| Year |
Citation |
Score |
| 2022 |
Duncan CJA, Skouboe MK, Howarth S, Hollensen AK, Chen R, Børresen ML, Thompson BJ, Stremenova Spegarova J, Hatton CF, Stæger FF, Andersen MK, Whittaker J, Paludan SR, Jørgensen SE, Thomsen MK, ... ... Zhou S, et al. Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic. The Journal of Experimental Medicine. 219. PMID 35442417 DOI: 10.1084/jem.20212427 |
0.382 |
|
| 2020 |
Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin K, Li L, ... ... Zhou S, et al. Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature Genetics. PMID 33353957 DOI: 10.1038/s41588-020-00760-4 |
0.413 |
|
| 2020 |
Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin K, Li L, ... ... Zhou S, et al. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature Genetics. PMID 33199917 DOI: 10.1038/s41588-020-00725-7 |
0.414 |
|
| 2019 |
Keller-Baruch J, Forgetta V, Manousaki D, Zhou S, Richards JB. 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. PMID 31821593 DOI: 10.1002/Jbmr.3937 |
0.31 |
|
| 2019 |
Zhou S, Xie P, Quoibion A, Ambalavanan A, Dionne-Laporte A, Spiegelman D, Bourassa CV, Xiong L, Dion PA, Rouleau GA. Genetic architecture and adaptations of Nunavik Inuit. Proceedings of the National Academy of Sciences of the United States of America. PMID 31332017 DOI: 10.1073/Pnas.1810388116 |
0.5 |
|
| 2018 |
Ambalavanan A, Chaumette B, Zhou S, Xie P, He Q, Spiegelman D, Dionne-Laporte A, Bourassa CV, Therrien M, Rochefort D, Xiong L, Dion PA, Joober R, Rapoport JL, Girard SL, et al. 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. PMID 30378261 DOI: 10.1002/Ajmg.B.32683 |
0.454 |
|
| 2018 |
Ruskey JA, Zhou S, Santiago R, Franche LA, Alam A, Roncière L, Spiegelman D, Fon EA, Trempe JF, Kalia LV, Postuma RB, Dupre N, Rivard GE, Assouline S, Amato D, et al. The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics. PMID 29920646 DOI: 10.1111/Cge.13405 |
0.375 |
|
| 2018 |
Walcott BP, Winkler EA, Zhou S, Birk H, Guo D, Koch MJ, Stapleton CJ, Spiegelman D, Dionne-Laporte A, Dion PA, Kahle KT, Rouleau GA, Lawton MT. Identification of a rare pathway mutation in a non-syndromic human brain arteriovenous malformation via exome sequencing. Human Genome Variation. 5: 18001. PMID 29844917 DOI: 10.1038/Hgv.2018.1 |
0.466 |
|
| 2018 |
Li J, Ruskey JA, Arnulf I, Dauvilliers Y, Hu MTM, Högl B, Leblond CS, Zhou S, Ambalavanan A, Ross JP, Bourassa CV, Spiegelman D, Laurent SB, Stefani A, Charley Monaca C, et al. 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. PMID 29756641 DOI: 10.1002/Mds.27385 |
0.602 |
|
| 2018 |
Wang B, Bao S, Zhang Z, Zhou X, Wang J, Fan Y, Zhang Y, Li Y, Chen L, Jia Y, Li J, Li M, Zheng W, Mu N, Wang L, ... ... Zhou S, et al. A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population. Neurobiology of Aging. PMID 29656768 DOI: 10.1016/J.Neurobiolaging.2018.03.006 |
0.482 |
|
| 2018 |
Zhou S, Gan-Or Z, Ambalavanan A, Lai D, Xie P, Bourassa CV, Strong S, Ross JP, Dionne-Laporte A, Spiegelman D, Dupré N, Foroud TM, Xiong L, Dion PA, Rouleau GA. Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Scientific Reports. 8: 4356. PMID 29531279 DOI: 10.1038/S41598-018-21603-7 |
0.665 |
|
| 2018 |
Zhou S, Dion PA, Rouleau GA. Genetics of Intracranial Aneurysms. Stroke. PMID 29437983 DOI: 10.1161/Strokeaha.117.018152 |
0.405 |
|
| 2018 |
Mohtashami S, He Q, Ruskey JA, Zhou S, Dion PA, Allen RP, Earley CJ, Fon EA, Xiong L, Dupre N, Dauvilliers Y, Rouleau GA, Gan-Or Z. TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects. Journal of Molecular Neuroscience : Mn. PMID 29404899 DOI: 10.1007/S12031-018-1031-4 |
0.457 |
|
| 2017 |
Skotte L, Koch A, Yakimov V, Zhou S, Søborg B, Andersson M, Michelsen SW, Navne JE, Mistry JM, Dion PA, Pedersen ML, Børresen ML, Rouleau GA, Geller F, Melbye M, et al. CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders. Circulation. Cardiovascular Genetics. 10. PMID 28611031 DOI: 10.1161/Circgenetics.116.001618 |
0.434 |
|
| 2016 |
Gan-Or Z, Zhou S, Johnson A, Montplaisir JY, Allen RP, Earley CJ, Desautels A, Dion PA, Xiong L, Rouleau GA. Case-Control and Family-Based Association Study of Specific Variants in Restless Legs Syndrome. Movement Disorders Clinical Practice. 3: 460-464. PMID 30363591 DOI: 10.1002/Mdc3.12306 |
0.51 |
|
| 2016 |
Zhou S, Ambalavanan A, Rochefort D, Xie P, Bourassa CV, Hince P, Dionne-Laporte A, Spiegelman D, Gan-Or Z, Mirarchi C, Zaharieva V, Dupré N, Kobayashi H, Hitomi T, Harada K, et al. RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population. American Journal of Human Genetics. PMID 27745834 DOI: 10.1016/J.Ajhg.2016.09.001 |
0.559 |
|
| 2016 |
Manousaki D, Kent JW, Haack K, Zhou S, Xie P, Greenwood CM, Brassard P, Newman DE, Cole S, Umans JG, Rouleau G, Comuzzie AG, Richards JB. Toward Precision Medicine: TBC1D4 Disruption Is Common Among the Inuit and Leads to Underdiagnosis of Type 2 Diabetes. Diabetes Care. PMID 27561922 DOI: 10.2337/Dc16-0769 |
0.401 |
|
| 2015 |
Ambalavanan A, Girard SL, Ahn K, Zhou S, Dionne-Laporte A, Spiegelman D, Bourassa CV, Gauthier J, Hamdan FF, Xiong L, Dion PA, Joober R, Rapoport J, Rouleau GA. De novo variants in sporadic cases of childhood onset schizophrenia. European Journal of Human Genetics : Ejhg. PMID 26508570 DOI: 10.1038/Ejhg.2015.218 |
0.499 |
|
| 2015 |
Gan-Or Z, Zhou S, Ambalavanan A, Leblond CS, Xie P, Johnson A, Spiegelman D, Allen RP, Earley CJ, Desautels A, Montplaisir JY, Dion PA, Xiong L, Rouleau GA. Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome. Sleep Medicine. 16: 1151-5. PMID 26298793 DOI: 10.1016/J.Sleep.2015.06.002 |
0.483 |
|
| 2015 |
Zhou S, Xiong L, Xie P, Ambalavanan A, Bourassa CV, Dionne-Laporte A, Spiegelman D, Turcotte Gauthier M, Henrion E, Diallo O, Dion PA, Rouleau GA. Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. Plos One. 10: e0128255. PMID 26010953 DOI: 10.1371/Journal.Pone.0128255 |
0.506 |
|
| 2015 |
Fu L, Zhou S, Rouleau G, Silviu-Dan F. Clinical and Genetic Investigation in a Family Segregating Different Types of Angioedema, Including a Case of Hereditary Angioedema Type-III Journal of Allergy and Clinical Immunology. 135: AB197. DOI: 10.1016/J.Jaci.2014.12.1579 |
0.456 |
|
| 2012 |
Daoud H, Zhou S, Noreau A, Sabbagh M, Belzil V, Dionne-Laporte A, Tranchant C, Dion P, Rouleau GA. Exome sequencing reveals SPG11 mutations causing juvenile ALS. Neurobiology of Aging. 33: 839.e5-9. PMID 22154821 DOI: 10.1016/J.Neurobiolaging.2011.11.012 |
0.658 |
|
| 2011 |
Girard SL, Gauthier J, Noreau A, Xiong L, Zhou S, Jouan L, Dionne-Laporte A, Spiegelman D, Henrion E, Diallo O, Thibodeau P, Bachand I, Bao JY, Tong AH, Lin CH, et al. Increased exonic de novo mutation rate in individuals with schizophrenia. Nature Genetics. 43: 860-3. PMID 21743468 DOI: 10.1038/Ng.886 |
0.467 |
|
| 2011 |
Wang B, Yu C, Xi YB, Cai HC, Wang J, Zhou S, Zhou S, Wu Y, Yan YB, Ma X, Xie L. A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family. Human Mutation. 32: E1939-47. PMID 21031598 DOI: 10.1002/humu.21386 |
0.327 |
|
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