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The Polygenic and Monogenic Basis of Blood Traits and Diseases
112 auth.
D. Vuckovic,
Erik L. Bao,
P. Akbari,
C. Lareau,
A. Mousas,
T. Jiang,
Ming-Huei Chen,
L. Raffield,
M. Tardaguila,
J. Huffman,
S. Ritchie,
Karyn Megy,
H. Ponstingl,
C. Penkett,
Patrick K. Albers,
...
Emilie M. Wigdor,
S. Sakaue,
A. Moscati,
Regina Manansala,
K. S. Lo,
Huijun Qian,
M. Akiyama,
Traci M. Bartz,
Y. Ben-Shlomo,
A. Beswick,
J. Bork-Jensen,
E. Bottinger,
Jennifer A. Brody,
F. V. van Rooij,
K. Chitrala,
P. Wilson,
H. Choquet,
J. Danesh,
E. di Angelantonio,
N. Dimou,
Jingzhong Ding,
P. Elliott,
T. Esko,
M. Evans,
S. Felix,
J. Floyd,
L. Broer,
N. Grarup,
Michael H. Guo,
Qi Guo,
A. Greinacher,
J. Haessler,
T. Hansen,
J. Howson,
Wei Huang,
E. Jorgenson,
T. Kacprowski,
M. Kähönen,
Y. Kamatani,
M. Kanai,
Savita Karthikeyan,
F. Koskeridis,
L. Lange,
T. Lehtimäki,
A. Linneberg,
Yongmei Liu,
L. Lyytikäinen,
A. Manichaikul,
K. Matsuda,
K. Mohlke,
N. Mononen,
Y. Murakami,
G. Nadkarni,
K. Nikus,
N. Pankratz,
O. Pedersen,
Michael H. Preuss,
B. Psaty,
O. Raitakari,
S. Rich,
Benjamin A. T. Rodriguez,
Jonathan D. Rosen,
J. Rotter,
P. Schubert,
Cassandra N. Spracklen,
P. Surendran,
Hua Tang,
J. Tardif,
M. Ghanbari,
U. Völker,
H. Völzke,
N. Watkins,
S. Weiss,
N. Cai,
Kousik Kundu,
S. Watt,
Klaudia Walter,
A. Zonderman,
Kelly Cho,
Yun Li,
R. Loos,
J. Knight,
M. Georges,
O. Stegle,
E. Evangelou,
Y. Okada,
David J. Roberts,
M. Inouye,
Andrew D. Johnson,
P. Auer,
W. Astle,
A. Reiner,
A. Butterworth,
W. Ouwehand,
G. Lettre,
V. Sankaran,
N. Soranzo
|
8 |
2020 |
8
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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
110 auth.
Ming-Huei Chen,
L. Raffield,
A. Mousas,
S. Sakaue,
J. Huffman,
A. Moscati,
B. Trivedi,
T. Jiang,
P. Akbari,
D. Vuckovic,
Erik L. Bao,
Xue Zhong,
Regina Manansala,
V. Laplante,
Minhui Chen,
...
K. S. Lo,
Huijun Qian,
C. Lareau,
M. Beaudoin,
K. Hunt,
M. Akiyama,
Traci M. Bartz,
Y. Ben-Shlomo,
A. Beswick,
J. Bork-Jensen,
E. Bottinger,
Jennifer A. Brody,
F. V. Rooij,
K. Chitrala,
Kelly Cho,
H. Choquet,
A. Correa,
J. Danesh,
E. Angelantonio,
N. Dimou,
Jingzhong Ding,
P. Elliott,
T. Esko,
M. Evans,
J. Floyd,
L. Broer,
N. Grarup,
Michael H. Guo,
A. Greinacher,
J. Haessler,
T. Hansen,
J. Howson,
Q. Huang,
Wei Huang,
E. Jorgenson,
T. Kacprowski,
M. Kähönen,
Y. Kamatani,
M. Kanai,
Savita Karthikeyan,
F. Koskeridis,
L. Lange,
T. Lehtimäki,
M. Lerch,
A. Linneberg,
Yongmei Liu,
L. Lyytikäinen,
A. Manichaikul,
H. Martin,
K. Matsuda,
K. Mohlke,
N. Mononen,
Y. Murakami,
G. Nadkarni,
M. Nauck,
K. Nikus,
W. Ouwehand,
N. Pankratz,
O. Pedersen,
Michael H. Preuss,
B. Psaty,
O. Raitakari,
David J. Roberts,
S. Rich,
Benjamin A. T. Rodriguez,
Jonathan D. Rosen,
J. Rotter,
P. Schubert,
Cassandra N. Spracklen,
P. Surendran,
Hua Tang,
J. Tardif,
R. Trembath,
M. Ghanbari,
U. Völker,
H. Völzke,
N. Watkins,
A. Zonderman,
P. Wilson,
Yun Li,
A. Butterworth,
J. Gauchat,
C. Chiang,
Bingshan Li,
R. Loos,
W. Astle,
E. Evangelou,
D. Heel,
V. Sankaran,
Y. Okada,
N. Soranzo,
Andrew D. Johnson,
A. Reiner,
P. Auer,
G. Lettre
|
8 |
2020 |
8
🐜
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🐜
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
78 auth.
M. H. Kowalski,
Huijun Qian,
Ziyi Hou,
Jonathan D. Rosen,
Amanda L. Tapia,
Y. Shan,
D. Jain,
Maria Argos,
D. Arnett,
C. Avery,
K. Barnes,
L. Becker,
Stephanie A. Bien,
J. Bis,
J. Blangero,
...
E. Boerwinkle,
D. Bowden,
S. Buyske,
Jianwen Cai,
M. Cho,
S. Choi,
H. Choquet,
L. Cupples,
M. Cushman,
M. Daya,
P. S. Vries,
P. Ellinor,
N. Faraday,
M. Fornage,
S. Gabriel,
S. Ganesh,
M. Graff,
N. Gupta,
Jiang He,
S. Heckbert,
Bertha A Hidalgo,
C. Hodonsky,
M. Irvin,
Andrew D. Johnson,
E. Jorgenson,
R. Kaplan,
S. Kardia,
T. Kelly,
C. Kooperberg,
J. Lasky-Su,
R. Loos,
S. Lubitz,
R. Mathias,
Caitlin P. McHugh,
C. Montgomery,
Jee-Young Moon,
A. Morrison,
Nicholette D. Palmer,
N. Pankratz,
G. Papanicolaou,
J. Peralta,
P. Peyser,
S. Rich,
J. Rotter,
E. Silverman,
Jennifer A. Smith,
N. Smith,
K. Taylor,
T. Thornton,
H. Tiwari,
R. Tracy,
Tao Wang,
S. Weiss,
L. Weng,
K. Wiggins,
James G. Wilson,
L. Yanek,
S. Zöllner,
Kari North,
P. Auer,
L. Raffield,
A. Reiner,
Yun Li
|
7 |
2019 |
7
🐜
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🐜
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Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
13 auth.
N. Matoba,
Dan Liang,
Huaigu Sun,
Nil Aygün,
J. McAfee,
Jessica E. Davis,
L. Raffield,
Huijun Qian,
J. Piven,
Yun Li,
...
S. Kosuri,
H. Won,
J. Stein
|
6 |
2020 |
6
🐜
|
|
🐜
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Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium
73 auth.
B. Lin,
Kelsey E. Grinde,
Jennifer A. Brody,
C. Breeze,
L. Raffield,
J. Mychaleckyj,
T. Thornton,
James A. Perry,
L. Baier,
L. de las Fuentes,
Xiuqing Guo,
Benjamin D. Heavner,
R. Hanson,
Y. Hung,
Huijun Qian,
...
C. Hsiung,
Shih-Jen Hwang,
M. R. Irvin,
D. Jain,
T. Kelly,
S. Kobes,
L. Lange,
J. Lash,
Yun Li,
Xiaoming Liu,
Xuenan Mi,
S. Musani,
G. Papanicolaou,
A. Parsa,
A. Reiner,
S. Salimi,
W. Sheu,
A. Shuldiner,
K. Taylor,
A. Smith,
Jennifer A. Smith,
A. Tin,
Dhananjay Vaidya,
R. Wallace,
Kenichi Yamamoto,
S. Sakaue,
K. Matsuda,
Y. Kamatani,
Y. Momozawa,
L. Yanek,
B. Young,
Wei Zhao,
Y. Okada,
G. Abecasis,
B. Psaty,
D. Arnett,
E. Boerwinkle,
Jianwen Cai,
Ida Yii-Der Chen,
A. Correa,
L. Cupples,
Jiang He,
S. Kardia,
C. Kooperberg,
R. Mathias,
B. Mitchell,
D. Nickerson,
S. Turner,
R. Vasan,
J. Rotter,
D. Levy,
H. Kramer,
A. Köttgen,
TOPMed Kidney Working Group,
S. Rich,
D. Lin,
S. Browning,
N. Franceschini
|
5 |
2021 |
5
🐜
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|
🐬
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SMNN: Batch Effect Correction for Single-cell RNA-seq data via Supervised Mutual Nearest Neighbor Detection
Yuchen Yang,
Gang Li,
Huijun Qian,
K. Wilhelmsen,
Yin Shen,
Yun Li
|
4 |
2019 |
4
🐬
|
|
🐜
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Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women
11 auth.
N. Franceschini,
J. Kopp,
A. Barac,
L. Martin,
Yun Li,
Huijun Qian,
...
A. Reiner,
M. Pollak,
R. Wallace,
W. Rosamond,
C. Winkler
|
4 |
2018 |
4
🐜
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|
🐜
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Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations
36 auth.
Jia Wen,
Munan Xie,
Bryce T Rowland,
Jonathan D. Rosen,
Quan Sun,
Jiawen Chen,
Amanda L. Tapia,
Huijun Qian,
M. H. Kowalski,
Y. Shan,
K. Young,
M. Graff,
Maria Argos,
C. Avery,
Stephanie A. Bien,
...
S. Buyske,
J. Yin,
H. Choquet,
M. Fornage,
C. Hodonsky,
E. Jorgenson,
C. Kooperberg,
R. Loos,
Yongmei Liu,
Jee-Young Moon,
K. North,
S. Rich,
J. Rotter,
Jennifer A. Smith,
Wei Zhao,
Lulu Shang,
Tao Wang,
Xiang Zhou,
A. Reiner,
L. Raffield,
Yun Li
|
3 |
2021 |
3
🐜
|
|
🐜
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Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction.
47 auth.
G. Jia,
J. Ping,
Xingyi Guo,
Yaohua Yang,
Ran Tao,
Bingshan Li,
S. Ambs,
M. Barnard,
Yu Chen,
M. García-Closas,
Jian Gu,
Jennifer J Hu,
Dezheng Huo,
Esther M. John,
Christopher I. Li,
...
James L. Li,
K. Nathanson,
B. Nemesure,
O. Olopade,
Tuya Pal,
Michael F Press,
M. Sanderson,
Dale R. Sandler,
X. Shu,
M. Troester,
S. Yao,
P. Adejumo,
Thomas U Ahearn,
A. Brewster,
A. Hennis,
T. Makumbi,
P. Ndom,
Katie M. O’Brien,
Andrew F Olshan,
M. Oluwasanu,
Sonya Reid,
Eboneé N. Butler,
Maosheng Huang,
A. Ntekim,
Huijun Qian,
Haoyu Zhang,
C. Ambrosone,
Q. Cai,
J. Long,
Julie R. Palmer,
C. Haiman,
Wei Zheng
|
3 |
2024 |
3
🐜
|
|
🐜
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Common genetic risk variants identified in the SPARK cohort implicate DDHD2 as a novel autism risk gene
13 auth.
N. Matoba,
Dan Liang,
Huaigu Sun,
Nil Aygün,
J. McAfee,
Jessica E. Davis,
L. Raffield,
Huijun Qian,
J. Piven,
Yun Li,
...
S. Kosuri,
H. Won,
J. Stein
|
1 |
2020 |
1
🐜
|
