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🦁
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Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
32 auth.
A. Sturm,
J. Knowles,
S. Gidding,
Z. Ahmad,
C. Ahmed,
C. Ballantyne,
S. Baum,
M. Bourbon,
A. Carrié,
M. Cuchel,
S. D. de Ferranti,
J. Defesche,
T. Freiberger,
R. Hershberger,
G. Hovingh,
...
L. Karayan,
J. Kastelein,
I. Kindt,
S. Lane,
S. Leigh,
M. Linton,
P. Mata,
W. Neal,
B. Nordestgaard,
R. Santos,
M. Harada‐Shiba,
E. Sijbrands,
N. Stitziel,
S. Yamashita,
K. Wilemon,
D. Ledbetter,
D. Rader
|
8 |
2018 |
8
🦁
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|
🐜
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Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps
26 auth.
A. Adeyemo,
Mary K. Balaconis,
Deanna R. Darnes,
S. Fatumo,
Palmira Granados Moreno,
C. Hodonsky,
M. Inouye,
M. Kanai,
Kazuto Kato,
B. Knoppers,
A. Lewis,
Alicia R. Martin,
M. McCarthy,
M. Meyer,
Y. Okada,
...
J. B. Richards,
Lucas D Richter,
S. Ripatti,
C. Rotimi,
S. Sanderson,
A. Sturm,
R. Verdugo,
E. Widén,
C. Willer,
G. Wojcik,
A. Zhou
|
8 |
2021 |
8
🐜
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|
🐜
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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome
19 auth.
A. Adler,
V. Novelli,
A. Amin,
E. Abiusi,
M. Care,
E. Nannenberg,
H. Feilotter,
S. Amenta,
D. Mazzà,
H. Bikker,
...
A. Sturm,
John Garcia,
M. Ackerman,
R. E. Hershberger,
M. Perez,
W. Zareba,
J. Ware,
A. Wilde,
M. Gollob
|
7 |
2020 |
7
🐜
|
|
🐢
|
Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
9 auth.
K. Musunuru,
R. Hershberger,
S. Day,
N. J. Klinedinst,
A. Landstrom,
V. Parikh,
...
Siddharth K. Prakash,
C. Semsarian,
A. Sturm
|
7 |
2020 |
7
🐢
|
|
🐜
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Reappraisal of Reported Genes for Sudden Arrhythmic Death
19 auth.
S. M. Hosseini,
R. Kim,
S. Udupa,
Gregory Costain,
R. Jobling,
Eriskay J Liston,
Seema M. Jamal,
Marta Szybowska,
C. Morel,
S. Bowdin,
...
John Garcia,
M. Care,
A. Sturm,
V. Novelli,
M. Ackerman,
J. Ware,
R. Hershberger,
A. Wilde,
M. Gollob
|
7 |
2018 |
7
🐜
|
|
🐜
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Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
44 auth.
Kandamurugu Manickam,
A. Buchanan,
Marci L. B. Schwartz,
M. L. Hallquist,
Janet L. Williams,
A. Rahm,
H. Rocha,
J. Savatt,
Alyson Evans,
Loren Butry,
Amanda L. Lazzeri,
D’Andra M. Lindbuchler,
Carroll N. Flansburg,
R. Leeming,
V. Vogel,
...
Matthew S. Lebo,
H. Mason-Suares,
Derick Hoskinson,
N. Abul-Husn,
F. Dewey,
J. Overton,
J. Reid,
A. Baras,
H. Willard,
C. McCormick,
Sarath Babu Krishna Murthy,
Dustin N. Hartzel,
Korey A. Kost,
Daniel R. Lavage,
A. Sturm,
Lauren R. Frisbie,
T. Person,
R. Metpally,
Monica A. Giovanni,
L. Lowry,
J. Leader,
M. Ritchie,
D. Carey,
A. Justice,
H. L. Kirchner,
W. Faucett,
Marc S. Williams,
David H. Ledbetter,
M. Murray
|
7 |
2018 |
7
🐜
|
|
🐜
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A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
23 auth.
Marci L. B. Schwartz,
C. McCormick,
Amanda L. Lazzeri,
D’Andra M. Lindbuchler,
M. L. Hallquist,
Kandamurugu Manickam,
A. Buchanan,
A. Rahm,
Monica A. Giovanni,
Lauren R. Frisbie,
...
Carroll N. Flansburg,
F. D. Davis,
A. Sturm,
C. Nicastro,
Matthew S. Lebo,
H. Mason-Suares,
Lisa Mahanta,
D. Carey,
Janet L. Williams,
Marc S. Williams,
D. Ledbetter,
W. Faucett,
M. Murray
|
7 |
2017 |
7
🐜
|
|
🐜
|
Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
16 auth.
Megan C. Roberts,
W. D. Dotson,
Christopher DeVore,
E. Bednar,
Deborah J. Bowen,
T. Ganiats,
R. Green,
Georgia Hurst,
A. Philp,
C. Ricker,
...
A. Sturm,
A. Trepanier,
Janet L. Williams,
H. Zierhut,
K. Wilemon,
H. Hampel
|
7 |
2018 |
7
🐜
|
|
🐜
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International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia
22 auth.
G. Watts,
S. Gidding,
R. Hegele,
F. Raal,
A. Sturm,
L. Jones,
Mitchell N. Sarkies,
Khalid Al-Rasadi,
D. Blom,
Magdalena Daccord,
...
S. D. de Ferranti,
E. Folco,
P. Libby,
P. Mata,
Hapizah Nawawi,
U. Ramaswami,
K. Ray,
C. Stefanutti,
S. Yamashita,
J. Pang,
G. Thompson,
R. D. Santos
|
6 |
2023 |
6
🐜
|
|
🐬
|
Homocysteine and MTHFR Mutations Relation to Thrombosis and Coronary Artery Disease
E. Varga,
A. Sturm,
C. Misita,
S. Moll
|
6 |
2005 |
6
🐬
|
|
🐜
|
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
39 auth.
C. Haggerty,
S. Damrauer,
M. Levin,
David L. Birtwell,
D. Carey,
Alicia M Golden,
Dustin N. Hartzel,
Yirui Hu,
R. Judy,
M. Kelly,
R. Kember,
H. Kirchner,
J. Leader,
Lusha W. Liang,
Chris McDermott-Roe,
...
A. Babu,
M. Morley,
Zachariah B. Nealy,
T. Person,
Arichanah Pulenthiran,
Aeron M. Small,
D. Smelser,
R. Stahl,
A. Sturm,
Heather Williams,
A. Baras,
K. Margulies,
T. Cappola,
F. Dewey,
A. Verma,
Xinyuan Zhang,
A. Correa,
Michael E. Hall,
James G. Wilson,
M. Ritchie,
D. Rader,
M. Murray,
Brandon K. Fornwalt,
Z. Arany
|
6 |
2019 |
6
🐜
|
