1. A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects. Issue 4 (16th September 2009) Authors: Posch, Maximilian G; Gramlich, Michael; Sunde, Margaret; Schmitt, Katharina R; Lee, Stella H Y; Richter, Silke; Kersten, Andrea; Perrot, Andreas; Panek, Anna N; Al Khatib, Iman H; Nemer, Georges; Mégarbané, André; Dietz, Rainer; Stiller, Brigitte; Berger, Felix; Harvey, Richard P; Özcelik, Cemil Journal: Journal of medical genetics Issue: Volume 47:Issue 4(2010) Page Start: 230 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Homozygous Frameshift Mutation in the HOXC13 Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family. Issue 4 (5th March 2013) Authors: Farooq, Muhammad; Kurban, Mazen; Fujimoto, Atsushi; Fujikawa, Hiroki; Abbas, Ossama; Nemer, Georges; Saliba, Jessica; Sleiman, Rima; Tofaili, Mona; Kibbi, Abdul‐Ghani; Ito, Masaaki; Shimomura, Yutaka Journal: Human mutation Issue: Volume 34:Issue 4(2013:Apr.) Page Start: 578 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Absolute quantification of gene expression in drug discovery using RT-qPCR: Case of a drug used in the treatment of leishmaniasis. (31st December 2022) Authors: Al Khoury, Charbel; Nemer, Georges; Guillot, Jacques; Tokajian, Sima Journal: Research in veterinary science Issue: Volume 153(2022) Page Start: 17 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Comparative characterization of sun exposed and sun protected skin‐derived mesenchymal‐like stem cells in variegate porphyria and healthy individuals. Issue 3 (11th December 2020) Authors: Safi, Rémi; Malek, Elie; Nemer, Georges; Sayed, Reem; Eid, Edward; Khalil, Samar; Nasser, Nourhane; Abbas, Ossama; Mohsen‐Kanson, Tala; Kurban, Mazen Journal: Photodermatology, photoimmunology & photomedicine Issue: Volume 37:Issue 3(2021) Page Start: 202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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. Issue 3 (December 2018) Authors: Hariri, Hadla; Kurban, Mazen; Al-Haddad, Christiane; Fahed, Akl C.; Poladian, Sarin; Khalil, Athar; Abbas, Oussama; Arabi, Mariam; Bitar, Fadi; Nemer, Georges Journal: Journal of dermatological science Issue: Volume 92:Issue 3(2018) Page Start: 237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy. (October 2020) Authors: 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. Journal: Circulation Issue: Volume 13:Number 5(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. GATA4 Loss‐of‐Function Mutations Underlie Familial Tetralogy of Fallot. Issue 12 (17th September 2013) Authors: Yang, Yi‐Qing; Gharibeh, Lara; Li, Ruo‐Gu; Xin, Yuan‐Feng; Wang, Juan; Liu, Zhong‐Min; Qiu, Xing‐Biao; Xu, Ying‐Jia; Xu, Lei; Qu, Xin‐Kai; Liu, Xu; Fang, Wei‐Yi; Huang, Ri‐Tai; Xue, Song; Nemer, Georges Journal: Human mutation Issue: Volume 34:Issue 12(2013:Dec.) Page Start: 1662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient. Issue 2 (20th December 2015) Authors: Kassab, Kameel; Hariri, Hadla; Gharibeh, Lara; Fahed, Akl C.; Zein, Manal; El‐Rassy, Inaam; Nemer, Mona; El‐Rassi, Issam; Bitar, Fadi; Nemer, Georges Journal: Molecular genetics & genomic medicine Issue: Volume 4:Issue 2(2016) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetics of inherited cardiocutaneous syndromes: a review. Issue 2 (22nd November 2016) Authors: Bardawil, Tara; Khalil, Samar; Bergqvist, Christina; Abbas, Ossama; Kibbi, Abdul Ghani; Bitar, Fadi; Nemer, Georges; Kurban, Mazen Journal: Open heart Issue: Volume 3:Issue 2(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. In silico evidence of beauvericin antiviral activity against SARS-CoV-2. (February 2022) Authors: Al Khoury, Charbel; Bashir, Zainab; Tokajian, Sima; Nemer, Nabil; Merhi, Georgi; Nemer, Georges Journal: Computers in biology and medicine Issue: Volume 141(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗