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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
27 auth.
J. Rioux,
J. Rioux,
R. Xavier,
K. Taylor,
M. Silverberg,
P. Goyette,
A. Huett,
Todd Green,
Petric Kuballa,
M. Barmada,
L. Datta,
Y. Shugart,
A. Griffiths,
S. Targan,
A. Ippoliti,
...
E. Bernard,
L. Mei,
D. Nicolae,
M. Regueiro,
L. P. Schumm,
A. Steinhart,
J. Rotter,
R. Duerr,
Judy H. Cho,
M. J. Daly,
M. J. Daly,
S. Brant
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10 |
2007 |
10
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Mapping Human Genetic Diversity in Asia
92 auth.
M. Abdulla,
Ikhlak Ahmed,
A. Assawamakin,
J. Bhak,
S. Brahmachari,
G. Calacal,
A. Chaurasia,
Chien-Hsiun Chen,
Jieming Chen,
Yuan-Tsong Chen,
Jiayou Chu,
E. M. Cutiongco-de la Paz,
Maria Corazon Abogado De Ungria,
F. Delfin,
J. Edo,
...
S. Fuchareon,
H. Ghang,
T. Gojobori,
Junsong Han,
Sheng-Feng Ho,
B. Hoh,
Wei Huang,
H. Inoko,
P. Jha,
T. Jinam,
Li Jin,
Jongsun Jung,
D. Kangwanpong,
Jatupol Kampuansai,
G. Kennedy,
Preeti Khurana,
Hyung-Lae Kim,
Kwang-Joong Kim,
Sangsoo Kim,
Woo-Yeon Kim,
K. Kimm,
R. Kimura,
T. Koike,
S. Kulawonganunchai,
Vikrant Kumar,
P. Lai,
Jong-Young Lee,
Sunghoon Lee,
Edison T. Liu,
P. Majumder,
Kiran Kumar Mandapati,
S. Marzuki,
Wayne Mitchell,
M. Mukerji,
K. Naritomi,
C. Ngamphiw,
N. Niikawa,
N. Nishida,
B. Oh,
S. Oh,
J. Ohashi,
A. Oka,
R. Ong,
C. Padilla,
P. Palittapongarnpim,
Henry B. Perdigon,
M. Phipps,
E. Png,
Y. Sakaki,
Jazelyn M. Salvador,
Yuliana Sandraling,
V. Scaria,
M. Seielstad,
Mohd Sidek,
Amit Sinha,
M. Srikummool,
H. Sudoyo,
S. Sugano,
H. Suryadi,
Yoshiyuki Suzuki,
K. Tabbada,
Adrian Tan,
K. Tokunaga,
S. Tongsima,
Lilian P Villamor,
Eric Wang,
Ying Wang,
Haifeng Wang,
Jer-Yuarn Wu,
Hua-sheng Xiao,
Shuhua Xu,
Jin Ok Yang,
Y. Shugart,
H. Yoo,
W. Yuan,
Guoping Zhao,
B. Zilfalil
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9 |
2009 |
9
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|
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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
8 auth.
Susan E. Hong,
Y. Shugart,
David T. Huang,
S. A. Shahwan,
P. Grant,
J. Hourihane,
...
N. Martin,
Christopher A. Walsh
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9 |
2000 |
9
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Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis
97 auth.
P. Arnold,
Kathleen D Askland,
C. Barlassina,
L. Bellodi,
O. Bienvenu,
D. Black,
M. Bloch,
H. Brentani,
C. Burton,
B. Camarena,
C. Cappi,
D. Cath,
M. Cavallini,
D. Conti,
E. Cook,
...
V. Coric,
B. Cullen,
D. Cusi,
L. Davis,
R. Delorme,
D. Denys,
E. Derks,
V. Eapen,
C. Edlund,
L. Erdman,
P. Falkai,
M. Figee,
A. Fyer,
D. Geller,
F. Goes,
H. Grabe,
M. Grados,
B. Greenberg,
E. Grünblatt,
Wei Guo,
G. Hanna,
S. Hemmings,
A. Hounie,
Michael Jenicke,
Clare L. Keenan,
J. Kennedy,
E. Khramtsova,
A. Konkashbaev,
J. Knowles,
Janice Krasnow,
C. Lange,
N. Lanzagorta,
M. Leboyer,
L. Lennertz,
Bingbin Li,
K. Liang,
C. Lochner,
F. Macciardi,
B. Maher,
W. Maier,
M. Marconi,
C. Mathews,
Manuel Matthesien,
J. McCracken,
N. McLaughlin,
E. Miguel,
R. Moessner,
D. Murphy,
B. Neale,
G. Nestadt,
P. Nestadt,
H. Nicolini,
Ericka Nurmi,
L. Osiecki,
D. Pauls,
J. Piacentini,
D. Posthuma,
A. Pulver,
H. Qin,
S. Rasmussen,
S. Rauch,
M. Richter,
M. Riddle,
S. Ripke,
S. Ruhrmann,
A. Sampaio,
J. Samuels,
J. Scharf,
Y. Shugart,
J. Smit,
Dan J Stein,
S. E. Stewart,
M. Turiel,
H. Vallada,
J. Veenstra-VanderWeele,
M. Wagner,
S. Walitza,
Ying Wang,
J. Wendland,
N. Vulink,
Dongmei Yu,
G. Zai
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8 |
2018 |
8
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|
🐜
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Exome sequencing and the genetic basis of complex traits
19 auth.
Adam Kiezun,
K. Garimella,
R. Do,
N. Stitziel,
B. Neale,
P. McLaren,
N. Gupta,
P. Sklar,
P. Sullivan,
J. Moran,
...
C. Hultman,
P. Lichtenstein,
P. Magnusson,
T. Lehner,
Y. Shugart,
A. Price,
P. D. Bakker,
S. Purcell,
S. Sunyaev
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8 |
2012 |
8
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|
🐜
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Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome
14 auth.
R. J. Ferland,
W. Eyaid,
R. Collura,
L. D. Tully,
R. Hill,
D. Al-Nouri,
A. Al-Rumayyan,
M. Topçu,
G. Gascon,
A. Bodell,
...
Y. Shugart,
M. Ruvolo,
C. Walsh,
C. Walsh
|
8 |
2004 |
8
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|
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Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex
12 auth.
V. Sheen,
V. Ganesh,
M. Topçu,
G. Sébire,
A. Bodell,
R. Hill,
...
P. Grant,
Y. Shugart,
J. Imitola,
S. Khoury,
R. Guerrini,
Christopher A. Walsh
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8 |
2004 |
8
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|
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Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
131 auth.
L. Davis,
Dongmei Yu,
Clare L. Keenan,
E. Gamazon,
A. Konkashbaev,
E. Derks,
B. Neale,
Jian Yang,
S. H. Lee,
P. Evans,
C. Barr,
L. Bellodi,
F. Benarroch,
G. Berrio,
O. Bienvenu,
...
M. Bloch,
R. Blom,
R. Bruun,
C. Budman,
B. Camarena,
D. Campbell,
C. Cappi,
Julio C. Cardona Silgado,
D. Cath,
M. Cavallini,
D. Chavira,
S. Chouinard,
D. Conti,
E. Cook,
V. Coric,
B. Cullen,
D. Deforce,
R. Delorme,
Y. Dion,
C. Edlund,
K. Egberts,
P. Falkai,
T. Fernandez,
Patience J. Gallagher,
H. Garrido,
D. Geller,
S. Girard,
H. Grabe,
M. Grados,
B. Greenberg,
V. Gross‐Tsur,
S. Haddad,
G. Heiman,
S. Hemmings,
A. Hounie,
C. Illmann,
J. Jankovic,
M. Jenike,
J. Kennedy,
R. King,
B. Kremeyer,
R. Kurlan,
N. Lanzagorta,
M. Leboyer,
J. Leckman,
L. Lennertz,
Chunyu Liu,
C. Lochner,
T. Lowe,
F. Macciardi,
J. McCracken,
L. McGrath,
S. C. Mesa Restrepo,
R. Moessner,
J. Morgan,
H. Muller,
D. Murphy,
A. Naarden,
W. Ochoa,
R. Ophoff,
L. Osiecki,
A. Pakstis,
M. Pato,
C. Pato,
J. Piacentini,
C. Pittenger,
Y. Pollak,
S. Rauch,
T. Renner,
V. Reus,
M. Richter,
M. Riddle,
M. Robertson,
Roxana Romero,
M. Rosário,
D. Rosenberg,
G. Rouleau,
S. Ruhrmann,
A. Ruiz-Linares,
A. Sampaio,
J. Samuels,
P. Sandor,
B. Sheppard,
H. Singer,
J. Smit,
Dan J Stein,
E. Strengman,
J. Tischfield,
Ana V. Valencia Duarte,
H. Vallada,
F. van Nieuwerburgh,
J. Veenstra-VanderWeele,
S. Walitza,
Ying Wang,
J. Wendland,
H. Westenberg,
Y. Shugart,
E. Miguel,
W. McMahon,
M. Wagner,
H. Nicolini,
D. Posthuma,
G. Hanna,
P. Heutink,
D. Denys,
P. Arnold,
B. Oostra,
G. Nestadt,
N. Freimer,
D. Pauls,
N. Wray,
S. E. Stewart,
C. Mathews,
J. Knowles,
N. Cox,
J. Scharf
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8 |
2013 |
8
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|
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Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus–related hepatocellular carcinoma
64 auth.
D. Jiang,
Jielin Sun,
G. Cao,
Yao Liu,
D. Lin,
Yu Gao,
Weihua Ren,
Xi-Dai Long,
Hong-xing Zhang,
Xiaopin Ma,
Zhong Wang,
Wei Jiang,
Tao-yang Chen,
Yong Gao,
Liangdan Sun,
...
J. Long,
Huixing Huang,
Dan Wang,
Hongjie Yu,
Pengyin Zhang,
Li-Sha Tang,
Bo Peng,
H. Cai,
Ting Liu,
P. Zhou,
Fang Liu,
Xiao-ling Lin,
S. Tao,
B. Wan,
He-xi Ge Sai-Yin,
L. Qin,
Jianhua Yin,
Li Liu,
Chen Wu,
Y. Pei,
Yuan-Feng Zhou,
Y. Zhai,
P. Lu,
A. Tan,
X. Zuo,
Jia Fan,
Jiang Chang,
Xiaoli Gu,
Nengjin Wang,
Yang Li,
Yin‐kun Liu,
Kan Zhai,
Hongwei Zhang,
Zhibin Hu,
Jun Liu,
Q. Yi,
Y. Xiang,
R. Shi,
Q. Ding,
W. Zheng,
X. Shu,
Z. Mo,
Y. Shugart,
Xuejun Zhang,
Gangqiao Zhou,
Hongbing Shen,
S. Zheng,
Jianfeng Xu,
Long Yu
|
8 |
2012 |
8
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|
🐜
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Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4
30 auth.
B. Feng,
Wei Huang,
Y. Shugart,
Ming K. Lee,
Feng Zhang,
J. Xia,
Hui-Yun Wang,
Teng-bo Huang,
Shao Jian,
Ping Huang,
Qi-sheng Feng,
Li-xi Huang,
Xing-juan Yu,
Duang Li,
Li-Zheng Chen,
...
W. Jia,
Yan Fang,
Hui-ming Huang,
Jing-Liu Zhu,
Xiao-ming Liu,
Yan Zhao,
Wang-Qing Liu,
M. Deng,
Wei-han Hu,
Shao‐xiong Wu,
H. Mo,
M. Hong,
M. King,
Zhu Chen,
Y. Zeng
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7 |
2002 |
7
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Localization of Usher syndrome type II to chromosome 1q.
9 auth.
William J. Kimberling,
M. D. Weston,
Claes Möller,
Sandra L.H. Davenport,
Y. Shugart,
Ira A. Priluck,
...
Alessandro Martini,
M. Milani,
Richard J.H. Smith
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7 |
1990 |
7
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|
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Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
41 auth.
S. Giraud,
Changzhi Zhang,
O. Serova-Sinilnikova,
V. Wautot,
J. Salandre,
N. Buisson,
C. Waterlot,
C. Bauters,
N. Porchet,
J. Aubert,
P. Emy,
G. Cadiot,
B. Delemer,
O. Chabre,
P. Niccoli,
...
F. Leprat,
F. Duron,
B. Emperauger,
P. Cougard,
P. Goudet,
É. Sarfati,
J. Riou,
Sylvie Guichard,
Michel Rodier,
A. Meyrier,
P. Caron,
M. Vantyghem,
Michel Assayag,
J. Peix,
M. Pugeat,
V. Rohmer,
M. Vallotton,
G. Lenoir,
P. Gaudray,
C. Proye,
B. Conte‐Devolx,
P. Chanson,
Y. Shugart,
D. Goldgar,
A. Murat,
A. Calender
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7 |
1998 |
7
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