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Increased risk of death and de novo chronic kidney disease following reversible acute kidney injury.
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H. Kirchner,
E. Norfolk,
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2012 |
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Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
54 auth.
F. Dewey,
M. Murray,
J. Overton,
L. Habegger,
J. Leader,
Samantha N. Fetterolf,
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C. Hout,
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R. Metpally,
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Monica A. Giovanni,
H. Kirchner,
S. Balasubramanian,
...
N. Abul-Husn,
Dustin N. Hartzel,
Daniel R. Lavage,
Korey A. Kost,
Jonathan S. Packer,
Alexander E. Lopez,
John Penn,
Semanti Mukherjee,
Nehal Gosalia,
Manoj Kanagaraj,
Alexander Hanbo Li,
L. Mitnaul,
Lance J. Adams,
T. Person,
K. Praveen,
A. Marcketta,
Matthew S. Lebo,
C. Austin-Tse,
H. Mason-Suares,
S. Bruse,
S. Mellis,
R. Phillips,
N. Stahl,
A. Murphy,
A. Economides,
K. Skelding,
C. Still,
J. Elmore,
I. Borecki,
G. Yancopoulos,
F. D. Davis,
W. Faucett,
O. Gottesman,
M. Ritchie,
A. Shuldiner,
J. Reid,
D. Ledbetter,
A. Baras,
D. Carey
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2016 |
8
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Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease.
26 auth.
F. Dewey,
V. Gusarova,
C. O’Dushlaine,
O. Gottesman,
Jesus Trejos,
Charleen Hunt,
C. V. van Hout,
L. Habegger,
D. Buckler,
Ka-man V Lai,
J. Leader,
M. Murray,
M. Ritchie,
H. Kirchner,
David H. Ledbetter,
...
John Penn,
Alexander E. Lopez,
I. Borecki,
J. Overton,
J. Reid,
D. Carey,
A. Murphy,
G. Yancopoulos,
A. Baras,
J. Gromada,
A. Shuldiner
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8 |
2016 |
8
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The Geisinger MyCode Community Health Initiative: an electronic health record-linked biobank for Precision Medicine research
11 auth.
D. Carey,
Samantha N. Fetterolf,
F. D. Davis,
W. Faucett,
H. Kirchner,
U. Mirshahi,
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M. Murray,
D. Smelser,
G. Gerhard,
D. Ledbetter,
Genet Med Author
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8 |
2015 |
8
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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
146 auth.
A. Schmidt,
D. Swerdlow,
D. Swerdlow,
M. V. Holmes,
M. Holmes,
R. Patel,
R. Patel,
Z. Fairhurst-Hunter,
D. Lyall,
F. Hartwig,
B. Horta,
E. Hyppönen,
C. Power,
M. Moldovan,
Max Moldovan,
...
E. V. Iperen,
G. Hovingh,
I. Demuth,
K. Norman,
E. Steinhagen-Thiessen,
Juri Demuth,
L. Bertram,
L. Bertram,
Tian Liu,
S. Coassin,
J. Willeit,
S. Kiechl,
K. Willeit,
D. Mason,
John Wright,
R. Morris,
Goya Wanamethee,
P. Whincup,
Y. Ben-Shlomo,
S. McLachlan,
J. Price,
M. Kivimäki,
C. Welch,
A. Sánchez-Gálvez,
P. Marques-Vidal,
A. Nicolaides,
A. Nicolaides,
A. Panayiotou,
N. Onland-Moret,
Y. Schouw,
G. Matullo,
G. Fiorito,
S. Guarrera,
C. Sacerdote,
N. Wareham,
C. Langenberg,
R. Scott,
J. Luan,
M. Bobák,
S. Malyutina,
A. Pająk,
R. Kubínová,
A. Tamošiūnas,
H. Pikhart,
L. Husemoen,
N. Grarup,
O. Pedersen,
T. Hansen,
A. Linneberg,
K. Simonsen,
J. Cooper,
S. Humphries,
M. Brilliant,
Terrie E. Kitchner,
H. Hakonarson,
D. Carrell,
C. McCarty,
H. Kirchner,
E. Larson,
D. Crosslin,
M. Andrade,
D. Roden,
J. Denny,
C. Carty,
Stephen J Hancock,
J. Attia,
E. Holliday,
M. O’Donnell,
S. Yusuf,
M. Chong,
G. Paré,
P. Harst,
M. A. Said,
R. N. Eppinga,
N. Verweij,
H. Snieder,
T. Christen,
D. Mook-Kanamori,
S. Gustafsson,
L. Lind,
E. Ingelsson,
E. Ingelsson,
E. Ingelsson,
R. Pazoki,
O. Franco,
A. Hofman,
A. Uitterlinden,
A. Dehghan,
A. Dehghan,
A. Teumer,
S. Baumeister,
M. Dörr,
M. Lerch,
U. Völker,
H. Völzke,
J. Ward,
J. Pell,
Danny J. Smith,
T. Meade,
A. M. Zee,
E. Baranova,
R. Young,
I. Ford,
A. Campbell,
S. Padmanabhan,
M. Bots,
D. Grobbee,
P. Froguel,
P. Froguel,
Dorothée Thuillier,
B. Balkau,
A. Bonnefond,
A. Bonnefond,
B. Cariou,
M. Smart,
Y. Bao,
M. Kumari,
A. Mahajan,
P. Ridker,
D. Chasman,
A. Reiner,
L. Lange,
M. Ritchie,
M. Ritchie,
F. Asselbergs,
J. Casas,
B. Keating,
D. Preiss,
D. Preiss,
A. Hingorani,
N. Sattar
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2017 |
8
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
164 auth.
J. Flannick,
J. Mercader,
C. Fuchsberger,
M. Udler,
A. Mahajan,
J. Wessel,
Tanya M. Teslovich,
Lizz Caulkins,
R. Koesterer,
F. Barajas-Olmos,
T. Blackwell,
E. Boerwinkle,
Jennifer A. Brody,
Federico Centeno-Cruz,
Ling Chen,
...
Siying Chen,
Cecilia Contreras-Cubas,
E. Córdova,
A. Correa,
M. Cortés,
R. DeFronzo,
L. Dolan,
Kimberly L Drews,
A. Elliott,
J. Floyd,
S. Gabriel,
M. Garay-Sevilla,
H. García-Ortiz,
M. Gross,
Sohee Han,
N. Heard-Costa,
A. Jackson,
M. Jørgensen,
H. Kang,
M. Kelsey,
Bong-Jo Kim,
H. Koistinen,
J. Kuusisto,
J. Leader,
A. Linneberg,
Ching‐Ti Liu,
Jianjun Liu,
V. Lyssenko,
A. Manning,
A. Marcketta,
J. M. Malacara-Hernández,
A. Martinez-Hernandez,
K. Matsuo,
E. Mayer‐Davis,
E. Mendoza-Caamal,
K. Mohlke,
A. Morrison,
Anne W. Ndungu,
Maggie CY Ng,
C. O’Dushlaine,
Anthony J. Payne,
C. Pihoker,
W. Post,
Michael H. Preuss,
B. Psaty,
R. Vasan,
N. Rayner,
A. Reiner,
C. Revilla-Monsalve,
N. Robertson,
N. Santoro,
C. Schurmann,
Wing Yee So,
X. Soberón,
H. Stringham,
T. Strom,
Claudia Ht Tam,
F. Thameem,
B. Tomlinson,
Jason M. Torres,
R. Tracy,
R. V. van Dam,
M. Vujković,
Shuai Wang,
R. Welch,
D. Witte,
T. Wong,
G. Atzmon,
N. Barzilai,
J. Blangero,
L. Bonnycastle,
D. Bowden,
J. Chambers,
E. Chan,
Ching-Yu Cheng,
Yoon Shin Cho,
F. Collins,
P. D. de Vries,
R. Duggirala,
B. Glaser,
Clicerio Gonzalez,
M. Gonzalez,
L. Groop,
J. Kooner,
S. Kwak,
M. Laakso,
D. Lehman,
P. Nilsson,
T. Spector,
E. Tai,
T. Tuomi,
J. Tuomilehto,
James G. Wilson,
C. Aguilar-Salinas,
E. Bottinger,
B. Burke,
D. Carey,
J. Chan,
J. Dupuis,
P. Frossard,
S. Heckbert,
M. Y. Hwang,
Young Jin Kim,
H. Kirchner,
Jong-Young Lee,
Juyoung Lee,
R. Loos,
Ronald Cw Ma,
A. Morris,
C. O’Donnell,
C. Palmer,
J. Pankow,
Kyong Soo Park,
A. Rasheed,
D. Saleheen,
X. Sim,
K. Small,
Yik Ying Teo,
C. Haiman,
C. Hanis,
B. Henderson,
L. Orozco,
Teresa Tusié-Luna,
F. Dewey,
A. Baras,
C. Gieger,
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R. Sladek,
J. Meigs,
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N. Burtt,
L. Scott,
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J. Florez,
M. McCarthy,
M. Boehnke
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7 |
2019 |
7
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Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
115 auth.
L. Wain,
L. Wain,
N. Shrine,
M. Artigas,
A. Erzurumluoglu,
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L. Bossini‐Castillo,
M. Obeidat,
A. Henry,
M. Portelli,
R. Hall,
C. Billington,
T. Rimington,
A. Fenech,
C. John,
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T. Blake,
V. Jackson,
R. Allen,
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A. Campbell,
D. Porteous,
M. Järvelin,
M. Järvelin,
M. Wielscher,
A. James,
J. Hui,
N. Wareham,
J. Zhao,
James F. Wilson,
Peter K. Joshi,
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R. Rawal,
H. Schulz,
M. Imboden,
N. Probst-Hensch,
S. Karrasch,
C. Gieger,
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O. Polašek,
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M. Kähönen,
I. Surakka,
I. Surakka,
V. Vitart,
C. Hayward,
T. Lehtimäki,
O. Raitakari,
David M. Evans,
A. J. Henderson,
C. Pennell,
Carol A. Wang,
P. Sly,
E. Wan,
R. Busch,
B. Hobbs,
A. Litonjua,
D. Sparrow,
A. Gulsvik,
P. Bakke,
J. Crapo,
T. Beaty,
N. Hansel,
R. Mathias,
I. Ruczinski,
K. Barnes,
Y. Bossé,
P. Joubert,
M. Berge,
C. Brandsma,
P. Paré,
D. Sin,
D. Nickle,
K. Hao,
O. Gottesman,
F. Dewey,
S. Bruse,
D. Carey,
H. Kirchner,
Stefan Jonsson,
G. Thorleifsson,
I. Jónsdóttir,
I. Jónsdóttir,
T. Gislason,
K. Stefánsson,
K. Stefánsson,
C. Schurmann,
G. Nadkarni,
E. Bottinger,
R. Loos,
R. Walters,
Zhengming Chen,
I. Millwood,
J. Vaucher,
O. Kurmi,
Liming Li,
Liming Li,
A. Hansell,
C. Brightling,
C. Brightling,
E. Zeggini,
M. Cho,
E. Silverman,
I. Sayers,
G. Trynka,
A. Morris,
D. Strachan,
I. Hall,
M. Tobin,
M. Tobin
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7 |
2017 |
7
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The risk of tuberculosis in children after close exposure: a systematic review and individual-participant meta-analysis
99 auth.
L. Martinez,
Olivia Cords,
C. Horsburgh,
J. Andrews,
C. Acuña-Villaorduña,
S. Ahuja,
N. Altet,
O. Augusto,
Davit Baliashvili,
S. Basu,
M. Becerra,
M. Bonnet,
W. Boom,
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H. Zar,
J. Zellweger,
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2020 |
7
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Prediction of mortality from 12-lead electrocardiogram voltage data using a deep neural network
22 auth.
S. Raghunath,
Alvaro E. Ulloa Cerna,
Linyuan Jing,
D. vanMaanen,
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M. Stumpe,
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John M. Pfeifer,
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B. Delisle,
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Dominik Beer,
C. Haggerty,
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2019 |
7
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Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
21 auth.
A. Zheutlin,
A. Zheutlin,
J. Dennis,
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2019 |
7
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Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease
44 auth.
A. Khera,
H. Won,
G. Peloso,
C. O’Dushlaine,
Dajiang J. Liu,
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P. Natarajan,
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R. McPherson,
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H. Watkins,
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J. Danesh,
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G. Abecasis,
D. Saleheen,
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S. Kathiresan
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2017 |
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