|
🐜
|
Initial sequencing and comparative analysis of the mouse genome.
222 auth.
R. Waterston,
K. Lindblad-Toh,
E. Birney,
J. Rogers,
J. F. Abril,
P. Agarwal,
R. Agarwala,
R. Ainscough,
M. Alexandersson,
Peter An,
S. Antonarakis,
J. Attwood,
R. Baertsch,
J. Bailey,
K. Barlow,
...
S. Beck,
E. M. Berry,
B. Birren,
Toby Bloom,
P. Bork,
M. Botcherby,
Nicolas L. Bray,
M. Brent,
Daniel G. Brown,
Stephen Brown,
C. Bult,
J. Burton,
Jonathan Butler,
R. Campbell,
Piero Carninci,
S. Cawley,
Francesca Chiaromonte,
A. Chinwalla,
D. Church,
M. Clamp,
C. Clee,
F. Collins,
L. Cook,
R. Copley,
A. Coulson,
O. Couronne,
James A. Cuff,
V. Curwen,
T. Cutts,
M. Daly,
R. David,
J. Davies,
K. Delehaunty,
J. Deri,
E. Dermitzakis,
Colin N. Dewey,
N. Dickens,
M. Diekhans,
S. Dodge,
I. Dubchak,
D. Dunn,
S. Eddy,
L. Elnitski,
Richard D Emes,
P. Eswara,
E. Eyras,
A. Felsenfeld,
Ginger A. Fewell,
P. Flicek,
Karen Foley,
W. Frankel,
L. Fulton,
R. Fulton,
T. Furey,
D. Gage,
R. Gibbs,
Gwênlyn Glusman,
S. Gnerre,
N. Goldman,
L. Goodstadt,
D. Grafham,
T. Graves,
E. Green,
S. Gregory,
R. Guigó,
M. Guyer,
R. Hardison,
D. Haussler,
Y. Hayashizaki,
Deana W. LaHillier,
A. Hinrichs,
W. Hlavina,
T. Holzer,
F. Hsu,
A. Hua,
T. Hubbard,
A. Hunt,
I. Jackson,
D. Jaffe,
L. S. Johnson,
Matthew C. Jones,
T. A. Jones,
A. Joy,
Michael Kamal,
E. Karlsson,
D. Karolchik,
A. Kasprzyk,
J. Kawai,
Evan Keibler,
C. Kells,
W. Kent,
Andrew W. Kirby,
D. Kolbe,
I. Korf,
R. Kucherlapati,
E. Kulbokas,
D. Kulp,
Tom Landers,
J. Leger,
Steven Leonard,
Ivica Letunic,
R. Levine,
Jia Li,
Ming Li,
C. Lloyd,
S. Lucas,
Bin Ma,
D. Maglott,
E. Mardis,
L. Matthews,
E. Mauceli,
John Mayer,
M. McCarthy,
W. McCombie,
Stuart Mclaren,
K. McLay,
J. McPherson,
J. Meldrim,
B. Meredith,
J. Mesirov,
W. Miller,
T. Miner,
Emmanuel Mongin,
K. Montgomery,
M. Morgan,
R. Mott,
J. Mullikin,
D. Muzny,
W. Nash,
J. Nelson,
M. Nhan,
R. Nicol,
Z. Ning,
C. Nusbaum,
M. O’Connor,
Y. Okazaki,
K. Oliver,
E. Overton-Larty,
L. Pachter,
Genís Parra,
K. Pepin,
Jane L. Peterson,
P. Pevzner,
R. Plumb,
C. Pohl,
Alexander Poliakov,
Tracy C. Ponce,
C. Ponting,
Simon C. Potter,
M. Quail,
A. Reymond,
B. Roe,
K. Roskin,
E. Rubin,
A. Rust,
R. Santos,
V. Sapojnikov,
Brian Schultz,
J. Schultz,
M. Schwartz,
S. Schwartz,
C. Scott,
S. Seaman,
S. Searle,
Ted Sharpe,
A. Sheridan,
R. Shownkeen,
S. Sims,
J. Singer,
G. Slater,
A. Smit,
Douglas Smith,
B. Spencer,
Arne Stabenau,
N. Stange-thomann,
C. Sugnet,
M. Suyama,
G. Tesler,
J. Thompson,
D. Torrents,
E. Trevaskis,
J. Tromp,
C. Ucla,
A. Ureta-Vidal,
J. Vinson,
A. Niederhausern,
C. Wade,
M. Wall,
R. Weber,
R. Weiss,
M. Wendl,
A. West,
K. Wetterstrand,
R. Wheeler,
S. Whelan,
Jamey Wierzbowski,
D. Willey,
Sophie T. Williams,
R. Wilson,
E. Winter,
K. Worley,
D. Wyman,
Shan Yang,
Shiaw-Pyng Yang,
E. Zdobnov,
M. Zody,
E. Lander
|
12 |
2002 |
12
🐜
|
|
🐜
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Rare coding variants in ten genes confer substantial risk for schizophrenia
111 auth.
T. Singh,
T. Poterba,
D. Curtis,
H. Akil,
M. A. Al Eissa,
J. Barchas,
N. Bass,
T. Bigdeli,
G. Breen,
E. Bromet,
Peter F. Buckley,
W. Bunney,
J. Bybjerg-Grauholm,
W. Byerley,
S. Chapman,
...
Wei J. Chen,
C. Churchhouse,
N. Craddock,
C. Cusick,
L. DeLisi,
S. Dodge,
M. Escamilla,
S. Eskelinen,
A. Fanous,
S. Faraone,
A. Fiorentino,
L. Francioli,
S. Gabriel,
D. Gage,
S. G. Gagliano Taliun,
A. Ganna,
G. Genovese,
D. Glahn,
J. Grove,
M. Hall,
E. Hämäläinen,
H. Heyne,
M. Holi,
D. Hougaard,
D. Howrigan,
Hailiang Huang,
H. Hwu,
R. Kahn,
H. Kang,
K. Karczewski,
G. Kirov,
J. Knowles,
F. Lee,
D. Lehrer,
F. Lescai,
D. Malaspina,
S. Marder,
S. Mccarroll,
A. McIntosh,
H. Medeiros,
L. Milani,
C. Morley,
D. Morris,
P. Mortensen,
R. Myers,
M. Nordentoft,
N. O’Brien,
A. M. Olivares,
D. Ongur,
W. Ouwehand,
D. Palmer,
T. Paunio,
D. Quested,
M. Rapaport,
E. Rees,
B. Rollins,
F. Satterstrom,
A. Schatzberg,
E. Scolnick,
L. Scott,
Sally Sharp,
P. Sklar,
J. Smoller,
J. Sobell,
M. Solomonson,
E. Stahl,
C. Stevens,
J. Suvisaari,
G. Tiao,
S. Watson,
N. Watts,
D. Blackwood,
A. Børglum,
B. Cohen,
A. Corvin,
T. Esko,
N. Freimer,
S. Glatt,
C. Hultman,
A. McQuillin,
A. Palotie,
C. Pato,
M. Pato,
A. Pulver,
D. St. Clair,
M. Tsuang,
M. Vawter,
J. Walters,
T. Werge,
R. Ophoff,
Patrick F. Sullivan,
M. Owen,
M. Boehnke,
M. O’Donovan,
B. Neale,
M. Daly
|
8 |
2022 |
8
🐜
|
|
🐜
|
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
72 auth.
Jack M. Fu,
F. Satterstrom,
Minshi Peng,
H. Brand,
Ryan L. Collins,
Shan Dong,
Brie Wamsley,
L. Klei,
Lily Wang,
Stephanie P Hao,
C. Stevens,
C. Cusick,
M. Babadi,
E. Banks,
Brett L. Collins,
...
S. Dodge,
S. Gabriel,
L. Gauthier,
Samuel K. Lee,
Lindsay Liang,
A. Ljungdahl,
B. Mahjani,
Laura G. Sloofman,
A. Smirnov,
M. Barbosa,
C. Betancur,
A. Brusco,
B. Chung,
E. Cook,
M. Cuccaro,
E. Domenici,
G. Ferrero,
J. Gargus,
G. Herman,
I. Hertz-Picciotto,
P. Maciel,
D. Manoach,
M. Passos-Bueno,
A. Persico,
A. Renieri,
J. Sutcliffe,
F. Tassone,
E. Trabetti,
Gabriele Campos,
S. Cardaropoli,
D. Carli,
Marcus C. Y. Chan,
C. Fallerini,
E. Giorgio,
A. C. Girardi,
Emily Hansen-Kiss,
S. L. Lee,
Carla Lintas,
Yunin J. Ludeña,
Rachel Nguyen,
Lisa Pavinato,
M. Pericak-Vance,
I. Pessah,
R. Schmidt,
Moyra J. Smith,
C. I. Costa,
S. Trajkova,
J. Wang,
M. Yu,
D. Cutler,
Silvia De Rubeis,
J. Buxbaum,
M. Daly,
B. Devlin,
K. Roeder,
Stephan J Sanders,
M. Talkowski
|
8 |
2022 |
8
🐜
|
|
🐜
|
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
17 auth.
Maura Costello,
M. Fleharty,
Justin Abreu,
Y. Farjoun,
S. Ferriera,
Laurie Holmes,
Brian Granger,
L. Green,
Tom Howd,
Tamara Mason,
...
Gina Vicente,
Michael Dasilva,
W. Brodeur,
Timothy DeSmet,
S. Dodge,
N. Lennon,
S. Gabriel
|
7 |
2017 |
7
🐜
|
|
🐜
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia
42 auth.
T. Singh,
T. Poterba,
D. Curtis,
H. Akil,
M. A. Al Eissa,
J. Barchas,
N. Bass,
T. Bigdeli,
G. Breen,
E. Bromet,
P. Buckley,
W. Bunney,
J. Bybjerg-Grauholm,
W. Byerley,
S. Chapman,
...
W. Chen,
C. Churchhouse,
N. Craddock,
C. Curtis,
C. Cusick,
L. DeLisi,
S. Dodge,
M. Escamilla,
S. Eskelinen,
A. Fanous,
S. Faraone,
A. Fiorentino,
L. Francioli,
S. Gabriel,
D. Gage,
S. G. Gagliano Taliun,
A. Ganna,
G. Genovese,
D. Glahn,
J. Grove,
M. Hall,
E. Hamalainen,
H. Heyne,
M. Holi,
D. Hougaard,
D. Howrigan,
H. Huang
|
6 |
2020 |
6
🐜
|
|
🐜
|
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.
235 auth.
H. Zouk,
E. Venner,
N. Lennon,
D. Muzny,
Debra J. Abrams,
Samuel E. Adunyah,
Ladia H. Albertson-Junkans,
Darren C. Ames,
Paul S. Appelbaum,
Samuel Aronson,
S. Aufox,
Lawrence J. Babb,
Adithya Balasubramanian,
Hana Bangash,
Melissa A. Basford,
...
L. Bastarache,
Samantha Baxter,
Meckenzie Behr,
Barbara Benoit,
E. Bhoj,
S. Bielinski,
S. Bland,
C. Blout,
K. Borthwick,
Erwin P. Bottinger,
Mark J. Bowser,
Harrison Brand,
Murray H. Brilliant,
W. Brodeur,
Pedro J. Caraballo,
D. Carrell,
Andrew Carroll,
B. Almoguera,
Lisa Castillo,
Victor M. Castro,
Gauthami Chandanavelli,
Theodore Chiang,
R. L. Chisholm,
K. Christensen,
Wendy K. Chung,
Christopher G. Chute,
Brittany City,
Beth Cobb,
John J. Connolly,
Paul K. Crane,
Katherine D. Crew,
D. Crosslin,
Mariza de Andrade,
Jessica De la Cruz,
Shawn Denson,
Joshua C. Denny,
Tim DeSmet,
O. Dikilitas,
Christopher Friedrich,
Stephanie M. Fullerton,
Birgit H Funke,
S. Gabriel,
V. Gainer,
A. Gharavi,
A. Glazer,
J. Glessner,
Jessica Goehringer,
A. Gordon,
Chet Graham,
Robert C. Green,
Justin H. Gundelach,
J. Dayal,
Heather S. Hain,
H. Hakonarson,
M. Harden,
John Harley,
M. Harr,
Andrea L. Hartzler,
M. G. Hayes,
S. Hebbring,
Nora B. Henrikson,
Andrew Hershey,
Christin Hoell,
Ingrid A. Holm,
K. M. Howell,
G. Hripcsak,
Jianhong Hu,
Gail P. Jarvik,
J. Jayaseelan,
Yunyun Jiang,
Yoonjung Yoonie Joo,
Sheethal Jose,
N. Josyula,
A. Justice,
Sara E Kalla,
D. Kalra,
Elizabeth W Karlson,
Melissa A. Kelly,
Brendan J. Keating,
E. Kenny,
Dustin Key,
K. Kiryluk,
Terrie E. Kitchner,
B. Klanderman,
Eric W Klee,
D. Kochan,
V. Korchina,
L. Kottyan,
C. Kovar,
Emily M. Kudalkar,
I. Kullo,
Philip Lammers,
E. Larson,
Matthew S. Lebo,
Magalie S Leduc,
Ming Ta Michael Lee,
K. Leppig,
Nancy D. Leslie,
Rongling Li,
Wayne H. Liang,
Chiao-Feng Lin,
J. Linder,
N. Lindor,
T. Lingren,
J. Linneman,
Cong Liu,
Wen Liu,
Xiuping Liu,
John Lynch,
Hayley Lyon,
Alyssa Macbeth,
Harshad S. Mahadeshwar,
Lisa Mahanta,
Brad Malin,
Teri A Manolio,
M. Marasà,
Keith Marsolo,
Michael J. Dinsmore,
S. Dodge,
Elizabeth D. Hynes,
Phil Dunlea,
Todd L. Edwards,
Christine M. Eng,
D. Fasel,
A. Fedotov,
Q. Feng,
M. Fleharty,
Andrea Foster,
R. Freimuth,
Michelle L McGowan,
Elizabeth M. McNally,
Jim Meldrim,
F. Mentch,
J. Mosley,
S. Mukherjee,
Thomas E. Mullen,
Jesse Muniz,
David R. Murdock,
Shawn N. Murphy,
M. Murugan,
M. Myers,
B. Namjou,
Yizhao Ni,
A. Obeng,
R. Onofrio,
Casey Overby Taylor,
T. Person,
Josh F. Peterson,
Lynn Petukhova,
Cassandra J. Pisieczko,
Siddharth Pratap,
C. Prows,
M. Puckelwartz,
A. Rahm,
Ritika Raj,
J. Ralston,
A. Ramaprasan,
Andrea Ramirez,
Luke V. Rasmussen,
L. Rasmussen-Torvik,
H. Rasouly,
Soumya Raychaudhuri,
M. Ritchie,
Catherine Rives,
Beenish Riza,
Dan M. Roden,
E. Rosenthal,
Avni Santani,
D. Schaid,
Steven E. Scherer,
Stuart Scott,
Aaron Scrol,
Soumitra Sengupta,
Ning Shang,
Himanshu Sharma,
Richard R. Sharp,
Rajbir Singh,
P. Sleiman,
Kara Slowik,
Joshua C. Smith,
Maureen E. Smith,
J. Smoller,
Sunghwan Sohn,
I. Stanaway,
J. Starren,
Mary Stroud,
J. Su,
Kasia Tolwinski,
S. V. Van Driest,
Sean M. Vargas,
Matthew Varugheese,
David Veenstra,
M. Verbitsky,
Gina Vicente,
Michael Wagner,
K. Walker,
Theresa L. Walunas,
Liwen Wang,
Qiaoyan Wang,
Wei-Qi Wei,
Scott T. Weiss,
Georgia L. Wiesner,
Q. Wells,
Chunhua Weng,
Peter S. White,
Ken L. Wiley,
Janet L. Williams,
Marc S. Williams,
Michael W. Wilson,
Leora Witkowski,
Laura Woods,
Betty Woolf,
Tsung-Jung Wu,
J. Wynn,
Yaping Yang,
Victoria Yi,
Ge Zhang,
Lan Zhang,
H. L. Rehm,
R. A. Gibbs
|
6 |
2019 |
6
🐜
|
|
🐜
|
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility
130 auth.
A. Sazonovs,
C. Stevens,
G. Venkataraman,
K. Yuan,
B. Avila,
M. Abreu,
T. Ahmad,
M. Allez,
A. Ananthakrishnan,
G. Atzmon,
A. Baras,
J. Barrett,
N. Barzilai,
L. Beaugerie,
Ashley H Beecham,
...
C. Bernstein,
A. Bitton,
B. Bokemeyer,
A. Chan,
D. Chung,
I. Cleynen,
J. Cosnes,
D. Cutler,
A. Daly,
O. Damas,
L. Datta,
Noor B. Dawany,
M. Devoto,
S. Dodge,
E. Ellinghaus,
L. Fachal,
M. Farkkila,
W. Faubion,
M. Ferreira,
D. Franchimont,
S. Gabriel,
T. Ge,
M. Georges,
K. Gettler,
M. Giri,
Benjamin Glaser,
S. Goerg,
P. Goyette,
D. Graham,
E. Hämäläinen,
T. Haritunians,
G. Heap,
M. Hiltunen,
M. Hoeppner,
J. Horowitz,
P. Irving,
V. Iyer,
C. Jalas,
J. Kelsen,
H. Khalili,
B. Kirschner,
K. Kontula,
J. Koskela,
S. Kugathasan,
J. Kupčinskas,
C. Lamb,
M. Laudes,
C. Lévesque,
A. Levine,
J. Lewis,
C. Liefferinckx,
B. Loescher,
E. Louis,
J. Mansfield,
Sandra May,
J. McCauley,
E. Mengesha,
M. Mni,
P. Moayyedi,
C. J. Moran,
R. Newberry,
Sirimon O’Charoen,
David T. Okou,
B. Oldenburg,
H. Ostrer,
A. Palotie,
J. Paquette,
J. Pekow,
I. Peter,
M. Pierik,
C. Ponsioen,
Nikolas Pontikos,
N. Prescott,
A. Pulver,
Souad Rahmouni,
D. Rice,
P. Saavalainen,
B. Sands,
R. Sartor,
E. Schiff,
S. Schreiber,
L. P. Schumm,
A. Segal,
P. Seksik,
R. Shawky,
S. Sheikh,
M. Silverberg,
A. Simmons,
Jurgita Skeiceviciene,
H. Sokol,
M. Solomonson,
Hari Somineni,
Dylan Sun,
S. Targan,
D. Turner,
H. Uhlig,
A. E. van der Meulen,
S. Vermeire,
S. Verstockt,
M. Voskuil,
H. Winter,
J. Young,
R. Duerr,
A. Franke,
S. Brant,
Judy H. Cho,
R. Weersma,
M. Parkes,
R. Xavier,
M. Rivas,
J. Rioux,
D. McGovern,
Hailiang Huang,
C. Anderson,
M. Daly
|
6 |
2022 |
6
🐜
|
|
🐜
|
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations
39 auth.
Alicia R. Martin,
Elizabeth G. Atkinson,
S. Chapman,
A. Stevenson,
Rocky E. Stroud,
T. Abebe,
D. Akena,
Melkam Alemayehu,
F. Ashaba,
L. Atwoli,
Tera Bowers,
L. Chibnik,
M. Daly,
Timothy DeSmet,
S. Dodge,
...
A. Fekadu,
S. Ferriera,
B. Gelaye,
Stella Gichuru,
W. Injera,
R. James,
S. Kariuki,
Gabriel Kigen,
K. Koenen,
E. Kwobah,
Joseph Kyebuzibwa,
L. Majara,
H. Musinguzi,
Rehema M. Mwema,
B. Neale,
Carter P Newman,
C. Newton,
Joseph K. Pickrell,
R. Ramesar,
Welelta Shiferaw,
Dan J Stein,
Solomon Teferra,
C. van der Merwe,
Z. Zingela
|
5 |
2020 |
5
🐜
|
|
🐜
|
Pathogen discovery from human tissue by sequence-based computational subtraction.
12 auth.
Yaohui Xu,
N. Stange-thomann,
G. Weber,
R. Bo,
S. Dodge,
R. David,
...
Karen Foley,
J. Beheshti,
N. Harris,
B. Birren,
E. Lander,
M. Meyerson
|
5 |
2003 |
5
🐜
|
|
🐜
|
Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform
39 auth.
Gilad Almogy,
Mark Pratt,
Florian C. Oberstrass,
Linda Lee,
Dan J. Mazur,
Nate Beckett,
Omer Barad,
Ilya Soifer,
Eddie Perelman,
Yoav Etzioni,
Martin Sosa,
April Jung,
Tyson Clark,
G. Lithwick-Yanai,
Sarah Pollock,
...
Gil Hornung,
Maya Levy,
M. Coole,
Tom Howd,
Megan Shand,
Y. Farjoun,
James Emery,
Giles Hall,
Samuel K. Lee,
Takuto Sato,
Ricky Magner,
Sophie Low,
Andrew Bernier,
Bharathi Gandi,
Jack Stohlman,
Corey M. Nolet,
Siobhán Donovan,
B. Blumenstiel,
Michelle Cipicchio,
S. Dodge,
E. Banks,
N. Lennon,
S. Gabriel,
D. Lipson
|
5 |
2022 |
5
🐜
|
|
🐜
|
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
65 auth.
Jack M. Fu,
F. Satterstrom,
Minshi Peng,
H. Brand,
Ryan L. Collins,
Shan Dong,
L. Klei,
C. Stevens,
C. Cusick,
M. Babadi,
E. Banks,
B. Collins,
S. Dodge,
S. Gabriel,
L. Gauthier,
...
Samuel K. Lee,
Lindsay Liang,
A. Ljungdahl,
B. Mahjani,
Laura G. Sloofman,
A. Smirnov,
M. Barbosa,
A. Brusco,
B. Chung,
M. Cuccaro,
E. Domenici,
G. Ferrero,
J. Gargus,
G. Herman,
I. Hertz-Picciotto,
P. Maciel,
D. Manoach,
M. Passos-Bueno,
A. Persico,
A. Renieri,
F. Tassone,
E. Trabetti,
Gabriele Campos,
Marcus C. Y. Chan,
C. Fallerini,
E. Giorgio,
A. Girard,
Emily Hansen-Kiss,
S. L. Lee,
Carla Lintas,
Yunin J. Ludeña,
Rachel Nguyen,
Lisa Pavinato,
M. Pericak-Vance,
Isaac Pessah,
E. Riberi,
R. Schmidt,
Moyra J. Smith,
Claudia I. C. Souza,
S. Trajkova,
J. Wang,
M. Yu,
D. Cutler,
Silvia De Rubeis,
J. Buxbaum,
M. Daly,
B. Devlin,
K. Roeder,
Stephan J Sanders,
M. Talkowski
|
5 |
2021 |
5
🐜
|
|
🐜
|
Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility
127 auth.
A. Sazonovs,
C. Stevens,
G. Venkataraman,
K. Yuan,
B. Avila,
M. Abreu,
T. Ahmad,
M. Allez,
A. Ananthakrishnan,
G. Atzmon,
A. Baras,
J. Barrett,
N. Barzilai,
L. Beaugerie,
Ashley H Beecham,
...
C. Bernstein,
A. Bitton,
B. Bokemeyer,
A. Chan,
D. Chung,
I. Cleynen,
J. Cosnes,
D. Cutler,
A. Daly,
O. Damas,
L. Datta,
Noor B. Dawany,
M. Devoto,
S. Dodge,
E. Ellinghaus,
L. Fachal,
M. Farkkila,
W. Faubion,
M. Ferreira,
D. Franchimont,
S. Gabriel,
M. Georges,
K. Gettler,
M. Giri,
B. Glaser,
S. Goerg,
P. Goyette,
D. Graham,
E. Hämäläinen,
T. Haritunians,
Graham A. R. Heap,
M. Hiltunen,
M. Hoeppner,
J. Horowitz,
P. Irving,
V. Iyer,
C. Jalas,
J. Kelsen,
H. Khalili,
B. Kirschner,
K. Kontula,
J. Koskela,
S. Kugathasan,
J. Kupčinskas,
C. Lamb,
M. Laudes,
A. Levine,
James Lewis,
C. Liefferinckx,
B. Loescher,
É. Louis,
J. Mansfield,
Sandra May,
J. McCauley,
E. Mengesha,
M. Mni,
P. Moayyedi,
C. J. Moran,
R. Newberry,
Sirimon O’Charoen,
David T. Okou,
B. Oldenburg,
H. Ostrer,
A. Palotie,
J. Pekow,
I. Peter,
M. Pierik,
C. Ponsioen,
Nikolas Pontikos,
N. Prescott,
A. Pulver,
Souad Rahmouni,
D. Rice,
P. Saavalainen,
B. Sands,
R. Sartor,
E. Schiff,
S. Schreiber,
L. Schuum,
A. Segal,
P. Seksik,
R. Shawky,
S. Sheikh,
M. Silverberg,
A. Simmons,
Jurgita Skeiceviciene,
H. Sokol,
M. Solomonson,
Hari Somineni,
Dylan Sun,
S. Targan,
D. Turner,
H. Uhlig,
A. E. van der Meulen,
S. Vermeire,
S. Verstockt,
M. Voskuil,
H. Winter,
J. Young,
R. Duerr,
A. Franke,
S. Brant,
Judy H. Cho,
R. Weersma,
M. Parkes,
R. Xavier,
M. Rivas,
J. Rioux,
D. McGovern,
Hailiang Huang,
C. Anderson,
M. Daly
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