F. Petit
发表
P. Elliott,
M. Jarvelin,
C. Gieger,
2011,
Nature.
Véronique Geoffroy,
Claire Redin,
Corinne Stoetzel,
2012,
Journal of Medical Genetics.
C. Rooryck,
G. Lefort,
P. Jonveaux,
2013,
European Journal of Human Genetics.
F. Escande,
F. Fellmann,
M. Ros,
2020,
Nature Communications.
F. Petit,
Charlotte Avet,
Chantal Denoyelle,
2018,
PloS one.
E. Bertini,
C. Garel,
R. Touraine,
2012,
Orphanet Journal of Rare Diseases.
P. Byers,
M. Holder-Espinasse,
W. Lissens,
2017,
Journal of Medical Genetics.
A. Afenjar,
T. Roscioli,
A. Verloes,
2018,
neurogenetics.
M. Holder-Espinasse,
D. Lacombe,
D. Bonneau,
2010,
European journal of medical genetics.
A. Munnich,
I. Simonic,
S. Mehta,
2012,
Journal of Medical Genetics.
B. Yalcin,
A. Boland,
A. Houllier,
2022,
Nature Communications.
A. Kremer,
M. Knapen,
L. V. van Zutven,
2016,
Molecular Cytogenetics.
Gianluca Bontempi,
J. Vermeesch,
T. Lenaerts,
2017,
Genome Medicine.
Y. Crow,
P. Revy,
D. Duffy,
2019,
The Journal of experimental medicine.
X. Coumoul,
F. Petit,
J. Cohen‐Tannoudji,
2020,
Chemosphere.
A. Vanderver,
Y. Crow,
Naoki Kitabayashi,
2017,
Neuropediatrics.
A. Vanderver,
Y. Crow,
Naoki Kitabayashi,
2017,
Neuropediatrics.
B. Cardinaud,
J. Epelbaum,
F. Petit,
2004,
The European journal of neuroscience.
M. Holder-Espinasse,
B. Delobel,
B. Duban-Bedu,
2012,
Clinical genetics.
F. Petit,
T. Smol,
R. Caumes,
2017,
European Journal of Human Genetics.
A. Noegel,
S. Lyonnet,
C. Becker,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
L. Faivre,
F. Escande,
O. Fruchart,
2015,
Clinical genetics.
L. Faivre,
C. Thauvin-Robinet,
F. Petit,
2022,
European journal of medical genetics.
C. V. van Ravenswaaij-Arts,
T. Frebourg,
S. Coutant,
2020,
Human mutation.
B. Papsin,
R. Zechi-Ceide,
N. M. Kokitsu-Nakata,
2022,
Human mutation.
Jason M. Johnson,
A. Munnich,
M. Cunningham,
2014,
American journal of medical genetics. Part A.
A. Munnich,
M. Bitner-Glindzicz,
E. Tobias,
2013,
Journal of Medical Genetics.
J. Rosenfeld,
C. Shaw,
Soo-Mi Park,
2022,
American journal of medical genetics. Part A.
Denise L. Perry,
J. Rosenfeld,
A. Reymond,
2018,
Human mutation.
R. Touraine,
N. Chassaing,
P. Jouk,
2020,
Human mutation.
F. Petit,
C. Kordon,
C. Loudes,
2000,
Neuroendocrinology.
F. Escande,
J. Amiel,
M. Delrue,
2014,
Clinical genetics.
Mathieu Nacher,
S. Mazières,
J. Dugoujon,
2014,
Blood cells, molecules & diseases.
M. Diana,
E. Darcq,
F. Petit,
2022,
Biological Psychiatry.
A. Visel,
L. Pennacchio,
S. Lyonnet,
2013,
Human mutation.
S. Peineau,
J. Epelbaum,
F. Petit,
2004
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R. Touraine,
A. Toutain,
N. Chassaing,
2021,
Clinical genetics.
B. Weschke,
M. Seifert,
A. Kaindl,
2020,
Journal of Human Genetics.
J. Hurst,
C. Farra,
A. Toutain,
2019,
European Journal of Human Genetics.
A. Munnich,
N. Baena,
A. Verloes,
2014,
Human mutation.
C. Chiaverini,
C. Philippe,
S. Hadj-Rabia,
2019,
The Journal of investigative dermatology.
R. Barker,
Karolina Pircs,
Marcella Birtele,
2022,
Stem cell reports.
N. Boddaert,
G. Canaud,
F. Branle,
2022,
The Journal of experimental medicine.
L. Storme,
J. Andrieux,
F. Petit,
2014,
American journal of medical genetics. Part A.
F. Petit,
C. Roche-Lestienne,
T. Smol,
2020,
bioRxiv.
C. Ravel,
F. Petit,
A. Gougeon,
2017,
Scientific Reports.
Allison G. Dempsey,
M. Owen,
R. Buckner,
2021,
Translational Psychiatry.
S. Peineau,
J. Epelbaum,
F. Petit,
2000,
Journal of neurophysiology.
A. Munnich,
C. Bole-Feysot,
P. Nitschké,
2013,
American journal of human genetics.
W. Chung,
J. Mulliken,
R. Helaers,
2017,
Circulation.
J. Andrieux,
B. Delobel,
P. Gosset,
2010,
Fertility and sterility.
K. Devriendt,
J. Clayton-Smith,
S. Bhaskar,
2017,
American journal of human genetics.
A. Munnich,
C. Fallet-Bianco,
I. Gut,
2021,
Journal of Medical Genetics.
A. Destrée,
R. De Rycke,
N. Goemans,
2019,
Genetics in Medicine.
A. Munnich,
P. Nitschké,
D. Lacombe,
2015,
Human mutation.
G. Cooper,
P. Fergelot,
K. Devriendt,
2020,
European Journal of Human Genetics.
J. Rosenfeld,
L. Vissers,
H. Peeters,
2021,
Genome medicine.
C. Bult,
P. Donahoe,
P. Giampietro,
2021,
medRxiv.
F. Petit,
G. Garrel,
J. Cohen‐Tannoudji,
2019,
The Journal of endocrinology.
N. Ahituv,
K. Sears,
F. Petit,
2017,
Nature Reviews Genetics.
F. Escande,
J. Andrieux,
B. Keren,
2015,
European Journal of Human Genetics.
A. Toutain,
J. Andrieux,
F. Petit,
2011,
European journal of medical genetics.
Tyler H. Garvin,
D. Dickel,
A. Visel,
2020,
Cell.
M. Lemaître,
L. Vallée,
B. Gilbert-Dussardier,
2015,
European journal of medical genetics.
J. Saurin,
A. Hovnanian,
B. Fournier,
2022,
Genes, chromosomes & cancer.
S. Julia,
E. Pasmant,
A. Sabbagh,
2021,
Cancers.
Timothy J. Edwards,
Ryan J. Dean,
H. Peeters,
2018,
American journal of human genetics.
S. Peineau,
P. Dournaud,
J. Epelbaum,
2003,
The Journal of physiology.
C. Has,
S. Kárpáti,
F. Petit,
2016,
The British journal of dermatology.
D. Steinemann,
W. Hofmann,
B. Schlegelberger,
2020,
Clinical genetics.
I. Treilleux,
I. Ray-Coquard,
R. Rimokh,
2015,
Carcinogenesis.
R. Touraine,
C. Chiaverini,
J. Rivière,
2017,
Genetics in Medicine.
F. Escande,
J. Andrieux,
B. Demeer,
2013,
European journal of medical genetics.
S. Mazières,
J. Chiaroni,
P. Bailly,
2016,
Malaria Journal.
H. Galehdari,
T. Frebourg,
R. Maroofian,
2020,
European journal of medical genetics.
D. Nickerson,
Yin Shen,
M. Bamshad,
2021,
Nature Communications.
J. Epelbaum,
F. Petit,
C. Kordon,
2002,
Neuroendocrinology.
Justyna A. Karolak,
H. Mefford,
W. Chung,
2019,
American journal of human genetics.
B. Gilbert-Dussardier,
K. Chennen,
O. Poch,
2019,
Clinical genetics.
P. Jouk,
F. Escande,
C. Goizet,
2020,
Human mutation.
J. Melki,
N. Philip,
Salima El-Chehadeh,
2019,
European Journal of Human Genetics.
T. Strom,
K. Devriendt,
J. Clayton-Smith,
2018,
European Journal of Human Genetics.
F. Giuliano,
F. Escande,
A. Dieux,
2020,
Human mutation.
F. Petit,
T. Smol,
S. Manouvrier-Hanu,
2021,
European journal of medical genetics.
K. Devriendt,
H. Firth,
S. Julia,
2013,
European journal of medical genetics.
D. Ley,
F. Petit,
B. Nelken,
2019,
Ophthalmic genetics.
Jocelyn Laporte,
Luciano Merlini,
Christophe Béroud,
2012,
Human mutation.
J. Clayton-Smith,
R. Loffroy,
C. Chiaverini,
2021,
Genetics in Medicine.
T. Strom,
K. Devriendt,
J. Clayton-Smith,
2018,
European Journal of Human Genetics.
J. Rivière,
A. Verloes,
J. Thevenon,
2017,
Clinical genetics.
M. Gut,
I. Gut,
J. Melki,
2016,
American journal of human genetics.
J. Millán,
J. Roume,
J. Salles,
2015,
Molecular genetics and metabolism.
F. Escande,
F. Petit,
M. Figeac,
2015,
European Journal of Human Genetics.
G. Jondeau,
J. M. van de Kamp,
C. Boileau,
2014,
Cardiology in the Young.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
M. Lyons,
C. Depienne,
R. Person,
2021,
Human genetics.
F. Escande,
B. Delobel,
V. Cormier-Daire,
2018,
European Journal of Human Genetics.
D. Wieczorek,
S. Mansour,
A. Moore,
2013,
European Journal of Human Genetics.
F. Petit,
G. Garrel,
J. Cohen‐Tannoudji,
2019,
Medecine sciences : M/S.
C. Genestie,
F. Petit,
J. Cohen‐Tannoudji,
2019,
Oncogene.
A. Munnich,
S. Julia,
A. Toutain,
2019,
Genetics in Medicine.
V. Dissanayake,
F. Escande,
F. Petit,
2019,
BMC Medical Genetics.
Blepharocheilodontic syndrome is a CDH1 pathway–related disorder due to mutations in CDH1 and CTNND1
F. Escande,
P. Guerreschi,
F. Petit,
2017,
Genetics in Medicine.
A. Toutain,
B. Donadille,
L. Faivre,
2023,
PloS one.
J. Andrieux,
B. Delobel,
F. Leprêtre,
2008,
European journal of medical genetics.
L. Vallée,
E. Bieth,
J. Cuisset,
2011,
Muscle & nerve.
S. Peineau,
P. Dournaud,
J. Epelbaum,
2012
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B. Klink,
C. Bénéteau,
J. Thevenon,
2022,
Clinical genetics.
R. Porcher,
É. Marijon,
A. Lazarus,
2019,
Circulation.
J. Melki,
A. Toutain,
A. Verloes,
2021,
Orphanet Journal of Rare Diseases.
C. Rooryck,
L. Pasquier,
E. Colin,
2023,
Frontiers in Genetics.
N. Boutry,
F. Petit,
C. Vanlerberghe,
2018,
Clinical genetics.
A. Toutain,
F. Escande,
B. Isidor,
2017,
Clinical genetics.
A. Green,
Alison M. Male,
F. McKenzie,
2019,
Genetics in Medicine.
B. O’Roak,
A. Munnich,
G. Jondeau,
2020,
Journal of Medical Genetics.
C. Genestie,
J. Katzenellenbogen,
I. Treilleux,
2021,
The Journal of pathology.
J. Lupski,
J. Buchan,
G. Pazour,
2022,
Kidney international.
J. Hurst,
C. Farra,
A. Toutain,
2019,
European Journal of Human Genetics.
J. Andrieux,
M. Blyth,
J. Cuisset,
2015,
European journal of medical genetics.
F. Escande,
A. Moncla,
J. Martinovic,
2019,
American journal of medical genetics. Part A.
A. Toutain,
N. Philip,
P. Jouk,
2023,
BMC Health Services Research.
E. Quelennec,
J. Amiel,
F. Petit,
2020,
Stem cell research.
J. Thevenon,
L. Faivre,
F. Escande,
2020,
Human mutation.
A. Toutain,
B. Donadille,
L. Faivre,
2022,
European journal of medical genetics.
Saskia M. J. Hopman,
L. Vissers,
R. Pfundt,
2023,
American journal of human genetics.
M. Yvert,
F. Rivier,
N. Leboucq,
2022,
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.
A. De Paepe,
J. Andrieux,
Toshiyuki Yamamoto,
2016,
European journal of medical genetics.
P. Underhill,
S. Mazières,
J. Chiaroni,
2018,
European Journal of Human Genetics.
C. Fantini-Hauwel,
P. Antoine,
O. Boute,
2017,
Journal of Genetic Counseling.
L. Storme,
J. Andrieux,
S. Bouquillon,
2011,
European Journal of Medical Genetics.
F. Petit,
J. Laverrière,
J. Cohen‐Tannoudji,
2019,
Epigenetics & Chromatin.
Allison G. Dempsey,
S. Spence,
D. Ledbetter,
2012,
Journal of Medical Genetics.
F. Petit,
F. Renaud,
S. Lejeune,
2020,
Genetics in Medicine.
F. Petit,
J. Laverrière,
J. Cohen‐Tannoudji,
2019,
Epigenetics & Chromatin.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
P. Elliott,
M. Jarvelin,
C. Gieger,
2021
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A. Munnich,
P. Nitschké,
D. Lacombe,
2015,
Human Mutation.
P. Underhill,
S. Mazières,
J. Chiaroni,
2018,
European Journal of Human Genetics.
S. Mundlos,
A. Boland,
S. Ohno,
2024,
Nature communications.