Marina Kennerson

5.3k citations

95 papers · 3.0k indexed · 1 hit paper · h-index 27

Neurology top 1%
- Neurological diseases and metabolism 31
- Botulinum Toxin and Related Neurological Disorders 7
- Amyotrophic Lateral Sclerosis Research 7
Cellular and Molecular Neuroscience top 1%
- Hereditary Neurological Disorders 59
- Genetic Neurodegenerative Diseases 34
Neurology top 1%
- Neurological diseases and metabolism 31
- Botulinum Toxin and Related Neurological Disorders 7
- Amyotrophic Lateral Sclerosis Research 7
Genetics top 2%
- Neurogenetic and Muscular Disorders Research 14
Cell Biology top 2%
- Cellular Mechanics and Interactions 8
- Cellular transport and secretion 8

Co-authors: Garth A. Nicholson Vincent Timmerman Peter De Jonghe Ian P. Blair Danqing Zhu Michaela Auer‐Grumbach Jeffery M. Vance Kenneth H. Fischbeck
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Nature Genetics (3 papers)Journal of the American College of Cardiology (1 paper)Brain (3 papers)
Partner nations: Australia United States Malaysia

In The Last Decade

Marina Kennerson

92 papers receiving 2.9k citations

Hit Papers

align trajectories log scale

Peers

Countries citing papers authored by Marina Kennerson

Since Specialization

Citations

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

Fields of papers citing papers by Marina Kennerson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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

20 of 20 papers shown

#	Work
1	Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders Annals of Clinical and Translational Neurology ·Laura Ivete Rudaks,Igor Stevanovski,Dennis Yeow,Andre L. M. Reis,Sanjog R. Chintalaphani,Pak Leng Cheong,Hasindu Gamaarachchi,Lisa Worgan,Kate Ahmad,Mike Hayes,Andrew Hannaford,Samuel Kim,Victor S.C. Fung,G. Michael Hálmagyi,Andrew J. Martin,David Manser,Michel Tchan,(unknown),Marina Kennerson,Ira W. Deveson,Kishore R. Kumar	2025	3
2	Long-read sequencing for diagnosis of genetic myopathies BMJ Neurology Open ·Dennis Yeow,Laura Ivete Rudaks,Ryan L. Davis,Karl Ng,Roula Ghaoui,Pak Leng Cheong,Gianina Ravenscroft,Marina Kennerson,Ira W. Deveson,Kishore R. Kumar	2025	1
3	A missense mutation in human INSC causes peripheral neuropathy EMBO Molecular Medicine ·Jui‐Yu Yeh,Hua‐Chuan Chao,Cheng-Li Hong,Yu-Chien Hung,Fei‐Yang Tzou,Cheng-Tsung Hsiao,Jeng‐Lin Li,Wenjie Chen,Cheng‐Ta Chou,Yu‐Shuen Tsai,Yi‐Chu Liao,Yu‐Chun Lin,Suewei Lin,Shu‐Yi Huang,Marina Kennerson,Yi‐Chung Lee,Chih‐Chiang Chan	2024	0
4	An Inversion Affecting the GCH1 Gene as a Novel Finding in Dopa‐Responsive Dystonia Movement Disorders Clinical Practice ·Shadi El‐Wahsh,Avi Fellner,Matthew Hobbs,Joe Copty,Ira W. Deveson,Igor Stevanovski,Marion Stoll,Danqing Zhu,Ramesh K. Narayanan,Bianca R. Grosz,Lisa Worgan,Pak Leng Cheong,Dennis Yeow,Laura Ivete Rudaks,Md Mehedi Hasan,Vanessa M. Hayes,Marina Kennerson,Kishore R. Kumar,Mike Hayes	2024	2
5	Advances and challenges in modeling inherited peripheral neuropathies using iPSCs Experimental & Molecular Medicine ·Jonas Van Lent,Robert Prior,Gonzalo Pérez Siles,Anthony N. Cutrupi,Marina Kennerson,Tim Vangansewinkel,Esther Wolfs,Bipasha Mukherjee-Clavin,Zachary S. Nevin,Luke M. Judge,Bruce R. Conklin,Henna Tyynismaa,Alex Clark,David Bennett,Ludo Van Den Bosch,Mario Saporta,Vincent Timmerman	2024	10
6	An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches The Cerebellum ·Laura Ivete Rudaks,Dennis Yeow,Karl Ng,Ira W. Deveson,Marina Kennerson,Kishore R. Kumar	2024	16
7	Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards Journal of Neurology Neurosurgery & Psychiatry ·J. Parmar,Nigel G. Laing,Marina Kennerson,Gianina Ravenscroft	2024	6
8	A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing Journal of the Peripheral Nervous System ·Bianca R. Grosz,J. Parmar,Melina Ellis,Samantha J. Bryen,Cas Simons,Andre L. M. Reis,Igor Stevanovski,Ira W. Deveson,Garth A. Nicholson,Nigel G. Laing,Mathew Wallis,Gianina Ravenscroft,Kishore R. Kumar,Steve Vucic,Marina Kennerson	2024	1
9	A humanized yeast model reveals dominant-negative properties of neuropathy-associated alanyl-tRNA synthetase mutations Human Molecular Genetics ·Rebecca Meyer‐Schuman,Sheila Marte,T.J. Smith,Shawna Feely,Marina Kennerson,Garth A. Nicholson,Mike E Shy,Kristin S. Koutmou,Anthony Antonellis	2023	7
10	Identity-by-descent analysis of CMTX3 links three families through a common founder Journal of Human Genetics ·Lyndal Henden,Bianca R. Grosz,Melina Ellis,Garth A. Nicholson,Marina Kennerson,Kelly L. Williams	2022	3
11	Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy Journal of the Peripheral Nervous System ·Bianca R. Grosz,Igor Stevanovski,Sara Negri,Melina Ellis,Stephanie L. Barnes,Stephen Reddel,Steve Vucic,Garth A. Nicholson,Andrea Cortese,Kishore R. Kumar,Ira W. Deveson,Marina Kennerson	2022	9
12	Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis Journal of Neurology Neurosurgery & Psychiatry ·Antonia Carroll,P. James B. Dyck,Mamede de Carvalho,Marina Kennerson,Mary M. Reilly,Matthew C. Kiernan,Steve Vucic	2022	60
13	Novel gene–intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy Brain ·Anthony N. Cutrupi,Ramesh K. Narayanan,Gonzalo Pérez‐Siles,Bianca R. Grosz,Kaitao Lai,Alexandra Boyling,Melina Ellis,Ruby C.Y. Lin,Brent Neumann,Di Mao,Motonari Uesugi,Garth A. Nicholson,Steve Vucic,Mario Saporta,Marina Kennerson	2022	9
14	Revisiting the pathogenic mechanism of the GJB1 5’ UTR c.-103C > T mutation causing CMTX1 Neurogenetics ·Bianca R. Grosz,John Svaren,Gonzalo Pérez‐Siles,Garth A. Nicholson,Marina Kennerson	2021	2
15	CD300f epitopes are specific targets for acute myeloid leukemia with monocytic differentiation Molecular Oncology ·Edward Abadir,Robin Gasiorowski,Kaitao Lai,Fiona Kupresanin,Adelina Romano,Pablo A. Silveira,Kevin Lo,Phillip D. Fromm,Marina Kennerson,Harry Iland,P. Joy Ho,P. Mark Hogarth,Kenneth F. Bradstock,Derek N.J. Hart,Georgina J. Clark	2019	7
16	A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene Human Molecular Genetics ·Marina Kennerson,Eppie M. Yiu,David Chuang,Aditi Kidambi,Shih-Chia Tso,C. Ly,Rama Chaudhry,Alexander P. Drew,Gary Rance,Martin B. Delatycki,Stephan Züchner,Monique M. Ryan,Garth A. Nicholson	2013	56
17	Modafinil Effects during Acute Continuous Positive Airway Pressure Withdrawal: A Randomized Crossover Double-Blind Placebo-controlled Trial American Journal of Respiratory and Critical Care Medicine ·Shaun C. Williams,Nathaniel S. Marshall,Marina Kennerson,Naomi L. Rogers,Peter Y. Liu,Ronald R. Grunstein	2010	30
18	Determinants of Serum-Induced SIRT1 Expression in Older Men: The CHAMP Study The Journals of Gerontology Series A ·David G. Le Couteur,V.L. Benson,Aisling C. McMahon,Fiona Blyth,David J. Handelsman,Markus J. Seibel,Marina Kennerson,Vasi Naganathan,Robert G. Cumming,Rafael de Cabo	2010	19
19	A Rapid and Definitive Test for Charcot-Marie-Tooth 1A and Hereditary Neuropathy with Liability to Pressure Palsies Using Multiplexed Real-Time PCR Genetic Testing ·Peter Lorentzos,Thomas Kaiser,Marina Kennerson,Garth A. Nicholson	2003	17
20	Mutational studies in X-linked Charcot-Marie-Tooth disease (CMTX) The American Journal of Human Genetics ·Annia K. Cherryson,Leone Yeung,Marina Kennerson,Garth A. Nicholson	1994	10

About Marina Kennerson

Marina Kennerson is a scholar working on Neurology, Cellular and Molecular Neuroscience and Genetics, having authored 95 papers that have together received 3.0k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (59 papers), Genetic Neurodegenerative Diseases (34 papers), Neurological diseases and metabolism (31 papers), Neurogenetic and Muscular Disorders Research (14 papers), Cellular Mechanics and Interactions (8 papers), Cellular transport and secretion (8 papers), Botulinum Toxin and Related Neurological Disorders (7 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). The work is most often cited by research in Neurology (658 citations), Cellular and Molecular Neuroscience (1.4k citations) and Neurology (762 citations). Marina Kennerson has collaborated with scholars based in Australia, United States and Malaysia. Frequent co-authors include Garth A. Nicholson, Vincent Timmerman, Peter De Jonghe, Ian P. Blair, Danqing Zhu, Michaela Auer‐Grumbach, Jeffery M. Vance, Kenneth H. Fischbeck, Klaus Wagner and Stephan Züchner. Their work appears in journals such as Nature Genetics, Journal of the American College of Cardiology and Brain.

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