A multi-objective robust stochastic programming model for disaster relief logistics under uncertainty von Bozorgi-Amiri, Ali, Jabalameli, M. S., Mirzapour Al-e-Hashem, S. M. J.

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Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer’s disease, providing new insights into its disease mechanisms von Wang, Zhen, Zhang, Quanwei, Lin, Jhih-Rong, Jabalameli, M. Reza, Mitra, Joydeep, Nguyen, Nha, Zhang, Zhengdong D.

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Substance abuse and the risk of severe COVID-19: Mendelian randomization confirms the causal role of opioids but hints a negative causal effect for cannabinoids von Jabalameli, M Reza, Zhang, Zhengdong D

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Polygenic prediction of human longevity on the supposition of pervasive pleiotropy von Jabalameli, M. Reza, Lin, Jhih-Rong, Zhang, Quanwei, Wang, Zhen, Mitra, Joydeep, Nguyen, Nha, Gao, Tina, Khusidman, Mark, Sathyan, Sanish, Atzmon, Gil, Milman, Sofiya, Vijg, Jan, Barzilai, Nir, Zhang, Zhengdong D.

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Molecular insights into the role of AMPA receptors in the synaptic plasticity, pathogenesis and treatment of epilepsy: therapeutic potentials of perampanel and antisense oligonucle... von Charsouei, Saeid, Jabalameli, M. Reza, Karimi-Moghadam, Amin

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Fuzzy multi-choice goal programming von Bankian-Tabrizi, Behzad, Shahanaghi, Kamran, Saeed Jabalameli, M.

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Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly von Pengelly, Reuben J, Greville-Heygate, Stephanie, Schmidt, Susanne, Seaby, Eleanor G, Jabalameli, M Reza, Mehta, Sarju G, Parker, Michael J, Goudie, David, Fagotto-Kaufmann, Christine, Mercer, Catherine, Debant, Anne, Ennis, Sarah, Baralle, Diana

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Gene-dense autosomal chromosomes show evidence for increased selection von Jabalameli, M Reza, Horscroft, Clare, Vergara-Lope, Alejandra, Pengelly, Reuben J, Collins, Andrew

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Understanding the disease genome: gene essentiality and the interplay of selection, recombination and mutation von Pengelly, Reuben J, Vergara-Lope, Alejandra, Alyousfi, Dareen, Jabalameli, M Reza, Collins, Andrew

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Chronic tophaceous gout von Jabalameli, M, Bagherifard, A, Hadi, H, Behshad, V, Ghaffari, S

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Genomic expansion of Aldh1a1 protects beavers against high metabolic aldehydes from lipid oxidation von Zhang, Quanwei, Tombline, Gregory, Ablaeva, Julia, Zhang, Lei, Zhou, Xuming, Smith, Zachary, Zhao, Yang, Xiaoli, Alus M., Wang, Zhen, Lin, Jhih-Rong, Jabalameli, M. Reza, Mitra, Joydeep, Nguyen, Nha, Vijg, Jan, Seluanov, Andrei, Gladyshev, Vadim N., Gorbunova, Vera, Zhang, Zhengdong D.

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Unravelling genetic components of longevity von Jabalameli, M Reza, Zhang, Zhengdong D

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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia von Lin, Jhih-Rong, Zhao, Yingjie, Jabalameli, M. Reza, Nguyen, Nha, Mitra, Joydeep, Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Owen, Michael J., Williams, Nigel M., Bassett, Anne S., McDonald-McGinn, Donna M., Gur, Raquel E., Bearden, Carrie E., Morrow, Bernice E., Lachman, Herbert M., Zhang, Zhengdong D.

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Prepatellar subcutaneous calcifications in systemic sclerosis von Jabalameli, M, Bagherifard, A, Zabihiyeganeh, M, Nejadikelarijani, A, Ghaffari, S

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Exome sequencing identifies a disease variant of the mitochondrial ATP‐Mg/Pi carrier SLC25A25 in two families with kidney stones von Jabalameli, M. Reza, Fitzpatrick, Fiona M., Colombo, Roberto, Howles, Sarah A., Leggatt, Gary, Walker, Valerie, Wiberg, Akira, Kunji, Edmund R. S., Ennis, Sarah

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Linkage disequilibrium maps for European and African populations constructed from whole genome sequence data von Vergara-Lope, Alejandra, Jabalameli, M. Reza, Horscroft, Clare, Ennis, Sarah, Collins, Andrew, Pengelly, Reuben J.

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The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibility von Bahreini, Seyed Amir, Jabalameli, M. Reza, Saadatnia, Mohammad, Zahednasab, Hamid

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The design of resilient food supply chain networks prone to epidemic disruptions von Gholami-Zanjani, Seyed Mohammad, Klibi, Walid, Jabalameli, Mohammad Saeed, Pishvaee, Mir Saman

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Rare genetic coding variants associated with human longevity and protection against age-related diseases von Lin, Jhih-Rong, Sin-Chan, Patrick, Napolioni, Valerio, Torres, Guillermo G, Mitra, Joydeep, Zhang, Quanwei, Jabalameli, M Reza, Wang, Zhen, Nguyen, Nha, Gao, Tina, Laudes, Matthias, Görg, Siegfried, Franke, Andre, Nebel, Almut, Greicius, Michael D, Atzmon, Gil, Ye, Kenny, Gorbunova, Vera, Ladiges, Warren C, Shuldiner, Alan R, Niedernhofer, Laura J, Robbins, Paul D, Milman, Sofiya, Suh, Yousin, Vijg, Jan, Barzilai, Nir, Zhang, Zhengdong D

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Are IL2 promoter polymorphisms associated with MS in Iranian patients? - We Do Not Know von Jabalameli, M. R., Zahednasab, H.

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