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Akl C. Fahed
Akl C. Fahed
Harvard Medical School
Bestätigte E-Mail-Adresse bei mail.harvard.edu
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Zitiert von
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Genetics of congenital heart disease: the glass half empty
AC Fahed, BD Gelb, JG Seidman, CE Seidman
Circulation research 112 (4), 707-720, 2013
7072013
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
AC Fahed, M Wang, JR Homburger, AP Patel, AG Bick, CL Neben, C Lai, ...
Nature communications 11 (1), 3635, 2020
3212020
Familial hypercholesterolemia: the lipids or the genes?
AC Fahed, GM Nemer
Nutrition & Metabolism 8, 1-12, 2011
1292011
Diet, genetics, and disease: a focus on the Middle East and North Africa region
AC Fahed, AKM El-Hage-Sleiman, TI Farhat, GM Nemer
Journal of Nutrition and Metabolism 2012, 2012
1052012
Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions
AC Fahed, IK Jang
Nature Reviews Cardiology 18 (10), 724-734, 2021
862021
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study
TR Tromp, ML Hartgers, GK Hovingh, AJ Vallejo-Vaz, KK Ray, H Soran, ...
The Lancet 399 (10326), 719-728, 2022
832022
Association of rare pathogenic DNA variants for familial hypercholesterolemia, hereditary breast and ovarian cancer syndrome, and lynch syndrome with disease risk in adults …
AP Patel, M Wang, AC Fahed, H Mason-Suares, D Brockman, R Pelletier, ...
JAMA network open 3 (4), e203959-e203959, 2020
822020
Heart failure in congenital heart disease: a confluence of acquired and congenital
AC Fahed, AE Roberts, S Mital, NK Lakdawala
Heart failure clinics 10 (1), 219-227, 2014
672014
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation
AC Fahed, RM Safa, FF Haddad, FF Bitar, RR Andary, MT Arabi, ST Azar, ...
Molecular genetics and metabolism 102 (2), 181-188, 2011
662011
UBQLN2 mutation causing heterogeneous X‐linked dominant neurodegeneration
AC Fahed, B McDonough, CM Gouvion, KL Newell, LS Dure, M Bebin, ...
Annals of neurology 75 (5), 793-798, 2014
652014
Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype
K Shibbani, AC Fahed, L Al‐Shaar, M Arabi, G Nemer, F Bitar, ...
Clinical genetics 85 (2), 127-137, 2014
622014
Translational medicine in the era of big data and machine learning
WS Weintraub, AC Fahed, JS Rumsfeld
Circulation Research 123 (11), 1202-1204, 2018
432018
Connecting the lines between hypogonadism and atherosclerosis
AC Fahed, JM Gholmieh, ST Azar
International Journal of Endocrinology 2012, 2012
432012
NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
OK Abou Hassan, AC Fahed, M Batrawi, M Arabi, MM Refaat, ...
Scientific reports 5 (1), 8848, 2015
422015
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease
AP Patel, M Wang, Y Ruan, S Koyama, SL Clarke, X Yang, C Tcheandjieu, ...
Nature Medicine 29 (7), 1793-1803, 2023
352023
Design and user experience testing of a polygenic score report: a qualitative study of prospective users
DG Brockman, L Petronio, JS Dron, BC Kwon, T Vosburg, L Nip, A Tang, ...
BMC Medical Genomics 14, 1-20, 2021
352021
Students’ perceptions of peer-organized extra-curricular research course during medical school: a qualitative study
B Nazha, RH Salloum, AC Fahed, M Nabulsi
PloS one 10 (3), e0119375, 2015
332015
Transethnic transferability of a genome-wide polygenic score for coronary artery disease
AC Fahed, KG Aragam, G Hindy, YDI Chen, K Chaudhary, A Dobbyn, ...
Circulation: Genomic and Precision Medicine 14 (1), e003092, 2021
312021
GATA 5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
K Kassab, H Hariri, L Gharibeh, AC Fahed, M Zein, I El‐Rassy, M Nemer, ...
Molecular Genetics & Genomic Medicine 4 (2), 160-171, 2016
312016
Association of the interaction between familial hypercholesterolemia variants and adherence to a healthy lifestyle with risk of coronary artery disease
AC Fahed, M Wang, AP Patel, E Ajufo, DJ Maamari, KG Aragam, ...
JAMA network open 5 (3), e222687-e222687, 2022
252022
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