F. Bernier
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Peter N. Robinson,
M. Reijnders,
J. Hehir-Kwa,
2019,
Front. Genet..
Steven J. M. Jones,
S. Scherer,
B. Fernandez,
2014,
American journal of human genetics.
F. Bernier,
Renee Spaetgens,
2006,
Cardiology clinics.
David C. Katz,
Nathan M. Young,
B. Hallgrímsson,
2019,
Seminars in cell & developmental biology.
K. Boycott,
T. Hartley,
F. Bernier,
2019,
Genetics in Medicine.
Fadya Omar,
F. Bernier,
D. Marshall,
2020,
Genetics in Medicine.
Melody N. Grohs,
Jess E. Reynolds,
C. Lebel,
2019,
Environmental Health.
M. Hicks,
F. Bernier,
J. Lemay,
2008,
Journal of developmental and behavioral pediatrics : JDBP.
F. Bernier,
S. Crawford,
R. Lowry,
2020,
American journal of medical genetics. Part A.
Lijia Huang,
D. Lacombe,
F. Bernier,
2013,
Human mutation.
F. Alkuraya,
J. Majewski,
F. Bernier,
2015,
American journal of human genetics.
F. Bernier,
J. Hatfield,
Jonathan W. Martin,
2019,
Environmental research.
A. Paterson,
J. Brooks,
I. Birol,
2022,
BMC Genomic Data.
F. Bernier,
J. Robinson,
D. Gilchrist,
2011,
Journal of Genetic Counseling.
F. Bernier,
J. Parboosingh,
P. Bridge,
2005,
Journal of Medical Genetics.
F. Bernier,
J. Hatfield,
Jonathan W. Martin,
2020,
Environment international.
David C. Katz,
Jordan J. Bannister,
B. Hallgrímsson,
2022,
IEEE Journal of Biomedical and Health Informatics.
K. Boycott,
F. Bernier,
A. Innes,
2008,
American journal of medical genetics. Part A.
E. Zackai,
J. Clayton-Smith,
R. Scott,
2016,
American journal of medical genetics. Part A.
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
F. Bernier,
A. Innes,
J. Vance,
2018,
Life Science Alliance.
Colin A. Johnson,
Teunis J. P. van Dam,
J. Shendure,
2015,
Nature Cell Biology.
F. Bernier,
O. Caluseriu,
J. Lazier,
2016,
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.
K. Boycott,
F. Bernier,
S. Shetty,
2007,
Clinical dysmorphology.
K. Boycott,
T. Hartley,
F. Bernier,
2022,
BMJ Open.
M. Brudno,
K. Boycott,
K. Kernohan,
2022,
American journal of human genetics.
K. Gripp,
K. Boycott,
T. Hartley,
2014,
American journal of human genetics.
C. Ober,
C. Beaulieu,
R. Sparkes,
2017,
American journal of medical genetics. Part A.
S. Robertson,
F. Bernier,
A. Bankier,
1999,
American journal of medical genetics.
David C. Katz,
Jordan J. Bannister,
Jacinda R. Larson,
2020,
Genetics in Medicine.
H. Ouellette-Kuntz,
F. Bernier,
D. Dewey,
2013,
Journal of Autism and Developmental Disorders.
Q. Doan,
C. Lebel,
C. Beaulieu,
2017,
BMJ Open.
L. Shaffer,
M. Somerville,
B. Morrow,
2005,
American journal of human genetics.
P. Birembaut,
F. Bernier,
B. Lardennois,
1981,
Journal d'urologie.
Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency
K. Schwarz,
T. Giese,
R. Lifton,
2017,
The Journal of clinical investigation.
A. Ekici,
R. Abou Jamra,
F. Bernier,
2014,
American journal of human genetics.
Seonhee Kim,
P. Grant,
D. Harris,
2020,
Human molecular genetics.
E. Zackai,
M. Brudno,
K. Boycott,
2015,
Clinical genetics.
B. Fernandez,
B. Knoppers,
K. Boycott,
2015,
Journal of Medical Genetics.
F. Bamforth,
F. Bernier,
P. Grundy,
1996,
American journal of medical genetics.
S. Schwartz,
C. Lee,
C. Morton,
2001,
Human molecular genetics.
F. Bernier,
L. Lafay-Cousin,
D. Strother,
2009,
American journal of medical genetics. Part A.
M. Tarnopolsky,
B. Brais,
O. Suchowersky,
2020,
Movement disorders clinical practice.
M. Tarnopolsky,
K. Boycott,
D. Bulman,
2018,
Clinical genetics.
A. Fulton,
D. Schneidman-Duhovny,
A. Rajkovic,
2016,
European Journal of Human Genetics.
P. Pavlidis,
F. Bernier,
A. Chudley,
2014,
BMC Medical Genetics.
B. Fernandez,
K. Boycott,
T. Hartley,
2017,
Clinical genetics.
B. Fernandez,
C. Polychronakos,
M. Tarnopolsky,
2015,
Clinical genetics.
S. D. Fraser,
F. Bernier,
A. Innes,
2020,
bioRxiv.
S. D. Fraser,
P. Gordon,
F. Bernier,
2020
.
C. Ober,
R. Hegele,
O. Suchowersky,
2013,
American journal of human genetics.
C. Ober,
R. Hegele,
O. Suchowersky,
2013
.
R. Sparkes,
F. Bernier,
J. Chernos,
2008,
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.
F. Bernier,
A. Innes,
K. Bone,
2017,
Prenatal diagnosis.
S. Scherer,
A. C. Lionel,
C. Marshall,
2016,
Journal of Medical Genetics.
F. Bernier,
D. Dewey,
2016,
Current Developmental Disorders Reports.
F. Bernier,
Jing Liu,
R. Lowry,
2011,
Genetics research international.
D. Valle,
N. Sobreira,
J. Majewski,
2015,
Human mutation.
F. Bernier,
A. Innes,
J. Parboosingh,
2016,
American journal of medical genetics. Part A.
Jay Shendure,
Michael J Bamshad,
Deborah A Nickerson,
2012,
American journal of human genetics.
K. Boycott,
F. Bernier,
A. Innes,
2018,
American journal of medical genetics. Part A.
F. Bernier,
F. Snyder,
D. R. Mcleod,
1996,
Journal of Inherited Metabolic Disease.
C. Bönnemann,
K. Boycott,
F. Bernier,
2017,
Clinical genetics.
F. Bernier,
A. Innes,
J. Parboosingh,
2013,
American journal of medical genetics. Part A.
K. Boycott,
F. Bernier,
A. Innes,
2007,
American journal of medical genetics. Part A.
F. Bernier,
N. Letourneau,
G. Giesbrecht,
2014,
Biological research for nursing.
F. Bernier,
J. Hatfield,
Jonathan W. Martin,
2020,
Environment international.
F. Bernier,
D. Dewey,
S. Crawford,
2005,
Prenatal Diagnosis.
A. Kirton,
F. Bernier,
I. Rebeyka,
2013,
American journal of medical genetics. Part A.
Carol Dobson-Stone,
Maria Fraser,
Lorraine Southam,
2000,
European Journal of Human Genetics.
Orion J. Buske,
M. Brudno,
B. Knoppers,
2021,
Genetics in Medicine.
F. Bernier,
R. Lowry,
J. Chernos,
2000,
Genetic testing.
L. Mccargar,
M. O’Beirne,
M. Eliasziw,
2014,
Maternal & child nutrition.
H. Ouellette-Kuntz,
F. Bernier,
D. Dewey,
2013,
Journal of Autism and Developmental Disorders.
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Beryl B. Cummings,
Carol J. Saunders,
C. Saunders,
2019,
Acta Neuropathologica.
F. Bernier,
J. Parboosingh,
F. Kardelen,
2013,
American journal of medical genetics. Part A.
Q. Doan,
C. Lebel,
C. Beaulieu,
2017
.
A. Kirton,
F. Bernier,
C. Chee,
2014,
Pediatrics.
E. Puffenberger,
C. Ober,
R. Hegele,
2015,
Human mutation.
C. Morin,
F. Bernier,
L. Bélanger,
2004,
Sleep medicine.
C. Ober,
C. Beaulieu,
R. Sparkes,
2017,
American Journal of Medical Genetics. Part A.
Colin A. Johnson,
C. Ober,
R. Hegele,
2011,
American journal of human genetics.
F. Baas,
S. Ferdinandusse,
R. Wanders,
2018,
European Journal of Human Genetics.
L. Mccargar,
M. O’Beirne,
M. Eliasziw,
2017,
Environmental Health.
F. Bernier,
S. Nakaji,
I. Takahashi,
2017
.
K. Boycott,
T. Hartley,
F. Bernier,
2021,
Genetics in Medicine.
X. Wei,
F. Bernier,
D. Fruitman,
2011,
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.
M. Shaw,
J. Gécz,
M. Brudno,
2021,
European Journal of Human Genetics.
F. Bernier,
P. Macleod,
A. Chudley,
2008,
Molecular Cytogenetics.
Benedikt Hallgrímsson,
David C. Katz,
Nils D Forkert,
2020,
Sensors.
F. Bernier,
A. Innes,
C. Greenberg,
2003,
American journal of medical genetics. Part A.
H. Ouellette-Kuntz,
F. Bernier,
A. Chudley,
2012,
Chronic diseases and injuries in Canada.
F. Bernier,
D. Thorburn,
A. Boneh,
2002,
Neurology.
F. Bernier,
J. Hatfield,
Jonathan W. Martin,
2019,
Environmental toxicology and chemistry.
F. Bernier,
A. Innes,
J. Parboosingh,
2018,
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.
F. Bernier,
Julia Tagoe,
S. Christian,
2021,
Journal of community genetics.
E. Zackai,
M. Brudno,
K. Boycott,
2014,
Nature Communications.
M. Hicks,
F. Bernier,
J. Lemay,
2008,
Journal of developmental and behavioral pediatrics : JDBP.
F. Bernier,
A. Innes,
J. Parboosingh,
2013,
American journal of medical genetics. Part A.