Martin B Delatycki
Overview
Explore the profile of Martin B Delatycki including associated specialties, affiliations and a list of published articles.
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Articles
322
Citations
5519
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Recent Articles
1.
Indelicato E, Delatycki M, Farmer J, Franca Jr M, Perlman S, Rai M, et al.
Nat Rev Neurol
. 2025 Mar;
PMID: 40032987
Friedreich ataxia (FRDA) is a rare multisystem, life-limiting disease and is the most common early-onset inherited ataxia in populations of European, Arab and Indian descent. In recent years, substantial progress...
2.
Rafehi H, Fearnley L, Read J, Snell P, Davies K, Scott L, et al.
Genome Res
. 2025 Feb;
PMID: 40015980
The cerebellar ataxias (CAs) are a heterogeneous group of disorders characterized by progressive incoordination. Seventeen repeat expansion (RE) loci have been identified as the primary genetic cause and account for...
3.
Zhang G, Chen J, Johnstone D, Delatycki M, Allen K, Olynyk J
Med J Aust
. 2025 Feb;
PMID: 40013463
No abstract available.
4.
Delatycki M, Kirk E, Laing N
N Engl J Med
. 2025 Feb;
392(9):930.
PMID: 40009814
No abstract available.
5.
Freeman L, Archibald A, Dive L, Delatycki M, Kirk E, Laing N, et al.
Eur J Hum Genet
. 2024 Nov;
33(2):194-198.
PMID: 39587355
Reproductive genetic carrier screening (RGCS) provides information about people's chance of having children with certain genetic conditions, to inform reproductive decision making. RGCS at population scale requires a robust and...
6.
Kirk E, Delatycki M, Archibald A, Tutty E, Caruana J, Halliday J, et al.
N Engl J Med
. 2024 Nov;
391(20):1877-1889.
PMID: 39565987
Background: Genomic sequencing technology allows for identification of reproductive couples with an increased chance, as compared with that in the general population, of having a child with an autosomal recessive...
7.
Naghipour S, Corben L, Hulme A, Dottori M, Delatycki M, Lees J, et al.
Mov Disord
. 2024 Nov;
40(2):226-230.
PMID: 39559924
No abstract available.
8.
Martyn M, Lee L, Jan A, Tytherleigh R, Lynch F, Mighton C, et al.
Genet Med
. 2024 Nov;
27(2):101327.
PMID: 39548854
Purpose: Families of children in pediatric acute care who are offered ultrarapid genomic sequencing are making complex decisions during a high-stress period. To reduce complexity for families and clinicians, we...
9.
Milne S, Roberts M, Williams S, Chua J, Grootendorst A, Agostinelli G, et al.
Ann Neurol
. 2024 Nov;
97(3):409-424.
PMID: 39520242
Objective: Rehabilitation is thought to reduce ataxia severity in individuals with hereditary cerebellar ataxia (HCA). This multicenter, randomized controlled superiority trial aimed to examine the efficacy of a 30-week goal-directed...
10.
Cortese A, Beecroft S, Facchini S, Curro R, Cabrera-Serrano M, Stevanovski I, et al.
Nat Commun
. 2024 Oct;
15(1):8955.
PMID: 39419991
No abstract available.