Nigel F. Clarke

6.8k citations

60 papers · 2.3k indexed · h-index 29

Genetics top 1%
- Neurogenetic and Muscular Disorders Research 18
Cardiology and Cardiovascular Medicine top 2%
- Cardiomyopathy and Myosin Studies 30
Molecular Biology top 5%
- Muscle Physiology and Disorders 42
- RNA Research and Splicing 8
- Nuclear Structure and Function 7
Cell Biology top 5%
- Cellular transport and secretion 5
- Cellular Mechanics and Interactions 4
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 10

Co-authors: Kathryn N. North Nigel G. Laing Norma B. Romero Leigh B. Waddell Sandra T. Cooper James J. Dowling Alan H. Beggs Sarah A. Sandaradura
Cited by: Genetics Cardiology and Cardiovascular Medicine Molecular Biology
Journals: Neuromuscular Disorders (17 papers)Annals of Neurology (7 papers)European Journal of Human Genetics (4 papers)
Partner nations: Australia United States France

In The Last Decade

Nigel F. Clarke

59 papers receiving 2.3k citations

Peers

Countries citing papers authored by Nigel F. Clarke

Since Specialization

Citations

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

Fields of papers citing papers by Nigel F. Clarke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nigel F. Clarke. 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 Nigel F. Clarke. The network helps show where Nigel F. Clarke may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Cardiac Amyloidosis Secondary to Light-Chain Deposition: The Effect of Daratumumab on Clinical Heart Failure Progression in an Elderly Male Heart Lung and Circulation ·Daniele Barbaro,Nigel F. Clarke,Premkumar Ravishankar,K. Teo,Noemi Horvath,Ito Tetsufumi	2024	0
2	Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseases npj Genomic Medicine ·Deborah Schofield,Khurshid Alam,Ossama Awad,Rupendra Shrestha,Daniel G. MacArthur,Mark R. Davis,Nigel G. Laing,Nigel F. Clarke,Joshua Burns,Sandra T. Cooper,Kathryn N. North,Sarah A. Sandaradura,Gina O’Grady	2017	59
3	Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect Neuromuscular Disorders ·Yiran Guo,Minal Menezes,Manoj P. Menezes,Jinlong Liang,Dong Li,Lisa G. Riley,Nigel F. Clarke,P. Ian Andrews,Lifeng Tian,Richard Webster,Fengxiang Wang,Xuanzhu Liu,Yulan Shen,David R. Thorburn,Brendan J. Keating,Andrew G. Engel,Håkon Håkonarson,John Christodoulou,Xun Xu	2014	15
4	Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine European Journal of Human Genetics ·Gina O’Grady,Heather Best,Emily C. Oates,Simranpreet Kaur,Amanda Charlton,Susan Brammah,Jaya Punetha,Akanchha Kesari,Kathryn N. North,Biljana Ilkovski,Eric P. Hoffman,Nigel F. Clarke	2014	16
5	A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies Neuromuscular Disorders ·Nigel F. Clarke,Kimberly Amburgey,James W. Teener,Sandra Camelo‐Piragua,Akanchha Kesari,Jaya Punetha,Leigh B. Waddell,Mark R. Davis,Nigel G. Laing,Nicole Monnier,Kathryn N. North,Eric P. Hoffman,James J. Dowling	2013	29
6	Congenital myopathies Handbook of clinical neurology ·Norma B. Romero,Nigel F. Clarke	2013	43
7	Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations European Journal of Human Genetics ·Homa Tajsharghi,Simon Hammans,Christopher Lindberg,Alexander Lossos,Nigel F. Clarke,Ingrid Mazanti,Leigh B. Waddell,Yakov Fellig,Nicola Foulds,Nguyen Thi Thu,Richard Webster,Olayinka Raheem,Bjarne Udd,Zohar Argov,Anders Oldfors	2013	28
8	Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledge American Journal of Medical Genetics Part A ·Emily C. Oates,Jonathan M. Payne,Sheryl Foster,Nigel F. Clarke,Kathryn N. North	2013	29
9	Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late‐onset cerebellar ataxia Muscle & Nerve ·Giorgio Tasca,Zagaa Odgerel,Mauro Monforte,Stefania Aurino,Nigel F. Clarke,Leigh B. Waddell,Bjarne Udd,Enzo Ricci,Lev G. Goldfarb	2012	22
10	Mapping domains and mutations on the skeletal muscle ryanodine receptor channel Trends in Molecular Medicine ·H. Leonenko,Francesco Zorzato,Nigel F. Clarke,Susan Treves	2012	44
11	Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5 Neurology ·C. Sbert,Johanna Palmio,Tiina Suominen,M. G. Nasyrova,Anni Evilä,Yasutaro Sataké,Giorgio Tasca,Leigh B. Waddell,Nigel F. Clarke,Alexandru Barboi,Peter Hackman,Bjarne Udd	2012	82
12	Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch Journal of Neuropathology & Experimental Neurology ·Leigh B. Waddell,Frances A. Lemckert,Xi Zheng,Patak,Frances J. Evesson,Maria da Graça Lucas Vieira,Angela Lek,育代梶谷,Pei‐Hui Lin,Nigel F. Clarke,Andrew P. Landstrom,Michael J. Ackerman,Noah Weisleder,Jianjie Ma,Kathryn N. North,Sandra T. Cooper	2011	72
13	Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion Human Mutation ·Nigel F. Clarke,Leigh B. Waddell,Sandra T. Cooper,Margaret M. Perry,Robert L. Smith,Andrew J. Kornberg,Francesco Muntoni,Suzanne Lillis,Volker Straub,Kate Bushby,Michela Guglieri,Mary D. King,Michael A. Farrell,Isabelle Marty,Joël Lunardi,Nicole Monnier,Kathryn N. North	2010	126
14	POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardation European Journal of Medical Genetics ·Aklass Dara,C Bouchet,Susana Quijano‐Roy,Sandrine Vuillaumier‐Barrot,Nigel F. Clarke,Sylvie Odent,Diana Rodriguez,Norma B. Romero,Makiko Ōsawa,Tamao Endo,Tsuyoshi Wakita,Nathalie Séta,Pascale Guicheney	2008	20
15	Mutations in TPM3 are a common cause of congenital fiber type disproportion Annals of Neurology ·Nigel F. Clarke,Hanna Kolski,Danielle E. Dye,Esther Lim,Robert L. Smith,Rakesh Patel,Michael Fahey,Rémi Bellance,Norma B. Romero,Edward S. Johnson,Annick Labarre‐Vila,Nicole Monnier,Nigel G. Laing,Kathryn N. North	2008	102
16	Skeletal Muscle Disease Due to Mutations in Tropomyosin, Troponin and Cofilin Advances in experimental medicine and biology ·Nigel F. Clarke	2008	19
17	C.P.1.04 Defining diagnostic boundaries for congenital fibre type disproportion Neuromuscular Disorders ·Nigel F. Clarke,Robert L. Smith,Andrew J. Kornberg,Lloyd K. Shield,J. I. Manson,Alan H. Beggs,Kathryn N. North	2007	1
18	The pathogenesis of ACTA1‐related congenital fiber type disproportion Annals of Neurology ·Nigel F. Clarke,Biljana Ilkovski,Sandra T. Cooper,Valentina A. Valova,Phillip J. Robinson,Ikuya Nonaka,Juanjuan Feng,Steven B. Marston,Kathryn N. North	2007	49
19	SEPN1: Associated with congenital fiber‐type disproportion and insulin resistance Annals of Neurology ·Nigel F. Clarke,Warren Kidson,Susana Quijano‐Roy,B. Estournet,Ana Ferreiro,Pascale Guicheney,James Manson,Andrew J. Kornberg,Lloyd K. Shield,Kathryn N. North	2006	114
20	Congenital Fiber Type Disproportion—30 Years On Journal of Neuropathology & Experimental Neurology ·Nigel F. Clarke,Kathryn N. North	2003	60

About Nigel F. Clarke

Nigel F. Clarke is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Developmental Biology, Molecular Biology and Cellular and Molecular Neuroscience, having authored 60 papers that have together received 2.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (42 papers), Cardiomyopathy and Myosin Studies (30 papers), Neurogenetic and Muscular Disorders Research (18 papers), Genetic Neurodegenerative Diseases (10 papers), RNA Research and Splicing (8 papers), Nuclear Structure and Function (7 papers), Cellular transport and secretion (5 papers) and Cellular Mechanics and Interactions (4 papers). The work is most often cited by research in Genetics (738 citations), Cardiology and Cardiovascular Medicine (1.1k citations), Molecular Biology (1.8k citations), Cell Biology (328 citations) and Cellular and Molecular Neuroscience (343 citations). Nigel F. Clarke has collaborated with scholars based in Australia, United States and France. Frequent co-authors include Kathryn N. North, Nigel G. Laing, Norma B. Romero, Leigh B. Waddell, Sandra T. Cooper, James J. Dowling, Alan H. Beggs, Sarah A. Sandaradura, Andrew J. Kornberg and Daniel G. MacArthur. Their work appears in journals such as Neuromuscular Disorders, Annals of Neurology, European Journal of Human Genetics, Neurology and Brain.

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