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Michael A. Iacocca
Michael A. Iacocca
Deep Genomics
在 deepgenomics.com 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Improving reporting standards for polygenic scores in risk prediction studies
H Wand, SA Lambert, C Tamburro, MA Iacocca, JW O'Sullivan, C Sillari, ...
Nature, 2020
3452020
Severe hypertriglyceridemia is primarily polygenic
JS Dron, J Wang, H Cao, AD McIntyre, MA Iacocca, JR Menard, ...
Journal of clinical lipidology 13 (1), 80-88, 2019
1892019
ClinVar database of global familial hypercholesterolemia‐associated DNA variants
MA Iacocca, JR Chora, A Carrié, T Freiberger, SE Leigh, JC Defesche, ...
Human mutation 39 (11), 1631-1640, 2018
1102018
The clinical genome resource (ClinGen) familial hypercholesterolemia variant curation expert panel consensus guidelines for LDLR variant classification
JR Chora, MA Iacocca, L Tichý, H Wand, CL Kurtz, H Zimmermann, ...
Genetics in Medicine 24 (2), 293-306, 2022
832022
Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia
MA Iacocca, J Wang, JS Dron, JF Robinson, AD McIntyre, H Cao, ...
Journal of lipid research 58 (11), 2202-2209, 2017
792017
Recent advances in genetic testing for familial hypercholesterolemia
MA Iacocca, RA Hegele
Expert review of molecular diagnostics 17 (7), 641-651, 2017
712017
Six years’ experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias
JS Dron, J Wang, AD McIntyre, MA Iacocca, JF Robinson, MR Ban, H Cao, ...
BMC Medical Genomics 13, 1-15, 2020
652020
Whole-gene duplication of PCSK9 as a novel genetic mechanism for severe familial hypercholesterolemia
MA Iacocca, J Wang, S Sarkar, JS Dron, T Lagace, AD McIntyre, P Lau, ...
Canadian Journal of Cardiology 34 (10), 1316-1324, 2018
502018
Role of DNA copy number variation in dyslipidemias
MA Iacocca, RA Hegele
Current Opinion in Lipidology 29 (2), 125-132, 2018
442018
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines
CG Preston, MW Wright, R Madhavrao, SM Harrison, JL Goldstein, X Luo, ...
Genome medicine 14 (1), 6, 2022
402022
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia
JS Dron, J Wang, AJ Berberich, MA Iacocca, H Cao, P Yang, J Knoll, ...
Journal of Lipid Research 59 (8), 1529-1535, 2018
322018
Progress in finding pathogenic DNA copy number variations in dyslipidemia.
MA Iacocca, JS Dron, RA Hegele
Current opinion in lipidology, 2019
242019
ClinGen Familial Hypercholesterolemia Expert Panel. The clinical genome resource (clingen) familial hypercholesterolemia variant curation expert panel consensus guidelines for …
JR Chora, MA Iacocca, L Tichý, H Wand, CL Kurtz, H Zimmermann, ...
Genet Med 24 (2), 293-306, 2022
162022
Genetic determinants of myocardial infarction risk in familial hypercholesterolemia
PJ Zhao, MR Ban, MA Iacocca, AD McIntyre, J Wang, RA Hegele
CJC open 1 (5), 225-230, 2019
102019
Efficacy of evolocumab in monogenic vs polygenic hypercholesterolemia
T Lee, MA Iacocca, MR Ban, RA Hegele
CJC open 1 (3), 115-118, 2019
82019
ClinGen FH Variant Curation Expert Panel
MA Iacocca, JR Chora, A Carrié, T Freiberger, SE Leigh, JC Defesche, ...
ClinVar database of global familial hypercholesterolemia-associated DNA …, 2018
72018
ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines
CG Preston, MW Wright, R Madhavrao, SM Harrison, JL Goldstein, X Luo, ...
medRxiv, 2021.02. 12.21251663, 2021
22021
Improving the genetic diagnosis of familial hypercholesterolemia
M Iacocca
The University of Western Ontario (Canada), 2019
22019
DNA copy number variation screening in familial hypercholesterolemia-related genes
RAH MA Iacocca, J Wang, JS Dron, H Cao, JF Robinson, AD McIntyre
Atherosclerosis 275, e79, 2018
22018
Adaptation of ACMG/AMP Guidelines for Standardized Variant Interpretation in Familial Hypercholesterolemia
MA Iacocca, J Chora, A Carrie, SE Leigh, L Tichy, MT DiStefano, ...
Atherosclerosis Supplements 32, 51, 2018
22018
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