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Items: 1 to 20 of 67

1.

Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.

Healy J, Bourgey M, Richer C, Sinnett D, Roy-Gagnon MH.

J Biomed Biotechnol. 2010;2010:369534. doi: 10.1155/2010/369534. Epub 2010 Jun 9.

2.

Transmission of HLA-DP variants from parents to children with B-cell precursor acute lymphoblastic leukemia: log-linear analysis using the case-parent design.

Taylor M, Bergemann TL, Hussain A, Thompson PD, Spector L.

Hum Immunol. 2011 Oct;72(10):897-903. doi: 10.1016/j.humimm.2011.05.011. Epub 2011 May 24.

PMID:
21645570
3.

Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia.

Healy J, Bélanger H, Beaulieu P, Larivière M, Labuda D, Sinnett D.

Blood. 2007 Jan 15;109(2):683-92. Epub 2006 Sep 28.

4.

Studying parents and grandparents to assess genetic contributions to early-onset disease.

Weinberg CR.

Am J Hum Genet. 2003 Feb;72(2):438-47. Epub 2003 Jan 17.

5.
6.

Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.

Prasad RB, Hosking FJ, Vijayakrishnan J, Papaemmanuil E, Koehler R, Greaves M, Sheridan E, Gast A, Kinsey SE, Lightfoot T, Roman E, Taylor M, Pritchard-Jones K, Stanulla M, Schrappe M, Bartram CR, Houlston RS, Kumar R, Hemminki K.

Blood. 2010 Mar 4;115(9):1765-7. doi: 10.1182/blood-2009-09-241513. Epub 2009 Dec 30.

7.

No evidence for association between TGFB1 promoter SNPs and the risk of childhood pre-B acute lymphoblastic leukemia among French Canadians.

Healy J, Roy-Gagnon MH, Sinnett D.

Haematologica. 2009 Jul;94(7):1034-5. doi: 10.3324/haematol.2009.005991. Epub 2009 Jun 2. No abstract available.

8.

Novel associations between activating killer-cell immunoglobulin-like receptor genes and childhood leukemia.

Almalte Z, Samarani S, Iannello A, Debbeche O, Duval M, Infante-Rivard C, Amre DK, Sinnett D, Ahmad A.

Blood. 2011 Aug 4;118(5):1323-8. doi: 10.1182/blood-2010-10-313791. Epub 2011 May 25.

9.

Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia.

Parimi N, Tromp G, Kuivaniemi H, Nien JK, Gomez R, Romero R, Goddard KA.

BMC Med Genet. 2008 Jul 3;9:60. doi: 10.1186/1471-2350-9-60.

10.

Evaluation of offspring and maternal genetic effects on disease risk using a family-based approach: the "pent" design.

Mitchell LE, Weinberg CR.

Am J Epidemiol. 2005 Oct 1;162(7):676-85. Epub 2005 Aug 10.

11.

Informative missingness in genetic association studies: case-parent designs.

Allen AS, Rathouz PJ, Satten GA.

Am J Hum Genet. 2003 Mar;72(3):671-80. Epub 2003 Feb 14.

12.

Analysis of genetic interactions involving maternal and offspring genotypes at different Loci: power simulation and application to testicular cancer.

Nsengimana J, Barrett JH.

Genet Epidemiol. 2012 Sep;36(6):612-21. doi: 10.1002/gepi.21655. Epub 2012 Jun 27.

13.

A hybrid design for studying genetic influences on risk of diseases with onset early in life.

Weinberg CR, Umbach DM.

Am J Hum Genet. 2005 Oct;77(4):627-36. Epub 2005 Aug 31.

14.

Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population.

Jiang L, Liang J, Jiang M, Yu X, Zheng J, Liu H, Wu D, Zhou Y.

Eur J Haematol. 2011 Mar;86(3):199-205. doi: 10.1111/j.1600-0609.2010.01562.x. Epub 2011 Jan 25.

PMID:
21166880
15.
16.

Impact of glutathione S-transferase gene deletion on early relapse in childhood B-precursor acute lymphoblastic leukemia.

Takanashi M, Morimoto A, Yagi T, Kuriyama K, Kano G, Imamura T, Hibi S, Todo S, Imashuku S.

Haematologica. 2003 Nov;88(11):1238-44.

17.

Combined 677CC/1298AC genotypes of methylenetetrahydrofolate reductase (MTHFR ) reduce susceptibility to precursor B lymphoblastic leukemia in a Chinese population.

Lv L, Wu C, Sun H, Zhu S, Yang Y, Chen X, Fu H, Bao L.

Eur J Haematol. 2010 Jun;84(6):506-12. doi: 10.1111/j.1600-0609.2010.01430.x. Epub 2010 Mar 30.

PMID:
20374270
18.

Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test.

Sinsheimer JS, Palmer CG, Woodward JA.

Genet Epidemiol. 2003 Jan;24(1):1-13.

PMID:
12508251
19.

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease.

Yamada R, Tanaka T, Unoki M, Nagai T, Sawada T, Ohnishi Y, Tsunoda T, Yukioka M, Maeda A, Suzuki K, Tateishi H, Ochi T, Nakamura Y, Yamamoto K.

Am J Hum Genet. 2001 Mar;68(3):674-85. Epub 2001 Feb 14.

20.

Genetic variations in CD14 promoter and acute lymphoblastic leukemia susceptibility in a Chinese population.

Yu X, Zhang C, Sun A, Jiang L, Zheng J, You Y, Wu D, Zhou Y.

DNA Cell Biol. 2011 Oct;30(10):777-82. doi: 10.1089/dna.2011.1223. Epub 2011 Apr 10.

PMID:
21476947
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