Tracy L. Young-Pearse, Ph.D. - Publications

Neurology Harvard University/Brigham and Women's 
Development, schizophrenia, Alzheimer's disease

280 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
2020 Sanderson JB, De S, Jiang H, Rovere M, Jin M, Zaccagnini L, Hays Watson A, De Boni L, Lagomarsino VN, Young-Pearse TL, Liu X, Pochapsky TC, Hyman BT, Dickson DW, Klenerman D, et al. Analysis of α-synuclein species enriched from cerebral cortex of humans with sporadic dementia with Lewy bodies. Brain Communications. 2: fcaa010. PMID 32280944 DOI: 10.1093/braincomms/fcaa010  0.64
2020 Rice HC, Marcassa G, Chrysidou I, Horré K, Young-Pearse TL, Müller UC, Saito T, Saido TC, Vassar R, de Wit J, De Strooper B. Contribution of GABAergic interneurons to amyloid-β plaque pathology in an APP knock-in mouse model. Molecular Neurodegeneration. 15: 3. PMID 31915042 DOI: 10.1186/S13024-019-0356-Y  0.56
2019 Corbett GT, Wang Z, Hong W, Colom-Cadena M, Rose J, Liao M, Asfaw A, Hall TC, Ding L, DeSousa A, Frosch MP, Collinge J, Harris DA, Perkinton MS, Spires-Jones TL, ... Young-Pearse TL, et al. PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteins. Acta Neuropathologica. PMID 31853635 DOI: 10.1007/S00401-019-02114-9  0.44
2019 Pescosolido MF, Kavanaugh BC, Pochet N, Schmidt M, Jerskey BA, Rogg JM, De Jager PL, Young-Pearse TL, Liu JS, Morrow EM. Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108. PMID 31192222 DOI: 10.1159/000496341  0.8
2018 Srikanth P, Lagomarsino VN, Pearse RV, Liao M, Ghosh S, Nehme R, Seyfried N, Eggan K, Young-Pearse TL. Convergence of independent DISC1 mutations on impaired neurite growth via decreased UNC5D expression. Translational Psychiatry. 8: 245. PMID 30410030 DOI: 10.1038/S41398-018-0281-9  0.44
2018 Jin M, O'Nuallain B, Hong W, Boyd J, Lagomarsino VN, O'Malley TT, Liu W, Vanderburg CR, Frosch MP, Young-Pearse T, Selkoe DJ, Walsh DM. An in vitro paradigm to assess potential anti-Aβ antibodies for Alzheimer's disease. Nature Communications. 9: 2676. PMID 29992960 DOI: 10.1038/S41467-018-05068-W  0.64
2018 Srikanth P, Lagomarsino VN, Muratore CR, Ryu SC, He A, Taylor WM, Zhou C, Arellano M, Young-Pearse TL. Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids. Translational Psychiatry. 8: 77. PMID 29643329 DOI: 10.1038/S41398-018-0122-X  0.44
2018 Guix FX, Corbett GT, Cha DJ, Mustapic M, Liu W, Mengel D, Chen Z, Aikawa E, Young-Pearse T, Kapogiannis D, Selkoe DJ, Walsh DM. Detection of Aggregation-Competent Tau in Neuron-Derived Extracellular Vesicles. International Journal of Molecular Sciences. 19. PMID 29495441 DOI: 10.3390/Ijms19030663  0.64
2017 Muratore CR, Zhou C, Liao M, Fernandez MA, Taylor WM, Lagomarsino VN, Pearse RV, Rice HC, Negri JM, He A, Srikanth P, Callahan DG, Shin T, Zhou M, Bennett DA, ... ... Young-Pearse TL, et al. Cell-type Dependent Alzheimer's Disease Phenotypes: Probing the Biology of Selective Neuronal Vulnerability. Stem Cell Reports. PMID 29153990 DOI: 10.1016/J.Stemcr.2017.10.015  0.64
2017 Wang Z, Jackson RJ, Hong W, Taylor WM, Corbett GT, Moreno A, Liu W, Li S, Frosch MP, Slutsky I, Young-Pearse T, Spires-Jones TL, Walsh DM. Human brain-derived Aβ oligomers bind to synapses and disrupt synaptic activity in a manner that requires APP. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29101243 DOI: 10.1523/Jneurosci.2009-17.2017  0.44
2017 Callahan DG, Taylor WM, Tilearcio M, Cavanaugh T, Selkoe DJ, Young-Pearse TL. Embryonic mosaic deletion of APP results in displaced Reelin-expressing cells in the cerebral cortex. Developmental Biology. PMID 28284905 DOI: 10.1016/J.Ydbio.2017.03.007  0.64
2016 Liao MC, Muratore CR, Gierahn TM, Sullivan SE, Srikanth P, De Jager PL, Love JC, Young-Pearse TL. Single-Cell Detection of Secreted Aβ and sAPPα from Human IPSC-Derived Neurons and Astrocytes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 1730-46. PMID 26843653 DOI: 10.1523/Jneurosci.2735-15.2016  0.8
2015 Young-Pearse TL, Morrow EM. Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities. Current Opinion in Neurobiology. 36: 66-73. PMID 26517284 DOI: 10.1016/J.Conb.2015.10.006  0.8
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  0.6
2015 Sullivan SE, Young-Pearse T. Induced pluripotent stem cells as a discovery tool for Alzheimer׳s disease. Brain Research. PMID 26459988 DOI: 10.1016/J.Brainres.2015.10.005  0.8
2015 Srikanth P, Han K, Callahan DG, Makovkina E, Muratore CR, Lalli MA, Zhou H, Boyd JD, Kosik KS, Selkoe DJ, Young-Pearse TL. Genomic DISC1 Disruption in hiPSCs Alters Wnt Signaling and Neural Cell Fate. Cell Reports. PMID 26299970 DOI: 10.1016/J.Celrep.2015.07.061  0.8
2015 Kanmert D, Cantlon A, Muratore CR, Jin M, O'Malley TT, Lee G, Young-Pearse TL, Selkoe DJ, Walsh DM. C-Terminally Truncated Forms of Tau, But Not Full-Length Tau or Its C-Terminal Fragments, Are Released from Neurons Independently of Cell Death. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 10851-65. PMID 26224867 DOI: 10.1523/Jneurosci.0387-15.2015  0.8
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  0.6
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  0.6
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, 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  0.6
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, 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  0.6
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, 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  0.6
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  0.6
2014 Muratore CR, Srikanth P, Callahan DG, Young-Pearse TL. Comparison and optimization of hiPSC forebrain cortical differentiation protocols. Plos One. 9: e105807. PMID 25165848 DOI: 10.1371/Journal.Pone.0105807  0.8
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  0.6
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  0.6
2014 Preitner N, Quan J, Nowakowski DW, Hancock ML, Shi J, Tcherkezian J, Young-Pearse TL, Flanagan JG. APC is an RNA-binding protein, and its interactome provides a link to neural development and microtubule assembly. Cell. 158: 368-82. PMID 25036633 DOI: 10.1016/J.Cell.2014.05.042  0.8
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, 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  0.6
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  0.6
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, 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  0.6
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  0.6
2014 Srikanth P, Young-Pearse TL. Stem cells on the brain: modeling neurodevelopmental and neurodegenerative diseases using human induced pluripotent stem cells. Journal of Neurogenetics. 28: 5-29. PMID 24628482 DOI: 10.3109/01677063.2014.881358  0.8
2014 Muratore CR, Rice HC, Srikanth P, Callahan DG, Shin T, Benjamin LN, Walsh DM, Selkoe DJ, Young-Pearse TL. The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons. Human Molecular Genetics. 23: 3523-36. PMID 24524897 DOI: 10.1093/Hmg/Ddu064  0.8
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  0.6
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  0.6
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  0.6
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, 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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2013 . Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus. Human Molecular Genetics. 22: 4653-60. PMID 23836780 DOI: 10.1093/Hmg/Ddt293  0.6
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, et al. Genetic loci for retinal arteriolar microcirculation. Plos One. 8: e65804. PMID 23776548 DOI: 10.1371/Journal.Pone.0065804  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
2013 Rice HC, Young-Pearse TL, Selkoe DJ. Systematic evaluation of candidate ligands regulating ectodomain shedding of amyloid precursor protein. Biochemistry. 52: 3264-77. PMID 23597280 DOI: 10.1021/Bi400165F  0.8
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2012 Rice HC, Townsend M, Bai J, Suth S, Cavanaugh W, Selkoe DJ, Young-Pearse TL. Pancortins interact with amyloid precursor protein and modulate cortical cell migration. Development (Cambridge, England). 139: 3986-96. PMID 22992957 DOI: 10.1242/Dev.082909  0.8
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  0.6
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  0.6
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, 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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
2012 Taniguchi Y, Young-Pearse T, Sawa A, Kamiya A. In utero electroporation as a tool for genetic manipulation in vivo to study psychiatric disorders: from genes to circuits and behaviors. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 18: 169-79. PMID 21551077 DOI: 10.1177/1073858411399925  0.8
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, 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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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, 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  0.6
2010 Rice H, Suth S, Cavanaugh W, Bai J, Young-Pearse TL. In utero electroporation followed by primary neuronal culture for studying gene function in subset of cortical neurons. Journal of Visualized Experiments : Jove. PMID 20972409 DOI: 10.3791/2103  0.8
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  0.6
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  0.6
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, 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  0.6
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, 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  0.6
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  0.6
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  0.6
2010 Young-Pearse TL, Suth S, Luth ES, Sawa A, Selkoe DJ. Biochemical and functional interaction of disrupted-in-schizophrenia 1 and amyloid precursor protein regulates neuronal migration during mammalian cortical development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 10431-40. PMID 20685985 DOI: 10.1523/Jneurosci.1445-10.2010  0.8
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
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, 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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2008 Young-Pearse TL, Chen AC, Chang R, Marquez C, Selkoe DJ. Secreted APP regulates the function of full-length APP in neurite outgrowth through interaction with integrin beta1. Neural Development. 3: 15. PMID 18573216 DOI: 10.1186/1749-8104-3-15  0.8
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2007 Young-Pearse TL, Bai J, Chang R, Zheng JB, LoTurco JJ, Selkoe DJ. A critical function for beta-amyloid precursor protein in neuronal migration revealed by in utero RNA interference. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 14459-69. PMID 18160654 DOI: 10.1523/Jneurosci.4701-07.2007  0.8
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2006 Young-Pearse TL, Ivic L, Kriegstein AR, Cepko CL. Characterization of mice with targeted deletion of glycine receptor alpha 2. Molecular and Cellular Biology. 26: 5728-34. PMID 16847326 DOI: 10.1128/Mcb.00237-06  0.8
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
2005 Lawrence MG, Kramarevsky NY, Christiansen SP, Wright MM, Young TL, Summers CG. Glaucoma following cataract surgery in children: surgically modifiable risk factors. Transactions of the American Ophthalmological Society. 103: 46-55. PMID 17057787  0.6
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  0.6
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  0.6
2005 Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL. Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity. Molecular Vision. 11: 501-8. PMID 16052165  0.6
2005 Nelin LD, Chicoine LG, Reber KM, English BK, Young TL, Liu Y. Cytokine-induced endothelial arginase expression is dependent on epidermal growth factor receptor. American Journal of Respiratory Cell and Molecular Biology. 33: 394-401. PMID 15994432 DOI: 10.1165/rcmb.2005-0039OC  0.6
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  0.6
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  0.6
2005 Shantakumar S, Gammon MD, Eng SM, Sagiv SK, Gaudet MM, Teitelbaum SL, Britton JA, Terry MB, Paykin A, Young TL, Wang LW, Wang Q, Stellman SD, Beyea J, Hatch M, et al. Residential environmental exposures and other characteristics associated with detectable PAH-DNA adducts in peripheral mononuclear cells in a population-based sample of adult females. Journal of Exposure Analysis and Environmental Epidemiology. 15: 482-90. PMID 15856074 DOI: 10.1038/Sj.Jea.7500426  0.6
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  0.6
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  0.6
2005 Nagy AL, Neriani KE, Young TL. Effects of target and distractor heterogeneity on search for a color target. Vision Research. 45: 1885-99. PMID 15797778 DOI: 10.1016/j.visres.2005.01.007  0.6
2005 Young TL, Matsuda T, Cepko CL. The noncoding RNA taurine upregulated gene 1 is required for differentiation of the murine retina. Current Biology : Cb. 15: 501-12. PMID 15797018 DOI: 10.1016/j.cub.2005.02.027  0.6
2005 Scavello GS, Paluru PC, Zhou J, White PS, Rappaport EF, Young TL. Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes. Molecular Vision. 11: 97-110. PMID 15723005  0.6
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  0.6
2004 Young TL. Dissecting the genetics of human high myopia: a molecular biologic approach. Transactions of the American Ophthalmological Society. 102: 423-45. PMID 15747770  0.6
2004 Paluru PC, Scavello GS, Ganter WR, Young TL. Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia. Molecular Vision. 10: 917-22. PMID 15592176  0.6
2004 Nagy AL, Neriani KE, Young TL. Color mechanisms used in selecting stimuli for attention and making discriminations. Visual Neuroscience. 21: 295-9. PMID 15518203 DOI: 10.1017/S0952523804213190  0.6
2004 Rowan S, Chen CM, Young TL, Fisher DE, Cepko CL. Transdifferentiation of the retina into pigmented cells in ocular retardation mice defines a new function of the homeodomain gene Chx10. Development (Cambridge, England). 131: 5139-52. PMID 15459106 DOI: 10.1242/Dev.01300  0.6
2004 Ahmed ZM, Li XC, Powell SD, Riazuddin S, Young TL, Ramzan K, Ahmad Z, Luscombe S, Dhillon K, MacLaren L, Ploplis B, Shotland LI, Ives E, Riazuddin S, Friedman TB, et al. Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan. Bmc Medical Genetics. 5: 24. PMID 15447792 DOI: 10.1186/1471-2350-5-24  0.6
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  0.6
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  0.6
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  0.6
2004 Young TL, Cepko CL. A role for ligand-gated ion channels in rod photoreceptor development. Neuron. 41: 867-79. PMID 15046720 DOI: 10.1016/S0896-6273(04)00141-2  0.6
2004 Young TL, Scavello GS, Paluru PC, Choi JD, Rappaport EF, Rada JA. Microarray analysis of gene expression in human donor sclera. Molecular Vision. 10: 163-76. PMID 15041956  0.6
2004 Chicoine LG, Paffett ML, Young TL, Nelin LD. Arginase inhibition increases nitric oxide production in bovine pulmonary arterial endothelial cells. American Journal of Physiology. Lung Cellular and Molecular Physiology. 287: L60-8. PMID 14977627 DOI: 10.1152/Ajplung.00194.2003  0.6
2004 Hawkins JL, Young TL. Collagenous colitis treated successfully with budesonide. Tennessee Medicine : Journal of the Tennessee Medical Association. 97: 29-30. PMID 14968684  0.6
2004 Livesey FJ, Young TL, Cepko CL. An analysis of the gene expression program of mammalian neural progenitor cells. Proceedings of the National Academy of Sciences of the United States of America. 101: 1374-9. PMID 14734810 DOI: 10.1073/pnas.0307014101  0.6
2003 Hennessy MB, Young TL, O'Leary SK, Maken DS. Social preferences of developing guinea pigs (Cavia porcellus) from the preweaning to the periadolescent periods. Journal of Comparative Psychology (Washington, D.C. : 1983). 117: 406-13. PMID 14717642 DOI: 10.1037/0735-7036.117.4.406  0.6
2003 Young TL, Ireson C. Effectiveness of school-based telehealth care in urban and rural elementary schools. Pediatrics. 112: 1088-94. PMID 14595051 DOI: 10.1542/peds.112.5.1088  0.6
2003 Young TL, Guo XD, King RA, Johnson JM, Rada JA. Identification of genes expressed in a human scleral cDNA library. Molecular Vision. 9: 508-14. PMID 14551531  0.6
2003 Young TL. Ophthalmic genetics/inherited eye disease. Current Opinion in Ophthalmology. 14: 296-303. PMID 14502058 DOI: 10.1097/00055735-200310000-00011  0.6
2003 Cryns K, Sivakumaran TA, Van den Ouweland JM, Pennings RJ, Cremers CW, Flothmann K, Young TL, Smith RJ, Lesperance MM, Van Camp G. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Human Mutation. 22: 275-87. PMID 12955714 DOI: 10.1002/Humu.10258  0.6
2003 Weiserbs KF, Jacobson JS, Begg MD, Wang LW, Wang Q, Agrawal M, Norkus EP, Young TL, Santella RM. A cross-sectional study of polycyclic aromatic hydrocarbon-DNA adducts and polymorphism of glutathione S-transferases among heavy smokers by race/ethnicity. Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals. 8: 142-55. PMID 12775499 DOI: 10.1080/1354750031000086269  0.6
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  0.6
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  0.6
2002 Hennessy MB, Voith VL, Young TL, Hawke JL, Centrone J, McDowell AL, Linden F, Davenport GM. Exploring human interaction and diet effects on the behavior of dogs in a public animal shelter. Journal of Applied Animal Welfare Science : Jaaws. 5: 253-73. PMID 16221077 DOI: 10.1207/S15327604Jaws0504_01  0.6
2002 Hennessy MB, Voith VL, Hawke JL, Young TL, Centrone J, McDowell AL, Linden F, Davenport GM. Effects of a program of human interaction and alterations in diet composition on activity of the hypothalamic-pituitary-adrenal axis in dogs housed in a public animal shelter. Journal of the American Veterinary Medical Association. 221: 65-71. PMID 12420826 DOI: 10.2460/Javma.2002.221.65  0.6
2002 Pronovost PJ, Angus DC, Dorman T, Robinson KA, Dremsizov TT, Young TL. Physician staffing patterns and clinical outcomes in critically ill patients: a systematic review. Jama. 288: 2151-62. PMID 12413375 DOI: 10.1001/Jama.288.17.2151  0.6
2002 Gammon MD, Santella RM, Neugut AI, Eng SM, Teitelbaum SL, Paykin A, Levin B, Terry MB, Young TL, Wang LW, Wang Q, Britton JA, Wolff MS, Stellman SD, Hatch M, et al. Environmental toxins and breast cancer on Long Island. I. Polycyclic aromatic hydrocarbon DNA adducts. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 11: 677-85. PMID 12163319  0.6
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  0.6
2002 Scott RL, Butcher JN, Young TL, Gomez N. The Hispanic MMPI-A across five countries. Journal of Clinical Psychology. 58: 407-17. PMID 11920694 DOI: 10.1002/Jclp.1152  0.6
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  0.6
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  0.6
2001 Young TL, Ives E, Lynch E, Person R, Snook S, MacLaren L, Cater T, Griffin A, Fernandez B, Lee MK, King MC, Cator T. Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. Human Molecular Genetics. 10: 2509-14. PMID 11709538 DOI: 10.1093/Hmg/10.22.2509  0.6
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.  0.6
2001 Young TL, D'angelo SL, Davis J. Impact of a school-based health center on emergency department use by elementary school students. The Journal of School Health. 71: 196-8. PMID 11393932  0.6
2001 Washington RL, Bernhardt DT, Gomez J, Johnson MD, Martin TJ, Rowland TW, Small E, LeBlanc C, Krein C, Malina R, Young JC, Reed FE, Anderson S, Bolduc S, Bar-Or O, et al. Organized sports for children and preadolescents. Pediatrics. 107: 1459-62. PMID 11389277 DOI: 10.1542/peds.107.6.1459  0.6
2000 Jacobson JS, Begg MD, Wang LW, Wang Q, Agarwal M, Norkus E, Singh VN, Young TL, Yang D, Santella RM. Effects of a 6-month vitamin intervention on DNA damage in heavy smokers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 9: 1303-11. PMID 11142415  0.6
2000 Ramjiganesh T, Roy S, Nicolosi RJ, Young TL, McIntyre JC, Fernandez ML. Corn husk oil lowers plasma LDL cholesterol concentrations by decreasing cholesterol absorption and altering hepatic cholesterol metabolism in guinea pigs. The Journal of Nutritional Biochemistry. 11: 358-66. PMID 11044630 DOI: 10.1016/S0955-2863(00)00091-7  0.6
2000 Halpern MT, Khan ZM, Young TL, Battista C. Economic model of sustained-release bupropion hydrochloride in health plan and work site smoking-cessation programs. American Journal of Health-System Pharmacy : Ajhp : Official Journal of the American Society of Health-System Pharmacists. 57: 1421-9. PMID 10938982  0.6
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 and Strabismus. 37: 149-55. PMID 10845415  0.6
2000 Santella RM, Gammon MD, Zhang YJ, Motykiewicz G, Young TL, Hayes SC, Terry MB, Schoenberg JB, Brinton LA, Bose S, Teitelbaum SL, Hibshoosh H. Immunohistochemical analysis of polycyclic aromatic hydrocarbon-DNA adducts in breast tumor tissue. Cancer Letters. 154: 143-9. PMID 10806302 DOI: 10.1016/S0304-3835(00)00367-0  0.6
2000 Belliveau MJ, Young TL, Cepko CL. Late retinal progenitor cells show intrinsic limitations in the production of cell types and the kinetics of opsin synthesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 2247-54. PMID 10704500 DOI: 10.1523/Jneurosci.20-06-02247.2000  0.6
1999 Young TL, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM. American Journal of Human Genetics. 65: 1680-7. PMID 10577922 DOI: 10.1086/302686  0.6
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  0.6
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  0.6
1999 Adams EK, Young TL. Costs of smoking: a focus on maternal, childhood, and other short-run costs. Medical Care Research and Review : McRr. 56: 3-29. PMID 10189774  0.6
1999 Young TL, Penney L, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31. American Journal of Human Genetics. 64: 900-4. PMID 10053027 DOI: 10.1086/302301  0.6
1999 Woods MO, Young TL, Parfrey PS, Hefferton D, Green JS, Davidson WS. Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus. Genomics. 55: 2-9. PMID 9888993 DOI: 10.1006/Geno.1998.5626  0.6
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  0.6
1998 Young TL, Zimmerman R. Clueless: parental knowledge of risk behaviors of middle school students. Archives of Pediatrics & Adolescent Medicine. 152: 1137-9. PMID 9811294 DOI: 10.1001/Archpedi.152.11.1137  0.6
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  0.6
1998 Kushner BJ, Arthur BW, Mazow ML, Medow NB, Young TL. Grand rounds #51: a case of consecutive exotropia after medial rectus recession for Duane syndrome. Binocular Vision & Strabismus Quarterly. 13: 188-92. PMID 9780416  0.6
1998 Whyatt RM, Bell DA, Jedrychowski W, Santella RM, Garte SJ, Cosma G, Manchester DK, Young TL, Cooper TB, Ottman R, Perera FP. Polycyclic aromatic hydrocarbon-DNA adducts in human placenta and modulation by CYP1A1 induction and genotype. Carcinogenesis. 19: 1389-92. PMID 9744534 DOI: 10.1093/Carcin/19.8.1389  0.6
1998 Young TL, Woods MO, Parfrey PS, Green JS, O'Leary E, Hefferton D, Davidson WS. Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype. American Journal of Medical Genetics. 78: 461-7. PMID 9714014 DOI: 10.1002/(Sici)1096-8628(19980806)78:5<461::Aid-Ajmg12>3.0.Co;2-D  0.6
1998 Whyatt RM, Santella RM, Jedrychowski W, Garte SJ, Bell DA, Ottman R, Gladek-Yarborough A, Cosma G, Young TL, Cooper TB, Randall MC, Manchester DK, Perera FP. Relationship between ambient air pollution and DNA damage in Polish mothers and newborns. Environmental Health Perspectives. 106: 821-6. PMID 9646044 DOI: 10.2307/3434196  0.6
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  0.6
1998 Simpson KJ, Young TL. The Harrison Healthy Kids Center: a comprehensive elementary school-based health program. The Journal of School Health. 68: 116-9. PMID 9608454  0.6
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  0.6
1998 Richardson SC, Young TL. Liver biopsy-associated hemobilia treated conservatively. Tennessee Medicine : Journal of the Tennessee Medical Association. 91: 141-2. PMID 9564248  0.6
1998 McQuaid K, Young TL. Rigid gas permeable contact lens changes in the aphakic infant. The Clao Journal : Official Publication of the Contact Lens Association of Ophthalmologists, Inc. 24: 36-40. PMID 9474452  0.6
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  0.6
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  0.6
1997 Dickey C, Santella RM, Hattis D, Tang D, Hsu Y, Cooper T, Young TL, Perera FP. Variability in PAH-DNA adduct measurements in peripheral mononuclear cells: implications for quantitative cancer risk assessment. Risk Analysis : An Official Publication of the Society For Risk Analysis. 17: 649-56. PMID 9404054 DOI: 10.1111/J.1539-6924.1997.Tb00905.X  0.6
1997 Mathieu A, Payne JF, Fancey LL, Santella RM, Young TL. Polycyclic aromatic hydrocarbon-DNA adducts in beluga whales from the Arctic. Journal of Toxicology and Environmental Health. 51: 1-4. PMID 9169056 DOI: 10.1080/00984109708984006  0.6
1997 Cheung JC, Summers CG, Young TL. Myopia predicts better outcome in persistent hyperplastic primary vitreous. Journal of Pediatric Ophthalmology and Strabismus. 34: 170-6. PMID 9168422  0.6
1997 Mooney LA, Bell DA, Santella RM, Van Bennekum AM, Ottman R, Paik M, Blaner WS, Lucier GW, Covey L, Young TL, Cooper TB, Glassman AH, Perera FP. Contribution of genetic and nutritional factors to DNA damage in heavy smokers. Carcinogenesis. 18: 503-9. PMID 9067549 DOI: 10.1093/Carcin/18.3.503  0.6
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  0.6
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 and Strabismus. 33: 268-70. PMID 8880623  0.6
1996 Mumford JL, Williams K, Wilcosky TC, Everson RB, Young TL, Santella RM. A sensitive color ELISA for detecting polycyclic aromatic hydrocarbon-DNA adducts in human tissues. Mutation Research. 359: 171-7. PMID 8618549 DOI: 10.1016/S0165-1161(96)90264-2  0.6
1995 Santella RM, Perera FP, Young TL, Zhang YJ, Chiamprasert S, Tang D, Wang LW, Beachman A, Lin JH, DeLeo VA. Polycyclic aromatic hydrocarbon-DNA and protein adducts in coal tar treated patients and controls and their relationship to glutathione S-transferase genotype. Mutation Research. 334: 117-24. PMID 7885362 DOI: 10.1016/0165-1161(95)90001-2  0.6
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  0.6
1995 Tang D, Santella RM, Blackwood AM, Young TL, Mayer J, Jaretzki A, Grantham S, Tsai WY, Perera FP. A molecular epidemiological case-control study of lung cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 4: 341-6. PMID 7655328  0.6
1995 Rush DR, Stelmach WJ, Young TL, Kirchdoerfer LJ, Scott-Lennox J, Holverson HE, Sabesin SM, Nicholas TA. Clinical effectiveness and quality of life with ranitidine vs placebo in gastroesophageal reflux disease patients: a clinical experience network (CEN) study. The Journal of Family Practice. 41: 126-36. PMID 7636452  0.6
1994 Green RC, Narod SA, Morasse J, Young TL, Cox J, Fitzgerald GW, Tonin P, Ginsburg O, Miller S, Jothy S. Hereditary nonpolyposis colon cancer: analysis of linkage to 2p15-16 places the COCA1 locus telomeric to D2S123 and reveals genetic heterogeneity in seven Canadian families. American Journal of Human Genetics. 54: 1067-77. PMID 8198129  0.6
1994 Grinberg-Funes RA, Singh VN, Perera FP, Bell DA, Young TL, Dickey C, Wang LW, Santella RM. Polycyclic aromatic hydrocarbon-DNA adducts in smokers and their relationship to micronutrient levels and the glutathione-S-transferase M1 genotype. Carcinogenesis. 15: 2449-54. PMID 7955090 DOI: 10.1093/carcin/15.11.2449  0.6
1993 Kozma CM, Schulz RM, Dickson WM, Dye JT, Cox ER, Holdford DA, Michael L, Yates WN, Young TL. Economic impact of cost-containment strategies in third party programmes in the US. Part II. Pharmacoeconomics. 4: 187-202. PMID 10146922 DOI: 10.2165/00019053-199304030-00004  0.6
1993 Young TL, Ziylan S, Schaffer DB. The ophthalmologic manifestations of the cardio-facio-cutaneous syndrome. Journal of Pediatric Ophthalmology and Strabismus. 30: 48-52. PMID 8455127  0.6
1993 Santella RM, Hemminki K, Tang DL, Paik M, Ottman R, Young TL, Savela K, Vodickova L, Dickey C, Whyatt R. Polycyclic aromatic hydrocarbon-DNA adducts in white blood cells and urinary 1-hydroxypyrene in foundry workers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 2: 59-62. PMID 8420613  0.6
1993 Mumford JL, Lee X, Lewtas J, Young TL, Santella RM. DNA adducts as biomarkers for assessing exposure to polycyclic aromatic hydrocarbons in tissues from Xuan Wei women with high exposure to coal combustion emissions and high lung cancer mortality. Environmental Health Perspectives. 99: 83-7. PMID 8319664  0.6
1992 Young TL, Schaffer DB, Cohen AR. Infantile glaucoma associated with the Diamond-Blackfan syndrome. Journal of Pediatric Ophthalmology and Strabismus. 29: 55-8. PMID 1583582  0.6
1992 Hertle RW, Katowitz JA, Young TL, Quinn GE, Farber MG. Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome. Ophthalmology. 99: 347-55. PMID 1565446  0.6
1992 Perera FP, Hemminki K, Gryzbowska E, Motykiewicz G, Michalska J, Santella RM, Young TL, Dickey C, Brandt-Rauf P, De Vivo I. Molecular and genetic damage in humans from environmental pollution in Poland. Nature. 360: 256-8. PMID 1436106 DOI: 10.1038/360256A0  0.6
1992 Santella RM, Grinberg-Funes RA, Young TL, Dickey C, Singh VN, Wang LW, Perera FP. Cigarette smoking related polycyclic aromatic hydrocarbon-DNA adducts in peripheral mononuclear cells. Carcinogenesis. 13: 2041-5. PMID 1423873 DOI: 10.1093/carcin/13.11.2041  0.6
1992 Klegar KL, Young TL. Pill-induced esophageal injury. Journal of the Tennessee Medical Association. 85: 417-8. PMID 1405622  0.6
1991 Santella RM, Zhang YJ, Young TL, Lee BM, Lu XQ. Monitoring human exposure to environmental carcinogens. Advances in Experimental Medicine and Biology. 283: 165-81. PMID 2068984  0.6
1991 Perera F, Mayer J, Santella RM, Brenner D, Jeffrey A, Latriano L, Smith S, Warburton D, Young TL, Tsai WY. Biologic markers in risk assessment for environmental carcinogens. Environmental Health Perspectives. 90: 247-54. PMID 2050068 DOI: 10.2307/3430875  0.6
1990 Hemminki K, Randerath K, Reddy MV, Putman KL, Santella RM, Perera FP, Young TL, Phillips DH, Hewer A, Savela K. Postlabeling and immunoassay analysis of polycyclic aromatic hydrocarbons--adducts of deoxyribonucleic acid in white blood cells of foundry workers. Scandinavian Journal of Work, Environment & Health. 16: 158-62. PMID 2382118 DOI: 10.5271/sjweh.1798  0.6
1990 Santella RM, Yang XY, Hsieh LL, Young TL, Lu XQ, Stefanidis M, Perera FP. Immunologic methods for the detection of carcinogen adducts in humans. Basic Life Sciences. 53: 33-44. PMID 2282041  0.6
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  0.6
1990 Young TL, Higginbotham EJ, Zou XL, Farber MD. Effects of topical glaucoma drugs on fistulized rabbit conjunctiva. Ophthalmology. 97: 1423-7. PMID 2255514  0.6
1990 Perera F, Jeffrey A, Santella RM, Brenner D, Mayer J, Latriano L, Smith S, Young TL, Tsai WY, Hemminki K. Macromolecular adducts and related biomarkers in biomonitoring and epidemiology of complex exposures. Iarc Scientific Publications. 164-80. PMID 2228114  0.6
1990 Young TL, Habraken Y, Ludlum DB, Santella RM. Development of monoclonal antibodies recognizing 7-(2-hydroxyethyl)guanine and imidazole ring-opened 7-(2-hydroxyethyl)guanine. Carcinogenesis. 11: 1685-9. PMID 2208583 DOI: 10.1093/carcin/11.10.1685  0.6
1990 Santella RM, Yang XY, Hsieh LL, Young TL. Immunologic methods for the detection of carcinogen adducts in humans. Progress in Clinical and Biological Research. 340: 247-57. PMID 2199982  0.6
1989 Young TL, Lubitz RM. Cylindrical battery ingestion: a case of endoscopic retrieval. Journal of the Tennessee Medical Association. 82: 415-6. PMID 2761248  0.6
1989 Perera F, Mayer J, Jaretzki A, Hearne S, Brenner D, Young TL, Fischman HK, Grimes M, Grantham S, Tang MX. Comparison of DNA adducts and sister chromatid exchange in lung cancer cases and controls. Cancer Research. 49: 4446-51. PMID 2743334  0.6
1989 Joondeph BC, Young TL, Saran BR. Multiple scleral ruptures after blunt ocular trauma. American Journal of Ophthalmology. 108: 744. PMID 2596565  0.6
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  0.6
1988 Young TL, Santella RM. Development of techniques to monitor for exposure to vinyl chloride: monoclonal antibodies to ethenoadenosine and ethenocytidine. Carcinogenesis. 9: 589-92. PMID 3356066 DOI: 10.1093/carcin/9.4.589  0.6
1988 Perera FP, Santella RM, Brenner D, Young TL, Weinstein IB. Application of biological markers to the study of lung cancer causation and prevention. Iarc Scientific Publications. 451-9. PMID 3198231  0.6
1988 Santella RM, Weston A, Perera FP, Trivers GT, Harris CC, Young TL, Nguyen D, Lee BM, Poirier MC. Interlaboratory comparison of antisera and immunoassays for benzo[a]pyrene-diol-epoxide-I-modified DNA. Carcinogenesis. 9: 1265-9. PMID 3133129 DOI: 10.1093/carcin/9.7.1265  0.6
1988 Perera FP, Hemminki K, Young TL, Brenner D, Kelly G, Santella RM. Detection of polycyclic aromatic hydrocarbon-DNA adducts in white blood cells of foundry workers. Cancer Research. 48: 2288-91. PMID 3127049  0.6
1986 Young TL, Rogers KD. School performance characteristics preceding onset of smoking in high school students. American Journal of Diseases of Children (1960). 140: 257-9. PMID 3946359 DOI: 10.1001/archpedi.1986.02140170083038  0.6
1985 Young TL, Achkar E, Tuthill R, Ferguson DR. Chronic active hepatitis induced by nitrofurantoin. Cleveland Clinic Quarterly. 52: 253-6. PMID 4028427  0.6
1983 Dyer ML, Young TL, Kattine AA, Wilson DD. Blastomycosis in a Papanicolaou Smear. Report of a case with possible venereal transmission. Acta Cytologica. 27: 285-7. PMID 6575545  0.6
1982 Gordon R, Burford IR, Young TL. Uptake of Lipids by the Entomophilic Nematode Romanomermis culicivorax. Journal of Nematology. 14: 492-5. PMID 19295741  0.6
1980 Young TL, Reisinger KS. Wall socket electrical burns: relevance to health education? Pediatrics. 65: 825-7. PMID 7367094  0.6
1974 Young TL, Huang FK, Shan C, Yeh L. [Clinicopathological conference no. 19: dizziness, headache, vomiting and obscure vision]. Zhonghua Yi Xue Za Zhi. 580-4. PMID 4214143  0.6
1974 Young TL, Huang FK, Shan C, Yeh L. [Clinicopathological conference. No. 16. Fever, right-upper side abdominal pain, hepatomegaly]. Zhonghua Yi Xue Za Zhi. 6: 381-4. PMID 4211346  0.6
1971 Young TL. Endodontic cultures: can they be justified? Dental Student. 49: 40 passim. PMID 5278425  0.6
1971 Young TL. Endodontic cultures: can they be justified? Contact Point. 65-7. PMID 5277242  0.6
1963 YOUNG TL. Family neuropsychiatry. Diseases of the Nervous System. 24: 243-6. PMID 14002833  0.6
1952 SOMMERS SC, YOUNG TL. Oxyphil parathyroid adenomas. The American Journal of Pathology. 28: 673-89. PMID 14943803  0.6
1951 YOUNG TL. Insomnia. The New Orleans Medical and Surgical Journal. 104: 195-7. PMID 14882512  0.6
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