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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

• Axel Freischmidt, Thomas Wieland, +37 authors Jochen Hans Weishaupt
• Nature Neuroscience
• 2015

Amyotrophic lateral sclerosis (ALS) is a genetically heterogeneous neurodegenerative syndrome hallmarked by adult-onset loss of motor neurons. We performed exome sequencing of 252 familial ALS (fALS)… (More)

Short term load forecasting for small scale power system using fuzzy logic

• M. F. I. Khamis, Zuhairi Baharudin, N. H. Hamid, M. F. Abdullah, Frida Nordin
• 2011 Fourth International Conference on Modeling…
• 2011

Load forecasting has an important role in planning and operations in power generation plant. Many new forecasting systems have been presented and proposed in recent years. Gas District Cooling (GDC)… (More)

Development of Al-Mu'awwidhah computing for personal data protection against abnormal attacks

• A. F. Shamsudin, Joseph A Ibrahim, T. M. Sembok, Frida Nordin, Jamshed Hashim, Wan Sabri Wan Yusof
• 2013 5th International Conference on Information…
• 2013

Personal data is constantly being compromised not just by the normal identity thefts but also abnormal attacks. The Islamic concept of Al-Mu'awwidhah inspired the discovery of non-parametric… (More)

Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis

• Yasuyuki Ohta, Geneviève Soucy, +10 authors Jean-Pierre Julien
• Human molecular genetics
• 2016

Recent genetic studies yielded conflicting results regarding a role for the variant chromogranin B (CHGB)P413L allele as a disease modifier in ALS. Moreover, potential deleterious effects of the… (More)

Sequence variations in C9orf72 downstream of the hexanucleotide repeat region and its effect on repeat-primed PCR interpretation: a large multinational screening study.

• Angelica Nordin, Chizuru Akimoto, +26 authors Peter Munch Andersen
• Amyotrophic lateral sclerosis & frontotemporal…
• 2017

A large GGGGCC-repeat expansion mutation (HREM) in C9orf72 is the most common known cause of ALS and FTD in European populations. Sequence variations immediately downstream of the HREM region have… (More)

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