H. Azaiez
发表
Andrew R. Grant,
Marina T. DiStefano,
H. Rehm,
2019,
bioRxiv.
Alex Chapin,
Margaret Kenna,
Heidi L Rehm,
2018,
bioRxiv.
T. Casavant,
D. Kolbe,
T. Braun,
2020,
Human Genetics.
S. Riazuddin,
Z. Ahmed,
M. Shahzad,
2020,
bioRxiv.
J. W. Askew,
Katherine R. Smith,
M. Bahlo,
2018,
Genetics in Medicine.
D. Kolbe,
Richard J. H. Smith,
P. Huygen,
2014,
Human mutation.
H. Rehm,
H. Kremer,
K. Avraham,
2018,
bioRxiv.
Christina M. Sloan,
D. Kolbe,
Yamato Kubota,
2015,
The Annals of otology, rhinology, and laryngology.
D. Kolbe,
M. Farhadi,
M. Azizi,
2016,
Archives of Iranian medicine.
W. Kimberling,
T. Yang,
C. Nishimura,
2007,
Human Genetics.
Y. Raphael,
H. Kremer,
Sherri M Jones,
2018,
PloS one.
C. Petit,
D. Weil,
S. Abdelhak,
2015,
Annals of human genetics.
K. Kindt,
Uzma Shaukat,
S. Riazuddin,
2018,
Human molecular genetics.
S. Abdelhak,
L. Romdhane,
K. Dellagi,
2013,
Journal of Community Genetics.
A. El-Amraoui,
K. Alagramam,
T. Haaf,
2020,
bioRxiv.
T. Yang,
J. Bodurtha,
B. Peters,
2021,
Human genetics.
S. Abdelhak,
O. Messaoud,
H. Ouragini,
2012,
Archives of Dermatological Research.
S. Abdelhak,
S. Boubaker,
M. Mokni,
2011,
Journal of Genetics.
Christina M. Sloan,
D. Kolbe,
C. Sloan,
2015,
The Annals of otology, rhinology, and laryngology.
H. Azaiez,
G. Camp,
Richard J. H. Smith,
2006
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S. Abdelhak,
L. Romdhane,
K. Dellagi,
2012,
Orphanet Journal of Rare Diseases.
Richard J. H. Smith,
H. Azaiez,
K. Booth,
2020,
International journal of molecular sciences.
Christina M. Sloan,
D. Kolbe,
C. Sloan,
2016,
Clinical genetics.
D. Kolbe,
K. Frees,
C. Nishimura,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
T. Yang,
J. Bodurtha,
B. Peters,
2021,
Human Genetics.
A. Pandya,
C. Petit,
D. Weil,
2005,
Journal of Medical Genetics.
Andrew R. Grant,
Marina T. DiStefano,
I. Krantz,
2021,
Genetics in Medicine.
Allen C. Simpson,
W. Kimberling,
K. Avraham,
2015,
PLoS genetics.
Owen White,
Amiel A. Dror,
Carlo Colantuoni,
2020,
Nature Methods.
Adam P. DeLuca,
Matthew S. Lebo,
Janeen L Andorf,
2014,
Genome Biology.
Daniel Nilsson,
Peter Szolovits,
Karen Eilbeck,
2014,
Genome Biology.
S. Abdelhak,
L. Romdhane,
K. Dellagi,
2013,
Journal of Community Genetics.
Amy E. Weaver,
D. Kolbe,
K. Frees,
2016,
Human Genetics.
Bernd Fritzsch,
I. Jahan,
Richard J. H. Smith,
2018,
Front. Genet..
K. Kahrizi,
H. Najmabadi,
K. Frees,
2018,
Human mutation.
T. Casavant,
D. Kolbe,
T. Braun,
2018,
American journal of human genetics.
Richard J. H. Smith,
H. Azaiez,
K. Booth,
2015,
The Annals of otology, rhinology, and laryngology.
Christina M. Sloan,
D. Kolbe,
S. Iwasaki,
2015,
The Annals of otology, rhinology, and laryngology.
Richard J. H. Smith,
H. Azaiez,
K. Booth,
2015
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Richard J. H. Smith,
Thomas L. Casavant,
Todd E. Scheetz,
2014,
Bioinform..
CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival
Steve D. M. Brown,
P. Avan,
S. Picaud,
2017,
EMBO molecular medicine.
Allen C. Simpson,
M. Schnieders,
K. Kahrizi,
2015,
American journal of medical genetics. Part A.
Christina M. Sloan,
Amy E. Weaver,
D. Kolbe,
2014,
Genome Medicine.
D. Kolbe,
R. Santos-Cortez,
A. Wonkam,
2016,
Clinical genetics.
K Cryns,
G Van Camp,
P J Govaerts,
2004,
Journal of Medical Genetics.
D. Tellería,
Richard J. H. Smith,
P. Huygen,
2020,
Scientific Reports.
Thomas L Casavant,
Todd E Scheetz,
E Ann Black-Ziegelbein,
2014,
American journal of human genetics.
Y. Fukushima,
D. Kolbe,
Richard J. H. Smith,
2016,
The Annals of otology, rhinology, and laryngology.
A. El-Amraoui,
K. Alagramam,
T. Haaf,
2021,
Human genetics.
K. Kahrizi,
H. Najmabadi,
H. Azaiez,
2020,
Journal of Human Genetics.
Mallory R. Tollefson,
Amy E. Weaver,
T. Casavant,
2023,
Research square.
Allen C. Simpson,
W. Kimberling,
Richard J. H. Smith,
2017
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I. Schrauwen,
H. Azaiez,
H. Moteki,
2016,
BioMed research international.
Adam P. DeLuca,
Allen C. Simpson,
T. Casavant,
2016,
The Annals of otology, rhinology, and laryngology.
Allen C. Simpson,
M. Farhadi,
K. Kahrizi,
2015,
Journal of Medical Genetics.
Christina M. Sloan,
D. Kolbe,
C. Sloan,
2015,
The Annals of otology, rhinology, and laryngology.
Allen C. Simpson,
T. Casavant,
T. Scheetz,
2015
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J. Soulier,
S. Abdelhak,
K. Dellagi,
2014,
Molecular genetics & genomic medicine.
T. Casavant,
D. Kolbe,
T. Braun,
2020,
Human Genetics.
M. Nothnagel,
F. Bahrami,
K. Kahrizi,
2020,
Clinical genetics.
S. Riazuddin,
Z. Ahmed,
M. Shahzad,
2020,
Human Genetics.
S. Abdelhak,
M. Nagara,
H. Azaiez,
2012,
Diagnostic Pathology.
Y. Raphael,
M. Brilliant,
S. Riazuddin,
2010,
American journal of human genetics.
A. Pandya,
H. Kremer,
L. Hoefsloot,
2010,
Clinical genetics.
K. Kahrizi,
H. Najmabadi,
Richard J. H. Smith,
2018,
Journal of Medical Genetics.
M. Tekin,
A. El-Amraoui,
D. Duman,
2018,
Clinical genetics.
H. Rehm,
D. Kolbe,
C. Morton,
2021,
European Journal of Human Genetics.
H. Rehm,
D. Kolbe,
C. Morton,
2021,
European Journal of Human Genetics.
D. Kolbe,
M. Schnieders,
Yingyue Li,
2016,
Journal of the American Society of Nephrology : JASN.
S. Abdelhak,
O. Messaoud,
M. B. rekaya,
2013
.
Andrew R. Grant,
H. P. Kang,
Marina T. DiStefano,
2018,
Genetics in Medicine.
Richard J. H. Smith,
H. Azaiez,
G. Camp,
2004,
Human mutation.
Amy E. Weaver,
D. Kolbe,
J. Kamholz,
2020,
Ophthalmic genetics.
S. Leal,
S. Riazuddin,
T. Friedman,
2023,
Clinical genetics.
H. Azaiez,
Richard J. H. Smith,
2007,
The Laryngoscope.
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss
Richard J. H. Smith,
H. Azaiez,
K. Booth,
2022,
Human Genetics.
Allen C. Simpson,
M. Farhadi,
K. Kahrizi,
2015,
Journal of Medical Genetics.
Andrew R. Grant,
Marina T. DiStefano,
H. Rehm,
2019,
Genetics in Medicine.
Mallory R. Tollefson,
Amy E. Weaver,
T. Casavant,
2023,
Human Genetics.
K. Kahrizi,
H. Najmabadi,
H. Azaiez,
2020,
Journal of Human Genetics.
Diana L. Kolbe,
Hela Azaiez,
Sean S. Ephraim,
2016,
Human Genetics.
C. Srisailapathy,
H. Azaiez,
Jeffrey Justin Margret,
2024,
Advanced genetics.