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M. Annoussamy · SciRah

Researcher profile · Semantic Scholar

M. Annoussamy

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M. Annoussamy — researcher profile on SciRah

h-index: 15
Works: 62
Citations: 974

Most-cited papers

Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study
A. Chabanon, A. Seferian, A. Daron, Y. Péréon +18 more
2018PLoS ONE147 citations Open access
Semantic Scholar
Nusinersen in patients older than 7 months with spinal muscular atrophy type 1
K. Aragon-Gawińska, A. Seferian, A. Daron, E. Gargaun +14 more
2018Neurology109 citations
Semantic Scholar
Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study
M. Annoussamy, A. Seferian, A. Daron, Y. Péréon +18 more
2020Annals of Clinical and Translational Neurology108 citations Open access
Semantic Scholar
Change in mechanical properties of wheat straw due to decomposition and moisture.
M. Annoussamy, G. Richard, S. Recous, J. Guérif
200095 citations
Semantic Scholar
Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
A. Seferian, A. Moraux, M. Annoussamy, A. Canal +20 more
2015PLoS ONE76 citations Open access
Semantic Scholar
Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy
J. Hogrel, C. Wary, A. Moraux, N. Azzabou +13 more
2016Neurology68 citations Open access
Semantic Scholar
Upper Limb Evaluation and One-Year Follow Up of Non-Ambulant Patients with Spinal Muscular Atrophy: An Observational Multicenter Trial
A. Seferian, A. Moraux, A. Canal, V. Decostre +18 more
2015PLoS ONE66 citations Open access
Semantic Scholar
X-linked myotubular myopathy
M. Annoussamy, C. Lilien, T. Gidaro, E. Gargaun +20 more
2019Neurology58 citations Open access
Semantic Scholar
First regulatory qualification of a digital primary endpoint to measure treatment efficacy in DMD
Laurent Servais, D. Eggenspieler, Margaux Poleur, M. Grelet +3 more
2023Nature Medicine37 citations Open access
Semantic Scholar
Hierarchical Bayesian modelling of disease progression to inform clinical trial design in centronuclear myopathy
Eve Fouarge, A. Monseur, B. Boulanger, M. Annoussamy +9 more
2021Orphanet Journal of Rare Diseases31 citations Open access
Semantic Scholar
Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype
L. Servais, M. Montus, C. Le Guiner, R. ben Yaou +17 more
2015Journal of Neuromuscular Diseases30 citations Open access
Semantic Scholar
Normative data on spontaneous stride velocity, stride length, and walking activity in a non-controlled environment
Margaux Poleur, A. Ulinici, A. Daron, O. Schneider +6 more
2021Orphanet Journal of Rare Diseases24 citations Open access
Semantic Scholar
Myostatin: a Circulating Biomarker Correlating with Disease in Myotubular Myopathy Mice and Patients
C. Koch, S. Buono, A. Menuet, A. Robé +24 more
2020Molecular Therapy: Methods & Clinical Development22 citations Open access
Semantic Scholar
Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy
C. Lilien, H. Reyngoudt, A. Seferian, T. Gidaro +10 more
2021Annals of Clinical and Translational Neurology17 citations Open access
Semantic Scholar
Diagnosing X-linked Myotubular Myopathy – A German 20-year Follow Up Experience
A. Gangfuss, D. Schmitt, A. Roos, F. Braun +3 more
2020Journal of Neuromuscular Diseases17 citations Open access
Semantic Scholar
Stride Velocity 95th Centile Detects Decline in Ambulatory Function Over Shorter Intervals than the 6-Minute Walk Test or North Star Ambulatory Assessment in Duchenne Muscular Dystrophy
Michael Rabbia, Maitea Guridi Ormazabal, H. Staunton, Klaas Veenstra +4 more
2024Journal of Neuromuscular Diseases15 citations Open access
Semantic Scholar
Quantitative nuclear magnetic resonance imaging detects subclinical changes over 1 year in skeletal muscle of GNE myopathy
T. Gidaro, H. Reyngoudt, Julien Louër, A. Béhin +9 more
2019Journal of Neurology13 citations
Semantic Scholar
Quantitative measures of motor development in Angelman syndrome
Jessica Duis, Austin Skinner, Robert Carson, Arnaud Gouelle +5 more
2023American Journal of Medical Genetics. Part A9 citations Open access
Semantic Scholar
O.41Sunfish part 1: 18-month safety and exploratory outcomes of risdiplam (RG7916) treatment in patients with type 2 or 3 spinal muscular atrophy
E. Mercuri, G. Baranello, Janbernd Kirschner, L. Servais +10 more
2019Neuromuscular Disorders4 citations
Semantic Scholar
P.398 - Rimeporide: safety, tolerability and pharmacokinetic results from a phase Ib study in DMD boys as well as exploratory biomarkers
Teresa Gidaro, L. Servais, S. Previtali, A. Zambon +16 more
20174 citations
Semantic Scholar
Longitudinal data of the European prospective natural history study of patients with type 2 and 3 spinal muscular atrophy
A. Chabanon, M. Annoussamy, A. Daron, Yann Péréon +16 more
20173 citations
Semantic Scholar
Baseline data from a European prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy – NatHis-SMA
A. Chabanon, Y. Péréon, A. Daron, C. Cances +15 more
20163 citations
Semantic Scholar
FP.12 Application for primary endpoint qualification of the 95th centile of stride velocity (SV95C) in Duchenne muscular dystrophy
M. Annoussamy, D. Eggenspieler, A. Seferian, E. Mercuri +16 more
2022Neuromuscular Disorders2 citations Open access
Semantic Scholar
SMA THERAPIES I
K. Aragon-Gawińska, A. Seferian, L. Brande, A. Daron +17 more
2018Neuromuscular Disorders2 citations
Semantic Scholar
P.429 - Innovative home activity monitoring in non-ambulant patients with spinal muscular atrophy: a multicenter observational trial
E. Gargaun, A. Seferian, G. Quicke, A. Moraux +15 more
20172 citations
Semantic Scholar
ActiMyo home monitoring in adult patients with limb girdle muscular dystrophy type 2B and facioscapulohumeral muscular dystrophy in study ATYR 1940-C-004
Teresa Gidaro, A. Moraux, M. Grelet, E. Gasnier +12 more
20172 citations
Semantic Scholar
11P Autosomal dominant centronuclear myopathy caused by variants in the DNM2 gene – Results of an international, prospective natural history study
F. Braun, A. Seferian, A. Béhin, F. Fer +6 more
2024Neuromuscular Disorders1 citations
Semantic Scholar
DMD/BMD – OUTCOME MEASURES
M. Poleur, A. Ulinici, A. Daron, O. Schneider +6 more
2021Neuromuscular Disorders1 citations Open access
Semantic Scholar
OUTCOME MEASURES
M. Annoussamy, D. Eggenspieler, P. Strijbos, M. Rabbia +3 more
2021Neuromuscular Disorders1 citations
Semantic Scholar
SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES
C. Lilien, M. Annoussamy, M. Polleur, A. Seferian +4 more
2020Neuromuscular Disorders1 citations
Semantic Scholar
OUTCOME MEASURES
M. Annoussamy, D. Eggenspieler, P. Furlong, L. Servais
2020Neuromuscular Disorders1 citations
Semantic Scholar
Data from: X-linked myotubular myopathy: a prospective international natural history study
M. Annoussamy, C. Lilien, T. Gidaro, E. Gargaun +20 more
20191 citations
Semantic Scholar
P.200Feasibility and baseline values of continuous movement measurement in patients with centronuclear myopathy by using ActiMyo®
M. Annoussamy, E. Gasnier, J. Baets, U. Schara +16 more
2019Neuromuscular Disorders1 citations
Semantic Scholar
Treatment by nusinersen in spinal muscular atrophy type 1 patients older than 7 months, 14 months follow-up
Karolina Aragon-Gawińska, A. Seferian, L. Brande, A. Daron +17 more
20181 citations
Semantic Scholar
Baseline data from patients with myotubular myopathy enrolled in a European prospective and longitudinal natural history study
M. Annoussamy, C. Lilien, Teresa Gidaro, E. Gargaun +15 more
20161 citations
Semantic Scholar
Natural history and functional status of patients with myotubular myopathy enrolled in a prospective and longitudinal study
N. R'guiba, M. Annoussamy, R. Cardaş, C. Lilien +16 more
20151 citations
Semantic Scholar
T.P.9
A. Le Moing, A. Totoescu-Seferian, A. Moraux, E. Dorvaux +7 more
20141 citations
Semantic Scholar
14P X-linked myotubular myopathy: 3-year follow-up of a prospective international natural history
A. Seferian, M. Annoussamy, F. Fer, C. Lilien +15 more
2024Neuromuscular Disorders0 citations
Semantic Scholar
Table of Contents, Volume 191A, Number 7, July 2023
My Vuong Hermansen, L. Wekre, I. Lidal, Ashlee Joan Macalino +37 more
2023American Journal of Medical Genetics. Part A0 citations Open access
Semantic Scholar
P.46 Magneto-inertial wearable device: Upper limb trajectory identification in non-ambulant patients with spinal muscular atrophy
C. Lilien, A. Tricot, M. Annoussamy, M. Polleur +6 more
2022Neuromuscular Disorders0 citations
Semantic Scholar
P.222 Wearable inertial sensors for longitudinal follow-up of patients with amyotrophic lateral sclerosis.
M. Poleur, M. Annoussamy, L. Clavel, L. Buscemi +6 more
2022Neuromuscular Disorders0 citations
Semantic Scholar
OUTCOME MEASURES
M. Annoussamy, D. Eggenspieler, E. Camino, B. Porter +6 more
2021Neuromuscular Disorders0 citations
Semantic Scholar
SMA – OUTCOME MEASURES AND REGISTRIES
M. Poleur, M. Annoussamy, D. Eggenspieler, S. Delstanche +2 more
2021Neuromuscular Disorders0 citations Open access
Semantic Scholar
OUTCOME MEASURES
L. Servais, T. Gidaro, A. Seferian, E. Gasnier +5 more
2019Neuromuscular Disorders0 citations
Semantic Scholar
P.217Patterns of disease progression in patients with spinal muscular atrophy type 3 using the motor function measure
A. Seferian, M. Annoussamy, A. Chabanon, C. Cances +9 more
2019Neuromuscular Disorders0 citations
Semantic Scholar
P.107Clinical changes over time in patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study
M. Annoussamy, J. Baets, W. De Ridder, D. Duchěne +14 more
2019Neuromuscular Disorders0 citations
Semantic Scholar
CONGENITAL MYOPATHIES (CNM)
M. Annoussamy, C. Lilien, T. Gidaro, V. Chê +16 more
2018Neuromuscular Disorders0 citations
Semantic Scholar
Baseline characteristics of patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study
M. Annoussamy, A. Grange, C. Lilien, V. Chê +11 more
20180 citations
Semantic Scholar
CONGENITAL MYOPATHIES (CNM)
M. Annoussamy, A. Grange, C. Lilien, V. Chê +10 more
2018Neuromuscular Disorders0 citations
Semantic Scholar
SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES
J. Hogrel, M. Annoussamy, A. Chabanon, A. Daron +16 more
2018Neuromuscular Disorders0 citations
Semantic Scholar

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