Tomoyuki Awano

1.3k total citations
14 papers, 957 citations indexed

About

Tomoyuki Awano is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Tomoyuki Awano has authored 14 papers receiving a total of 957 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Physiology. Recurrent topics in Tomoyuki Awano's work include Neurogenetic and Muscular Disorders Research (7 papers), RNA modifications and cancer (5 papers) and Neurological diseases and metabolism (3 papers). Tomoyuki Awano is often cited by papers focused on Neurogenetic and Muscular Disorders Research (7 papers), RNA modifications and cancer (5 papers) and Neurological diseases and metabolism (3 papers). Tomoyuki Awano collaborates with scholars based in United States, Sweden and South Korea. Tomoyuki Awano's co-authors include Umrao R. Monani, Martin L. Katz, Gary S. Johnson, Shahnawaz Khan, Dennis P. O’Brien, Gayle C. Johnson, Yuka Maeno-Hikichi, Lynn T. Landmesser, Joan R. Coates and Jeremy F. Taylor and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Tomoyuki Awano

14 papers receiving 941 citations

Peers

Countries citing papers authored by Tomoyuki Awano

Since Specialization

Citations

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

Fields of papers citing papers by Tomoyuki Awano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoyuki Awano

This figure shows the co-authorship network connecting the top 25 collaborators of Tomoyuki Awano. A scholar is included among the top collaborators of Tomoyuki Awano 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 Tomoyuki Awano. Tomoyuki Awano 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	A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses 2023 ·Neuron ·Jeong-Ki Kim, Narendra Nath Jha, Tomoyuki Awano, (unknown), Kishore Gollapalli, Emily Welby, (unknown), (unknown), Xueyong Wang, Zhihua Feng, (unknown), (unknown), Shunichi Homma, Chien‐Ping Ko, Lucı́a Tabares, Allison D. Ebert, Mark M. Rich, Umrao R. Monani	19
2	Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein 2017 ·Nature Communications ·Maoxue Tang, Guangping Gao, Carlos B. Rueda, Hang Yu, David N. Thibodeaux, Tomoyuki Awano, Kristin Engelstad, Maria J. Sanchez‐Quintero, Hong Yang, Fanghua Li, Huapeng Li, Qin Su, (unknown), Lynne C. Jones, (unknown), Jonathan McConathy, Elizabeth M. C. Hillman, Jeffrey L. Noebels, Darryl C. De Vivo, Umrao R. Monani	89
3	Motor neuronal repletion of the NMJ organizer, Agrin, modulates the severity of the spinal muscular atrophy disease phenotype in model mice 2017 ·Human Molecular Genetics ·Jeong-Ki Kim, (unknown), Tomoyuki Awano, Ruth Herbst, Umrao R. Monani	37
4	Breed Distribution of SOD1 Alleles Previously Associated with Canine Degenerative Myelopathy 2014 ·Journal of Veterinary Internal Medicine ·Rong Zeng, Joan R. Coates, Gayle C. Johnson, (unknown), (unknown), Tomoyuki Awano, Ana Kolicheski, Emma Ivansson, Michele Perloski, (unknown), Dennis P. O’Brien, Jiasen Guo, Martin L. Katz, (unknown), (unknown)	74
5	Spinal Muscular Atrophy: Journeying From Bench to Bedside 2014 ·Neurotherapeutics ·Tomoyuki Awano, Jeong-Ki Kim, Umrao R. Monani	31
6	Limited Phenotypic Effects of Selectively Augmenting the SMN Protein in the Neurons of a Mouse Model of Severe Spinal Muscular Atrophy 2012 ·PLoS ONE ·(unknown), Tomoyuki Awano, Gyu-Hwan Park, Umrao R. Monani	42
7	Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric ( SMN2 ) Gene 2010 ·Journal of Neuroscience ·(unknown), Yuka Maeno-Hikichi, Tomoyuki Awano, Lynn T. Landmesser, Umrao R. Monani	128
8	Characterization of extracellular DNA production and flocculation of the marine photosynthetic bacterium Rhodovulum sulfidophilum 2009 ·Applied Microbiology and Biotechnology ·Hiromichi Suzuki, (unknown), Tomoyuki Awano, So Umekage, (unknown), Yo Kikuchi	31
9	Genome-wide association analysis reveals aSOD1mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis 2009 ·Proceedings of the National Academy of Sciences ·Tomoyuki Awano, Gary S. Johnson, Claire M. Wade, Martin L. Katz, Gayle C. Johnson, Jeremy F. Taylor, Michele Perloski, Tara Biagi, (unknown), Sam Long, Philip A. March, Natasha J. Olby, G. Diane Shelton, Shahnawaz Khan, Dennis P. O’Brien, Kerstin Lindblad‐Toh, Joan R. Coates	182
10	A phosducin (PDC ) gene mutation does not cause progressive retinal atrophy in Korean miniature schnauzers 2008 ·Animal Genetics ·Manbok Jeong, Chun Han, Kristina Narfström, Tomoyuki Awano, Gary S. Johnson, (unknown), Je Kyung Seong, Kangmoon Seo	3
11	A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2 2007 ·Neurogenetics ·Xuhua Chen, Gary S. Johnson, Robert D. Schnabel, Jeremy F. Taylor, Gayle C. Johnson, Heidi G. Parker, Edward E. Patterson, Martin L. Katz, Tomoyuki Awano, (unknown), Dennis P. O’Brien	15
12	A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis 2006 ·Molecular Genetics and Metabolism ·Tomoyuki Awano, Martin L. Katz, Dennis P. O’Brien, Jeremy F. Taylor, Jason Evans, Shahnawaz Khan, István Sohár, Peter Lobel, Gary S. Johnson	106
13	A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis 2006 ·Molecular Genetics and Metabolism ·Tomoyuki Awano, Martin L. Katz, Dennis P. O’Brien, István Sohár, Peter Lobel, Joan R. Coates, Shahnawaz Khan, Gayle C. Johnson, Urs Giger, Gary S. Johnson	98
14	A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis 2004 ·Biochemical and Biophysical Research Communications ·Martin L. Katz, Shahnawaz Khan, Tomoyuki Awano, (unknown), A. N. Siakotos, Gary S. Johnson	102

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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