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Author

  • Nigel Laing
2016

What is the role for preconception carrier screening in neurology?

Laing, N., 2016, In : Advances in Clinical Neuroscience and Rehabilitation. 16, 1, p. 5-6 2 p.

Research output: Contribution to journalComment/debate

Open Access
2015

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

Sztal, T. E., Zhao, M., Williams, C., Oorschot, V., Parslow, A. C., Giousoh, A., Yuen, M., Hall, T. E., Costin, A., Ramm, G., Bird, P. I., Busch-Nentwich, E. M., Stemple, D. L., Currie, P. D., Cooper, S. T., Laing, N., Nowak, K. & Bryson-Richardson, R. J., Sep 2015, In : Acta Neuropathologica. 130, 3, p. 389-406

Research output: Contribution to journalArticle

Open Access
18 Citations (Scopus)
2016

Diagnosis and etiology of congenital muscular dystrophy: We are halfway there

O'Grady, G. L., Lek, M., Lamande, S. R., Waddell, L., Oates, E. C., Punetha, J., Ghaoui, R., Sandaradura, S. A., Best, H., Kaur, S., Davis, M., Laing, N. G., Muntoni, F., Hoffman, E., Macarthur, D. G., Clarke, N. F., Cooper, S. & North, K., 7 Jul 2016, In : Annals of Neurology. 80, 1, p. 101-111 11 p.

Research output: Contribution to journalArticle

20 Citations (Scopus)
2011

Fetal akinesia: review of the genetics of the neuromuscular causes

Ravenscroft, G., Sollis, E., Charles, A. K., North, K. A., Baynam, G. & Laing, N., 2011, In : Journal of Medical Genetics. 48, p. 793-801

Research output: Contribution to journalArticle

40 Citations (Scopus)
2016

Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy

Guimier, A., Gordon, C. T., Godard, F., Ravenscroft, G., Oufadem, M., Vasnier, C., Rambaud, C., Nitschke, P., Bole-Feysot, C., Masson, C., Dauger, S., Longman, C., Laing, N. G., Kugener, B., Bonnet, D., Bouvagnet, P., Di Filippo, S., Probst, V., Redon, R., Charron, P. & 7 others, Rötig, A., Lyonnet, S., Dautant, A., De Pontual, L., Di Rago, J-P., Delahodde, A. & Amiel, J., 1 Sep 2016, In : American Journal of Human Genetics. 99, 3, p. 666-673

Research output: Contribution to journalArticle

Open Access
13 Citations (Scopus)
2018

Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2

Lassuthova, P., Rebelo, A. P., Ravenscroft, G., Lamont, P. J., Davis, M. R., Manganelli, F., Feely, S. M., Bacon, C., Brožková, D. Š., Haberlova, J., Mazanec, R., Tao, F., Saghira, C., Abreu, L., Courel, S., Powell, E., Buglo, E., Bis, D. M., Baxter, M. F., Ong, R. W. & 14 others, Marns, L., Lee, Y. C., Bai, Y., Isom, D. G., Barro-Soria, R., Chung, K. W., Scherer, S. S., Larsson, H. P., Laing, N. G., Choi, B. O., Seeman, P., Shy, M. E., Santoro, L. & Zuchner, S., 1 Mar 2018, In : American Journal of Human Genetics. 102, 3, p. 505-514 10 p.

Research output: Contribution to journalArticle

Open Access
File
14 Citations (Scopus)
333 Downloads (Pure)
2014

Novel cofilin-2 (CFL2) four base pair deletion causing nemaline myopathy

Ong, R., Alsaman, A. S., Selcen, D., Arabshahi, A., Yau, K., Ravenscroft, G., Duff, R., Atkinson, V., Allcock, R. & Laing, N., 2014, In : Journal of Neurology, Neurosurgery and Psychiatry. 85, 9, p. 1058-1060

Research output: Contribution to journalLetter

11 Citations (Scopus)
2013

Cardiac α-actin over-expression therapy in dominant ACTA1 disease

Ravenscroft, G., Mcnamara, E., Griffiths, L. M., Papadimitriou, J., Hardeman, E. C., Bakker, T., Davies, K. E., Laing, N. & Nowak, K., 2013, In : Human Molecular Genetics. 22, 19, p. 3987-3997

Research output: Contribution to journalArticle

13 Citations (Scopus)
Open Access
7 Citations (Scopus)
2012

Nemaline Myopathy with Stiffness and Hypertonia associated with an ACTA1 Mutation

Jain, R. K., Jayawant, S., Squier, W., Muntoni, F., Sewry, C. A., Manzur, A., Quinlivan, R., Lillis, S., Jungbluth, H., Sparrow, J. C., Ravenscroft, G., Nowak, K., Memo, M., Marston, S. B. & Laing, N., 2012, In : Neurology. 78, p. 1100-1103

Research output: Contribution to journalReview article

30 Citations (Scopus)
2014

Clinical and genetic characterization of distal myopathies

Cabrera, M., Junckerstorff, R., Needham, M., Lamont, P. & Laing, N., 2014, 19th Congress of the World Muscle Society. United Kingdom: Elsevier, Vol. 24. p. 810

Research output: Chapter in Book/Conference paperConference paper

Adult onset distal and proximal myopathy with complete ophthalmoplegia and bulbar involvement due to de novo mutation in MYH2

Cabrera, M., Junckerstorff, R., Lamont, P. & Laing, N., 2014, 19th Congress of the World Muscle Society. United Kingdom: Elsevier, Vol. 24. p. 796-797

Research output: Chapter in Book/Conference paperConference paper

Novel CHKB mutation expands the megaconial muscular dystrophy phenotype

Cabrera-Serrano, M., Junckerstorff, R., Atkinson, V., Sivadorai, P., Allcock, R., Lamont, P. J. & Laing, N., 2014, In : Muscle and Nerve. 51, 1, p. 140-143

Research output: Contribution to journalArticle

10 Citations (Scopus)
2018

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant

Sedghi, M., Salari, M., Moslemi, A. R., Kariminejad, A., Davis, M., Goullée, H., Olsson, B., Laing, N. & Tajsharghi, H., 1 Dec 2018, In : Neurology: Genetics. 4, 6, e295.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence

Bonnin, E., Cabochette, P., Filosa, A., Jühlen, R., Komatsuzaki, S., Hezwani, M., Dickmanns, A., Martinelli, V., Vermeersch, M., Supply, L., Martins, N., Pirenne, L., Ravenscroft, G., Lombard, M., Port, S., Spillner, C., Janssens, S., Roets, E., Van Dorpe, J., Lammens, M. & 6 others, Kehlenbach, R. H., Ficner, R., Laing, N. G., Hoffmann, K., Vanhollebeke, B. & Fahrenkrog, B., 1 Dec 2018, In : PLoS Genetics. 14, 12, e1007845.

Research output: Contribution to journalArticle

Open Access
6 Citations (Scopus)
2014

Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy

Yuen, M., Sandaradura, S. A., Dowling, J. J., Kostyukova, A. S., Moroz, N. A., Quinlan, K. G. R., Lehtokari, V. L., Ravenscroft, G., Todd, E., Ceyhan-Birsoy, O., Gokhin, D. S., Maluenda, J., Lek, M., Nolent, F., Pappas, C. T., Novak, S. M., D'Amico, A., Malfatti, E., Thomas, B. P., Gabriel, S. B. & 37 others, Gupta, N., Daly, M. J., Ilkovski, B., Houweling, P. J., Davidson, A. E., Swanson, L. C., Brownstein, C. A., Gupta, V. A., Medne, L., Shannon, P., Martin, N., Bick, D. P., Flisberg, A., Holmberg, E. E., Van Den Bergh, P., Lapunzina, P., Waddell, L. B., Sloboda, D. D., Bertini, E. S., Chitayat, D. A., Telfer, W. R., Laquerrière, A., Gregorio, C. C., Ottenheijm, C. A. C., Bönnemann, C. G., Pelin, K., Beggs, A. H., Hayashi, Y., Roméro, N. B., Laing, N., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V. M., Macarthur, D. G., North, K. N. & Clarke, N. F., Nov 2014, In : Journal of Clinical Investigation. 124, 11, p. 4693-4708

Research output: Contribution to journalArticle

88 Citations (Scopus)
2019

TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor

Kariminejad, A., Dahl-Halvarsson, M., Ravenscroft, G., Afroozan, F., Keshavarz, E., Zonooz, M. F., Najmabadi, H., Goullee, H., Davis, M., Laing, N. & Tajsharghi, H., Jul 2019, In : European Journal of Human Genetics. 27, p. 314-314 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

2011

Clinical utility gene card for: Laing distal myopathy

Lamont, P., Wallefeld, W., Davis, M., Udd, B. & Laing, N., 2011, In : European Journal of Human Genetics. 8 December 2010, p. 3 pages

Research output: Contribution to journalReview article

2 Citations (Scopus)
2013

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations

Ravenscroft, G., Thompson, E. M., Todd, E., Yau, K. S., Kresoje, N., Sivadorai, P., Friend, K., Riley, K., Manton, N. D., Blumbergs, P., Fietz, M., Duff, R., Davis, M. R., Allcock, R. & Laing, N., 2013, In : Neuromuscular Disorders. 23, p. 165-169

Research output: Contribution to journalArticle

23 Citations (Scopus)
2016

Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria

Ravenscroft, G., Di Donato, N., Hahn, G., Davis, M. R., Craven, P. D., Poke, G., Neas, K. R., Neuhann, T. M., Dobyns, W. B. & Laing, N. G., Nov 2016, In : Neuromuscular Disorders. 26, 11, p. 744-748

Research output: Contribution to journalArticle

23 Citations (Scopus)
2012

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy

Martilla, M., Lemola, E., Wallefeld, W., Memo, M., Donner, K., Laing, N., Marston, S., Grönholm, M. & Wallgren-Pettersen, C., 2012, In : Biochemical Journal. 442, p. 231-239

Research output: Contribution to journalArticle

Open Access
35 Citations (Scopus)

Is newborn screening for Duchenne muscular dystrophy ethically justifiable?

Bayley, K. L. & Laing, N., 2012, In : Future Neurology. 7, p. 363-365

Research output: Contribution to journalArticle

2015

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Todd, E., Yau, K., Ong, R., Slee, J., Mcgillivray, G., Barnett, C. P., Haliloglu, G., Talim, B., Akcoren, Z., Kariminejad, A., Cairns, A., Clarke, N. F., Freckmann, M. L., Romero, N. B., Williams, D., Sewry, C. A., Colley, A., Ryan, M. M., Kiraly-Borri, C., Sivadorai, P. & 6 others, Allcock, R., Beeson, D., Maxwell, S., Davis, M. R., Laing, N. & Ravenscroft, G., 17 Nov 2015, In : Orphanet Journal of Rare Diseases. 10, 1, 14 p., 148.

Research output: Contribution to journalArticle

Open Access
51 Citations (Scopus)
2017

Outcomes of an international workshop on preconception expanded carrier screening: Some considerations for governments

Molster, C. M., Lister, K., Metternick-Jones, S., Baynam, G., Clarke, A. J., Straub, V., Dawkins, H. J. S. & Laing, N., 24 Feb 2017, In : Frontiers in Public Health. 5, FEB, 25.

Research output: Contribution to journalArticle

Open Access
9 Citations (Scopus)

New era in genetics of early-onset muscle disease: Breakthroughs and challenges

Ravenscroft, G., Davis, M. R., Lamont, P., Forrest, A. & Laing, N. G., Apr 2017, In : Seminars in Cell and Developmental Biology. 64, p. 160-170 11 p.

Research output: Contribution to journalReview article

12 Citations (Scopus)
2015

Clinical utility gene card for: Nemaline myopathy - update 2015

Nowak, K., Davis, M. R., Wallgren-Pettersson, C., Lamont, P. J. & Laing, N., Nov 2015, In : European Journal of Human Genetics. 23, 11, p. e1-e5 5 p.

Research output: Contribution to journalArticle

Open Access
File
8 Citations (Scopus)
188 Downloads (Pure)
2017

BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

Cabrera-Serrano, M., Rivas-Infante, E., Mavillard, F., Morar, B., Comas, D., Carvajal, A., Avila, R., Muelas, N., Olive, M., Diaz, J., Verges, E., Romero, N., Laporte, J., Vilchez, J., Laing, N., Kalaydjieva, L. & Paradas, C., Oct 2017, In : Neuromuscular Disorders. 27, p. S172-S173 2 p.

Research output: Contribution to journalAbstract/Meeting Abstract

2019

Expanded reproductive carrier screening-how can we do the most good and cause the least harm?

Delatycki, M. B., Laing, N. & Kirk, E., May 2019, In : European Journal of Human Genetics. 27, 5, p. 669-670 2 p.

Research output: Contribution to journalEditorial

2 Citations (Scopus)
2017

What prospective parents need to know about gene tests such as ‘prepair’

Ravenscroft, G., Farrar, M., Laing, N. & Ong, R., 17 Nov 2017, The Conversation.

Research output: Contribution to specialist publicationArticle

2014

Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (MYH7) Distal Myopathy

Lamont, P. J., Wallefeld, W., Hilton- Jones, D., Udd, B., Argov, Z., Barboi, A. C., Bonneman, C., Boycott, K. M., Bushby, K. M. D., Connolly, A. M., Davies, N. P., Beggs, A. H., Cox, G. F., Dastgir, J., Dechene, E. T., Gooding, R., Jungbluth, H., Muelas, N., Palmio, J., Penttilä, S. & 10 others, Schmedding, E., Suominen, T., Straub, V. W., Staples, C. I., Van Den Bergh, P. Y. K., Vílchez, J. J., Wagner, K. R., Wheeler, P. G., Wraige, E. A. & Laing, N., Jul 2014, In : Human Mutation. 35, 7, p. 868-879

Research output: Contribution to journalArticle

49 Citations (Scopus)
2013

Skeletal muscle α-actin diseases (actinopathies): Pathology and mechanisms

Nowak, K., Ravenscroft, G. & Laing, N., 2013, In : Acta Neuropathologica. 125, 1, p. 19-32

Research output: Contribution to journalReview article

Open Access
File
61 Citations (Scopus)
461 Downloads (Pure)
2015

Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita

Ravenscroft, G., Nolent, F., Rajagopalan, S., Meireles, A. M., Paavola, K. J., Gaillard, D., Alanio, E., Buckland, M., Arbuckle, S., Krivanek, M., Maluenda, J., Pannell, S., Gooding, R., Ong, R., Allcock, R., Carvalho, E. D. F., Carvalho, M. D. F., Kok, F., Talbot, W. S., Melki, J. & 1 others, Laing, N., 4 Jun 2015, In : The American Journal of Human Genetics. 96, 6, p. 955-961

Research output: Contribution to journalArticle

Open Access
50 Citations (Scopus)
2017

Genetic and histological characterisation of excitation-contraction coupling related structural myopathy cohort

Beecroft, S., Choi, R., McLean, C., Olive, M., Ryan, M., Davis, M., Laing, N., Launikonis, B. & Ravenscroft, G., Oct 2017, In : Neuromuscular Disorders. 27, p. S97-S97 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

2018

Genetics of neuromuscular fetal akinesia in the genomics era

Beecroft, S. J., Lombard, M., Mowat, D., McLean, C., Cairns, A., Davis, M., Laing, N. G. & Ravenscroft, G., 1 Aug 2018, In : Journal of Medical Genetics. 55, 8, p. 505-514 10 p.

Research output: Contribution to journalReview article

10 Citations (Scopus)
2016

Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization

O'Grady, G. L., Best, H. A., Sztal, T. E., Schartner, V., Sanjuan-Vazquez, M., Donkervoort, S., Abath Neto, O., Sutton, R. B., Ilkovski, B., Romero, N. B., Stojkovic, T., Dastgir, J., Waddell, L. B., Boland, A., Hu, Y., Williams, C., Ruparelia, A. A., Maisonobe, T., Peduto, A. J., Reddel, S. W. & 22 others, Lek, M., Tukiainen, T., Cummings, B. B., Joshi, H., Nectoux, J., Brammah, S., Deleuze, J. F., Ing, V. O., Ramm, G., Ardicli, D., Nowak, K., Talim, B., Topaloglu, H., Laing, N., North, K. N., Macarthur, D. G., Friant, S., Clarke, N. F., Bryson-Richardson, R. J., Bönnemann, C. G., Laporte, J. & Cooper, S. T., 3 Nov 2016, In : American Journal of Human Genetics. 99, 5, p. 1086-1105

Research output: Contribution to journalArticle

Open Access
13 Citations (Scopus)
2011

Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

Duff, R., Tay, V., Hackman, P., Ravenscroft, G., Mclean, C., Kennedy, P., Steinbach, A., Schöffler, W., Van Der Ven, P. F. M., Fürst, D. O., Song, J., Dijnović-Carugo, K., Penttilä, S., Raheem, O., Reardon, K., Malandrini, A., Gambelli, S., Villanova, M., Nowak, K., Williams, D. R. & 4 others, Landers, J. E., Brown Jr, R. H., Udd, B. & Laing, N., 2011, In : American Journal of Human Genetics. 88, p. 1-6

Research output: Contribution to journalArticle

Open Access
74 Citations (Scopus)
2017

Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseases

Schofield, D., Alam, K., Douglas, L., Shrestha, R., MacArthur, D. G., Davis, M., Laing, N. G., Clarke, N. F., Burns, J., Cooper, S. T., North, K. N., Sandaradura, S. A. & O'Grady, G. L., 2017, In : Genome Medicine. 2

Research output: Contribution to journalArticle

Open Access
29 Citations (Scopus)
2018
7 Citations (Scopus)
2019

Recessive MYH7-related myopathy in two families

Beecroft, S. J., van de Locht, M., de Winter, J. M., Ottenheijm, C. A., Sewry, C. A., Mohammed, S., Ryan, M. M., Woodcock, I. R., Sanders, L., Gooding, R., Davis, M. R., Oates, E. C., Laing, N. G., Ravenscroft, G., McLean, C. A. & Jungbluth, H., Jun 2019, In : Neuromuscular Disorders. 29, 6, p. 456-467 12 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)
2018

Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant

Sandaradura, S. A., Bournazos, A., Mallawaarachchi, A., Cummings, B. B., Waddell, L. B., Jones, K. J., Troedson, C., Sudarsanam, A., Nash, B. M., Peters, G. B., Algar, E. M., Macarthur, D. G., North, K. N., Brammah, S., Charlton, A., Laing, N. G., Wilson, M. J., Davis, M. R. & Cooper, S. T., Mar 2018, In : Human Mutation. 39, 3, p. 383-388

Research output: Contribution to journalArticle

Open Access
12 Citations (Scopus)

Dejerine–Sottas disease in childhood—Genetic and sonographic heterogeneity

Hobbelink, S. M. R., Brockley, C. R., Kennedy, R. A., Carroll, K., de Valle, K., Rao, P., Davis, M. R., Laing, N. G., Voermans, N. C., Ryan, M. M. & Yiu, E. M., 1 Apr 2018, In : Brain and Behavior. 8, 4, e00919.

Research output: Contribution to journalArticle

Open Access
File
2 Citations (Scopus)
126 Downloads (Pure)
2015

Use of whole-exome sequencing for diagnosis of limb-girdle muscular dystrophy: Outcomes and lessons learned

Ghaoui, R., Cooper, S. T., Lek, M., Jones, K., Corbett, A., Reddel, S. W., Needham, M., Liang, C., Waddell, L. B., Nicholson, G., O'Grady, G., Kaur, S., Ong, R., Davis, M., Sue, C. M., Laing, N., North, K. N., Macarthur, D. G. & Clarke, N. F., Dec 2015, In : JAMA Neurology. 72, 12, p. 1424-1432

Research output: Contribution to journalArticle

75 Citations (Scopus)

A Germline MTOR Mutation in Aboriginal Australian Siblings with Intellectual Disability, Dysmorphism, Macrocephaly, and Small Thoraces

Baynam, G., Overkov, A., Davis, M., Mina, K., Schofield, L., Allcock, R., Laing, N., Cook, M., Dawkins, H. & Goldblatt, J., 2015, In : American Journal of Medical Genetics, Part A. 167, 7, p. 1659-1667

Research output: Contribution to journalArticle

20 Citations (Scopus)
2014

Distal arthrogryposis type 5D with novel clinical features and compound heterozygous mutations in ECEL1

Barnett, C. P., Todd, E. J., Ong, R., Davis, M. R., Atkinson, V., Allcock, R., Laing, N. & Ravenscroft, G., 2014, In : American Journal of Medical Genetics, Part A. 164, 7, p. 1846-1849

Research output: Contribution to journalLetter

9 Citations (Scopus)
2017

Do titin developmental isoforms contribute to the pathogenesis of congenital titinopathy?

Oates, E., Yau, K., Jones, K., Smith, J., Cummings, B., Farrar, M., Cooper, S., Lek, M., Hoffman, E., Straub, V., Ferreiro, A., Udd, B., Beggs, A., Bonnemann, C., North, K., MacArthur, D., Granzier, H., Muntoni, F., Davis, M. & Laing, N., Oct 2017, In : Neuromuscular Disorders. 27, p. S237-S238 2 p.

Research output: Contribution to journalAbstract/Meeting Abstract

2019

International perspectives on the implementation of reproductive carrier screening

Delatycki, M. B., Alkuraya, F., Archibald, A., Castellani, C., Cornel, M., Grody, W. W., Henneman, L., Ioannides, A. S., Kirk, E., Laing, N., Lucassen, A., Massie, J., Schuurmans, J., Thong, M-K., van Langen, I. & Zlotogora, J., 29 Nov 2019, In : Prenatal Diagnosis. 10 p.

Research output: Contribution to journalReview article

1 Citation (Scopus)
2018

Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstruction

Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M. L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A. & 7 others, Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R. & Laing, N. G., 1 Sep 2018, In : Neurogastroenterology and Motility. 30, 9, e13371.

Research output: Contribution to journalArticle

4 Citations (Scopus)
2011

Nemaline Myopathies

Wallgren-Pettersson, C., Sewry, C. A., Nowak, K. & Laing, N., 2011, In : SEMINARS IN PEDIATRIC NEUROLOGY. 18, p. 230-238

Research output: Contribution to journalArticle

100 Citations (Scopus)
2013

Genetics of Muscle Disease

Nowak, K., Lamont, P. & Laing, N., 2013, MUSCLE DISEASE Pathology and Genetics. Weller, R. O. (ed.). Second Edition ed. United Kingdom: John Wiley & Sons, p. 375

Research output: Chapter in Book/Conference paperChapter

2 Citations (Scopus)
2017

Variable cardiac α-actin (Actc1) expression in early adult skeletal muscle correlates with promoter methylation

Boutilier, J. K., Taylor, R. L., Ram, R., McNamara, E., Nguyen, Q., Goullée, H., Chandler, D., Mehta, M., Balmer, L., Laing, N. G., Morahan, G. & Nowak, K. J., 26 Aug 2017, In : Biochimica et Biophysica Acta: international journal of biochemistry and biophysics. 1860, 10, p. 1025-1036 12 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)