Robert Wojciechowski, Ph.D. - Publications

Affiliations: 
2008 Johns Hopkins University, Baltimore, MD 
Area:
Epidemiology, Genetics, Ophthalmology

42 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
2022 Patasova K, Khawaja AP, Wojciechowski R, Mahroo OA, Falchi M, Rahi JS, Hammond CJ, Hysi PG. A genome-wide analysis of 340 318 participants identifies four novel loci associated with the age of first spectacle wear. Human Molecular Genetics. PMID 35220419 DOI: 10.1093/hmg/ddac048  0.374
2020 Hysi PG, Choquet H, Khawaja AP, Wojciechowski R, Tedja MS, Yin J, Simcoe MJ, Patasova K, Mahroo OA, Thai KK, Cumberland PM, Melles RB, Verhoeven VJM, Vitart V, Segre A, et al. Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Nature Genetics. PMID 32231278 DOI: 10.1038/S41588-020-0599-0  0.449
2020 Craig JE, Han X, Qassim A, Hassall M, Cooke Bailey JN, Kinzy TG, Khawaja AP, An J, Marshall H, Gharahkhani P, Igo RP, Graham SL, Healey PR, Ong JS, Zhou T, ... ... Wojciechowski R, et al. Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature Genetics. PMID 31959993 DOI: 10.1038/S41588-019-0556-Y  0.32
2018 Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, ... Wojciechowski R, et al. Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8. The British Journal of Ophthalmology. PMID 29925512 DOI: 10.1136/Bjophthalmol-2018-312064  0.363
2018 Khawaja AP, Cooke Bailey JN, Wareham NJ, Scott RA, Simcoe M, Igo RP, Song YE, Wojciechowski R, Cheng CY, Khaw PT, Pasquale LR, Haines JL, Foster PJ, Wiggs JL, Hammond CJ, et al. Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. Nature Genetics. PMID 29785010 DOI: 10.1038/S41588-018-0126-8  0.379
2017 Wojciechowski R, Cheng CY. INVOLVEMENT OF MULTIPLE MOLECULAR PATHWAYS IN THE GENETICS OF OCULAR REFRACTION AND MYOPIA. Retina (Philadelphia, Pa.). PMID 28406858 DOI: 10.1097/Iae.0000000000001518  0.379
2017 Springelkamp H, Iglesias AI, Mishra A, Höhn R, Wojciechowski R, Khawaja AP, Nag A, Wang YX, Wang JJ, Cuellar-Partida G, Gibson J, Cooke Bailey JN, Vithana EN, Gharahkhani P, Boutin T, et al. New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Human Molecular Genetics. PMID 28073927 DOI: 10.1093/Hmg/Ddw399  0.381
2016 Fan Q, Guo X, Tideman JW, Williams KM, Yazar S, Hosseini SM, Howe LD, Pourcain BS, Evans DM, Timpson NJ, McMahon G, Hysi PG, Krapohl E, Wang YX, Jonas JB, ... ... Wojciechowski R, et al. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium. Scientific Reports. 6: 25853. PMID 27174397 DOI: 10.1038/Srep25853  0.438
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, 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  0.443
2015 Tkatchenko AV, Tkatchenko TV, Guggenheim JA, Verhoeven VJ, Hysi PG, Wojciechowski R, Singh PK, Kumar A, Thinakaran G, Williams C. APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans. Plos Genetics. 11: e1005432. PMID 26313004 DOI: 10.1371/Journal.Pgen.1005432  0.349
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, 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  0.475
2014 Simpson CL, Wojciechowski R, Oexle K, Murgia F, Portas L, Li X, Verhoeven VJ, Vitart V, Schache M, Hosseini SM, Hysi PG, Raffel LJ, Cotch MF, Chew E, Klein BE, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Plos One. 9: e107110. PMID 25233373 DOI: 10.1371/Journal.Pone.0107110  0.423
2014 Hysi PG, Cheng CY, Springelkamp H, Macgregor S, Bailey JN, Wojciechowski R, Vitart V, Nag A, Hewitt AW, Höhn R, Venturini C, Mirshahi A, Ramdas WD, Thorleifsson G, Vithana E, et al. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics. 46: 1126-30. PMID 25173106 DOI: 10.1038/Ng.3087  0.426
2014 Kavitha S, Zebardast N, Palaniswamy K, Wojciechowski R, Chan ES, Friedman DS, Venkatesh R, Ramulu PY. Family history is a strong risk factor for prevalent angle closure in a South Indian population. Ophthalmology. 121: 2091-7. PMID 24974379 DOI: 10.1016/J.Ophtha.2014.05.001  0.34
2014 Hysi PG, Wojciechowski R, Rahi JS, Hammond CJ. Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future. Investigative Ophthalmology & Visual Science. 55: 3344-51. PMID 24876304 DOI: 10.1167/Iovs.14-14149  0.427
2014 Hysi PG, Mahroo OA, Cumberland P, Wojciechowski R, Williams KM, Young TL, Mackey DA, Rahi JS, Hammond CJ. Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts. Jama Ophthalmology. 132: 50-6. PMID 24264139 DOI: 10.1001/Jamaophthalmol.2013.6022  0.41
2014 Fan Q, Wojciechowski R, Kamran Ikram M, Cheng CY, Chen P, Zhou X, Pan CW, Khor CC, Tai ES, Aung T, Wong TY, Teo YY, Saw SM. Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies. Human Molecular Genetics. 23: 546-54. PMID 24014484 DOI: 10.1093/Hmg/Ddt431  0.424
2013 Simpson CL, Wojciechowski R, Yee SS, Soni P, Bailey-Wilson JE, Stambolian D. Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort. Molecular Vision. 19: 2173-86. PMID 24227913  0.392
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, ... ... Wojciechowski R, 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  0.384
2013 Duvesh R, Verma A, Venkatesh R, Kavitha S, Ramulu PY, Wojciechowski R, Sundaresan P. Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure. Investigative Ophthalmology & Visual Science. 54: 5624-8. PMID 23847314 DOI: 10.1167/Iovs.13-12186  0.401
2013 Wojciechowski R, Hysi PG. Focusing in on the complex genetics of myopia. Plos Genetics. 9: e1003442. PMID 23593034 DOI: 10.1371/Journal.Pgen.1003442  0.307
2013 Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Human Molecular Genetics. 22: 2754-64. PMID 23474815 DOI: 10.1093/Hmg/Ddt116  0.473
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, 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  0.476
2013 Wojciechowski R, Yee SS, Simpson CL, Bailey-Wilson JE, Stambolian D. Matrix metalloproteinases and educational attainment in refractive error: evidence of gene-environment interactions in the Age-Related Eye Disease Study. Ophthalmology. 120: 298-305. PMID 23098370 DOI: 10.1016/J.Ophtha.2012.07.078  0.336
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, 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  0.469
2012 Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, et al. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Human Genetics. 131: 1467-80. PMID 22665138 DOI: 10.1007/S00439-012-1176-0  0.586
2011 Simpson CL, Justice CM, Krishnan M, Wojciechowski R, Sung H, Cai J, Green T, Lewis D, Behneman D, Wilson AF, Bailey-Wilson JE. Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data. Bmc Proceedings. 5: S83. PMID 22373393 DOI: 10.1186/1753-6561-5-S9-S83  0.557
2011 Liu YC, Chou P, Wojciechowski R, Lin PY, Liu CJ, Chen SJ, Liu JH, Hsu WM, Cheng CY. Power vector analysis of refractive, corneal, and internal astigmatism in an elderly Chinese population: the Shihpai Eye Study. Investigative Ophthalmology & Visual Science. 52: 9651-7. PMID 22110083 DOI: 10.1167/Iovs.11-7641  0.314
2011 Wojciechowski R. Nature and nurture: The complex genetics of myopia and refractive error Clinical Genetics. 79: 301-320. PMID 21155761 DOI: 10.1111/J.1399-0004.2010.01592.X  0.415
2010 Wojciechowski R, Bailey-Wilson JE, Stambolian D. Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families. Investigative Ophthalmology & Visual Science. 51: 4989-95. PMID 20484597 DOI: 10.1167/Iovs.10-5474  0.389
2009 Kim Y, Wojciechowski R, Sung H, Mathias RA, Wang L, Klein AP, Lenroot RK, Malley J, Bailey-Wilson JE. Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects. Bmc Proceedings. 3: S64. PMID 20018058 DOI: 10.1186/1753-6561-3-S7-S64  0.4
2009 Wojciechowski R, Bailey-Wilson JE, Stambolian D. Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36. Molecular Vision. 15: 1398-406. PMID 19626131  0.344
2009 Wojciechowski R, Stambolian D, Ciner E, Ibay G, Holmes TN, Bailey-Wilson JE. Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study. Investigative Ophthalmology & Visual Science. 50: 2024-32. PMID 19151385 DOI: 10.1167/Iovs.08-2848  0.498
2009 Ciner E, Ibay G, Wojciechowski R, Dana D, Holmes TN, Bailey-Wilson JE, Stambolian D. Genome-wide scan of African-American and white families for linkage to myopia. American Journal of Ophthalmology. 147: 512-517.e2. PMID 19026404 DOI: 10.1016/J.Ajo.2008.09.004  0.406
2008 Ciner E, Wojciechowski R, Ibay G, Bailey-Wilson JE, Stambolian D. Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15. Genetic Epidemiology. 32: 454-63. PMID 18293391 DOI: 10.1002/Gepi.20318  0.509
2007 Peet JA, Cotch MF, Wojciechowski R, Bailey-Wilson JE, Stambolian D. Heritability and familial aggregation of refractive error in the Old Order Amish. Investigative Ophthalmology & Visual Science. 48: 4002-6. PMID 17724179 DOI: 10.1167/Iovs.06-1388  0.324
2006 Wojciechowski R, Moy C, Ciner E, Ibay G, Reider L, Bailey-Wilson JE, Stambolian D. Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36. Human Genetics. 119: 389-99. PMID 16501916 DOI: 10.1007/S00439-006-0153-X  0.508
2005 Klein AP, Tsai YY, Duggal P, Gillanders EM, Barnhart M, Mathias RA, Dusenberry IP, Turiff A, Chines PS, Goldstein J, Wojciechowski R, Hening W, Pugh EW, Bailey-Wilson JE. Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits. Bmc Genetics. 6: S20. PMID 16451629 DOI: 10.1186/1471-2156-6-S1-S20  0.583
2005 Wojciechowski R, Congdon N, Bowie H, Munoz B, Gilbert D, West SK. Heritability of refractive error and familial aggregation of myopia in an elderly American population. Investigative Ophthalmology & Visual Science. 46: 1588-92. PMID 15851555 DOI: 10.1167/Iovs.04-0740  0.4
2005 Wojciechowski R, Congdon N, Bowie H, Munoz B, Gilbert D, West S. Familial aggregation of hyperopia in an elderly population of siblings in Salisbury, Maryland. Ophthalmology. 112: 78-83. PMID 15629824 DOI: 10.1016/J.Ophtha.2004.07.026  0.357
2005 Congdon N, Broman KW, Lai H, Munoz B, Bowie H, Gilbert D, Wojciechowski R, West SK. Cortical, but not posterior subcapsular, cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors. Ophthalmology. 112: 73-7. PMID 15629823 DOI: 10.1016/J.Ophtha.2004.07.012  0.348
2004 Congdon N, Broman KW, Lai H, Munoz B, Bowie H, Gilber D, Wojciechowski R, Alston C, West SK. Nuclear cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors. Investigative Ophthalmology & Visual Science. 45: 2182-6. PMID 15223793 DOI: 10.1167/Iovs.03-1163  0.373
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