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Results: 1 to 20 of 256

1.

Genetic Variants Associated with Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants.

Hartnett ME, Morrison MA, Smith S, Yanovitch TL, Young TL, Colaizy T, Momany A, Dagle J, Carlo WA, Clark EA, Page GP, Murray J, DeAngelis MM, Cotten CM.

Invest Ophthalmol Vis Sci. 2014 Aug 12. pii: IOVS-14-14841. doi: 10.1167/iovs.14-14841. [Epub ahead of print]

PMID:
25118269
[PubMed - as supplied by publisher]
2.

Myopia in Young Adults Is Inversely Related to an Objective Marker of Ocular Sun Exposure: The Western Australian Raine Cohort Study.

McKnight CM, Sherwin JC, Yazar S, Forward H, Tan AX, Hewitt AW, Pennell CE, McAllister IL, Young TL, Coroneo MT, Mackey DA.

Am J Ophthalmol. 2014 Jul 26. pii: S0002-9394(14)00454-1. doi: 10.1016/j.ajo.2014.07.033. [Epub ahead of print]

PMID:
25072831
[PubMed - as supplied by publisher]
3.

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.

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, Corre T, de Boer RA, Goel A, Johnson T, Khor CC; LifeLines Cohort Study, Lluís-Ganella C, Luan J, Lyytikäinen LP, Nolte IM, Sim X, Sõber S, van der Most PJ, Verweij N, Zhao JH, Amin N, Boerwinkle E, Bouchard C, Dehghan A, Eiriksdottir G, Elosua R, Franco OH, Gieger C, Harris TB, Hercberg S, Hofman A, James AL, Johnson AD, Kähönen M, Khaw KT, Kutalik Z, Larson MG, Launer LJ, Li G, Liu J, Liu K, Morrison AC, Navis G, Ong RT, Papanicolau GJ, Penninx BW, Psaty BM, Raffel LJ, Raitakari OT, Rice K, Rivadeneira F, Rose LM, Sanna S, Scott RA, Siscovick DS, Stolk RP, Uitterlinden AG, Vaidya D, van der Klauw MM, Vasan RS, Vithana EN, Völker U, Völzke H, Watkins H, Young TL, Aung T, Bochud M, Farrall M, Hartman CA, Laan M, Lakatta EG, Lehtimäki T, Loos RJ, Lucas G, Meneton P, Palmer LJ, Rettig R, Snieder H, Tai ES, Teo YY, van der Harst P, Wareham NJ, Wijmenga C, Wong TY, Fornage M, Gudnason V, Levy D, Palmas W, Ridker PM, Rotter JI, van Duijn CM, Witteman JC, Chakravarti A, Rao DC.

Am J Hum Genet. 2014 Jul 3;95(1):24-38. doi: 10.1016/j.ajhg.2014.05.010. Epub 2014 Jun 19.

PMID:
24954895
[PubMed - in process]
4.

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.

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, Guo X, Sheu WH, Delahanty R, Guo X, Kubo M, Yamamoto K, Ohkubo T, Go MJ, Liu JJ, Gan W, Chen CC, Gao Y, Li S, Lee NR, Wu C, Zhou X, Song H, Yao J, Lee IT, Long J, Tsunoda T, Akiyama K, Takashima N, Cho YS, Ong RT, Lu L, Chen CH, Tan A, Rice TK, Adair LS, Gui L, Allison M, Lee WJ, Cai Q, Isomura M, Umemura S, Kim YJ, Seielstad M, Hixson J, Xiang YB, Isono M, Kim BJ, Sim X, Lu W, Nabika T, Lee J, Lim WY, Gao YT, Takayanagi R, Kang DH, Wong TY, Hsiung CA, Wu IC, Juang JM, Shi J, Choi BY, Aung T, Hu F, Kim MK, Lim WY, Wang TD, Shin MH, Lee J, Ji BT, Lee YH, Young TL, Shin DH, Chun BY, Cho MC, Han BG, Hwu CM, Assimes TL, Absher D, Yan X, Kim E, Kuo JZ, Kwon S, Taylor KD, Chen YD, Rotter JI, Qi L, Zhu D, Wu T, Mohlke KL, Gu D, Mo Z, Wu JY, Lin X, Miki T, Tai ES, Lee JY, Kato N, Shu XO, Tanaka T.

Hum Mol Genet. 2014 May 26. pii: ddu248. [Epub ahead of print]

PMID:
24861553
[PubMed - as supplied by publisher]
5.

X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.

Stanton SG, Griffin A, Stockley TL, Brown C, Young TL, Benteau T, Abdelfatah N.

Am J Audiol. 2014 Jun;23(2):190-200. doi: 10.1044/2014_AJA-13-0040.

PMID:
24687041
[PubMed - in process]
6.

Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.

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, Liu J, Liao J, Ye X, Wang Y, Lu L, Young TL, Lee J, Thai AC, Cheng CY, van Dam RM, Friedlander Y, Heng CK, Koh WP, Chen CH, Chang LC, Pan WH, Qi Q, Isono M, Zheng W, Cai Q, Gao Y, Yamamoto K, Ohnaka K, Takayanagi R, Kita Y, Ueshima H, Hsiung CA, Cui J, Sheu WH, Rotter JI, Chen YD, Hsu C, Okada Y, Kubo M, Takahashi A, Tanaka T, van Rooij FJ, Ganesh SK, Huang J, Huang T, Yuan J, Hwang JY; CHARGE Hematology Working Group, Gross MD, Assimes TL, Miki T, Shu XO, Qi L, Chen YT, Lin X, Aung T, Wong TY, Teo YY, Kim BJ, Kato N, Tai ES.

Diabetes. 2014 Jul;63(7):2551-62. doi: 10.2337/db13-1815. Epub 2014 Mar 19.

PMID:
24647736
[PubMed - in process]
7.

What is the appropriate age cut-off for cycloplegia in refraction?

Sanfilippo PG, Chu BS, Bigault O, Kearns LS, Boon MY, Young TL, Hammond CJ, Hewitt AW, Mackey DA.

Acta Ophthalmol. 2014 Sep;92(6):e458-62. doi: 10.1111/aos.12388. Epub 2014 Mar 19.

PMID:
24641244
[PubMed - in process]
8.

The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.

Milting H, Klauke B, Christensen AH, Müsebeck J, Walhorn V, Grannemann S, Münnich T, Sarić T, Rasmussen TB, Jensen HK, Mogensen J, Baecker C, Romaker E, Laser KT, Zu Knyphausen E, Kassner A, Gummert J, Judge DP, Connors S, Hodgkinson K, Young TL, van der Zwaag PA, van Tintelen JP, Anselmetti D.

Eur Heart J. 2014 Mar 27. [Epub ahead of print]

PMID:
24598986
[PubMed - as supplied by publisher]
9.

A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort.

Nag A, Venturini C, Small KS; International Glaucoma Genetics Consortium, Young TL, Viswanathan AC, Mackey DA, Hysi PG, Hammond C.

Hum Mol Genet. 2014 Jun 15;23(12):3343-8. doi: 10.1093/hmg/ddu050. Epub 2014 Feb 11.

PMID:
24518671
[PubMed - in process]
Free PMC Article
10.

Refraction issues in childhood: when to prescribe glasses.

Choy AP, Wasserman BN, Young TL, Nelson LB.

J Pediatr Ophthalmol Strabismus. 2014 Jan-Feb;51(1):7-9. doi: 10.3928/01913913-20130719-01. No abstract available.

PMID:
24512587
[PubMed - indexed for MEDLINE]
11.

Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts.

Hysi PG, Mahroo OA, Cumberland P, Wojciechowski R, Williams KM, Young TL, Mackey DA, Rahi JS, Hammond CJ.

JAMA Ophthalmol. 2014 Jan;132(1):50-6. doi: 10.1001/jamaophthalmol.2013.6022.

PMID:
24264139
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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.

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, Wong TY, Teo YY, Tai ES.

PLoS One. 2013 Nov 7;8(11):e79767. doi: 10.1371/journal.pone.0079767. eCollection 2013.

PMID:
24244560
[PubMed - in process]
Free PMC Article
13.

Scleral micro-RNA signatures in adult and fetal eyes.

Metlapally R, Gonzalez P, Hawthorne FA, Tran-Viet KN, Wildsoet CF, Young TL.

PLoS One. 2013 Oct 21;8(10):e78984. doi: 10.1371/journal.pone.0078984. eCollection 2013.

PMID:
24205357
[PubMed - in process]
Free PMC Article
14.

Birth order and myopia.

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.

Ophthalmic Epidemiol. 2013 Dec;20(6):375-84. doi: 10.3109/09286586.2013.848457. Epub 2013 Oct 29.

PMID:
24168726
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.

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, Timpson NJ, Evans DM, Montgomery GW, Mishra A, Wang YX, Wang JJ, Rochtchina E, Polasek O, Wright AF, Amin N, van Leeuwen EM, Wilson JF, Pennell CE, van Duijn CM, de Jong PT, Vingerling JR, Zhou X, Chen P, Li R, Tay WT, Zheng Y, Chew M; Consortium for Refractive Error and Myopia, Burdon KP, Craig JE, Iyengar SK, Igo RP Jr, Lass JH Jr; Fuchs' Genetics Multi-Center Study Group, Chew EY, Haller T, Mihailov E, Metspalu A, Wedenoja J, Simpson CL, Wojciechowski R, Höhn R, Mirshahi A, Zeller T, Pfeiffer N, Lackner KJ; Wellcome Trust Case Control Consortium 2, Bettecken T, Meitinger T, Oexle K, Pirastu M, Portas L, Nag A, Williams KM, Yonova-Doing E, Klein R, Klein BE, Hosseini SM, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group, Makela KM, Lehtimaki T, Kahonen M, Raitakari O, Yoshimura N, Matsuda F, Chen LJ, Pang CP, Yip SP, Yap MK, Meguro A, Mizuki N, Inoko H, Foster PJ, Zhao JH, Vithana E, Tai ES, Fan Q, Xu L, Campbell H, Fleck B, Rudan I, Aung T, Hofman A, Uitterlinden AG, Bencic G, Khor CC, Forward H, Pärssinen O, Mitchell P, Rivadeneira F, Hewitt AW, Williams C, Oostra BA, Teo YY, Hammond CJ, Stambolian D, Mackey DA, Klaver CC, Wong TY, Saw SM, Baird PN.

Am J Hum Genet. 2013 Aug 8;93(2):264-77. doi: 10.1016/j.ajhg.2013.06.016.

PMID:
24144296
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.

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, Gan W, He CT, Hsiung CA, Hwu CM, Ichihara S, Igase M, Jo J, Kato N, Kawamoto R, Kuzawa CW, Lee JJ, Liu J, Lu L, McDade TW, Osawa H, Sheu WH, Teo Y, Vadlamudi S, Van Dam RM, Wang Y, Xiang YB, Yamamoto K, Ye X, Young TL, Zheng W, Zhu J, Shu XO, Shin C, Jee SH, Chuang LM, Miki T, Yokota M, Lin X, Mohlke KL, Tai ES.

Hum Mol Genet. 2014 Feb 15;23(4):1108-19. doi: 10.1093/hmg/ddt488. Epub 2013 Oct 8.

PMID:
24105470
[PubMed - in process]
17.

Whole genome expression profiling of normal human fetal and adult ocular tissues.

Young TL, Hawthorne F, Feng S, Luo X, St Germain E, Wang M, Metlapally R.

Exp Eye Res. 2013 Nov;116:265-78. doi: 10.1016/j.exer.2013.08.009. Epub 2013 Sep 7.

PMID:
24016867
[PubMed - indexed for MEDLINE]
18.

What is your diagnosis? Osteosarcoma.

Frankel CS, Young TL, Alvarez-Berger F, Spencer CP.

J Am Vet Med Assoc. 2013 Aug 1;243(3):329-31. doi: 10.2460/javma.243.3.329. No abstract available.

PMID:
23865872
[PubMed - indexed for MEDLINE]
19.

Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?

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, Wang JJ, Klaver CC, Boerwinkle E, Klein R, Siscovick DS, Jensen RA, Gudnason V, Smith AV, Teo YY, Wong TY, Tai ES, Heng CK, Friedlander Y.

PLoS One. 2013 Jul 2;8(7):e67650. doi: 10.1371/journal.pone.0067650. Print 2013.

PMID:
23844046
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.

Blue Mountains Eye Study (BMES); Wellcome Trust Case Control Consortium 2 (WTCCC2).

Hum Mol Genet. 2013 Nov 15;22(22):4653-60. doi: 10.1093/hmg/ddt293. Epub 2013 Jul 7.

PMID:
23836780
[PubMed - indexed for MEDLINE]
Free PMC Article

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