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🐜
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
14 auth.
R. Green,
J. Berg,
W. Grody,
Sarah S. Kalia,
B. Korf,
C. Martin,
A. McGuire,
R. Nussbaum,
Julianne M. O’Daniel,
K. Ormond,
...
H. Rehm,
M. Watson,
Marc S. Williams,
L. Biesecker
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11 |
2013 |
11
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|
🐜
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Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource
24 auth.
Natasha T. Strande,
E. Riggs,
A. Buchanan,
O. Ceyhan-Birsoy,
Marina T. DiStefano,
S. Dwight,
J. Goldstein,
R. Ghosh,
Bryce A. Seifert,
Tam P. Sneddon,
...
M. W. Wright,
L. Milko,
J. Cherry,
Monica A. Giovanni,
M. Murray,
Julianne M. O’Daniel,
E. Ramos,
Avni Santani,
Avni Santani,
A. F. Scott,
S. Plon,
H. Rehm,
C. Martin,
J. Berg
|
8 |
2017 |
8
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|
🐬
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Survey of U.S. Public Attitudes Towards Pharmacogenetic Testing
S. Haga,
Julianne M. O’Daniel,
Genevieve M. Tindall,
I. Lipkus,
R. Agans
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6 |
2011 |
6
🐬
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|
🐜
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A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation
24 auth.
J. Hunter,
Stephanie A. Irving,
L. Biesecker,
A. Buchanan,
B. Jensen,
Kristy Lee,
C. Martin,
L. Milko,
Kristin R. Muessig,
Annie D. Niehaus,
...
Julianne M. O’Daniel,
M. Piper,
E. Ramos,
S. Schully,
A. F. Scott,
A. Slavotinek,
N. Sobreira,
Natasha T. Strande,
Meredith A. Weaver,
Elizabeth M. Webber,
Marc S. Williams,
J. Berg,
J. Evans,
K. Goddard
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6 |
2016 |
6
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|
🐜
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Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
10 auth.
C. Rehder,
Lora J. H. Bean,
D. Bick,
E. Chao,
W. Chung,
Soma Das,
...
Julianne M. O’Daniel,
H. Rehm,
V. Shashi,
L. Vincent
|
6 |
2021 |
6
🐜
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|
🐜
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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
19 auth.
J. Berg,
A. K. Foreman,
Julianne M. O’Daniel,
J. Booker,
Lacey J. Boshe,
T. Carey,
K. Crooks,
B. Jensen,
E. Juengst,
Kristy Lee,
...
Daniel K. Nelson,
B. Powell,
C. Powell,
M. Roche,
C. Skrzynia,
Natasha T. Strande,
K. Weck,
K. Wilhelmsen,
J. Evans
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6 |
2015 |
6
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|
🦁
|
Public Perspectives on Returning Genetics and Genomics Research Results
Julianne M. O’Daniel,
S. Haga
|
6 |
2011 |
6
🦁
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|
🐜
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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
27 auth.
Tamara S. Roman,
Stephanie B. Crowley,
M. Roche,
A. K. Foreman,
Julianne M. O’Daniel,
Bryce A. Seifert,
Kristy Lee,
A. Brandt,
C. Gustafson,
Daniela M. DeCristo,
Natasha T. Strande,
L. Ramkissoon,
L. Milko,
Phillips Owen,
Sayanty Roy,
...
M. Xiong,
Ryan S. Paquin,
Rita M. Butterfield,
Megan A. Lewis,
Katherine J Souris,
D. Bailey,
C. Rini,
J. Booker,
B. Powell,
K. Weck,
C. Powell,
J. Berg
|
6 |
2020 |
6
🐜
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|
🐜
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Genomic Risk Profiling: Attitudes and Use in Personal and Clinical Care of Primary Care Physicians Who Offer Risk Profiling
7 auth.
S. Haga,
Madeline M. Carrig,
Julianne M. O’Daniel,
L. Orlando,
Ley A. Killeya‐Jones,
G. Ginsburg,
...
Alex H Cho
|
6 |
2011 |
6
🐜
|
|
🦁
|
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories
39 auth.
Julianne M. O’Daniel,
H. Mclaughlin,
L. Amendola,
S. Bale,
J. Berg,
D. Bick,
K. Bowling,
E. Chao,
W. Chung,
L. Conlin,
G. Cooper,
Soma Das,
Joshua L. Deignan,
M. Dorschner,
J. Evans,
...
A. Ghazani,
K. Goddard,
M. Gornick,
Kelly D. Hagman,
T. Hambuch,
M. Hegde,
L. Hindorff,
I. Holm,
G. Jarvik,
Amy K. Johnson,
Lindsey C. Mighion,
M. Morra,
S. Plon,
Sumit Punj,
C. Richards,
A. Santani,
B. Shirts,
N. Spinner,
Sha Tang,
K. Weck,
S. Wolf,
Yaping Yang,
H. L. Rehm,
H. L. Rehm
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6 |
2016 |
6
🦁
|
|
🐜
|
Germline Analysis from Tumor–Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings
17 auth.
Bryce A. Seifert,
Julianne M. O’Daniel,
K. Amin,
Daniel S Marchuk,
N. Patel,
J. Parker,
A. Hoyle,
Lisle E. Mose,
Andrew Marron,
M. Hayward,
...
C. Bizon,
K. Wilhelmsen,
J. Evans,
H. Earp,
N. Sharpless,
D. Hayes,
J. Berg
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6 |
2016 |
6
🐜
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