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High-throughput discovery of novel developmental phenotypes
159 auth.
M. Dickinson,
A. Flenniken,
Xiao Ji,
L. Teboul,
M. Wong,
Jacqueline K. White,
T. Meehan,
W. Weninger,
Henrik Westerberg,
H. Adissu,
Candice N. Baker,
Lynette R. Bower,
James M. Brown,
L. B. Caddle,
Francesco Chiani,
...
Dave Clary,
James Cleak,
M. Daly,
J. Denegre,
B. Doe,
M. Dolan,
Sarah Edie,
H. Fuchs,
V. Gailus-Durner,
A. Galli,
A. Gambadoro,
Juan J. Gallegos,
Shiying Guo,
N. Horner,
Chih-Wei Hsu,
S. Johnson,
Sowmya Kalaga,
L. C. Keith,
L. Lanoue,
T. Lawson,
M. Lek,
M. Mark,
S. Marschall,
J. Mason,
Melissa L. McElwee,
S. Newbigging,
L. Nutter,
Kevin A. Peterson,
R. Ramírez‐Solís,
D. Rowland,
E. Ryder,
K. Samocha,
J. Seavitt,
M. Selloum,
Zsombor Szoke-Kovacs,
Masaru Tamura,
Amanda G. Trainor,
Ilinca Tudose,
S. Wakana,
Jonathan Warren,
O. Wendling,
David B. West,
Leeyean Wong,
A. Yoshiki,
M. Mckay,
Barbara Urban,
C. Lund,
Erin D. Froeter,
Taylor LaCasse,
A. Mehalow,
Emily R. Gordon,
L. Donahue,
R. Taft,
P. Kutney,
S. Dion,
L. Goodwin,
S. Kales,
Rachel Urban,
K. Palmer,
F. Pertuy,
D. Bitz,
Bruno Weber,
Patrice Goetz-Reiner,
Hughes Jacobs,
E. le Marchand,
Amal El Amri,
Leila El Fertak,
Hamid Ennah,
D. Ali-Hadji,
A. Ayadi,
Marie Wattenhofer-Donzé,
S. Jacquot,
P. André,
M. Birling,
G. Pavlovic,
T. Sorg,
Iva Frank Morse Benso,
Iva Morse,
Frank Benso,
Michelle E. Carol Jackie Samantha Stewart Copley Harrison Joynson,
M. Stewart,
Caroline Copley,
J. Harrison,
Sam Joynson,
Ruolin Guo,
D. Qu,
S. Spring,
Lisa X. Yu,
J. Ellegood,
L. Morikawa,
Xueyuan Shang,
P. Feugas,
A. Creighton,
P. Castellanos Pentón,
Ozge Danisment,
Nicola Griggs,
Catherine Tudor,
A. Green,
Cecilia Icoresi Mazzeo,
E. Siragher,
Charlotte Lillistone,
E. Tuck,
Diane Gleeson,
Debarati Sethi,
T. Bayzetinova,
Jonathan Burvill,
Bishoy Habib,
Lauren Weavers,
R. Maswood,
Evelina Miklejewska,
Michael Woods,
E. Grau,
Stuart Newman,
Caroline Sinclair,
Ellen Brown,
Shinya Mizuho Ayumi Ayabe Iwama Murakami,
Shinya Ayabe,
M. Iwama,
A. Murakami,
W. Wurst,
D. MacArthur,
G. Tocchini-Valentini,
Xiang Gao,
Paul Flicek,
A. Bradley,
W. Skarnes,
M. Justice,
H. Parkinson,
Mark W. Moore,
S. Wells,
R. Braun,
K. Svenson,
M. D. de Angelis,
Y. Hérault,
T. Mohun,
A. Mallon,
R. Henkelman,
Steve D. M. Brown,
D. Adams,
K. Lloyd,
C. McKerlie,
A. Beaudet,
M. Bucan,
S. Murray
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9 |
2016 |
9
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Glypican-3–Deficient Mice Exhibit Developmental Overgrowth and Some of the Abnormalities Typical of Simpson-Golabi-Behmel Syndrome
26 auth.
D. Cano-Gauci,
D. Cano-Gauci,
Howard H. Song,
Howard H. Song,
Huiling Yang,
Huiling Yang,
C. McKerlie,
B. Choo,
B. Choo,
W. Shi,
W. Shi,
R. Pullano,
R. Pullano,
T. Piscione,
S. Grisaru,
...
Shawn Soon,
L. Sedlackova,
A. Tanswell,
T. Mak,
T. Mak,
H. Yeger,
G. Lockwood,
G. Lockwood,
N. Rosenblum,
J. Filmus,
J. Filmus
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8 |
1999 |
8
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The mammalian gene function resource: the international knockout mouse consortium
84 auth.
A. Bradley,
K. Anastassiadis,
A. Ayadi,
J. Battey,
C. Bell,
M. Birling,
Joanna Bottomley,
Steve D. M. Brown,
Antje Bürger,
C. Bult,
Wendy Bushell,
F. Collins,
C. Desaintes,
B. Doe,
A. Economides,
...
J. Eppig,
R. Finnell,
R. Finnell,
C. Fletcher,
M. Fray,
D. Frendewey,
Roland H. Friedel,
R. Friedel,
F. Grosveld,
Jens Hansen,
Y. Hérault,
G. Hicks,
A. Hörlein,
Richard Houghton,
M. H. Angelis,
D. Huylebroeck,
V. Iyer,
P. Jong,
J. Kadin,
Cornelia Kaloff,
K. Kennedy,
M. Koutsourakis,
K. C. K. Lloyd,
S. Marschall,
J. Mason,
C. McKerlie,
M. P. McLeod,
H. V. Melchner,
Mark W. Moore,
A. Mujica,
A. Mujica,
A. Nagy,
M. Nefedov,
L. Nutter,
G. Pavlovic,
J. Peterson,
J. Pollock,
R. Ramírez‐Solís,
D. Rancourt,
M. Raspa,
J. Remacle,
M. Ringwald,
B. Rosen,
N. Rosenthal,
J. Rossant,
P. R. Noppinger,
Edward Ryder,
J. Schick,
F. Schnütgen,
P. Schofield,
C. Seisenberger,
M. Selloum,
E. Simpson,
W. Skarnes,
D. Smedley,
D. Smedley,
W. Stanford,
A. F. Stewart,
Kevin R. Stone,
Kate Swan,
Hamsa D. Tadepally,
L. Teboul,
G. Tocchini-Valentini,
D. Valenzuela,
A. West,
K. Yamamura,
Y. Yoshinaga,
W. Wurst,
W. Wurst
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8 |
2012 |
8
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C5L2 is critical for the biological activities of the anaphylatoxins C5a and C3a
10 auth.
N. Chen,
C. Mirtsos,
Daniel Suh,
Yong-Chen Lu,
Wen-Jye Lin,
C. McKerlie,
...
TaeWeon Lee,
H. Baribault,
H. Tian,
W. Yeh
|
8 |
2007 |
8
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Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
17 auth.
Ming Chen,
D. Tomkins,
W. Auerbach,
C. McKerlie,
H. Youssoufian,
Lili Liu,
O. Gan,
M. Carreau,
A. Auerbach,
T. Groves,
...
C. Guidos,
M. Freedman,
J. Cross,
D. Percy,
J. Dick,
A. Joyner,
M. Buchwald
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8 |
1996 |
8
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|
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A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia
35 auth.
A. Flenniken,
L. Osborne,
Nicole Anderson,
N. Ciliberti,
Craig Fleming,
J. Gittens,
Xiang-qun Gong,
L. Kelsey,
Crystal S Lounsbury,
Luisa Moreno,
B. Nieman,
K. Peterson,
D. Qu,
W. Roscoe,
Qing Shao,
...
Dan Tong,
Gregory I L Veitch,
I. Voronina,
I. Vukobradovic,
G. Wood,
Yonghong Zhu,
R. Zirngibl,
J. Aubin,
Donglin Bai,
B. Bruneau,
M. Grynpas,
J. Henderson,
R. Henkelman,
C. McKerlie,
J. Sled,
W. Stanford,
D. Laird,
G. Kidder,
S. Adamson,
J. Rossant
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7 |
2005 |
7
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Prevalence of sexual dimorphism in mammalian phenotypic traits
202 auth.
N. Karp,
J. Mason,
A. Beaudet,
Y. Benjamini,
Lynette R. Bower,
R. Braun,
Steve D. M. Brown,
E. Chesler,
M. Dickinson,
A. Flenniken,
H. Fuchs,
M. Angelis,
Xiang Gao,
Shiying Guo,
Simon Greenaway,
...
R. Heller,
Y. Hérault,
M. Justice,
N. Kurbatova,
C. Lelliott,
K. Lloyd,
A. Mallon,
J. Mank,
H. Masuya,
C. McKerlie,
T. Meehan,
R. Mott,
S. Murray,
H. Parkinson,
R. Ramírez‐Solís,
Luis A. Santos,
J. Seavitt,
D. Smedley,
T. Sorg,
A. Speak,
K. Steel,
K. Svenson,
Y. Obata,
Tomohiro Suzuki,
Masaru Tamura,
H. Kaneda,
T. Furuse,
Kimio Kobayashi,
I. Miura,
Ikuko Yamada,
Nobuhiko Tanaka,
A. Yoshiki,
Shinya Ayabe,
Dave Clary,
H. Tolentino,
Michael Schuchbauer,
Todd Tolentino,
Joseph Aprile,
Sheryl M. Pedroia,
L. Kelsey,
I. Vukobradovic,
Zorana Berberovic,
Celeste Owen,
D. Qu,
Ruolin Guo,
S. Newbigging,
L. Morikawa,
Napoleon Law,
Xueyuan Shang,
P. Feugas,
Yanchun Wang,
Mohammad Eskandarian,
Yingchun Zhu,
L. Nutter,
P. Pentón,
Valerie Laurin,
Shannon Clarke,
Qing Lan,
Khondoker Sohel,
David Miller,
Gregory Clark,
Jane Hunter,
Jorge Cabezas,
Mohammed Bubshait,
Tr Carroll,
Sandra Tondat,
Suzanne MacMaster,
M. Pereira,
M. Gertsenstein,
Ozge Danisment,
E. Jacob,
A. Creighton,
Gillian T. Sleep,
James Clark,
L. Teboul,
M. Fray,
Adam Caulder,
Jorik Loeffler,
G. Codner,
James Cleak,
S. Johnson,
Zsombor Szoke-Kovacs,
A. Radage,
M. Maritati,
J. Mianné,
Wendy Gardiner,
Susan Allen,
H. Cater,
M. Stewart,
Piia Keskivali-Bond,
Caroline Sinclair,
Ellen Brown,
B. Doe,
H. Wardle-Jones,
Evelyn Grau,
Nicola Griggs,
Mike Woods,
Helen Kundi,
M. Griffiths,
Christian Kipp,
David G. Melvin,
N. P. Raj,
S. Holroyd,
David J. Gannon,
Rafael Alcantara,
A. Galli,
Y. Hooks,
Catherine Tudor,
A. Green,
F. Kussy,
E. Tuck,
E. Siragher,
Simon A. Maguire,
D. Lafont,
Valerie E. Vancollie,
Selina Pearson,
Amy S. Gates,
Mark Sanderson,
Carl Shannon,
Lauren F. E. Anthony,
M. Sumowski,
R. McLaren,
A. Świątkowska,
Christopher Isherwood,
E. Cambridge,
Heather M. Wilson,
Susana Caetano,
C. Mazzeo,
M. Dąbrowska,
Charlotte Lillistone,
J. Estabel,
A. K. Maguire,
Laura-Anne Roberson,
G. Pavlovic,
M. Birling,
Wattenhofer-Donze Marie,
S. Jacquot,
A. Ayadi,
D. Ali-Hadji,
Philippe Charles,
P. André,
E. le Marchand,
Amal El Amri,
Laurent Vasseur,
Antonio Aguilar-Pimentel,
L. Becker,
Irina Treise,
K. Moreth,
T. Stoeger,
O. Amarie,
F. Neff,
W. Wurst,
R. Bekeredjian,
M. Ollert,
T. Klopstock,
J. Calzada-Wack,
S. Marschall,
R. Brommage,
R. Steinkamp,
C. Lengger,
Manuela A. Östereicher,
H. Maier,
Claudia Stoeger,
S. Leuchtenberger,
A. Yildrim,
L. Garrett,
S. Hölter,
Annemarie Zimprich,
C. Seisenberger,
Antje Bürger,
J. Graw,
O. Eickelberg,
A. Zimmer,
Eckhard Wolf,
D. Busch,
M. Klingenspor,
C. Schmidt‐Weber,
V. Gailus-Durner,
J. Beckers,
B. Rathkolb,
J. Rozman,
S. Wakana,
David B. West,
S. Wells,
Henrik Westerberg,
Shay Yaacoby,
Jacqueline K. White
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7 |
2017 |
7
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Disease Model Discovery from 3,328 Gene Knockouts by The International Mouse Phenotyping Consortium
63 auth.
T. Meehan,
N. Conte,
David B. West,
Julius O. B. Jacobsen,
J. Mason,
Jonathan Warren,
Chen Ck,
Ilinca Tudose,
Mike Relac,
Peter Matthews,
N. Karp,
Luis A. Santos,
T. Fiegel,
Natalie Ring,
Henrik Westerberg,
...
Simon Greenaway,
D. Sneddon,
Hugh Morgan,
G. Codner,
M. Stewart,
James B. Brown,
N. Horner,
M. Haendel,
N. Washington,
C. Mungall,
Corey L. Reynolds,
Juan J. Gallegos,
Gailus-Durner,
T. Sorg,
G. Pavlovic,
Lynette R. Bower,
M. Oore,
Iva Morse,
Xiang Gao,
G. Tocchini-Valentini,
Y. Obata,
Soo Ick Cho,
J. Seong,
J. Seavitt,
A. Beaudet,
M. Dickinson,
Y. Hérault,
W. urst,
de Angelis Mh,
Lloyd Kck,
A. Flenniken,
Nutter Lmj,
S. Newbigging,
C. McKerlie,
M. Justice,
S. Murray,
K. Svenson,
R. Braun,
Jacqui White,
A. Bradley,
Paul Flicek,
S. Wells,
W. Skarnes,
D. Adams,
Helen E. Parkinson,
A. Mallon,
Brown Sdm.,
D. Smedley
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7 |
2017 |
7
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|
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Atelectasis causes alveolar injury in nonatelectatic lung regions.
10 auth.
S. Tsuchida,
D. Engelberts,
V. Peltekova,
N. Hopkins,
H. Frndova,
P. Babyn,
...
C. McKerlie,
M. Post,
P. McLoughlin,
B. Kavanagh
|
7 |
2006 |
7
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Neto1 Is a Novel CUB-Domain NMDA Receptor–Interacting Protein Required for Synaptic Plasticity and Learning
14 auth.
David Ng,
G. Pitcher,
R. Szilard,
A. Sertié,
Marijana Kanisek,
S. Clapcote,
T. Lipina,
Lorraine V. Kalia,
D. Joo,
C. McKerlie,
...
M. Cortez,
J. Roder,
M. Salter,
R. Mcinnes
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7 |
2009 |
7
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|
🐬
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Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia.
Jasmine C. Wong,
N. Alon,
C. McKerlie,
Jun R Huang,
M. Meyn,
M. Buchwald
|
7 |
2003 |
7
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