Stacey S. Cherny - Publications

Affiliations: 
The University of Hong Kong, San Francisco, Hong Kong Island, Hong Kong 
Area:
statistical genetics

151 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  1
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  0.36
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.36
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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.  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2009 Cherny SS. QTL methodology in behavior genetics Handbook of Behavior Genetics. 35-45. DOI: 10.1007/978-0-387-76727-7_3  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2008 Cherny SS. Variance components and related methods for mapping quantitative trait loci Sociological Methods and Research. 37: 227-250. DOI: 10.1177/0049124108324524  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2001 Abecasis GR, Cherny SS, Cookson WO, Cardon LR. GRR: graphical representation of relationship errors. Bioinformatics (Oxford, England). 17: 742-3. PMID 11524377  1
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  1
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  1
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  1
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  1
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  1
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.  1
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  1
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  1
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  1
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  1
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  1
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  1
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.  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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