| Year |
Citation |
Score |
| 2019 |
Leung KH, Luo S, Kwarteng R, Chen SG, Yap MKH, Huang CL, Yip SP. The myopia susceptibility locus vasoactive intestinal peptide receptor 2 (VIPR2) contains variants with opposite effects. Scientific Reports. 9: 18165. PMID 31796800 DOI: 10.1038/S41598-019-54619-8 |
0.702 |
|
| 2019 |
Huang Y, Kee CS, Hocking PM, Williams C, Yip SP, Guggenheim JA. A Genome-Wide Association Study for Susceptibility to Visual Experience-Induced Myopia. Investigative Ophthalmology & Visual Science. 60: 559-569. PMID 30721303 DOI: 10.1167/Iovs.18-25597 |
0.311 |
|
| 2018 |
Zaki H, Gasmelseed N, Abdalla B, Yip S. Association of toll-like receptor 2 polymorphisms with susceptibility to pulmonary tuberculosis in Sudanese Egyptian Journal of Medical Human Genetics. 19: 261-265. DOI: 10.1016/J.Ejmhg.2018.01.001 |
0.456 |
|
| 2017 |
Liao X, Yap MKH, Leung KH, Kao PYP, Liu LQ, Yip SP. Genetic Association Study of KCNQ5 Polymorphisms with High Myopia. Biomed Research International. 2017: 3024156. PMID 28884119 DOI: 10.1155/2017/3024156 |
0.723 |
|
| 2017 |
Yip SP, Leung KH, Kao PYP, Yap MKH. AB015. The relationship between copy number variations and high myopia in Chinese: a case-control study Annals of Eye Science. 2: AB015-AB015. DOI: 10.21037/Aes.2017.Ab015 |
0.621 |
|
| 2016 |
Kao PY, Leung KH, Chan LW, Yip SP, Yap MK. Pathway analysis of complex diseases for GWAS, extending to consider rare variants, multi-omics and interactions. Biochimica Et Biophysica Acta. PMID 27888147 DOI: 10.1016/J.Bbagen.2016.11.030 |
0.632 |
|
| 2016 |
Fan Q, Verhoeven VJ, Wojciechowski R, Barathi VA, Hysi PG, Guggenheim JA, Höhn R, Vitart V, Khawaja AP, Yamashiro K, Hosseini SM, Lehtimäki T, Lu Y, Haller T, Xie J, ... ... Yip SP, et al. Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nature Communications. 7: 11008. PMID 27020472 DOI: 10.1038/Ncomms11008 |
0.414 |
|
| 2015 |
Wang F, Chan LW, Tsui NB, Wong SC, Siu PM, Yip SP, Yung BY. Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia. Biomed Research International. 2015: 610595. PMID 25961029 DOI: 10.1155/2015/610595 |
0.316 |
|
| 2015 |
Yuan C, Yip SP, Wu VW, Kwong DL, Cheuk IW, Ying M. Association between genetic polymorphisms and carotid atherosclerosis in patients treated with radiotherapy for nasopharyngeal carcinoma. Radiation Oncology (London, England). 10: 39. PMID 25880731 DOI: 10.1186/S13014-015-0341-8 |
0.312 |
|
| 2015 |
Miyake M, Yamashiro K, Tabara Y, Suda K, Morooka S, Nakanishi H, Khor CC, Chen P, Qiao F, Nakata I, Akagi-Kurashige Y, Gotoh N, Tsujikawa A, Meguro A, Kusuhara S, ... ... Yip SP, et al. Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Nature Communications. 6: 6689. PMID 25823570 DOI: 10.1038/Ncomms7689 |
0.696 |
|
| 2015 |
Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, ... ... Yip SP, et al. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics. 134: 131-46. PMID 25367360 DOI: 10.1007/S00439-014-1500-Y |
0.436 |
|
| 2014 |
Koh SP, Yip SP, Lee KK, Chan CC, Lau SM, Kho CS, Lau CK, Lin SY, Lau YM, Wong LG, Au KL, Wong KF, Chu RW, Yu PH, Chow EY, et al. Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. Bmc Genetics. 15: 147. PMID 25526816 DOI: 10.1186/S12863-014-0147-Y |
0.515 |
|
| 2014 |
Cheuk IW, Yip SP, Kwong DL, Wu VW. Association of XRCC1 and XRCC3 gene haplotypes with the development of radiation-induced fibrosis in patients with nasopharyngeal carcinoma. Molecular and Clinical Oncology. 2: 553-558. PMID 24940494 DOI: 10.3892/Mco.2014.276 |
0.436 |
|
| 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, ... Yip SP, et al. Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. The Journal of Clinical Investigation. 123: 4909-17. PMID 24216480 DOI: 10.1172/Jci69277 |
0.458 |
|
| 2013 |
Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, ... ... Yip SP, et al. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics. 93: 264-77. PMID 24144296 DOI: 10.1016/J.Ajhg.2013.06.016 |
0.333 |
|
| 2013 |
Yiu WC, Yap MK, Fung WY, Ng PW, Yip SP. Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. Plos One. 8: e61805. PMID 23637909 DOI: 10.1371/Journal.Pone.0061805 |
0.481 |
|
| 2013 |
Yip SP, Li CC, Yiu WC, Hung WH, Lam WW, Lai MC, Ng PW, Fung WY, Chu PH, Jiang B, Chan HH, Yap MK. A novel missense mutation in the NYX gene associated with high myopia. Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists). 33: 346-53. PMID 23406521 DOI: 10.1111/Opo.12036 |
0.31 |
|
| 2013 |
Verhoeven VJ, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GH, McMahon G, ... ... Yip SP, et al. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nature Genetics. 45: 314-8. PMID 23396134 DOI: 10.1038/Ng.2554 |
0.386 |
|
| 2013 |
Verhoeven VJM, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GHS, McMahon G, ... ... Yip SP, et al. Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Nature Genetics (2013) 45 (314-318)) Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712B |
0.324 |
|
| 2012 |
Zhu MM, Yap MK, Ho DW, Fung WY, Ng PW, Gu YS, Yip SP. Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case-control study in Chinese. Bmc Medical Genetics. 13: 64. PMID 22857148 DOI: 10.1186/1471-2350-13-64 |
0.415 |
|
| 2012 |
Ho DW, Yap MK, Ng PW, Fung WY, Yip SP. Association of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus. Plos One. 7: e40238. PMID 22792142 DOI: 10.1371/Journal.Pone.0040238 |
0.397 |
|
| 2012 |
Zaki HY, Leung KH, Yiu WC, Gasmelseed N, Elwali NE, Yip SP. Common polymorphisms in TLR4 gene associated with susceptibility to pulmonary tuberculosis in the Sudanese. The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease. 16: 934-40. PMID 22525209 DOI: 10.5588/Ijtld.11.0517 |
0.709 |
|
| 2012 |
Mak JY, Yap MK, Fung WY, Ng PW, Yip SP. Association of IGF1 gene haplotypes with high myopia in Chinese adults. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 209-16. PMID 22332214 DOI: 10.1001/Archophthalmol.2011.365 |
0.459 |
|
| 2012 |
Ho DW, Yap MK, Yip SP. UPDG: utilities package for data analysis of pooled DNA GWAS. Bmc Genetics. 13: 1. PMID 22252406 DOI: 10.1186/1471-2156-13-1 |
0.319 |
|
| 2011 |
Ho DW, Yiu WC, Yap MK, Fung WY, Ng PW, Yip SP. Genotyping performance assessment of whole genome amplified DNA with respect to multiplexing level of assay and its period of storage. Plos One. 6: e26119. PMID 22022531 DOI: 10.1371/Journal.Pone.0026119 |
0.404 |
|
| 2011 |
Yip SP, Leung KH, Ng PW, Fung WY, Sham PC, Yap MK. Evaluation of proteoglycan gene polymorphisms as risk factors in the genetic susceptibility to high myopia. Investigative Ophthalmology & Visual Science. 52: 6396-403. PMID 21743019 DOI: 10.1167/Iovs.11-7639 |
0.723 |
|
| 2011 |
Jiang B, Yap MK, Leung KH, Ng PW, Fung WY, Lam WW, Gu YS, Yip SP. PAX6 haplotypes are associated with high myopia in Han chinese. Plos One. 6: e19587. PMID 21589860 DOI: 10.1371/Journal.Pone.0019587 |
0.714 |
|
| 2011 |
Yip SP, Leung KH, Fung WY, Ng PW, Sham PC, Yap MK. A DNA pooling-based case-control study of myopia candidate genes COL11A1, COL18A1, FBN1, and PLOD1 in a Chinese population. Molecular Vision. 17: 810-21. PMID 21527992 |
0.695 |
|
| 2011 |
Leung KH, Yiu WC, Yap MK, Ng PW, Fung WY, Sham PC, Yip SP. Systematic investigation of the relationship between high myopia and polymorphisms of the MMP2, TIMP2, and TIMP3 genes by a DNA pooling approach. Investigative Ophthalmology & Visual Science. 52: 3893-900. PMID 21421877 DOI: 10.1167/Iovs.11-7286 |
0.699 |
|
| 2010 |
Yu YS, Wang LL, Shen Y, Yap MK, Yip SP, Han W. Investigation of the association between all-trans-retinol dehydrogenase (RDH8) polymorphisms and high myopia in Chinese. Journal of Zhejiang University. Science. B. 11: 836-41. PMID 21043051 DOI: 10.1631/Jzus.B1000001 |
0.497 |
|
| 2009 |
Zha Y, Leung KH, Lo KK, Fung WY, Ng PW, Shi MG, Yap MK, Yip SP. TGFB1 as a susceptibility gene for high myopia: a replication study with new findings. Archives of Ophthalmology (Chicago, Ill. : 1960). 127: 541-8. PMID 19365037 DOI: 10.1001/Archophthalmol.2008.623 |
0.726 |
|
| 2009 |
Han W, Leung KH, Fung WY, Mak JY, Li YM, Yap MK, Yip SP. Association of PAX6 polymorphisms with high myopia in Han Chinese nuclear families. Investigative Ophthalmology & Visual Science. 50: 47-56. PMID 19124844 DOI: 10.1167/Iovs.07-0813 |
0.718 |
|
| 2008 |
Song YQ, Ho DW, Karppinen J, Kao PY, Fan BJ, Luk KD, Yip SP, Leong JC, Cheah KS, Sham P, Chan D, Cheung KM. Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern Chinese. Bmc Medical Genetics. 9: 38. PMID 18439317 DOI: 10.1186/1471-2350-9-38 |
0.356 |
|
| 2008 |
Song YQ, Cheung KM, Ho DW, Poon SC, Chiba K, Kawaguchi Y, Hirose Y, Alini M, Grad S, Yee AF, Leong JC, Luk KD, Yip SP, Karppinen J, Cheah KS, et al. Association of the asporin D14 allele with lumbar-disc degeneration in Asians. American Journal of Human Genetics. 82: 744-7. PMID 18304494 DOI: 10.1016/J.Ajhg.2007.12.017 |
0.413 |
|
| 2008 |
Tang WC, Yap MK, Yip SP. A review of current approaches to identifying human genes involved in myopia. Clinical & Experimental Optometry : Journal of the Australian Optometrical Association. 91: 4-22. PMID 18045248 DOI: 10.1111/J.1444-0938.2007.00181.X |
0.682 |
|
| 2008 |
Kao P, Chan D, Cheah K, Cheung K, Ho D, Karppinen J, Leong J, Luk K, Yip S, Song Y, Sham P. Genome-wide association study of Degenerative Disc Disease (DDD) Spine. 53. DOI: 10.1097/01.Brs.0000320212.35379.B8 |
0.3 |
|
| 2008 |
Leung KH, Yip SP. Single strand conformation polymorphism (SSCP) analysis Molecular Biomethods Handbook: Second Edition. 117-131. DOI: 10.1007/978-1-60327-375-6_9 |
0.659 |
|
| 2008 |
Leung KH, Yip SP. Denaturing high-performance liquid chromatography (DHPLC) for nucleic acid analysis Molecular Biomethods Handbook: Second Edition. 89-106. DOI: 10.1007/978-1-60327-375-6_7 |
0.633 |
|
| 2007 |
Yip SP, Lai SK, Wong ML. Systematic sequence analysis of the human fucosyltransferase 2 (FUT2) gene identifies novel sequence variations and alleles. Transfusion. 47: 1369-80. PMID 17655580 DOI: 10.1111/J.1537-2995.2007.01280.X |
0.397 |
|
| 2007 |
Chan KY, Ching JC, Xu MS, Cheung AN, Yip SP, Yam LY, Lai ST, Chu CM, Wong AT, Song YQ, Huang FP, Liu W, Chung PH, Leung GM, Chow EY, et al. Association of ICAM3 genetic variant with severe acute respiratory syndrome. The Journal of Infectious Diseases. 196: 271-80. PMID 17570115 DOI: 10.1086/518892 |
0.407 |
|
| 2007 |
Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK. Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population. Molecular Vision. 13: 534-44. PMID 17438518 |
0.712 |
|
| 2007 |
Leung KH, Yip SP, Wong WS, Yiu LS, Chan KK, Lai WM, Chow EY, Lin CK, Yam WC, Chan KS. Sex- and age-dependent association of SLC11A1 polymorphisms with tuberculosis in Chinese: a case control study. Bmc Infectious Diseases. 7: 19. PMID 17371589 DOI: 10.1186/1471-2334-7-19 |
0.678 |
|
| 2007 |
Virtanen IM, Song YQ, Cheung KM, Ala-Kokko L, Karppinen J, Ho DW, Luk KD, Yip SP, Leong JC, Cheah KS, Sham P, Chan D. Phenotypic and population differences in the association between CILP and lumbar disc disease. Journal of Medical Genetics. 44: 285-8. PMID 17220213 DOI: 10.1136/Jmg.2006.047076 |
0.407 |
|
| 2006 |
Han W, Yap MK, Wang J, Yip SP. Family-based association analysis of hepatocyte growth factor (HGF) gene polymorphisms in high myopia. Investigative Ophthalmology & Visual Science. 47: 2291-9. PMID 16723436 DOI: 10.1167/Iovs.05-1344 |
0.403 |
|
| 2006 |
Yip SP, Choi PS, Lee SY, Leung KH, El-Zawahri MM, Luqmani YA. ABO blood group in Kuwaitis: detailed allele frequency distribution and identification of novel alleles. Transfusion. 46: 773-9. PMID 16686845 DOI: 10.1111/J.1537-2995.2006.00796.X |
0.672 |
|
| 2006 |
Cheung KM, Chan D, Karppinen J, Chen Y, Jim JJ, Yip SP, Ott J, Wong KK, Sham P, Luk KD, Cheah KS, Leong JC, Song YQ. Association of the Taq I allele in vitamin D receptor with degenerative disc disease and disc bulge in a Chinese population. Spine. 31: 1143-8. PMID 16648751 DOI: 10.1097/01.Brs.0000216530.41838.D3 |
0.332 |
|
| 2006 |
Han W, Shen Y, Wang J, Yip S, Yap MKH. [Establishing the linkage disequilibrium pattern for the all-trans-retinol dehydrogenase (RDH8) gene]. Chinese Journal of Ophthalmology. 42: 642-648. DOI: 10.3760/J:Issn:0412-4081.2006.07.015 |
0.499 |
|
| 2005 |
Jim JJ, Noponen-Hietala N, Cheung KM, Ott J, Karppinen J, Sahraravand A, Luk KD, Yip SP, Sham PC, Song YQ, Leong JC, Cheah KS, Ala-Kokko L, Chan D. The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration. Spine. 30: 2735-42. PMID 16371896 DOI: 10.1097/01.Brs.0000190828.85331.Ef |
0.329 |
|
| 2004 |
Han W, Yip SP, Wang J, Yap MKH. Using denaturing HPLC for SNP discovery and genotyping, and establishing the linkage disequilibrium pattern for the all-trans-retinol dehydrogenase (RDH8) gene Journal of Human Genetics. 49: 16-23. PMID 14661078 DOI: 10.1007/S10038-003-0100-9 |
0.506 |
|
| 2003 |
Yip SP, Lee SY, To SS, Wong ML. Improved real-time PCR assay for homogeneous multiplex genotyping of four CYP2C9 alleles with hybridization probes. Clinical Chemistry. 49: 2109-11. PMID 14633897 DOI: 10.1373/Clinchem.2003.023622 |
0.435 |
|
| 2003 |
Yip SP, Pun SF, Leung KH, Lee SY. Rapid, simultaneous genotyping of five common Southeast Asian beta-thalassemia mutations by multiplex minisequencing and denaturing HPLC. Clinical Chemistry. 49: 1656-9. PMID 14500591 DOI: 10.1373/49.10.1656 |
0.618 |
|
| 2003 |
Yip SP, Leung KH, Lin CK. Extent and distribution of linkage disequilibrium around the SLC11A1 locus. Genes and Immunity. 4: 212-21. PMID 12700596 DOI: 10.1038/Sj.Gene.6363944 |
0.691 |
|
| 2002 |
Yip SP. Sequence variation at the human ABO locus Annals of Human Genetics. 66: 1-27. PMID 12014997 DOI: 10.1017/S0003480001008995 |
0.481 |
|
| 2000 |
Yip SP. Single-tube multiplex PCR-SSCP analysis distinguishes 7 common ABO alleles and readily identifies new alleles Blood. 95: 1487-1492. DOI: 10.1182/Blood.V95.4.1487.004K53_1487_1492 |
0.447 |
|
| 1999 |
Yip SP, Putt W, Hopkinson DA, Whitehouse DB. Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1) Annals of Human Genetics. 63: 129-140. PMID 10738524 DOI: 10.1046/J.1469-1809.1999.6320129.X |
0.483 |
|
| 1999 |
Yip SP, Lovegrove JU, Rana NA, Hopkinson DA, Whitehouse DB. Mapping recombination hotspots in human phosphoglucomutase (PGM1) Human Molecular Genetics. 8: 1699-1706. PMID 10441333 DOI: 10.1093/Hmg/8.9.1699 |
0.414 |
|
| 1996 |
Yip SP, Choy WL, Chan CW, Choi CH. The absence of a B allele in acquired B blood group phenotype confirmed by a DNA based genotyping method. Journal of Clinical Pathology. 49: 180-1. PMID 8655692 DOI: 10.1136/Jcp.49.2.180 |
0.324 |
|
| 1995 |
Yip SP, Yow CM, Lewis WH. DNA polymorphism at the ABO locus in the Chinese population of Hong Kong. Human Heredity. 45: 266-71. PMID 7590758 DOI: 10.1159/000154311 |
0.386 |
|
| 1993 |
Yip SP, Lewis WH. No association found between C3 alleles and scar hypertrophy. Burns : Journal of the International Society For Burn Injuries. 19: 297-301. PMID 8395174 DOI: 10.1016/0305-4179(93)90116-P |
0.334 |
|
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