|
🐜
|
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
24 auth.
Alienke J. Monsuur,
Paul I. W. de Bakker,
Paul I. W. de Bakker,
B. Alizadeh,
A. Zhernakova,
M. Bevova,
E. Strengman,
L. Franke,
R. Slot,
M. V. Belzen,
...
M. V. Belzen,
I. Lavrijsen,
B. Diosdado,
M. J. Daly,
M. J. Daly,
Chris J. J. Mulder,
M. Mearin,
M. Mearin,
Jos W. R. Meijer,
G. A. Meijer,
E. V. Oort,
M. Wapenaar,
B. Koeleman,
C. Wijmenga
|
8 |
2005 |
8
🐜
|
|
🐜
|
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP.
19 auth.
A. Zhernakova,
E. M. Festen,
L. Franke,
L. Franke,
G. Trynka,
C. V. Diemen,
Alienke J. Monsuur,
M. Bevova,
R. Nijmeijer,
R. Slot,
...
R. Heijmans,
H. Boezen,
D. Heel,
A. A. V. Bodegraven,
P. Stokkers,
C. Wijmenga,
C. Wijmenga,
J. Crusius,
R. Weersma
|
8 |
2008 |
8
🐜
|
|
🐜
|
Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases.
15 auth.
A. Zhernakova,
B. Alizadeh,
M. Bevova,
Miek A. van Leeuwen,
M. Coenen,
B. Franke,
L. Franke,
M. Posthumus,
D. V. van Heel,
G. van der Steege,
...
T. Radstake,
P. Barrera,
B. Roep,
B. Koeleman,
C. Wijmenga
|
7 |
2007 |
7
🐜
|
|
🐜
|
Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.
24 auth.
R. Taft,
A. Vanderver,
R. Leventer,
Stephen A. Damiani,
Cas Simons,
S. Grimmond,
David J. Miller,
Johanna L Schmidt,
P. Lockhart,
K. Pope,
...
Kelin Ru,
J. Crawford,
T. Rosser,
I. D. de Coo,
M. Juneja,
I. Verma,
P. Prabhakar,
S. Blaser,
J. Raiman,
P. Pouwels,
M. Bevova,
T. Abbink,
M. S. van der Knaap,
N. Wolf
|
7 |
2013 |
7
🐜
|
|
🐜
|
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites
12 auth.
M. Wapenaar,
Alienke J. Monsuur,
A. A. V. Bodegraven,
R. Weersma,
M. Bevova,
R. Linskens,
...
P. Howdle,
G. Holmes,
Cjj Mulder,
G. Dijkstra,
D. Heel,
C. Wijmenga
|
7 |
2007 |
7
🐜
|
|
🐢
|
Using mouse models to dissect the genetics of obesity.
G. Brockmann,
M. Bevova
|
7 |
2002 |
7
🐢
|
|
🐜
|
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
28 auth.
B. Nota,
E. Struys,
A. Pop,
E. Jansen,
M. F. Fernandez Ojeda,
Warsha A. Kanhai,
M. Kranendijk,
S. J. V. van Dooren,
M. Bevova,
E. Sistermans,
A. Nieuwint,
M. Barth,
T. Ben-Omran,
G. Hoffmann,
P. de Lonlay,
...
M. McDonald,
A. Meberg,
A. Muntau,
J. Nuoffer,
R. Parini,
M. Read,
A. Renneberg,
R. Santer,
Thomas Strahleck,
E. Van Schaftingen,
M. S. van der Knaap,
C. Jakobs,
G. Salomons
|
7 |
2013 |
7
🐜
|
|
🐜
|
The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases
24 auth.
F. Kurreeman,
G. Goulielmos,
B. Alizadeh,
B. Rueda,
J. Houwing-Duistermaat,
E. Sánchez,
M. Bevova,
T. Radstake,
M. Vonk,
E. Galanakis,
...
N. Ortego,
W. Verduyn,
M. Zervou,
B. Roep,
B. Dema,
L. Espino,
E. Urcelay,
D. Boumpas,
L. H. van den Berg,
C. Wijmenga,
B. Koeleman,
T. Huizinga,
R. Toes,
Javier Martín
|
6 |
2009 |
6
🐜
|
|
🐜
|
Direct chromosome-length haplotyping by single-cell sequencing
9 auth.
David Porubsky,
A. Sanders,
Niek van Wietmarschen,
E. Falconer,
M. Hills,
D. Spierings,
...
M. Bevova,
V. Guryev,
P. Lansdorp
|
5 |
2016 |
5
🐜
|
|
🐜
|
Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1
16 auth.
C. Bettencourt,
Justo García Yébenes,
J. López-Sendón,
Orr Shomroni,
Xingqian Zhang,
Shu-Bing Qian,
I. Bakker,
S. Heetveld,
R. Ros,
B. Quintáns,
...
M. Sobrido,
M. Bevova,
S. Jain,
M. Bugiani,
P. Heutink,
P. Rizzu
|
5 |
2015 |
5
🐜
|
