sirui zhou
Affiliations: | McGill University (Montreal Neurological Institute) |
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| Duncan CJA, Skouboe MK, Howarth S, et al. (2022) Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic. The Journal of Experimental Medicine. 219 |
| Bakker MK, van der Spek RAA, van Rheenen W, et al. (2020) Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature Genetics |
| Bakker MK, van der Spek RAA, van Rheenen W, et al. (2020) Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature Genetics |
| Keller-Baruch J, Forgetta V, Manousaki D, et al. (2019) Genetically decreased circulating vascular endothelial growth factor and osteoporosis outcomes: A Mendelian randomization study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research |
| Zhou S, Xie P, Quoibion A, et al. (2019) Genetic architecture and adaptations of Nunavik Inuit. Proceedings of the National Academy of Sciences of the United States of America |
| Ambalavanan A, Chaumette B, Zhou S, et al. (2018) Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics |
| Ruskey JA, Zhou S, Santiago R, et al. (2018) The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics |
| Walcott BP, Winkler EA, Zhou S, et al. (2018) Identification of a rare pathway mutation in a non-syndromic human brain arteriovenous malformation via exome sequencing. Human Genome Variation. 5: 18001 |
| Li J, Ruskey JA, Arnulf I, et al. (2018) Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Movement Disorders : Official Journal of the Movement Disorder Society |
| Wang B, Bao S, Zhang Z, et al. (2018) A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population. Neurobiology of Aging |