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Prevalence of common disease-associated variants in Asian Indians.

Pemberton TJ, Mehta NU, Witonsky D, Di Rienzo A, Allayee H, Conti DV, Patel PI.

BMC Genet. 2008 Feb 4;9:13. doi: 10.1186/1471-2156-9-13.


Low levels of genetic divergence across geographically and linguistically diverse populations from India.

Rosenberg NA, Mahajan S, Gonzalez-Quevedo C, Blum MG, Nino-Rosales L, Ninis V, Das P, Hegde M, Molinari L, Zapata G, Weber JL, Belmont JW, Patel PI.

PLoS Genet. 2006 Dec;2(12):e215.


Association of CFH, LOC387715, and HTRA1 polymorphisms with exudative age-related macular degeneration in a northern Chinese population.

Xu Y, Guan N, Xu J, Yang X, Ma K, Zhou H, Zhang F, Snellingen T, Jiao Y, Liu X, Wang N, Liu N.

Mol Vis. 2008 Jul 28;14:1373-81.


Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients.

Kaur I, Katta S, Hussain A, Hussain N, Mathai A, Narayanan R, Hussain A, Reddy RK, Majji AB, Das T, Chakrabarti S.

Invest Ophthalmol Vis Sci. 2008 May;49(5):1771-6. doi: 10.1167/iovs.07-0560.


Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans.

Chandak GR, Ward KJ, Yajnik CS, Pandit AN, Bavdekar A, Joglekar CV, Fall CH, Mohankrishna P, Wilkin TJ, Metcalf BS, Weedon MN, Frayling TM, Hattersley AT.

BMC Med Genet. 2006 Oct 10;7:76.


8q24 and 17q prostate cancer susceptibility loci in a multiethnic Asian cohort.

Chan JY, Li H, Singh O, Mahajan A, Ramasamy S, Subramaniyan K, Kanesvaran R, Sim HG, Chong TW, Teo YY, Chia SE, Tan MH, Chowbay B.

Urol Oncol. 2013 Nov;31(8):1553-60. doi: 10.1016/j.urolonc.2012.02.009. Epub 2012 May 5.


Variation at diabetes- and obesity-associated Loci may mirror neutral patterns of human population diversity and diabetes prevalence in India.

Raj SM, Halebeedu P, Kadandale JS, Mirazon Lahr M, Gallego Romero I, Yadhav JR, Iliescu M, Rai N, Crivellaro F, Chaubey G, Villems R, Thangaraj K, Muniyappa K, Chandra HS, Kivisild T.

Ann Hum Genet. 2013 Sep;77(5):392-408. doi: 10.1111/ahg.12028. Epub 2013 Jul 1.


Analysis of CFH, TLR4, and APOE polymorphism in India suggests the Tyr402His variant of CFH to be a global marker for age-related macular degeneration.

Kaur I, Hussain A, Hussain N, Das T, Pathangay A, Mathai A, Hussain A, Nutheti R, Nirmalan PK, Chakrabarti S.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3729-35.


Hypertension-susceptibility gene prevalence in the Pacific Islands and associations with hypertension in Melanesia.

Furusawa T, Naka I, Yamauchi T, Natsuhara K, Eddie R, Kimura R, Nakazawa M, Ishida T, Inaoka T, Matsumura Y, Ataka Y, Ohtsuka R, Ohashi J.

J Hum Genet. 2013 Mar;58(3):142-9. doi: 10.1038/jhg.2012.147. Epub 2013 Jan 17.


Functional variants of IL4 and IL6 genes and risk of tobacco-related oral carcinoma in high-risk Asian Indians.

Gaur P, Mittal M, Mohanti B, Das S.

Oral Dis. 2011 Oct;17(7):720-6. doi: 10.1111/j.1601-0825.2011.01831.x. Epub 2011 Jul 20.


Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians.

Akhter MS, Biswas A, Rashid H, Devi L, Behari M, Saxena R.

J Neurol Sci. 2014 Sep 15;344(1-2):69-75. doi: 10.1016/j.jns.2014.06.025. Epub 2014 Jun 20.


Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US.

Been LF, Ralhan S, Wander GS, Mehra NK, Singh J, Mulvihill JJ, Aston CE, Sanghera DK.

BMC Med Genet. 2011 Jan 24;12:18. doi: 10.1186/1471-2350-12-18.


Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.

Rivera A, Fisher SA, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Weber BH.

Hum Mol Genet. 2005 Nov 1;14(21):3227-36. Epub 2005 Sep 20.


A common complement C3 variant is associated with protection against wet age-related macular degeneration in a Japanese population.

Yanagisawa S, Kondo N, Miki A, Matsumiya W, Kusuhara S, Tsukahara Y, Honda S, Negi A.

PLoS One. 2011;6(12):e28847. doi: 10.1371/journal.pone.0028847. Epub 2011 Dec 12.


A study on genetic variants of Fibroblast growth factor receptor 2 (FGFR2) and the risk of breast cancer from North India.

Siddiqui S, Chattopadhyay S, Akhtar MS, Najm MZ, Deo SV, Shukla NK, Husain SA.

PLoS One. 2014 Oct 21;9(10):e110426. doi: 10.1371/journal.pone.0110426. eCollection 2014.


The involvement of complement factor B and complement component C2 in an Indian cohort with age-related macular degeneration.

Kaur I, Katta S, Reddy RK, Narayanan R, Mathai A, Majji AB, Chakrabarti S.

Invest Ophthalmol Vis Sci. 2010 Jan;51(1):59-63. doi: 10.1167/iovs.09-4135. Epub 2009 Aug 20.


Analyses of single nucleotide polymorphisms and haplotype linkage of LOC387715 and the HTRA1 gene in exudative age-related macular degeneration in a Chinese cohort.

Jiang H, Qu Y, Dang G, Zhang X, Yin N, Zhang Y, Bi H, Pan X, Xu X, Zhou F, Dai H.

Retina. 2009 Jul-Aug;29(7):974-9. doi: 10.1097/IAE.0b013e3181a3b90e.


LOC387715/HTRA1 polymorphisms, smoking and combined effects on exudative age-related macular degeneration in a Korean population.

Lee SJ, Kim NR, Chin HS.

Clin Exp Ophthalmol. 2010 Oct;38(7):698-704. doi: 10.1111/j.1442-9071.2010.02316.x. Epub 2010 Jun 30.


Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk.

Sanghera DK, Ortega L, Han S, Singh J, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Ferrell RE, Nath SK, Kamboh MI.

BMC Med Genet. 2008 Jul 3;9:59. doi: 10.1186/1471-2350-9-59.

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