| Year |
Citation |
Score |
| 2020 |
Knol MJ, Lu D, Traylor M, Adams HH, Rafael J Romero J, Smith AV, Fornage M, Hofer E, Liu J, Hostettler IC, Luciano M, Trompet S, Giese AK, Hilal S, van den Akker EB, ... ... Yang Q, et al. Association of common genetic variants with brain microbleeds: A Genome-wide Association Study. Neurology. PMID 32913026 DOI: 10.1212/Wnl.0000000000010852 |
0.329 |
|
| 2020 |
Jaworek T, Ryan KA, Gaynor BJ, McArdle PF, Stine OC, OConnor TD, Lopez H, Aparicio HJ, Gao Y, Lin X, Groves ML, Flaherty ML, Liu S, Yang Q, Wilson J, et al. Exome Array Analysis of Early-Onset Ischemic Stroke. Stroke. STROKEAHA120031357. PMID 32912094 DOI: 10.1161/Strokeaha.120.031357 |
0.31 |
|
| 2020 |
Armstrong NJ, Mather KA, Sargurupremraj M, Knol MJ, Malik R, Satizabal CL, Yanek LR, Wen W, Gudnason VG, Dueker ND, Elliott LT, Hofer E, Bis J, Jahanshad N, Li S, ... ... Yang Q, et al. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities. Stroke. STROKEAHA119027544. PMID 32517579 DOI: 10.1161/Strokeaha.119.027544 |
0.307 |
|
| 2019 |
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, ... ... Yang Q, et al. Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics. PMID 31636452 DOI: 10.1038/S41588-019-0511-Y |
0.323 |
|
| 2019 |
Tin A, Marten J, Halperin Kuhns VL, Li Y, Wuttke M, Kirsten H, Sieber KB, Qiu C, Gorski M, Yu Z, Giri A, Sveinbjornsson G, Li M, Chu AY, Hoppmann A, ... ... Yang Q, et al. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics. PMID 31578528 DOI: 10.1038/S41588-019-0504-X |
0.351 |
|
| 2019 |
Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, Giri A, Sieber KB, Qiu C, Kirsten H, Tin A, Chu AY, Bansal N, Feitosa MF, Wang L, ... ... Yang Q, et al. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature Communications. 10: 4130. PMID 31511532 DOI: 10.1038/S41467-019-11576-0 |
0.366 |
|
| 2019 |
Mishra A, Chauhan G, Violleau MH, Vojinovic D, Jian X, Bis JC, Li S, Saba Y, Grenier-Boley B, Yang Q, Bartz TM, Hofer E, Soumaré A, Peng F, Duperron MG, et al. Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects. Brain : a Journal of Neurology. PMID 30859180 DOI: 10.1093/Brain/Awz024 |
0.368 |
|
| 2018 |
Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, Traglia M, Ahluwalia TS, Akiyama M, Appel EVR, Arking DE, Arnold A, Astrup A, Beekman M, ... ... Yang Q, et al. Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Nature Communications. 9: 4455. PMID 30367059 DOI: 10.1038/S41467-018-06356-1 |
0.315 |
|
| 2018 |
Tin A, Li Y, Brody JA, Nutile T, Chu AY, Huffman JE, Yang Q, Chen MH, Robinson-Cohen C, Macé A, Liu J, Demirkan A, Sorice R, Sedaghat S, Swen M, et al. Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels. Nature Communications. 9: 4228. PMID 30315176 DOI: 10.1038/S41467-018-06620-4 |
0.341 |
|
| 2017 |
Kong P, Wu R, Lan Y, He W, Yang C, Yin C, Yang Q, Jiang C, Xu D, Xia L. Association between Mismatch-repair Genetic variation and the Risk of Multiple Primary Cancers: A Meta-Analysis. Journal of Cancer. 8: 3296-3308. PMID 29158803 DOI: 10.7150/Jca.19810 |
0.325 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Yang Q, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.348 |
|
| 2017 |
Gorski M, van der Most PJ, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, ... ... Yang Q, et al. 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific Reports. 7: 45040. PMID 28452372 DOI: 10.1038/Srep45040 |
0.357 |
|
| 2017 |
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, ... ... Yang Q, et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics. PMID 28416818 DOI: 10.1038/Ng.3843 |
0.336 |
|
| 2017 |
McMahon GM, Hwang SJ, Clish CB, Tin A, Yang Q, Larson MG, Rhee EP, Li M, Levy D, O'Donnell CJ, Coresh J, Young JH, Gerszten RE, Fox CS. Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease. Kidney International. PMID 28302371 DOI: 10.1016/J.Kint.2017.01.007 |
0.349 |
|
| 2017 |
de Vries PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen MH, Wang JJ, Attia JR, Marioni RE, Steri M, Weng LC, Pool R, Grossmann V, ... ... Yang Q, et al. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Plos One. 12: e0167742. PMID 28107422 DOI: 10.1371/Journal.Pone.0167742 |
0.302 |
|
| 2017 |
Chung J, Ma Y, Zhang X, Yang Q, Beecham GW, Lunetta KL, Mez J, Haines JL, Pericak-Vance MA, Schellenberg GD, Jun GR, Farrer LA. Bivariate Genome-Wide Association Study Of Neuropathologic Features Of Alzheimer’S Disease Alzheimers & Dementia. 13: 217. DOI: 10.1016/J.Jalz.2017.07.094 |
0.304 |
|
| 2016 |
van Rooij FJ, Qayyum R, Smith AV, Zhou Y, Trompet S, Tanaka T, Keller MF, Chang LC, Schmidt H, Yang ML, Chen MH, Hayes J, Johnson AD, Yanek LR, Mueller C, ... ... Yang Q, et al. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. American Journal of Human Genetics. PMID 28017375 DOI: 10.1016/J.Ajhg.2016.11.016 |
0.35 |
|
| 2016 |
Rhee EP, Yang Q, Yu B, Liu X, Cheng S, Deik A, Pierce KA, Bullock K, Ho JE, Levy D, Florez JC, Kathiresan S, Larson MG, Vasan RS, Clish CB, et al. An exome array study of the plasma metabolome. Nature Communications. 7: 12360. PMID 27453504 DOI: 10.1038/Ncomms12360 |
0.359 |
|
| 2016 |
Wu H, Liao Q, Chillrud SN, Yang Q, Huang L, Bi J, Yan B. Environmental Exposure to Cadmium: Health Risk Assessment and its Associations with Hypertension and Impaired Kidney Function. Scientific Reports. 6: 29989. PMID 27411493 DOI: 10.1038/Srep29989 |
0.442 |
|
| 2016 |
Yang QY, Xu XR, Jiao J, He LH, Yu SF, Gu GZ, Chen GS, Zhou WH, Wu H, Li YH. [Association between grainyhead-like 2 gene polymorphisms and noise-induced hearing loss]. Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences. 48: 409-413. PMID 27318899 |
0.445 |
|
| 2016 |
Xu X, Yang Q, Jiao J, He L, Yu S, Wang J, Gu G, Chen G, Zhou W, Wu H, Li Y, Zhang H. Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study. International Journal of Environmental Research and Public Health. 13. PMID 27271650 DOI: 10.3390/ijerph13060561 |
0.463 |
|
| 2016 |
Cui X, Chen K, Xing H, Yang Q, Krishna R, Bao Z, Wu H, Zhou W, Dong X, Han Y, Li B, Ren Q, Zaworotko MJ, Chen B. Pore chemistry and size control in hybrid porous materials for acetylene capture from ethylene. Science (New York, N.Y.). PMID 27198674 DOI: 10.1126/Science.Aaf2458 |
0.393 |
|
| 2016 |
Zhang Z, Zhang Z, Lu H, Yang Q, Wu H, Wang J. Microglial Polarization and Inflammatory Mediators After Intracerebral Hemorrhage. Molecular Neurobiology. PMID 26894396 DOI: 10.1007/s12035-016-9785-6 |
0.417 |
|
| 2016 |
Li J, Li C, Wang G, Liu Z, Chen P, Yang Q, Dong N, Wu H, Liu Z, Li W. APR-246/PRIMA-1Met Inhibits and Reverses Squamous Metaplasia in Human Conjunctival Epithelium. Investigative Ophthalmology & Visual Science. 57: 444-52. PMID 26868746 DOI: 10.1167/iovs.15-17519 |
0.408 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.328 |
|
| 2016 |
Wu H, Wu T, Han X, Wan J, Jiang C, Chen W, Lu H, Yang Q, Wang J. Cerebroprotection by the neuronal PGE2 receptor EP2 after intracerebral hemorrhage in middle-aged mice. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. PMID 26746866 DOI: 10.1177/0271678X15625351 |
0.414 |
|
| 2016 |
Zhang Y, Zou HY, Shi P, Yang Q, Tang LJ, Jiang JH, Wu HL, Yu RQ. Determination of benzo[a]pyrene in cigarette mainstream smoke by using mid-infrared spectroscopy associated with a novel chemometric algorithm. Analytica Chimica Acta. 902: 43-9. PMID 26703252 DOI: 10.1016/J.Aca.2015.10.029 |
0.396 |
|
| 2015 |
Li XW, Shi BY, Yang QL, Wu J, Wu HM, Wang YF, Wu ZJ, Fan YM, Wang YP. Epigenetic regulation of CDH1 exon 8 alternative splicing in gastric cancer. Bmc Cancer. 15: 954. PMID 26674321 DOI: 10.1186/s12885-015-1983-5 |
0.423 |
|
| 2015 |
Teumer A, Tin A, Sorice R, Gorski M, Yeo NC, Chu AY, Li M, Li Y, Mijatovic V, Ko YA, Taliun D, Luciani A, Chen MH, Yang Q, Foster MC, et al. Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes. Diabetes. PMID 26631737 DOI: 10.2337/Db15-1313 |
0.319 |
|
| 2015 |
Fan L, Zhang Y, Wang F, Yang Q, Tan J, Renata G, Wu H, Song C, Jin B. Multifunctional all-in-one drug delivery systems for tumor targeting and sequential release of three different anti-tumor drugs. Biomaterials. 76: 399-407. PMID 26561936 DOI: 10.1016/j.biomaterials.2015.10.069 |
0.388 |
|
| 2015 |
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V, Hottenga JJ, Trompet S, Müller-Nurasyid M, Zhao JH, Brody JA, ... ... Yang Q, et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics. PMID 26561523 DOI: 10.1093/Hmg/Ddv454 |
0.342 |
|
| 2015 |
Chen MH, Yang Q. RVFam: An R Package for Rare Variant Association Analysis with Family Data. Bioinformatics (Oxford, England). PMID 26508760 DOI: 10.1093/Bioinformatics/Btv609 |
0.314 |
|
| 2015 |
Chen X, Yang Q, Li H, Li H, Hong Y, Pan L, Chen N, Zhu F, Chi X, Zhu W, Chen M, Liu H, Yang Z, Zhang E, Wang T, et al. Transcriptome-wide sequencing provides insights into geocarpy in peanut (Arachis hypogaea L.). Plant Biotechnology Journal. PMID 26502832 DOI: 10.1111/pbi.12487 |
0.431 |
|
| 2015 |
Zhou C, Chen Z, Lu X, Wu H, Yang Q, Xu D. Icaritin activates JNK-dependent mPTP necrosis pathway in colorectal cancer cells. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. PMID 26427664 DOI: 10.1007/s13277-015-4134-3 |
0.427 |
|
| 2015 |
Wu H, Meng Q, Yang Q, Zhang M, Lu K, Wei Z. Large-Area Polyimide/SWCNT Nanocable Cathode for Flexible Lithium-Ion Batteries. Advanced Materials (Deerfield Beach, Fla.). PMID 26418281 DOI: 10.1002/adma.201502241 |
0.381 |
|
| 2015 |
Fan L, Yang Q, Tan J, Qiao Y, Wang Q, He J, Wu H, Zhang Y. Dual loading miR-218 mimics and Temozolomide using AuCOOH@FA-CS drug delivery system: promising targeted anti-tumor drug delivery system with sequential release functions. Journal of Experimental & Clinical Cancer Research : Cr. 34: 106. PMID 26407971 DOI: 10.1186/s13046-015-0216-8 |
0.4 |
|
| 2015 |
Ibrahim-Verbaas CA, Bressler J, Debette S, Schuur M, Smith AV, Bis JC, Davies G, Trompet S, Smith JA, Wolf C, Chibnik LB, Liu Y, Vitart V, Kirin M, Petrovic K, ... ... Yang Q, et al. GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Molecular Psychiatry. PMID 25869804 DOI: 10.1038/Mp.2015.37 |
0.345 |
|
| 2015 |
Tang W, Cushman M, Green D, Rich SS, Lange LA, Yang Q, Tracy RP, Tofler GH, Basu S, Wilson JG, Keating BJ, Weng LC, Taylor HA, Jacobs DR, Delaney JA, et al. Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans. American Journal of Hematology. 90: 534-40. PMID 25779970 DOI: 10.1002/Ajh.24005 |
0.338 |
|
| 2015 |
Huang X, Xu Y, Yang Q, Chen J, Zhang T, Li Z, Guo C, Chen H, Wu H, Li N. Efficacy and biological safety of lopinavir/ritonavir based anti-retroviral therapy in HIV-1-infected patients: a meta-analysis of randomized controlled trials. Scientific Reports. 5: 8528. PMID 25704206 DOI: 10.1038/srep08528 |
0.414 |
|
| 2015 |
Chauhan G, Adams HH, Bis JC, Weinstein G, Yu L, Töglhofer AM, Smith AV, van der Lee SJ, Gottesman RF, Thomson R, Wang J, Yang Q, Niessen WJ, Lopez OL, Becker JT, et al. Association of Alzheimer's disease GWAS loci with MRI markers of brain aging. Neurobiology of Aging. 36: 1765.e7-16. PMID 25670335 DOI: 10.1016/J.Neurobiolaging.2014.12.028 |
0.337 |
|
| 2015 |
Rannikmäe K, Davies G, Thomson PA, Bevan S, Devan WJ, Falcone GJ, Traylor M, Anderson CD, Battey TW, Radmanesh F, Deka R, Woo JG, Martin LJ, Jimenez-Conde J, Selim M, ... ... Yang Q, et al. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology. 84: 918-26. PMID 25653287 DOI: 10.1212/Wnl.0000000000001309 |
0.302 |
|
| 2015 |
Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, ... ... Yang Q, et al. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Molecular Psychiatry. 20: 183-92. PMID 25644384 DOI: 10.1038/Mp.2014.188 |
0.361 |
|
| 2015 |
Wu H, Wu T, Hua W, Dong X, Gao Y, Zhao X, Chen W, Cao W, Yang Q, Qi J, Zhou J, Wang J. PGE2 receptor agonist misoprostol protects brain against intracerebral hemorrhage in mice. Neurobiology of Aging. 36: 1439-50. PMID 25623334 DOI: 10.1016/j.neurobiolaging.2014.12.029 |
0.419 |
|
| 2015 |
Lopez LM, Hill WD, Harris SE, Valdes Hernandez M, Munoz Maniega S, Bastin ME, Bailey E, Smith C, McBride M, McClure J, Graham D, Dominiczak A, Yang Q, Fornage M, Ikram MA, et al. Genes from a translational analysis support a multifactorial nature of white matter hyperintensities. Stroke; a Journal of Cerebral Circulation. 46: 341-7. PMID 25586835 DOI: 10.1161/Strokeaha.114.007649 |
0.319 |
|
| 2015 |
Gorski M, Tin A, Garnaas M, McMahon GM, Chu AY, Tayo BO, Pattaro C, Teumer A, Chasman DI, Chalmers J, Hamet P, Tremblay J, Woodward M, Aspelund T, Eiriksdottir G, ... ... Yang Q, et al. Genome-wide association study of kidney function decline in individuals of European descent. Kidney International. 87: 1017-29. PMID 25493955 DOI: 10.1038/Ki.2014.361 |
0.352 |
|
| 2014 |
Gong Z, Zhang S, Zeng Z, Wu H, Yang Q, Xiong F, Shi L, Yang J, Zhang W, Zhou Y, Zeng Y, Li X, Xiang B, Peng S, Zhou M, et al. LOC401317, a p53-regulated long non-coding RNA, inhibits cell proliferation and induces apoptosis in the nasopharyngeal carcinoma cell line HNE2. Plos One. 9: e110674. PMID 25422887 DOI: 10.1371/Journal.Pone.0110674 |
0.42 |
|
| 2014 |
Gao C, Wang C, Liu B, Wu H, Yang Q, Jin J, Li H, Dong S, Gao G, Zhang H. Intermittent hypoxia preconditioning-induced epileptic tolerance by upregulation of monocarboxylate transporter 4 expression in rat hippocampal astrocytes. Neurochemical Research. 39: 2160-9. PMID 25146899 DOI: 10.1007/s11064-014-1411-2 |
0.4 |
|
| 2014 |
Wu H, Dong F, Wang Y, Xiao Q, Yang Q, Zhao J, Quinn TJ, Chen SD, Liu J. Catechol-O-methyltransferase Val158Met polymorphism: modulation of wearing-off susceptibility in a Chinese cohort of Parkinson's disease. Parkinsonism & Related Disorders. 20: 1094-6. PMID 25108642 DOI: 10.1016/j.parkreldis.2014.07.011 |
0.441 |
|
| 2014 |
Yang Q, Ren ZH, Chickooree D, Wu HJ, Tan HY, Wang K, He ZJ, Gong CJ, Ram V, Zhang S. The effect of early detection of anterolateral thigh free flap crisis on the salvage success rate, based on 10 years of experience and 1072 flaps. International Journal of Oral and Maxillofacial Surgery. 43: 1059-63. PMID 25022830 DOI: 10.1016/j.ijom.2014.06.003 |
0.394 |
|
| 2014 |
Scharpf RB, Mireles L, Yang Q, Köttgen A, Ruczinski I, Susztak K, Halper-Stromberg E, Tin A, Cristiano S, Chakravarti A, Boerwinkle E, Fox CS, Coresh J, Linda Kao WH. Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations. Bmc Genetics. 15: 81. PMID 25007794 DOI: 10.1186/1471-2156-15-81 |
0.347 |
|
| 2014 |
Weng LC, Tang W, Rich SS, Smith NL, Redline S, O'Donnell CJ, Basu S, Reiner AP, Delaney JA, Tracy RP, Palmer CD, Young T, Yang Q, Folsom AR, Cushman M. A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups. Thrombosis Research. 134: 462-7. PMID 24908450 DOI: 10.1016/J.Thromres.2014.05.018 |
0.304 |
|
| 2014 |
McMahon GM, Olden M, Garnaas M, Yang Q, Liu X, Hwang SJ, Larson MG, Goessling W, Fox CS. Sequencing of LRP2 reveals multiple rare variants associated with urinary trefoil factor-3. Journal of the American Society of Nephrology : Jasn. 25: 2896-905. PMID 24876117 DOI: 10.1681/Asn.2013111240 |
0.353 |
|
| 2014 |
Williams SR, Yang Q, Chen F, Liu X, Keene KL, Jacques P, Chen WM, Weinstein G, Hsu FC, Beiser A, Wang L, Bookman E, Doheny KF, Wolf PA, Zilka M, et al. Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. Plos Genetics. 10: e1004214. PMID 24651765 DOI: 10.1371/Journal.Pgen.1004214 |
0.353 |
|
| 2014 |
Huang J, Huffman JE, Yamakuchi M, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, ... ... Yang Q, et al. Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1093-101. PMID 24578379 DOI: 10.1161/Atvbaha.113.302088 |
0.354 |
|
| 2014 |
Li X, Yang Q, Yu H, Wu L, Zhao Y, Zhang C, Yue X, Liu Z, Wu H, Haffty BG, Feng Z, Hu W. LIF promotes tumorigenesis and metastasis of breast cancer through the AKT-mTOR pathway. Oncotarget. 5: 788-801. PMID 24553191 DOI: 10.18632/oncotarget.1772 |
0.422 |
|
| 2014 |
O'Seaghdha CM, Tin A, Yang Q, Katz R, Liu Y, Harris T, Astor B, Coresh J, Fox CS, Kao WH, Shlipak MG. Association of a cystatin C gene variant with cystatin C levels, CKD, and risk of incident cardiovascular disease and mortality. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 63: 16-22. PMID 23932088 DOI: 10.1053/J.Ajkd.2013.06.015 |
0.318 |
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| 2013 |
O'Seaghdha CM, Wu H, Yang Q, Kapur K, Guessous I, Zuber AM, Köttgen A, Stoudmann C, Teumer A, Kutalik Z, Mangino M, Dehghan A, Zhang W, Eiriksdottir G, Li G, et al. Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. Plos Genetics. 9: e1003796. PMID 24068962 DOI: 10.1371/Journal.Pgen.1003796 |
0.54 |
|
| 2013 |
Hafeez F, Neboori HJ, Harigopal M, Wu H, Haffty BG, Yang Q, Schiff D, Moran MS. Is Ki-67 expression prognostic for local relapse in early-stage breast cancer patients treated with breast conservation therapy (BCT)? International Journal of Radiation Oncology, Biology, Physics. 87: 344-8. PMID 23910708 DOI: 10.1016/j.ijrobp.2013.05.052 |
0.43 |
|
| 2013 |
Chen J, Li W, Huang X, Guo C, Zou R, Yang Q, Zhang H, Zhang T, Chen H, Wu H. Evaluating total lymphocyte count as a surrogate marker for CD4 cell count in the management of HIV-infected patients in resource-limited settings: a study from China. Plos One. 8: e69704. PMID 23874985 DOI: 10.1371/journal.pone.0069704 |
0.397 |
|
| 2013 |
Jones T, Neboori H, Wu H, Yang Q, Haffty BG, Evans S, Higgins S, Moran MS. Are breast cancer subtypes prognostic for nodal involvement and associated with clinicopathologic features at presentation in early-stage breast cancer? Annals of Surgical Oncology. 20: 2866-72. PMID 23661183 DOI: 10.1245/s10434-013-2994-6 |
0.434 |
|
| 2013 |
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, et al. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics. 45: 145-54. PMID 23263486 DOI: 10.1038/Ng.2500 |
0.34 |
|
| 2012 |
Yang Q, Wang Y. Methods for Analyzing Multivariate Phenotypes in Genetic Association Studies. Journal of Probability and Statistics. 2012: 652569. PMID 24748889 DOI: 10.1155/2012/652569 |
0.317 |
|
| 2012 |
Chen MH, Huang J, Chen WM, Larson MG, Fox CS, Vasan RS, Seshadri S, O'Donnell CJ, Yang Q. Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study. Plos One. 7: e51589. PMID 23284720 DOI: 10.1371/Journal.Pone.0051589 |
0.345 |
|
| 2012 |
Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin SY, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD, Smith NL, Williams SM, Ikram MA, Kleber ME, Becker DM, ... ... Yang Q, et al. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood. 120: 4873-81. PMID 22990020 DOI: 10.1182/Blood-2012-06-436188 |
0.364 |
|
| 2012 |
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, et al. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human Molecular Genetics. 21: 5329-43. PMID 22962313 DOI: 10.1093/Hmg/Dds369 |
0.355 |
|
| 2012 |
Liu C, Yang Q, Hwang SJ, Sun F, Johnson AD, Shirihai OS, Vasan RS, Levy D, Schwartz F. Association of genetic variation in the mitochondrial genome with blood pressure and metabolic traits. Hypertension. 60: 949-56. PMID 22949535 DOI: 10.1161/Hypertensionaha.112.196519 |
0.318 |
|
| 2012 |
Liang Y, Wu H, Lei R, Chong RA, Wei Y, Lu X, Tagkopoulos I, Kung SY, Yang Q, Hu G, Kang Y. Transcriptional network analysis identifies BACH1 as a master regulator of breast cancer bone metastasis. The Journal of Biological Chemistry. 287: 33533-44. PMID 22875853 DOI: 10.1074/Jbc.M112.392332 |
0.44 |
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| 2012 |
Köttgen A, Yang Q, Shimmin LC, Tin A, Schaeffer C, Coresh J, Liu X, Rampoldi L, Hwang SJ, Boerwinkle E, Hixson JE, Kao WH, Fox CS. Association of estimated glomerular filtration rate and urinary uromodulin concentrations with rare variants identified by UMOD gene region sequencing. Plos One. 7: e38311. PMID 22693617 DOI: 10.1371/Journal.Pone.0038311 |
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Neboori HJ, Haffty BG, Wu H, Yang Q, Aly A, Goyal S, Schiff D, Moran MS, Golhar R, Chen C, Moore D, Ganesan S. Low p53 binding protein 1 (53BP1) expression is associated with increased local recurrence in breast cancer patients treated with breast-conserving surgery and radiotherapy. International Journal of Radiation Oncology, Biology, Physics. 83: e677-83. PMID 22520477 DOI: 10.1016/j.ijrobp.2012.01.089 |
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O'Seaghdha CM, Yang Q, Wu H, Hwang SJ, Fox CS. Performance of a genetic risk score for CKD stage 3 in the general population. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 59: 19-24. PMID 21995970 DOI: 10.1053/J.Ajkd.2011.08.030 |
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Rao M, Mottl AK, Cole SA, Umans JG, Freedman BI, Bowden DW, Langefeld CD, Fox CS, Yang Q, Cupples A, Iyengar SK, Hunt SC, Trikalinos TA. Meta-analysis of genome-wide linkage scans for renal function traits. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 27: 647-56. PMID 21622988 DOI: 10.1093/Ndt/Gfr255 |
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Foster MC, Yang Q, Hwang SJ, Hoffmann U, Fox CS. Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study. Bmc Medical Genetics. 12: 148. PMID 22044751 DOI: 10.1186/1471-2350-12-148 |
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Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, Mallick S, Myers S, Tandon A, Spencer C, Palmer CD, Adeyemo AA, Akylbekova EL, Cupples LA, Divers J, ... ... Yang Q, et al. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. American Journal of Human Genetics. 89: 368-81. PMID 21907010 DOI: 10.1016/J.Ajhg.2011.07.025 |
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Lovely RS, Yang Q, Massaro JM, Wang J, D'Agostino RB, O'Donnell CJ, Shannon J, Farrell DH. Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 31: 2345-52. PMID 21757653 DOI: 10.1161/Atvbaha.111.232710 |
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Fornage M, Debette S, Bis JC, Schmidt H, Ikram MA, Dufouil C, Sigurdsson S, Lumley T, DeStefano AL, Fazekas F, Vrooman HA, Shibata DK, Maillard P, Zijdenbos A, Smith AV, ... ... Yang Q, et al. Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. Annals of Neurology. 69: 928-39. PMID 21681796 DOI: 10.1002/Ana.22403 |
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Yang Q, He H, Li H, Tian H, Zhang J, Zhai L, Chen J, Wu H, Yi G, He ZH, Peng X. NOA1 functions in a temperature-dependent manner to regulate chlorophyll biosynthesis and Rubisco formation in rice. Plos One. 6: e20015. PMID 21625436 DOI: 10.1371/journal.pone.0020015 |
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Pasaniuc B, Zaitlen N, Lettre G, Chen GK, Tandon A, Kao WH, Ruczinski I, Fornage M, Siscovick DS, Zhu X, Larkin E, Lange LA, Cupples LA, Yang Q, Akylbekova EL, et al. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. Plos Genetics. 7: e1001371. PMID 21541012 DOI: 10.1371/Journal.Pgen.1001371 |
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Zeng G, Tang T, Wu HJ, You WH, Luo JK, Lin Y, Liang QH, Li XQ, Huang X, Yang QD. Salvianolic acid B protects SH-SY5Y neuroblastoma cells from 1-methyl-4-phenylpyridinium-induced apoptosis. Biological & Pharmaceutical Bulletin. 33: 1337-42. PMID 20686228 DOI: 10.1248/bpb.33.1337 |
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Yang Q, Wu H, Guo CY, Fox CS. Analyze multivariate phenotypes in genetic association studies by combining univariate association tests. Genetic Epidemiology. 34: 444-54. PMID 20583287 DOI: 10.1002/Gepi.20497 |
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Chen MH, Larson MG, Hsu YH, Peloso GM, Guo CY, Fox CS, Atwood LD, Yang Q. A three-stage approach for genome-wide association studies with family data for quantitative traits. Bmc Genetics. 11: 40. PMID 20470424 DOI: 10.1186/1471-2156-11-40 |
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Johnson AD, Kavousi M, Smith AV, Chen MH, Dehghan A, Aspelund T, Lin JP, van Duijn CM, Harris TB, Cupples LA, Uitterlinden AG, Launer L, Hofman A, Rivadeneira F, Stricker B, ... Yang Q, et al. Genome-wide association meta-analysis for total serum bilirubin levels. Human Molecular Genetics. 18: 2700-10. PMID 19414484 DOI: 10.1093/Hmg/Ddp202 |
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Liu C, Yang Q, Adrienne Cupples L, Meigs JB, Dupuis J. Selection of the most informative individuals from families with multiple siblings for association studies. Genetic Epidemiology. 33: 299-307. PMID 19025786 DOI: 10.1002/Gepi.20380 |
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Kottgen A, Kao WHL, Hwang SJ, Boerwinkle E, Yang Q, Levy D, Benjamin EJ, Larson MG, Astor BC, Coresh J, Fox CS. Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis risk in Communities Studies Bmc Medical Genetics. 9. PMID 18522750 DOI: 10.1186/1471-2350-9-49 |
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Chen MH, Cui J, Guo CY, Cupples LA, Van Eerdewegh P, Dupuis J, Yang Q. Joint modeling of linkage and association using affected sib-pair data. Bmc Proceedings. 1: S38. PMID 18466536 DOI: 10.1186/1753-6561-1-S1-S38 |
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Yang Q, Biernacka JM, Chen MH, Houwing-Duistermaat JJ, Bergemann TL, Basu S, Fan R, Liu L, Bourgey M, Clerget-Darpoux F, Lin WY, Elston RC, Cupples LA, Apprey V, Cui J, et al. Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4. Genetic Epidemiology. 31: S34-42. PMID 18046758 DOI: 10.1002/Gepi.20278 |
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Yang Q, Kathiresan S, Lin JP, Tofler GH, O'Donnell CJ. Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. Bmc Medical Genetics. 8: S12. PMID 17903294 DOI: 10.1186/1471-2350-8-S1-S12 |
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Hwang SJ, Yang Q, Meigs JB, Pearce EN, Fox CS. A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. Bmc Medical Genetics. 8: S10. PMID 17903292 DOI: 10.1186/1471-2350-8-S1-S10 |
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Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB, Demissie S, DeStefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, ... ... Yang Q, et al. The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. Bmc Medical Genetics. 8: S1. PMID 17903291 DOI: 10.1186/1471-2350-8-S1-S1 |
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Lin J, O'Donnell CJ, Jin L, Fox C, Yang Q, Cupples LA. Evidence for linkage of red blood cell size and count: genome-wide scans in the Framingham Heart Study. American Journal of Hematology. 82: 605-610. PMID 17211848 DOI: 10.1002/Ajh.20868 |
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Li S, Teumer A, Knol MJ, Yang Q, Seshadri S. P1-004: GENOME-WIDE ASSOCIATION STUDY OF 11,785 INDIVIDUALS IDENTIFIES SEVEN LOCI ASSOCIATED WITH BRAIN-DERIVED NEUROTROPHIC FACTOR Alzheimer's & Dementia. 14: P262-P262. DOI: 10.1016/J.Jalz.2018.06.005 |
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Kathiresan S, Gabriel SB, Yang Q, Lochner AL, Larson MG, Levy D, Tofler GH, Hirschhorn JN, O'Donnell CJ. Comprehensive survey of common genetic variation at the plasminogen activator inhibitor-1 locus and relations to circulating plasminogen activator inhibitor-1 levels Circulation. 112: 1728-1735. PMID 16172282 DOI: 10.1161/Circulationaha.105.547836 |
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Hofmann MA, Yang Q, Harja E, Kedia P, Gregersen PK, Cupples LA, Schmidt AM, Hudson BI. The RAGE Gly82Ser polymorphism is not associated with cardiovascular disease in the Framingham offspring study. Atherosclerosis. 182: 301-5. PMID 16159602 DOI: 10.1016/J.Atherosclerosis.2005.02.006 |
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Fox CS, Yang Q, Cupples LA, Guo CY, Atwood LD, Murabito JM, Levy D, Mendelsohn ME, Housman DE, Shearman AM. Sex-specific association between estrogen receptor-alpha gene variation and measures of adiposity: the Framingham Heart Study. The Journal of Clinical Endocrinology and Metabolism. 90: 6257-62. PMID 16144952 DOI: 10.1210/Jc.2005-0670 |
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McDermott DH, Yang Q, Kathiresan S, Cupples LA, Massaro JM, Keaney JF, Larson MG, Vasan RS, Hirschhorn JN, O'Donnell CJ, Murphy PM, Benjamin EJ. CCL2 polymorphisms are associated with serum monocyte chemoattractant protein-1 levels and myocardial infarction in the Framingham Heart Study Circulation. 112: 1113-1120. PMID 16116069 DOI: 10.1161/Circulationaha.105.543579 |
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Yang Q, Lai CQ, Parnell L, Cupples LA, Adiconis X, Zhu Y, Wilson PW, Housman DE, Shearman AM, D'Agostino RB, Ordovas JM. Genome-wide linkage analyses and candidate gene fine mapping for HDL3 cholesterol: the Framingham Study. Journal of Lipid Research. 46: 1416-25. PMID 15805549 DOI: 10.1194/Jlr.M400382-Jlr200 |
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Fox CS, Yang Q, Guo CY, Cupples LA, Wilson PW, Levy D, Meigs JB. Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study. Kidney International. 67: 70-4. PMID 15610229 DOI: 10.1111/J.1523-1755.2005.00056.X |
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Fox CS, Yang Q, Cupples LA, Guo CY, Larson MG, Leip EP, Wilson PW, Levy D. Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study. Journal of the American Society of Nephrology : Jasn. 15: 2457-61. PMID 15339995 DOI: 10.1097/01.Asn.0000135972.13396.6F |
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Djoussé L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, ... ... Yang Q, et al. Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics. 5: 109-14. PMID 15029481 DOI: 10.1007/S10048-004-0175-2 |
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Yang Q, Tofler GH, Cupples LA, Larson MG, Feng D, Lindpaintner K, Levy D, D'Agostino RB, O'Donnell CJ. A genome-wide search for genes affecting circulating fibrinogen levels in the Framingham Heart Study. Thrombosis Research. 110: 57-64. PMID 12877910 DOI: 10.1016/S0049-3848(03)00288-3 |
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Cupples LA, Yang Q, Demissie S, Copenhafer D, Levy D. Description of the Framingham Heart Study data for Genetic Analysis Workshop 13. Bmc Genetics. 4: S2. PMID 14975070 DOI: 10.1186/1471-2156-4-S1-S2 |
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