Familial Hypercholesterolemia: The Lipids or the Genes?

por Fahed, Akl C, Nemer, Georges M
Publicado 2011

Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis

por Fahed, Akl C., Nassar, Anwar H.
Publicado 2012

Connecting the Lines between Hypogonadism and Atherosclerosis

por Fahed, Akl C., Gholmieh, Joanna M., Azar, Sami T.
Publicado 2012

The potential of polygenic scores to improve cost and efficiency of clinical trials

por Fahed, Akl C., Philippakis, Anthony A., Khera, Amit V.
Publicado 2022

Students’ Perceptions of Peer-Organized Extra-Curricular Research Course during Medical School: A Qualitative Study

por Nazha, Bassel, Salloum, Rony H., Fahed, Akl C., Nabulsi, Mona
Publicado 2015

Diet, Genetics, and Disease: A Focus on the Middle East and North Africa Region

por Fahed, Akl C., El-Hage-Sleiman, Abdul-Karim M., Farhat, Theresa I., Nemer, Georges M.
Publicado 2012

Massive underrepresentation of Arabs in genomic studies of common disease

por Bhattacharya, Romit, Chen, NingNing, Shim, Injeong, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S., Fahed, Akl C.
Publicado 2023

GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient

por Kassab, Kameel, Hariri, Hadla, Gharibeh, Lara, Fahed, Akl C., Zein, Manal, El‐Rassy, Inaam, Nemer, Mona, El‐Rassi, Issam, Bitar, Fadi, Nemer, Georges
Publicado 2015

Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course

por Urbut, Sarah M., Cho, So Mi Jemma, Paruchuri, Kaavya, Truong, Buu, Haidermota, Sara, Peloso, Gina, Hornsby, Whitney, Philippakis, Anthony, Fahed, Akl C., Natarajan, Pradeep
Publicado 2023

Variable expressivity and co‐occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy

por Fahed, Akl C., Khalaf, Ruby, Salloum, Rony, Andary, Rabih R., Safa, Raya, El‐Rassy, Inaam, Moubarak, Elie, Azar, Sami T., Bitar, Fadi F., Nemer, Georges
Publicado 2016

Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia

por Fahed, Akl C., Shibbani, Kamel, Andary, Rabih R., Arabi, Mariam T., Habib, Robert H., Nguyen, Denis D., Haddad, Fady F., Moubarak, Elie, Nemer, Georges, Azar, Sami T., Bitar, Fadi F.
Publicado 2017

Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease

por Fahed, Akl C., Wang, Minxian, Patel, Aniruddh P., Ajufo, Ezimamaka, Maamari, Dimitri J., Aragam, Krishna G., Brockman, Deanna G., Vosburg, Trish, Ellinor, Patrick T., Ng, Kenney, Khera, Amit V.
Publicado 2022

Exploring the link between Gilbert’s syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals

por Kartoun, Uri, Fahed, Akl C, Kany, Shinwan, Singh, Pulkit, Khurshid, Shaan, Patel, Aniruddh P, Batra, Puneet, Philippakis, Anthony, Khera, Amit V, Lubitz, Steven A, Ellinor, Patrick T, Anand, Vibha, Ng, Kenney
Publicado 2023

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

por Abou Hassan, Ossama K., Fahed, Akl C., Batrawi, Manal, Arabi, Mariam, Refaat, Marwan M., DePalma, Steven R., Seidman, J. G., Seidman, Christine E., Bitar, Fadi F., Nemer, Georges M.
Publicado 2015

MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record

por Urbut, Sarah M., Yeung, Ming Wai, Khurshid, Shaan, Cho, So Mi Jemma, Schuermans, Art, German, Jakob, Taraszka, Kodi, Fahed, Akl C., Ellinor, Patrick, Trinquart, Ludovic, Parmigiani, Giovanni, Gusev, Alexander, Natarajan, Pradeep
Publicado 2023

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

por Kamar, Amina, Fahed, Akl C., Shibbani, Kamel, El-Hachem, Nehme, Bou-Slaiman, Salim, Arabi, Mariam, Kurban, Mazen, Seidman, Jonathan G., Seidman, Christine E., Haidar, Rachid, Baydoun, Elias, Nemer, Georges, Bitar, Fadi
Publicado 2017

Clinical utility of polygenic scores for cardiometabolic disease in Arabs

por Shim, Injeong, Kuwahara, Hiroyuki, Chen, NingNing, Hashem, Mais O., AlAbdi, Lama, Abouelhoda, Mohamed, Won, Hong-Hee, Natarajan, Pradeep, Ellinor, Patrick T., Khera, Amit V., Gao, Xin, Alkuraya, Fowzan S., Fahed, Akl C.
Publicado 2023

Design and user experience testing of a polygenic score report: a qualitative study of prospective users

por Brockman, Deanna G., Petronio, Lia, Dron, Jacqueline S., Kwon, Bum Chul, Vosburg, Trish, Nip, Lisa, Tang, Andrew, O’Reilly, Mary, Lennon, Niall, Wong, Bang, Ng, Kenney, Huang, Katherine H., Fahed, Akl C., Khera, Amit V.
Publicado 2021

Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy

por Fahed, Akl C., Nemer, Georges, Bitar, Fadi F., Arnaout, Samir, Abchee, Antoine B., Batrawi, Manal, Khalil, Athar, Abou Hassan, Ossama K., DePalma, Steven R., McDonough, Barbara, Arabi, Mariam T., Ware, James S., Seidman, Jonathan G., Seidman, Christine E.
Publicado 2020

Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease

por Maamari, Dimitri J., Brockman, Deanna G., Aragam, Krishna, Pelletier, Renée C., Folkerts, Emma, Neben, Cynthia L., Okumura, Sydney, Hull, Leland E., Philippakis, Anthony A., Natarajan, Pradeep, Ellinor, Patrick T., Ng, Kenney, Zhou, Alicia Y., Khera, Amit V., Fahed, Akl C.
Publicado 2022