| Year |
Citation |
Score |
| 2020 |
Adhikari AN, Currier RJ, Tang H, Turgeon CT, Nussbaum RL, Srinivasan R, Sunderam U, Kwok PY, Brenner SE, Gavrilov D, Puck JM, Gallagher R. Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing. International Journal of Neonatal Screening. 6. PMID 32802992 DOI: 10.3390/Ijns6020041 |
0.303 |
|
| 2020 |
Nandakumar P, Lee D, Hoffmann TJ, Ehret GB, Arking D, Ranatunga D, Li M, Grove ML, Boerwinkle E, Schaefer C, Kwok PY, Iribarren C, Risch N, Chakravarti A. Analysis of putative cis-regulatory elements regulating blood pressure variation. Human Molecular Genetics. PMID 32436959 DOI: 10.1093/Hmg/Ddaa098 |
0.36 |
|
| 2020 |
Young E, Abid HZ, Kwok PY, Riethman H, Xiao M. Comprehensive Analysis of Human Subtelomeres by Whole Genome Mapping. Plos Genetics. 16: e1008347. PMID 31986135 DOI: 10.1371/Journal.Pgen.1008347 |
0.649 |
|
| 2019 |
Heft IE, Mostovoy Y, Levy-Sakin M, Ma W, Stevens AJ, Pastor S, McCaffrey J, Boffelli D, Martin DI, Xiao M, Kennedy MA, Kwok PY, Sikela JM. The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome. Genetics. PMID 31754017 DOI: 10.1534/Genetics.119.302782 |
0.354 |
|
| 2019 |
Wong KHY, Levy-Sakin M, Ma W, Gonzaludo N, Mak ACY, Vaka D, Poon A, Chu C, Lao R, Balamir M, Grenville Z, Wong N, Kane JP, Kwok PY, Malloy MJ, et al. Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis. Molecular Genetics & Genomic Medicine. e1007. PMID 31617323 DOI: 10.1002/Mgg3.1007 |
0.302 |
|
| 2019 |
Demaerel W, Mostovoy Y, Yilmaz F, Vervoort L, Pastor S, Hestand MS, Swillen A, Vergaelen E, Geiger EA, Coughlin CR, Chow SK, McDonald-McGinn D, Morrow B, Kwok PY, Xiao M, et al. The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401. PMID 31481461 DOI: 10.1101/Gr.248682.119 |
0.323 |
|
| 2019 |
Leung AK, Liu MC, Li L, Lai YY, Chu C, Kwok PY, Ho PL, Yip KY, Chan TF. OMMA enables population-scale analysis of complex genomic features and phylogenomic relationships from nanochannel-based optical maps. Gigascience. 8. PMID 31289833 DOI: 10.1093/Gigascience/Giz079 |
0.539 |
|
| 2019 |
Chaisson MJP, Sanders AD, Zhao X, Malhotra A, Porubsky D, Rausch T, Gardner EJ, Rodriguez OL, Guo L, Collins RL, Fan X, Wen J, Handsaker RE, Fairley S, Kronenberg ZN, ... ... Kwok PY, et al. Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature Communications. 10: 1784. PMID 30992455 DOI: 10.1038/S41467-018-08148-Z |
0.618 |
|
| 2019 |
Levy-Sakin M, Pastor S, Mostovoy Y, Li L, Leung AKY, McCaffrey J, Young E, Lam ET, Hastie AR, Wong KHY, Chung CYL, Ma W, Sibert J, Rajagopalan R, Jin N, ... ... Kwok PY, et al. Genome maps across 26 human populations reveal population-specific patterns of structural variation. Nature Communications. 10: 1025. PMID 30833565 DOI: 10.1038/S41467-019-08992-7 |
0.691 |
|
| 2018 |
Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, ... ... Kwok PY, et al. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. American Journal of Human Genetics. 103: 319-327. PMID 30193136 DOI: 10.1016/J.Ajhg.2018.08.007 |
0.305 |
|
| 2018 |
Wong KHY, Levy-Sakin M, Kwok PY. De novo human genome assemblies reveal spectrum of alternative haplotypes in diverse populations. Nature Communications. 9: 3040. PMID 30072691 DOI: 10.1038/S41467-018-05513-W |
0.343 |
|
| 2018 |
Hoffmann TJ, Theusch E, Haldar T, Ranatunga DK, Jorgenson E, Medina MW, Kvale MN, Kwok PY, Schaefer C, Krauss RM, Iribarren C, Risch N. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics. PMID 29507422 DOI: 10.1038/S41588-018-0064-5 |
0.358 |
|
| 2017 |
Li L, Leung AK, Kwok TP, Lai YYY, Pang IK, Chung GT, Mak ACY, Poon A, Chu C, Li M, Wu JJK, Lam ET, Cao H, Lin C, Sibert J, ... ... Kwok PY, et al. OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps. Genome Biology. 18: 230. PMID 29195502 DOI: 10.1186/S13059-017-1356-2 |
0.673 |
|
| 2017 |
Wang J, Gao S, Mostovoy Y, Kang Y, Zagoskin M, Sun Y, Zhang B, White LK, Easton A, Nutman TB, Kwok PY, Hu S, Nielsen MK, Davis RE. Comparative genome analysis of programmed DNA elimination in nematodes. Genome Research. PMID 29118011 DOI: 10.1101/Gr.225730.117 |
0.316 |
|
| 2017 |
Bassaganyas L, Freedman G, Vaka D, Wan E, Lao R, Chen F, Kvale M, Currier RJ, Puck JM, Kwok PY. Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification. Human Mutation. PMID 29067733 DOI: 10.1002/Humu.23356 |
0.314 |
|
| 2017 |
Young E, Pastor S, Rajagopalan R, McCaffrey J, Sibert J, Mak AC, Kwok PY, Riethman H, Xiao M. High-throughput single-molecule mapping links subtelomeric variants and long-range haplotypes with specific telomeres. Nucleic Acids Research. PMID 28180280 DOI: 10.1093/Nar/Gkx017 |
0.656 |
|
| 2017 |
Leung AK, Kwok TP, Wan R, Xiao M, Kwok PY, Yip KY, Chan TF. OMBlast: alignment tool for optical mapping using a seed-and-extend approach. Bioinformatics (Oxford, England). 33: 311-319. PMID 28172448 DOI: 10.1093/Bioinformatics/Btw620 |
0.52 |
|
| 2016 |
Ge X, Gong H, Dumas K, Litwin J, Phillips JJ, Waisfisz Q, Weiss MM, Hendriks Y, Stuurman KE, Nelson SF, Grody WW, Lee H, Kwok PY, Shieh JT. Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation. Npj Genomic Medicine. 1. PMID 28868155 DOI: 10.1038/Npjgenmed.2016.36 |
0.396 |
|
| 2016 |
Hoffmann TJ, Ehret GB, Nandakumar P, Ranatunga D, Schaefer C, Kwok PY, Iribarren C, Chakravarti A, Risch N. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Nature Genetics. PMID 27841878 DOI: 10.1038/Ng.3715 |
0.321 |
|
| 2016 |
Roberts JD, Yang J, Gladstone RA, Longoria J, Whitman IR, Dewland TA, Miller C, Robles A, Poon A, Seiler B, Laframboise WA, Olgin JE, Kwok PY, Marcus GM. Atrial Fibrillation Associated Genetic Variants and Left Atrial Histology: Evaluation for Molecular Sub-Phenotypes. Journal of Cardiovascular Electrophysiology. PMID 27574037 DOI: 10.1111/Jce.13083 |
0.361 |
|
| 2016 |
Lemaitre RN, Bartz TM, King IB, Brody JA, McKnight B, Sotoodehnia N, Rea TD, Johnson CO, Mozaffarian D, Hesselson S, Kwok PY, Siscovick DS. Circulating n-3 fatty acids and trans-fatty acids, PLA2G2A gene variation and sudden cardiac arrest. Journal of Nutritional Science. 5: e12. PMID 27313848 DOI: 10.1017/Jns.2016.2 |
0.726 |
|
| 2016 |
Mostovoy Y, Levy-Sakin M, Lam J, Lam ET, Hastie AR, Marks P, Lee J, Chu C, Lin C, Džakula Ž, Cao H, Schlebusch SA, Giorda K, Schnall-Levin M, Wall JD, ... Kwok PY, et al. A hybrid approach for de novo human genome sequence assembly and phasing. Nature Methods. PMID 27159086 DOI: 10.1038/Nmeth.3865 |
0.575 |
|
| 2016 |
Mak AC, Tang PL, Cleveland C, Smith MH, Connolly MK, Katsumoto TR, Wolters PJ, Kwok PY, Criswell LA. Whole Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 27111861 DOI: 10.1002/Art.39721 |
0.373 |
|
| 2015 |
Mak AC, Lai YY, Lam ET, Kwok TP, Leung AK, Poon A, Mostovoy Y, Hastie AR, Stedman W, Anantharaman T, Andrews W, Zhou X, Pang AW, Dai H, Chu C, ... ... Kwok PY, et al. Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays. Genetics. PMID 26510793 DOI: 10.1534/Genetics.115.183483 |
0.694 |
|
| 2015 |
Tranah GJ, Yaffe K, Katzman SM, Lam ET, Pawlikowska L, Kwok PY, Schork NJ, Manini TM, Kritchevsky S, Thomas F, Newman AB, Harris TB, Coleman AL, Gorin MB, Helzner EP, et al. Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 26328603 DOI: 10.1093/Gerona/Glv097 |
0.691 |
|
| 2015 |
Pendleton M, Sebra R, Pang AW, Ummat A, Franzen O, Rausch T, Stütz AM, Stedman W, Anantharaman T, Hastie A, Dai H, Fritz MH, Cao H, Cohain A, Deikus G, ... ... Kwok PY, et al. Assembly and diploid architecture of an individual human genome via single-molecule technologies. Nature Methods. PMID 26121404 DOI: 10.1038/Nmeth.3454 |
0.333 |
|
| 2015 |
Kvale MN, Hesselson S, Hoffmann TJ, Cao Y, Chan D, Connell S, Croen LA, Dispensa BP, Eshragh J, Finn A, Gollub J, Iribarren C, Jorgenson E, Kushi LH, Lao R, ... ... Kwok PY, et al. Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. PMID 26092718 DOI: 10.1534/Genetics.115.178905 |
0.741 |
|
| 2015 |
Lapham K, Kvale MN, Lin J, Connell S, Croen LA, Dispensa BP, Fang L, Hesselson S, Hoffmann TJ, Iribarren C, Jorgenson E, Kushi LH, Ludwig D, Matsuguchi T, McGuire WB, ... ... Kwok PY, et al. Automated Assay of Telomere Length Measurement and Informatics for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. 200: 1061-72. PMID 26092717 DOI: 10.1534/Genetics.115.178624 |
0.698 |
|
| 2015 |
Banda Y, Kvale MN, Hoffmann TJ, Hesselson SE, Ranatunga D, Tang H, Sabatti C, Croen LA, Dispensa BP, Henderson M, Iribarren C, Jorgenson E, Kushi LH, Ludwig D, Olberg D, ... ... Kwok PY, et al. Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. PMID 26092716 DOI: 10.1534/Genetics.115.178616 |
0.712 |
|
| 2015 |
Wu D, Mandal S, Choi A, Anderson A, Prochazkova M, Perry H, Gil-Da-Silva-Lopes VL, Lao R, Wan E, Tang PL, Kwok PY, Klein O, Zhuan B, Slavotinek AM. DLX4 is associated with orofacial clefting and abnormal jaw development. Human Molecular Genetics. 24: 4340-52. PMID 25954033 DOI: 10.1093/Hmg/Ddv167 |
0.331 |
|
| 2015 |
Chen J, Hackett CS, Zhang S, Song YK, Bell RJ, Molinaro AM, Quigley DA, Balmain A, Song JS, Costello JF, Gustafson WC, Van Dyke T, Kwok PY, Khan J, Weiss WA. The genetics of splicing in neuroblastoma. Cancer Discovery. 5: 380-95. PMID 25637275 DOI: 10.1158/2159-8290.Cd-14-0892 |
0.61 |
|
| 2015 |
Roberts JD, Longoria J, Poon A, Gollob MH, Dewland TA, Kwok PY, Olgin JE, Deo RC, Marcus GM. Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation. Circulation. Cardiovascular Genetics. 8: 50-7. PMID 25406240 DOI: 10.1161/Circgenetics.114.000650 |
0.325 |
|
| 2015 |
Ge X, Kwok PY, Shieh JT. Prioritizing genes for X-linked diseases using population exome data. Human Molecular Genetics. 24: 599-608. PMID 25217573 DOI: 10.1093/Hmg/Ddu473 |
0.343 |
|
| 2015 |
Cao H, Hastie A, Pang A, Andrews W, Anantharaman T, Chan T, Saghbini M, Sadoski H, Austin M, Dzakula Z, Dickinson T, Holmlin E, Xun X, Kwok P, Rossi M. Abstract 4746: Mapping the “dark matter” of cancer genome - Long repeats, complex structural variations with nanochannel technology Cancer Research. 75: 4746-4746. DOI: 10.1158/1538-7445.Am2015-4746 |
0.337 |
|
| 2014 |
Deo RC, Musso G, Tasan M, Tang P, Poon A, Yuan C, Felix JF, Vasan RS, Beroukhim R, De Marco T, Kwok PY, MacRae CA, Roth FP. Prioritizing causal disease genes using unbiased genomic features. Genome Biology. 15: 534. PMID 25633252 DOI: 10.1186/S13059-014-0534-8 |
0.38 |
|
| 2014 |
Hackett CS, Quigley DA, Wong RA, Chen J, Cheng C, Song YK, Wei JS, Pawlikowska L, Bao Y, Goldenberg DD, Nguyen K, Gustafson WC, Rallapalli SK, Cho YJ, Cook JM, ... ... Kwok PY, et al. Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma. Cell Reports. 9: 1034-46. PMID 25437558 DOI: 10.1016/J.Celrep.2014.09.046 |
0.706 |
|
| 2014 |
Wall JD, Tang LF, Zerbe B, Kvale MN, Kwok PY, Schaefer C, Risch N. Estimating genotype error rates from high-coverage next-generation sequence data. Genome Research. 24: 1734-9. PMID 25304867 DOI: 10.1101/Gr.168393.113 |
0.316 |
|
| 2014 |
Hariani GD, Lam ET, Lam EJ, Havener T, Kwok PY, McLeod HL, Wagner MJ, Motsinger-Reif AA. Application of next generation sequencing to CEPH cell lines to discover variants associated with FDA approved chemotherapeutics. Bmc Research Notes. 7: 360. PMID 24924344 DOI: 10.1186/1756-0500-7-360 |
0.592 |
|
| 2014 |
O'Bleness M, Searles VB, Dickens CM, Astling D, Albracht D, Mak AC, Lai YY, Lin C, Chu C, Graves T, Kwok PY, Wilson RK, Sikela JM. Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome. Bmc Genomics. 15: 387. PMID 24885025 DOI: 10.1186/1471-2164-15-387 |
0.327 |
|
| 2014 |
Evans DS, Calton MA, Kim MJ, Kwok PY, Miljkovic I, Harris T, Koster A, Liu Y, Tranah GJ, Ahituv N, Hsueh WC, Vaisse C. Genetic association study of adiposity and melanocortin-4 receptor (MC4R) common variants: replication and functional characterization of non-coding regions. Plos One. 9: e96805. PMID 24820477 DOI: 10.1371/Journal.Pone.0096805 |
0.431 |
|
| 2014 |
Wander PL, Hochner H, Sitlani CM, Enquobahrie DA, Lumley T, Lawrence GM, Burger A, Savitsky B, Manor O, Meiner V, Hesselson S, Kwok PY, Siscovick DS, Friedlander Y. Maternal genetic variation accounts in part for the associations of maternal size during pregnancy with offspring cardiometabolic risk in adulthood. Plos One. 9: e91835. PMID 24670385 DOI: 10.1371/Journal.Pone.0091835 |
0.679 |
|
| 2014 |
Lemaitre RN, Johnson CO, Hesselson S, Sotoodehnia N, Sotoodhenia N, McKnight B, Sitlani CM, Rea TD, King IB, Kwok PY, Mak A, Li G, Brody J, Larson E, Mozaffarian D, et al. Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 471-7. PMID 24418166 DOI: 10.1016/J.Hrthm.2014.01.008 |
0.693 |
|
| 2014 |
Lawrence GM, Shulman S, Friedlander Y, Sitlani CM, Burger A, Savitsky B, Granot-Hershkovitz E, Lumley T, Kwok PY, Hesselson S, Enquobahrie D, Wander PL, Manor O, Siscovick DS, Hochner H. Associations of maternal pre-pregnancy and gestational body size with offspring longitudinal change in BMI. Obesity (Silver Spring, Md.). 22: 1165-71. PMID 24124160 DOI: 10.1002/Oby.20643 |
0.693 |
|
| 2014 |
Hariani GD, Lam ET, Havener T, Kwok PY, McLeod HL, Wagner MJ, Motsinger-Reif AA. Correction: Application of next generation sequencing to CEPH cell lines to discover variants associated with FDA approved chemotherapeutics Bmc Research Notes. 7. DOI: 10.1186/1756-0500-7-652 |
0.534 |
|
| 2014 |
Chen J, Hackett CS, Zhang S, Song YK, Molinaro A, Quigley DA, Balmain A, Gustafson WC, Dyke TAV, Kwok P, Khan J, Weiss WA. Abstract 3413: A genetic analysis of splicing in neuroblastoma identifies opposing functions for FUBP1 splice variants in MYC regulation Cancer Research. 74: 3413-3413. DOI: 10.1158/1538-7445.Am2014-3413 |
0.646 |
|
| 2013 |
Bendjilali N, Kim H, Weinsheimer S, Guo DE, Kwok PY, Zaroff JG, Sidney S, Lawton MT, McCulloch CE, Koeleman BP, Klijn CJ, Young WL, Pawlikowska L. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. Plos One. 8: e71434. PMID 24098321 DOI: 10.1371/Journal.Pone.0071434 |
0.607 |
|
| 2013 |
Martin PM, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok PY, Moon RT, Cheyette BN. A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational Psychiatry. 3: e301. PMID 24002087 DOI: 10.1038/Tp.2013.75 |
0.547 |
|
| 2013 |
Tamraz B, Fukushima H, Wolfe AR, Kaspera R, Totah RA, Floyd JS, Ma B, Chu C, Marciante KD, Heckbert SR, Psaty BM, Kroetz DL, Kwok PY. OATP1B1-related drug-drug and drug-gene interactions as potential risk factors for cerivastatin-induced rhabdomyolysis. Pharmacogenetics and Genomics. 23: 355-64. PMID 23652407 DOI: 10.1097/Fpc.0B013E3283620C3B |
0.729 |
|
| 2013 |
Hastie AR, Dong L, Smith A, Finklestein J, Lam ET, Huo N, Cao H, Kwok PY, Deal KR, Dvorak J, Luo MC, Gu Y, Xiao M. Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome. Plos One. 8: e55864. PMID 23405223 DOI: 10.1371/Journal.Pone.0055864 |
0.58 |
|
| 2013 |
Bergen AW, Javitz HS, Krasnow R, Nishita D, Michel M, Conti DV, Liu J, Lee W, Edlund CK, Hall S, Kwok PY, Benowitz NL, Baker TB, Tyndale RF, Lerman C, et al. Nicotinic acetylcholine receptor variation and response to smoking cessation therapies. Pharmacogenetics and Genomics. 23: 94-103. PMID 23249876 DOI: 10.1097/Fpc.0B013E32835Cdabd |
0.315 |
|
| 2013 |
Levin AM, Mathias RA, Huang L, Roth LA, Daley D, Myers RA, Himes BE, Romieu I, Yang M, Eng C, Park JE, Zoratti K, Gignoux CR, Torgerson DG, Galanter JM, ... ... Kwok PY, et al. A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations. The Journal of Allergy and Clinical Immunology. 131: 1176-84. PMID 23146381 DOI: 10.1016/J.Jaci.2012.10.002 |
0.391 |
|
| 2013 |
Shen L, Hoffmann T, Kvale M, Sakoda L, Banda Y, Kwok P, Risch N, Jorgenson E, Schaefer C. PS3-15: Genome-Wide Association Study of Anxiety Disorders: Early Results from Kaiser Permanente's Research Program on Genes, Environment, and Health (RPGEH) Clinical Medicine & Research. 11: 149-149. DOI: 10.3121/Cmr.2013.1176.Ps3-15 |
0.308 |
|
| 2013 |
Jorgenson E, Sciortino S, Shen L, Ranatunga D, Hoffmann T, Kvale M, Banda Y, Kwok P, Walter L, Risch N, Schaefer C. B4-4: Genome-Wide Association Study of Macular Degeneration: Early Results from the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) Clinical Medicine & Research. 11: 146-147. DOI: 10.3121/Cmr.2013.1176.B4-4 |
0.36 |
|
| 2013 |
Hastie AR, Dong L, Smith A, Finklestein J, Lam ET, Huo N, Cao H, Kwok PY, Deal KR, Dvorak J, Luo MC, Gu Y, Xiao M. Correction: Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome (PLoS ONE) Plos One. 8. DOI: 10.1371/annotation/8629ed33-c566-4543-b657-eea1792f384c |
0.527 |
|
| 2012 |
Khush KK, Pawlikowska L, Menza RL, Goldstein BA, Hayden V, Nguyen J, Kim H, Poon A, Sapru A, Matthay MA, Kwok PY, Young WL, Baxter-Lowe LA, Zaroff JG. Beta-adrenergic receptor polymorphisms and cardiac graft function in potential organ donors. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 12: 3377-86. PMID 22994654 DOI: 10.1111/J.1600-6143.2012.04266.X |
0.605 |
|
| 2012 |
Lam ET, Hastie A, Lin C, Ehrlich D, Das SK, Austin MD, Deshpande P, Cao H, Nagarajan N, Xiao M, Kwok PY. Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly. Nature Biotechnology. 30: 771-6. PMID 22797562 DOI: 10.1038/Nbt.2303 |
0.586 |
|
| 2012 |
Johnson CO, Lemaitre RN, Fahrenbruch CE, Hesselson S, Sotoodehnia N, McKnight B, Rice KM, Kwok PY, Siscovick DS, Rea TD. Common variation in fatty acid genes and resuscitation from sudden cardiac arrest Circulation: Cardiovascular Genetics. 5: 422-429. PMID 22661490 DOI: 10.1161/Circgenetics.111.961912 |
0.68 |
|
| 2012 |
Tranah GJ, Lam ET, Katzman SM, Nalls MA, Zhao Y, Evans DS, Yokoyama JS, Pawlikowska L, Kwok PY, Mooney S, Kritchevsky S, Goodpaster BH, Newman AB, Harris TB, Manini TM, et al. Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly. Biochimica Et Biophysica Acta. 1817: 1691-700. PMID 22659402 DOI: 10.1016/J.Bbabio.2012.05.012 |
0.71 |
|
| 2012 |
Floyd JS, Kaspera R, Marciante KD, Weiss NS, Heckbert SR, Lumley T, Wiggins KL, Tamraz B, Kwok PY, Totah RA, Psaty BM. A screening study of drug-drug interactions in cerivastatin users: An adverse effect of clopidogrel Clinical Pharmacology and Therapeutics. 91: 896-904. PMID 22419147 DOI: 10.1038/Clpt.2011.295 |
0.698 |
|
| 2012 |
Lam ET, Bracci PM, Holly EA, Chu C, Poon A, Wan E, White K, Kwok PY, Pawlikowska L, Tranah GJ. Mitochondrial DNA sequence variation and risk of pancreatic cancer. Cancer Research. 72: 686-95. PMID 22174369 DOI: 10.1158/0008-5472.Can-11-1682 |
0.721 |
|
| 2011 |
Birnbaum RY, Hayashi G, Cohen I, Poon A, Chen H, Lam ET, Kwok PY, Birk OS, Liao W. Association analysis identifies ZNF750 regulatory variants in psoriasis. Bmc Medical Genetics. 12: 167. PMID 22185198 DOI: 10.1186/1471-2350-12-167 |
0.625 |
|
| 2011 |
Durinck S, Ho C, Wang NJ, Liao W, Jakkula LR, Collisson EA, Pons J, Chan SW, Lam ET, Chu C, Park K, Hong SW, Hur JS, Huh N, Neuhaus IM, ... ... Kwok PY, et al. Temporal dissection of tumorigenesis in primary cancers. Cancer Discovery. 1: 137-43. PMID 21984974 DOI: 10.1158/2159-8290.Cd-11-0028 |
0.515 |
|
| 2011 |
Hoffmann TJ, Zhan Y, Kvale MN, Hesselson SE, Gollub J, Iribarren C, Lu Y, Mei G, Purdy MM, Quesenberry C, Rowell S, Shapero MH, Smethurst D, Somkin CP, Van den Eeden SK, ... ... Kwok PY, et al. Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. Genomics. 98: 422-30. PMID 21903159 DOI: 10.1016/J.Ygeno.2011.08.007 |
0.731 |
|
| 2011 |
Aouizerat BE, Vittinghoff E, Musone SL, Pawlikowska L, Kwok PY, Olgin JE, Tseng ZH. GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. Bmc Cardiovascular Disorders. 11: 29. PMID 21658281 DOI: 10.1186/1471-2261-11-29 |
0.783 |
|
| 2011 |
Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, Cao Y, Cawley S, Chung E, Connell S, Eshragh J, Ewing M, Gollub J, Henderson M, Hubbell E, Iribarren C, ... ... Kwok PY, et al. Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics. 98: 79-89. PMID 21565264 DOI: 10.1016/J.Ygeno.2011.04.005 |
0.745 |
|
| 2011 |
Chen H, Poon A, Yeung C, Helms C, Pons J, Bowcock AM, Kwok PY, Liao W. A genetic risk score combining ten psoriasis risk loci improves disease prediction. Plos One. 6: e19454. PMID 21559375 DOI: 10.1371/Journal.Pone.0019454 |
0.352 |
|
| 2011 |
Swarbrick MM, Evans DS, Valle MI, Favre H, Wu SH, Njajou OT, Li R, Zmuda JM, Miljkovic I, Harris TB, Kwok PY, Vaisse C, Hsueh WC. Replication and extension of association between common genetic variants in SIM1 and human adiposity. Obesity (Silver Spring, Md.). 19: 2394-403. PMID 21512513 DOI: 10.1038/Oby.2011.79 |
0.385 |
|
| 2011 |
Marciante KD, Durda JP, Heckbert SR, Lumley T, Rice K, McKnight B, Totah RA, Tamraz B, Kroetz DL, Fukushima H, Kaspera R, Bis JC, Glazer NL, Li G, Austin TR, ... ... Kwok PY, et al. Cerivastatin, genetic variants, and the risk of rhabdomyolysis. Pharmacogenetics and Genomics. 21: 280-8. PMID 21386754 DOI: 10.1097/Fpc.0B013E328343Dd7D |
0.714 |
|
| 2011 |
Musone SL, Taylor KE, Nititham J, Chu C, Poon A, Liao W, Lam ET, Ma A, Kwok PY, Criswell LA. Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases. Genes and Immunity. 12: 176-82. PMID 21326317 DOI: 10.1038/Gene.2010.64 |
0.801 |
|
| 2011 |
Mikhak B, Weinsheimer S, Pawlikowska L, Poon A, Kwok PY, Lawton MT, Chen Y, Zaroff JG, Sidney S, McCulloch CE, Young WL, Kim H. Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations. Cerebrovascular Diseases (Basel, Switzerland). 31: 338-45. PMID 21212665 DOI: 10.1159/000322601 |
0.631 |
|
| 2011 |
Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Kwok PY, et al. Common variants in P2RY11 are associated with narcolepsy. Nature Genetics. 43: 66-71. PMID 21170044 DOI: 10.1038/Ng.734 |
0.738 |
|
| 2011 |
Durinck S, Ho C, Wang NJ, Liao W, Jakkula LR, Collisson EA, Pons J, Chan S, Lam ET, Chu C, Park K, Hong S, Hur JS, Huh N, Neuhaus IM, ... ... Kwok P, et al. Timing chromosomal abnormalities using mutation data Genome Biology. 12: P39. DOI: 10.1186/Gb-2011-12-S1-P39 |
0.525 |
|
| 2010 |
Njajou OT, Blackburn EH, Pawlikowska L, Mangino M, Damcott CM, Kwok PY, Spector TD, Newman AB, Harris TB, Cummings SR, Cawthon RM, Shuldiner AR, Valdes AM, Hsueh WC. A common variant in the telomerase RNA component is associated with short telomere length. Plos One. 5: e13048. PMID 20885959 DOI: 10.1371/Journal.Pone.0013048 |
0.566 |
|
| 2010 |
Kaspera R, Naraharisetti SB, Tamraz B, Sahele T, Cheesman MJ, Kwok PY, Marciante K, Heckbert SR, Psaty BM, Totah RA. Cerivastatin in vitro metabolism by CYP2C8 variants found in patients experiencing rhabdomyolysis. Pharmacogenetics and Genomics. 20: 619-29. PMID 20739906 DOI: 10.1097/Fpc.0B013E32833Ecace |
0.726 |
|
| 2010 |
Li Y, Liao W, Cargill M, Chang M, Matsunami N, Feng BJ, Poon A, Callis-Duffin KP, Catanese JJ, Bowcock AM, Leppert MF, Kwok PY, Krueger GG, Begovich AB. Carriers of rare missense variants in IFIH1 are protected from psoriasis. The Journal of Investigative Dermatology. 130: 2768-72. PMID 20668468 DOI: 10.1038/Jid.2010.214 |
0.309 |
|
| 2010 |
Reekie K, Metspalu A, Chanock SJ, Liu ET, Mardis ER, Scherer SW, Kwok PY, Brookes AJ. HGV2009 meeting: bigger and better studies provide more answers and more questions. Human Mutation. 31: 886-8. PMID 20506253 DOI: 10.1002/Humu.21270 |
0.327 |
|
| 2010 |
Otte C, Wüst S, Zhao S, Pawlikowska L, Kwok PY, Whooley MA. Glucocorticoid receptor gene, low-grade inflammation, and heart failure: the Heart and Soul study. The Journal of Clinical Endocrinology and Metabolism. 95: 2885-91. PMID 20371666 DOI: 10.1210/Jc.2009-2251 |
0.62 |
|
| 2010 |
Su H, Kim H, Pawlikowska L, Kitamura H, Shen F, Cambier S, Markovics J, Lawton MT, Sidney S, Bollen AW, Kwok PY, Reichardt L, Young WL, Yang GY, Nishimura SL. Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis. The American Journal of Pathology. 176: 1018-27. PMID 20019187 DOI: 10.2353/Ajpath.2010.090453 |
0.597 |
|
| 2010 |
Wan E, Akana M, Pons J, Chen J, Musone S, Kwok PY, Liao W. Green technologies for room temperature nucleic acid storage Current Issues in Molecular Biology. 12: 135-142. PMID 19801719 |
0.756 |
|
| 2010 |
Scherer ML, Nalls MA, Pawlikowska L, Ziv E, Mitchell G, Huntsman S, Hu D, Sutton-Tyrrell K, Lakatta EG, Hsueh WC, Newman AB, Tandon A, Kim L, Kwok PY, Sung A, et al. Admixture mapping of ankle-arm index: identification of a candidate locus associated with peripheral arterial disease. Journal of Medical Genetics. 47: 1-7. PMID 19586928 DOI: 10.1136/Jmg.2008.064808 |
0.603 |
|
| 2009 |
Weinsheimer S, Kim H, Pawlikowska L, Chen Y, Lawton MT, Sidney S, Kwok PY, McCulloch CE, Young WL. EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Circulation. Cardiovascular Genetics. 2: 476-82. PMID 20031623 DOI: 10.1161/Circgenetics.109.883595 |
0.636 |
|
| 2009 |
Tseng ZH, Vittinghoff E, Musone SL, Lin F, Whiteman D, Pawlikowska L, Kwok PY, Olgin JE, Aouizerat BE. Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 6: 1745-50. PMID 19959123 DOI: 10.1016/J.Hrthm.2009.08.031 |
0.783 |
|
| 2009 |
Otte C, Wüst S, Zhao S, Pawlikowska L, Kwok PY, Whooley MA. Glucocorticoid receptor gene and depression in patients with coronary heart disease: the Heart and Soul Study-2009 Curt Richter Award Winner. Psychoneuroendocrinology. 34: 1574-81. PMID 19783104 DOI: 10.1016/J.Psyneuen.2009.08.016 |
0.631 |
|
| 2009 |
Trivedi NN, Tamraz B, Chu C, Kwok PY, Caughey GH. Human subjects are protected from mast cell tryptase deficiency despite frequent inheritance of loss-of-function mutations. The Journal of Allergy and Clinical Immunology. 124: 1099-105.e1-4. PMID 19748655 DOI: 10.1016/J.Jaci.2009.07.026 |
0.751 |
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| 2009 |
Ha Choi J, Wah Yee S, Kim MJ, Nguyen L, Ho Lee J, Kang JO, Hesselson S, Castro RA, Stryke D, Johns SJ, Kwok PY, Ferrin TE, Goo Lee M, Black BL, Ahituv N, et al. Identification and characterization of novel polymorphisms in the basal promoter of the human transporter, MATE1 Pharmacogenetics and Genomics. 19: 770-780. PMID 19745787 DOI: 10.1097/Fpc.0B013E328330Eeca |
0.71 |
|
| 2009 |
Hesselson SE, Matsson P, Shima JE, Fukushima H, Yee SW, Kobayashi Y, Gow JM, Ha C, Ma B, Poon A, Johns SJ, Stryke D, Castro RA, Tahara H, Choi JH, ... ... Kwok PY, et al. Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. Plos One. 4: e6942. PMID 19742321 DOI: 10.1371/Journal.Pone.0006942 |
0.716 |
|
| 2009 |
Panici JA, Wang F, Bonkowski MS, Spong A, Bartke A, Pawlikowska L, Kwok PY, Masternak MM. Is altered expression of hepatic insulin-related genes in growth hormone receptor knockout mice due to GH resistance or a difference in biological life spans? The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 64: 1126-33. PMID 19706698 DOI: 10.1093/Gerona/Glp111 |
0.58 |
|
| 2009 |
Pawlikowska L, Hu D, Huntsman S, Sung A, Chu C, Chen J, Joyner AH, Schork NJ, Hsueh WC, Reiner AP, Psaty BM, Atzmon G, Barzilai N, Cummings SR, Browner WS, ... Kwok PY, et al. Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. Aging Cell. 8: 460-72. PMID 19489743 DOI: 10.1111/J.1474-9726.2009.00493.X |
0.739 |
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| 2009 |
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Hong SS, Honda Y, Honda M, Högl B, ... ... Kwok PY, et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nature Genetics. 41: 708-11. PMID 19412176 DOI: 10.1038/Ng.372 |
0.783 |
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| 2009 |
Brookes AJ, Chanock SJ, Hudson TJ, Peltonen L, Abecasis G, Kwok PY, Scherer SW. Genomic variation in a global village: Report of the 10th Annual Human Genome Variation Meeting 2008 Human Mutation. 30: 1134-1138. PMID 19384970 DOI: 10.1002/Humu.21008 |
0.345 |
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| 2009 |
Walston JD, Matteini AM, Nievergelt C, Lange LA, Fallin DM, Barzilai N, Ziv E, Pawlikowska L, Kwok P, Cummings SR, Kooperberg C, LaCroix A, Tracy RP, Atzmon G, Lange EM, et al. Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults. Experimental Gerontology. 44: 350-5. PMID 19249341 DOI: 10.1016/J.Exger.2009.02.004 |
0.615 |
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| 2009 |
Xiao M, Wan E, Chu C, Hsueh WC, Cao Y, Kwok PY. Direct determination of haplotypes from single DNA molecules Nature Methods. 6: 199-201. PMID 19198595 DOI: 10.1038/Nmeth.1301 |
0.37 |
|
| 2009 |
Chen Y, Teranishi K, Li S, Yee SW, Hesselson S, Stryke D, Johns SJ, Ferrin TE, Kwok P, Giacomini KM. Genetic variants in multidrug and toxic compound extrusion-1, hMATE1, alter transport function. The Pharmacogenomics Journal. 9: 127-36. PMID 19172157 DOI: 10.1038/Tpj.2008.19 |
0.718 |
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| 2009 |
Tahara H, Yee SW, Urban TJ, Hesselson S, Castro RA, Kawamoto M, Stryke D, Johns SJ, Ferrin TE, Kwok PY, Giacomini KM. Functional genetic variation in the basal promoter of the organic cation/carnitine transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5). The Journal of Pharmacology and Experimental Therapeutics. 329: 262-71. PMID 19141711 DOI: 10.1124/Jpet.108.146449 |
0.741 |
|
| 2009 |
Yee SW, Shima JE, Hesselson S, Nguyen L, De Val S, Lafond RJ, Kawamoto M, Johns SJ, Stryke D, Kwok PY, Ferrin TE, Black BL, Gurwitz D, Ahituv N, Giacomini KM. Identification and characterization of proximal promoter polymorphisms in the human concentrative nucleoside transporter 2 (SLC28A2). The Journal of Pharmacology and Experimental Therapeutics. 328: 699-707. PMID 19098160 DOI: 10.1124/Jpet.108.147207 |
0.745 |
|
| 2009 |
Kim H, Hysi PG, Pawlikowska L, Poon A, Burchard EG, Zaroff JG, Sidney S, Ko NU, Achrol AS, Lawton MT, McCulloch CE, Kwok PY, Young WL. Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation. Cerebrovascular Diseases (Basel, Switzerland). 27: 176-82. PMID 19092239 DOI: 10.1159/000185609 |
0.629 |
|
| 2009 |
Bodian DL, Chan TF, Poon A, Schwarze U, Yang K, Byers PH, Kwok PY, Klein TE. Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships. Human Molecular Genetics. 18: 463-71. PMID 18996919 DOI: 10.1093/Hmg/Ddn374 |
0.514 |
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| 2009 |
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SS, Honda Y, Honda M, Högl B, Longstreth WT, ... ... Kwok P, et al. Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus Nature Genetics. 41: 859-859. DOI: 10.1038/Ng0709-859B |
0.753 |
|
| 2009 |
Kwok P. Continental SNPs go public: New ancestry informative markers for follow‐up association studies Human Mutation. 30. DOI: 10.1002/Humu.20965 |
0.333 |
|
| 2008 |
Musone SL, Taylor KE, Lu TT, Nititham J, Ferreira RC, Ortmann W, Shifrin N, Petri MA, Kamboh MI, Manzi S, Seldin MF, Gregersen PK, Behrens TW, Ma A, Kwok PY, et al. Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus. Nature Genetics. 40: 1062-4. PMID 19165919 DOI: 10.1038/Ng.202 |
0.772 |
|
| 2008 |
Yang JJ, Burchard EG, Choudhry S, Johnson CC, Ownby DR, Favro D, Chen J, Akana M, Ha C, Kwok PY, Krajenta R, Havstad SL, Joseph CL, Seibold MA, Shriver MD, et al. Differences in allergic sensitization by self-reported race and genetic ancestry. The Journal of Allergy and Clinical Immunology. 122: 820-827.e9. PMID 19014772 DOI: 10.1016/J.Jaci.2008.07.044 |
0.558 |
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| 2008 |
Kim H, Hysi PG, Pawlikowska L, Choudhry S, González Burchard E, Kwok PY, Sidney S, McCulloch CE, Young WL. Population stratification in a case-control study of brain arteriovenous malformation in Latinos. Neuroepidemiology. 31: 224-8. PMID 18841030 DOI: 10.1159/000160215 |
0.603 |
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| 2008 |
Tseng ZH, Aouizerat BE, Pawlikowska L, Vittinghoff E, Lin F, Whiteman D, Poon A, Herrington D, Howard TD, Varosy PD, Hulley SB, Malloy M, Kane J, Kwok PY, Olgin JE. Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 5: 814-21. PMID 18534365 DOI: 10.1016/J.Hrthm.2008.03.016 |
0.6 |
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| 2008 |
Nickerson DA, Ankener W, Delahunty C, Kwok PY. Genotyping by ligation assays. Current Protocols in Human Genetics. Unit 2.6. PMID 18428270 DOI: 10.1002/0471142905.Hg0206S10 |
0.311 |
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| 2008 |
Liu Y, Helms C, Liao W, Zaba LC, Duan S, Gardner J, Wise C, Miner A, Malloy MJ, Pullinger CR, Kane JP, Saccone S, Worthington J, Bruce I, Kwok PY, et al. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. Plos Genetics. 4: e1000041. PMID 18369459 DOI: 10.1371/Journal.Pgen.1000041 |
0.373 |
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| 2008 |
Ko NU, Rajendran P, Kim H, Rutkowski M, Pawlikowska L, Kwok PY, Higashida RT, Lawton MT, Smith WS, Zaroff JG, Young WL. Endothelial nitric oxide synthase polymorphism (-786T->C) and increased risk of angiographic vasospasm after aneurysmal subarachnoid hemorrhage. Stroke; a Journal of Cerebral Circulation. 39: 1103-8. PMID 18309169 DOI: 10.1161/Strokeaha.107.496596 |
0.558 |
|
| 2008 |
Chan TF, Poon A, Basu A, Addleman NR, Chen J, Phong A, Byers PH, Klein TE, Kwok PY. Natural variation in four human collagen genes across an ethnically diverse population. Genomics. 91: 307-14. PMID 18272325 DOI: 10.1016/J.Ygeno.2007.12.008 |
0.697 |
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| 2007 |
Ha C, Kwok P. The Template-Directed Dye-Incorporation Assay with Fluorescence Polarization Detection (FP-TDI). Csh Protocols. 2007. PMID 21356946 DOI: 10.1101/Pdb.Prot4844 |
0.319 |
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| 2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Kwok PY, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.667 |
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| 2007 |
Tingley WG, Pawlikowska L, Zaroff JG, Kim T, Nguyen T, Young SG, Vranizan K, Kwok PY, Whooley MA, Conklin BR. Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation. Proceedings of the National Academy of Sciences of the United States of America. 104: 8461-6. PMID 17485678 DOI: 10.1073/Pnas.0610393104 |
0.62 |
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| 2007 |
Xiao M, Gordon MP, Phong A, Ha C, Chan TF, Cai D, Selvin PR, Kwok PY. Determination of haplotypes from single DNA molecules: a method for single-molecule barcoding. Human Mutation. 28: 913-21. PMID 17443670 DOI: 10.1002/Humu.20528 |
0.515 |
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| 2007 |
Reich D, Patterson N, Ramesh V, De Jager PL, McDonald GJ, Tandon A, Choy E, Hu D, Tamraz B, Pawlikowska L, Wassel-Fyr C, Huntsman S, Waliszewska A, Rossin E, Li R, ... ... Kwok PY, et al. Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels. American Journal of Human Genetics. 80: 716-26. PMID 17357077 DOI: 10.1086/513206 |
0.786 |
|
| 2007 |
Shah SJ, Tingley WG, Zaroff JG, Pawlikowska L, Kwok P, Whooley MA. Genetic Determinants of Cardiac Contractile Function in Caucasians Journal of Cardiac Failure. 13: S73-S74. DOI: 10.1016/J.Cardfail.2007.06.305 |
0.61 |
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| 2006 |
Chan TF, Ha C, Phong A, Cai D, Wan E, Leung L, Kwok PY, Xiao M. A simple DNA stretching method for fluorescence imaging of single DNA molecules. Nucleic Acids Research. 34: e113. PMID 16971459 DOI: 10.1093/Nar/Gkl593 |
0.507 |
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| 2006 |
Kwok PY. Genome-wide association studies getting more complicated but help is on the way. Human Genomics. 2: 341-2. PMID 16848970 DOI: 10.1186/1479-7364-2-6-341 |
0.44 |
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| 2006 |
Zaroff JG, Pawlikowska L, Miss JC, Yarlagadda S, Ha C, Achrol A, Kwok PY, McCulloch CE, Lawton MT, Ko N, Smith W, Young WL. Adrenoceptor polymorphisms and the risk of cardiac injury and dysfunction after subarachnoid hemorrhage. Stroke; a Journal of Cerebral Circulation. 37: 1680-5. PMID 16728691 DOI: 10.1161/01.Str.0000226461.52423.Dd |
0.609 |
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| 2006 |
Pawlikowska L, Poon KY, Achrol AS, McCulloch CE, Ha C, Lum K, Zaroff JG, Ko NU, Johnston SC, Sidney S, Marchuk DA, Lawton MT, Kwok PY, Young WL. Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations. Neurosurgery. 58: 838-43; discussion 8. PMID 16639317 DOI: 10.1227/01.Neu.0000209605.18358.E5 |
0.568 |
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| 2006 |
Koboldt DC, Miller RD, Kwok PY. Distribution of human SNPs and its effect on high-throughput genotyping. Human Mutation. 27: 249-54. PMID 16425292 DOI: 10.1002/Humu.20286 |
0.377 |
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| 2006 |
Chen Y, Pawlikowska L, Yao JS, Shen F, Zhai W, Achrol AS, Lawton MT, Kwok PY, Yang GY, Young WL. Interleukin-6 involvement in brain arteriovenous malformations. Annals of Neurology. 59: 72-80. PMID 16278864 DOI: 10.1002/Ana.20697 |
0.586 |
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| 2006 |
Zaroff JG, Pawlikowska L, Miss JC, Yarlagadda S, Ha C, Achrol A, Kwok PY, McCulloch CE, Lawton MT, Ko N, Smith W, Young WL. Response to letter by Atanassova [7] Stroke. 37: 2873. DOI: 10.1161/01.Str.0000248200.15086.97 |
0.576 |
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| 2005 |
Pawlikowska L, Tran MN, Achrol AS, Ha C, Burchard E, Choudhry S, Zaroff J, Lawton MT, Castro R, McCulloch CE, Marchuk D, Kwok PY, Young WL. Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 36: 2278-80. PMID 16179574 DOI: 10.1161/01.Str.0000182253.91167.Fa |
0.628 |
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| 2005 |
Swarbrick MM, Waldenmaier B, Pennacchio LA, Lind DL, Cavazos MM, Geller F, Merriman R, Ustaszewska A, Malloy M, Scherag A, Hsueh WC, Rief W, Mauvais-Jarvis F, Pullinger CR, Kane JP, ... ... Kwok PY, et al. Lack of support for the association between GAD2 polymorphisms and severe human obesity. Plos Biology. 3: e315. PMID 16122350 DOI: 10.1371/Journal.Pbio.0030315 |
0.339 |
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| 2005 |
Xiao M, Kwok P. Kinetic fluorescence-quenching detection assay for allele frequency estimation. Methods of Molecular Biology. 311: 115-123. PMID 16100403 DOI: 10.1385/1-59259-957-5:115 |
0.365 |
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| 2005 |
Miller RD, Phillips MS, Jo I, Donaldson MA, Studebaker JF, Addleman N, Alfisi SV, Ankener WM, Bhatti HA, Callahan CE, Carey BJ, Conley CL, Cyr JM, Derohannessian V, Donaldson RA, ... ... Kwok PY, et al. High-density single-nucleotide polymorphism maps of the human genome. Genomics. 86: 117-26. PMID 15961272 DOI: 10.1016/J.Ygeno.2005.04.012 |
0.393 |
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| 2005 |
Reiner AP, Ziv E, Lind DL, Nievergelt CM, Schork NJ, Cummings SR, Phong A, Burchard EG, Harris TB, Psaty BM, Kwok PY. Population structure, admixture, and aging-related phenotypes in African American adults: the Cardiovascular Health Study. American Journal of Human Genetics. 76: 463-77. PMID 15660291 DOI: 10.1086/428654 |
0.367 |
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| 2005 |
Freimuth RR, Marsh S, Xiao M, Kwok P, McLeod HL. Identification of genetic polymorphisms in 40 chemotherapy pathway genes Clinical Pharmacology & Therapeutics. 77. DOI: 10.1016/J.Clpt.2004.12.132 |
0.403 |
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| 2004 |
Marsh S, Xiao M, Yu J, Ahluwalia R, Minton M, Freimuth RR, Kwok PY, McLeod HL. Pharmacogenomic assessment of carboxylesterases 1 and 2. Genomics. 84: 661-8. PMID 15475243 DOI: 10.1016/J.Ygeno.2004.07.008 |
0.392 |
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| 2004 |
Pawlikowska L, Tran MN, Achrol AS, McCulloch CE, Ha C, Lind DL, Hashimoto T, Zaroff J, Lawton MT, Marchuk DA, Kwok PY, Young WL. Polymorphisms in genes involved in inflammatory and angiogenic pathways and the risk of hemorrhagic presentation of brain arteriovenous malformations. Stroke; a Journal of Cerebral Circulation. 35: 2294-300. PMID 15331795 DOI: 10.1161/01.Str.0000141932.44613.B1 |
0.626 |
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| 2004 |
Kwok PY, Xiao M. Single-molecule analysis for molecular haplotyping. Human Mutation. 23: 442-6. PMID 15108275 DOI: 10.1002/Humu.20020 |
0.398 |
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| 2003 |
Kwok P. High-throughput genotyping with primer extension fluorescent polarization detection. Current Protocols in Human Genetics. 39. PMID 18428360 DOI: 10.1002/0471142905.Hg0211S39 |
0.313 |
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| 2003 |
Xiao M, Kwok P. DNA analysis by fluorescence quenching detection. Genome Research. 13: 932-939. PMID 12727909 DOI: 10.1101/Gr.987803 |
0.369 |
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| 2003 |
Miller RD, Duan S, Lovins EG, Kloss EF, Kwok PY. Efficient high-throughput resequencing of genomic DNA. Genome Research. 13: 717-20. PMID 12654721 DOI: 10.1101/Gr.886203 |
0.367 |
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| 2003 |
Xiao M, Latif SM, Kwok P. Kinetic FP-TDI assay for SNP allele frequency determination. Biotechniques. 34: 190-197. PMID 12545559 DOI: 10.2144/03341Dd08 |
0.388 |
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| 2003 |
Kwok PY, Duan S. SNP discovery by direct DNA sequencing Methods in Molecular Biology (Clifton, N.J.). 212: 71-84. PMID 12491904 DOI: 10.1385/1-59259-327-5:071 |
0.334 |
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| 2003 |
Speckman RA, Wright Daw JA, Helms C, Duan S, Cao L, Taillon-Miller P, Kwok PY, Menter A, Bowcock AM. Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility. Human Genetics. 112: 34-41. PMID 12483297 DOI: 10.1007/S00439-002-0851-Y |
0.362 |
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| 2003 |
Kwok PY. Making 'random amplification' predictable in whole genome analysis. Trends in Biotechnology. 20: 411-2. PMID 12220898 DOI: 10.1016/S0167-7799(02)02034-6 |
0.351 |
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| 2002 |
Fan J, Surti U, Taillon-Miller P, Hsie L, Kennedy GC, Hoffner L, Ryder T, Mutch DG, Kwok P. Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping. Genomics. 79: 58-62. PMID 11827458 DOI: 10.1006/Geno.2001.6676 |
0.405 |
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| 2002 |
Kwok PY. Methods for genotyping single nucleotide polymorphisms. Annual Review of Genomics and Human Genetics. 2: 235-58. PMID 11701650 DOI: 10.1146/Annurev.Genom.2.1.235 |
0.408 |
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| 2002 |
Miller RD, Kwok PY. The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine. Human Molecular Genetics. 10: 2195-8. PMID 11673401 DOI: 10.1093/Hmg/10.20.2195 |
0.405 |
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| 2002 |
Vieux EF, Kwok P, Miller RD. Primer design for PCR and sequencing in high-throughput analysis of SNPs. Biotechniques. 32: 28-32. DOI: 10.2144/Jun0202 |
0.34 |
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| 2001 |
Kwok P. Genetic Association by Whole-Genome Analysis? Science. 294: 1669-1670. PMID 11721042 DOI: 10.1126/Science.1066921 |
0.382 |
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| 2001 |
White PS, Kwok P, Oefner P, Brookes AJ. 3rd International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis: SNPs: 'some notable progress'. European Journal of Human Genetics. 9: 316-318. PMID 11313777 DOI: 10.1038/Sj.Ejhg.5200616 |
0.375 |
|
| 2001 |
Brookes AJ, Kwok P, White PS, Oefner PJ. SNiPpets from the Third International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis, September 8–11, 2000, Taos, New Mexico, USA Human Mutation. 17: 241-242. PMID 11295820 DOI: 10.1002/Humu.19 |
0.358 |
|
| 2001 |
Kwok PY. High-throughput genotyping assay approaches. Pharmacogenomics. 1: 95-100. PMID 11258600 DOI: 10.1517/14622416.1.1.95 |
0.358 |
|
| 2001 |
Kwok PY. Approaches to allele frequency determination. Pharmacogenomics. 1: 231-5. PMID 11256594 DOI: 10.1517/14622416.1.2.231 |
0.365 |
|
| 2001 |
Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, ... ... Kwok PY, et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature. 409: 928-33. PMID 11237013 DOI: 10.1038/35057149 |
0.408 |
|
| 2001 |
Miller RD, Taillon-Miller P, Kwok P. Regions of low single-nucleotide polymorphism incidence in human and orangutan xq: deserts and recent coalescences. Genomics. 71: 78-88. PMID 11161800 DOI: 10.1006/Geno.2000.6417 |
0.382 |
|
| 2001 |
Hsu TM, Law SM, Duan S, Neri BP, Kwok P. Genotyping single-nucleotide polymorphisms by the invader assay with dual-color fluorescence polarization detection. Clinical Chemistry. 47: 1373-1377. DOI: 10.1093/Clinchem/47.8.1373 |
0.345 |
|
| 2000 |
Taillon-Miller P, Bauer-Sardiña I, Saccone NL, Putzel J, Laitinen T, Cao A, Kere J, Pilia G, Rice JP, Kwok PY. Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28. Nature Genetics. 25: 324-8. PMID 10888883 DOI: 10.1038/77100 |
0.368 |
|
| 2000 |
Taillon-Miller P, Kwok P. A high-density single-nucleotide polymorphism map of Xq25-q28. Genomics. 65: 195-202. PMID 10857743 DOI: 10.1006/Geno.2000.6165 |
0.356 |
|
| 2000 |
Kwok P. Finding a Needle in a Haystack: Detection and Quantification of Rare Mutant Alleles Are Coming of Age Clinical Chemistry. 46: 593-594. DOI: 10.1093/Clinchem/46.5.593 |
0.328 |
|
| 1999 |
Kwok PY, Gu Z. Single nucleotide polymorphism libraries: why and how are we building them? Molecular Medicine Today. 5: 538-43. PMID 10562720 DOI: 10.1016/S1357-4310(99)01601-9 |
0.381 |
|
| 1999 |
Pulai JI, Zakeri H, Kwok PY, Kim JH, Wu J, Schonfeld G. Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation. American Journal of Medical Genetics. 80: 218-20. PMID 9843041 DOI: 10.1002/(Sici)1096-8628(19981116)80:3<218::Aid-Ajmg7>3.0.Co;2-0 |
0.306 |
|
| 1999 |
Taillon-Miller P, Piernot EE, Kwok P. Efficient Approach to Unique Single-Nucleotide Polymorphism Discovery Genome Research. 9: 499-505. DOI: 10.1101/Gr.9.5.499 |
0.381 |
|
| 1999 |
Chen X, Levine L, Kwok P. Fluorescence Polarization in Homogeneous Nucleic Acid Analysis Genome Research. 9: 492-498. DOI: 10.1101/Gr.9.5.492 |
0.325 |
|
| 1998 |
Gu Z, Hillier L, Kwok PY. Single nucleotide polymorphism hunting in cyberspace. Human Mutation. 12: 221-5. PMID 9744471 DOI: 10.1002/(Sici)1098-1004(1998)12:4<221::Aid-Humu1>3.0.Co;2-I |
0.357 |
|
| 1998 |
Landegren U, Nilsson M, Kwok PY. Reading bits of genetic information: methods for single-nucleotide polymorphism analysis. Genome Research. 8: 769-76. PMID 9724323 DOI: 10.1101/Gr.8.8.769 |
0.337 |
|
| 1998 |
Taillon-Miller P, Gu Z, Li Q, Hillier L, Kwok P. Overlapping Genomic Sequences: A Treasure Trove of Single-Nucleotide Polymorphisms Genome Research. 8: 748-754. PMID 9685323 DOI: 10.1101/Gr.8.7.748 |
0.386 |
|
| 1998 |
Kwok PY, Chen X. Detection of single nucleotide variations. Genetic Engineering. 20: 125-34. PMID 9666557 DOI: 10.1007/978-1-4899-1739-3_6 |
0.353 |
|
| 1998 |
Chen X, Livak KJ, Kwok PY. A homogeneous, ligase-mediated DNA diagnostic test. Genome Research. 8: 549-56. PMID 9582198 DOI: 10.1101/Gr.8.5.549 |
0.386 |
|
| 1997 |
Taillon-Miller P, Bauer-Sardiña I, Zakeri H, Hillier L, Mutch DG, Kwok P. The Homozygous Complete Hydatidiform Mole: A Unique Resource for Genome Studies ☆ Genomics. 46: 307-310. PMID 9417922 DOI: 10.1006/Geno.1997.5042 |
0.402 |
|
| 1996 |
Kwok PY, Deng Q, Zakeri H, Taylor SL, Nickerson DA. Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs. Genomics. 31: 123-6. PMID 8808290 DOI: 10.1006/Geno.1996.0019 |
0.357 |
|
| 1994 |
Gnirke A, Iadonato SP, Kwok PY, Olson MV. Physical calibration of yeast artificial chromosome contig maps by RecA-assisted restriction endonuclease (RARE) cleavage. Genomics. 24: 199-210. PMID 7698741 DOI: 10.1006/Geno.1994.1607 |
0.573 |
|
| 1992 |
Kwok PY, Gremaud MF, Nickerson DA, Hood L, Olson MV. Automatable screening of yeast artificial-chromosome libraries based on the oligonucleotide-ligation assay. Genomics. 13: 935-41. PMID 1505984 DOI: 10.1016/0888-7543(92)90004-C |
0.529 |
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