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A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
13 auth.
L. Botto,
K. May,
P. Fernhoff,
P. Fernhoff,
A. Correa,
K. Coleman,
S. Rasmussen,
Robert K Merritt,
L. O’Leary,
L. Wong,
...
E. Elixson,
W. Mahle,
R. Campbell
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9 |
2003 |
9
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Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect.
7 auth.
W. Mahle,
J. Crisalli,
K. Coleman,
R. Campbell,
V. Tam,
R. Vincent,
...
K. Kanter
|
6 |
2003 |
6
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Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
23 auth.
Z. Ou,
P. Stankiewicz,
Z. Xia,
Amy M. Breman,
B. Dawson,
Joanna Wiszniewska,
P. Szafranski,
M. L. Cooper,
M. Rao,
L. Shao,
...
S. South,
K. Coleman,
P. Fernhoff,
M. Deray,
S. Rosengren,
E. Roeder,
Victoria B. Enciso,
A. C. Chinault,
Ankita Patel,
Sung-Hae L. Kang,
C. Shaw,
J. Lupski,
S. Cheung
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6 |
2011 |
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
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6 |
2020 |
6
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Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo‐cardio‐facial/digeorge/22q11.2 deletion syndrome patients
33 auth.
T. Guo,
D. McDonald-McGinn,
A. Blonska,
A. Shanske,
A. Bassett,
E. Chow,
Mark J. Bowser,
M. Sheridan,
F. Beemer,
K. Devriendt,
A. Swillen,
J. Breckpot,
M. C. Digilio,
B. Marino,
B. Dallapiccola,
...
C. Carpenter,
Xin Zheng,
Jacob Johnson,
Jonathan H. Chung,
A. M. Higgins,
N. Philip,
T. Simon,
K. Coleman,
D. Heine-Suñer,
J. Rosell,
W. Kates,
M. Devoto,
E. Goldmuntz,
E. Zackai,
Tao Wang,
R. Shprintzen,
B. Emanuel,
B. Morrow
|
6 |
2011 |
6
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Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
57 auth.
Maria Delio,
T. Guo,
D. McDonald-McGinn,
E. Zackai,
Sean B. Herman,
M. Kaminetzky,
A. M. Higgins,
K. Coleman,
C. Chow,
M. Jalbrzikowski,
C. Bearden,
Alice Bailey,
A. Vangkilde,
L. Olsen,
C. Olesen,
...
F. Skovby,
T. Werge,
L. Templin,
T. Busa,
N. Philip,
A. Swillen,
J. Vermeesch,
K. Devriendt,
Maude Schneider,
S. Dahoun,
S. Eliez,
K. Schoch,
S. Hooper,
V. Shashi,
J. Samanich,
R. Marion,
Thérèse Van Amelsvoort,
E. Boot,
P. Klaassen,
Sasja N. Duijff,
J. Vorstman,
Tracy Yuen,
C. Silversides,
E. Chow,
A. Bassett,
A. Frisch,
Abraham Weizman,
D. Gothelf,
Maria Niarchou,
M. V. D. van den Bree,
M. Owen,
D. H. Suñer,
Jordi Rosell Andreo,
M. Armando,
S. Vicari,
M. Digilio,
A. Auton,
W. Kates,
Tao Wang,
R. Shprintzen,
B. Emanuel,
B. Morrow
|
5 |
2013 |
5
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Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
32 auth.
E. Mlynarski,
M. Sheridan,
Michael Xie,
T. Guo,
S. Racedo,
D. McDonald-McGinn,
Xiaowu Gai,
E. Chow,
J. Vorstman,
A. Swillen,
K. Devriendt,
J. Breckpot,
M. Digilio,
B. Marino,
B. Dallapiccola,
...
N. Philip,
T. Simon,
A. Roberts,
M. Piotrowicz,
C. Bearden,
S. Eliez,
D. Gothelf,
K. Coleman,
W. Kates,
M. Devoto,
E. Zackai,
D. Heine-Suñer,
T. Shaikh,
A. Bassett,
E. Goldmuntz,
B. Morrow,
B. Emanuel
|
5 |
2015 |
5
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A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: Implications for clinical evaluation and treatment
O. Ousley,
Kimberly Rockers,
M. Dell,
K. Coleman,
J. Cubells
|
5 |
2007 |
5
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Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
10 auth.
T. Guo,
Jonathan H. Chung,
Tao Wang,
D. McDonald-McGinn,
W. Kates,
Wanda Hawuła,
...
K. Coleman,
E. Zackai,
B. Emanuel,
B. Morrow
|
5 |
2015 |
5
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Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: A preliminary report
H. Ross,
Ying Guo,
K. Coleman,
O. Ousley,
Andrew H. Miller
|
5 |
2013 |
5
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