Said El Shamieh (S El Shamieh, Said El-Shamieh)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 21

Top Venues

Journal of cardiovascular development and disease

Genes

Journal of personalized medicine

BMJ open science

Beirut Arab University

Université de Lorraine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Beirut Arab University Aug 01 2019

Lebanon

Associate Professor

Beirut Arab University Sep 01 2016

Lebanon

Assistant Professor :: Medical Laboratory Sciences

Beirut Arab University Jan 02 2015 - Aug 31 2016

Lebanon

Lecturer :: Faculty of Sciences

Institut de la vision Dec 03 2012 - Dec 01 2014

France

Postdoctoral Fellow :: Genetics

Education History

Université de Lorraine Nov 01 2009 - Sep 01 2012

France

PHD :: Health and Life Sciences

Université de Lorraine Sep 01 2007 - Sep 01 2009

France

MSC :: Health and Life Sciences

Université Libanaise Sep 01 2003 - Sep 01 2007

Lebanon

BSC

Publications

Lama Jaffal, Mariam Ibrahim, Said El Shamieh
Analysis of rod-cone dystrophy genes reveals unique mutational patterns. BMJ open science 6 (1) (2022)
Lama Jaffal, Mariam Ibrahim, Said El Shamieh
Analysis of rod-cone dystrophy genes reveals unique mutational patterns. BMJ open science 6 (1) (2022)
Lama Jaffal, Zamzam Mrad, Mariam Ibrahim, Ali Salami, Isabelle Audo, Christina Zeitz, Said El Shamieh
The research output of rod-cone dystrophy genetics. Orphanet journal of rare diseases 17 (1) (2022)
Hana M A Fakhoury, Said El Shamieh, Amru Rifai, Hani Tamim, Rajaa Fakhoury
Vitamin D Related Gene Polymorphisms and Cholesterol Levels in a Mediterranean Population. Journal of cardiovascular development and disease 9 (4) (2022)
Christina Zeitz, Marco Nassisi, Caroline Laurent-Coriat, Camille Andrieu, Fiona Boyard, Christel Condroyer, Vanessa Démontant, Aline Antonio, Marie-Elise Lancelot, Helen Frederiksen, Barbara Kloeckener-Gruissem, Said El Shamieh, Xavier Zanlonghi, Isabelle Meunier, Anne-Françoise Roux, Saddek Mohand-Saïd, José Alain Sahel, Isabelle Audo
CHM mutation spectrum and disease: An update at the time of human therapeutic trials. Human mutation 42 (4) (2021)
Said El Shamieh, Ali Salami, Mirna Fawaz, Rania Jounblat, Mirna Waked, Rajaa Fakhoury
rs6837671A>G in FAM13A Is a Trans-Ethnic Genetic Variant Interacting with Vitamin D Levels to Affect Chronic Obstructive Pulmonary Disease. Journal of personalized medicine 11 (2) (2021)
Said El Shamieh, Maria G Stathopoulou, Amélie Bonnefond, Ndeye Coumba Ndiaye, Cécile Lecoeur, David Meyre, Sébastien Dadé, Pia Chedid, Ali Salami, Payman Shahabi, George V Dedoussis, Philippe Froguel, Sophie Visvikis-Siest
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French children. Clinical chemistry and laboratory medicine 58 (11) (2021)
Lama Jaffal, Hawraa Joumaa, Zamzam Mrad, Christina Zeitz, Isabelle Audo, Said El Shamieh
The genetics of rod-cone dystrophy in Arab countries: a systematic review. European journal of human genetics : EJHG 29 (6) (2020)
Khaled Naja, Ali Salami, Said El Shamieh, Rajaa Fakhoury
rs622342 in SLC22A1, CYP2C9*2 and CYP2C9*3 and Glycemic Response in Individuals with Type 2 Diabetes Mellitus Receiving Metformin/Sulfonylurea Combination Therapy: 6-Month Follow-Up Study. Journal of personalized medicine 10 (2) (2020)
Pia Chedid, Ali Salami, Said El Shamieh
The Association of rs1898830 in Toll-Like Receptor 2 with Lipids and Blood Pressure. Journal of cardiovascular development and disease 7 (3) (2020)
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, Charles Helou, George Cherfan, Kazem Zibara, Isabelle Audo, Christina Zeitz, Said El Shamieh
Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes. Genes 10 (12) (2019)
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, Charles Helou, Christel Condroyer, Maya El Dor, Georges Cherfan, Christina Zeitz, Isabelle Audo, Kazem Zibara, Said El Shamieh
Novel Missense Mutations in BEST1 Are Associated with Bestrophinopathies in Lebanese Patients. Genes 10 (2) (2019)
Ali Salami, Christy Costanian, Said El Shamieh
rs2569190A>G in CD14 is Independently Associated with Hypercholesterolemia: A Brief Report. Journal of cardiovascular development and disease 6 (4) (2019)
Elise Boulanger-Scemama, Saddek Mohand-Saïd, Said El Shamieh, Vanessa Démontant, Christel Condroyer, Aline Antonio, Christelle Michiels, Fiona Boyard, Jean-Paul Saraiva, Mélanie Letexier, José-Alain Sahel, Christina Zeitz, Isabelle Audo
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies. International journal of molecular sciences 20 (19) (2019)
Said El Shamieh, Fatima Saleh, Shafka Assaad, Fadi Farhat
Next-generation sequencing reveals mutations in RB1, CDK4 and TP53 that may promote chemo-resistance to palbociclib in ovarian cancer. Drug metabolism and personalized therapy 34 (2) (2019)
Ali Salami, Said El Shamieh
Association between SNPs of Circulating Vascular Endothelial Growth Factor Levels, Hypercholesterolemia and Metabolic Syndrome. Medicina (Kaunas, Lithuania) 55 (8) (2019)
Vesna Gorenjak, Dwaine R Vance, Alexandros M Petrelis, Maria G Stathopoulou, Sébastien Dadé, Said El Shamieh, Helena Murray, Christine Masson, John Lamont, Peter Fitzgerald, Sophie Siest
Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy population. PloS one 14 (8) (2019)
Cécile Méjécase, S Mohand-Saïd, Said El Shamieh, A Antonio, C Condroyer, S Blanchard, M Letexier, J-P Saraiva, José Alain Sahel, Isabelle Audo, Christina Zeitz
A novel nonsense variant in REEP6 is involved in a sporadic rod-cone dystrophy case. Clinical genetics 93 (3) (2019)
Cécile Méjécase, Aurélie Hummel, Saddek Mohand-Saïd, Camille Andrieu, Said El Shamieh, Aline Antonio, Christel Condroyer, Fiona Boyard, Marine Foussard, Steven Blanchard, Mélanie Letexier, Jean-Paul Saraiva, José Alain Sahel, Christina Zeitz, Isabelle Audo
Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophy. Clinical genetics 95 (2) (2018)
Isabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, Xavier Zanlonghi, Christel Condroyer, Vanessa Démontant, Fiona Boyard, Aline Antonio, Cécile Méjécase, Said El Shamieh, José Alain Sahel, Christina Zeitz
MERTK mutation update in inherited retinal diseases. Human mutation 39 (7) (2018)
Said El Shamieh, Cécile Méjécase, Matteo Bertelli, Angélique Terray, Christelle Michiels, Christel Condroyer, Stéphane Fouquet, Maxime Sadoun, Emmanuelle Clérin, Binqian Liu, Thierry Léveillard, Olivier Goureau, José-Alain Sahel, Isabelle Audo, Christina Zeitz
Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy. Genes 8 (10) (2017)

Said El Shamieh.css-eqlu8i{font-size:small;padding-left:4px;} (S El Shamieh, Said El-Shamieh)

Publication Activity (10 Years)

Top Topics

Top Venues

Said El Shamieh (S El Shamieh, Said El-Shamieh)