| 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 |
0.383 |
|
| 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 |
0.415 |
|
| 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 |
0.416 |
|
| 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 |
0.311 |
|
| 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 |
0.501 |
|
| 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 |
0.455 |
|
| 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 |
0.376 |
|
| 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 |
0.467 |
|
| 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 |
0.604 |
|
| 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 |
0.667 |
|
| 2018 |
Zhou S, Dion PA, Rouleau GA. Genetics of Intracranial Aneurysms. Stroke. PMID 29437983 DOI: 10.1161/Strokeaha.117.018152 |
0.406 |
|
| 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 |
0.459 |
|
| 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 |
0.435 |
|
| 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 |
0.512 |
|
| 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 |
0.561 |
|
| 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 |
0.402 |
|
| 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 |
0.5 |
|
| 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 |
0.484 |
|
| 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 |
0.507 |
|
| 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 |
0.457 |
|
| 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 |
0.468 |
|
| 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 |
0.328 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2020 |
Trajanoska K, Seppala LJ, Medina-Gomez C, Hsu YH, Zhou S, van Schoor NM, de Groot LCPGM, Karasik D, Richards JB, Kiel DP, Uitterlinden AG, Perry JRB, van der Velde N, Day FR, Rivadeneira F. Genetic basis of falling risk susceptibility in the UK Biobank Study. Communications Biology. 3: 543. PMID 32999390 DOI: 10.1038/s42003-020-01256-x |
0.298 |
|
| 2009 |
Wang B, Wang J, Liu J, Ni F, Yan J, Zhou S, Mu Y, Cao Y, Ma X. Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese. Endocrine. 36: 16-9. PMID 19507064 DOI: 10.1007/s12020-009-9205-z |
0.28 |
|
| 2008 |
Wang B, Tan S, Yang Z, Xie YC, Wang J, Zhou S, Li S, Zheng C, Ma X. Association between Alzheimer's disease and the NOS3 gene Glu298Asp polymorphism in Chinese. Journal of Molecular Neuroscience : Mn. 34: 173-6. PMID 18183499 DOI: 10.1007/s12031-007-9026-6 |
0.273 |
|
| 2019 |
Mokry LE, Zhou S, Guo C, Scott RA, Devey L, Langenberg C, Wareham N, Waterworth D, Cardon L, Sanseau P, Davey Smith G, Richards JB. Interleukin-18 as a drug repositioning opportunity for inflammatory bowel disease: A Mendelian randomization study. Scientific Reports. 9: 9386. PMID 31253830 DOI: 10.1038/S41598-019-45747-2 |
0.267 |
|
| 2021 |
Povysil G, Butler-Laporte G, Shang N, Wang C, Khan A, Alaamery M, Nakanishi T, Zhou S, Forgetta V, Eveleigh RJM, Bourgey M, Aziz N, Jones SJ, Knoppers B, Scherer SW, et al. Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. The Journal of Clinical Investigation. PMID 34043590 DOI: 10.1172/JCI147834 |
0.266 |
|
| 2020 |
Povysil G, Butler-Laporte G, Shang N, Weng C, Khan A, Alaamery M, Nakanishi T, Zhou S, Forgetta V, Eveleigh R, Bourgey M, Aziz N, Jones S, Knoppers B, Scherer S, et al. Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19. Medrxiv : the Preprint Server For Health Sciences. PMID 33398295 DOI: 10.1101/2020.12.18.20248226 |
0.265 |
|
| 2014 |
Pan H, Suo P, Liu C, Wang J, Zhou S, Ma X, Wang B. The ESR1 gene in unexplained recurrent spontaneous abortion. Systems Biology in Reproductive Medicine. 60: 161-4. PMID 24568551 DOI: 10.3109/19396368.2013.877540 |
0.263 |
|
| 2008 |
Wang B, Wang J, Zhou S, Tan S, He X, Yang Z, Xie YC, Li S, Zheng C, Ma X. The association of mitochondrial aldehyde dehydrogenase gene (ALDH2) polymorphism with susceptibility to late-onset Alzheimer's disease in Chinese. Journal of the Neurological Sciences. 268: 172-5. PMID 18201725 DOI: 10.1016/j.jns.2007.12.006 |
0.256 |
|
| 2019 |
Cerani A, Zhou S, Forgetta V, Morris JA, Trajanoska K, Rivadeneira F, Larsson SC, Michaëlsson K, Richards JB. Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study. Bmj (Clinical Research Ed.). 366: l4410. PMID 31371314 DOI: 10.1136/Bmj.L4410 |
0.25 |
|
| 2020 |
Lu T, Zhou S, Wu H, Forgetta V, Greenwood CMT, Richards JB. Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33110269 DOI: 10.1038/s41436-020-01007-7 |
0.247 |
|
| 2023 |
Butler-Laporte G, Farjoun J, Nakanishi T, Lu T, Abner E, Chen Y, Hultström M, Metspalu A, Milani L, Mägi R, Nelis M, Hudjashov G, Yoshiji S, Ilboudo Y, Liang KYH, ... ... Zhou S, et al. HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases. Communications Biology. 6: 1113. PMID 37923823 DOI: 10.1038/s42003-023-05496-5 |
0.243 |
|
| 2008 |
Wang B, Xie YC, Yang Z, Peng D, Wang J, Zhou S, Li S, Ma X. Lack of an association between Alzheimer's disease and the cystatin C (CST3) gene G73A polymorphism in Mainland Chinese. Dementia and Geriatric Cognitive Disorders. 25: 461-4. PMID 18408364 DOI: 10.1159/000125670 |
0.242 |
|
| 2011 |
Wang B, Meng D, Wang J, Liu S, Zhou S, Miao Z, Han L, Chu N, Zhang K, Ma X, Li C. Genetic association of polymorphism rs1333049 with gout. Rheumatology (Oxford, England). 50: 1559-61. PMID 21558165 DOI: 10.1093/rheumatology/ker135 |
0.241 |
|
| 2021 |
Nakanishi T, Cerani A, Forgetta V, Zhou S, Allen RJ, Leavy OC, Koido M, Assayag D, Jenkins RG, Wain LV, Yang IV, Lathrop GM, Wolters PJ, Schwartz DA, Richards JB. Genetically increased circulating FUT3 level leads to reduced risk of Idiopathic Pulmonary Fibrosis: a Mendelian Randomisation Study. The European Respiratory Journal. PMID 34172473 DOI: 10.1183/13993003.03979-2020 |
0.24 |
|
| 2010 |
Ni F, Wen Q, Wang B, Zhou S, Wang J, Mu Y, Ma X, Cao Y. Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure. Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology. 26: 246-9. PMID 20222838 DOI: 10.3109/09513590903225358 |
0.236 |
|
| 2023 |
Trajanoska K, Bhérer C, Taliun D, Zhou S, Richards JB, Mooser V. From target discovery to clinical drug development with human genetics. Nature. 620: 737-745. PMID 37612393 DOI: 10.1038/s41586-023-06388-8 |
0.224 |
|
| 2011 |
Feng WX, Mokrousov I, Wang BB, Nelson H, Jiao WW, Wang J, Sun L, Zhou SR, Xiao J, Gu Y, Wu XR, Ma X, Shen A. Tag SNP polymorphism of CCL2 and its role in clinical tuberculosis in Han Chinese pediatric population. Plos One. 6: e14652. PMID 21556333 DOI: 10.1371/journal.pone.0014652 |
0.22 |
|
| 2023 |
Lu T, Forgetta V, Zhou S, Richards JB, Greenwood CM. Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 37830501 DOI: 10.1002/jbmr.4920 |
0.218 |
|
| 2010 |
Zhou S, Huriletemuer, Wang J, Zhang C, Zhao S, Wang de S, Wang B, Ma X. Absence of association on aldehyde dehydrogenase 2 (ALDH2) polymorphism with Mongolian Alzheimer patients. Neuroscience Letters. 468: 312-5. PMID 19914339 DOI: 10.1016/j.neulet.2009.11.022 |
0.216 |
|
| 2023 |
Chen Y, Lu T, Pettersson-Kymmer U, Stewart ID, Butler-Laporte G, Nakanishi T, Cerani A, Liang KYH, Yoshiji S, Willett JDS, Su CY, Raina P, Greenwood CMT, Farjoun Y, Forgetta V, ... ... Zhou S, et al. Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nature Genetics. 55: 44-53. PMID 36635386 DOI: 10.1038/s41588-022-01270-1 |
0.212 |
|
| 2008 |
Wang B, Zhou S, Yang Z, Xie YC, Wang J, Zhang P, Lv Z, Zheng C, Ma X. Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease. Journal of the Neurological Sciences. 270: 148-51. PMID 18396294 DOI: 10.1016/j.jns.2008.02.021 |
0.211 |
|
| 2011 |
Wang B, Suo P, Chen B, Wei Z, Yang L, Zhou S, Wang J, Cao Y, Ma X. Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women. Human Reproduction (Oxford, England). 26: 950-4. PMID 21296802 DOI: 10.1093/humrep/der001 |
0.211 |
|
| 2010 |
Zhou S, Huriletemuer, Wang J, Wang B, Zhao S, Wang de S, Zhang C, Ma X. Association analysis between polymorphism rs2373115 of gene GRB-associated binding protein 2 and Mongolian Alzheimer patients. Neuroscience Letters. 480: 4-6. PMID 20188796 DOI: 10.1016/j.neulet.2010.02.047 |
0.205 |
|
| 2021 |
Zhou S, Butler-Laporte G, Nakanishi T, Morrison DR, Afilalo J, Afilalo M, Laurent L, Pietzner M, Kerrison N, Zhao K, Brunet-Ratnasingham E, Henry D, Kimchi N, Afrasiabi Z, Rezk N, et al. A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity. Nature Medicine. PMID 33633408 DOI: 10.1038/s41591-021-01281-1 |
0.199 |
|
| 2023 |
Zhou S, Sosina OA, Bovijn J, Laurent L, Sharma V, Akbari P, Forgetta V, Jiang L, Kosmicki JA, Banerjee N, Morris JA, Oerton E, Jones M, LeBlanc MG, Idone V, et al. Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis. Nature Genetics. 55: 1277-1287. PMID 37558884 DOI: 10.1038/s41588-023-01444-5 |
0.198 |
|
| 2010 |
Wang B, Zhou S, Wang J, Liu J, Ni F, Yan J, Mu Y, Cao Y, Ma X. Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome. Reproductive Biomedicine Online. 21: 344-8. PMID 20705511 DOI: 10.1016/j.rbmo.2010.04.013 |
0.196 |
|
| 2010 |
Huriletemuer, Wang B, Wang J, Wang G, Zhang C, Zhao S, Zhou S, Ma X, Wang de S. APOE epsilon4 is a high-risk factor for Alzheimer's disease in the Mongolian population. Journal of the Neurological Sciences. 288: 167-9. PMID 19819468 DOI: 10.1016/j.jns.2009.08.058 |
0.193 |
|
| 2010 |
Mu Y, Liu J, Wang B, Wen Q, Wang J, Yan J, Zhou S, Ma X, Cao Y. Interleukin 1 beta (IL-1β) promoter C [-511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome. Endocrine. 37: 71-5. PMID 20963558 DOI: 10.1007/s12020-009-9268-x |
0.187 |
|
| 2009 |
Wang B, Zhou S, Wang J, Liu J, Ni F, Liu C, Yan J, Mu Y, Cao Y, Ma X. Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in Chinese women. Endocrine. 35: 198-203. PMID 19191034 DOI: 10.1007/s12020-009-9152-8 |
0.182 |
|
| 2021 |
Wu H, Forgetta V, Zhou S, Bhatnagar SR, Paré G, Richards JB. A Polygenic Risk Score for Low-density Lipoprotein Cholesterol is Associated with Risk of Ischemic Heart Disease and Enriches for Individuals with Familial Hypercholesterolemia. Circulation. Genomic and Precision Medicine. PMID 33440130 DOI: 10.1161/CIRCGEN.120.003106 |
0.174 |
|
| 2012 |
Wang B, Zhou S, Hong F, Wang J, Liu X, Cai Y, Wang F, Feng T, Ma X. Association analysis between the tag SNP for sonic hedgehog rs9333613 polymorphism and male sexual orientation. Journal of Andrology. 33: 951-4. PMID 21940988 DOI: 10.2164/jandrol.110.012849 |
0.173 |
|
| 2011 |
Wang J, Chen Q, Wang L, Zhou S, Cheng L, Xie X, Huang G, Wang B, Ma X. Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese minority groups. International Journal of Cardiology. 148: 102-4. PMID 21262546 DOI: 10.1016/j.ijcard.2010.05.041 |
0.172 |
|
| 2011 |
Feng W, Mokrousov I, Wang B, Nelson H, Jiao W, Wang J, Sun L, Zhou S, Xiao J, Gu Y, Wu X, Ma X, Shen A. Correction: Tag SNP Polymorphism of CCL2 and Its Role in Clinical Tuberculosis in Han Chinese Pediatric Population Plos One. 6. DOI: 10.1371/annotation/675f01a0-0f6e-4eb5-8cb1-ee8c5b5cbfe3 |
0.169 |
|
| 2010 |
Zhou S, Wang B, Ni F, Wang J, Cao Y, Ma X. GPR3 may not be a potential candidate gene for premature ovarian failure. Reproductive Biomedicine Online. 20: 53-5. PMID 20158988 DOI: 10.1016/j.rbmo.2009.10.013 |
0.168 |
|
| 2023 |
Willett JDS, Lu T, Nakanishi T, Yoshiji S, Butler-Laporte G, Zhou S, Farjoun Y, Richards JB. Colocalization of expression transcripts with COVID-19 outcomes is rare across cell states, cell types and organs. Human Genetics. 142: 1461-1476. PMID 37640912 DOI: 10.1007/s00439-023-02590-w |
0.162 |
|
| 2011 |
Liu J, Wang B, Wei Z, Zhou P, Zu Y, Zhou S, Wen Q, Wang J, Cao Y, Ma X. Mutational analysis of human bone morphogenetic protein 15 in Chinese women with polycystic ovary syndrome. Metabolism: Clinical and Experimental. 60: 1511-4. PMID 22014425 DOI: 10.1016/j.metabol.2010.10.006 |
0.16 |
|
| 2023 |
Nakanishi T, Willett J, Farjoun Y, Allen RJ, Guillen-Guio B, Adra D, Zhou S, Richards JB. Alternative splicing in lung influences COVID-19 severity and respiratory diseases. Nature Communications. 14: 6198. PMID 37794074 DOI: 10.1038/s41467-023-41912-4 |
0.156 |
|
| 2011 |
Chen B, Suo P, Wang B, Wang J, Yang L, Zhou S, Zhu Y, Ma X, Cao Y. Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure. Reproductive Biology and Endocrinology : Rb&E. 9: 75. PMID 21624127 DOI: 10.1186/1477-7827-9-75 |
0.147 |
|
| 2024 |
Lu T, Chen Y, Yoshiji S, Ilboudo Y, Forgetta V, Zhou S, Greenwood CM. Circulating metabolite abundances associated with risks of bipolar disorder, schizophrenia, and depression: a Mendelian randomization study. Biological Psychiatry. PMID 38705554 DOI: 10.1016/j.biopsych.2024.04.016 |
0.136 |
|
| 2022 |
Paranjpe I, Jayaraman P, Su CY, Zhou S, Chen S, Thompson R, Del Valle DM, Kenigsberg E, Zhao S, Jaladanki S, Chaudhary K, Ascolillo S, Vaid A, Kumar A, Kozlova E, et al. Proteomic Characterization of Acute Kidney Injury in Patients Hospitalized with SARS-CoV2 Infection. Medrxiv : the Preprint Server For Health Sciences. PMID 36093350 DOI: 10.1101/2021.12.09.21267548 |
0.134 |
|
| 2023 |
Nadkarni G, Paranjpe I, Jayaraman P, Su CY, Zhou S, Chen S, Valle DD, Thompson R, Kenigsberg E, Zhao S, Jaladanki S, Chaudhary K, Ascolillo S, Vaid A, Gonzalez-Kozlova E, et al. Proteomic Characterization of Acute Kidney Injury in Patients Hospitalized with SARS-CoV2 Infection. Research Square. PMID 36993735 DOI: 10.21203/rs.3.rs-2379226/v1 |
0.132 |
|
| 2010 |
Wang B, Mu Y, Ni F, Zhou S, Wang J, Cao Y, Ma X. Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure. Reproductive Biomedicine Online. 20: 499-503. PMID 20219431 DOI: 10.1016/j.rbmo.2010.01.008 |
0.122 |
|
| 2024 |
Sun J, Guo H, Zhang S, Nie Y, Zhou S, Zeng Y, Sun Y. Machine learning-based integration develops an immunogenic cell death-derived lncRNA signature for predicting prognosis and immunotherapy response in lung adenocarcinoma. Scientific Reports. 14: 11724. PMID 38778157 DOI: 10.1038/s41598-024-62569-z |
0.12 |
|
| 2024 |
Zhou SR, Zhu YS, Yuan WT, Pan XY, Wang T, Chen XD. Hepatocyte growth factor promotes retinal pigment epithelium cell activity through MET/AKT signaling pathway. International Journal of Ophthalmology. 17: 806-814. PMID 38766346 DOI: 10.18240/ijo.2024.05.03 |
0.12 |
|
| 2024 |
Sun J, Guo H, Nie Y, Zhou S, Zeng Y, Sun Y. Deciphering the heterogeneity dominated by tumor-associated macrophages for survival prognostication and prediction of immunotherapy response in lung adenocarcinoma. Scientific Reports. 14: 9276. PMID 38653742 DOI: 10.1038/s41598-024-60132-4 |
0.12 |
|
| 2024 |
Ling Z, Zhou S, Zhou Y, Zhong W, Su Z, Qin Z. Protective role of madecassoside from Centella asiatica against protein L-isoaspartyl methyltransferase deficiency-induced neurodegeneration. Neuropharmacology. 109834. PMID 38181970 DOI: 10.1016/j.neuropharm.2023.109834 |
0.118 |
|
| 2011 |
Wang J, Xie X, Zhou S, Huang G, Ma X, Suo P, Zhou S, Wang B, Ma X. The study of copy number variations in the regions of NOTCH1 among Chinese VSD and TOF patients. International Journal of Cardiology. 147: 444-6. PMID 21277031 DOI: 10.1016/j.ijcard.2010.04.029 |
0.114 |
|
| 2024 |
Li J, Wang F, Li Z, Feng J, Men Y, Han J, Xia J, Zhang C, Han Y, Chen T, Zhao Y, Zhou S, Da Y, Chai G, Hao J. Integrative multi-omics analysis identifies genetically supported druggable targets and immune cell specificity for myasthenia gravis. Journal of Translational Medicine. 22: 302. PMID 38521921 DOI: 10.1186/s12967-024-04994-2 |
0.112 |
|
| 2023 |
Su CY, Zhou S, Gonzalez-Kozlova E, Butler-Laporte G, Brunet-Ratnasingham E, Nakanishi T, Jeon W, Morrison DR, Laurent L, Afilalo J, Afilalo M, Henry D, Chen Y, Carrasco-Zanini J, Farjoun Y, et al. Circulating proteins to predict COVID-19 severity. Scientific Reports. 13: 6236. PMID 37069249 DOI: 10.1038/s41598-023-31850-y |
0.111 |
|
| 2023 |
Yoshiji S, Butler-Laporte G, Lu T, Willett JDS, Su CY, Nakanishi T, Morrison DR, Chen Y, Liang K, Hultström M, Ilboudo Y, Afrasiabi Z, Lan S, Duggan N, DeLuca C, ... ... Zhou S, et al. Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity. Nature Metabolism. 1-17. PMID 36805566 DOI: 10.1038/s42255-023-00742-w |
0.111 |
|
| 2010 |
Wang B, Wen Q, Ni F, Zhou S, Wang J, Cao Y, Ma X. Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure. Clinical Endocrinology. 72: 135-6. PMID 19438907 DOI: 10.1111/j.1365-2265.2009.03613.x |
0.11 |
|
| 2010 |
Wang B, Wang J, Zheng Y, Zhou S, Zheng J, Wang F, Ma X, Zeng Z. A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China. Pathology. 42: 674-80. PMID 21080879 DOI: 10.3109/00313025.2010.523696 |
0.109 |
|
| 2021 |
Chen Y, Forgetta V, Richards JB, Zhou S. Health Effects of Calcium: Evidence From Mendelian Randomization Studies. Jbmr Plus. 5: e10542. PMID 34761146 DOI: 10.1002/jbm4.10542 |
0.108 |
|
| 2022 |
Lu T, Forgetta V, Greenwood CMT, Zhou S, Richards JB. Circulating Proteins Influencing Psychiatric Disease: A Mendelian Randomization Study. Biological Psychiatry. PMID 36280454 DOI: 10.1016/j.biopsych.2022.08.015 |
0.108 |
|
| 2020 |
Sun X, Zhou S, He X, Wang Y, Cui W. Sex-Specific Association between Serum 25-Hydroxyvitamin D and Metabolic Risk Factors in T2DM Patients. International Journal of Endocrinology. 2020: 9238719. PMID 32565795 DOI: 10.1155/2020/9238719 |
0.108 |
|
| 2020 |
Butler-Laporte G, Nakanishi T, Mooser V, Renieri A, Amitrano S, Zhou S, Chen Y, Forgetta V, Richards JB. The effect of angiotensin-converting enzyme levels on Covid-19 susceptibility and severity: a Mendelian randomization study. International Journal of Epidemiology. PMID 33349849 DOI: 10.1093/ije/dyaa229 |
0.101 |
|
| 2021 |
Nilsson KH, Henning P, Shahawy ME, Nethander M, Andersen TL, Ejersted C, Wu J, Gustafsson KL, Koskela A, Tuukkanen J, Souza PPC, Tuckermann J, Lorentzon M, Ruud LE, Lehtimäki T, ... ... Zhou S, et al. RSPO3 is important for trabecular bone and fracture risk in mice and humans. Nature Communications. 12: 4923. PMID 34389713 DOI: 10.1038/s41467-021-25124-2 |
0.099 |
|
| 2023 |
Zhou S, Zhou Y, Zhong W, Su Z, Qin Z. Involvement of protein L-isoaspartyl methyltransferase in the physiopathology of neurodegenerative diseases: Possible substrates associated with synaptic function. Neurochemistry International. 170: 105606. PMID 37657764 DOI: 10.1016/j.neuint.2023.105606 |
0.095 |
|
| 2020 |
Zhou S, Morris JA, Oerton E, Forgetta V, Langenberg C, Richards JB. Large-scale genomics and proteomics to identify novel circulating biomarkers for bone density Bone Reports. 13: 100338. DOI: 10.1016/j.bonr.2020.100338 |
0.093 |
|
| 2024 |
Smith-Byrne K, Hedman Å, Dimitriou M, Desai T, Sokolov AV, Schioth HB, Koprulu M, Pietzner M, Langenberg C, Atkins J, Penha RC, McKay J, Brennan P, Zhou S, Richards BJ, et al. Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers. Nature Communications. 15: 3621. PMID 38684708 DOI: 10.1038/s41467-024-46834-3 |
0.084 |
|
| 2024 |
Zhu W, Zhou S, Zhang J, Li L, Liu P, Xiong W. Differentiation of Native Vertebral Osteomyelitis: A Comprehensive Review of Imaging Techniques and Future Applications. Medical Science Monitor : International Medical Journal of Experimental and Clinical Research. 30: e943168. PMID 38555491 DOI: 10.12659/MSM.943168 |
0.073 |
|
| 2019 |
Wei J, Luo X, Zhou S, He X, Zheng J, Sun X, Cui W. Associations between iron status and insulin resistance in Chinese children and adolescents: findings from the China Health and Nutrition Survey. Asia Pacific Journal of Clinical Nutrition. 28: 819-825. PMID 31826380 DOI: 10.6133/apjcn.201912_28(4).0019 |
0.073 |
|
| 2023 |
Paranjpe I, Jayaraman P, Su CY, Zhou S, Chen S, Thompson R, Del Valle DM, Kenigsberg E, Zhao S, Jaladanki S, Chaudhary K, Ascolillo S, Vaid A, Gonzalez-Kozlova E, Kauffman J, et al. Proteomic characterization of acute kidney injury in patients hospitalized with SARS-CoV2 infection. Communications Medicine. 3: 81. PMID 37308534 DOI: 10.1038/s43856-023-00307-8 |
0.071 |
|
| 2022 |
Smith-Byrne K, Cerani A, Guida F, Zhou S, Agudo A, Aleksandrova K, Barricarte A, Rodríguez-Barranco M, Borchers CH, Gram IT, Han J, Amos CI, Hung RJ, Grankvist K, Nøst TH, et al. Circulating Isovalerylcarnitine and Lung Cancer Risk: Evidence from Mendelian Randomization and Pre-Diagnostic Blood Measurements. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 35839461 DOI: 10.1158/1055-9965.EPI-21-1033 |
0.071 |
|
| 2024 |
Brunet-Ratnasingham E, Morin S, Randolph HE, Labrecque M, Bélair J, Lima-Barbosa R, Pagliuzza A, Marchitto L, Hultström M, Niessl J, Cloutier R, Sreng Flores AM, Brassard N, Benlarbi M, Prévost J, ... ... Zhou S, et al. Sustained IFN signaling is associated with delayed development of SARS-CoV-2-specific immunity. Nature Communications. 15: 4177. PMID 38755196 DOI: 10.1038/s41467-024-48556-y |
0.07 |
|
| 2022 |
Butler-Laporte G, Gonzalez-Kozlova E, Su CY, Zhou S, Nakanishi T, Brunet-Ratnasingham E, Morrison D, Laurent L, Afilalo J, Afilalo M, Henry D, Chen Y, Carrasco-Zanini J, Farjoun Y, Pietzner M, et al. The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals. Clinical Proteomics. 19: 34. PMID 36171541 DOI: 10.1186/s12014-022-09371-z |
0.07 |
|
| 2021 |
Su Z, Ren N, Ling Z, Sheng L, Zhou S, Guo C, Ke Z, Xu T, Qin Z. Differential expression of microRNAs associated with neurodegenerative diseases and diabetic nephropathy in protein L-isoaspartyl methyltransferase-deficient mice. Cell Biology International. PMID 34314072 DOI: 10.1002/cbin.11679 |
0.07 |
|
| 2023 |
Guo H, Sun J, Zhang S, Nie Y, Zhou S, Zeng Y. Progress in understanding and treating idiopathic pulmonary fibrosis: recent insights and emerging therapies. Frontiers in Pharmacology. 14: 1205948. PMID 37608885 DOI: 10.3389/fphar.2023.1205948 |
0.067 |
|
| 2021 |
Butler-Laporte G, Nakanishi T, Mooser V, Morrison DR, Abdullah T, Adeleye O, Mamlouk N, Kimchi N, Afrasiabi Z, Rezk N, Giliberti A, Renieri A, Chen Y, Zhou S, Forgetta V, et al. Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study. Plos Medicine. 18: e1003605. PMID 34061844 DOI: 10.1371/journal.pmed.1003605 |
0.066 |
|
| 2010 |
Liu C, Wang J, Zhou S, Wang B, Ma X. Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population. Reproductive Biology and Endocrinology : Rb&E. 8: 114. PMID 20920206 DOI: 10.1186/1477-7827-8-114 |
0.059 |
|
| 2022 |
Butler-Laporte G, Gonzalez-Kozlova E, Su CY, Zhou S, Nakanishi T, Brunet-Ratnasingham E, Morrison D, Laurent L, Aflalo J, Aflalo M, Henry D, Chen Y, Carrasco-Zanini J, Farjoun Y, Pietzner M, et al. Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals. Clinical Proteomics. 19: 40. PMID 36376796 DOI: 10.1186/s12014-022-09378-6 |
0.057 |
|
| 2023 |
Sun X, Yan T, Li Z, Zhou S, Peng W, Cui W, Xu J, Cao ZB, Shi L, Wang Y. Effects of Endurance Exercise and Vitamin D Supplementation on Insulin Resistance and Plasma Lipidome in Middle-Aged Adults with Type 2 Diabetes. Nutrients. 15. PMID 37447353 DOI: 10.3390/nu15133027 |
0.056 |
|
| 2024 |
Cao Y, Tan X, Shen J, Liu F, Xu Y, Chen Y, Zhou S, Qiu T, Li D, Zhao Q, Zhao K. Morinda Officinalis-derived extracellular vesicle-like particles: Anti-osteoporosis effect by regulating MAPK signaling pathway. Phytomedicine : International Journal of Phytotherapy and Phytopharmacology. 129: 155628. PMID 38663117 DOI: 10.1016/j.phymed.2024.155628 |
0.052 |
|
| 2023 |
Tan X, Xu Y, Zhou S, Pan M, Cao Y, Cai X, Zhao Q, Zhao K. Advances in the Study of Plant-Derived Vesicle-Like Nanoparticles in Inflammatory Diseases. Journal of Inflammation Research. 16: 4363-4372. PMID 37795493 DOI: 10.2147/JIR.S421124 |
0.049 |
|
| 2024 |
Zhou S, Zhu W, Guo H, Nie Y, Sun J, Liu P, Zeng Y. Microbes for lung cancer detection: feasibility and limitations. Frontiers in Oncology. 14: 1361879. PMID 38779090 DOI: 10.3389/fonc.2024.1361879 |
0.047 |
|
| 2019 |
Xiao H, Huang W, Xiong K, Ruan S, Yuan C, Mo G, Tian R, Zhou S, She R, Ye P, Liu B, Deng J. Osteochondral repair using scaffolds with gradient pore sizes constructed with silk fibroin, chitosan, and nano-hydroxyapatite. International Journal of Nanomedicine. 14: 2011-2027. PMID 30962685 DOI: 10.2147/IJN.S191627 |
0.037 |
|
| 2022 |
Sun X, Xiao W, Li Z, Zhou S, Dong M, Huang C, Ma Y, Gou B. Does vitamin D supplementation improve bone health, body composition and physical performance beyond endurance exercise in patients with type 2 diabetes: A secondary analysis of randomized controlled trial. Frontiers in Physiology. 13: 1003572. PMID 36246136 DOI: 10.3389/fphys.2022.1003572 |
0.027 |
|
| 2021 |
Brunet-Ratnasingham E, Anand SP, Gantner P, Dyachenko A, Moquin-Beaudry G, Brassard N, Beaudoin-Bussières G, Pagliuzza A, Gasser R, Benlarbi M, Point F, Prévost J, Laumaea A, Niessl J, Nayrac M, ... ... Zhou S, et al. Integrated immunovirological profiling validates plasma SARS-CoV-2 RNA as an early predictor of COVID-19 mortality. Science Advances. 7: eabj5629. PMID 34826237 DOI: 10.1126/sciadv.abj5629 |
0.021 |
|
| 2018 |
Guo J, Sun X, Wu J, Chang Q, Higuchi M, Li W, Zhou S, Wang Y. The current practice and future promise of integration of exercise science and medicine in China Global Health Journal. 2: 31-35. DOI: 10.1016/s2414-6447(19)30157-5 |
0.01 |
|
| Hide low-probability matches. |