Fahed, Akl
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coauthor of: Natarajan, Pradeep
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Wild Edible Plants: Promoting Dietary Diversity in Poor Communities of Lebanon
author list: IBSAR
published in: Wild Edible Plants: Promoting Dietary Diversity in Poor Communities of Lebanon
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Diet, genetics, and disease: a focus on the middle East and north Africa region.
PubMed Identifier: 22536488
author list: Fahed AC, El-Hage-Sleiman AK, Farhat TI, Nemer GM
published in: Journal of nutrition and metabolism
information resource reference: Diet, genetics, and disease: a focus on the middle East and north Africa region. J Nutr Metab. 2012; 2012:109037.
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Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation.
PubMed Identifier: 21145767
author list: Fahed AC, Safa RM, Haddad FF, Bitar FF, Andary RR, Arabi MT, Azar ST, Nemer G
published in: Molecular genetics and metabolism
information resource reference: Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation. Mol Genet Metab. 2011 Feb; 102(2):181-8.
journal title abbreviation: Mol Genet Metab
publication date: 2010-11-11T00:00:00
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Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype.
PubMed Identifier: 23379544
author list: Shibbani K, Fahed AC, Al-Shaar L, Arabi M, Nemer G, Bitar F, Majdalani M
published in: Clinical genetics
information resource reference: Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype. Clin Genet. 2014 Feb; 85(2):127-37.
journal title abbreviation: Clin Genet
publication date: 2013-03-12T00:00:00
year: 2013
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linked author: Fahed, Akl
linked information resource: Subclinical Burden of Coronary Artery Calcium in Patients With Coarctation of the Aorta.

Subclinical Burden of Coronary Artery Calcium in Patients With Coarctation of the Aorta.
PubMed Identifier: 30424867
author list: Krishnamurthy Y, Stefanescu Schmidt AC, Bittner DO, Scholtz JE, Bui A, Reddy R, Youniss MA, Donohoe K, Flannery LD, Fahed AC, Ghoshhajra BB, DeFaria Yeh D, Bhatt AB
published in: The American journal of cardiology
information resource reference: Subclinical Burden of Coronary Artery Calcium in Patients With Coarctation of the Aorta. Am J Cardiol. 2019 01 15; 123(2):323-328.
journal title abbreviation: Am J Cardiol
publication date: 2018-10-21T00:00:00
year: 2018
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linked information resource: Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis.

Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis.
PubMed Identifier: 30514661
author list: Hariri H, Kurban M, Al-Haddad C, Fahed AC, Poladian S, Khalil A, Abbas O, Arabi M, Bitar F, Nemer G
published in: Journal of dermatological science
information resource reference: Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis. J Dermatol Sci. 2018 Dec; 92(3):237-244.
journal title abbreviation: J Dermatol Sci
publication date: 2018-11-10T00:00:00
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Familial hypercholesterolemia: the lipids or the genes?
PubMed Identifier: 21513517
author list: Fahed AC, Nemer GM
published in: Nutrition & metabolism
information resource reference: Familial hypercholesterolemia: the lipids or the genes? Nutr Metab (Lond). 2011 Apr 22; 8(1):23.
journal title abbreviation: Nutr Metab (Lond)
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linked information resource: Translational Medicine in the Era of Big Data and Machine Learning.

Translational Medicine in the Era of Big Data and Machine Learning.
PubMed Identifier: 30571466
author list: Weintraub WS, Fahed AC, Rumsfeld JS
published in: Circulation research
information resource reference: Translational Medicine in the Era of Big Data and Machine Learning. Circ Res. 2018 11 09; 123(11):1202-1204.
journal title abbreviation: Circ Res
publication date: 2018-11-09T00:00:00
year: 2018
type: Academic Article
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https://connects.catalyst.harvard.edu/Profiles/profile/117509573
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Plaque, Atherosclerotic
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Blankstein, Ron
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Khera, Amit
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linked author: Fahed, Akl
linked information resource: https://connects.catalyst.harvard.edu/Profiles/profile/151798059

https://connects.catalyst.harvard.edu/Profiles/profile/151798059
PubMed Identifier: 32347951
author list: Patel AP, Wang M, Fahed AC, Mason-Suares H, Brockman D, Pelletier R, Amr S, Machini K, Hawley M, Witkowski L, Koch C, Philippakis A, Cassa CA, Ellinor PT, Kathiresan S, Ng K, Lebo M, Khera AV
published in: JAMA network open
information resource reference: Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History. JAMA Netw Open. 2020 04 01; 3(4):e203959.
journal title abbreviation: JAMA Netw Open
publication date: 2020-04-01T00:00:00
year: 2020
type: Academic Article
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label: Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.

Authorship 1277348
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linked information resource: Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.
PubMed Identifier: 32820175
author list: Fahed AC, Wang M, Homburger JR, Patel AP, Bick AG, Neben CL, Lai C, Brockman D, Philippakis A, Ellinor PT, Cassa CA, Lebo M, Ng K, Lander ES, Zhou AY, Kathiresan S, Khera AV
published in: Nature communications
information resource reference: Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nat Commun. 2020 08 20; 11(1):3635.
journal title abbreviation: Nat Commun
publication date: 2020-08-20T00:00:00
year: 2020
type: Academic Article
type: Article
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Authorship 1281666
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author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.

Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.
PubMed Identifier: 32885985
author list: Fahed AC, Nemer G, Bitar FF, Arnaout S, Abchee AB, Batrawi M, Khalil A, Abou Hassan OK, DePalma SR, McDonough B, Arabi MT, Ware JS, Seidman JG, Seidman CE
published in: Circulation. Genomic and precision medicine
information resource reference: Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy. Circ Genom Precis Med. 2020 10; 13(5):444-452.
journal title abbreviation: Circ Genom Precis Med
publication date: 2020-09-04T00:00:00
year: 2020
type: Academic Article
type: Article
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Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.
PubMed Identifier: 33284643
author list: Fahed AC, Aragam KG, Hindy G, Chen YI, Chaudhary K, Dobbyn A, Krumholz HM, Sheu WHH, Rich SS, Rotter JI, Chowdhury R, Cho J, Do R, Ellinor PT, Kathiresan S, Khera AV
published in: Circulation. Genomic and precision medicine
information resource reference: Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease. Circ Genom Precis Med. 2021 02; 14(1):e003092.
journal title abbreviation: Circ Genom Precis Med
publication date: 2020-12-07T00:00:00
year: 2020
type: Academic Article
type: Article
type: Document
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Authorship 1312741
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linked information resource: Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.

Authorship 1353532
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linked information resource: Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions.

Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions.
PubMed Identifier: 33953381
author list: Fahed AC, Jang IK
published in: Nature reviews. Cardiology
information resource reference: Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions. Nat Rev Cardiol. 2021 10; 18(10):724-734.
journal title abbreviation: Nat Rev Cardiol
publication date: 2021-05-05T00:00:00
year: 2021
type: Academic Article
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Urbut, Sarah
eCommons Login: sau120
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linked information resource: [The "short Achilles tendon" syndrome: a new entity of the diabetic foot].

[The "short Achilles tendon" syndrome: a new entity of the diabetic foot].
PubMed Identifier: 9463016
author list: Lormeau B, Fahed A, Marminc L, Miossec P, Valensi P, Attali JR
published in: Diabetes & metabolism
information resource reference: [The "short Achilles tendon" syndrome: a new entity of the diabetic foot]. Diabetes Metab. 1997 Nov; 23(5):443-7.
journal title abbreviation: Diabetes Metab
publication date: 1997-11-01T00:00:00
year: 1997
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1400600
type: Authorship
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linked author: Fahed, Akl
linked information resource: Design and user experience testing of a polygenic score report: a qualitative study of prospective users.

Design and user experience testing of a polygenic score report: a qualitative study of prospective users.
PubMed Identifier: 34598685
author list: Brockman DG, Petronio L, Dron JS, Kwon BC, Vosburg T, Nip L, Tang A, O'Reilly M, Lennon N, Wong B, Ng K, Huang KH, Fahed AC, Khera AV
published in: BMC medical genomics
information resource reference: Design and user experience testing of a polygenic score report: a qualitative study of prospective users. BMC Med Genomics. 2021 10 01; 14(1):238.
journal title abbreviation: BMC Med Genomics
publication date: 2021-10-01T00:00:00
year: 2021
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1436215
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linked author: Fahed, Akl
linked information resource: CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine?

Authorship 1442438
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linked author: Fahed, Akl
linked information resource: Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease.

Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease.
PubMed Identifier: 35294538
author list: Fahed AC, Wang M, Patel AP, Ajufo E, Maamari DJ, Aragam KG, Brockman DG, Vosburg T, Ellinor PT, Ng K, Khera AV
published in: JAMA network open
information resource reference: Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease. JAMA Netw Open. 2022 03 01; 5(3):e222687.
journal title abbreviation: JAMA Netw Open
publication date: 2022-03-01T00:00:00
year: 2022
type: Academic Article
type: Article
type: Document
type: Information Resource

CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine?
PubMed Identifier: 35254917
author list: Maamari DJ, Jaffer FA, Khera AV, Fahed AC
published in: Circulation
information resource reference: CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine? Circulation. 2022 03 08; 145(10):721-723.
journal title abbreviation: Circulation
publication date: 2022-03-07T00:00:00
year: 2022
type: Academic Article
type: Article
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The potential of polygenic scores to improve cost and efficiency of clinical trials.
PubMed Identifier: 35614072
author list: Fahed AC, Philippakis AA, Khera AV
published in: Nature communications
information resource reference: The potential of polygenic scores to improve cost and efficiency of clinical trials. Nat Commun. 2022 05 25; 13(1):2922.
journal title abbreviation: Nat Commun
publication date: 2022-05-25T00:00:00
year: 2022
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linked information resource: The potential of polygenic scores to improve cost and efficiency of clinical trials.

Authorship 1501622
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linked information resource: Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis.

Authorship 1500523
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linked information resource: Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.

Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.
PubMed Identifier: 36147540
author list: Maamari DJ, Brockman DG, Aragam K, Pelletier RC, Folkerts E, Neben CL, Okumura S, Hull LE, Philippakis AA, Natarajan P, Ellinor PT, Ng K, Zhou AY, Khera AV, Fahed AC
published in: JACC. Advances
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Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis.
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Genetic and clinical factors underlying a self-reported family history of heart disease.
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Exploring the link between Gilbert's syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals.
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author list: Kartoun U, Fahed AC, Kany S, Singh P, Khurshid S, Patel AP, Batra P, Philippakis A, Khera AV, Lubitz SA, Ellinor PT, Anand V, Ng K
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PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm.
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information resource reference: PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm. J Nucl Cardiol. 2023 10; 30(5):2187-2190.
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linked information resource: A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.

A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
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linked information resource: Clinical utility of polygenic scores for cardiometabolic disease in Arabs.

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linked information resource: Pragmatic Approach to Applying Polygenic Risk Scores to Diverse Populations.

Pragmatic Approach to Applying Polygenic Risk Scores to Diverse Populations.
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Clinical utility of polygenic scores for cardiometabolic disease in Arabs.
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linked information resource: Clinical applications of polygenic risk score for coronary artery disease through the life course.

Clinical applications of polygenic risk score for coronary artery disease through the life course.
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linked information resource: Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course.

MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record.
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Massive underrepresentation of Arabs in genomic studies of common disease.
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Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course.
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linked information resource: Machine Learning in Invasive and Noninvasive Coronary Angiography.

Machine Learning in Invasive and Noninvasive Coronary Angiography.
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linked information resource: PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm.

PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm.
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author list: Qamar I, Grewal S, Fahed AC, Weiner R, Tawakol A, Osborne MT
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Authorship 1634807
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linked information resource: The Role of Genetics in Advancing Cardiometabolic Drug Development.

The Role of Genetics in Advancing Cardiometabolic Drug Development.
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Authorship 1651908
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linked information resource: Ocular manifestations of severe familial hypercholesterolemia.

Ocular manifestations of severe familial hypercholesterolemia.
PubMed Identifier: 38737271
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MSGene: a multistate model using genetic risk and the electronic health record applied to lifetime risk of coronary artery disease.
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author list: Urbut SM, Yeung MW, Khurshid S, Cho SMJ, Schuermans A, German J, Taraszka K, Paruchuri K, Fahed AC, Ellinor PT, Trinquart L, Parmigiani G, Gusev A, Natarajan P
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Authorship 1658461
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linked information resource: Polygenic Background Modifies Risk of Coronary Artery Disease Among Individuals With Heterozygous Familial Hypercholesterolemia.

Polygenic Background Modifies Risk of Coronary Artery Disease Among Individuals With Heterozygous Familial Hypercholesterolemia.
PubMed Identifier: 38938725
author list: Reeskamp LF, Shim I, Dron JS, Ibrahim S, Tromp TR, Fahed AC, Patel AP, Hutten BA, Stroes ESG, Hovingh GK, Khera AV
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information resource reference: Polygenic Background Modifies Risk of Coronary Artery Disease Among Individuals With Heterozygous Familial Hypercholesterolemia. JACC Adv. 2023 Nov; 2(9):100662.
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linked information resource: Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbidities.

Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbidities.
PubMed Identifier: 38959863
author list: Kim MS, Shim I, Fahed AC, Do R, Park WY, Natarajan P, Khera AV, Won HH
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Allan and Gill Gray Professor of Medicine in the Field of Cardiology
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Lecturer on Medicine, Part-time
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Research Associate in Medicine
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Authorship 1687979
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linked information resource: Integrating Clinical, Genetic, and Electrocardiogram-Based Artificial Intelligence to Estimate Risk of Incident Atrial Fibrillation.

Authorship 1684113
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linked information resource: Polygenic Risk Is Associated With Long-Term Coronary Plaque Progression and High-Risk Plaque.

Authorship 1685402
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Authorship 1686826
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linked information resource: Does Mechanical Circulatory Support-Assisted Percutaneous Coronary Intervention Improve Left Ventricular Function?

Integrating Clinical, Genetic, and Electrocardiogram-Based Artificial Intelligence to Estimate Risk of Incident Atrial Fibrillation.
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author list: Kany S, Rämö JT, Friedman SF, Weng LC, Roselli C, Kim MS, Fahed AC, Lubitz SA, Maddah M, Ellinor PT, Khurshid S
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information resource reference: Integrating Clinical, Genetic, and Electrocardiogram-Based Artificial Intelligence to Estimate Risk of Incident Atrial Fibrillation. medRxiv. 2024 Aug 14.
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Polygenic Risk Is Associated With Long-Term Coronary Plaque Progression and High-Risk Plaque.
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Instability of high polygenic risk classification and mitigation by integrative scoring.
PubMed Identifier: 39211853
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Does Mechanical Circulatory Support-Assisted Percutaneous Coronary Intervention Improve Left Ventricular Function?
PubMed Identifier: 39131479
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Authorship 490202
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linked information resource: Connecting the Lines between Hypogonadism and Atherosclerosis.

Authorship 665171
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linked information resource: Pregnancy in a woman with homozygous familial hypercholesterolemia not on low-density lipoprotein apheresis.

Pregnancy in a woman with homozygous familial hypercholesterolemia not on low-density lipoprotein apheresis.
PubMed Identifier: 23946902
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linked information resource: Multivariate genomic analysis of 5?million people elucidates the genetic architecture of shared components of the metabolic syndrome.

Multivariate genomic analysis of 5?million people elucidates the genetic architecture of shared components of the metabolic syndrome.
PubMed Identifier: 39349817
author list: Park S, Kim S, Kim B, Kim DS, Kim J, Ahn Y, Kim H, Song M, Shim I, Jung SH, Cho C, Lim S, Hong S, Jo H, Fahed AC, Natarajan P, Ellinor PT, Torkamani A, Park WY, Yu TY, Myung W, Won HH
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Authorship 74759
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linked information resource: Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype.

Assistant Professor of Medicine
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Genomic Drivers of Coronary Artery Disease and Risk of Future Outcomes After Coronary Angiography.
PubMed Identifier: 39836422
author list: Supriami K, Urbut SM, Tello-Ayala JR, Unlu O, Friedman SF, Abou-Karam R, Koyama S, Uddin MM, Pomerantsev E, Lu MT, Honigberg MC, Aragam KG, Doshi-Velez F, Patel AP, Natarajan P, Ellinor PT, Fahed AC
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Polygenic Risk Scores in Human Disease.
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linked information resource: Polygenic Risk Scores in Human Disease.

Authorship 1724062
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linked information resource: Genomic Drivers of Coronary Artery Disease and Risk of Future Outcomes After Coronary Angiography.

Authorship 1724605
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linked information resource: Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course.

Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course.
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author list: Urbut SM, Cho SMJ, Paruchuri K, Truong B, Haidermota S, Peloso GM, Hornsby WE, Philippakis A, Fahed AC, Natarajan P
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Authorship 1730583
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linked information resource: Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk Scores.

Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk Scores.
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author list: Khan N, Shaar A, Kunji K, Khan A, Elshrif M, Bashir M, Ali MT, Al Haj Zen A, Kiryluk K, Nemer G, Fahed AC, Saad M
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Instability of high polygenic risk classification and mitigation by integrative scoring.
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linked information resource: Heart failure in congenital heart disease: a confluence of acquired and congenital.

Heart failure in congenital heart disease: a confluence of acquired and congenital.
PubMed Identifier: 24275306
author list: Fahed AC, Roberts AE, Mital S, Lakdawala NK
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information resource reference: Heart failure in congenital heart disease: a confluence of acquired and congenital. Heart Fail Clin. 2014 Jan; 10(1):219-27.
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Machine Learning-Based Plasma Protein Risk Score Improves Atrial Fibrillation Prediction Over Clinical and Genomic Models.
PubMed Identifier: 40525300
author list: Kim MS, Khurshid S, Kany S, Weng LC, Urbut S, Roselli C, Wijdeveld LFJM, Jurgens SJ, Rämö JT, Ellinor PT, Fahed AC
published in: Circulation. Genomic and precision medicine
information resource reference: Machine Learning-Based Plasma Protein Risk Score Improves Atrial Fibrillation Prediction Over Clinical and Genomic Models. Circ Genom Precis Med. 2025 Aug; 18(4):e004943.
journal title abbreviation: Circ Genom Precis Med
publication date: 2025-06-17T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Instructor in Medicine
is primary position: true
position in department: Medicine
position in division: Cardiology
sort order: 1
type: Position
HR job title: Instructor in Medicine
position in organization: Massachusetts General Hospital

Electrocardiogram-Based Artificial Intelligence to Identify Coronary Artery Disease.
PubMed Identifier: 40749517
author list: Kany S, Friedman SF, Al-Alusi M, Khurshid S, Rämö JT, Pipilas D, Pirruccello JP, Reeder C, Philippakis AA, Ho JE, Maddah M, Ellinor PT, Fahed AC
published in: JACC. Advances
information resource reference: Electrocardiogram-Based Artificial Intelligence to Identify Coronary Artery Disease. JACC Adv. 2025 Sep; 4(9):102041.
journal title abbreviation: JACC Adv
publication date: 2025-07-31T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

AHA PREVENT Equations and Cardiovascular Disease Risk in Diverse Health Care Populations.
PubMed Identifier: 40669956
author list: Cho SMJ, Levin M, Chen R, Samarakoon R, Judy R, Hartmann K, Postupaka D, Viscosi V, Farber-Eger E, Fahed AC, Honigberg MC, Patel CJ, Hornsby W, Wells QS, Damrauer SM, Do R, Natarajan P
published in: Journal of the American College of Cardiology
information resource reference: AHA PREVENT Equations and Cardiovascular Disease Risk in Diverse Health Care Populations. J Am Coll Cardiol. 2025 Jul 22; 86(3):181-192.
journal title abbreviation: J Am Coll Cardiol
publication date: 2025-07-22T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 706758
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Low-density lipoprotein levels and not mutation status predict intima-media thickness in familial hypercholesterolemia.

Authorship 706759
type: Authorship
linked author: Fahed, Akl
linked information resource: "Mutations in Human Genetic Disease", edited by David N. Cooper and Jian-Min Chen

"Mutations in Human Genetic Disease", edited by David N. Cooper and Jian-Min Chen
author list: Akl C. Fahed and Georges M. Nemer
published in: Genetic Causes of Syndromic and Non-Syndromic Congenital Heart Disease
information resource reference: "Mutations in Human Genetic Disease", edited by David N. Cooper and Jian-Min Chen. Genetic Causes of Syndromic and Non-Syndromic Congenital Heart Disease. 2012.
publication date: 2012-10-12T00:00:00
year: 2012
type: Academic Article
type: Article
type: Document
type: Information Resource

Low-density lipoprotein levels and not mutation status predict intima-media thickness in familial hypercholesterolemia.
PubMed Identifier: 24120234
author list: Fahed AC, Habib RH, Nemer GM, Azar ST, Andary RR, Arabi MT, Moubarak EM, Bitar FF, Haddad FF
published in: Annals of vascular surgery
information resource reference: Low-density lipoprotein levels and not mutation status predict intima-media thickness in familial hypercholesterolemia. Ann Vasc Surg. 2014 Feb; 28(2):421-6.
journal title abbreviation: Ann Vasc Surg
publication date: 2013-10-09T00:00:00
year: 2013
type: Academic Article
type: Article
type: Document
type: Information Resource

Contributions of Common, Rare, and Somatic Genetic Variants to Incidence of Atrial Fibrillation.
PubMed Identifier: 41060636
author list: Zhang R, Kim MS, Yin W, Liao S, Zhu X, Yang X, Yu K, Sui Y, Roselli C, Khurshid S, Chen Q, A Y, Zhao H, Xu T, Huang X, Pu J, Liu Z, Natarajan P, Zhai G, Ellinor PT, Wang M, Fahed AC
published in: JAMA cardiology
information resource reference: Contributions of Common, Rare, and Somatic Genetic Variants to Incidence of Atrial Fibrillation. JAMA Cardiol. 2025 Dec 01; 10(12):1240-1248.
journal title abbreviation: JAMA Cardiol
publication date: 2025-12-01T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Outcomes after coronary angiography in individuals with elevated lipoprotein(a).
PubMed Identifier: 41231412
author list: Supriami K, Faaborg-Andersen CC, Cho SMJ, Tello-Ayala JR, Abou-Karam R, Pomerantsev E, Viscosi V, Haidermota S, Hornsby W, Natarajan P, Ellinor PT, Honigberg MC, Fahed AC
published in: European journal of preventive cardiology
information resource reference: Outcomes after coronary angiography in individuals with elevated lipoprotein(a). Eur J Prev Cardiol. 2025 Nov 13.
journal title abbreviation: Eur J Prev Cardiol
publication date: 2025-11-13T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Blood Pressure Polygenic Score Predicts Long-Term Blood Pressure Control and Treatment-Resistant Hypertension.
PubMed Identifier: 41532316
author list: Cho SMJ, Ruan Y, Lee HH, Koyama S, Juraschek SP, Allen NB, Yang E, McEvoy JW, Secemsky EA, Honigberg MC, Fahed AC, Patel AP, Hornsby WE, Natarajan P
published in: Hypertension (Dallas, Tex. : 1979)
information resource reference: Blood Pressure Polygenic Score Predicts Long-Term Blood Pressure Control and Treatment-Resistant Hypertension. Hypertension. 2026 Mar; 83(3):e26399.
journal title abbreviation: Hypertension
publication date: 2026-01-14T00:00:00
year: 2026
type: Academic Article
type: Article
type: Document
type: Information Resource

Traumatic Spinal Cord Injury and Subsequent Risk of Developing Chronic Cardiovascular, Neurologic, Psychiatric, and Endocrine Disorders.
PubMed Identifier: 41186949
author list: Mashlah A, Marini S, Mills H, Yahya T, Radmanesh F, Chalif J, Zusman BE, Bernstock JD, Al Mansi MH, Grashow R, Abd-El-Barr MM, Zaidi HA, Lu Y, Salim A, Fahed AC, Manley GT, Halabi C, Digiorgio A, Zafonte R, Izzy S
published in: JAMA network open
information resource reference: Traumatic Spinal Cord Injury and Subsequent Risk of Developing Chronic Cardiovascular, Neurologic, Psychiatric, and Endocrine Disorders. JAMA Netw Open. 2025 Nov 03; 8(11):e2541157.
journal title abbreviation: JAMA Netw Open
publication date: 2025-11-03T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Genomics reveals eleven obesity endotypes with distinct biological and phenotypic signatures.
PubMed Identifier: 40630572
author list: Kim MS, Song M, Kim H, Park S, Shim I, Lim S, Kim B, Chen X, Sui Y, Jemma Cho SM, Koyama S, Yun JS, Natarajan P, Ellinor PT, Fahed AC, Won HH
published in: medRxiv : the preprint server for health sciences
information resource reference: Genomics reveals eleven obesity endotypes with distinct biological and phenotypic signatures. medRxiv. 2025 Jul 02.
journal title abbreviation: medRxiv
publication date: 2025-07-02T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Genetics of Cholesterol and Coronary Disease Risk across Six Global Ancestries.
PubMed Identifier: 41147828
author list: Urbut SM, Chen Q, Sui Y, Misra A, Koyama S, Hornsby W, Peloso GM, Finer S, van Heel DA, Ito K, Alkuraya F, Fahed AC, Wang M, Natarajan P
published in: NEJM evidence
information resource reference: Genetics of Cholesterol and Coronary Disease Risk across Six Global Ancestries. NEJM Evid. 2025 Nov; 4(11):EVIDoa2500105.
journal title abbreviation: NEJM Evid
publication date: 2025-10-28T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Genetics and context for precision health in Greater Boston.
PubMed Identifier: 41298473
author list: Koyama S, Wang Y, Paruchuri K, Uddin MM, Cho SMJ, Urbut SM, Sui Y, Fahed AC, Kamineni H, Haidermota S, Hornsby WE, Green RC, Daly MJ, Neale BM, Ellinor PT, Smoller JW, Slaugenhaupt SA, Lebo MS, Karlson EW, Martin AR, Natarajan P
published in: Nature communications
information resource reference: Genetics and context for precision health in Greater Boston. Nat Commun. 2025 Nov 26; 16(1):11661.
journal title abbreviation: Nat Commun
publication date: 2025-11-26T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Polygenic Risk Based Detection and Treatment of Subclinical Coronary Atherosclerosis in the PROACT Clinical Trials.
PubMed Identifier: 41706060
author list: Abou-Karam R, Kim MS, Jemma Cho SM, Bitar F, Gady S, Cheng F, Thompson AG, Karlson EW, Natarajan P, Ellinor PT, Foldyna B, Ghebremichael MS, Atlas SJ, Ridker PM, Lu MT, Fahed AC
published in: Journal of the American College of Cardiology
information resource reference: Polygenic Risk Based Detection and Treatment of Subclinical Coronary Atherosclerosis in the PROACT Clinical Trials. J Am Coll Cardiol. 2026 Feb 06.
journal title abbreviation: J Am Coll Cardiol
publication date: 2026-02-06T00:00:00
year: 2026
type: Academic Article
type: Article
type: Document
type: Information Resource

Patel, Aniruddh
eCommons Login: APP11
first name: Aniruddh
last name: Patel
full name: Aniruddh Pradip Patel, M.D.
has faculty rank: Assistant Professor
Person ID: 127398
person in primary position: Assistant Professor of Medicine
type: Agent
type: Person
preferred title: Assistant Professor of Medicine

Authorship 735192
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.

UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.
PubMed Identifier: 24771548
author list: Fahed AC, McDonough B, Gouvion CM, Newell KL, Dure LS, Bebin M, Bick AG, Seidman JG, Harter DH, Seidman CE
published in: Annals of neurology
information resource reference: UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration. Ann Neurol. 2014 May; 75(5):793-798.
journal title abbreviation: Ann Neurol
publication date: 2014-05-09T00:00:00
year: 2014
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1776010
type: Authorship
author rank in publication: 8
linked author: Fahed, Akl
linked information resource: Genetics and context for precision health in Greater Boston.

Authorship 1777543
type: Authorship
author rank in publication: 10
linked author: Fahed, Akl
linked information resource: AHA PREVENT Equations and Cardiovascular Disease Risk in Diverse Health Care Populations.

Authorship 1778958
type: Authorship
author rank in publication: 22
linked author: Fahed, Akl
linked information resource: Contributions of Common, Rare, and Somatic Genetic Variants to Incidence of Atrial Fibrillation.

Authorship 1780145
type: Authorship
author rank in publication: 15
linked author: Fahed, Akl
linked information resource: Traumatic Spinal Cord Injury and Subsequent Risk of Developing Chronic Cardiovascular, Neurologic, Psychiatric, and Endocrine Disorders.

Authorship 1781902
type: Authorship
author rank in publication: 16
linked author: Fahed, Akl
linked information resource: Polygenic Risk Based Detection and Treatment of Subclinical Coronary Atherosclerosis in the PROACT Clinical Trials.

Authorship 1784703
type: Authorship
author rank in publication: 11
linked author: Fahed, Akl
linked information resource: Blood Pressure Polygenic Score Predicts Long-Term Blood Pressure Control and Treatment-Resistant Hypertension.

Authorship 1777573
type: Authorship
author rank in publication: 11
linked author: Fahed, Akl
linked information resource: Machine Learning-Based Plasma Protein Risk Score Improves Atrial Fibrillation Prediction Over Clinical and Genomic Models.

Authorship 1777999
type: Authorship
author rank in publication: 13
linked author: Fahed, Akl
linked information resource: Electrocardiogram-Based Artificial Intelligence to Identify Coronary Artery Disease.

Authorship 1779619
type: Authorship
author rank in publication: 15
linked author: Fahed, Akl
linked information resource: Genomics reveals eleven obesity endotypes with distinct biological and phenotypic signatures.

Authorship 1780933
type: Authorship
author rank in publication: 13
linked author: Fahed, Akl
linked information resource: Outcomes after coronary angiography in individuals with elevated lipoprotein(a).

Authorship 1782488
type: Authorship
author rank in publication: 12
linked author: Fahed, Akl
linked information resource: Genetics of Cholesterol and Coronary Disease Risk across Six Global Ancestries.

Authorship 1813473
type: Authorship
author rank in publication: 3
linked author: Fahed, Akl
linked information resource: Grant Funding for Immigrant Cardiovascular Health Research in the US and Canada.

Authorship 1816861
type: Authorship
author rank in publication: 6
linked author: Fahed, Akl
linked information resource: Predictors of Variability in Coronary Flow Reserve and Microvascular Resistance Measurement Using the Bolus Thermodilution Technique.

Authorship 1818328
type: Authorship
author rank in publication: 13
linked author: Fahed, Akl
linked information resource: Comprehensive benchmarking single and multi ancestry polygenic score methods with the PGS-hub platform.

Authorship 1830661
type: Authorship
author rank in publication: 7
linked author: Fahed, Akl
linked information resource: Multicenter Prospective Assessment of Coronary Microvascular Dysfunction: Primary Results of the FlowLab Study.

Authorship 1847038
type: Authorship
author rank in publication: 16
linked author: Fahed, Akl
linked information resource: ACE inhibition increases Alzheimer's disease risk by promoting tau phosphorylation.

Authorship 1851906
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: Unraveling the genetic blueprint of coronary artery disease: The role of polygenic risk scores in risk prediction.

Comprehensive benchmarking single and multi ancestry polygenic score methods with the PGS-hub platform.
PubMed Identifier: 41580418
author list: Chen X, Wang F, Zhao H, Hao J, A Y, Yang X, Xu T, Zhou Y, Chen Q, Zhang R, Yu K, Zaib K, Fahed AC, Zhai G, Wang M
published in: Nature communications
information resource reference: Comprehensive benchmarking single and multi ancestry polygenic score methods with the PGS-hub platform. Nat Commun. 2026 Jan 25; 17(1).
journal title abbreviation: Nat Commun
publication date: 2026-01-25T00:00:00
year: 2026
type: Academic Article
type: Article
type: Document
type: Information Resource

ACE inhibition increases Alzheimer's disease risk by promoting tau phosphorylation.
PubMed Identifier: 40832424
author list: Kim MS, Park S, Kim JH, Myung W, Song M, Do R, Nho K, Kim E, Hwang S, Yu Z, Natarajan P, Kim HJ, Son HJ, Park WY, Sui Y, Fahed AC, Ellinor PT, Ali M, Gong K, Cruchaga C, Yon DK, Seo J, Shin JY, Jo DG, Won HH
published in: medRxiv : the preprint server for health sciences
information resource reference: ACE inhibition increases Alzheimer's disease risk by promoting tau phosphorylation. medRxiv. 2025 Aug 12.
journal title abbreviation: medRxiv
publication date: 2025-08-12T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Predictors of Variability in Coronary Flow Reserve and Microvascular Resistance Measurement Using the Bolus Thermodilution Technique.
PubMed Identifier: 41195810
author list: Galo J, Maksoud A, Shah S, Toleva O, Kobayashi Y, Fahed AC, Shlofmitz E, Sharma A, Buijs JOD, Spinelli J, Rapoza R, Bergmark B, Hashim H
published in: Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
information resource reference: Predictors of Variability in Coronary Flow Reserve and Microvascular Resistance Measurement Using the Bolus Thermodilution Technique. Catheter Cardiovasc Interv. 2026 Jan; 107(1):153-161.
journal title abbreviation: Catheter Cardiovasc Interv
publication date: 2025-11-06T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Unraveling the genetic blueprint of coronary artery disease: The role of polygenic risk scores in risk prediction.
PubMed Identifier: 41561400
author list: El Ghazawi A, Fahed AC, Fawaz N, Fakih Y, Alam S, Refaat M
published in: American heart journal plus : cardiology research and practice
information resource reference: Unraveling the genetic blueprint of coronary artery disease: The role of polygenic risk scores in risk prediction. Am Heart J Plus. 2026 Feb; 62:100712.
journal title abbreviation: Am Heart J Plus
publication date: 2026-01-02T00:00:00
year: 2026
type: Academic Article
type: Article
type: Document
type: Information Resource

Multicenter Prospective Assessment of Coronary Microvascular Dysfunction: Primary Results of the FlowLab Study.
PubMed Identifier: 41014809
author list: Bergmark BA, Shah S, Toleva O, Maksoud A, Kearney KE, Kobayashi Y, Fahed AC, Hashim H, Sharma A, Blair J, Chehab BM, Kanakadandi U, Jaffer FA, Jeremias A, Gross DA, Baljepally R, Ali ZA, Reddy G, Shlofmitz E, Moussa I, Zhang S, Murphy SA, Ahmed S, Spinelli J, Meinen J, Rapoza RJ, Sabatine MS
published in: JACC. Advances
information resource reference: Multicenter Prospective Assessment of Coronary Microvascular Dysfunction: Primary Results of the FlowLab Study. JACC Adv. 2025 Nov; 4(11 Pt 1):102179.
journal title abbreviation: JACC Adv
publication date: 2025-09-26T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Grant Funding for Immigrant Cardiovascular Health Research in the US and Canada.
PubMed Identifier: 41329490
author list: Bedrouni W, Bedrouni M, Fahed AC, Anand SS, Bessissow A, Touyz R, Huynh T
published in: JAMA network open
information resource reference: Grant Funding for Immigrant Cardiovascular Health Research in the US and Canada. JAMA Netw Open. 2025 Dec 01; 8(12):e2546110.
journal title abbreviation: JAMA Netw Open
publication date: 2025-12-01T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Assistant Professor of Medicine
is primary position: true
position in department: Medicine
position in division: Cardiology
sort order: 1
type: Position
HR job title: Assistant Professor of Medicine
position in organization: Massachusetts General Hospital

Authorship 743679
type: Authorship
author rank in publication: 4
linked author: Fahed, Akl
linked information resource: P569A novel role for NFATC1 in patients with both congenital heart disease and glaucoma.

Authorship 743680
type: Authorship
author rank in publication: 3
linked author: Fahed, Akl
linked information resource: P329GATA5: a key player in congenital heart diseases.

P569A novel role for NFATC1 in patients with both congenital heart disease and glaucoma.
PubMed Identifier: 25020296
author list: Hariri H, Farhat T, Khalaf R, Fahed A, Al-Haddad C, Arabi M, Bitar F, Nemer G
published in: Cardiovascular research
information resource reference: P569A novel role for NFATC1 in patients with both congenital heart disease and glaucoma. Cardiovasc Res. 2014 Jul 15; 103 Suppl 1:S102.
journal title abbreviation: Cardiovasc Res
publication date: 2014-06-27T00:00:00
year: 2014
type: Academic Article
type: Article
type: Document
type: Information Resource

P329GATA5: a key player in congenital heart diseases.
PubMed Identifier: 25020719
author list: Kassab K, Hariri H, Fahed A, El-Rassi I, Bitar F, Nemer G
published in: Cardiovascular research
information resource reference: P329GATA5: a key player in congenital heart diseases. Cardiovasc Res. 2014 Jul 15; 103 Suppl 1:S59-60.
journal title abbreviation: Cardiovasc Res
publication date: 2014-06-27T00:00:00
year: 2014
type: Academic Article
type: Article
type: Document
type: Information Resource

Professor of Medicine
is primary position: true
position in department: Medicine
position in division: Cardiology
sort order: 1
type: Position
HR job title: Professor of Medicine
position in organization: Massachusetts General Hospital

Authorship 370893
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia.

Authorship 781531
type: Authorship
author rank in publication: 3
linked author: Fahed, Akl
linked information resource: Students' perceptions of peer-organized extra-curricular research course during medical school: a qualitative study.

Authorship 781532
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.

Students' perceptions of peer-organized extra-curricular research course during medical school: a qualitative study.
PubMed Identifier: 25764441
author list: Nazha B, Salloum RH, Fahed AC, Nabulsi M
published in: PloS one
information resource reference: Students' perceptions of peer-organized extra-curricular research course during medical school: a qualitative study. PLoS One. 2015; 10(3):e0119375.
journal title abbreviation: PLoS One
publication date: 2015-03-12T00:00:00
year: 2015
type: Academic Article
type: Article
type: Document
type: Information Resource

NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.
PubMed Identifier: 25742962
author list: Abou Hassan OK, Fahed AC, Batrawi M, Arabi M, Refaat MM, DePalma SR, Seidman JG, Seidman CE, Bitar FF, Nemer GM
published in: Scientific reports
information resource reference: NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity. Sci Rep. 2015 Mar 06; 5:8848.
journal title abbreviation: Sci Rep
publication date: 2015-03-06T00:00:00
year: 2015
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 298625
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Cystic mucinous tumors of the urachus: carcinoma in situ or adenoma of unknown malignant potential?

Authorship 243251
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Diet, genetics, and disease: a focus on the middle East and north Africa region.

Authorship 462288
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation.

Authorship 815254
type: Authorship
author rank in publication: 5
linked author: Fahed, Akl
linked information resource: A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy?

A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy?
PubMed Identifier: 26174680
author list: Gharibeh L, El-Rassy I, Soubra A, Safa R, Fahed A, Tanos R, Arabi M, Kambris Z, Bitar F, Nemer G
published in: Journal of genetics
information resource reference: A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy? J Genet. 2015 Jun; 94(2):309-12.
journal title abbreviation: J Genet
publication date: 2015-06-01T00:00:00
year: 2015
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 861581
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: The Muscle-Bound Heart.

Authorship 861582
type: Authorship
linked author: Fahed, Akl
linked information resource: Journal of the American College of Cardiology

Journal of the American College of Cardiology
author list: Fahed AC, Nemer G, Bitar FF, Arnaout S, Abchee AB, Ware J, Batrawi M, DePalma SR, McDonough B, Arabi MT, Seidman JG, Seidman CE
published in: The R21C Mutation in Troponin I has a Founder Effect in South Lebanon and Causes Malignant Hypertrophic Cardiomyopathy
information resource reference: Journal of the American College of Cardiology. The R21C Mutation in Troponin I has a Founder Effect in South Lebanon and Causes Malignant Hypertrophic Cardiomyopathy. 2015; 65(10S).
publication date: 2015-02-01T00:00:00
year: 2015
type: Academic Article
type: Article
type: Document
type: Information Resource

The Muscle-Bound Heart.
PubMed Identifier: 26920199
author list: Refaat MM, Fahed AC, Hassanieh S, Hotait M, Arabi M, Skouri H, Seidman JG, Seidman CE, Bitar FF, Nemer G
published in: Cardiac electrophysiology clinics
information resource reference: The Muscle-Bound Heart. Card Electrophysiol Clin. 2016 Mar; 8(1):223-31.
journal title abbreviation: Card Electrophysiol Clin
publication date: 2016-03-01T00:00:00
year: 2016
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 876273
type: Authorship
author rank in publication: 4
linked author: Fahed, Akl
linked information resource: GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.

GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.
PubMed Identifier: 27066509
author list: Kassab K, Hariri H, Gharibeh L, Fahed AC, Zein M, El-Rassy I, Nemer M, El-Rassi I, Bitar F, Nemer G
published in: Molecular genetics & genomic medicine
information resource reference: GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient. Mol Genet Genomic Med. 2016 Mar; 4(2):160-71.
journal title abbreviation: Mol Genet Genomic Med
publication date: 2015-12-20T00:00:00
year: 2015
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 884882
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy.

Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy.
PubMed Identifier: 27247956
author list: Fahed AC, Khalaf R, Salloum R, Andary RR, Safa R, El-Rassy I, Moubarak E, Azar ST, Bitar FF, Nemer G
published in: Molecular genetics & genomic medicine
information resource reference: Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy. Mol Genet Genomic Med. 2016 May; 4(3):283-91.
journal title abbreviation: Mol Genet Genomic Med
publication date: 2016-02-24T00:00:00
year: 2016
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 92157
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Genetics of congenital heart disease: the glass half empty.

Assistant Professor
sort order: 2
type: Faculty Rank

Full Professor
sort order: 0
type: Faculty Rank

Instructor
sort order: 4
type: Faculty Rank

Lecturer
sort order: 3
type: Faculty Rank

Other Faculty
sort order: 5
type: Faculty Rank

Authorship 624981
type: Authorship
linked author: Fahed, Akl
linked information resource: Wild Edible Plants: Promoting Dietary Diversity in Poor Communities of Lebanon

Authorship 454178
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Familial hypercholesterolemia: the lipids or the genes?

Authorship 982502
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: Yellow plaques on the hands of a 10-year-old girl.

Yellow plaques on the hands of a 10-year-old girl.
PubMed Identifier: 28522056
author list: Saliba EC, Fahed AC
published in: Journal of the American Academy of Dermatology
information resource reference: Yellow plaques on the hands of a 10-year-old girl. J Am Acad Dermatol. 2017 Jun; 76(6):e193-e194.
journal title abbreviation: J Am Acad Dermatol
publication date: 2017-06-01T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

Genetics of congenital heart disease: the glass half empty.
PubMed Identifier: 23410880
author list: Fahed AC, Gelb BD, Seidman JG, Seidman CE
published in: Circulation research
information resource reference: Genetics of congenital heart disease: the glass half empty. Circ Res. 2013 Feb 15; 112(4):707-20.
journal title abbreviation: Circ Res
publication date: 2013-02-15T00:00:00
year: 2013
type: Academic Article
type: Article
type: Document
type: Information Resource

The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia.
PubMed Identifier: 22487947
author list: Fahed AC, Bitar FF, Khalaf RI, Moubarak EM, Azar ST, Nemer GM
published in: Endocrine
information resource reference: The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia. Endocrine. 2012 Oct; 42(2):445-8.
journal title abbreviation: Endocrine
publication date: 2012-04-10T00:00:00
year: 2012
type: Academic Article
type: Article
type: Document
type: Information Resource

185 Cambridge St
type: Address
address line 1: MGH Cardiovascular Research Center
address line 2: Richard B. Simches Research Center
address line 3: 185 Cambridge St
city: Boston
postal code: 02114
state or province: MA

Cystic mucinous tumors of the urachus: carcinoma in situ or adenoma of unknown malignant potential?
PubMed Identifier: 22704322
author list: Fahed AC, Nonaka D, Kanofsky JA, Huang WC
published in: The Canadian journal of urology
information resource reference: Cystic mucinous tumors of the urachus: carcinoma in situ or adenoma of unknown malignant potential? Can J Urol. 2012 Jun; 19(3):6310-3.
journal title abbreviation: Can J Urol
publication date: 2012-06-01T00:00:00
year: 2012
type: Academic Article
type: Article
type: Document
type: Information Resource

Connecting the Lines between Hypogonadism and Atherosclerosis.
PubMed Identifier: 22518131
author list: Fahed AC, Gholmieh JM, Azar ST
published in: International journal of endocrinology
information resource reference: Connecting the Lines between Hypogonadism and Atherosclerosis. Int J Endocrinol. 2012; 2012:793953.
journal title abbreviation: Int J Endocrinol
publication date: 2012-02-16T00:00:00
year: 2012
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1034898
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: Frequency of Guideline-Based Statin Therapy in Adults With Congenital Heart Disease.

Frequency of Guideline-Based Statin Therapy in Adults With Congenital Heart Disease.
PubMed Identifier: 29268935
author list: Flannery LD, Fahed AC, DeFaria Yeh D, Youniss MA, Barinsky GL, Stefanescu Schmidt AC, Benavidez OJ, Meigs JB, Bhatt AB
published in: The American journal of cardiology
information resource reference: Frequency of Guideline-Based Statin Therapy in Adults With Congenital Heart Disease. Am J Cardiol. 2018 02 15; 121(4):485-490.
journal title abbreviation: Am J Cardiol
publication date: 2017-11-23T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1037165
type: Authorship
author rank in publication: 2
linked author: Fahed, Akl
linked information resource: A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects.

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects.
PubMed Identifier: 29326753
author list: Kamar A, Fahed AC, Shibbani K, El-Hachem N, Bou-Slaiman S, Arabi M, Kurban M, Seidman JG, Seidman CE, Haidar R, Baydoun E, Nemer G, Bitar F
published in: Frontiers in genetics
information resource reference: A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects. Front Genet. 2017; 8:217.
journal title abbreviation: Front Genet
publication date: 2017-12-18T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1042127
type: Authorship
author rank in publication: 1
linked author: Fahed, Akl
linked information resource: Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia.

Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia.
PubMed Identifier: 28761763
author list: Fahed AC, Shibbani K, Andary RR, Arabi MT, Habib RH, Nguyen DD, Haddad FF, Moubarak E, Nemer G, Azar ST, Bitar FF
published in: Cholesterol
information resource reference: Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia. Cholesterol. 2017; 2017:3685265.
journal title abbreviation: Cholesterol
publication date: 2017-07-06T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource