Ingrid Brænne
发表
Jason H. Moore,
J. Erdmann,
H. Schunkert,
2018,
Circulation. Genomic and precision medicine.
Andrew D. Johnson,
K. Hao,
N. Samani,
2015,
Arteriosclerosis, thrombosis, and vascular biology.
J. Friedman,
K. Lohmann,
A. Hicks,
2016,
Movement disorders : official journal of the Movement Disorder Society.
E. Altenmüller,
P. Bauer,
K. Lohmann,
2017,
Genes.
E. Watrin,
K. Wendt,
D. Braunholz,
2015,
Human mutation.
N. Samani,
J. Björkegren,
J. Erdmann,
2018,
Scientific Reports.
T. Wieland,
J. Erdmann,
C. Hengstenberg,
2015,
European Journal of Human Genetics.
P. Deloukas,
J. Erdmann,
C. Hengstenberg,
2014,
BMC Cardiovascular Disorders.
M. Nöthen,
J. Ott,
N. Samani,
2013,
Nature.
P. Bingley,
E. Bonifacio,
J. Ilonen,
2021,
Scientific Reports.
J. Erdmann,
K. Lohmann,
Tian Liu,
2015
.
A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A
J. Erdmann,
H. Schunkert,
Z. Aherrahrou,
2019,
The Thoracic and Cardiovascular Surgeon.
J. Erdmann,
K. Lohmann,
Tian Liu,
2015,
European Journal of Human Genetics.
V. Salomaa,
M. Laakso,
N. Samani,
2017,
Scientific Reports.
N. Brüggemann,
K. Lohmann,
L. Bertram,
2014,
Journal of Neurology.
K. Lohmann,
L. Kalaydjieva,
V. Kostic,
2016,
Movement disorders : official journal of the Movement Disorder Society.
V. Salomaa,
M. Laakso,
N. Samani,
2017,
PloS one.
A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A
Dogra,
J. Erdmann,
H. Schunkert,
2019,
Scientific Reports.
Kai Labusch,
Amir Madany Mamlouk,
Ingrid Brænne,
2010,
ICANN.
M. Nöthen,
J. Ott,
N. Samani,
2013,
Nature.
K. Lohmann,
L. Kalaydjieva,
V. Kostic,
2016,
Movement disorders : official journal of the Movement Disorder Society.