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Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions
19 auth.
M. D’Amelio,
I. Ricci,
R. Sacco,
Xudong Liu,
L. D'agruma,
L. Muscarella,
V. Guarnieri,
R. Militerni,
C. Bravaccio,
M. Elia,
...
C. Schneider,
R. Melmed,
S. Trillo,
T. Pascucci,
S. Puglisi-Allegra,
K. Reichelt,
F. Macciardi,
J. Holden,
A. Persico
|
7 |
2005 |
7
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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
11 auth.
E. Rajcan-Separovic,
C. Harvard,
Xudong Liu,
B. Mcgillivray,
J. Hall,
Y. Qiao,
...
J. Hurlburt,
J. Hildebrand,
E. Mickelson,
J. Holden,
M. Lewis
|
7 |
2006 |
7
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Comorbid and inflammatory characteristics of genetic subtypes of clonal hematopoiesis.
18 auth.
Elina K Cook,
T. Izukawa,
S. Young,
G. Rosen,
M. Jamali,
Liying Zhang,
Dylan Johnson,
E. Bain,
J. Hilland,
C. K. Ferrone,
...
J. Buckstein,
J. Francis,
B. Momtaz,
Amy J. M. McNaughton,
Xudong Liu,
Brooke Snetsinger,
R. Buckstein,
M. Rauh
|
6 |
2019 |
6
🐜
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A DRD1 haplotype is associated with risk for autism spectrum disorders in male‐only affected sib‐pair families
J. A. Hettinger,
Xudong Liu,
C. Schwartz,
R. Michaelis,
J. Holden
|
6 |
2008 |
6
🐬
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|
🦁
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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
9 auth.
Xudong Liu,
Natalia Novosedlik,
Ami Wang,
Melissa L. Hudson,
I. Cohen,
A. Chudley,
...
C. Forster-Gibson,
S. Lewis,
J. Holden
|
6 |
2009 |
6
🦁
|
|
🐜
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Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders
14 auth.
P. Malenfant,
Xudong Liu,
Melissa L. Hudson,
Y. Qiao,
M. Hrynchak,
N. Riendeau,
M. J. Hildebrand,
Ira L. Cohen,
A. Chudley,
C. Forster-Gibson,
...
Elizabeth C. R. Mickelson,
E. Rajcan-Separovic,
M. E. S. Lewis,
Jeanette J. A. Holden
|
6 |
2011 |
6
🐜
|
|
🦁
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Population- and Family-Based Studies Associate the MTHFR Gene with Idiopathic Autism in Simplex Families
7 auth.
Xudong Liu,
F. Solehdin,
I. Cohen,
Maripaz G. Gonzalez,
E. Jenkins,
M. E. S. Lewis,
...
J. Holden
|
6 |
2011 |
6
🦁
|
|
🐜
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DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families
9 auth.
J. A. Hettinger,
Xudong Liu,
Melissa L. Hudson,
Alana Lee,
I. Cohen,
R. Michaelis,
...
C. Schwartz,
S. Lewis,
J. Holden
|
5 |
2012 |
5
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Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind.
C. Lackner,
M. Sabbagh,
Elizabeth V. Hallinan,
Xudong Liu,
J. Holden
|
5 |
2012 |
5
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