Nicholas E. Johnson

3.5k citations

101 papers · 1.8k indexed · h-index 26

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Botulinum Toxin and Related Neurological Disorders

Papers in ⓘ

Cellular and Molecular Neuroscience 63
- Genetic Neurodegenerative Diseases 56
- Hereditary Neurological Disorders 13
Neurology 35
- Parkinson's Disease Mechanisms and Treatments 23
- Botulinum Toxin and Related Neurological Disorders 12

Co-authors: Chad Heatwole (31 shared papers)Michael McDermott (13 shared papers)Nuran Dilek (15 shared papers)Richard T. Moxley (12 shared papers)William B. Martens (8 shared papers)Rabi Tawil (8 shared papers)Jeffrey Statland (15 shared papers)Elizabeth Luebbe (11 shared papers)
Journals: Muscle & Nerve (23 papers)Neurology (21 papers)Neuromuscular Disorders (7 papers)Journal of Neuromuscular Diseases (4 papers)Neurology Genetics (4 papers)
Partner nations: United States Canada Italy

In The Last Decade

Nicholas E. Johnson

92 papers receiving 1.8k citations

Peers

Countries citing papers authored by Nicholas E. Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Nicholas E. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas E. Johnson. 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 Nicholas E. Johnson. The network helps show where Nicholas E. Johnson may publish in the future.

Co-authors

The 25 scholars most cited alongside Nicholas E. Johnson, 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 Nicholas E. Johnson Line = papers co-authored together Nicholas E. Johnson links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 101 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1) Neurology ·Chad Heatwole, Rita Bode, Nicholas E. Johnson, Christine Quinn, William B. Martens, Michael McDermott, Nan Rothrock, Charles A. Thornton, Barbara G. Vickrey, David Victorson, Richard T. Moxley	2012	156
2	Review of the Diagnosis and Treatment of Periodic Paralysis Muscle & Nerve ·Jeffrey Statland, Bertrand Fontaine, Michael G. Hanna, Nicholas E. Johnson, John T. Kissel, Valeria Sansone, Perry B. Shieh, Rabi Tawil, Jaya Trivedi, Stephen C. Cannon, Robert C. Griggs	2017	138
3	Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program Neurology ·Nicholas E. Johnson, Russell J. Butterfield, Katie Mayne, Tara Newcomb, Carina Imburgia, Diane M. Dunn, Brett Duval, Marcia L. Feldkamp, Robert B. Weiss	2021	85
4	Quality-of-life in Charcot–Marie–Tooth disease: The patient’s perspective Neuromuscular Disorders ·Nicholas E. Johnson, Chad Heatwole, Nuran Dilek, Janet E. Sowden, Callyn A. Kirk, Denise Shereff, Michael E. Shy, David N. Herrmann	2014	67
5	p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models Nature Genetics ·Edward J. Grow, B. D. Weaver, Christina M. Smith, Jingtao Guo, Paula Stein, Sean Shadle, Peter G. Hendrickson, Nicholas E. Johnson, Russell J. Butterfield, Roberta Menafra, Susan L. Kloet, Silvère M. van der Maarel, Carmen J. Williams, Bradley R. Cairns	2021	67
6	Patient Reported Impact of Symptoms in Spinal Muscular Atrophy (PRISM-SMA) Neurology ·Phillip Mongiovi, Nuran Dilek, Connie Garland, Michael Hunter, John T. Kissel, Elizabeth Luebbe, Michael McDermott, Nicholas E. Johnson, Chad Heatwole	2018	58
7	Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databases Genetics in Medicine ·Wei Liu, Sander Pajusalu, Nicole J. Lake, Geyu Zhou, Nilah M. Ioannidis, Plavi Mittal, Nicholas E. Johnson, Conrad C. Weihl, Bradley A. Williams, Douglas E. Albrecht, Laura Rufibach, Monkol Lek	2019	57
8	Myotonic Muscular Dystrophies CONTINUUM Lifelong Learning in Neurology ·Nicholas E. Johnson	2019	55
9	Patient‐identified disease burden in facioscapulohumeral muscular dystrophy Muscle & Nerve ·Nicholas E. Johnson, Christine Quinn, Eileen Eastwood, Rabi Tawil, Chad Heatwole	2012	52
10	Patient-Reported Symptoms in Facioscapulohumeral Muscular Dystrophy (PRISM-FSHD) Neurology ·Johanna Hamel, Nicholas E. Johnson, Rabi Tawil, William B. Martens, Nuran Dilek, Michael McDermott, Chad Heatwole	2019	49
11	Myotonic Dystrophy Health Index: Initial evaluation of a disease‐specific outcome measure Muscle & Nerve ·Chad Heatwole, Rita Bode, Nicholas E. Johnson, Jeanne Dekdebrun, Nuran Dilek, Mark Heatwole, James E. Hilbert, Elizabeth Luebbe, William B. Martens, Michael McDermott, Nan Rothrock, Charles A. Thornton, Barbara G. Vickrey, David Victorson, Richard T. Moxley	2013	47
12	Plasma Exchange versus Intravenous Immunoglobulin for Myasthenia Gravis Crisis: An Acute Hospital Cost Comparison Study Journal of Clinical Neuromuscular Disease ·Chad Heatwole, Nicholas E. Johnson, Robert G. Holloway, Katia Noyes	2011	45
13	Patient-Reported Impact of Symptoms in Myotonic Dystrophy Type 2 (PRISM-2) Neurology ·Chad Heatwole, Nicholas E. Johnson, Rita Bode, Jeanne Dekdebrun, Nuran Dilek, James E. Hilbert, Elizabeth Luebbe, William B. Martens, Michael McDermott, Christine Quinn, Nan Rothrock, Charles A. Thornton, Barbara G. Vickrey, David Victorson, Richard T. Moxley	2015	45
14	Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1 Neurology Clinical Practice ·Nicholas E. Johnson, Eugenio Zapata‐Aldana, Nathalie Angeard, Tetsuo Ashizawa, Kiera N. Berggren, Chiara Marini‐Bettolo, Tina Duong, Anne‐Berit Ekström, Valeria Sansone, Cuixia Tian, Leah Hellerstein, Craig Campbell	2019	39
15	Parent‐reported multi‐national study of the impact of congenital and childhood onset myotonic dystrophy Developmental Medicine & Child Neurology ·Nicholas E. Johnson, Anne‐Berit Ekström, Craig Campbell, Man Hung, Heather Adams, Wei Chen, Elizabeth Luebbe, James E. Hilbert, Richard T. Moxley, Chad Heatwole	2015	38
16	Myotonic Dystrophy: From Bench to Bedside Seminars in Neurology ·Chad Heatwole, Nicholas E. Johnson	2012	38
17	Mexiletine in Myotonic Dystrophy Type 1 Neurology ·Chad Heatwole, Elizabeth Luebbe, Spencer Rosero, Katy Eichinger, William B. Martens, James E. Hilbert, Jeanne Dekdebrun, Nuran Dilek, Christine Zizzi, Nicholas E. Johnson, Araya Puwanant, Rabi Tawil, Giovanni Schifitto, Christopher A. Beck, J. Franklin Richeson, Wojciech Zaręba, Charles A. Thornton, Michael McDermott, Richard T. Moxley	2020	37
18	Management of Charcot–Marie–Tooth disease: improving long-term care with a multidisciplinary approach Journal of Multidisciplinary Healthcare ·Nicholas E. Johnson, Donald McCorquodale, Evan M Pucillo	2016	33
19	Myotonic dystrophy health index: Correlations with clinical tests and patient function Muscle & Nerve ·Chad Heatwole, Rita Bode, Nicholas E. Johnson, Jeanne Dekdebrun, Nuran Dilek, Katy Eichinger, James E. Hilbert, Eric L. Logigian, Elizabeth Luebbe, William B. Martens, Michael McDermott, Shree Pandya, Araya Puwanant, Nan Rothrock, Charles A. Thornton, Barbara G. Vickrey, David Victorson, Richard T. Moxley	2015	33
20	Effects of weakness of orofacial muscles on swallowing and communication in FSHD Neurology ·Karlien Mul, Kiera N. Berggren, Mattie Y. Sills, Ayla McCalley, Baziel G.M. van Engelen, Nicholas E. Johnson, Jeffrey Statland	2019	33

About Nicholas E. Johnson

Nicholas E. Johnson is a scholar working on Cellular and Molecular Neuroscience, Neurology, Genetics, Molecular Biology and Neurology, having authored 101 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (56 papers), Muscle Physiology and Disorders (32 papers), Parkinson's Disease Mechanisms and Treatments (23 papers), Mitochondrial Function and Pathology (20 papers), Hereditary Neurological Disorders (13 papers), Botulinum Toxin and Related Neurological Disorders (12 papers), Neurogenetic and Muscular Disorders Research (12 papers) and Cardiomyopathy and Myosin Studies (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (953 citations), Neurology (612 citations), Genetics (285 citations), Molecular Biology (1.0k citations) and Psychiatry and Mental health (133 citations). Nicholas E. Johnson has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Chad Heatwole, Michael McDermott, Nuran Dilek, Richard T. Moxley, William B. Martens, Rabi Tawil, Jeffrey Statland, Elizabeth Luebbe, Christine Quinn and Charles A. Thornton. Their work appears in journals such as Muscle & Nerve, Neurology, Neuromuscular Disorders, Journal of Neuromuscular Diseases and Neurology 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.

Explore authors with similar magnitude of impact