☰

Tami L. Young, Ph.D. - Publications

Affiliations: 
2003 Loma Linda University, Loma Linda, United States 
Area:
Clinical Psychology, Cognitive Psychology
Tree Info Similar researchers PubMed Report error

0/249 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
Low-probability matches (unlikely to be authored by this person)
2021 Tideman JWL, Pärssinen O, Haarman AEG, Khawaja AP, Wedenoja J, Williams KM, Biino G, Ding X, Kähönen M, Lehtimäki T, Raitakari OT, Cheng CY, Jonas JB, Young TL, Bailey-Wilson JE, et al. Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. Jama Ophthalmology. PMID 33830181 DOI: 10.1001/jamaophthalmol.2021.0497  0.01
2021 Gharahkhani P, Jorgenson E, Hysi P, Khawaja AP, Pendergrass S, Han X, Ong JS, Hewitt AW, Segrè AV, Rouhana JM, Hamel AR, Igo RP, Choquet H, Qassim A, Josyula NS, ... ... Young TL, et al. Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Nature Communications. 12: 1258. PMID 33627673 DOI: 10.1038/s41467-020-20851-4  0.01
2020 Young TL, Whisenhunt KN, Jin J, LaMartina SM, Martin SM, Souma T, Limviphuvadh V, Suri F, Souzeau E, Zhang X, Dan Y, Anagnos E, Carmona S, Jody NM, Stangel N, et al. SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma. Investigative Ophthalmology & Visual Science. 61: 6. PMID 33027505 DOI: 10.1167/iovs.61.12.6  0.01
2020 Fan Q, Pozarickij A, Tan NYQ, Guo X, Verhoeven VJM, Vitart V, Guggenheim JA, Miyake M, Tideman JWL, Khawaja AP, Zhang L, MacGregor S, Höhn R, Chen P, Biino G, ... ... Young TL, et al. Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Communications Biology. 3: 133. PMID 32193507 DOI: 10.1038/s42003-020-0802-y  0.01
2019 Bradfield Y, Barbosa T, Blodi B, Tompson SW, McLellan GJ, Struck M, Young TL. Comparative Intraoperative Anterior Segment OCT Findings in Pediatric Patients with and without Glaucoma. Ophthalmology. Glaucoma. 2: 232-239. PMID 32672544 DOI: 10.1016/j.ogla.2019.04.006  0.01
2019 Wong YL, Hysi P, Cheung G, Tedja M, Hoang QV, Tompson SWJ, Whisenhunt KN, Verhoeven VJM, Zhao W, Hess M, Wong CW, Kifley A, Hosoda Y, Haarman AEG, Hopf S, ... ... Young TL, et al. Correction: Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium. Plos One. 14: e0223942. PMID 31600355 DOI: 10.1371/Journal.Pone.0223942  0.01
2019 Wong YL, Hysi P, Cheung G, Tedja M, Hoang QV, Tompson SWJ, Whisenhunt KN, Verhoeven V, Zhao W, Hess M, Wong CW, Kifley A, Hosoda Y, Haarman AEG, Hopf S, ... ... Young TL, et al. Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium. Plos One. 14: e0220143. PMID 31415580 DOI: 10.1371/journal.pone.0220143  0.01
2019 Seow WJ, Ngo CS, Pan H, Barathi VA, Tompson SW, Whisenhunt KN, Vithana E, Chong YS, Juo SH, Hysi P, Young TL, Karnani N, Saw SM. In-utero epigenetic factors are associated with early-onset myopia in young children. Plos One. 14: e0214791. PMID 31100065 DOI: 10.1371/Journal.Pone.0214791  0.01
2018 Lupton MK, Medland SE, Gordon SD, Goncalves T, MacGregor S, Mackey DA, Young TL, Duffy DL, Visscher PM, Wray NR, Nyholt DR, Bain L, Ferreira MA, Henders AK, Wallace L, et al. Accuracy of Inferred APOE Genotypes, for a Range of Genotyping Arrays and Imputation Reference Panels. Journal of Alzheimer's Disease : Jad. PMID 29865051 DOI: 10.3233/Jad-171104  0.01
2018 Tedja MS, Wojciechowski R, Hysi PG, Eriksson N, Furlotte NA, Verhoeven VJM, Iglesias AI, Meester-Smoor MA, Tompson SW, Fan Q, Khawaja AP, Cheng CY, Höhn R, Yamashiro K, Wenocur A, ... ... Young TL, et al. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nature Genetics. PMID 29808027 DOI: 10.1038/s41588-018-0127-7  0.01
2017 Thomson BR, Souma T, Tompson SW, Onay T, Kizhatil K, Siggs OM, Feng L, Whisenhunt KN, Yanovitch TL, Kalaydjieva L, Azmanov DN, Finzi S, Tanna CE, Hewitt AW, Mackey DA, ... ... Young TL, et al. Angiopoietin-1 is required for Schlemm's canal development in mice and humans. The Journal of Clinical Investigation. PMID 29106382 DOI: 10.1172/Jci95545  0.01
2017 Tompson SW, Young TL. Assaying the Effects of Splice Site Variants by Exon Trapping in a Mammalian Cell Line. Bio-Protocol. 7. PMID 28758139 DOI: 10.21769/BioProtoc.2281  0.01
2017 Cuellar-Partida G, Williams KM, Yazar S, Guggenheim JA, Hewitt AW, Williams C, Wang JJ, Kho PF, Saw SM, Cheng CY, Wong TY, Aung T, Young TL, Tideman JWL, Jonas JB, et al. Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study. International Journal of Epidemiology. PMID 28586461 DOI: 10.1093/Ije/Dyx068  0.01
2017 Kloss BA, Tompson SW, Whisenhunt KN, Quow KL, Huang SJ, Pavelec DM, Rosenberg T, Young TL. Exome Sequence Analysis of 14 Families With High Myopia. Investigative Ophthalmology & Visual Science. 58: 1982-1990. PMID 28384719 DOI: 10.1167/iovs.16-20883  0.01
2017 Vicente LP, Finzi S, Susanna R, Young TL. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study. Arquivos Brasileiros De Oftalmologia. 80: 49-51. PMID 28380103 DOI: 10.5935/0004-2749.20170013  0.01
2017 Jin ZB, Wu J, Huang XF, Feng CY, Cai XB, Mao JY, Xiang L, Wu KC, Xiao X, Kloss BA, Li Z, Liu Z, Huang S, Shen M, Cheng FF, ... ... Young TL, et al. Trio-based exome sequencing arrests de novo mutations in early-onset high myopia. Proceedings of the National Academy of Sciences of the United States of America. PMID 28373534 DOI: 10.1073/pnas.1615970114  0.01
2017 Tompson SW, Johnson C, Abbott D, Bakall B, Soler V, Yanovitch TL, Whisenhunt KN, Klemm T, Rozen S, Stone EM, Johnson M, Young TL. Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genetics. 1-8. PMID 28095098 DOI: 10.1080/13816810.2016.1275018  0.01
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, ... ... Young TL, 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  0.01
2016 Tkatchenko AV, Luo X, Tkatchenko TV, Vaz C, Tanavde VM, Maurer-Stroh S, Zauscher S, Gonzalez P, Young TL. Large-Scale microRNA Expression Profiling Identifies Putative Retinal miRNA-mRNA Signaling Pathways Underlying Form-Deprivation Myopia in Mice. Plos One. 11: e0162541. PMID 27622715 DOI: 10.1371/Journal.Pone.0162541  0.01
2016 Kuo AN, Verkicharla PK, McNabb RP, Cheung CY, Hilal S, Farsiu S, Chen C, Wong TY, Ikram MK, Cheng CY, Young TL, Saw SM, Izatt JA. Posterior Eye Shape Measurement With Retinal OCT Compared to MRI. Investigative Ophthalmology & Visual Science. 57: OCT196-OCT203. PMID 27409473 DOI: 10.1167/Iovs.15-18886  0.01
2016 Souma T, Tompson SW, Thomson BR, Siggs OM, Kizhatil K, Yamaguchi S, Feng L, Limviphuvadh V, Whisenhunt KN, Maurer-Stroh S, Yanovitch TL, Kalaydjieva L, Azmanov DN, Finzi S, Mauri L, ... ... Young TL, et al. Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity. The Journal of Clinical Investigation. PMID 27270174 DOI: 10.1172/Jci85830  0.01
2016 Frerichs L, Kim M, Dave G, Cheney A, Hassmiller Lich K, Jones J, Young TL, Cene CW, Varma DS, Schaal J, Black A, Striley CW, Vassar S, Sullivan G, Cottler LB, et al. Stakeholder Perspectives on Creating and Maintaining Trust in Community-Academic Research Partnerships. Health Education & Behavior : the Official Publication of the Society For Public Health Education. PMID 27230272 DOI: 10.1177/1090198116648291  0.01
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, ... ... Young TL, 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  0.01
2016 Sanfilippo PG, Chu BS, Bigault O, Kearns LS, Boon MY, Young TL, Hammond CJ, Hewitt AW, Mackey DA. Response: Cycloplegia in refraction: age and cycloplegics. Acta Ophthalmologica. PMID 27167468 DOI: 10.1111/aos.13082  0.01
2016 Swanton AR, Young TL, Peek-Asa C. Characteristics of Fatal Agricultural Injuries by Production Type. Journal of Agricultural Safety and Health. 22: 75-85. PMID 27024994  0.01
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, ... ... Young TL, 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  0.01
2016 Hodgkinson KA, Howes AJ, Boland P, Shen XS, Stuckless S, Young TL, Curtis F, Collier A, Parfrey PS, Connors SP. Long-Term Clinical Outcome of Arrhythmogenic Right Ventricular Cardiomyopathy in Individuals With a p.S358L Mutation in TMEM43 Following Implantable Cardioverter Defibrillator Therapy. Circulation. Arrhythmia and Electrophysiology. 9. PMID 26966288 DOI: 10.1161/Circep.115.003589  0.01
2016 Swanton AR, Young TL, Peek-Asa C. Characteristics of fatal agricultural injuries by production type Journal of Agricultural Safety and Health. 22: 75-85. DOI: 10.13031/jash.22.11244  0.01
2016 Young TL, Williams J, Nelson-Gardell D, Edwards SL, Thorington VA. Assessing the Helpfulness of One Parenting Assistance Helpline Journal of Child and Family Studies. 1-10. DOI: 10.1007/S10826-016-0387-8  0.01
2015 Etchegary H, Enright G, Audas R, Pullman D, Young TL, Hodgkinson K. Perceived economic burden associated with an inherited cardiac condition: a qualitative inquiry with families affected by arrhythmogenic right ventricular cardiomyopathy. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26513349 DOI: 10.1038/Gim.2015.132  0.01
2015 Kato N, Loh M, Takeuchi F, Verweij N, Wang X, Zhang W, Kelly TN, Saleheen D, Lehne B, Mateo Leach I, Drong AW, Abbott J, Wahl S, Tan ST, Scott WR, ... ... Young TL, et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nature Genetics. 47: 1282-93. PMID 26390057 DOI: 10.1038/Ng.3405  0.01
2015 Swanton AR, Young TL, Leinenkugel K, Torner JC, Peek-Asa C. Nonfatal tractor-related injuries presenting to a state trauma system. Journal of Safety Research. 53: 97-102. PMID 25934002 DOI: 10.1016/J.Jsr.2015.03.002  0.01
2015 Black K, Dobbs D, Young TL. Aging in community: mobilizing a new paradigm of older adults as a core social resource. Journal of Applied Gerontology : the Official Journal of the Southern Gerontological Society. 34: 219-43. PMID 25681387 DOI: 10.1177/0733464812463984  0.01
2015 Springelkamp H, Mishra A, Hysi PG, Gharahkhani P, Höhn R, Khor CC, Cooke Bailey JN, Luo X, Ramdas WD, Vithana E, Koh V, Yazar S, Xu L, Forward H, Kearns LS, ... ... Young TL, et al. Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Genetic Epidemiology. 39: 207-16. PMID 25631615 DOI: 10.1002/Gepi.21886  0.01
2015 He M, Xu M, Zhang B, Liang J, Chen P, Lee JY, Johnson TA, Li H, Yang X, Dai J, Liang L, Gui L, Qi Q, Huang J, Li Y, ... ... Young T, et al. Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. Human Molecular Genetics. 24: 1791-800. PMID 25429064 DOI: 10.1093/Hmg/Ddu583  0.01
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, ... ... Young TL, 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  0.01
2015 Hwang JY, Sim X, Wu Y, Liang J, Tabara Y, Hu C, Hara K, Tam CH, Cai Q, Zhao Q, Jee S, Takeuchi F, Go MJ, Ong RT, Ohkubo T, ... ... Young TL, et al. Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. Diabetes. 64: 291-8. PMID 25187374 DOI: 10.2337/Db14-0563  0.01
2015 Milting H, Klauke B, Christensen AH, Müsebeck J, Walhorn V, Grannemann S, Münnich T, Šari? T, Rasmussen TB, Jensen HK, Mogensen J, Baecker C, Romaker E, Laser KT, zu Knyphausen E, ... Young TL, et al. The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus. European Heart Journal. 36: 872-81. PMID 24598986 DOI: 10.1093/Eurheartj/Ehu077  0.01
2015 Swanton AR, Young TL, Leinenkugel K, Torner JC, Peek-Asa C. Nonfatal tractor-related injuries presenting to a state trauma system Journal of Safety Research. 53: 97-102. DOI: 10.1016/j.jsr.2015.03.002  0.01
2015 Young TL, Turnage-Butterbaugh I, Degges-White S, Mossing S. Wellness among undergraduate students on academic probation: Implications for college counselors Journal of College Counseling. 18: 222-232. DOI: 10.1002/Jocc.12016  0.01
2014 Etchegary H, Pullman D, Simmonds C, Young TL, Hodgkinson K. 'It had to be done': genetic testing decisions for arrhythmogenic right ventricular cardiomyopathy. Clinical Genetics. PMID 25263618 DOI: 10.1111/cge.12513  0.01
2014 Springelkamp H, Höhn R, Mishra A, Hysi PG, Khor CC, Loomis SJ, Bailey JN, Gibson J, Thorleifsson G, Janssen SF, Luo X, Ramdas WD, Vithana E, Nongpiur ME, Montgomery GW, ... ... Young TL, et al. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications. 5: 4883. PMID 25241763 DOI: 10.1038/ncomms5883  0.01
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, ... ... Young TL, 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  0.01
2014 Hartnett ME, Morrison MA, Smith S, Yanovitch TL, Young TL, Colaizy T, Momany A, Dagle J, Carlo WA, Clark EA, Page G, Murray J, DeAngelis MM, Cotten CM. Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants. Investigative Ophthalmology & Visual Science. 55: 6194-203. PMID 25118269 DOI: 10.1167/Iovs.14-14841  0.01
2014 McKnight CM, Sherwin JC, Yazar S, Forward H, Tan AX, Hewitt AW, Pennell CE, McAllister IL, Young TL, Coroneo MT, Mackey DA. Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort study. American Journal of Ophthalmology. 158: 1079-85. PMID 25072831 DOI: 10.1016/j.ajo.2014.07.033  0.01
2014 Simino J, Shi G, Bis JC, Chasman DI, Ehret GB, Gu X, Guo X, Hwang SJ, Sijbrands E, Smith AV, Verwoert GC, Bragg-Gresham JL, Cadby G, Chen P, Cheng CY, ... ... Young TL, et al. Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. American Journal of Human Genetics. 95: 24-38. PMID 24954895 DOI: 10.1016/J.Ajhg.2014.05.010  0.01
2014 Wen W, Zheng W, Okada Y, Takeuchi F, Tabara Y, Hwang JY, Dorajoo R, Li H, Tsai FJ, Yang X, He J, Wu Y, He M, Zhang Y, Liang J, ... ... Young TL, et al. Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. Human Molecular Genetics. 23: 5492-504. PMID 24861553 DOI: 10.1093/Hmg/Ddu248  0.01
2014 Stanton SG, Griffin A, Stockley TL, Brown C, Young TL, Benteau T, Abdelfatah N. X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care. American Journal of Audiology. 23: 190-200. PMID 24687041 DOI: 10.1044/2014_Aja-13-0040  0.01
2014 Chen P, Takeuchi F, Lee JY, Li H, Wu JY, Liang J, Long J, Tabara Y, Goodarzi MO, Pereira MA, Kim YJ, Go MJ, Stram DO, Vithana E, Khor CC, ... ... Young TL, et al. Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians. Diabetes. 63: 2551-62. PMID 24647736 DOI: 10.2337/Db13-1815  0.01
2014 Sanfilippo PG, Chu BS, Bigault O, Kearns LS, Boon MY, Young TL, Hammond CJ, Hewitt AW, Mackey DA. What is the appropriate age cut-off for cycloplegia in refraction? Acta Ophthalmologica. 92: e458-62. PMID 24641244 DOI: 10.1111/aos.12388  0.01
2014 Nag A, Venturini C, Small KS, Young TL, Viswanathan AC, Mackey DA, Hysi PG, Hammond C. A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort. Human Molecular Genetics. 23: 3343-8. PMID 24518671 DOI: 10.1093/hmg/ddu050  0.01
2014 Choy AP, Wasserman BN, Young TL, Nelson LB. Refraction issues in childhood: when to prescribe glasses. Journal of Pediatric Ophthalmology and Strabismus. 51: 7-9. PMID 24512587 DOI: 10.3928/01913913-20130719-01  0.01
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  0.01
2014 Wu Y, Gao H, Li H, Tabara Y, Nakatochi M, Chiu YF, Park EJ, Wen W, Adair LS, Borja JB, Cai Q, Chang YC, Chen P, Croteau-Chonka DC, Fogarty MP, ... ... Young TL, et al. A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2. Human Molecular Genetics. 23: 1108-19. PMID 24105470 DOI: 10.1093/Hmg/Ddt488  0.01
2014 Lim SH, St Germain E, Tran-Viet KN, Staffieri S, Marino M, Dollfus PH, Nading EB, Crowe S, Gole G, Perdomo-Trujillo Y, Haybittel M, Elder J, Pelletier V, Traboulsi E, Mackey D, ... Young TL, et al. Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia. Ophthalmic Genetics. 35: 1-6. PMID 23802135 DOI: 10.3109/13816810.2012.752017  0.01
2014 Young TL, Hee K, Lennon AJ, Egan RJ, Wilkie O, Yao Y. Design and characterization of an adhesion strength tester for evaluating metal contacts on silicon solar cells 2014 Ieee 40th Photovoltaic Specialist Conference, Pvsc 2014. 2550-2553. DOI: 10.1109/PVSC.2014.6925450  0.01
2014 Young TL. The Journal of Intergenerational Relationships: Honoring Traditions and Welcoming Innovation Journal of Intergenerational Relationships. 12: 95-98. DOI: 10.1080/15350770.2014.902291  0.01
2014 Ohrt JH, Ener E, Porter J, Young TL. Group Leader Reflections on Their Training and Experience: Implications for Group Counselor Educators and Supervisors Journal For Specialists in Group Work. 39: 95-124. DOI: 10.1080/01933922.2014.883004  0.01
2014 Karr DJ, Levin AV, Traboulsi EI, Young TL. AAP AAPOS workshop: your genetics toolbox: concepts and conditions every pediatric ophthalmologist should know Journal of American Association For Pediatric Ophthalmology and Strabismus. 18: e43. DOI: 10.1016/j.jaapos.2014.07.138  0.01
2014 Young TL, Hawthorne F, Feng S, Luo X, St. Germain E, Wang M, Metlapally R. Corrigendum to "Whole genome expression profiling of normal human fetal and adult ocular tissues" [Exp. Eye Res. 116 (2013) 265-278] DOI: 10.1016/j.exer.2013.08.009 Experimental Eye Research. 127: 299. DOI: 10.1016/j.exer.2013.12.013  0.01
2013 Chen P, Ong RT, Tay WT, Sim X, Ali M, Xu H, Suo C, Liu J, Chia KS, Vithana E, Young TL, Aung T, Lim WY, Khor CC, Cheng CY, et al. A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry. Plos One. 8: e79767. PMID 24244560 DOI: 10.1371/Journal.Pone.0079767  0.01
2013 Metlapally R, Gonzalez P, Hawthorne FA, Tran-Viet KN, Wildsoet CF, Young TL. Scleral micro-RNA signatures in adult and fetal eyes. Plos One. 8: e78984. PMID 24205357 DOI: 10.1371/journal.pone.0078984  0.01
2013 Guggenheim JA, McMahon G, Northstone K, Mandel Y, Kaiserman I, Stone RA, Lin X, Saw SM, Forward H, Mackey DA, Yazar S, Young TL, Williams C. Birth order and myopia. Ophthalmic Epidemiology. 20: 375-84. PMID 24168726 DOI: 10.3109/09286586.2013.848457  0.01
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, 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  0.01
2013 Young TL, Hawthorne F, Feng S, Luo X, St Germain E, Wang M, Metlapally R. Whole genome expression profiling of normal human fetal and adult ocular tissues. Experimental Eye Research. 116: 265-78. PMID 24016867 DOI: 10.1016/j.exer.2013.08.009  0.01
2013 Frankel CS, Young TL, Alvarez-Berger F, Spencer CP. What is your diagnosis? Osteosarcoma. Journal of the American Veterinary Medical Association. 243: 329-31. PMID 23865872 DOI: 10.2460/javma.243.3.329  0.01
2013 Dorajoo R, Li R, Ikram MK, Liu J, Froguel P, Lee J, Sim X, Ong RT, Tay WT, Peng C, Young TL, Blakemore AI, Cheng CY, Aung T, Mitchell P, et al. Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? Plos One. 8: e67650. PMID 23844046 DOI: 10.1371/Journal.Pone.0067650  0.01
2013 Sim X, Jensen RA, Ikram MK, Cotch MF, Li X, MacGregor S, Xie J, Smith AV, Boerwinkle E, Mitchell P, Klein R, Klein BE, Glazer NL, Lumley T, McKnight B, ... ... Young TL, et al. Genetic loci for retinal arteriolar microcirculation. Plos One. 8: e65804. PMID 23776548 DOI: 10.1371/Journal.Pone.0065804  0.01
2013 Yazar S, Mishra A, Ang W, Kearns LS, Mountain JA, Pennell C, Montgomery GW, Young TL, Hammond CJ, Macgregor S, Mackey DA, Hewitt AW. Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study. Molecular Vision. 19: 1238-46. PMID 23761726  0.01
2013 Knachel HC, Benin V, Moddeman WE, Birkbeck JC, Kestner TA, Young TL. Characterization by NMR of reactants and products of hydrofluoroether isomers, CF3(CF2)3OCH3 and (CF3)2C(F)CF2OCH3, reacting with isopropyl alcohol. Magnetic Resonance in Chemistry : Mrc. 51: 407-13. PMID 23703707 DOI: 10.1002/mrc.3964  0.01
2013 Tran-Viet KN, Powell C, Barathi VA, Klemm T, Maurer-Stroh S, Limviphuvadh V, Soler V, Ho C, Yanovitch T, Schneider G, Li YJ, Nading E, Metlapally R, Saw SM, Goh L, ... ... Young TL, et al. Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. American Journal of Human Genetics. 92: 820-6. PMID 23643385 DOI: 10.1016/j.ajhg.2013.04.005  0.01
2013 Nag A, Venturini C, Hysi PG, Arno M, Aldecoa-Otalora Astarloa E, Macgregor S, Hewitt AW, Young TL, Mitchell P, Viswanathan AC, Mackey DA, Hammond CJ. Copy number variation at chromosome 5q21.2 is associated with intraocular pressure. Investigative Ophthalmology & Visual Science. 54: 3607-12. PMID 23599335 DOI: 10.1167/Iovs.13-11952  0.01
2013 Lechner J, Dash DP, Muszynska D, Hosseini M, Segev F, George S, Frazer DG, Moore JE, Kaye SB, Young T, Simpson DA, Churchill AJ, Héon E, Willoughby CE. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Investigative Ophthalmology & Visual Science. 54: 3215-23. PMID 23599324 DOI: 10.1167/Iovs.13-11781  0.01
2013 Tran-Viet KN, Soler V, Quiette V, Powell C, Yanovitch T, Metlapally R, Luo X, Katsanis N, Nading E, Young TL. Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes. Molecular Vision. 19: 759-66. PMID 23592912  0.01
2013 Chang L, Pan CW, Ohno-Matsui K, Lin X, Cheung GC, Gazzard G, Koh V, Hamzah H, Tai ES, Lim SC, Mitchell P, Young TL, Aung T, Wong TY, Saw SM. Myopia-related fundus changes in Singapore adults with high myopia. American Journal of Ophthalmology. 155: 991-999.e1. PMID 23499368 DOI: 10.1016/J.Ajo.2013.01.016  0.01
2013 Abdelfatah N, McComiskey DA, Doucette L, Griffin A, Moore SJ, Negrijn C, Hodgkinson KA, King JJ, Larijani M, Houston J, Stanton SG, Young TL. Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL. European Journal of Human Genetics : Ejhg. 21: 1112-9. PMID 23443030 DOI: 10.1038/Ejhg.2013.5  0.01
2013 Wang BY, Stojanovi? S, Turner DA, Young TL, Hadad CM, Badji? JD. The entrapment of chiral guests with gated baskets: can a kinetic discrimination of enantiomers be governed through gating? Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4767-75. PMID 23436252 DOI: 10.1002/Chem.201204344  0.01
2013 Hawthorne F, Feng S, Metlapally R, Li YJ, Tran-Viet KN, Guggenheim JA, Malecaze F, Calvas P, Rosenberg T, Mackey DA, Venturini C, Hysi PG, Hammond CJ, Young TL. Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2. Investigative Ophthalmology & Visual Science. 54: 2076-86. PMID 23422819 DOI: 10.1167/iovs.12-11102  0.01
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, ... ... Young TL, 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  0.01
2013 Hawthorne FA, Young TL. Genetic contributions to myopic refractive error: Insights from human studies and supporting evidence from animal models. Experimental Eye Research. 114: 141-9. PMID 23379998 DOI: 10.1016/j.exer.2012.12.015  0.01
2013 Doucette L, Green J, Black C, Schwartzentruber J, Johnson GJ, Galutira D, Young TL. Molecular genetics of achromatopsia in Newfoundland reveal genetic heterogeneity, founder effects and the first cases of Jalili syndrome in North America. Ophthalmic Genetics. 34: 119-29. PMID 23362848 DOI: 10.3109/13816810.2013.763993  0.01
2013 Soler VJ, Tran-Viet KN, Galiacy SD, Limviphuvadh V, Klemm TP, St Germain E, Fournié PR, Guillaud C, Maurer-Stroh S, Hawthorne F, Suarez C, Kantelip B, Afshari NA, Creveaux I, Luo X, ... ... Young TL, et al. Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis. Journal of Medical Genetics. 50: 246-54. PMID 23349227 DOI: 10.1136/jmedgenet-2012-101325  0.01
2013 McClements M, Davies WI, Michaelides M, Young T, Neitz M, MacLaren RE, Moore AT, Hunt DM. Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. Investigative Ophthalmology & Visual Science. 54: 1361-9. PMID 23322568 DOI: 10.1167/iovs.12-11156  0.01
2013 Lopes MC, Hysi PG, Verhoeven VJ, Macgregor S, Hewitt AW, Montgomery GW, Cumberland P, Vingerling JR, Young TL, van Duijn CM, Oostra B, Uitterlinden AG, Rahi JS, Mackey DA, Klaver CC, et al. Identification of a candidate gene for astigmatism. Investigative Ophthalmology & Visual Science. 54: 1260-7. PMID 23322567 DOI: 10.1167/Iovs.12-10463  0.01
2013 Lu Y, Vitart V, Burdon KP, Khor CC, Bykhovskaya Y, Mirshahi A, Hewitt AW, Koehn D, Hysi PG, Ramdas WD, Zeller T, Vithana EN, Cornes BK, Tay WT, Tai ES, ... ... Young TL, et al. Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics. 45: 155-63. PMID 23291589 DOI: 10.1038/Ng.2506  0.01
2013 Lim SH, Tran-Viet KN, Yanovitch TL, Freedman SF, Klemm T, Call W, Powell C, Ravichandran A, Metlapally R, Nading EB, Rozen S, Young TL. CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States. American Journal of Ophthalmology. 155: 508-517.e5. PMID 23218701 DOI: 10.1016/j.ajo.2012.09.012  0.01
2013 Haywood AF, Merner ND, Hodgkinson KA, Houston J, Syrris P, Booth V, Connors S, Pantazis A, Quarta G, Elliott P, McKenna W, Young TL. Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada. European Heart Journal. 34: 1002-11. PMID 23161701 DOI: 10.1093/Eurheartj/Ehs383  0.01
2013 Abdelfatah N, Merner N, Houston J, Benteau T, Griffin A, Doucette L, Stockley T, Lauzon JL, Young TL. A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect. Human Mutation. 34: 66-9. PMID 22911656 DOI: 10.1002/Humu.22205  0.01
2013 Hodgkinson KA, Connors SP, Merner N, Haywood A, Young TL, McKenna WJ, Gallagher B, Curtis F, Bassett AS, Parfrey PS. The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43. Clinical Genetics. 83: 321-31. PMID 22725725 DOI: 10.1111/j.1399-0004.2012.01919.x  0.01
2013 Chan RV, Leo SW, Young T. A 7-year-old child seeking treatment for progressive myopia. Journal of Pediatric Ophthalmology and Strabismus. 48: 135-7. PMID 21598874 DOI: 10.3928/01913913-20110503-01  0.01
2013 Stoltz KB, Young TL. Applications of Motivational Interviewing in Career Counseling: Facilitating Career Transition Journal of Career Development. 40: 329-346. DOI: 10.1177/0894845312455508  0.01
2013 Park NS, Dobbs D, Carrion IV, Young TL, Salmon JR, Roff LL. Social Relationships of African American and Hispanic Older Assisted Living Residents: Exploring the Role of Race and Ethnicity Journal of Housing For the Elderly. 27: 369-391. DOI: 10.1080/02763893.2013.813427  0.01
2013 Young TL. Using Motivational Interviewing Within the Early Stages of Group Development Journal For Specialists in Group Work. 38: 169-181. DOI: 10.1080/01933922.2013.764369  0.01
2013 Young TL, Reysen R, Eskridge T, Ohrt JH. Personal Growth Groups: Measuring Outcome and Evaluating Impact Journal For Specialists in Group Work. 38: 52-67. DOI: 10.1080/01933922.2012.745915  0.01
2013 Young TL, Janke MC. Perceived Benefits and Concerns of Older Adults in a Community Intergenerational Program: Does Race Matter? Activities, Adaptation and Aging. 37: 121-140. DOI: 10.1080/01924788.2013.784852  0.01
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, ... ... Young TL, 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  0.01
2013 Young TL, Gutierrez D, Hagedorn WB. Does motivational interviewing (MI) work with nonaddicted clients? A controlled study measuring the effects of a brief training in MI on client outcomes Journal of Counseling and Development. 91: 313-320. DOI: 10.1002/J.1556-6676.2013.00099.X  0.01
2013 Young TL, Khazaeni LM, Bateman JB. Genetics of eye disease Harley's Pediatric Ophthalmology. 1-56.  0.01
2012 Mishra A, Yazar S, Hewitt AW, Mountain JA, Ang W, Pennell CE, Martin NG, Montgomery GW, Hammond CJ, Young TL, Macgregor S, Mackey DA. Genetic variants near PDGFRA are associated with corneal curvature in Australians. Investigative Ophthalmology & Visual Science. 53: 7131-6. PMID 22969067 DOI: 10.1167/Iovs.12-10489  0.01
2012 Okada Y, Sim X, Go MJ, Wu JY, Gu D, Takeuchi F, Takahashi A, Maeda S, Tsunoda T, Chen P, Lim SC, Wong TY, Liu J, Young TL, Aung T, et al. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nature Genetics. 44: 904-9. PMID 22797727 DOI: 10.1038/Ng.2352  0.01
2012 Fan Q, Barathi VA, Cheng CY, Zhou X, Meguro A, Nakata I, Khor CC, Goh LK, Li YJ, Lim W, Ho CE, Hawthorne F, Zheng Y, Chua D, Inoko H, ... ... Young TL, et al. Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. Plos Genetics. 8: e1002753. PMID 22685421 DOI: 10.1371/Journal.Pgen.1002753  0.01
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, ... ... Young TL, 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  0.01
2012 Ulmer M, Li J, Yaspan BL, Ozel AB, Richards JE, Moroi SE, Hawthorne F, Budenz DL, Friedman DS, Gaasterland D, Haines J, Kang JH, Lee R, Lichter P, Liu Y, ... ... Young T, et al. Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Investigative Ophthalmology & Visual Science. 53: 4468-74. PMID 22661486 DOI: 10.1167/Iovs.12-9784  0.01
2012 van Koolwijk LM, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, Janssen SF, Hewitt AW, Viswanathan AC, ten Brink JB, Hosseini SM, Amin N, Despriet DD, Willemse-Assink JJ, ... ... Young TL, et al. Common genetic determinants of intraocular pressure and primary open-angle glaucoma. Plos Genetics. 8: e1002611. PMID 22570627 DOI: 10.1371/Journal.Pgen.1002611  0.01
2012 Tran-Viet KN, St Germain E, Soler V, Powell C, Lim SH, Klemm T, Saw SM, Young TL. Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility. Molecular Vision. 18: 937-44. PMID 22539872  0.01
2012 Abbott D, Li YJ, Guggenheim JA, Metlapally R, Malecaze F, Calvas P, Rosenberg T, Paget S, Zayats T, Mackey DA, Feng S, Young TL. An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. Molecular Vision. 18: 720-9. PMID 22509102  0.01
2012 Mahoney K, Buckley D, Alam M, Penney S, Young TL, Parfrey P, Moore SJ. High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland. Epilepsy Research. 98: 140-7. PMID 21959335 DOI: 10.1016/J.Eplepsyres.2011.09.003  0.01
2012 Young TL. Sexuality, boundaries, and ethics Ethics and Professional Issues in Couple and Family Therapy. 89-106. DOI: 10.4324/9780203866245  0.01
2012 Young TL, Hagedorn WB. The effect of a brief training in motivational interviewing on trainee skill development Counselor Education and Supervision. 51: 82-97. DOI: 10.1002/J.1556-6978.2012.00006.X  0.01
2011 Fan Q, Zhou X, Khor CC, Cheng CY, Goh LK, Sim X, Tay WT, Li YJ, Ong RT, Suo C, Cornes B, Ikram MK, Chia KS, Seielstad M, Liu J, ... ... Young TL, et al. Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. Plos Genetics. 7: e1002402. PMID 22144915 DOI: 10.1371/Journal.Pgen.1002402  0.01
2011 Young BR, Young TL, Joyce MK, Kennedy SI, Atashbar MZ. Future opportunities for advancing glucose test device electronics. Journal of Diabetes Science and Technology. 5: 1077-86. PMID 22027300 DOI: 10.1177/193229681100500508  0.01
2011 Chang L, El-Dairi MA, Young TL, Bhatti MT. Retinal nerve fiber layer thickness in children with optic pathway gliomas. American Journal of Ophthalmology. 152: 504-5; author reply . PMID 21855679 DOI: 10.1016/j.ajo.2011.05.011  0.01
2011 Mackey DA, Hewitt AW, Ruddle JB, Vote B, Buttery RG, Toomes C, Metlapally R, Li YJ, Tran-Viet KN, Malecaze F, Calvas P, Rosenberg T, Guggenheim JA, Young TL. Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family. Molecular Vision. 17: 2118-28. PMID 21850187  0.01
2011 Young TL, Riggs M, Robinson JL. Childhood sexual abuse severity reconsidered: a factor structure of CSA characteristics. Journal of Child Sexual Abuse. 20: 373-95. PMID 21812543 DOI: 10.1080/10538712.2011.590124  0.01
2011 Schrader KA, Heravi-Moussavi A, Waters PJ, Senz J, Whelan J, Ha G, Eydoux P, Nielsen T, Gallagher B, Oloumi A, Boyd N, Fernandez BA, Young TL, Jones SJ, Hirst M, et al. Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities. The Journal of Pathology. 225: 12-8. PMID 21792934 DOI: 10.1002/Path.2941  0.01
2011 Leo SW, Young TL. An evidence-based update on myopia and interventions to retard its progression. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 15: 181-9. PMID 21596297 DOI: 10.1016/j.jaapos.2010.09.020  0.01
2011 Sanfilippo PG, Medland SE, Hewitt AW, Kearns LS, Ruddle JB, Sun C, Hammond CJ, Young TL, Martin NG, Mackey DA. Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science. 52: 5565-72. PMID 21498610 DOI: 10.1167/Iovs.11-7258  0.01
2011 Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P, Rao V, Aggarwal S, Paluru P, Bartoloni L, Young TL, Paoloni-Giacobino A, Morris MA, Nath SK, Antonarakis SE, et al. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. Investigative Ophthalmology & Visual Science. 52: 6814-9. PMID 21357393 DOI: 10.1167/iovs.10-6815  0.01
2011 Doucette L, Green J, Fernandez B, Johnson GJ, Parfrey P, Young TL. A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly. European Journal of Human Genetics : Ejhg. 19: 293-9. PMID 21150893 DOI: 10.1038/Ejhg.2010.210  0.01
2011 Li YJ, Goh L, Khor CC, Fan Q, Yu M, Han S, Sim X, Ong RT, Wong TY, Vithana EN, Yap E, Nakanishi H, Matsuda F, Ohno-Matsui K, Yoshimura N, ... ... Young TL, et al. Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology. 118: 368-75. PMID 21095009 DOI: 10.1016/J.Ophtha.2010.06.016  0.01
2011 SAW S, FAN Q, YOSHIMURA N, KHOR C, TAI E, GOH L, YOUNG T, LI Y. CTNND2 is a genetic variant for high myopia Acta Ophthalmologica. 89: 0-0. DOI: 10.1111/J.1755-3768.2011.2222.X  0.01
2011 Young TL, Yong JS, Cheong HP. Extending Linear discriminant analysis by using unlabeled data Proceedings - 11th Ieee International Conference On Computer and Information Technology, Cit 2011. 557-562. DOI: 10.1109/CIT.2011.52  0.01
2011 Young TL, Lambie GW, Hutchinson T, Thurston-Dyer J. The integration of reflectivity in developmental supervision: Implications for clinical supervisors Clinical Supervisor. 30: 1-18. DOI: 10.1080/07325223.2011.532019  0.01
2010 Chang L, El-Dairi MA, Frempong TA, Burner EL, Bhatti MT, Young TL, Leigh F. Optical coherence tomography in the evaluation of neurofibromatosis type-1 subjects with optic pathway gliomas. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 14: 511-7. PMID 21168074 DOI: 10.1016/j.jaapos.2010.08.014  0.01
2010 Yanovitch T, Wallace DK, Freedman SF, Enyedi LB, Kishnani P, Worley G, Crissman B, Burner E, Young TL. The accuracy of photoscreening at detecting treatable ocular conditions in children with Down syndrome. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 14: 472-7. PMID 21168069 DOI: 10.1016/j.jaapos.2010.09.016  0.01
2010 Ikram MK, Sim X, Xueling S, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, ... ... Young TL, et al. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. Plos Genetics. 6: e1001184. PMID 21060863 DOI: 10.1371/Journal.Pgen.1001184  0.01
2010 Young TL, Granic A, Yu Chen T, Haley CB, Edwards JD. Everyday reasoning abilities in persons with Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 2756-61. PMID 20939079 DOI: 10.1002/Mds.23379  0.01
2010 Lamoureux EL, Marella M, Chang B, Dirani M, Kah-Guan AE, Chia A, Young TL, Wong TY, Saw SM. Is the pediatric quality of life inventory valid for use in preschool children with refractive errors? Optometry and Vision Science : Official Publication of the American Academy of Optometry. 87: 813-22. PMID 20852452 DOI: 10.1097/Opx.0B013E3181F6Fb84  0.01
2010 Solouki AM, Verhoeven VJ, van Duijn CM, Verkerk AJ, Ikram MK, Hysi PG, Despriet DD, van Koolwijk LM, Ho L, Ramdas WD, Czudowska M, Kuijpers RW, Amin N, Struchalin M, Aulchenko YS, ... ... Young TL, et al. A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Nature Genetics. 42: 897-901. PMID 20835239 DOI: 10.1038/Ng.663  0.01
2010 Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, DeWan A, Sigurdsson A, Jonasdottir A, Gudjonsson SA, Magnusson KP, Stefansson H, Lam DS, Tam PO, Gudmundsdottir GJ, Southgate L, ... ... Young TL, et al. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics. 42: 906-9. PMID 20835238 DOI: 10.1038/Ng.661  0.01
2010 Hysi PG, Young TL, Mackey DA, Andrew T, Fernández-Medarde A, Solouki AM, Hewitt AW, Macgregor S, Vingerling JR, Li YJ, Ikram MK, Fai LY, Sham PC, Manyes L, Porteros A, et al. A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics. 42: 902-5. PMID 20835236 DOI: 10.1038/Ng.664  0.01
2010 Khor CC, Fan Q, Goh L, Tan D, Young TL, Li YJ, Seielstad M, Goh DL, Saw SM. Support for TGFB1 as a susceptibility gene for high myopia in individuals of Chinese descent. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 1081-4. PMID 20697017 DOI: 10.1001/archophthalmol.2010.149  0.01
2010 Dirani M, Zhou B, Hornbeak D, Chang BC, Gazzard G, Chia A, Ling Y, Selvaraj P, Young TL, Varma R, Wong TY, Saw SM. Prevalence and causes of decreased visual acuity in Singaporean Chinese preschoolers. The British Journal of Ophthalmology. 94: 1561-5. PMID 20576782 DOI: 10.1136/Bjo.2009.173104  0.01
2010 Lu Y, Dimasi DP, Hysi PG, Hewitt AW, Burdon KP, Toh T, Ruddle JB, Li YJ, Mitchell P, Healey PR, Montgomery GW, Hansell N, Spector TD, Martin NG, Young TL, et al. Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. Plos Genetics. 6: e1000947. PMID 20485516 DOI: 10.1371/Journal.Pgen.1000947  0.01
2010 Low W, Dirani M, Gazzard G, Chan YH, Zhou HJ, Selvaraj P, Au Eong KG, Young TL, Mitchell P, Wong TY, Saw SM. Family history, near work, outdoor activity, and myopia in Singapore Chinese preschool children. The British Journal of Ophthalmology. 94: 1012-6. PMID 20472747 DOI: 10.1136/Bjo.2009.173187  0.01
2010 Metlapally R, Ki CS, Li YJ, Tran-Viet KN, Abbott D, Malecaze F, Calvas P, Mackey DA, Rosenberg T, Paget S, Guggenheim JA, Young TL. Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort. Investigative Ophthalmology & Visual Science. 51: 4476-9. PMID 20435602 DOI: 10.1167/Iovs.09-4912  0.01
2010 Guggenheim JA, Zayats T, Hammond C, Young TL. Lumican and muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia. Eye (London, England). 24: 1411-2; author reply. PMID 20414262 DOI: 10.1038/eye.2010.55  0.01
2010 Macgregor S, Hewitt AW, Hysi PG, Ruddle JB, Medland SE, Henders AK, Gordon SD, Andrew T, McEvoy B, Sanfilippo PG, Carbonaro F, Tah V, Li YJ, Bennett SL, Craig JE, ... ... Young TL, et al. Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics. 19: 2716-24. PMID 20395239 DOI: 10.1093/Hmg/Ddq144  0.01
2010 Hornbeak DM, Dirani M, Sham WK, Li J, Young TL, Wong TY, Chong YS, Saw SM. Emerging trends in breastfeeding practices in Singaporean Chinese women: findings from a population-based study. Annals of the Academy of Medicine, Singapore. 39: 88-94. PMID 20237728  0.01
2010 Chia A, Dirani M, Chan YH, Gazzard G, Au Eong KG, Selvaraj P, Ling Y, Quah BL, Young TL, Mitchell P, Varma R, Wong TY, Saw SM. Prevalence of amblyopia and strabismus in young singaporean chinese children. Investigative Ophthalmology & Visual Science. 51: 3411-7. PMID 20207979 DOI: 10.1167/Iovs.09-4461  0.01
2010 Dellinger AE, Saw SM, Goh LK, Seielstad M, Young TL, Li YJ. Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays. Nucleic Acids Research. 38: e105. PMID 20142258 DOI: 10.1093/nar/gkq040  0.01
2010 Khor CC, Fan Q, Goh LK, Wong TY, Li YJ, Cheung N, Seielstad M, Goh DL, Young TL, Tai ES, Saw SM. Hepatocyte growth factor and retinal arteriolar diameter in Singapore Chinese. Ophthalmology. 117: 939-45. PMID 20122738 DOI: 10.1016/J.Ophtha.2009.09.055  0.01
2010 Dirani M, Zhang X, Goh LK, Young TL, Lee P, Saw SM. The role of vision in academic school performance. Ophthalmic Epidemiology. 17: 18-24. PMID 20100096 DOI: 10.3109/09286580903450320  0.01
2010 Dirani M, Chan YH, Gazzard G, Hornbeak DM, Leo SW, Selvaraj P, Zhou B, Young TL, Mitchell P, Varma R, Wong TY, Saw SM. Prevalence of refractive error in Singaporean Chinese children: the strabismus, amblyopia, and refractive error in young Singaporean Children (STARS) study. Investigative Ophthalmology & Visual Science. 51: 1348-55. PMID 19933197 DOI: 10.1167/Iovs.09-3587  0.01
2010 Ikram MK, Sim X, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BEK, Breteler MMB, Cheung N, Liew G, Mitchell P, Uitterlinden AG, Rivadeneira F, ... ... Young TL, et al. Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo Plos Genetics. 6. DOI: 10.1371/Annotation/841Bfadf-85D1-4059-894F-2863D73Fa963  0.01
2010 Drack AV, Young T. Fee for service genetic testing in ophthalmology: What is available, who should be tested, and who understands the results? Journal of American Association For Pediatric Ophthalmology and Strabismus. 14: e32. DOI: 10.1016/J.JAAPOS.2009.12.134  0.01
2010 Cabrera MT, Dirani M, Fan Q, Selvaraj P, Chia A, Saw SM, Gazzard G, Wong TY, Young TL, Varma R. Reply American Journal of Ophthalmology. 149: 523-524. DOI: 10.1016/j.ajo.2009.10.006  0.01
2010 Young TL. Myopia Ocular Disease: Mechanisms and Management. 424-432. DOI: 10.1016/B978-0-7020-2983-7.00055-3  0.01
2009 Nallasamy S, Davidson SL, Howell LJ, Hedrick H, Flake AW, Crombleholme TM, Adzick NS, Young TL. The effects of fetal surgery on retinopathy of prematurity development. Ophthalmology and Eye Diseases. 1: 13-9. PMID 23861606  0.01
2009 Young TL, Negash SM, Long RM. Enhancing sexual desire and intimacy via the metaphor of a problem child: utilizing structural-strategic family therapy. Journal of Sex & Marital Therapy. 35: 402-17. PMID 20183007 DOI: 10.1080/00926230903065971  0.01
2009 Hodgkinson K, Dicks E, Connors S, Young TL, Parfrey P, Pullman D. Translation of research discoveries to clinical care in arrhythmogenic right ventricular cardiomyopathy in Newfoundland and Labrador: lessons for health policy in genetic disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 859-65. PMID 20010364 DOI: 10.1097/Gim.0B013E3181C20Bb3  0.01
2009 Lavanya R, Jeganathan VS, Zheng Y, Raju P, Cheung N, Tai ES, Wang JJ, Lamoureux E, Mitchell P, Young TL, Cajucom-Uy H, Foster PJ, Aung T, Saw SM, Wong TY. Methodology of the Singapore Indian Chinese Cohort (SICC) eye study: quantifying ethnic variations in the epidemiology of eye diseases in Asians. Ophthalmic Epidemiology. 16: 325-36. PMID 19995197 DOI: 10.3109/09286580903144738  0.01
2009 Ronan SM, Tran-Viet KN, Burner EL, Metlapally R, Toth CA, Young TL. Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome. Archives of Ophthalmology (Chicago, Ill. : 1960). 127: 1511-9. PMID 19901218 DOI: 10.1001/archophthalmol.2009.273  0.01
2009 Mackey DA, Mackinnon JR, Brown SA, Kearns LS, Ruddle JB, Sanfilippo PG, Sun C, Hammond CJ, Young TL, Martin NG, Hewitt AW. Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 12: 441-54. PMID 19803772 DOI: 10.1375/Twin.12.5.441  0.01
2009 Sun C, Zhu G, Wong TY, Hewitt AW, Ruddle JB, Hodgson L, Montgomery GW, Young TL, Hammond CJ, Craig JE, Martin NG, He M, Mackey DA. Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye Study. Hypertension. 54: 788-95. PMID 19687348 DOI: 10.1161/Hypertensionaha.109.132902  0.01
2009 Hornbeak DM, Young TL. Myopia genetics: a review of current research and emerging trends. Current Opinion in Ophthalmology. 20: 356-62. PMID 19587595 DOI: 10.1097/ICU.0b013e32832f8040  0.01
2009 Zayats T, Young TL, Mackey DA, Malecaze F, Calvas P, Guggenheim JA. Quality of DNA extracted from mouthwashes. Plos One. 4: e6165. PMID 19582144 DOI: 10.1371/journal.pone.0006165  0.01
2009 Yanovitch T, Li YJ, Metlapally R, Abbott D, Viet KN, Young TL. Hepatocyte growth factor and myopia: genetic association analyses in a Caucasian population. Molecular Vision. 15: 1028-35. PMID 19471602  0.01
2009 Mahoney K, Moore SJ, Buckley D, Alam M, Parfrey P, Penney S, Merner N, Hodgkinson K, Young TL. Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A. Seizure. 18: 492-7. PMID 19464195 DOI: 10.1016/J.Seizure.2009.04.009  0.01
2009 Trager MJ, Dirani M, Fan Q, Gazzard G, Selvaraj P, Chia A, Wong TY, Young TL, Varma R, Saw SM. Testability of vision and refraction in preschoolers: the strabismus, amblyopia, and refractive error study in singaporean children. American Journal of Ophthalmology. 148: 235-241.e6. PMID 19426960 DOI: 10.1016/J.Ajo.2009.02.037  0.01
2009 Carbonaro F, Andrew T, Mackey DA, Young TL, Spector TD, Hammond CJ. Repeated measures of intraocular pressure result in higher heritability and greater power in genetic linkage studies. Investigative Ophthalmology & Visual Science. 50: 5115-9. PMID 19420339 DOI: 10.1167/iovs.09-3577  0.01
2009 Blanchard AA, Skliris GP, Watson PH, Murphy LC, Penner C, Tomes L, Young TL, Leygue E, Myal Y. Claudins 1, 3, and 4 protein expression in ER negative breast cancer correlates with markers of the basal phenotype. Virchows Archiv : An International Journal of Pathology. 454: 647-56. PMID 19387682 DOI: 10.1007/s00428-009-0770-6  0.01
2009 Metlapally R, Li YJ, Tran-Viet KN, Abbott D, Czaja GR, Malecaze F, Calvas P, Mackey D, Rosenberg T, Paget S, Zayats T, Owen MJ, Guggenheim JA, Young TL. COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Investigative Ophthalmology & Visual Science. 50: 4080-6. PMID 19387081 DOI: 10.1167/Iovs.08-3346  0.01
2009 Webb MP, Dicks EL, Green JS, Moore SJ, Warden GM, Gamberg JS, Davidson WS, Young TL, Parfrey PS. Autosomal recessive Bardet-Biedl syndrome: first-degree relatives have no predisposition to metabolic and renal disorders. Kidney International. 76: 215-23. PMID 19367329 DOI: 10.1038/Ki.2009.116  0.01
2009 Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, ... Young TL, et al. An international collaborative family-based whole-genome linkage scan for high-grade myopia. Investigative Ophthalmology & Visual Science. 50: 3116-27. PMID 19324860 DOI: 10.1167/Iovs.08-2781  0.01
2009 Rice A, Nsengimana J, Simmons IG, Toomes C, Hoole J, Willoughby CE, Cassidy F, Williams GA, George ND, Sheridan E, Young TL, Hunter TI, Barrett BT, Elliott DB, Bishop DT, et al. Replication of the recessive STBMS1 locus but with dominant inheritance. Investigative Ophthalmology & Visual Science. 50: 3210-7. PMID 19218600 DOI: 10.1167/iovs.07-1631  0.01
2009 Dirani M, Tong L, Gazzard G, Zhang X, Chia A, Young TL, Rose KA, Mitchell P, Saw SM. Outdoor activity and myopia in Singapore teenage children. The British Journal of Ophthalmology. 93: 997-1000. PMID 19211608 DOI: 10.1136/bjo.2008.150979  0.01
2009 Zayats T, Yanovitch T, Creer RC, McMahon G, Li YJ, Young TL, Guggenheim JA. Myocilin polymorphisms and high myopia in subjects of European origin. Molecular Vision. 15: 213-22. PMID 19180258  0.01
2009 Doucette L, Merner ND, Cooke S, Ives E, Galutira D, Walsh V, Walsh T, MacLaren L, Cater T, Fernandez B, Green JS, Wilcox ER, Shotland LI, Shotland L, Li XC, ... ... Young TL, et al. Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. European Journal of Human Genetics : Ejhg. 17: 554-64. PMID 19107147 DOI: 10.1038/Ejhg.2008.231  0.01
2009 Young TL. Molecular genetics of human myopia: an update. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 86: E8-E22. PMID 19104467 DOI: 10.1097/OPX.0b013e3181940655  0.01
2009 Metlapally R, Michaelides M, Bulusu A, Li YJ, Schwartz M, Rosenberg T, Hunt DM, Moore AT, Züchner S, Rickman CB, Young TL. Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies. Investigative Ophthalmology & Visual Science. 50: 1552-8. PMID 19098318 DOI: 10.1167/iovs.08-2455  0.01
2009 Ralston KD, Young TL, Buchheit RG. Electrochemical evaluation of constituent intermetallics in aluminum alloy 2024-T3 exposed to aqueous vanadate inhibitors Journal of the Electrochemical Society. 156. DOI: 10.1149/1.3076147  0.01
2009 McBrien NA, Young TL, Pang CP, Hammond C, Baird P, Saw S, Morgan IG, Mutti DO, Rose KA, Wallman J, Gentle A, Wildsoet CF, Gwiazda J, Schmid KL, Smith E, et al. Myopia: Recent Advances in Molecular Studies; Prevalence, Progression and Risk Factors; Emmetropization; Therapies; Optical Links; Peripheral Refraction; Sclera and Ocular Growth; Signalling Cascades; and Animal Models Optometry and Vision Science. 86: 45-66. DOI: 10.1097/01.Opx.0000344146.84135.68  0.01
2009 Young TL, Youn KK, Young KC. Au(I)-catalyzed cycloisomerization reaction of amide- or ester-tethered 1,6-enynes to bicyclo[3.2.0]hept-6-en-2-ones Journal of Organic Chemistry. 74: 7922-7934. DOI: 10.1021/jo901771p  0.01
2009 Young TL, Drack AV. 150: Genetics workshop: Part 1. The era of molecular ophthalmology Journal of American Association For Pediatric Ophthalmology and Strabismus. 13: e36-e37. DOI: 10.1016/j.jaapos.2008.12.161  0.01
2009 Drack AV, Young T. 131: Genetics workshop: Part 2. Genetic testing in ophthalmology: What is available, who should be tested, and who understands the results? Journal of American Association For Pediatric Ophthalmology and Strabismus. 13: e33. DOI: 10.1016/J.JAAPOS.2008.12.151  0.01
2009 Yanovitch TL, Wallace DK, Freedman SF, Enyedi LB, Young TL. 126: Success rates of adjustable and nonadjustable strabismus surgery in adults Journal of American Association For Pediatric Ophthalmology and Strabismus. 13: e32. DOI: 10.1016/J.JAAPOS.2008.12.097  0.01
2008 White T, Lu T, Metlapally R, Katowitz J, Kherani F, Wang TY, Tran-Viet KN, Young TL. Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia. Molecular Vision. 14: 2458-65. PMID 19112531  0.01
2008 Schneider A, Bardakjian TM, Zhou J, Hughes N, Keep R, Dorsainville D, Kherani F, Katowitz J, Schimmenti LA, Hummel M, Fitzpatrick DR, Young TL. Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters. American Journal of Medical Genetics. Part A. 146: 2794-8. PMID 18831064 DOI: 10.1002/Ajmg.A.32384  0.01
2008 Young TL, Young KC. Silver(I)-catalyzed facile synthesis of pyrazoles from propargyl N-sulfonylhydrazones Journal of Organic Chemistry. 73: 4698-4701. PMID 18489156 DOI: 10.1021/jo800663g  0.01
2008 Perman JA, Young TL, Stines E, Hamon J, Turner LM, Rowe MG. A community-driven obesity prevention and intervention in an elementary school. The Journal of the Kentucky Medical Association. 106: 104-8. PMID 18488968  0.01
2008 Yang J, Peek-Asa C, Jones MP, Nordstrom DL, Taylor C, Young TL, Zwerling C. Smoke alarms by type and battery life in rural households: a randomized controlled trial. American Journal of Preventive Medicine. 35: 20-4. PMID 18482822 DOI: 10.1016/J.Amepre.2008.03.020  0.01
2008 Wibbenmeyer LA, Kealey GP, Young TL, Newell IM, Lewis RW, Miller BR, Peek-Asa C. A prospective analysis of trash, brush, and grass burning behaviors. Journal of Burn Care & Research : Official Publication of the American Burn Association. 29: 441-5. PMID 18388580 DOI: 10.1097/BCR.0b013e3181710835  0.01
2008 Zhou J, Kherani F, Bardakjian TM, Katowitz J, Hughes N, Schimmenti LA, Schneider A, Young TL. Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. Molecular Vision. 14: 583-92. PMID 18385794  0.01
2008 Metlapally R, Li YJ, Tran-Viet KN, Bulusu A, White TR, Ellis J, Kao D, Young TL. Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia. Molecular Vision. 14: 387-93. PMID 18334955  0.01
2008 Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL. Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. American Journal of Human Genetics. 82: 809-21. PMID 18313022 DOI: 10.1016/J.Ajhg.2008.01.010  0.01
2008 Zayats T, Guggenheim JA, Hammond CJ, Young TL. Comment on 'A PAX6 gene polymorphism is associated with genetic predisposition to extreme myopia'. Eye (London, England). 22: 598-9; author reply . PMID 18219338 DOI: 10.1038/sj.eye.6703096  0.01
2008 Ralston KD, Chrisanti S, Young TL, Buchheit RG. Corrosion inhibition of aluminum alloy 2024-T3 by aqueous vanadium species Journal of the Electrochemical Society. 155. DOI: 10.1149/1.2907772  0.01
2007 Frankowski B, Gereige R, Grant L, Hyman D, Magalnick H, Mears CJ, Monteverdi G, Murray RD, Pattishall E, Roland M, Young TL, Taras H, Li SS, Joffe A, Behnke M, et al. The role of schools in combating illicit substance abuse Pediatrics. 120: 1379-1384. PMID 18055689 DOI: 10.1542/peds.2007-2905  0.01
2007 Smith GA, Baum CR, Dowd MD, Durbin DR, Gardner HG, Sege R, Turner MS, Weiss JC, Wright JL, Bull MJ, Agran PF, Brenner RA, Bryn S, Gilchrist J, Sinclair A, ... ... Young TL, et al. School transportation safety Pediatrics. 120: 213-220. PMID 17606581 DOI: 10.1542/peds.2007-1278  0.01
2007 Yang JH, Jun TG, Sung K, Jin HC, Young TL, Pyo WP. Repair of long-segment congenital tracheal stenosis Journal of Korean Medical Science. 22: 491-496. PMID 17596659 DOI: 10.3346/jkms.2007.22.3.491  0.01
2007 Nelin LD, Wang X, Zhao Q, Chicoine LG, Young TL, Hatch DM, English BK, Liu Y. MKP-1 switches arginine metabolism from nitric oxide synthase to arginase following endotoxin challenge. American Journal of Physiology. Cell Physiology. 293: C632-40. PMID 17442735 DOI: 10.1152/ajpcell.00137.2006  0.01
2007 Joffe A, Behnke ML, Knight JR, Kokotailo P, Sims TH, Williams JF, Kulig JW, Simkin D, Goldberg L, Levy S, Smith K, Murray RD, Frankowski BL, Gereige RS, Mears CJ, ... ... Young TL, et al. Testing for drugs of abuse in children and adolescents: Addendum - Testing in schools and at home Pediatrics. 119: 627-630. PMID 17332219 DOI: 10.1542/peds.2006-3688  0.01
2007 Nallasamy S, Paluru PC, Devoto M, Wasserman NF, Zhou J, Young TL. Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota. Molecular Vision. 13: 229-36. PMID 17327828  0.01
2007 Young TL, Metlapally R, Shay AE. Complex trait genetics of refractive error. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 38-48. PMID 17210850 DOI: 10.1001/archopht.125.1.38  0.01
2007 Thurber CA, Walton E, Murray RD, Frankowski BL, Gereige RS, Mears CJ, Roland MM, Young TL, Grant LM, Hyman D, Magalnick H, Monteverdi GJ, Pattishall EG, LaCursia N, Mazyck D, et al. Preventing and treating homesickness Pediatrics. 119: 192-201. PMID 17200288 DOI: 10.1542/peds.2006-2781  0.01
2007 Wook SK, Young TL, Jin HC, Sung K, Yang JH, Jun TG, Pyo WP. Kinking of internal thoracic artery graft without symptoms: Should it be revised? Heart Surgery Forum. 10: 264-267. DOI: 10.1532/HSF98.20071039  0.01
2006 Jadico SK, Young DA, Huebner A, Edmond JC, Pollock AN, McDonald-McGinn DM, Li YJ, Zackai EH, Young TL. Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 10: 521-7. PMID 17189145 DOI: 10.1016/j.jaapos.2006.07.012  0.01
2006 Johnson JM, Young TL, Rada JA. Small leucine rich repeat proteoglycans (SLRPs) in the human sclera: identification of abundant levels of PRELP. Molecular Vision. 12: 1057-66. PMID 17093390  0.01
2006 Jadico SK, Huebner A, McDonald-McGinn DM, Zackai EH, Young TL. Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 10: 435-44. PMID 17070479 DOI: 10.1016/j.jaapos.2006.06.008  0.01
2006 McCambridge TM, Bernhardt DT, Brenner JS, Congeni JA, Gomez JE, Gregory AJM, Gregory DB, Griesemer BA, Reed FE, Rice SG, Small EW, Stricker PR, LeBlanc C, Raynor J, Lindros JC, ... ... Young TL, et al. Active healthy living: Prevention of childhood obesity through increased physical activity Pediatrics. 117: 1834-1842. PMID 16651347 DOI: 10.1542/peds.2006-0472  0.01
2006 Zhou J, Rappaport EF, Tobias JW, Young TL. Differential gene expression in mouse sclera during ocular development. Investigative Ophthalmology & Visual Science. 47: 1794-802. PMID 16638983 DOI: 10.1167/iovs.05-0759  0.01
2006 Nallasamy S, Kherani F, Yaeger D, McCallum J, Kaur M, Devoto M, Jackson LG, Krantz ID, Young TL. Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation study. Archives of Ophthalmology (Chicago, Ill. : 1960). 124: 552-7. PMID 16606884 DOI: 10.1001/archopht.124.4.552  0.01
2006 Malleske DT, Rogers LK, Velluci SM, Young TL, Park MS, Long DW, Welty SE, Smith CV, Nelin LD. Hyperoxia increases hepatic arginase expression and ornithine production in mice. Toxicology and Applied Pharmacology. 215: 109-17. PMID 16554078 DOI: 10.1016/J.Taap.2006.02.002  0.01
2006 Egbert JE, Christiansen SP, Wright MM, Young TL, Summers CG. The natural history of glaucoma and ocular hypertension after pediatric cataract surgery. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 10: 54-7. PMID 16527681 DOI: 10.1016/j.jaapos.2005.07.002  0.01
2006 Stanley KP, Chicoine LG, Young TL, Reber KM, Lyons CR, Liu Y, Nelin LD. Gene transfer with inducible nitric oxide synthase decreases production of urea by arginase in pulmonary arterial endothelial cells. American Journal of Physiology. Lung Cellular and Molecular Physiology. 290: L298-306. PMID 16155089 DOI: 10.1152/ajplung.00140.2005  0.01
2006 Young TL, Sung K, Shin JO, Jeon ES. Disruption of dystrophin in acute fulminant coxsackieviral B4 infection Circulation. 113. DOI: 10.1161/CIRCULATIONAHA.105.541136  0.01
2005 Smith BT, Tasman WS, Young TL, Wilson ME, Raab EL, Paysse EA, Cox MS, Traboulsi EI, Anderson DR. Retinopathy of prematurity: Late complications in the baby boomer generation (1946-1964) Transactions of the American Ophthalmological Society. 103: 225-236. PMID 17057805  0.01
2005 Benni PB, Chen B, Dykes FD, Wagoner SF, Heard M, Tanner AJ, Young TL, Rais-Bahrami K, Rivera O, Short BL. Validation of the CAS neonatal NIRS system by monitoring vv-ECMO patients: preliminary results. Advances in Experimental Medicine and Biology. 566: 195-201. PMID 16594153 DOI: 10.1007/0-387-26206-7_27  0.01
2005 Payne AS, Yan AC, Ilyas E, Li W, Seykora JT, Young TL, Pawel BR, Honig PJ, Camacho J, Imaizumi S, Heymann WR, Schnur RE. Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype. Archives of Dermatology. 141: 1567-73. PMID 16365259 DOI: 10.1001/archderm.141.12.1567  0.01
2005 Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL. Identification of a novel locus on 2q for autosomal dominant high-grade myopia. Investigative Ophthalmology & Visual Science. 46: 2300-7. PMID 15980214 DOI: 10.1167/iovs.04-1423  0.01
2005 Zhou J, Young TL. Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia. Gene. 352: 10-9. PMID 15862761 DOI: 10.1016/j.gene.2005.02.019  0.01
2005 Heidary G, Ying GS, Maguire MG, Young TL. The association of astigmatism and spherical refractive error in a high myopia cohort. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 82: 244-7. PMID 15829852 DOI: 10.1097/01.Opx.0000159361.17876.96  0.01
2005 Hoffman JD, Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs. American Journal of Medical Genetics. Part A. 135: 96-8. PMID 15809999 DOI: 10.1002/ajmg.a.30688  0.01
2005 Descipio C, Schneider L, Young TL, Wasserman N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AA, et al. Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome. American Journal of Medical Genetics. Part A. 134: 3-11. PMID 15704124 DOI: 10.1002/ajmg.a.30573  0.01
2004 Tamhankar MA, Liu GT, Young TL, Sutton LN, Hurst RW. Acquired, isolated third nerve palsies in infants with cerebrovascular malformations. American Journal of Ophthalmology. 138: 484-6. PMID 15364238 DOI: 10.1016/j.ajo.2004.03.023  0.01
2004 Scavello GS, Paluru PC, Ganter WR, Young TL. Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia. Investigative Ophthalmology & Visual Science. 45: 2091-7. PMID 15223781 DOI: 10.1167/iovs.03-0933  0.01
2004 Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, et al. X-linked high myopia associated with cone dysfunction. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 897-908. PMID 15197065 DOI: 10.1001/Archopht.122.6.897  0.01
2004 Frattini A, Pangrazio A, Susani L, Sobacchi C, Mirolo M, Abinun M, Andolina M, Flanagan A, Horwitz EM, Mihci E, Notarangelo LD, Ramenghi U, Teti A, Van Hove J, Vujic D, ... Young T, et al. Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1740-7. PMID 14584882 DOI: 10.1359/jbmr.2003.18.10.1740  0.01
2003 Young TL. Ophthalmic genetics/inherited eye disease. Current Opinion in Ophthalmology. 14: 296-303. PMID 14502058 DOI: 10.1097/00055735-200310000-00011  0.01
2003 Paluru P, Ronan SM, Heon E, Devoto M, Wildenberg SC, Scavello G, Holleschau A, Mäkitie O, Cole WG, King RA, Young TL. New locus for autosomal dominant high myopia maps to the long arm of chromosome 17. Investigative Ophthalmology & Visual Science. 44: 1830-6. PMID 12714612 DOI: 10.1167/Iovs.02-0697  0.01
2003 North PE, Anthony DC, Young TL, Waner M, Brown HH, Brodsky MC. Retinal neovascular markers in retinopathy of prematurity: aetiological implications. The British Journal of Ophthalmology. 87: 275-8. PMID 12598436 DOI: 10.1136/Bjo.87.3.275  0.01
2002 Ahmed I, Tope WD, Young TL, Miller DM, Bloom KE. Neurocutaneous melanosis in association with encephalocraniocutaneous lipomatosis. Journal of the American Academy of Dermatology. 47: S196-200. PMID 12140461 DOI: 10.1067/mjd.2002.110073  0.01
2002 Jensen AA, Young TL. Inferior oblique muscle palsy following maxillectomy for squamous cell carcinoma. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 6: 51-3. PMID 11907480 DOI: 10.1067/mpa.2002.121325  0.01
2001 Engman JH, Egbert JE, Summers CG, Young TL. Efficacy of inferior oblique anterior transposition placement grading for dissociated vertical deviation. Ophthalmology. 108: 2045-50. PMID 11713077 DOI: 10.1016/S0161-6420(01)00801-6  0.01
2001 Elsas FJ, Collins M, Jones J, Kimble JA, Kline L, Witherspoon D, Roth AM, Demorest BH, Gilbert WS, Plotsky D, Jaafar M, Pilkerton AR, Mercer PA, Siatkowski RM, Clarkson J, ... ... Young TL, et al. Multicenter trial of Cryotherapy for Retinopathy of Prematurity: Ophthalmological outcomes at 10 years Archives of Ophthalmology. 119: 1110-1118. PMID 11483076 DOI: 10.1001/ARCHOPHT.119.8.1110  0.01
2001 Young TL, Atwood LD, Ronan SM, Dewan AT, Alvear AB, Peterson J, Holleschau A, King RA. Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis. Ophthalmic Genetics. 22: 69-75. PMID 11449316 DOI: 10.1076/opge.22.2.69.2233  0.01
2000 Young TL, Conahan BM, Summers CG, Egbert JE. Anterior Transposition of the Superior Oblique Tendon in the Treatment of Oculomotor Nerve Palsy and Its Influence on Postoperative Hypertropia Journal of Pediatric Ophthalmology & Strabismus. 37: 149-155. DOI: 10.3928/0191-3913-20000501-06  0.01
1999 Young TL, Bloom JN, Ruttum M, Sprunger DT, Weinstein JM. The IOLAB, Inc pediatric intraocular lens study. AAPOS Reasearch Committee. American Association for Pediatric Ophthalmology and Strabismus. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 3: 295-302. PMID 10532575 DOI: 10.1016/S1091-8531(99)70026-1  0.01
1999 Tripathi RK, Flanders DJ, Young TL, Oetting WS, Ramaiah A, King RA, Boissy RE, Nordlund JJ. Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 12: 187-92. PMID 10385915 DOI: 10.1111/J.1600-0749.1999.Tb00512.X  0.01
1998 Oetting WS, Armstrong CM, Ronan SM, Young TL, Sellers TA, King RA. Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detection. Electrophoresis. 19: 3079-83. PMID 9932797 DOI: 10.1002/Elps.1150191806  0.01
1998 Young TL, Ronan SM, Alvear AB, Wildenberg SC, Oetting WS, Atwood LD, Wilkin DJ, King RA. A second locus for familial high myopia maps to chromosome 12q. American Journal of Human Genetics. 63: 1419-24. PMID 9792869 DOI: 10.1086/302111  0.01
1998 Young TL, Ronan SM, Drahozal LA, Wildenberg SC, Alvear AB, Oetting WS, Atwood LD, Wilkin DJ, King RA. Evidence that a locus for familial high myopia maps to chromosome 18p. American Journal of Human Genetics. 63: 109-19. PMID 9634508 DOI: 10.1086/301907  0.01
1998 Weigel BJ, Pierpont ME, Young TL, Mutchler SB, Neglia JP. Retinoblastoma and Hirschsprung disease in a patient with interstitial deletion of chromosome 13. American Journal of Medical Genetics. 77: 285-8. PMID 9600737 DOI: 10.1002/(SICI)1096-8628(19980526)77:4<285::AID-AJMG7>3.0.CO;2-M  0.01
1997 Young TL, Anthony DC, Pierce E, Foley E, Smith LE. Histopathology and vascular endothelial growth factor in untreated and diode laser-treated retinopathy of prematurity. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 1: 105-10. PMID 10875087 DOI: 10.1016/S1091-8531(97)90008-2  0.01
1997 Young TL, Quinn GE, Baumgart S, Petersen RA, Schaffer DB. Extracorporeal membrane oxygenation causing asymmetric vasculopathy in neonatal infants. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 1: 235-40. PMID 10532770 DOI: 10.1016/S1091-8531(97)90044-6  0.01
1997 Young TL, Weis JR, Summers CG, Egbert JE. The association of strabismus, amblyopia, and refractive errors in spasmus nutans. Ophthalmology. 104: 112-7. PMID 9022113 DOI: 10.1016/S0161-6420(97)30353-4  0.01
1997 Cheung JC, Summers CG, Young TL. Myopia Predicts Better Outcome in Persistent Hyperplastic Primary Vitreous Journal of Pediatric Ophthalmology & Strabismus. 34: 170-176. DOI: 10.3928/0191-3913-19970501-08  0.01
1996 Young TL, Himelstein BP, Rebsamen SL, Ruchelli E, Quinn GE, Bunin N. Intraocular Ki-1 Lymphoma in a 2-Year-Old Boy Journal of Pediatric Ophthalmology & Strabismus. 33: 268-270. DOI: 10.3928/0191-3913-19960901-14  0.01
1995 Quinn GE, Berlin JA, Young TL, Ziylan S, Stone RA. Association of intraocular pressure and myopia in children. Ophthalmology. 102: 180-5. PMID 7862404 DOI: 10.1016/S0161-6420(95)31038-X  0.01
1995 Petrig BL, Young TL, Grunwald JE, Quinn GE, Riva CE. Laser Doppler velocimetry in retinal arteries of infants Lasers in Medical Science. 10: 267-272. DOI: 10.1007/BF02133619  0.01
1994 Morasse J, Green RC, Narod S, Young T, Tonin P, Morissette J, Weissenbach J, Khandjian EW, Rousseau F. Poster abstractGenetic heterogeneity in hereditary non-polyposis colon cancer as detected with molecular probes Clinical Biochemistry. 27: 200-201. DOI: 10.1016/0009-9120(94)90066-3  0.01
1993 Young TL, Ziylan S, Schaffer DB. The Ophthalmologic Manifestations of the Cardio-Facio-Cutaneous Syndrome Journal of Pediatric Ophthalmology & Strabismus. 30: 48-52. DOI: 10.3928/0191-3913-19930101-12  0.01
1992 Hertle RW, Katowitz JA, Young TL, Quinn GE, Farber MG. Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome. Ophthalmology. 99: 347-55. PMID 1565446 DOI: 10.1016/S0161-6420(92)31966-9  0.01
1992 Young TL, Schaffer DB, Cohen AR. Infantile Glaucoma Associated With the Diamond-Blackfan Syndrome Journal of Pediatric Ophthalmology & Strabismus. 29: 55-58. DOI: 10.3928/0191-3913-19920101-11  0.01
1990 Young TL, Büchi ER, Kaufman LM, Sugar J, Tso MO. Respiratory epithelium in a cystic choristoma of the limbus. Archives of Ophthalmology (Chicago, Ill. : 1960). 108: 1736-9. PMID 2256846 DOI: 10.1001/archopht.1990.01070140090036  0.01
1990 Young TL, Higginbotham EJ, Zou XL, Farber MD. Effects of topical glaucoma drugs on fistulized rabbit conjunctiva. Ophthalmology. 97: 1423-7. PMID 2255514 DOI: 10.1016/S0161-6420(90)32392-8  0.01
1989 Joondeph BC, Young TL, Saran BR. Multiple scleral ruptures after blunt ocular trauma. American Journal of Ophthalmology. 108: 744. PMID 2596565 DOI: 10.1016/0002-9394(89)90882-9  0.01
1989 Young TL, Robin JB, Holland GN, Hendricks RL, Paschal JF, Engstrom RE, Sugar J. Herpes simplex keratitis in patients with acquired immune deficiency syndrome. Ophthalmology. 96: 1476-9. PMID 2555761 DOI: 10.1016/S0161-6420(89)32706-0  0.01
Hide low-probability matches.