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Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
47 auth.
P. Horák,
M. Griffith,
Arpad M. Danos,
B. Pitel,
Subha Madhavan,
Xuelu Liu,
Cynthia Chow,
H. Williams,
Leigh Carmody,
Lisa Barrow-Laing,
D. Rieke,
S. Kreutzfeldt,
A. Stenzinger,
D. Tamborero,
Manuela Benary,
...
P. Rajagopal,
C. Ida,
Harry Lesmana,
L. Satgunaseelan,
J. Merker,
M. Tolstorukov,
P. Campregher,
J. Warner,
Shruti Rao,
Maya Natesan,
H. Shen,
J. Venstrom,
Somak Roy,
K. Tao,
R. Kanagal-Shamanna,
Xinjie Xu,
D. Ritter,
K. Pagel,
Kilannin Krysiak,
A. Dubuc,
Yassmine M N Akkari,
X. Li,
Jennifer Lee,
I. King,
G. Raca,
A. Wagner,
Marylin M. Li,
S. Plon,
S. Kulkarni,
O. Griffith,
D. Chakravarty,
D. Sonkin
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6 |
2022 |
6
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|
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A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
39 auth.
A. Wagner,
B. Walsh,
Georgia Mayfield,
D. Tamborero,
D. Sonkin,
Kilannin Krysiak,
J. Deu-Pons,
Ryan P. Duren,
Jianjiong Gao,
J. McMurry,
S. Patterson,
C. Del Vecchio Fitz,
B. Pitel,
O. Sezerman,
K. Ellrott,
...
J. Warner,
D. Rieke,
T. Aittokallio,
E. Cerami,
D. Ritter,
L. Schriml,
R. Freimuth,
M. Haendel,
G. Raca,
Subha Madhavan,
M. Baudis,
J. Beckmann,
R. Dienstmann,
D. Chakravarty,
X. Li,
S. Mockus,
O. Elemento,
N. Schultz,
N. López-Bigas,
M. Lawler,
Jeremy Goecks,
M. Griffith,
O. Griffith,
Adam A. Margolin
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6 |
2020 |
6
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🐜
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A harmonized meta-knowledgebase of clinical interpretations of cancer genomic variants
37 auth.
A. Wagner,
B. Walsh,
Georgia Mayfield,
D. Tamborero,
D. Sonkin,
Kilannin Krysiak,
J. Pons,
Ryan P. Duren,
Jianjiong Gao,
J. McMurry,
S. Patterson,
C. Del Vecchio Fitz,
O. Sezerman,
J. Warner,
D. Rieke,
...
T. Aittokallio,
E. Cerami,
D. Ritter,
L. Schriml,
R. Freimuth,
M. Haendel,
G. Raca,
Subha Madhavan,
M. Baudis,
J. Beckmann,
R. Dienstmann,
D. Chakravarty,
X. Li,
S. Mockus,
O. Elemento,
N. Schultz,
N. López-Bigas,
M. Lawler,
Jeremy Goecks,
M. Griffith,
O. Griffith,
Adam A. Margolin
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4 |
2018 |
4
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|
🐜
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Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
47 auth.
P. Horák,
M. Griffith,
Arpad M. Danos,
B. Pitel,
Subha Madhavan,
Xuelu Liu,
Cynthia Chow,
H. Williams,
Leigh Carmody,
Lisa Barrow-Laing,
D. Rieke,
S. Kreutzfeldt,
A. Stenzinger,
D. Tamborero,
Manuela Benary,
...
P. Rajagopal,
C. Ida,
Harry Lesmana,
L. Satgunaseelan,
J. Merker,
M. Tolstorukov,
P. Campregher,
J. Warner,
Shruti Rao,
Maya Natesan,
H. Shen,
J. Venstrom,
Somak Roy,
K. Tao,
R. Kanagal-Shamanna,
Xinjie Xu,
D. Ritter,
K. Pagel,
Kilannin Krysiak,
A. Dubuc,
Yassmine M N Akkari,
X. Li,
Jennifer Lee,
I. King,
G. Raca,
A. Wagner,
Marylin M. Li,
S. Plon,
S. Kulkarni,
O. Griffith,
D. Chakravarty,
D. Sonkin
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3 |
2022 |
3
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MolecularMatch LAB Integrates Knowledgebases for Collaborative Clinical Interpretation of Variation in Cancer
Ryan P. Duren,
Shane K. Neeley,
J. Welsh,
Nick Tackes,
X. Li,
Caleb F. Davis
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0 |
2017 |
0
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|
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Translational Research and Immunotherapy in Lung Cancer
11 auth.
J. Schoenhals,
E. Brooks,
M. Cortez,
S. Seyedin,
S. Niknam,
Xiaohong Wang,
...
Alexandra P. Cadena,
X. Li,
D. Gomez,
Z. Liao,
J. Welsh
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0 |
2016 |
0
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4. Coordinating variant interpretation knowledgebases improves clinical interpretation of genomic variants in cancers
13 auth.
A. Wagner,
B. Walsh,
D. Sonkin,
R. Dienstmann,
X. Li,
J. Beckmann,
Georgia Mayfield,
D. Tamborero,
N. López-Bigas,
Jeremy Goecks,
...
Adam A. Margolin,
M. Griffith,
O. Griffith
|
0 |
2018 |
0
🐜
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|
🐬
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Distinct mutations of MMR gene in colorectal cancer by targeted enrichment and high-throughput next generation sequencing
Kai Huang,
Huijing Chen,
Fangqi Liu,
Ye Xu,
X. Li,
P. Nan
|
0 |
2016 |
0
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