R. Sreenivasan
发表
R. Goto,
Meredith E K Calvert,
J. Saju,
2015,
Stem cell reports.
A. Sinclair,
P. Koopman,
K. McElreavey,
2018,
Human mutation.
V. Harley,
R. Sreenivasan,
D. Alankarage,
2016
.
V. Harley,
R. Sreenivasan,
2013
.
A. Sinclair,
J. Bowles,
P. Koopman,
2018,
Nature Communications.
A. Christoffels,
L. Orbán,
Junhui Jiang,
2014,
Biology of reproduction.
A. Sinclair,
J. Bowles,
P. Koopman,
2019,
Nature Communications.
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes
A. Sinclair,
W. Carré,
P. Touraine,
2021,
European Journal of Human Genetics.
S. Lyonnet,
V. Harley,
R. D. Iongh,
2017,
The Journal of Steroid Biochemistry and Molecular Biology.
A. Sinclair,
N. Dejucq-Rainsford,
J. Palvimo,
2020,
Maturitas.
K. Loveland,
M. Hedger,
R. Middendorff,
2018,
Reproduction.
P. Olsson,
L. Orbán,
R. Sreenivasan,
2009,
Molecular and Cellular Endocrinology.
L. Looijenga,
H. Stoop,
S. White,
2012,
PloS one.
A. Sinclair,
R. Sreenivasan,
Brittany Croft,
2019,
Encyclopedia of Endocrine Diseases.
A. Sinclair,
M. Weiss,
P. Koopman,
2021,
bioRxiv.
A. Sinclair,
F. Vialard,
C. Ravel,
2020,
Molecular human reproduction.
A. Munnich,
A. Molven,
O. Bruland,
2011,
Journal of Medical Genetics.
A. Sinclair,
J. Bowles,
P. Koopman,
2018,
Nature Communications.
A. Sinclair,
R. Sreenivasan,
Gabby Atlas,
2021,
Sexual Development.
W. C. Liew,
L. Orbán,
R. Bártfai,
2012,
PloS one.
A. Sinclair,
N. Gonen,
R. Sreenivasan,
2022,
Sexual Development.
R. Goto,
Meredith E K Calvert,
J. Saju,
2014,
Stem cell reports.
A. Sinclair,
S. Rahman,
S. Wortmann,
2022,
The Journal of clinical endocrinology and metabolism.
A. Sinclair,
C. Ravel,
E. Tucker,
2020,
Maturitas.
L. Ribas,
F. Piferrer,
W. C. Liew,
2017,
Proceedings of the National Academy of Sciences.
A. Christoffels,
L. Orbán,
R. Bártfai,
2008,
PloS one.
U. Grossniklaus,
Li-Yong Yuan,
R. Sreenivasan,
2007,
The Plant Cell Online.
N. McKenna,
S. Ochsner,
A. Pradhan,
2012,
The Journal of Biological Chemistry.
A. Sinclair,
F. Casagranda,
A. Compton,
2023,
Human Genetics.
Whole exome sequencing reveals copy number variants in individuals with disorders of sex development
A. Sinclair,
P. Touraine,
E. Tucker,
2022,
Molecular and Cellular Endocrinology.
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes
A. Sinclair,
W. Carré,
P. Touraine,
2021,
European Journal of Human Genetics.
R. Lovell-Badge,
V. Harley,
R. Sekido,
2012,
Chromosome Research.
J. van den Bergen,
K. Ayers,
Gorjana Robevska,
2024,
Genes.