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Stacey S. Cherny - Publications

Affiliations: 
The University of Hong Kong, Hong Kong Island, Hong Kong, Hong Kong 
Area:
statistical genetics
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Year Citation  Score
2022 Cherny SS, Williams FMK, Livshits G. Genetic and environmental correlational structure among metabolic syndrome endophenotypes. Annals of Human Genetics. PMID 35357000 DOI: 10.1111/ahg.12465  0.313
2020 Tubbs JD, Porsch RM, Cherny SS, Sham PC. The Genes We Inherit and Those We Don't: Maternal Genetic Nurture and Child BMI Trajectories. Behavior Genetics. PMID 32681386 DOI: 10.1007/S10519-020-10008-W  0.393
2020 Sham PC, Purcell SM, Cherny SS, Neale MC, Neale BM. Statistical Power and the Classical Twin Design. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 23: 87-89. PMID 32638684 DOI: 10.1017/Thg.2020.46  0.515
2020 Cherny SS, Livshits G, Wells HRR, Freidin MB, Malkin I, Dawson SJ, Williams FMK. Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank. European Journal of Human Genetics : Ejhg. PMID 32203203 DOI: 10.1038/S41431-020-0603-2  0.326
2018 Toulopoulou T, Zhang X, Cherny S, Dickinson D, Berman KF, Straub RE, Sham P, Weinberger DR. Polygenic risk score increases schizophrenia liability through cognition-relevant pathways. Brain : a Journal of Neurology. PMID 30535067 DOI: 10.1093/Brain/Awy279  0.349
2018 Tang CS, Zhuang X, Lam WY, Ngan ES, Hsu JS, Michelle YU, Man-Ting SO, Cherny SS, Ngo ND, Sham PC, Tam PK, Garcia-Barcelo MM. Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing. European Journal of Human Genetics : Ejhg. PMID 29483666 DOI: 10.1038/S41431-018-0129-Z  0.395
2017 McCormack M, Gui H, Ingason A, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, ... ... Cherny S, et al. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology. PMID 29288229 DOI: 10.1212/Wnl.0000000000004853  0.329
2017 Hsu JSJ, So M, Tang CSM, Anwarul K, Porsch RM, Wong C, Yu M, Yeung F, Xia H, Zhang R, Cherny SS, Chung PHY, Kenneth KYW, Sham PC, Ngo ND, et al. De novo mutations in Caudal Type Homeo Box Transcription Factor 2 (CDX2) in patients with persistent cloaca. Human Molecular Genetics. PMID 29177441 DOI: 10.1093/Hmg/Ddx406  0.313
2017 Gui H, Li M, Sham PC, Baum L, Kwan P, Cherny SS. Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 29150900 DOI: 10.1002/Ajmg.B.32607  0.404
2017 Tang CS, Dattani S, So MT, Cherny SS, Tam PKH, Sham PC, Garcia-Barcelo MM. Actionable secondary findings from whole-genome sequencing of 954 East Asians. Human Genetics. PMID 29128982 DOI: 10.1007/S00439-017-1852-1  0.362
2017 Lu X, Peloso GM, Liu DJ, Wu Y, Zhang H, Zhou W, Li J, Tang CS, Dorajoo R, Li H, Long J, Guo X, Xu M, Spracklen CN, Chen Y, ... ... Cherny SS, et al. Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease. Nature Genetics. PMID 29083407 DOI: 10.1038/Ng.3978  0.399
2017 Gui H, Kwan JS, Sham PC, Cherny SS, Li M. Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis. Genetics. PMID 28495956 DOI: 10.1534/Genetics.116.198150  0.45
2017 Cheng G, Chung PH, Chan EK, So MT, Sham PC, Cherny SS, Tam PK, Garcia-Barceló MM. Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis. Bmc Medical Genomics. 10: 22. PMID 28416017 DOI: 10.1186/S12920-017-0259-0  0.371
2017 Gui H, Kwok M, Baum L, Sham PC, Kwan P, Cherny SS. SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese. The Pharmacogenomics Journal. PMID 28398356 DOI: 10.1038/Tpj.2017.11  0.382
2017 Cheung CY, Tang CS, Xu A, Lee CH, Au KW, Xu L, Fong CH, Kwok KH, Chow WS, Woo YC, Yuen M, Cherny SS, Hai J, Cheung BM, Tan K, et al. An Exome-Chip Association Analysis in Chinese Reveals a Functional Missense Variant of Gckr that Regulates Fgf21 Levels. Diabetes. PMID 28385800 DOI: 10.2337/Db16-1384  0.352
2016 Wong JK, Campbell D, Ngo ND, Yeung F, Cheng G, Tang CS, Chung PH, Tran NS, So MT, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes. Bmc Medical Genomics. 9: 75. PMID 27955658 DOI: 10.1186/S12920-016-0236-Z  0.393
2016 Cheung CY, Tang CS, Xu A, Lee CH, Au KW, Xu L, Fong CH, Kwok KH, Chow WS, Woo YC, Yuen MM, Hai JS, Jin YL, Cheung BM, Tan KC, ... Cherny SS, et al. Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals. Diabetologia. PMID 27744525 DOI: 10.1007/S00125-016-4132-Z  0.3
2016 Tang CS, Gui H, Kapoor A, Kim JH, Luzón-Toro B, Pelet A, Burzynski G, Lantieri F, So MT, Berrios C, Shin HD, Fernández RM, Le TL, Verheij JB, Matera I, ... Cherny SS, et al. Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. Human Molecular Genetics. PMID 27702942 DOI: 10.1093/Hmg/Ddw333  0.394
2016 Trotta A, Iyegbe C, Di Forti M, Sham PC, Campbell DD, Cherny SS, Mondelli V, Aitchison KJ, Murray RM, Vassos E, Fisher HL. Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study. Plos One. 11: e0163319. PMID 27648571 DOI: 10.1371/Journal.Pone.0163319  0.352
2016 Zhao JV, Lam TH, Jiang C, Cherny SS, Liu B, Cheng KK, Zhang W, Leung GM, Schooling CM. A Mendelian randomization study of testosterone and cognition in men. Scientific Reports. 6: 21306. PMID 26864717 DOI: 10.1038/Srep21306  0.332
2016 Porsch RM, Middeldorp CM, Cherny SS, Krapohl E, van Beijsterveldt CE, Loukola A, Korhonen T, Pulkkinen L, Corley R, Rhee S, Kaprio J, Rose RR, Hewitt JK, Sham P, Plomin R, et al. Longitudinal heritability of childhood aggression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26786601 DOI: 10.1002/Ajmg.B.32420  0.35
2015 Tang CS, Zhang H, Cheung CY, Xu M, Ho JC, Zhou W, Cherny SS, Zhang Y, Holmen O, Au KW, Yu H, Xu L, Jia J, Porsch RM, Sun L, et al. Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. Nature Communications. 6: 10206. PMID 26690388 DOI: 10.1038/Ncomms10206  0.352
2015 Luzón-Toro B, Gui H, Ruiz-Ferrer M, Sze-Man Tang C, Fernández RM, Sham PC, Torroglosa A, Kwong-Hang Tam P, Espino-Paisán L, Cherny SS, Bleda M, Enguix-Riego Mdel V, Dopazo J, Antiñolo G, García-Barceló MM, et al. Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease. Scientific Reports. 5: 16473. PMID 26559152 DOI: 10.1038/Srep16473  0.39
2015 Zhang J, Zhang L, Zhang Y, Yang J, Guo M, Sun L, Pan HF, Hirankarn N, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, ... ... Cherny SS, et al. Gene-based meta-analysis of GWAS data identifies independent SNPs in ANXA6 as associated with SLE in Asian populations. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26202167 DOI: 10.1002/Art.39275  0.406
2015 Liu W, Wong JK, He Q, Wong EH, Tang CS, Zhang R, So MT, Wong KK, Nicholls J, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM, Xia H. Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism. Bmc Medical Genetics. 16: 49. PMID 26179878 DOI: 10.1186/S12881-015-0189-7  0.345
2015 Zhang Y, Wang Y, Yang J, Zhang J, Sun L, Hirankarn N, Pan HF, Lau CS, Chan TM, Lee TL, Leung AM, Mok CC, Zhang L, Shen JJ, Wong SN, ... ... Cherny SS, et al. Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. Arthritis Research & Therapy. 17: 67. PMID 25880549 DOI: 10.1186/S13075-015-0577-6  0.346
2015 Zhang Y, Yang J, Zhang J, Sun L, Hirankarn N, Pan HF, Lau CS, Chan TM, Lee TL, Leung AM, Mok CC, Zhang L, Wang Y, Shen JJ, Wong SN, ... ... Cherny SS, et al. Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations. Annals of the Rheumatic Diseases. PMID 25862617 DOI: 10.1136/Annrheumdis-2014-206367  0.38
2015 Zhang Y, Zhang J, Yang J, Wang Y, Zhang L, Zuo X, Sun L, Pan HF, Hirankarn N, Wang T, Chen R, Ying D, Zeng S, Shen JJ, Lee TL, ... ... Cherny SS, et al. Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus. Human Molecular Genetics. 24: 274-84. PMID 25149475 DOI: 10.1093/Hmg/Ddu429  0.371
2015 Garcia-Barceló M, Wong JKL, Ngo ND, Tran NS, Nguyen TL, Nguyen L, Sham P, Cherny S, Tam P. AB113. The first genetic study on congenital choledochal dilatation (CCD) implicates extracellular matrix proteins Annals of Translational Medicine. 3. DOI: 10.3978/J.Issn.2305-5839.2015.Ab113  0.341
2015 Cheng G, Garcia-Barceló M, Chung PH, Tang W, Wong EHM, Chan EK, So M, Ngo DN, Tran NS, Nguyen PAH, Sham P, Cherny SS, Nicholls JM, Tam PK. AB080. Genetic findings provide insight of biliary atresia patient complexity Annals of Translational Medicine. 3: 81. DOI: 10.3978/J.Issn.2305-5839.2015.Ab080  0.354
2014 Anney RJL, Avbersek A, Balding D, Baum L, Becker F, Berkovic SF, Bradfi JP, Brody LC, Buono RJ, Catarino CB, Cavalleri GL, Cherny SS, Chinthapalli K, Coffey AJ, Compston A, et al. Genetic determinants of common epilepsies: A meta-analysis of genome-wide association studies The Lancet Neurology. 13: 893-903. PMID 25087078 DOI: 10.1016/S1474-4422(14)70171-1  0.353
2014 Gui H, Jiang CQ, Cherny SS, Sham PC, Xu L, Liu B, Jin YL, Zhu T, Zhang WS, Thomas GN, Cheng KK, Lam TH. Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study. Neurobiology of Aging. 35: 2422.e3-8. PMID 24863667 DOI: 10.1016/J.Neurobiolaging.2014.04.022  0.33
2014 van Os J, Rutten BP, Myin-Germeys I, Delespaul P, Viechtbauer W, van Zelst C, Bruggeman R, Reininghaus U, Morgan C, Murray RM, Di Forti M, McGuire P, Valmaggia LR, Kempton MJ, ... ... Cherny SS, et al. Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin. 40: 729-36. PMID 24860087 DOI: 10.1093/Schbul/Sbu069  0.358
2014 Wong EH, So HC, Li M, Wang Q, Butler AW, Paul B, Wu HM, Hui TC, Choi SC, So MT, Garcia-Barcelo MM, McAlonan GM, Chen EY, Cheung EF, Chan RC, ... ... Cherny SS, et al. Common variants on Xq28 conferring risk of schizophrenia in Han Chinese. Schizophrenia Bulletin. 40: 777-86. PMID 24043878 DOI: 10.1093/Schbul/Sbt104  0.327
2014 Zhang J, Zhang Y, Yang J, Zhang L, Sun L, Pan HF, Hirankarn N, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, Wong SN, ... ... Cherny SS, et al. Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians. Human Molecular Genetics. 23: 524-33. PMID 24001599 DOI: 10.1093/Hmg/Ddt424  0.396
2013 Song YQ, Karasugi T, Cheung KM, Chiba K, Ho DW, Miyake A, Kao PY, Sze KL, Yee A, Takahashi A, Kawaguchi Y, Mikami Y, Matsumoto M, Togawa D, Kanayama M, ... ... Cherny SS, et al. Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. The Journal of Clinical Investigation. 123: 4909-17. PMID 24216480 DOI: 10.1172/Jci69277  0.376
2013 Wong EH, Ng CL, Lui VC, So MT, Cherny SS, Sham PC, Tam PK, Garcia-Barceló MM. Gene network analysis of candidate loci for human anorectal malformations. Plos One. 8: e69142. PMID 23936318 DOI: 10.1371/Journal.Pone.0069142  0.332
2013 Cheng G, Tang CS, Wong EH, Cheng WW, So MT, Miao X, Zhang R, Cui L, Liu X, Ngan ES, Lui VC, Chung PH, Chan IH, Liu J, Zhong W, ... ... Cherny SS, et al. Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. Journal of Hepatology. 59: 1285-91. PMID 23872602 DOI: 10.1016/J.Jhep.2013.07.021  0.406
2013 Cui L, Wong EH, Cheng G, Firmato de Almeida M, So MT, Sham PC, Cherny SS, Tam PK, Garcia-Barceló MM. Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia. Plos One. 8: e66631. PMID 23840513 DOI: 10.1371/Journal.Pone.0066631  0.355
2013 Ma RC, Hu C, Tam CH, Zhang R, Kwan P, Leung TF, Thomas GN, Go MJ, Hara K, Sim X, Ho JS, Wang C, Li H, Lu L, Wang Y, ... ... Cherny SS, et al. Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Diabetologia. 56: 1291-305. PMID 23532257 DOI: 10.1007/S00125-013-2874-4  0.32
2013 Gui H, Tang WK, So MT, Proitsi P, Sham PC, Tam PK, Ngan ES, Sau-Wai Ngan E, Cherny SS, Garcia-Barceló MM. RET and NRG1 interplay in Hirschsprung disease. Human Genetics. 132: 591-600. PMID 23400839 DOI: 10.1007/S00439-013-1272-9  0.372
2013 Yang W, Tang H, Zhang Y, Tang X, Zhang J, Sun L, Yang J, Cui Y, Zhang L, Hirankarn N, Cheng H, Pan HF, Gao J, Lee TL, Sheng Y, ... ... Cherny SS, et al. Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. American Journal of Human Genetics. 92: 41-51. PMID 23273568 DOI: 10.1016/J.Ajhg.2012.11.018  0.401
2013 Wong EH, Cui L, Ng CL, Tang CS, Liu XL, So MT, Yip BH, Cheng G, Zhang R, Tang WK, Yang W, Lau YL, Baum L, Kwan P, Sun LD, ... ... Cherny SS, et al. Genome-wide copy number variation study in anorectal malformations. Human Molecular Genetics. 22: 621-31. PMID 23108157 DOI: 10.1093/Hmg/Dds451  0.347
2012 Tang CS, Cheng G, So MT, Yip BH, Miao XP, Wong EH, Ngan ES, Lui VC, Song YQ, Chan D, Cheung K, Yuan ZW, Lei L, Chung PH, Liu XL, ... ... Cherny SS, et al. Genome-wide copy number analysis uncovers a new HSCR gene: NRG3. Plos Genetics. 8: e1002687. PMID 22589734 DOI: 10.1371/Journal.Pgen.1002687  0.31
2012 Hur YM, Cherny SS, Sham PC. Heritability of hallucinations in adolescent twins. Psychiatry Research. 199: 98-101. PMID 22578404 DOI: 10.1016/J.Psychres.2012.04.024  0.397
2012 Yang HC, Liang YJ, Chen JW, Chiang KM, Chung CM, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Leu HB, Yin WH, Chiu TY, Chern CL, ... ... Cherny SS, et al. Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. Plos One. 7: e32907. PMID 22479346 DOI: 10.1371/Journal.Pone.0032907  0.329
2012 Guo Y, Tomlinson B, Chu T, Fang YJ, Gui H, Tang CS, Yip BH, Cherny SS, Hur YM, Sham PC, Lam TH, Thomas NG. A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits. Plos One. 7: e31489. PMID 22384028 DOI: 10.1371/Journal.Pone.0031489  0.373
2012 Li MX, Yeung JM, Cherny SS, Sham PC. Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets. Human Genetics. 131: 747-56. PMID 22143225 DOI: 10.1007/S00439-011-1118-2  0.349
2012 Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, ... Cherny SS, et al. Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. Human Molecular Genetics. 21: 1184-9. PMID 22116939 DOI: 10.1093/Hmg/Ddr550  0.387
2012 Li R, Yang W, Zhang J, Hirankarn N, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, Lee TL, ... ... Cherny SS, et al. Association of CD247 with systemic lupus erythematosus in Asian populations. Lupus. 21: 75-83. PMID 22004975 DOI: 10.1177/0961203311422724  0.339
2012 Tang CS, Ngan ES, Tang WK, So MT, Cheng G, Miao XP, Leon TY, Leung BM, Hui KJ, Lui VH, Chen Y, Chan IH, Chung PH, Liu XL, Wong KK, ... ... Cherny SS, et al. Mutations in the NRG1 gene are associated with Hirschsprung disease. Human Genetics. 131: 67-76. PMID 21706185 DOI: 10.1007/S00439-011-1035-4  0.376
2011 So MT, Leon TY, Cheng G, Tang CS, Miao XP, Cornes BK, Diem NN, Cui L, Ngan ES, Lui VC, Wu XZ, Wang B, Wang H, Yuan ZW, Huang LM, ... ... Cherny SS, et al. RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients. Plos One. 6: e28986. PMID 22174939 DOI: 10.1371/Journal.Pone.0028986  0.313
2011 Gui H, Li M, Sham PC, Cherny SS. Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset. Bmc Research Notes. 4: 386. PMID 21981765 DOI: 10.1186/1756-0500-4-386  0.304
2011 Ong KL, Tso AW, Cherny SS, Sham PC, Lam TH, Lam KS, Cheung BM. Role of genetic variants in the gene encoding lipocalin-2 in the development of elevated blood pressure. Clinical and Experimental Hypertension (New York, N.Y. : 1993). 33: 484-91. PMID 21978028 DOI: 10.3109/10641963.2010.549276  0.327
2011 Ngan ES, Garcia-Barceló MM, Yip BH, Poon HC, Lau ST, Kwok CK, Sat E, Sham MH, Wong KK, Wainwright BJ, Cherny SS, Hui CC, Sham PC, Lui VC, Tam PK. Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans. The Journal of Clinical Investigation. 121: 3467-78. PMID 21841314 DOI: 10.1172/Jci43737  0.313
2011 So HC, Gui AH, Cherny SS, Sham PC. Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases. Genetic Epidemiology. 35: 310-7. PMID 21374718 DOI: 10.1002/Gepi.20579  0.374
2011 Zhang Y, Yang W, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Lee TL, Ho MH, Lee PP, Wong WH, Yang J, Zhang J, ... ... Cherny SS, et al. Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese. Genes and Immunity. 12: 231-4. PMID 21326321 DOI: 10.1038/Gene.2010.66  0.333
2011 Zhang L, Yang W, Ying D, Cherny SS, Hildebrandt F, Sham PC, Lau YL. Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data. Human Mutation. 32: 345-53. PMID 21309031 DOI: 10.1002/Humu.21432  0.353
2011 Ho JW, Choi SC, Lee YF, Hui TC, Cherny SS, Garcia-Barceló MM, Carvajal-Carmona L, Liu R, To SH, Yau TK, Chung CC, Yau CC, Hui SM, Lau PY, Yuen CH, et al. Replication study of SNP associations for colorectal cancer in Hong Kong Chinese. British Journal of Cancer. 104: 369-75. PMID 21179028 DOI: 10.1038/Sj.Bjc.6605977  0.331
2011 Ong KL, Tso AW, Leung RY, Cherny SS, Sham PC, Lam TH, Cheung BM, Lam KS. A genetic variant in the gene encoding adrenomedullin predicts the development of dysglycemia over 6.4 years in Chinese. Clinica Chimica Acta; International Journal of Clinical Chemistry. 412: 353-7. PMID 21075100 DOI: 10.1016/J.Cca.2010.11.007  0.333
2011 Yang J, Yang W, Hirankarn N, Ye DQ, Zhang Y, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, ... ... Cherny SS, et al. ELF1 is associated with systemic lupus erythematosus in Asian populations. Human Molecular Genetics. 20: 601-7. PMID 21044949 DOI: 10.1093/Hmg/Ddq474  0.344
2011 Garcia-Barceló MM, Miao X, Tang CS, So HC, Tang W, Leon TY, So M, Yip B, Chen RY, Cheung EF, Chen EY, Li T, Tam P, Cherny SS, Sham PC. No NRG1 V266L in Chinese patients with schizophrenia. Psychiatric Genetics. 21: 47-9. PMID 20978455 DOI: 10.1097/Ypg.0B013E328341355B  0.308
2011 Sham PC, Cherny SS, Hall MH. Statistical issues and approaches in endophenotype research Chinese Science Bulletin. 56: 3403-3408. DOI: 10.1007/S11434-011-4746-Y  0.434
2010 Li MX, Sham PC, Cherny SS, Song YQ. A knowledge-based weighting framework to boost the power of genome-wide association studies. Plos One. 5: e14480. PMID 21217833 DOI: 10.1371/Journal.Pone.0014480  0.38
2010 Toulopoulou T, Goldberg TE, Mesa IR, Picchioni M, Rijsdijk F, Stahl D, Cherny SS, Sham P, Faraone SV, Tsuang M, Weinberger DR, Seidman LJ, Murray RM. Impaired intellect and memory: a missing link between genetic risk and schizophrenia? Archives of General Psychiatry. 67: 905-13. PMID 20819984 DOI: 10.1001/Archgenpsychiatry.2010.99  0.373
2010 Ong KL, Li M, Tso AW, Xu A, Cherny SS, Sham PC, Tse HF, Lam TH, Cheung BM, Lam KS. Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese. European Journal of Endocrinology / European Federation of Endocrine Societies. 163: 251-7. PMID 20516205 DOI: 10.1530/Eje-10-0251  0.341
2010 Garcia-Barceló MM, Yeung MY, Miao XP, Tang CS, Cheng G, Chen G, So MT, Ngan ES, Lui VC, Chen Y, Liu XL, Hui KJ, Li L, Guo WH, Sun XB, ... ... Cherny SS, et al. Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. Human Molecular Genetics. 19: 2917-25. PMID 20460270 DOI: 10.1093/Hmg/Ddq196  0.399
2010 Tang CS, Sribudiani Y, Miao XP, de Vries AR, Burzynski G, So MT, Leon YY, Yip BH, Osinga J, Hui KJ, Verheij JB, Cherny SS, Tam PK, Sham PC, Hofstra RM, et al. Fine mapping of the 9q31 Hirschsprung's disease locus. Human Genetics. 127: 675-83. PMID 20361209 DOI: 10.1007/S00439-010-0813-8  0.341
2010 Ong KL, Tso AW, Cherny SS, Sham PC, Lam KS, Jiang CQ, Thomas GN, Lam TH, Cheung BM. A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men. Thrombosis and Haemostasis. 103: 728-35. PMID 20135074 DOI: 10.1160/Th09-10-0692  0.307
2010 Kung AW, Xiao SM, Cherny S, Li GH, Gao Y, Tso G, Lau KS, Luk KD, Liu JM, Cui B, Zhang MJ, Zhang ZL, He JW, Yue H, Xia WB, et al. Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. American Journal of Human Genetics. 86: 229-39. PMID 20096396 DOI: 10.1016/J.Ajhg.2009.12.014  0.334
2010 So HC, Fong PY, Chen RY, Hui TC, Ng MY, Cherny SS, Mak WW, Cheung EF, Chan RC, Chen EY, Li T, Sham PC. Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 103-13. PMID 19367581 DOI: 10.1002/Ajmg.B.30961  0.325
2009 Kwan JS, Cherny SS, Kung AW, Sham PC. Novel sib pair selection strategy increases power in quantitative association analysis. Behavior Genetics. 39: 571-9. PMID 19568925 DOI: 10.1007/S10519-009-9284-X  0.439
2009 Garcia-Barcelo MM, Tang CS, Ngan ES, Lui VC, Chen Y, So MT, Leon TY, Miao XP, Shum CK, Liu FQ, Yeung MY, Yuan ZW, Guo WH, Liu L, Sun XB, ... ... Cherny SS, et al. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Proceedings of the National Academy of Sciences of the United States of America. 106: 2694-9. PMID 19196962 DOI: 10.1073/Pnas.0809630105  0.377
2009 Sham PC, Cherny SS, Purcell S. Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci. Genetica. 136: 237-43. PMID 19127410 DOI: 10.1007/S10709-008-9349-4  0.464
2009 Brocklebank D, Gayán J, Andresen JM, Roberts SA, Young AB, Snodgrass SR, Penney JB, Ramos-Arroyo MA, Cha JJ, Rosas HD, Hersch SM, Feigin A, Cherny SS, Wexler NS, Housman DE, et al. Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 425-9. PMID 18712713 DOI: 10.1002/Ajmg.B.30826  0.383
2008 Yeung JM, Sham PC, Chan AS, Cherny SS. OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays. Bmc Genomics. 9: 636. PMID 19117518 DOI: 10.1186/1471-2164-9-636  0.337
2008 Hur YM, Kaprio J, Iacono WG, Boomsma DI, McGue M, Silventoinen K, Martin NG, Luciano M, Visscher PM, Rose RJ, He M, Ando J, Ooki S, Nonaka K, Lin CC, ... ... Cherny SS, et al. Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity (2005). 32: 1455-67. PMID 18779828 DOI: 10.1038/Ijo.2008.144  0.371
2008 Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE. Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32: 445-53. PMID 18481795 DOI: 10.1002/Gepi.20317  0.371
2008 Ong KL, Leung RY, Wong LY, Cherny SS, Sham PC, Lam TH, Lam KS, Cheung BM. Association of a polymorphism in the lipin 1 gene with systolic blood pressure in men. American Journal of Hypertension. 21: 539-45. PMID 18437145 DOI: 10.1038/Ajh.2008.21  0.303
2008 Garcia-Barceló MM, Fong PY, Tang CS, Miao XP, So MT, Yuan ZW, Li L, Guo WH, Liu L, Wang B, Sun XB, Huang LM, Tou JF, Wong KK, Ngan ES, ... ... Cherny SS, et al. Mapping of a Hirschsprung's disease locus in 3p21. European Journal of Human Genetics : Ejhg. 16: 833-40. PMID 18285831 DOI: 10.1038/Ejhg.2008.18  0.366
2008 Dyment DA, Cader MZ, Datta A, Broxholme SJ, Cherny SS, Willer CJ, Ramagopalan S, Herrera BM, Orton S, Chao M, Sadovnick AD, Hader M, Hader W, Ebers GC. A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 467-72. PMID 18081025 DOI: 10.1002/Ajmg.B.30620  0.319
2008 Cherny SS. Variance components and related methods for mapping quantitative trait loci Sociological Methods and Research. 37: 227-250. DOI: 10.1177/0049124108324524  0.382
2008 Sham PC, Cherny SS, Kao PYP, Song YQ, Chan D, Cheung KMC. (iii) Whole-genome association studies of complex diseases Current Orthopaedics. 22: 251-258. DOI: 10.1016/J.Cuor.2008.05.006  0.371
2007 Willer CJ, Dyment DA, Cherny S, Ramagopalan SV, Herrera BM, Morrison KM, Sadovnick AD, Risch NJ, Ebers GC. A genome-wide scan in forty large pedigrees with multiple sclerosis. Journal of Human Genetics. 52: 955-62. PMID 18000641 DOI: 10.1007/S10038-007-0194-6  0.42
2007 Goode EL, Cherny SS, Christian JC, Jarvik GP, de Andrade M. Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 10: 703-11. PMID 17903110 DOI: 10.1375/Twin.10.5.703  0.338
2007 Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X  0.321
2007 Hopfer CJ, Lessem JM, Hartman CA, Stallings MC, Cherny SS, Corley RP, Hewitt JK, Krauter KS, Mikulich-Gilbertson SK, Rhee SH, Smolen A, Young SE, Crowley TJ. A genome-wide scan for loci influencing adolescent cannabis dependence symptoms: evidence for linkage on chromosomes 3 and 9. Drug and Alcohol Dependence. 89: 34-41. PMID 17169504 DOI: 10.1016/J.Drugalcdep.2006.11.015  0.341
2007 Andresen JM, Gayán J, Cherny SS, Brocklebank D, Alkorta-Aranburu G, Addis EA, Cardon LR, Housman DE, Wexler NS. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. Journal of Medical Genetics. 44: 44-50. PMID 17018562 DOI: 10.1136/Jmg.2006.045153  0.384
2006 Posthuma D, Cherny SS, Boomsma DI. Introduction to the special issue: human linkage studies for behavioral traits. Behavior Genetics. 36: 1-3. PMID 16341906 DOI: 10.1007/S10519-005-9010-2  0.362
2004 Petrill SA, Lipton PA, Hewitt JK, Plomin R, Cherny SS, Corley R, DeFries JC. Genetic and environmental contributions to general cognitive ability through the first 16 years of life. Developmental Psychology. 40: 805-12. PMID 15355167 DOI: 10.1037/0012-1649.40.5.805  0.584
2004 Nash MW, Huezo-Diaz P, Williamson RJ, Sterne A, Purcell S, Hoda F, Cherny SS, Abecasis GR, Prince M, Gray JA, Ball D, Asherson P, Mann A, Goldberg D, McGuffin P, et al. Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships. Human Molecular Genetics. 13: 2173-82. PMID 15351774 DOI: 10.1093/Hmg/Ddh239  0.427
2004 Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/Pnas.0308679101  0.431
2004 Cherny SS, Sham PC, Cardon LR. Introduction to the Special Issue on Variance Components Methods for Mapping Quantitative Trait Loci Behavior Genetics. 34: 125-126. DOI: 10.1023/B:Bege.0000013938.54772.42  0.328
2003 Cader ZM, Noble-Topham S, Dyment DA, Cherny SS, Brown JD, Rice GP, Ebers GC. Significant linkage to migraine with aura on chromosome 11q24. Human Molecular Genetics. 12: 2511-7. PMID 12915447 DOI: 10.1093/Hmg/Ddg252  0.355
2003 Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ, Talcott JB, Stein JF, Monaco AP, Cardon LR. Use of multivariate linkage analysis for dissection of a complex cognitive trait. American Journal of Human Genetics. 72: 561-70. PMID 12587094 DOI: 10.1086/368201  0.43
2003 Purcell S, Cherny SS, Sham PC. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics (Oxford, England). 19: 149-50. PMID 12499305 DOI: 10.1093/Bioinformatics/19.1.149  0.395
2003 Bishop EG, Cherny SS, Corley R, Plomin R, DeFries JC, Hewitt JK. Development genetic analysis of general cognitive ability from 1 to 12 years in a sample of adoptees, biological siblings, and twins Intelligence. 31: 31-49. DOI: 10.1016/S0160-2896(02)00112-5  0.579
2002 Sham PC, Purcell S, Cherny SS, Abecasis GR. Powerful regression-based quantitative-trait linkage analysis of general pedigrees. American Journal of Human Genetics. 71: 238-53. PMID 12111667 DOI: 10.1086/341560  0.372
2002 Jawaid A, Bader JS, Purcell S, Cherny SS, Sham P. Optimal selection strategies for QTL mapping using pooled DNA samples. European Journal of Human Genetics : Ejhg. 10: 125-32. PMID 11938443 DOI: 10.1038/Sj.Ejhg.5200771  0.32
2002 Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nature Genetics. 30: 97-101. PMID 11731797 DOI: 10.1038/Ng786  0.387
2001 Abecasis GR, Cardon LR, Cookson WO, Sham PC, Cherny SS. Association analysis in a variance components framework. Genetic Epidemiology. 21: S341-6. PMID 11793695 DOI: 10.1002/Gepi.2001.21.S1.S341  0.405
2001 Cherny SS, Abecasis GR, Cookson WO, Sham PC, Cardon LR. The effect of genotype and pedigree error on linkage analysis: analysis of three asthma genome scans. Genetic Epidemiology. 21: S117-22. PMID 11793653 DOI: 10.1002/Gepi.2001.21.S1.S117  0.318
2001 Abecasis GR, Cherny SS, Cookson WO, Cardon LR. GRR: graphical representation of relationship errors. Bioinformatics (Oxford, England). 17: 742-3. PMID 11524377 DOI: 10.1093/Bioinformatics/17.8.742  0.332
2001 Purcell S, Cherny SS, Hewitt JK, Sham PC. Optimal sibship selection for genotyping in quantitative trait locus linkage analysis. Human Heredity. 52: 1-13. PMID 11359064 DOI: 10.1159/000053350  0.423
2001 Beekman M, Lakenberg N, Cherny SS, de Knijff P, Kluft CC, van Ommen GJ, Vogler GP, Frants RR, Boomsma DI, Slagboom PE. A powerful and rapid approach to human genome scanning using small quantities of genomic DNA. Genetical Research. 77: 129-34. PMID 11355568 DOI: 10.1017/S001667230100492X  0.355
2001 Abecasis GR, Cherny SS, Cardon LR. The impact of genotyping error on family-based analysis of quantitative traits. European Journal of Human Genetics : Ejhg. 9: 130-4. PMID 11313746 DOI: 10.1038/Sj.Ejhg.5200594  0.349
2001 Lessem JM, Cherny SS, Lessem JL. DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS macro. Bioinformatics (Oxford, England). 17: 371-2. PMID 11301308 DOI: 10.1093/Bioinformatics/17.4.371  0.309
2001 Cherny SS. Advances in Twin and Sib-Pair Analysis. The American Journal of Human Genetics. 69: 668. DOI: 10.1086/322935  0.39
2000 Sham PC, Sterne A, Purcell S, Cherny S, Webster M, Rijsdijk F, Asherson P, Ball D, Craig I, Eley T, Goldberg D, Gray J, Mann A, Owen M, Plomin R. GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Research : the Official Journal of the International Society For Twin Studies. 3: 316-22. PMID 11463153 DOI: 10.1375/136905200320565292  0.392
2000 Saudino KJ, Cherny SS, Plomin R. Parent ratings of temperament in twins: explaining the 'too low' DZ correlations. Twin Research : the Official Journal of the International Society For Twin Studies. 3: 224-33. PMID 11463143 DOI: 10.1375/136905200320565193  0.33
2000 Sham PC, Zhao JH, Cherny SS, Hewitt JK. Variance-Components QTL linkage analysis of selected and non-normal samples: conditioning on trait values. Genetic Epidemiology. 19: S22-8. PMID 11055366 DOI: 10.1002/1098-2272(2000)19:1+<::Aid-Gepi4>3.0.Co;2-S  0.342
2000 Sham PC, Cherny SS, Purcell S, Hewitt JK. Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data. American Journal of Human Genetics. 66: 1616-30. PMID 10762547 DOI: 10.1086/302891  0.375
1999 Talbot CJ, Nicod A, Cherny SS, Fulker DW, Collins AC, Flint J. High-resolution mapping of quantitative trait loci in outbred mice. Nature Genetics. 21: 305-8. PMID 10080185 DOI: 10.1038/6825  0.572
1999 Fulker DW, Cherny SS, Sham PC, Hewitt JK. Combined linkage and association sib-pair analysis for quantitative traits. American Journal of Human Genetics. 64: 259-67. PMID 9915965 DOI: 10.1086/302193  0.605
1999 Gayán J, Smith SD, Cherny SS, Cardon LR, Fulker DW, Brower AM, Olson RK, Pennington BF, DeFries JC. Quantitative-trait locus for specific language and reading deficits on chromosome 6p. American Journal of Human Genetics. 64: 157-64. PMID 9915954 DOI: 10.1086/302191  0.649
1999 Neale MC, Cherny SS, Sham PC, Whitfield JB, Heath AC, Birley AJ, Martin NG. Distinguishing population stratification from genuine allelic effects with Mx: Association of ADH2 with alcohol consumption Behavior Genetics. 29: 233-243. DOI: 10.1023/A:1021638122693  0.341
1998 Schmitz S, Cherny SS, Fulker DW. Increase in power through multivariate analyses. Behavior Genetics. 28: 357-63. PMID 9926617 DOI: 10.1023/A:1021669602220  0.587
1998 Petrill SA, Saudino K, Cherny SS, Emde RN, Fulker DW, Hewitt JK, Plomin R. Exploring the genetic and environmental etiology of high general cognitive ability in fourteen- to thirty-six-month-old twins. Child Development. 69: 68-74. PMID 9499557  0.577
1998 Petrill SA, Saudino K, Cherny SS, Emde RN, Fulker DW, Hewitt JK, Plomin R. Exploring the Genetic and Environmental Etiology of High General Cognitive Ability in Fourteen‐ to Thirty‐Six‐Month‐Old Twins Child Development. 69: 68-74. DOI: 10.1111/J.1467-8624.1998.Tb06133.X  0.616
1997 Petrill SA, Saudino K, Cherny SS, Emde RN, Hewitt JK, Fulker DW, Plomin R. Exploring the genetic etiology of low general cognitive ability from 14 to 36 months. Developmental Psychology. 33: 544-8. PMID 9149933 DOI: 10.1037/0012-1649.33.3.544  0.606
1997 Stallings MC, Cherny SS, Young SE, Miles DR, Hewitt JK, Fulker DW. The familial aggregation of depressive symptoms, antisocial behavior, and alcohol abuse. American Journal of Medical Genetics. 74: 183-91. PMID 9129721 DOI: 10.1002/(Sici)1096-8628(19970418)74:2<183::Aid-Ajmg14>3.0.Co;2-E  0.525
1996 Fulker DW, Cherny SS. An improved multipoint sib-pair analysis of quantitative traits. Behavior Genetics. 26: 527-32. PMID 8917952 DOI: 10.1007/Bf02359758  0.571
1995 Cardon LR, Fulker DW, Cherny SS. Linkage analysis of a common oligogenic disease using selected sib pairs. Genetic Epidemiology. 12: 741-6. PMID 8788002 DOI: 10.1002/Gepi.1370120635  0.588
1995 Fulker DW, Cherny SS, Cardon LR. Multipoint interval mapping of quantitative trait loci, using sib pairs. American Journal of Human Genetics. 56: 1224-33. PMID 7726180  0.506
1995 Hu S, Pattatucci AM, Patterson C, Li L, Fulker DW, Cherny SS, Kruglyak L, Hamer DH. Linkage between sexual orientation and chromosome Xq28 in males but not in females. Nature Genetics. 11: 248-56. PMID 7581447 DOI: 10.1038/Ng1195-248  0.52
1995 Fulker DW, Cherny SS. Genetic and environmental influences on cognition during childhood Population Research and Policy Review. 14: 283-300. DOI: 10.1007/Bf01074393  0.626
1994 Schmitz S, Cherny SS, Fulker DW, Mrazek DA. Genetic and environmental influences on early childhood behavior. Behavior Genetics. 24: 25-34. PMID 8192618 DOI: 10.1007/Bf01067926  0.59
1994 Cherny SS, Fulker DW, Corley RP, Plomin R, DeFries JC. Continuity and change in infant shyness from 14 to 20 months. Behavior Genetics. 24: 365-79. PMID 7993315 DOI: 10.1007/Bf01067538  0.688
1994 Cherny S, Fulker D, Emde R, Robinson J, Corley R, Reznick J, Plomin R, DeFries J. A Developmental-Genetic Analysis of Continuity and Change in the Bayley Mental Development Index from 14 to 24 Months: The MacArthur Longitudinal Twin Study Psychological Science. 5: 354-360. DOI: 10.1111/J.1467-9280.1994.Tb00285.X  0.693
1993 Rodriguez LA, Fulker DW, Cherny SS. A maximum-likelihood model-fitting approach to conducting a Hayman analysis of diallel tables with complete or missing data. Behavior Genetics. 23: 69-76. PMID 8476393 DOI: 10.1007/Bf01067555  0.549
1993 Benson JB, Cherny SS, Haith MM, Fulker DW. Rapid Assessment of Infant Predictors of Adult IQ: Midtwin-Midparent Analyses Developmental Psychology. 29: 434-447. DOI: 10.1037//0012-1649.29.3.434  0.505
1992 Cherny SS, Cardon LR, Fulker DW, DeFries JC. Differential heritability across levels of cognitive ability. Behavior Genetics. 22: 153-62. PMID 1596255 DOI: 10.1007/Bf01066994  0.652
1992 Cherny SS, DeFries JC, Fulker DW. Multiple regression analysis of twin data: a model-fitting approach. Behavior Genetics. 22: 489-97. PMID 1503550 DOI: 10.1007/Bf01066617  0.65
Low-probability matches (unlikely to be authored by this person)
2014 Toulopoulou T, van Haren N, Zhang X, Sham PC, Cherny SS, Campbell DD, Picchioni M, Murray R, Boomsma DI, Pol HH, Brouwer R, Schnack H, Fañanás L, Sauer H, Nenadic I, et al. Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry. PMID 25450228 DOI: 10.1038/Mp.2014.152  0.298
2011 So HC, Kwan JS, Cherny SS, Sham PC. Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening. American Journal of Human Genetics. 88: 548-65. PMID 21529750 DOI: 10.1016/J.Ajhg.2011.04.001  0.298
2018 Wong JKL, Gui H, Kwok M, Ng PW, Lui CHT, Baum L, Sham PC, Kwan P, Cherny SS. Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis. Neurology. Genetics. 4: e245. PMID 29904720 DOI: 10.1212/Nxg.0000000000000245  0.297
2016 Porsch RM, Merello E, De Marco P, Cheng G, Rodriguez L, So M, Sham PC, Tam PK, Capra V, Cherny SS, Garcia-Barcelo MM, Campbell DD. Sacral agenesis: a pilot whole exome sequencing and copy number study. Bmc Medical Genetics. 17: 98. PMID 28007035 DOI: 10.1186/S12881-016-0359-2  0.295
2012 Cheung BM, Ong KL, Tso AW, Leung RY, Xu A, Cherny SS, Sham PC, Lam TH, Lam KS. C-reactive protein as a predictor of hypertension in the Hong Kong Cardiovascular Risk Factor Prevalence Study (CRISPS) cohort. Journal of Human Hypertension. 26: 108-16. PMID 21270838 DOI: 10.1038/Jhh.2010.125  0.294
2010 Cornes BK, Tang CS, Leon TY, Hui KJ, So MT, Miao X, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population. Plos One. 5: e10918. PMID 20532249 DOI: 10.1371/Journal.Pone.0010918  0.29
2014 Gui H, Bao JY, Tang CS, So MT, Ngo DN, Tran AQ, Bui DH, Pham DH, Nguyen TL, Tong A, Lok S, Sham PC, Tam PK, Cherny SS, Garcia-Barcelo MM. Targeted next-generation sequencing on Hirschsprung disease: a pilot study exploits DNA pooling. Annals of Human Genetics. 78: 381-7. PMID 24947032 DOI: 10.1111/Ahg.12076  0.289
2015 Sha'ari HM, Haerian BS, Baum L, Tan HJ, Rafia MH, Kwan P, Cherny SS, Sham PC, Gui H, Raymond AA, Lim KS, Mohamed Z. Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study. Molecular Neurobiology. PMID 25876511 DOI: 10.1007/S12035-015-9150-1  0.288
2015 Toulopoulou T, van Haren N, Zhang X, Sham PC, Cherny SS, Campbell DD, Picchioni M, Murray R, Boomsma DI, Pol HH, Brouwer R, Schnack H, Fañanás L, Sauer H, Nenadic I, et al. Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry. PMID 26283640 DOI: 10.1038/Mp.2015.117  0.287
2011 Cheung BM, Ong KL, Tso AW, Leung RY, Cherny SS, Sham PC, Lam TH, Lam KS. Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene. European Journal of Endocrinology / European Federation of Endocrine Societies. 165: 571-7. PMID 21798961 DOI: 10.1530/Eje-11-0513  0.286
2009 Ong KL, Leung RY, Babinska A, Salifu MO, Ehrlich YH, Kornecki E, Wong LY, Tso AW, Cherny SS, Sham PC, Lam TH, Lam KS, Cheung BM. Elevated plasma level of soluble F11 receptor/junctional adhesion molecule-A (F11R/JAM-A) in hypertension. American Journal of Hypertension. 22: 500-5. PMID 19214165 DOI: 10.1038/Ajh.2009.23  0.285
2015 Haerian BS, Baum L, Kwan P, Cherny SS, Shin JG, Kim SE, Han BG, Tan HJ, Raymond AA, Tan CT, Mohamed Z. Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis. Molecular Neurobiology. PMID 26452361 DOI: 10.1007/S12035-015-9457-Y  0.283
2017 Gui H, Schriemer D, Cheng WW, Chauhan RK, Antiňolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, et al. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Genome Biology. 18: 48. PMID 28274275 DOI: 10.1186/S13059-017-1174-6  0.281
2008 Ong KL, Leung RY, Wong LY, Cherny SS, Sham PC, Lam TH, Lam KS, Cheung BM. Association of F11 receptor gene polymorphisms with central obesity and blood pressure. Journal of Internal Medicine. 263: 322-32. PMID 18067551 DOI: 10.1111/J.1365-2796.2007.01886.X  0.28
2010 Styrkarsdottir U, Halldorsson BV, Gudbjartsson DF, Tang NLS, Koh JM, Xiao SM, Kwok TCY, Kim GS, Chan JCN, Cherny S, Lee SH, Kwok A, Ho S, Gretarsdottir S, Kostic JP, et al. European bone mineral density loci are also associated with BMD in East-Asian populations Plos One. 5. PMID 20949110 DOI: 10.1371/Journal.Pone.0013217  0.278
2012 Tang CS, Cheng G, So M, Yip BH, Miao X, Wong EH, Ngan ES, Lui VC, Song Y, Chan D, Cheung K, Yuan Z, Lei L, Chung PH, Liu X, ... ... Cherny SS, et al. Correction: Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3 Plos Genetics. 8. DOI: 10.1371/Annotation/0Ffda9E0-Ba27-40C1-B766-Df58De9083D5  0.277
2008 Garcia-Barceló MM, Chi-Hang Lui V, Miao X, So MT, Yuk-yu Leon T, Yuan ZW, Li L, Liu L, Wang B, Sun XB, Huang LM, Tou JF, Sau-wai Ngan E, Cherny SS, Chan KW, et al. Mutational analysis of SHH and GLI3 in anorectal malformations. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 644-8. PMID 18655123 DOI: 10.1002/Bdra.20482  0.276
2012 Pang X, Liu C, Shi L, Liu R, Liang D, Li H, Cherny SS, Chen S. Utility of the trnH-psbA intergenic spacer region and its combinations as plant DNA barcodes: a meta-analysis. Plos One. 7: e48833. PMID 23155412 DOI: 10.1371/Journal.Pone.0048833  0.275
2012 Ngo DN, So MT, Gui H, Tran AQ, Bui DH, Cherny S, Tam PK, Nguyen TL, Garcia-Barcelo MM. Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations. Journal of Pediatric Surgery. 47: 1859-64. PMID 23084198 DOI: 10.1016/J.Jpedsurg.2012.05.020  0.273
1992 Becker G, Cherny SS. A FIVE-FACTOR NUCLEAR MODEL OF SOCIALLY DESIRABLE RESPONDING Social Behavior and Personality: An International Journal. 20: 163-191. DOI: 10.2224/Sbp.1992.20.3.163  0.268
2011 Cheung BM, Ong KL, Tso AW, Leung RY, Cherny SS, Sham PC, Thomas GN, Lam TH, Lam KS. Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese. American Journal of Hypertension. 24: 1331-7. PMID 21833041 DOI: 10.1038/Ajh.2011.141  0.268
2009 Ngan ES, Lang BH, Liu T, Shum CK, So MT, Lau DK, Leon TY, Cherny SS, Tsai SY, Lo CY, Khoo US, Tam PK, Garcia-Barceló MM. A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma. Journal of the National Cancer Institute. 101: 162-75. PMID 19176457 DOI: 10.1093/Jnci/Djn471  0.268
2015 Arscott P, Caleshu C, Kotzer K, Kreykes S, Kruisselbrink T, Orland K, Rigelsky C, Smith E, Spoonamore K, Haidle JL, Marvin M, Ackerman MJ, Hadi A, Mani A, Ommen S, ... Cherny S, et al. A Case for Inclusion of Genetic Counselors in Cardiac Care: A Case for Genetic Counselors. Cardiology in Review. PMID 26186385 DOI: 10.1097/CRD.0000000000000081  0.266
2019 Cherny SS, Freidin MB, Williams FMK, Livshits G. The analysis of causal relationships between blood lipid levels and BMD. Plos One. 14: e0212464. PMID 30794634 DOI: 10.1371/Journal.Pone.0212464  0.265
2022 Kasher M, Williams FMK, Freidin MB, Cherny SS, Malkin I, Livshits G. Insights into the pleiotropic relationships between chronic back pain and inflammation-related musculoskeletal conditions: rheumatoid arthritis and osteoporotic abnormalities. Pain. PMID 36017880 DOI: 10.1097/j.pain.0000000000002728  0.256
2011 Cheung BM, Ong KL, Tso AW, Cherny SS, Sham PC, Lam TH, Lam KS. Gamma-glutamyl transferase level predicts the development of hypertension in Hong Kong Chinese. Clinica Chimica Acta; International Journal of Clinical Chemistry. 412: 1326-31. PMID 21466796 DOI: 10.1016/J.Cca.2011.03.030  0.253
2011 Tang CS, Tang WK, So MT, Miao XP, Leung BM, Yip BH, Leon TY, Ngan ES, Lui VC, Chen Y, Chan IH, Chung PH, Liu XL, Wu XZ, Wong KK, ... ... Cherny SS, et al. Fine mapping of the NRG1 Hirschsprung's disease locus. Plos One. 6: e16181. PMID 21283760 DOI: 10.1371/journal.pone.0016181  0.25
2010 Ong KL, Tso AW, Lam KS, Cherny SS, Sham PC, Cheung BM. Using glycosylated hemoglobin to define the metabolic syndrome in United States adults. Diabetes Care. 33: 1856-8. PMID 20504895 DOI: 10.2337/Dc10-0190  0.246
2015 Campbell DD, Porsch RM, Cherny SS, Capra V, Merello E, De Marco P, Sham PC, Garcia-Barceló MM. Cost effective assay choice for rare disease study designs. Orphanet Journal of Rare Diseases. 10: 10. PMID 25648394 DOI: 10.1186/S13023-015-0226-9  0.243
2006 Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vrièze F, Kaleem M, et al. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. American Journal of Human Genetics. 78: 78-88. PMID 16385451 DOI: 10.1086/498851  0.243
2009 Cherny SS. QTL methodology in behavior genetics Handbook of Behavior Genetics. 35-45. DOI: 10.1007/978-0-387-76727-7_3  0.235
2001 Rijsdijk FV, Sham PC, Sterne A, Purcell S, McGuffin P, Farmer A, Goldberg D, Mann A, Cherny SS, Webster M, Ball D, Eley TC, Plomin R. Life events and depression in a community sample of siblings. Psychological Medicine. 31: 401-10. PMID 11305848 DOI: 10.1017/S0033291701003361  0.234
2016 Li Y, Samartzis D, Campbell D, Cherny S, Cheung KM, Luk KD, Karppinen J, Song Y, Cheah K, Chan D, Sham PC. Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study. The Spine Journal : Official Journal of the North American Spine Society. PMID 27157501 DOI: 10.1016/J.Spinee.2016.04.020  0.234
2020 Zhuang X, Ye R, So MT, Lam WY, Karim A, Yu M, Ngo ND, Cherny SS, Tam PK, Garcia-Barcelo MM, Tang CS, Sham PC. A random forest-based framework for genotyping and accuracy assessment of copy number variations. Nar Genomics and Bioinformatics. 2: lqaa071. PMID 33575619 DOI: 10.1093/nargab/lqaa071  0.23
2021 Jiang L, Jiang H, Dai S, Chen Y, Song Y, Tang CS, Pang SY, Ho SL, Wang B, Garcia-Barcelo MM, Tam PK, Cherny SS, Li MJ, Sham PC, Li M. Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases. Nucleic Acids Research. PMID 34931221 DOI: 10.1093/nar/gkab1234  0.222
2011 Sham PC, Cherny SS. Genetic Architecture of Complex Diseases Analysis of Complex Disease Association Studies. 1-13. DOI: 10.1016/B978-0-12-375142-3.10001-X  0.22
2014 Gui H, Tang W, So M, Proitsi P, Sham PC, Tam PK, Ngan ES, Cherny SS, Garcia-Barceló M. Erratum to: RET and NRG1 interplay in Hirschsprung disease Human Genetics. 133: 677-677. DOI: 10.1007/S00439-014-1429-1  0.218
2009 Cheung BM, Ong KL, Cherny SS, Sham PC, Tso AW, Lam KS. Diabetes prevalence and therapeutic target achievement in the United States, 1999 to 2006. The American Journal of Medicine. 122: 443-53. PMID 19375554 DOI: 10.1016/J.Amjmed.2008.09.047  0.217
1994 Becker G, Cherny SS. Gender-controlled measures of socially desirable responding. Journal of Clinical Psychology. 50: 746-52. PMID 7806652 DOI: 10.1002/1097-4679(199409)50:5<746::Aid-Jclp2270500512>3.0.Co;2-V  0.214
2014 Wasson K, Cherny S, Sanders TN, Hogan NS, Helzlsouer KJ. Who are you going to call? Primary care patients' disclosure decisions regarding direct-to-consumer genetic testing. Narrative Inquiry in Bioethics. 4: 53-68. PMID 24748260 DOI: 10.1353/Nib.2014.0026  0.197
2021 Kasher M, Freidin MB, Williams FM, Cherny SS, Malkin I, Livshits G. Shared Genetic Architecture Between Rheumatoid Arthritis and Varying Osteoporotic Phenotypes. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 34910834 DOI: 10.1002/jbmr.4491  0.185
2012 Gagne JR, Saudino KJ, Cherny SS. Genetic Influences on Temperament in Early Adolescence Nature, Nurture, and the Transition to Early Adolescence. DOI: 10.1093/acprof:oso/9780195157475.003.0011  0.183
2012 Guo Y, Tomlinson B, Chu T, Fang YJ, Gui H, Tang CS, Yip BH, Cherny SS, Hur Y, Sham PC, Lam TH, Thomas NG. Correction: A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits Plos One. 7. DOI: 10.1371/annotation/4415f88f-ab10-44dd-8ba9-1a57ade740c1  0.18
2021 Cherny SS, Livshits G, Wells HRR, Freidin MB, Malkin I, Dawson SJ, Williams FMK. Correction: Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank. European Journal of Human Genetics : Ejhg. PMID 33712805 DOI: 10.1038/s41431-021-00842-9  0.18
2016 Chiu YT, Wong JK, Choi SW, Sze KM, Ho DW, Chan LK, Lee JM, Man K, Cherny S, Yang WL, Wong CM, Sham PC, Ng IO. Novel pre-mRNA splicing of intronically integrated HBV generates oncogenic chimera in hepatocellular carcinoma. Journal of Hepatology. PMID 26867494 DOI: 10.1016/J.Jhep.2016.02.005  0.18
2011 Garcia-Barceló MM, Yeung MY, Miao XP, Tang CSM, Cheng G, So MT, Ngan EW, Lui VCH, Chen Y, Liu XL, Hui KJWS, Li L, Guo WH, Sun XB, Tou JF, ... ... Cherny SS, et al. Corrigendum: Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 Human Molecular Genetics. 20: 1048. DOI: 10.1093/hmg/ddq540  0.179
2022 Trpchevska N, Freidin MB, Broer L, Oosterloo BC, Yao S, Zhou Y, Vona B, Bishop C, Bizaki-Vallaskangas A, Canlon B, Castellana F, Chasman DI, Cherny S, Christensen K, Concas MP, et al. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss. American Journal of Human Genetics. PMID 35580588 DOI: 10.1016/j.ajhg.2022.04.010  0.177
2022 Kasher M, Williams FMK, Freidin MB, Malkin I, Cherny SS, Livshits G. Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis, and inflammation: discovering causal pathways. Human Molecular Genetics. PMID 35349660 DOI: 10.1093/hmg/ddac061  0.171
2006 Smemo S, Nowotny P, Hinrichs AL, Kauwe JS, Cherny S, Erickson K, Myers AJ, Kaleem M, Marlowe L, Gibson AM, Hollingworth P, O'Donovan MC, Morris CM, Holmans P, Lovestone S, et al. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology. 59: 21-6. PMID 16278862 DOI: 10.1002/Ana.20673  0.164
2024 Tarabeih N, Kalinkovich A, Ashkenazi S, Cherny SS, Shalata A, Livshits G. Relationships between Circulating Biomarkers and Body Composition Parameters in Patients with Metabolic Syndrome: A Community-Based Study. International Journal of Molecular Sciences. 25. PMID 38255954 DOI: 10.3390/ijms25020881  0.156
2001 Jawaid A, Purcell S, Cherny S, Sham P. A generalised threshold defined case-control selection strategy for QTL association mapping in pooled DNA samples American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 564-565.  0.134
2012 Bishop EG, Cherny SS, Hewitt JK. Developmental Analysis of IQ Nature, Nurture, and the Transition to Early Adolescence. DOI: 10.1093/acprof:oso/9780195157475.003.0002  0.131
2022 Kasher M, Cherny SS, Livshits G. Exploring potential shared genetic influences between rheumatoid arthritis and blood lipid levels. Atherosclerosis. 363: 48-56. PMID 36455308 DOI: 10.1016/j.atherosclerosis.2022.11.006  0.123
2020 Kasher M, Williams FMK, Freidin MB, Cherny S, Livshits G. An in-depth study of the associations between osteoarthritis- and osteoporosis-related phenotypes at different skeletal locations. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. PMID 32556517 DOI: 10.1007/s00198-020-05504-y  0.121
2013 Wasson K, Sanders TN, Hogan NS, Cherny S, Helzlsouer KJ. Primary care patients' views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study. Journal of Community Genetics. 4: 495-505. PMID 23832288 DOI: 10.1007/S12687-013-0156-Y  0.108
2022 Mullan KA, Anderson A, Shi YW, Ding JH, Ng CC, Chen Z, Baum L, Cherny S, Petrovski S, Sham PC, Lim KS, Liao WP, Kwan P. Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Epilepsia. PMID 35170024 DOI: 10.1111/epi.17182  0.099
2015 Baum L, Guo Y, Gui H, Sham PC, Cherny SS, Kwan P. A 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations Biochemistry and Molecular Biology: the Complexity of Human Traits and Diseases. 37-46.  0.078
2013 Samama CM, Lecoules N, Kierzek G, Claessens YE, Riou B, Rosencher N, Mismetti P, Sautet A, Barrellier MT, Apartsin K, Jonas M, Caeiro JR, van der Veen AH, Roy PM, Accetta R, ... ... Cherny S, et al. Comparison of fondaparinux with low molecular weight heparin for venous thromboembolism prevention in patients requiring rigid or semi-rigid immobilization for isolated non-surgical below-knee injury Journal of Thrombosis and Haemostasis. 11: 1833-1843. PMID 23965181 DOI: 10.1111/Jth.12395  0.074
2001 Cherny S, Mraz S, Su L, Harvell J, Kohler S. Heteroduplex analysis of T-cell receptor γ gene rearrangement as an adjuvant diagnostic tool in skin biopsies for erythroderma Journal of Cutaneous Pathology. 28: 351-355. PMID 11437940 DOI: 10.1034/j.1600-0560.2001.280703.x  0.069
2023 Cherny SS, Chowers M, Obolski U. Bayesian network modeling of patterns of antibiotic cross-resistance by bacterial sample source. Communications Medicine. 3: 61. PMID 37130943 DOI: 10.1038/s43856-023-00289-7  0.066
2022 Tarabeih N, Kalinkovich A, Shalata A, Cherny SS, Livshits G. Deciphering the Causal Relationships Between Low Back Pain Complications, Metabolic Factors, and Comorbidities. Journal of Pain Research. 15: 215-227. PMID 35125889 DOI: 10.2147/JPR.S349251  0.065
2011 Blagova OV, Nedostup AV, Dzemeshkevich SL, Sinitsyn VE, Sedov VP, Gagarina NV, Parshin VD, Cherny SS, Noskova MV, Troitskaya MP. Primary lymphoma of the heart: Difficulties in diagnosis and treatment Terapevticheskii Arkhiv. 83: 17-23. PMID 21675267  0.053
2014 Xu L, Jiang CQ, Lam TH, Zhang WS, Cherny SS, Thomas GN, Cheng KK. Sleep duration and memory in the elderly Chinese: longitudinal analysis of the Guangzhou Biobank Cohort Study. Sleep. 37: 1737-44. PMID 25364069 DOI: 10.5665/sleep.4162  0.051
2020 Cherny SS, Nevo D, Baraz A, Baruch S, Lewin-Epstein O, Stein GY, Obolski U. Revealing antibiotic cross-resistance patterns in hospitalized patients through Bayesian network modellingty. The Journal of Antimicrobial Chemotherapy. PMID 33020811 DOI: 10.1093/jac/dkaa408  0.043
2020 Cherny SS, Nevo D, Baraz A, Baruch S, Lewin-Epstein O, Stein GY, Obolski U. Erratum to: Revealing antibiotic cross-resistance patterns in hospitalized patients through Bayesian network modelling. The Journal of Antimicrobial Chemotherapy. PMID 33156899 DOI: 10.1093/jac/dkaa452  0.037
2014 Chirkov D, Panov L, Cherny S, Pylev I. Numerical simulation of full load surge in Francis turbines based on three-dimensional cavitating flow model Iop Conference Series: Earth and Environmental Science. 22. DOI: 10.1088/1755-1315/22/3/032036  0.034
2009 Cherny S, Chirkov D, Lapin V, Muranov A, Bannikov D, Miller M, Willberg D, Medvedev O, Alekseenko O. Two-dimensional modeling of the near-wellbore fracture tortuosity effect International Journal of Rock Mechanics and Mining Sciences. 46: 992-1000. DOI: 10.1016/j.ijrmms.2009.01.001  0.034
2006 Cherny S, Chirkov D, Lapin V, Lobareva I, Sharov S, Skorospelov V. 3D Euler flow simulation in hydro turbines: Unsteady analysis and automatic design Notes On Numerical Fluid Mechanics and Multidisciplinary Design. 93: 33-51. DOI: 10.1007/978-3-540-33844-4_4  0.031
2015 Briner A, Chavez JC, Nadezhdin S, Alekseenko O, Gurmen N, Cherny S, Kuranakov D, Lapin V. Impact of perforation tunnel orientation and length in horizontal wellbores on fracture initiation pressure in maximum tensile stress criterion model for tight gas fields in the Sultanate of Oman Spe Middle East Oil and Gas Show and Conference, Meos, Proceedings. 2015: 1432-1444.  0.028
2015 Shokin Y, Cherny S, Esipov D, Lapin V, Lyutov A, Kuranakov D. Three-dimensional model of fracture propagation from the cavity caused by quasi-static load or viscous fluid pumping Communications in Computer and Information Science. 549: 143-157. DOI: 10.1007/978-3-319-25058-8_15  0.026
2001 Kovenya V, Cherny S, Sharov S, Karamyshev V, Lebedev A. On some approaches to solve CFD problems Computers and Fluids. 30: 903-916. DOI: 10.1016/S0045-7930(01)00034-2  0.023
2012 Chirkov D, Avdyushenko A, Panov L, Bannikov D, Cherny S, Skorospelov V, Pylev I. CFD simulation of pressure and discharge surge in Francis turbine at off-design conditions Iop Conference Series: Earth and Environmental Science. 15. DOI: 10.1088/1755-1315/15/3/032038  0.023
2017 Tan Y, Lo K, Tse W, Chan CW, Lau K, Cherny SS, Lao L, Li L. Three Courses of Tianjiu Therapy in Sanfu Days for Chronic Asthma: A Clinic Efficacy Observation Trail Chinese Medicine. 8: 43-71. DOI: 10.4236/cm.2017.82005  0.015
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