Full Name
Mahmoud Abdul Hossein Pouladi
(not current staff)
Variants
Pouladi M.A.
 
Main Affiliation
 
 
Email
pouladi@nus.edu.sg
 

Publications

Refined By:
Type:  Article
Author:  Pouladi, M.A.
Department:  PAEDIATRICS

Results 1-5 of 5 (Search time: 0.005 seconds).

Issue DateTitleAuthor(s)
12018A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disabilityChia, P.H; Zhong, F.L; Niwa, S; Bonnard, C; Utami, K.H; Zeng, R; Lee, H; Eskin, A; Nelson, S.F; Xie, W.H; Al-Tawalbeh, S; El-Khateeb, M; Shboul, M; Pouladi, M.A ; Al-Raqad, M; Reversade, B 
26-Jan-2021A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental DefectsSahni, Geetika ; Chang, Shu-Yung ; Meng, Jeremy Teo Choon; Tan, Jerome Zu Yao; Fatien, Jean Jacques Clement; Bonnard, Carine; Utami, Kagistia Hana; Chan, Puck Wee; Tan, Thong Teck; Altunoglu, Umut; Kayserili, Hulya; Pouladi, Mahmoud ; Reversade, Bruno ; Toh, Yi-Chin 
3Oct-2019Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2Zeng, Ruizhu; Sidik, Harwin; Robinson, Kim S; Zhong, Franklin L; Reversade, Bruno ; Pouladi, Mahmoud A 
42020Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHengel, H.; Bosso-Lefèvre, C.; Grady, G.; Szenker-Ravi, E.; Li, H.; Pierce, S.; Lebigot, É.; Tan, T.-T.; Eio, M.Y.; Narayanan, G.; Utami, K.H.; Yau, M.; Handal, N.; Deigendesch, W.; Keimer, R.; Marzouqa, H.M.; Gunay-Aygun, M.; Muriello, M.J.; Verhelst, H.; Weckhuysen, S.; Mahida, S.; Naidu, S.; Thomas, T.G.; Lim, J.Y.; Tan, E.S.; Haye, D.; Willemsen, M.A.A.P.; Oegema, R.; Mitchell, W.G.; Pierson, T.M.; Andrews, M.V.; Willing, M.C.; Rodan, L.H.; Barakat, T.S.; van Slegtenhorst, M.; Gavrilova, R.H.; Martinelli, D.; Gilboa, T.; Tamim, A.M.; Hashem, M.O.; AlSayed, M.D.; Abdulrahim, M.M.; Al-Owain, M.; Awaji, A.; Mahmoud, A.A.H.; Faqeih, E.A.; Asmari, A.A.; Algain, S.M.; Jad, L.A.; Aldhalaan, H.M.; Helbig, I.; Koolen, D.A.; Riess, A.; Kraegeloh-Mann, I.; Bauer, P.; Gulsuner, S.; Stamberger, H.; Ng, A.Y.J.; Tang, S.; Tohari, S.; Keren, B.; Schultz-Rogers, L.E.; Klee, E.W.; Barresi, S.; Tartaglia, M.; Mor-Shaked, H.; Maddirevula, S.; Begtrup, A.; Telegrafi, A.; Pfundt, R.; Schüle, R.; Ciruna, B.; Bonnard, C.; Pouladi, M.A. ; Stewart, J.C.; Claridge-Chang, A.; Lefeber, D.J.; Alkuraya, F.S.; Mathuru, A.S.; Venkatesh, B. ; Barycki, J.J.; Simpson, M.A.; Jamuar, S.S.; Schöls, L.; Reversade, B. 
52019Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory featuresZiaei, A.; Xu, X.; Dehghani, L.; Bonnard, C.; Zellner, A.; Ng, A.Y.J.; Tohari, S.; Venkatesh, B. ; Haffner, C.; Reversade, B.; Shaygannejad, V.; Pouladi, M.A.