research in Molecular Biology (917 citations), Cancer Research (112 citations), Aging (13 citations), Oncology (182 citations) and Cellular and Molecular Neuroscience (117 citations). Nathan Harmston has collaborated with scholars based in Singapore, United Kingdom and United States. Frequent co-authors include Boris Lenhard, Enrico Petretto, David M. Virshup, Babita Madan, Malcolm Perry, Elizabeth Ing‐Simmons, Anja Barešić, Ge Tan, Matthias Merkenschlager and Jenefer Alam. Their work appears in journals such as Nature Communications, Journal of Clinical Investigation, Scientific Reports, Cell Reports and Cells.

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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