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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
80 auth.
R. Davies,
A. Fiksinski,
E. Breetvelt,
N. Williams,
S. Hooper,
Thomas Monfeuga,
A. Bassett,
M. Owen,
Raquel E. Gur,
B. Morrow,
D. McDonald-McGinn,
A. Swillen,
E. Chow,
M. V. D. van den Bree,
B. Emanuel,
...
J. Vermeesch,
Thérèse Van Amelsvoort,
C. Arango,
M. Armando,
L. Campbell,
J. Cubells,
S. Eliez,
S. García-Miñaúr,
D. Gothelf,
W. Kates,
K. Murphy,
C. Murphy,
D. Murphy,
N. Philip,
G. Repetto,
V. Shashi,
T. Simon,
D. H. Suñer,
S. Vicari,
S. Scherer,
Michael P. Epstein,
Stephen T. Warren,
S. Morrison,
S. Chawner,
C. Vingerhoets,
J. Breckpot,
E. Vergaelen,
A. Vogels,
Stephen Monks,
S. Prasad,
Corrado Sandini,
Maude Schneider,
J. Maeder,
D. Fraguas,
Rens Evers,
F. Tassone,
Jaume Morey-Canyelles,
O. Ousley,
K. Antshel,
W. Fremont,
Rosemarie Fritsch,
C. Ornstein,
E. Daly,
Gregory Costain,
Erik Boot,
T. Heung,
T. Crowley,
E. Zackai,
M. Calkins,
R. Gur,
Kathryn L. McCabe,
T. Busa,
K. Schoch,
M. Pontillo,
Sasja N. Duijff,
René S. Kahn,
Michiel L Houben,
L. Kushan,
M. Jalbrzikowski,
M. Carmel,
Ehud Mekori-Domachevsky,
E. Michaelovsky,
R. Weinberger,
C. Bearden,
J. Vorstman
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6 |
2020 |
6
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
124 auth.
I. Cleynen,
W. Engchuan,
M. Hestand,
T. Heung,
Aaron M. Holleman,
H. Johnston,
Thomas Monfeuga,
D. McDonald-McGinn,
R. Gur,
B. Morrow,
A. Swillen,
J. Vorstman,
C. Bearden,
E. Chow,
M. V. D. van den Bree,
...
B. Emanuel,
J. Vermeesch,
S. Warren,
M. Owen,
P. Chopra,
D. Cutler,
Richard Duncan,
Alex V. Kotlar,
J. Mulle,
Anna J. Voss,
M. Zwick,
Alexander Diacou,
A. Golden,
T. Guo,
Jhih-rong Lin,
Tao Wang,
Zhengdong D. Zhang,
Yingjie Zhao,
C. Marshall,
D. Merico,
Andrea Jin,
B. Lilley,
H. Salmons,
Oanh Tran,
P. Holmans,
A. Pardiñas,
J. Walters,
Wolfram Demaerel,
E. Boot,
N. Butcher,
Gregory Costain,
Chelsea Lowther,
Rens Evers,
Thérèse Van Amelsvoort,
E. V. van Duin,
C. Vingerhoets,
J. Breckpot,
K. Devriendt,
E. Vergaelen,
A. Vogels,
T. Crowley,
D. McGinn,
E. Moss,
Robert J. Sharkus,
Marta Unolt,
E. Zackai,
M. Calkins,
R. Gallagher,
R. Gur,
Sunny X. Tang,
R. Fritsch,
C. Ornstein,
G. Repetto,
E. Breetvelt,
Sasja N. Duijff,
A. Fiksinski,
H. Moss,
Maria Niarchou,
K. Murphy,
S. Prasad,
E. Daly,
M. Gudbrandsen,
C. Murphy,
D. Murphy,
Antonio Buzzanca,
F. Fabio,
M. Digilio,
M. Pontillo,
B. Marino,
S. Vicari,
K. Coleman,
J. Cubells,
O. Ousley,
M. Carmel,
D. Gothelf,
Ehud Mekori-Domachevsky,
E. Michaelovsky,
R. Weinberger,
Abraham Weizman,
L. Kushan,
M. Jalbrzikowski,
M. Armando,
S. Eliez,
Corrado Sandini,
Maude Schneider,
F. Béna,
K. Antshel,
W. Fremont,
W. Kates,
R. Belzeaux,
T. Busa,
N. Philip,
L. Campbell,
K. McCabe,
S. Hooper,
K. Schoch,
V. Shashi,
T. Simon,
F. Tassone,
C. Arango,
D. Fraguas,
S. García-Miñaúr,
Jaume Morey-Canyelles,
J. Rosell,
D. H. Suñer,
Jasna Raventos-Simic,
M. Epstein,
N. Williams,
A. Bassett
|
6 |
2020 |
6
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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
50 auth.
A. Bassett,
Chelsea Lowther,
D. Merico,
Gregory Costain,
E. Chow,
Thérèse Van Amelsvoort,
D. McDonald-McGinn,
R. Gur,
A. Swillen,
M. V. D. van den Bree,
K. Murphy,
D. Gothelf,
C. Bearden,
S. Eliez,
W. Kates,
...
N. Philip,
V. Sashi,
L. Campbell,
J. Vorstman,
J. Cubells,
G. Repetto,
T. Simon,
E. Boot,
T. Heung,
Rens Evers,
C. Vingerhoets,
E. V. van Duin,
E. Zackai,
E. Vergaelen,
K. Devriendt,
J. Vermeesch,
M. Owen,
C. Murphy,
Elena Michaelovosky,
L. Kushan,
Maude Schneider,
W. Fremont,
T. Busa,
S. Hooper,
K. McCabe,
Sasja N. Duijff,
K. Isaev,
G. Pellecchia,
John Wei,
Matthew J. Gazzellone,
S. Scherer,
B. Emanuel,
T. Guo,
B. Morrow,
C. Marshall
|
6 |
2017 |
6
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The 22q11 low copy repeats are characterized by unprecedented size and structural variability
18 auth.
Wolfram Demaerel,
Y. Mostovoy,
F. Yilmaz,
Lisanne Vervoort,
Steven Pastor,
M. Hestand,
A. Swillen,
E. Vergaelen,
E. Geiger,
C. Coughlin,
...
Stephen K. Chow,
D. McDonald-McGinn,
B. Morrow,
P. Kwok,
M. Xiao,
B. Emanuel,
T. Shaikh,
J. Vermeesch
|
5 |
2018 |
5
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|
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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
34 auth.
E. Boot,
N. Butcher,
S. Udow,
C. Marras,
K. Mok,
S. Kaneko,
M. Barrett,
P. Prontera,
B. Berman,
M. Masellis,
B. Dufournet,
K. Nguyen,
P. Charles,
E. Mutez,
T. Danaila,
...
A. Jacquette,
O. Colin,
S. Drapier,
M. Borg,
A. Fiksinski,
E. Vergaelen,
A. Swillen,
A. Vogels,
A. Plate,
C. Perandones,
T. Gasser,
Kristien Clerinx,
F. Bourdain,
K. Mills,
N. Williams,
N. Wood,
J. Booij,
A. Lang,
A. Bassett
|
5 |
2018 |
5
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🦁
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A pilot study on immuno-psychiatry in the 22q11.2 deletion syndrome: A role for Th17 cells in psychosis?
8 auth.
E. Vergaelen,
C. Schiweck,
Kristof Van Steeland,
Jacqueline Counotte,
W. Veling,
A. Swillen,
...
H. Drexhage,
S. Claes
|
5 |
2018 |
5
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Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology
10 auth.
S. Morrison,
S. Chawner,
Thérèse Van Amelsvoort,
A. Swillen,
C. Vingerhoets,
E. Vergaelen,
...
D. Linden,
S. Linden,
M. Owen,
M. V. D. van den Bree
|
4 |
2020 |
4
🐜
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|
🦁
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High prevalence of fatigue in adults with a 22q11.2 deletion syndrome
E. Vergaelen,
S. Claes,
S. Kempke,
A. Swillen
|
4 |
2017 |
4
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