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Functional impact of global rare copy number variation in autism spectrum disorders
176 auth.
D. Pinto,
A. Pagnamenta,
L. Klei,
R. Anney,
D. Merico,
R. Regan,
J. Conroy,
T. Magalhães,
C. Correia,
B. Abrahams,
J. Almeida,
E. Bacchelli,
Gary D Bader,
A. Bailey,
G. Baird,
...
A. Battaglia,
T. Berney,
N. Bolshakova,
S. Bölte,
P. Bolton,
T. Bourgeron,
Sean Brennan,
J. Brian,
S. Bryson,
A. Carson,
G. Casallo,
J. Casey,
B. Chung,
L. Cochrane,
Christina M. Corsello,
Emily L. Crawford,
Andrew Crossett,
C. Cytrynbaum,
G. Dawson,
M. Jonge,
R. Delorme,
Irene Drmic,
E. Duketis,
F. Duque,
A. Estes,
Penny Farrar,
B. Fernandez,
S. Folstein,
E. Fombonne,
C. Freitag,
J. Gilbert,
C. Gillberg,
J. Glessner,
J. Goldberg,
A. Green,
Jonathan Green,
Stephen J. Guter,
H. Hakonarson,
E. Heron,
M. Hill,
R. Holt,
J. Howe,
G. Hughes,
Vanessa Hus,
R. Igliozzi,
Cecilia Kim,
S. Klauck,
A. Kolevzon,
Olena Korvatska,
Vlad Kustanovich,
C. Lajonchere,
J. Lamb,
Magdalena Laskawiec,
M. Leboyer,
A. Couteur,
B. Leventhal,
A. C. Lionel,
Xiao-qing Liu,
C. Lord,
L. Lotspeich,
Sabata C. Lund,
E. Maestrini,
W. Mahoney,
Carine Mantoulan,
C. Marshall,
H. McConachie,
C. McDougle,
J. McGrath,
W. McMahon,
Alison K. Merikangas,
O. Migita,
N. Minshew,
G. Mirza,
J. Munson,
S. Nelson,
Carolyn Noakes,
A. Noor,
G. Nygren,
G. Oliveira,
K. Papanikolaou,
J. Parr,
B. Parrini,
T. Paton,
A. Pickles,
M. Pilorge,
J. Piven,
C. Ponting,
D. Posey,
A. Poustka,
F. Poustka,
Aparna Prasad,
J. Ragoussis,
Katy Renshaw,
Jessica Rickaby,
W. Roberts,
K. Roeder,
B. Rogé,
M. Rutter,
L. Bierut,
J. Rice,
Jeff Salt,
K. Sansom,
Daisuke Sato,
R. Segurado,
A. Sequeira,
Lili Senman,
N. Shah,
V. Sheffield,
L. Soorya,
I. Sousa,
O. Stein,
N. Sykes,
Vera Stoppioni,
Christina P Strawbridge,
R. Tancredi,
K. Tansey,
Bhooma Thiruvahindrapduram,
A. Thompson,
Susanne A. Thomson,
A. Tryfon,
J. Tsiantis,
H. Engeland,
J. Vincent,
F. Volkmar,
S. Wallace,
Kai Wang,
Zhouzhi Wang,
T. Wassink,
C. Webber,
R. Weksberg,
Kirsty Wing,
Kerstin Wittemeyer,
Shawn Wood,
B. Yaspan,
Danielle M Zurawiecki,
L. Zwaigenbaum,
J. Buxbaum,
R. Cantor,
E. Cook,
H. Coon,
M. Cuccaro,
B. Devlin,
S. Ennis,
L. Gallagher,
D. Geschwind,
M. Gill,
J. Haines,
Joachim Hallmayer,
Judith S Miller,
A. Monaco,
J. Nurnberger,
A. Paterson,
M. Pericak-Vance,
G. Schellenberg,
P. Szatmari,
A. Vicente,
V. Vieland,
E. Wijsman,
S. Scherer,
J. Sutcliffe,
C. Betancur
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10 |
2010 |
10 🐜
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Genetic heritability and shared environmental factors among twin pairs with autism.
16 auth.
J. Hallmayer,
Sue C. Cleveland,
Andrea Torres,
Jennifer M. Phillips,
B. Cohen,
Tiffany Torigoe,
Janet Miller,
A. Fedele,
Jack Collins,
K. Smith,
...
L. Lotspeich,
L. Croen,
S. Ozonoff,
C. Lajonchere,
J. Grether,
N. Risch
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10 |
2011 |
10 🐜
|
🐜
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements
138 auth.
P. Szatmari,
A. Paterson,
L. Zwaigenbaum,
W. Roberts,
J. Brian,
Xiao-qing Liu,
J. Vincent,
J. Skaug,
A. Thompson,
Lili Senman,
L. Feuk,
Cheng Qian,
S. Bryson,
Marshall B. Jones,
C. Marshall,
...
S. Scherer,
V. Vieland,
Christopher Bartlett,
L. Mangin,
R. Goedken,
Alberto Maria Segre,
M. Pericak-Vance,
M. Cuccaro,
J. Gilbert,
H. Wright,
R. Abramson,
C. Betancur,
T. Bourgeron,
C. Gillberg,
M. Leboyer,
J. Buxbaum,
K. Davis,
E. Hollander,
J. Silverman,
Joachim Hallmayer,
L. Lotspeich,
J. Sutcliffe,
J. Haines,
S. Folstein,
J. Piven,
T. Wassink,
V. Sheffield,
D. Geschwind,
M. Bucan,
W. Brown,
R. Cantor,
J. Constantino,
T. Gilliam,
M. Herbert,
C. Lajonchere,
D. Ledbetter,
Christa Lese-Martin,
Janet Miller,
S. Nelson,
C. Samango-Sprouse,
S. Spence,
M. State,
R. Tanzi,
H. Coon,
G. Dawson,
B. Devlin,
A. Estes,
P. Flodman,
L. Klei,
W. McMahon,
N. Minshew,
J. Munson,
E. Korvatska,
P. Rodier,
G. Schellenberg,
Moyra J. Smith,
M. Spence,
C. Stodgell,
P. Tepper,
E. Wijsman,
Chang-En Yu,
B. Rogé,
Carine Mantoulan,
Kerstin Wittemeyer,
A. Poustka,
B. Felder,
S. Klauck,
C. Schuster,
F. Poustka,
S. Bölte,
Sabine Feineis-Matthews,
Evelyn Herbrecht,
G. Schmötzer,
J. Tsiantis,
K. Papanikolaou,
E. Maestrini,
E. Bacchelli,
F. Blasi,
Simona Carone,
Claudio Toma,
H. van Engeland,
M. D. de Jonge,
C. Kemner,
F. Koop,
M. Langemeijer,
Channa T. Hijmans,
W. Staal,
G. Baird,
P. Bolton,
M. Rutter,
E. Weisblatt,
Jonathan Green,
C. Aldred,
J. Wilkinson,
A. Pickles,
A. Le Couteur,
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H. McConachie,
A. Bailey,
Kostas Francis,
Gemma Honeyman,
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J. Parr,
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A. Monaco,
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Kazuhiro Kobayashi,
J. Lamb,
I. Sousa,
N. Sykes,
E. Cook,
Stephen J. Guter,
B. Leventhal,
Jeff Salt,
C. Lord,
Christina M. Corsello,
Vanessa Hus,
D. Weeks,
F. Volkmar,
M. Tauber,
E. Fombonne,
A. Shih,
Kacie J. Meyer
|
10 |
2007 |
10 🐜
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🐜
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Common genetic variants on 5p14.1 associate with autism spectrum disorders
56 auth.
Kai Wang,
Haitao Zhang,
D. Ma,
M. Bucan,
J. Glessner,
B. Abrahams,
D. Salyakina,
M. Imieliński,
J. Bradfield,
P. Sleiman,
Cecilia Kim,
C. Hou,
E. Frackelton,
R. Chiavacci,
N. Takahashi,
...
T. Sakurai,
E. Rappaport,
C. Lajonchere,
J. Munson,
A. Estes,
Olena Korvatska,
J. Piven,
L. Sonnenblick,
A. I. A. Retuerto,
Edward I. Herman,
Hongmei Dong,
T. Hutman,
M. Sigman,
S. Ozonoff,
A. Klin,
Thomas Owley,
J. Sweeney,
Camille W. Brune,
R. Cantor,
R. Bernier,
J. Gilbert,
M. Cuccaro,
W. McMahon,
Judith N. Miller,
M. State,
T. Wassink,
H. Coon,
S. Levy,
R. Schultz,
J. Nurnberger,
J. Haines,
J. Sutcliffe,
E. Cook,
N. Minshew,
J. Buxbaum,
G. Dawson,
S. Grant,
D. Geschwind,
M. Pericak-Vance,
G. Schellenberg,
H. Hakonarson
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9 |
2009 |
9 🐜
|
🐜
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Microduplications of 16p11.2 are Associated with Schizophrenia
72 auth.
S. McCarthy,
Vladimir Makarov,
G. Kirov,
A. Addington,
J. McClellan,
Seungtai Yoon,
D. Perkins,
D. Dickel,
M. Kusenda,
O. Krastoshevsky,
V. Krause,
Ravinesh A. Kumar,
D. Grozeva,
D. Malhotra,
T. Walsh,
...
E. Zackai,
P. Kaplan,
J. Ganesh,
I. Krantz,
N. Spinner,
P. Roccanova,
A. Bhandari,
Kevin Pavon,
B. Lakshmi,
A. Leotta,
J. Kendall,
Yoon-ha Lee,
V. Vacic,
Sydney Gary,
L. Iakoucheva,
T. Crow,
S. Christian,
J. Lieberman,
S. Stroup,
T. Lehtimäki,
K. Puura,
C. Haldeman-Englert,
J. Pearl,
M. Goodell,
V. Willour,
P. DeRosse,
Jo Steele,
L. Kassem,
Jessica Wolff,
N. Chitkara,
F. McMahon,
A. Malhotra,
J. Potash,
T. Schulze,
M. Nöthen,
S. Cichon,
M. Rietschel,
E. Leibenluft,
Vlad Kustanovich,
C. Lajonchere,
J. Sutcliffe,
D. Skuse,
M. Gill,
L. Gallagher,
N. Mendell,
N. Craddock,
M. Owen,
M. O’Donovan,
T. Shaikh,
E. Susser,
L. DeLisi,
P. Sullivan,
C. Deutsch,
J. Rapoport,
D. Levy,
M. King,
J. Sebat
|
9 |
2009 |
9 🐜
|
🐜
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A genome-wide scan for common alleles affecting risk for autism
166 auth.
R. Anney,
L. Klei,
D. Pinto,
R. Regan,
J. Conroy,
T. Magalhães,
C. Correia,
B. Abrahams,
N. Sykes,
A. Pagnamenta,
J. Almeida,
E. Bacchelli,
A. Bailey,
G. Baird,
A. Battaglia,
...
T. Berney,
N. Bolshakova,
S. Bölte,
P. Bolton,
T. Bourgeron,
Sean Brennan,
J. Brian,
A. Carson,
G. Casallo,
J. Casey,
S. Chu,
L. Cochrane,
Christina M. Corsello,
Emily L. Crawford,
Andrew Crossett,
G. Dawson,
M. D. de Jonge,
R. Delorme,
Irene Drmic,
E. Duketis,
F. Duque,
A. Estes,
Penny Farrar,
B. Fernandez,
S. Folstein,
E. Fombonne,
C. Freitag,
J. Gilbert,
C. Gillberg,
J. Glessner,
J. Goldberg,
Jonathan Green,
Stephen J. Guter,
H. Hakonarson,
E. Heron,
M. Hill,
R. Holt,
J. Howe,
G. Hughes,
Vanessa Hus,
R. Igliozzi,
Cecilia Kim,
S. Klauck,
A. Kolevzon,
Olena Korvatska,
Vlad Kustanovich,
C. Lajonchere,
J. Lamb,
Magdalena Laskawiec,
M. Leboyer,
A. Le Couteur,
B. Leventhal,
A. C. Lionel,
Xiao-qing Liu,
C. Lord,
L. Lotspeich,
Sabata C. Lund,
E. Maestrini,
W. Mahoney,
Carine Mantoulan,
C. Marshall,
H. McConachie,
C. McDougle,
J. McGrath,
W. McMahon,
N. Melhem,
Alison K. Merikangas,
O. Migita,
N. Minshew,
G. Mirza,
J. Munson,
S. Nelson,
Carolyn Noakes,
A. Noor,
G. Nygren,
G. Oliveira,
K. Papanikolaou,
J. Parr,
B. Parrini,
T. Paton,
A. Pickles,
J. Piven,
D. Posey,
A. Poustka,
F. Poustka,
Aparna Prasad,
J. Ragoussis,
Katy Renshaw,
Jessica Rickaby,
W. Roberts,
K. Roeder,
B. Rogé,
M. Rutter,
L. Bierut,
J. Rice,
Jeff Salt,
K. Sansom,
Daisuke Sato,
R. Segurado,
Lili Senman,
N. Shah,
V. Sheffield,
L. Soorya,
I. Sousa,
Vera Stoppioni,
Christina P Strawbridge,
R. Tancredi,
K. Tansey,
Bhooma Thiruvahindrapduram,
A. Thompson,
Susanne A. Thomson,
A. Tryfon,
J. Tsiantis,
H. van Engeland,
J. Vincent,
F. Volkmar,
S. Wallace,
Kai Wang,
Zhouzhi Wang,
T. Wassink,
Kirsty Wing,
Kerstin Wittemeyer,
Shawn Wood,
B. Yaspan,
Danielle M Zurawiecki,
L. Zwaigenbaum,
C. Betancur,
J. Buxbaum,
R. Cantor,
E. Cook,
H. Coon,
M. Cuccaro,
L. Gallagher,
D. Geschwind,
M. Gill,
J. Haines,
Judith S Miller,
A. Monaco,
J. Nurnberger,
A. Paterson,
M. Pericak-Vance,
G. Schellenberg,
S. Scherer,
J. Sutcliffe,
P. Szatmari,
A. Vicente,
V. Vieland,
E. Wijsman,
B. Devlin,
S. Ennis,
Joachim Hallmayer
|
9 |
2010 |
9 🐜
|
🐜
|
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
39 auth.
Yong-hui Jiang,
R. Yuen,
Xin Jin,
Mingbang Wang,
Nong Chen,
Xueli Wu,
Jia Ju,
J. Mei,
Yujian Shi,
Mingze He,
Guangbiao Wang,
Jieqin Liang,
Zhe Wang,
D. Cao,
M. Carter,
...
Christina Chrysler,
Irene Drmic,
J. Howe,
L. Lau,
C. Marshall,
D. Merico,
T. Nalpathamkalam,
B. Thiruvahindrapuram,
A. Thompson,
M. Uddin,
S. Walker,
Jun Luo,
E. Anagnostou,
L. Zwaigenbaum,
R. Ring,
J. Wang,
C. Lajonchere,
Jun Wang,
A. Shih,
P. Szatmari,
Huanming Yang,
G. Dawson,
Yingrui Li,
S. Scherer
|
8 |
2013 |
8 🐜
|
🐜
|
Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes
36 auth.
M. Bucan,
B. Abrahams,
Kai Wang,
J. Glessner,
Edward I. Herman,
L. Sonnenblick,
A. I. Alvarez Retuerto,
M. Imieliński,
D. Hadley,
J. Bradfield,
Cecilia Kim,
Nicole B. Gidaya,
I. Lindquist,
T. Hutman,
M. Sigman,
...
Vlad Kustanovich,
C. Lajonchere,
A. Singleton,
Junhyong Kim,
T. Wassink,
W. McMahon,
Thomas Owley,
J. Sweeney,
H. Coon,
J. Nurnberger,
Mingyao Li,
R. Cantor,
N. Minshew,
J. Sutcliffe,
E. Cook,
G. Dawson,
J. Buxbaum,
S. Grant,
G. Schellenberg,
D. Geschwind,
H. Hakonarson
|
8 |
2009 |
8 🐜
|
🐜
|
Individual common variants exert weak effects on the risk for autism spectrum disorders
137 auth.
R. Anney,
L. Klei,
D. Pinto,
J. Almeida,
E. Bacchelli,
G. Baird,
N. Bolshakova,
S. Bölte,
P. Bolton,
T. Bourgeron,
Sean Brennan,
J. Brian,
J. Casey,
J. Conroy,
C. Correia,
...
Christina M. Corsello,
Emily L. Crawford,
M. D. de Jonge,
R. Delorme,
E. Duketis,
F. Duque,
A. Estes,
Penny Farrar,
B. Fernandez,
S. Folstein,
E. Fombonne,
J. Gilbert,
C. Gillberg,
J. Glessner,
A. Green,
Jonathan Green,
Stephen J. Guter,
E. Heron,
R. Holt,
J. Howe,
G. Hughes,
Vanessa Hus,
R. Igliozzi,
Suma Jacob,
G. Kenny,
Cecilia Kim,
A. Kolevzon,
Vlad Kustanovich,
C. Lajonchere,
J. Lamb,
Miriam Law-Smith,
M. Leboyer,
A. Le Couteur,
B. Leventhal,
Xiao-qing Liu,
Frances Lombard,
C. Lord,
L. Lotspeich,
Sabata C. Lund,
T. Magalhães,
Carine Mantoulan,
C. McDougle,
N. Melhem,
Alison K. Merikangas,
N. Minshew,
G. Mirza,
J. Munson,
Carolyn Noakes,
G. Nygren,
K. Papanikolaou,
A. Pagnamenta,
B. Parrini,
T. Paton,
A. Pickles,
D. Posey,
F. Poustka,
J. Ragoussis,
R. Regan,
W. Roberts,
K. Roeder,
B. Rogé,
M. Rutter,
S. Schlitt,
N. Shah,
V. Sheffield,
L. Soorya,
I. Sousa,
Vera Stoppioni,
N. Sykes,
R. Tancredi,
A. Thompson,
Susanne A. Thomson,
A. Tryfon,
J. Tsiantis,
H. van Engeland,
J. Vincent,
F. Volkmar,
J. Vorstman,
S. Wallace,
Kirsty Wing,
Kerstin Wittemeyer,
Shawn Wood,
Danielle M Zurawiecki,
L. Zwaigenbaum,
A. Bailey,
A. Battaglia,
R. Cantor,
H. Coon,
M. Cuccaro,
G. Dawson,
S. Ennis,
C. Freitag,
D. Geschwind,
J. Haines,
S. Klauck,
W. McMahon,
E. Maestrini,
Judith S Miller,
A. Monaco,
S. Nelson,
J. Nurnberger,
G. Oliveira,
J. Parr,
M. Pericak-Vance,
J. Piven,
G. Schellenberg,
S. Scherer,
A. Vicente,
T. Wassink,
E. Wijsman,
C. Betancur,
J. Buxbaum,
E. Cook,
L. Gallagher,
M. Gill,
Joachim Hallmayer,
A. Paterson,
J. Sutcliffe,
P. Szatmari,
V. Vieland,
H. Hakonarson,
B. Devlin
|
8 |
2012 |
8 🐜
|
🐜
|
A unified genetic theory for sporadic and inherited autism
12 auth.
Xiaoyue Zhao,
A. Leotta,
Vlad Kustanovich,
C. Lajonchere,
D. Geschwind,
Kiely Law,
...
Paul Law,
Shanping Qiu,
C. Lord,
J. Sebat,
Kenny Q. Ye,
M. Wigler
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8 |
2007 |
8 🐜
|
🐜
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Autistic social impairment in the siblings of children with pervasive developmental disorders.
8 auth.
J. Constantino,
C. Lajonchere,
M. Lutz,
Teddi Gray,
Anna M. Abbacchi,
K. McKenna,
...
Deepti Singh,
R. Todd
|
8 |
2006 |
8 🐜
|
🐜
|
Assessing behavioural and cognitive domains of autism spectrum disorders in rodents: current status and future perspectives
13 auth.
M. Kas,
Jeffrey C. Glennon,
J. Buitelaar,
Elodie Ey,
B. Biemans,
J. Crawley,
Robert H. Ring,
C. Lajonchere,
F. Esclassan,
J. Talpos,
...
L. P. Noldus,
J. P. H. Burbach,
T. Steckler
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6 |
2013 |
6 🐜
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🐢
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Cutaneous sensory spots and the “law of specific nerve energies”: history and development of ideas
U. Norrsell,
S. Finger,
C. Lajonchere
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6 |
1999 |
6 🐢
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