I. Zaharieva
发表
Courtney E. French,
F. Muntoni,
M. Tarnopolsky,
2021,
medRxiv.
E. Hoffman,
A. Pestronk,
R. Abresch,
2020,
European Journal of Human Genetics.
F. Muntoni,
L. Servais,
Haiyan Zhou,
2022,
Annals of clinical and translational neurology.
Julius O. B. Jacobsen,
Orion J. Buske,
D. Smedley,
2022,
Human mutation.
F. Muntoni,
N. Dlamini,
A. King,
2015,
Neuromuscular Disorders.
C. Krarup,
F. Muntoni,
P. Ruben,
2015,
Brain : a journal of neurology.
E. Hoffman,
E. Mercuri,
F. Muntoni,
2016,
American journal of human genetics.
Y. Hérault,
K. Mathews,
J. Dowling,
2019,
Neuromuscular Disorders.
Yusuke Nakamura,
Naoyuki Kamatani,
Michiaki Kubo,
2009,
Journal of Human Genetics.
F. Muntoni,
J. U-King-im,
I. Bodi,
2019,
Neuromuscular Disorders.
F. Muntoni,
T. Pierson,
E. Malfatti,
2018
.
F. Muntoni,
T. Pierson,
E. Malfatti,
2017,
Acta Neuropathologica.
F. Muntoni,
I. Nishino,
W. Liang,
2020,
Neuromuscular Disorders.
F. Muntoni,
L. Greensmith,
Haiyan Zhou,
2021,
Annals of clinical and translational neurology.
F. Muntoni,
R. Maroofian,
H. Houlden,
2022,
Annals of clinical and translational neurology.
H. Stefánsson,
R. Fossdal,
K. Stefánsson,
2018
.
K. Bushby,
F. Muntoni,
A. Ferlini,
2013,
PloS one.
M C O'Donovan,
M J Owen,
S Cichon,
2009,
Molecular Psychiatry.
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
M. Zeviani,
M. Pane,
E. Mercuri,
2017,
Human mutation.
Courtney E. French,
F. Muntoni,
M. Tarnopolsky,
2022,
Nature Communications.
F. Muntoni,
Haiyan Zhou,
M. Scoto,
2016,
Molecular therapy. Nucleic acids.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
G. Kirov,
D. Grozeva,
M. Owen,
2008,
Biological Psychiatry.
Susanne Walitza,
Herbert Roeyers,
Peter Holmans,
2012,
The American journal of psychiatry.
G. Kirov,
M. Owen,
M. O’Donovan,
2008,
BMC psychiatry.
F. Muntoni,
L. Servais,
Glyn Williams,
2018,
Human mutation.
M. Gill,
M. Owen,
M. O’Donovan,
2012,
The American journal of psychiatry.
E. Hoffman,
A. Pestronk,
R. Abresch,
2020,
European Journal of Human Genetics.
Joanna Poulton,
Francesco Muntoni,
Caroline A. Sewry,
2015
.
Yusuke Nakamura,
Naoyuki Kamatani,
Michiaki Kubo,
2013,
Psychiatric genetics.
G. Kirov,
M. Owen,
Y. Kamatani,
2011,
Genes, brain, and behavior.
G. Kirov,
M. Owen,
Yusuke Nakamura,
2009,
Journal of affective disorders.
A. Forrest,
F. Muntoni,
G. Ravenscroft,
2018,
Human molecular genetics.
G. Kirov,
M. Owen,
M. O’Donovan,
2010,
Biological Psychiatry.
I. Nelson,
C. Gilissen,
P. Chinnery,
2021,
European Journal of Human Genetics.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
K. Pelin,
F. Muntoni,
V. Lehtokari,
2015,
Journal of neuromuscular diseases.
F. Muntoni,
Silvio Alessandro Di Gioia,
A. O’Donnell-Luria,
2022,
Human mutation.
G. Pesole,
E. Bertini,
K. Bushby,
2016,
Journal of Cell Science.
F. Muntoni,
E. Pegoraro,
P. Bonaldo,
2014,
Neuromuscular Disorders.
P. Nilsson,
F. Muntoni,
R. Wolterbeek,
2017,
Scientific Reports.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2023,
Human Genomics.
H. Stefánsson,
R. Fossdal,
K. Stefánsson,
2010,
Lancet.
H. Stefánsson,
R. Fossdal,
K. Stefánsson,
2010,
BDJ.
F. Muntoni,
C. Sewry,
Lucy Feng,
2014,
Neuromuscular Disorders.
S. Scherer,
B. Franke,
M. Gill,
2012,
The American journal of psychiatry.
Beryl B. Cummings,
Kristen M. Laricchia,
A. O’Donnell-Luria,
2024,
Nature genetics.