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The Genotype-Tissue Expression (GTEx) project
127 auth.
J. Lonsdale,
Jeffrey A. Thomas,
Mike Salvatore,
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R. Hasz,
Gary Walters,
Fernando García,
Nancy Young,
B. Foster,
Michael Moser,
E. Karasik,
Bryan M. Gillard,
Kimberley D. Ramsey,
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Susan Sullivan,
J. Bridge,
Harold Magazine,
John Syron,
Johnelle Fleming,
L. Siminoff,
H. Traino,
M. Mosavel,
Laura K. Barker,
S. Jewell,
D. Rohrer,
D. Maxim,
Dana Filkins,
P. Harbach,
Eddie Cortadillo,
Bree D. Berghuis,
L. Turner,
E. Hudson,
Kristin Feenstra,
L. Sobin,
J. Robb,
Phillip Branton,
G. Korzeniewski,
C. Shive,
D. Tabor,
L. Qi,
K. Groch,
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Stephen A. Buia,
Angela M. Zimmerman,
Anna Smith,
R. Burges,
Karna L. Robinson,
Kimberly M. Valentino,
Debra Bradbury,
M. Cosentino,
Norma A. Diaz-Mayoral,
M. Kennedy,
T. Engel,
Penelope Williams,
Kenyon Erickson,
K. Ardlie,
W. Winckler,
G. Getz,
D. DeLuca,
D. MacArthur,
Manolis Kellis,
Alexander Thomson,
Taylor R. Young,
Ellen T. Gelfand,
M. Donovan,
Y. Meng,
George B. Grant,
D. Mash,
Yvonne Marcus,
Margaret J. Basile,
Jun Liu,
Jun Zhu,
Zhidong Tu,
N. Cox,
D. Nicolae,
E. Gamazon,
H. Im,
A. Konkashbaev,
J. Pritchard,
Matthew Stevens,
T. Flutre,
Xiaoquan Wen,
E. Dermitzakis,
T. Lappalainen,
R. Guigó,
Jean Monlong,
M. Sammeth,
D. Koller,
A. Battle,
S. Mostafavi,
M. McCarthy,
Manual Rivas,
J. Maller,
I. Rusyn,
A. Nobel,
F. Wright,
A. Shabalin,
M. Feolo,
N. Sharopova,
Anne Sturcke,
J. Paschal,
James M. Anderson,
E. Wilder,
L. Derr,
E. Green,
J. Struewing,
Gary F. Temple,
S. Volpi,
Joy T. Boyer,
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M. Guyer,
C. Ng,
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T. Insel,
S. Koester,
A. Little,
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H. Moore
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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
38 auth.
D. Ford,
D. Easton,
Michael R. Stratton,
S. Narod,
D. Goldgar,
P. Devilee,
D. Bishop,
B. Weber,
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J. Peto,
T. Rebbeck,
P. Tonin,
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R. Barkardottir,
J. Eyfjord,
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B. Ponder,
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J. Birch,
A. Lindblom,
D. Stoppa-Lyonnet,
Y. Bignon,
Å. Borg,
U. Hamann,
N. Haites,
Rodney J. Scott,
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L. Cannon-Albright,
A. Schofield,
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1998 |
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The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
9 auth.
J. Struewing,
P. Hartge,
S. Wacholder,
Sonya M. Baker,
M. Berlin,
M. McAdams,
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Michelle M. Timmerman,
L. Brody,
Margaret A. Tucker
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11 |
1997 |
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Germline p16 mutations in familial melanoma
9 auth.
C. Hussussian,
J. Struewing,
A. Goldstein,
P. Higgins,
D. Ally,
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W. Clark,
M. Tucker,
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10 |
1994 |
10
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Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
253 auth.
A. Barbeira,
Scott P. Dickinson,
Rodrigo Bonazzola,
Jiamao Zheng,
H. Wheeler,
Jason M. Torres,
E. Torstenson,
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Tzintzuni I. Garcia,
T. Edwards,
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K. Ardlie,
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Ellen T. Gelfand,
G. Getz,
Kane Hadley,
R. Handsaker,
Katherine H. Huang,
Seva Kashin,
K. Karczewski,
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Xiao Li,
D. MacArthur,
Jared L. Nedzel,
D. T. Nguyen,
M. Noble,
A. Segrè,
Casandra A. Trowbridge,
T. Tukiainen,
Nathan S. Abell,
Brunilda Balliu,
Ruth Barshir,
Omer Basha,
A. Battle,
G. Bogu,
A. Brown,
Christopher D. Brown,
Stephane E. Castel,
Lin S. Chen,
Colby Chiang,
D. Conrad,
Farhan N. Damani,
Joe R. Davis,
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E. Dermitzakis,
B. Engelhardt,
E. Eskin,
Pedro G. Ferreira,
L. Frésard,
E. Gamazon,
D. Garrido-Martín,
Ariel D. H. Gewirtz,
Genna Gliner,
Michael J. Gloudemans,
R. Guigó,
I. Hall,
Buhm Han,
Yuan He,
F. Hormozdiari,
C. Howald,
Brian Jo,
Eun Yong Kang,
Yungil Kim,
Sarah Kim-Hellmuth,
T. Lappalainen,
Gen Li,
Xin Li,
Boxiang Liu,
S. Mangul,
M. McCarthy,
Ian C. McDowell,
P. Mohammadi,
Jean Monlong,
S. Montgomery,
Manuel Muñoz-Aguirre,
Anne W. Ndungu,
A. Nobel,
Meritxell Oliva,
H. Ongen,
John Palowitch,
N. Panousis,
Panagiotis K. Papasaikas,
YoSon Park,
P. Parsana,
Anthony J. Payne,
Christine B. Peterson,
J. Quan,
F. Reverter,
C. Sabatti,
A. Saha,
M. Sammeth,
Alexandra J. Scott,
A. Shabalin,
Reza Sodaei,
M. Stephens,
B. Stranger,
B. Strober,
J. Sul,
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S. Urbut,
M. van de Bunt,
Gao Wang,
Xiaoquan Wen,
Fred A. Wright,
H. Xi,
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Zachary Zappala,
Judith B. Zaugg,
Yi-Hui Zhou,
J. Akey,
Daniel Bates,
Joanne Chan,
M. Claussnitzer,
Kathryn Demanelis,
Morgan Diegel,
J. Doherty,
A. Feinberg,
Maria S. Fernando,
J. Halow,
Kasper D. Hansen,
E. Haugen,
P. Hickey,
Lei Hou,
F. Jasmine,
Ruiqi Jian,
Lihua Jiang,
Audra K. Johnson,
R. Kaul,
Manolis Kellis,
M. Kibriya,
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J. B. Li,
Qin Li,
Xiao Li,
Jessica Lin,
Shin Lin,
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Latarsha J. Carithers,
P. Guan,
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Abhi Rao,
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Nicole C. Lockart,
Casey Martin,
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Richard Hasz,
Marcus Hunter,
Christopher Johns,
Mark Johnson,
G. Kopen,
W. F. Leinweber,
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Bernadette Mestichelli,
K. Myer,
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2016 |
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Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations.
41 auth.
S. Lakhani,
J. Jacquemier,
J. Sloane,
B. Gusterson,
T. Anderson,
M. V. Vijver,
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D. Venter,
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N. Haites,
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D. Goldgar,
...
S. Neuhausen,
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N. Spurr,
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J. Klijn,
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G. Lenoir,
R. Barkardottir,
V. Egilsson,
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H. Sobol,
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D. Easton
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9 |
1998 |
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The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies
12 auth.
C. McCarty,
R. Chisholm,
C. Chute,
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G. Jarvik,
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Rongling Li,
D. Masys,
M. Ritchie,
D. Roden,
J. Struewing,
Wendy A. Wolf
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9 |
2011 |
9
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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
7 auth.
J. Struewing,
D. Abeliovich,
T. Peretz,
N. Avishai,
M. Kaback,
F. Collins,
...
L. Brody
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9 |
1995 |
9
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Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations.
11 auth.
A. Goldstein,
M. Fraser,
J. Struewing,
C. Hussussian,
K. Ranade,
D. Zametkin,
...
Laura Fontaine,
Sara M. Organic,
N. Dracopoli,
W. Clark,
M. Tucker
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9 |
1995 |
9
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|
🐜
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A common coding variant in CASP8 is associated with breast cancer risk
79 auth.
A. Cox,
A. Dunning,
M. García-Closas,
S. Balasubramanian,
M. Reed,
K. Pooley,
S. Scollen,
C. Baynes,
B. Ponder,
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J. Lissowska,
L. Brinton,
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C. Axelsson,
Diana Torres,
U. Hamann,
C. Justenhoven,
H. Brauch,
J. Chang-Claude,
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A. Risch,
S. Wang-gohrke,
P. Schürmann,
N. Bogdanova,
T. Dörk,
R. Fagerholm,
Kirsimari Aaltonen,
C. Blomqvist,
H. Nevanlinna,
S. Seal,
A. Renwick,
M. Stratton,
N. Rahman,
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D. Hughes,
F. Odefrey,
P. Brennan,
A. Spurdle,
G. Chenevix-Trench,
J. Beesley,
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V. Kataja,
V. Kosma,
F. Couch,
J. Olson,
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R. Milne,
G. Ribas,
A. González-Neira,
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D. Easton
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9 |
2007 |
9
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Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation.
12 auth.
B. Modan,
P. Hartge,
G. Hirsh-Yechezkel,
A. Chetrit,
F. Lubin,
Uzi Beller,
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J. Menczer,
J. Struewing,
Margaret A. Tucker,
S. Wacholder
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8 |
2001 |
8
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The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
13 auth.
C. Oddoux,
J. Struewing,
C. Clayton,
S. Neuhausen,
L. Brody,
M. Kaback,
B. Haas,
L. Norton,
P. Borgen,
S. Jhanwar,
...
D. Goldgar,
H. Ostrer,
K. Offit
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8 |
1996 |
8
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Population-based study of risk of breast cancer in carriers of BRCA2 mutation
9 auth.
S. Thorlacius,
J. Struewing,
Patricia Hartage,
G. Olafsdóttir,
H. Sigvaldason,
L. Tryggvadottir,
...
S. Wacholder,
H. Tulinius,
J. Eyfjörd
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8 |
1998 |
8
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Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families
28 auth.
P. Tonin,
Barbara L. Weber,
K. Offit,
F. Couch,
T. Rebbeck,
S. Neuhausen,
A. Godwin,
M. Daly,
J. Wagner-Costalos,
D. B. Berman,
G. Grana,
Ellen Fox,
M. Kane,
R. Kolodner,
M. Krainer,
...
D. Haber,
J. Struewing,
E. Warner,
B. R. Rosen,
C. Lerman,
B. Peshkin,
Larry Norton,
O. Serova,
W. Foulkes,
H. Lynch,
G. Lenoir,
S. Narod,
J. Garber
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8 |
1996 |
8
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